Document jyn6gvbLQjVk7nLDEbdpao0XQ
933
1 IN THE UNITED STATES DISTRICT COURT
2 FOR THE EASTERN DISTRICT OF PENNSYLVANIA
3
4 IN RE: ASBESTOS PRODUCTS LIABILITY
5 LITIGATION {NO. VI)
6 CIVIL ACTION NO. MDL 875
7 CIVIL ACTION NO. 5-92-88
8X
9 This Document Relates To:
10 CONNED CORPORATION,. Plaintiff,
11 v.
12 UNION CARBIDE CHEMICALS AND
13 PLASTICS COMPANY, INC., Defendant and
14 Third-Party Plaintiff,
15 v.
16 OWENS-CORNING FIBERGLAS CORPORATION, ET AL.,
17 Third-Party Defendants.
---------------------------------------------------------------------------------------------------- x
18 KELLEY, DRYE & WARREN, L.L.P.
19 101 Park Avenue New York, New York 10178
20 July 7, 1999
21 10:35 a.m.
22 DEPOSITION OF DR. EDWARD ILGREN
23 PRIORITY-ONE COURT REPORTING SERVICES, INC.
24 899 Manor Road Staten Island, New York 10314
25 (718) 983-1234
Priority-One Court Reporting Services, Inc. (718) 983-1234
DUPLICATE
FILE COPY
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1 APPEARANCES:
2 STICH, ANGELL, KREIDLER,
BROWNSON & BALLOU, P.A.
3 The Crossings, Suite 120
250 Second Avenue South
4 Minneapolis, Minnesota 55401
BY: ROBERT D. BROWNSON, ESQ.
5 Attorneys for the Plaintiff,
Conwed Corporation
6
RUDNICK & WOLFE, ESQS.
7 203 N. Lasalle Street, Suite 1800
Chicago, Illinois 60601
a BY: MICHAEL R. GOLDMAN, ESQ.
Attorneys for the Plaintiff,
9 Conwed Corporation
10 FOLEY & LARDNER, ESQS. Firstar Center
11 777 East Wisconsin Avenue Milwaukee, Wisconsin 53202-5367
12 BY: TREVOR J. WILL, ESQ. Attorneys for the Defendant and
13 Third-Party Plaintiff, Union Carbide Chemicals and Plastics Company, Inc.
14 KELLEY, DRYE & WARREN, L.L.P.
15 101 Park Avenue New York, New York 10178
16 BY: ALAN J. GERSON, ESQ. Attorneys for the Defendant and
17 Third-Party Plaintiff, Union Carbide Chemicals and Plastics Company, Inc.
13
19
20
21
22
23
24
25
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1 INDEX
2 WITNESS NAME
PAGE NO.
3 DR. EDWARD ILGREN
4
5 Direct Examination by Mr. Brownson Cross-Examination by Mr. Will
6
937 1043
7 EXHIBITS
8 EXHIBIT NO.
PAGE NO.
9 P-39
10 P-40
11
Copy of "The American Journal of Pathology"
Copy of Dr. Kent Pinkerton's 1982 thesis
953 976
12 P-41
13 P-42
14
15 P-43
16
17
Copy of "The Annals of Occupational Hygiene"
Copy of "Effects of Electrostatic Charge on the Pathogenicity of Chrysotile Asbestos"
Copy of "Comparisons of the Pathogenicity of Long and Short Fibres of Chrysotile Asbestos in Rats"
980 999 1000
18 P-44 19 20
Copy of "The Sizes, Shapes and Mineralogy of Asbestos Structures that Induce Lung Tumors or Mesothelioma in AF/HAN Rats Following Inhalation"
1010
21 P-45 22
Copy of "American Review of Respiratory Disease" Volume 123 dated April 1981
1043
23 P-46 24
Copy of "American Review of Respiratory Disease" Volume 121 dated April 1980
1043
25
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1 REQUESTS
2 PAGE NO.
*
3 1025
Insert number of anomalous rat
4
5
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7
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10
11
12
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1 DR. EDWARD ILGREN, 2 called as a witness, having been first duly 3 resworn according to law, testifies as 4 follows: 5 6 7 DIRECT EXAMINATION BY MR. BROWNSON: 8 9 Q Good morning, Dr. Ilgren. We are 10 continuing here. Let me ask you, since last we 11 spoke, have you been out to Kings City or the 12 Coalinga deposit or Calidria mine? 13 A No. 14 Q Have you had an opportunity to see or 15 review any new information, since the time of our 16 last deposition, from the mine or the area out there? 17 A Say that again. New information from where? 18 Q From out of the Calidria mine or mill or 19 the deposit out there. I'm thinking in terms of any 20 medical records, any reports, any air sampling, 21 anything like that? 22 A No. 23 Q Have you read any information about any 24 cases of mesothelioma in the Kings City area? 25 A No.
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1 Q Have you examined or worked on any other
2 cases for Union Carbide, other than this particular
3 case involving Calidria exposure, since we last
4 spoke?
5 A Yes.
6 Q Do you know where that exposure arose
7 from. Was it a plant?
8 A Allegedly the ore bodies.
9 Q Was this any kind of an injury case or
10 did it involve a worker of some sort?
11 A
A policeman.
12 Q And this was a policeman where, in Kings
13 City?
14 A Highway patrol.
15 Q Now, I had heard something about a case
16 involving a policeman, and this must be the one; but
17 I confess to you, I don't have any particulars.
18 Is this a highway patrolman who alleges
19 he somehow got sick from working in the area of the
20 Coalinga ore deposit?
21 A You are asking me what healleged?
22 Q Well, what he is contending.
23 A
As I recall, he alleges to have gotten
24 his mesothelioma from Coalinga fibers that drifted
25 twenty miles through the air into his highway patrol
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car as he drove up and down Route 5 between 1978 and
1983 and also from two days of pig hunting on the ore
body.
Q Do you know, has this highway patrolman'
filed a lawsuit?
A Yes.
Q Do you know what his name is?
A Waggoner.
Q Do you know who his lawyer is?
A Wartnick, Chaber.
Q Do you know how his name is spelled?
A I think it's W-a-g-g-o-n-e-r.
Q Is Union Carbide a defendant in that suit
or is someone else the defendant; do you know?
A Union Carbide was a defendant and settled out.
Q Are there any remaining defendants, as
far as you know?
A There is one but I don't recall what the name
is.
Q Do you know if KCAC was a defendant?
A No, I don't know.
Q This highway patrolman Waggoner, is he
dead or alive, as far as you know?
A He died in January.
Q January of 1999?
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1A
Yea.
2 Q Do you know if this was a pleural
3 mesothelioma or a peritoneal?
4 MR. WILL: Objection. I object to the
5 form. He doesn't necessarily know it's a
6 mesothelioma.
7 Q Did Mr. Waggoner contend it was a pleural
8 or a peritoneal?
9 A I can't recall at the moment.
10 Q Do you know if any of his tissue was
11 preserved for examination?
12 A I don't know.
13 Q Are you still involved in the case or did
14 you cease your involvement?
15 A I'm still involved.
16 Q But you don't recall who this remaining
17 defendant in the case is?
18 A No.
19 Q Are you still involved for Union Carbide
20 or for somebody else?
21 A Somebody else.
22 Q Youjust can't recall who that is?
23 A I don't recall thename of the defendant.
24 Q Do you know, are there any other
25 exposures being alleged in this case, other than this
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1 Calidria exposure?
2 A Yes.
3 Q Is this other defendant, whose name you
4 can't recall, are they in it as a result of some
5 other exposure?
6 A Not to my knowledge.
7 Q How do they come in it in terms of the
8 Calidria exposure; do you know?
9 A I don't recall.
10 MR. WILL: By Calidria, are you referring
11 to the entire ore deposit?
12 MR. BROWNSON: That's a goodpoint.
13 Q I should say Coalinga exposure.
14 A
That's right.
15 Q Do you understand this other defendant to
16 be somehow a defendant related to the Coalinga ore
17 deposit, but it's not Union Carbide and it's not the
18 Calidria mine itself?
19 A
I don't know if it's the deposit or some other
20 aspect. I don't know precisely how the exposure
21 arises. Still, it's Coalinga.
22 Q Do you know any other scientists or
23 physicians who are working on that case, either on
24 behalf of Mr. Waggoner or on behalf of Union Carbide
25 or anyone else?
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1A
In this case, the wrongful death case?
2 Q Yes, the Waggoner case.
3 A No.
4 Q Is there anyone who worked on it at any
5 time that you know that is no longer involved?
6 A Yes.
7 Q Who is that?
8 A MarkShanker, Davis and Bill Nickelson.
9 Q Now, you said Mark Shanker?
10 A Yes.
11 Q And then you said Davis. You mean from
12 the University of Davis?
13 A Right.
14 Q And Nickelson?
15 A
Right.
16 Q What had Nickelson done on that case?
17 A I don't remember.
18 Q Do you know, was heattempting tocontend
19 that there was some sort of fiber drift, as he likes
20 to call it?
21 A " I think so,yes.
22 Q Was he attempting to make any
23 calculations that you are aware of?
24 A I can't remember hisdisclosure. I read it.
25 I can't remember the details.
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1 Q As far as you know, was there an expert
2 disclosure prepared by the lawyers that you read or
3 did you see any actual reports or depositions or
4 anything like that?
5 A From them?
6 Q From anybody else.
7A
Yes.
8 Q Yes?
9A
Yes.
10 Q What was it?
11 A An expert's disclosure.
12 Q So what you saw was an expert's
13 disclosure that the Wartnick firm prepared from
14 Nickelson?
15 A Yes, and Shanker.
16 Q You didn't see any of their actual work?
17 A
No, I don't think so.
18 Q Are you aware of any pathologist who has
19 examined the case at any time for anybody?
20 A That case?
21 Q Yes.
22 A No.
23 Q Is Dr. Chatfield involved in that case at
24 all?
25 A At the present time?
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1 Q Yes.
2 A No.
3 Q Do you know if heever was?
4 A I think so, but Ican't recall.
5 Q Do you know if he will be in the future?
6 MR. WILL: How can he know that?
7 MR. BROWNSON: He might have heard that
8 they were going to get some tissue and send it
9 to Dr. Chatfield.
10 Q I'm just asking if you know?
11 A I don't know.
12 Q Are you aware of any plans that Dr.
13 Chatfield will be involved in the case? That's all
14 I'm asking.
15 A No.
16 Q Now, let's turn to something a little
17 closer to your heart, which is your series of papers
18 in "Indoor Built Environment."
19 First of all, can you tell us anything
20 more about paper numbers 4 and/or 5? How are those
21 coming along?
22 Will those be published or when? Do you
23 have any information on that?
24 MR. WILL: Which one of those questions
25 are you asking him to answer?
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1 MR. BROWNSON: I can break it down.
2 Q Where does paper number 4 stand?
3A
Well, we hope to have it finished by the end
4 of the summer and the same with paper 5.
5 Q Is there any research ongoing at the
6 present time that you are doing in connection with
7 papers 4 or 5 or is your work done and you are now
8 just writing?
9A
My work is done. I'm writing.
10 Q How about Dr. Chatfield, id he still
11 doing any work; do you know?
12 A Not to my knowledge.
13 Q Have you made any additional examination
14 of the archived material from Drs. McConnell and
15 Pinkerton that you had looked at before in connection
16 with papers 4 or 5?
17 A
No.
18 Q Do you know when papers 4 and 5 might be
19 published?
20 A No.
21 Q Do you intend to publish them or have
22 them published in "Indoor Built Environment" or some
23 other --
24 A Yes.
25 Q In "Indoor Built Environment"?
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1 A Yes.
2 Q Now, I would like to turn your attention
3 to paper number 3 or installment number 3 of your
4 paper, which is entitled, "Lack of Biopersistence."
5 Do you have a copy there?
6A
I don't have one with me.
7 MR. BROWNSON: Do you have one for him,
8 Trevor?
9 MR. WILL: Actually, no.
10 MR. BROWNSON: Let's mark it as Exhibit
11 39.
12 MR. WILL: It's already been marked.
13 MR. BROWNSON: Do you know what number it
14 was?
15 MR. WILL: Well, it's 38.
16 MR. BROWNSON: We will call it Exhibit
17 38.
18 MR. WILL: Document entitled, "Coalinga
19 Fibre: A Short, Amphibole-Free Chrysotile"
20 was marked Defendant's Exhibit 38 for
21 identification last time, so the record is
22 clear.
23 .
Q You now have in front of you, Dr. Ilgren,
24 Exhibit number 38, which is the paper subtitled,
25 "Lack of Biopersistence," correct?
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1 A Correct.
2 Q Authored by you and Dr. Eric Chatfield?
3 A Yes. 4 Q Now, I will try to move through this in
5 fairly short order; but let's turn first to the
6 materials and methods section, which is the second
7 page of the paper on page 99.
8 Do you see that section?
9A
Yes.
10 Q First of all, are you the author of this
11 section?
12 A
I can't remember. I wrote a substantial part;
13 but I can't remember what Eric -- Eric might have
14 added something to it.
15 Q Do you know what he -- if he added to it,
16 do you know what that might be?
17 A I can't remember. We traded drafts.
18 Q As you sit here today, do you know
19 anything that specifically could have been authored
20 by Dr. Chatfield?
21 A No.
22 Q Now, with respect to the materials and
23 methods, as I understand that section in a scientific
24 paper, that's the section that informs the reader, up
25 front or towards the start of the paper, the nuts and
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1 bolts of the materials and methods, if you will; is
2 that correct?
3 A Yes.
4
Q
Let me ask you this.
Can you describe
5 for us specifically what you actually did; and by you
6 I mean you personally, in terms of the materials and
7 methods for paper number 3?
8 A Specifically with regards to what?
9 Q Well, anything that is described in the
10 materials and methods section. I'm trying to
11 understand the work that you did.
12 A Can youask me specifically what -- focus on
13 something and say that I do this, because I'm
14 confused.
15 Q Did you examine any tissue in connection
16 with paper number 3?
17 A No.
18 Q Did you do any microscopic analysis?
19 A No.
20 Q Do you know if Dr. ChatfieId did?
21 A I believe not.
22 Q Again, if we go to the materials and
23 methods section it states: "The methods used to
24 perform elemental analysis and the measurement of
25 asbestos fibre volume and density are as described by
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1 Pinkerton et al. [10]."
949
2 Do you see that?
3 A Yes.
4 Q Now, does that sentence describe some
5 work that you did or some work that Pinkerton did?
6A
At the end there I state, "All of the
7 morphometrical analyses were conducted by Professor
8 Kent Pinkerton."
9 Q So to speed this along, would it be fair
10 to say that all of the morphometrical analyses, which
11 is described in the materials section, was work done
12 by Pinkerton and not by you?
13 A Right.
14 MR. GERSON: We have to go off the record
15 for a moment.
16 MR. BROWNSON: Sure.
17 (A discussion is held off the record.)
18 Q The morphometrical analyses conducted by
19 Professor Kent Pinkerton, as described in the
20 materials and methods section of your paper, are
21 historical work by Pinkerton, aren't they?
22 A Historical?
23 Q In other words, they were done fifteen,
24 twenty years ago?
25 A Yes, that's true.
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1 Q They were not any new work done in
2 connection with this particular paper?
3A
Not, not to my knowledge, though, I don't
4 recall. He might have done something in 1994 or
5 1995; but I don't recall. I don't know exactly when
6 he stopped doing these analyses; but they certainly
7 weren't done in the past couple years.
8 Q And they were not done in connection with
9 this particular paper, were they?
10 A
Could you rephrase that?
11 Q Yes. Dr. Pinkerton's morphometrical
12 analyses, as the ones described in the materials and
13 methods section, were not done for purposes of this
14 paper, were they?
15 A
Well, I don't know. He asked me to help him
16 write up the work. So to that extent, I guess -- I
17 mean, they were aimed at forming a publication, which
18 presumably would have taken this form.
19 Q Well, when you say he asked you to write
20 up the work, he never came to you and asked you to
21 publish data on the work he had done back in the late
22 '70s and early '80s, did he?
23 A
No. In 1991, when we corresponded, he sent me
24 his data and said I'm free to write these up in
25 whatever form I want. So that's what I meant.
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1 Q And then when you undertook that task to
2 write these series of papers, you described the
3 materials and methods we see here on page 99,
4 correct?
5A
Right.
6 Q But you describe them as materials and
7 methods that had been done by Professor
8 Pinkerton at some point in the past?
9A
Right.
10 Q And the topic of paper number 3 is
11 biopersistence, right?
12 A
Right.
'
13 Q If we could generalize the theme of paper
14 number 3, would it be to go back to these old rat
15 studies that Dr. Pinkerton had done while a graduate
16 student and try to discern from these data the
17 biopersistence of these three kinds of asbestos in
18 the lungs of those rats?
19 A
With the exemption that, I think, he did some
20 work subsequent to being a graduate student, that
21 would be correct.
22 Q As I read through paper number 3, you
23 argue that the three different types of chrysotile
24 asbestos have different biopersistence in the lungs
25 of these rats in Dr. Pinkerton's study, correct?
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1 A Right.
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952
2 Q And you base that upon these various
3 measurements of silica found in the lung tissue of
4 those rats, correct?
5 A Partly.
6 Q Well, is there any -- was there any
7 measurement of actual asbestos fibers from the lungs
8 of those rats?
9 A Sure.
10 Q And where do we find that in your paper?
11 A
Fiber volume and density. There are three
12 indices. There is the silica ashings, that's the
13 morphometric fiber volume density; and then there is
14 the stuff that I noticed on the presence and absence
15 of dust-laden macrophages, which is on page 102
16 column 2 paragraph 4.
17 Q Did anyone do any microscopic analysis of
18 asbestos fibers in the lungs of these rats?
19 A Yes.
20 Q Where do we find that in your paper?
21 A
Well, it's table 2 and 3 and the column page
22 section I just told you about on page 102.
23 Q Where do I see in table 2 or 3 analysis
24 of asbestos fibers?
25 A
All fibers. One is a fiber volume, the volume
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1 of the tissue component under consideration occupied
2 by fiber and fiber density is the so-called density
3 or number of fibers present in, again, certain tissue
4 component as listed.
5 Q Let me ask this question. Did Dr.
6 Pinkerton actually count fibers in this tissue or did
7 he measure silica?
8A
No, in tables 2 or 3 they would be "fiber
9 counts."
10 Q So as you understand, Dr. Pinkerton
11 actually counted asbestos fibers in the tissue in
12 table 2 and 3?
13 A
Yes, per materials and methods citation, "The
14 methods used to perform elemental analysis and the
15 measurement of asbestos fibre volume and density are
16 as described by Pinkerton et al. [10]," which is his
17 1984 paper.
18 ' So the details of the manner in which the
19 fibers were counted were in the 1984 paper.
20 MR. BROWNSON: Let's mark this as Exhibit
21 39.
22 (A copy of "The American Journal of
23 Pathology" is marked as Plaintiff's Exhibit 39
24 for identification, as of this date.)
25 Q I will show you, doctor, what we marked
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as Exhibit 39, which is a paper of "The American
Journal of Pathology" by Dr. Pinkerton and some other
doctors entitled "Fiber Localization and Its
Relationship to Lung Reaction in Rats After Chronic
Inhalation of Chrysotile Asbestos."
My first question will be, is that paper
the reference 10 that is cited in your paper number
3, Exhibit 38?
A Yes.
Q So if I understand what you have told us,
the analysis of actual asbestos fibers as opposed to
measurements of silica that Dr. Pinkerton made in the
lungs of rats comes out of this paper, Exhibit 39?
A Yes.
Q Is there anything in that paper, which is
your reference, in Exhibit 39, which was published in
1984 by Dr. Pinkerton, that talks about the
biopersistence of the three types of chrysotile
asbestos to which these rats were exposed?
A I don't recall. I think it may allude to the
persistence of the Jeffrey fiber. I don't believe it
mentions UICC/B and Coalinga.
Q Now, going to your paper. Exhibit 39,
let's start then with the --
MR. GERSON: Exhibit 39?
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1 MR. BROWNSON: 38, sorry.
2 Q Let's start with the next heading after
3 materials and methods, which is entitled results.
4 Do you see that?
5 A Right.
6 Q Page 99?
7A
Yes.
3 Q Again, to try to summarize this, what you
9 have done, you have drawn some conclusions about the
10 biopersistence of these three different types of
11 asbestos by looking at the silica content
12 determination in the lungs of these rats and the
13 specific fiber density and volume changes within
14 different compartments of the lungs of the rats; is
15 that right?
16 A
And the presence and/or absence of
17 dust-related macrophages, but that's correct.
18 Q Let's start with the silica content
19 determinations of the lungs. First of all, did you
20 do any actual analytical work with respect to the
21 silica content determinations of the lungs of these
22 rats?
23 A No.
24 Q Again, this was work that Dr. Pinkerton
25 had done back in prior years?
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Yes, plus -- there were other data that fall
2 into this table that may or may not have been
3 Pinkerton's that I found at the NTP archive, namely,
4 the Jeffrey fiber one-day exposure twelve-month
5 follow-up. That's on page 100 top of column 2.
6 Q And you found that in the archive, but
7 you are not sure who actually did it?
8A
Yes, it was with the other raw data; but I'm
9 not sure whether -- Pinkerton did not send me the raw
10 data. The raw data, as enumerated in the table, came
11 out of the archive.
12 Q So this is some material that you found
13 in the archive; but you are not quite sure who
14 actually did it in the first place?
15 A That's right.
16 Q Now, with respect to the silica lung
17 content determination in these rats, as I understand
18 it, you looked at these various results that Dr.
19 Pinkerton had gotten back when he made the rats
20 inhale the three types of asbestos in the late '70s
21 and early '80s, correct?
22 A Right.
23 Q Again, you didn't actually look at any
24 rat lung tissue, you looked at the numbers generated
25 by Dr. Pinkerton when he did that work?
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1 A Or whoever, but that's right.
2 Q With the exception of this one thing you
3 just told us about, it was work by Dr. Pinkerton?
4 A To my knowledge, that's correct.
5 Q And then you basically published that
6 data from Dr. Pinkerton and/or this other unknown
7 person in paper number 3; and then you drew some
8 conclusions from it, correct?
9A
Right.
10 Q Again, focusing on the lung silica
11 content portion of this data, as I understand, what
12 that shows is how much silica was in the lungs of
13 these rats at different points of time, right?
14 A Right.
15 Q Silica is a component, if you will, of
16 chrysotile asbestos, right?
17 A Correct.
18 Q So at least with respect to the silica
19 lung content portion of your analysis, you are not
20 actually describing asbestos fibers per se, what you
21 are describing is the amount of silica which
22 presumably could have come from the asbestos fibers?
23 A Presumably, right.
24 Q Do you know, in fact, that all of the
25 silica in the lungs of these rats did come from the
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1 asbestos fibers or could some of it have come from
2 other places?
3A
It could have come from other places. I don't
4 know what they would have been. There is obviously
5 some in the control annals which weren't exposed.
6 So there is clearly some kicking around the lungs
7 which isn't asbestos derived.
8 Q Would you agree with me that a more
9 accurate way to determine how much asbestos is in the
10 lungs of rats would be to analyze the number of
11 asbestos fibers in those lungs as opposed to
12 measuring silica content?
13 A
Yes, we state that in the paper. I mean, this
14 has just been the traditional methods used by Vogner
15 and Davis and others in the past who also conclude or
16 point out, as you do, that it would be, perhaps, more
17 accurate, if you are interested in fiber localization
18 and identification, to look at the individual fibers.
19 Q As I understand, there is nothing we can
20 determine from looking at silica content with respect
21 to fiber length, is there?
22 A
No.
23 Q To do that, we actually have to look at
24 fibers, measure their lengths and count them and that
25 sort of thing?
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1 A Right.
2 Q Now, is there anything in paper number 3,
3 the biopersistence paper, which describes the size
4 distribution of the asbestos fibers which were found
5 in the lungs of these rats exposed by Dr. Pinkerton?
6 A Not to my knowledge.
7 Q If you had the opportunity to actually
3 design a study where you were going to make rats
9 inhale asbestos and then determine biopersistence,
10 would you agree that it would be interesting to
11 determine the size distribution of the fiber in the
12 asbestos the rats were breathing and how the
13 different sizes of fibers stayed or were cleared from
14 the lungs over time?
15 MR. GERSON: What is your question?
16 MR. BROWNSON: Read it back.
17 (The record is read back.)
18 A
He did it all in the '86 paper for Jeffrey,
19 but I don't know -- I couldn't find it for Coalinga
20 or UICC/B.
21 Q Just so the record is clear, by Jeffrey,
22 you mean the Jeffrey mine chrysotile asbestos?
23 A
Right.
24 Q Which is one of the three types of
25 asbestos that Dr. Pinkerton made the rats breathe?
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Right.
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960
2 Q So in a paper published by Dr. Pinkerton
3 in 1986, he shows how the different sizes or lengths
4 of the Jeffrey chrysotile asbestos persisted or was
5 cleared over time from the lungs of rats; but you
6 couldn't find that for the other two types, the
7 UICC/B chrysotile or the Coalinga chrysotile?
a A Right. I'm referring to my reference 9.
9 Q So would you agree with me that, in your
10 paper number 3, you then took Dr. Pinkerton's data
11 and tried to make some effort to determine how all
12 three types of asbestos persisted in the lungs of the
13 rats over time?
14 A Right.
15 Q And you had to do that yourself, because
16 Dr. Pinkerton did not -- had not done that, he had
17 just done it with one of the three, the Jeffrey,
18 right?
19 A Maybe I don't quite understand your question.
20 MR. GERSON: I don't either.
21 Q Is there any published data anywhere,
22 other than what you show in your paper number 3, that
23 shows the biopersistence of the Coalinga asbestos
24 that these rats in Dr. Pinkerton's study breathed?
25 A No.
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1 Q Is there any published data, other than
2 what you show in your paper number 3, that shows that
3 the biopersistence of the UICC/B asbestos that Dr.
4 Pinkerton's rats breathed?
5A
Not to my knowledge.
6 Q Again, to try to summarize, if we look at
7 the state of the published data from this rat
8 inhalation study that Dr. Pinkerton did, before you
9 published your paper number 3, we can find
10 information about the biopersistence of the Jeffrey
11 asbestos but not the other two?
12 A
No, I don't agree with that.
13 Q Where would we find the other two?
14 A
In terms of -- well, your question was about
15 biopersistence.
16 Q Right.
17 A
Can you read that question back?
18 (The record is read back.)
19 Q Now, I was excluding this paper. Maybe
20 the question was not clear. Let me ask a different
21 question.
22 Before you wrote your paper number 3 that
23 we are looking at, before then, was there any
24 published data showing the biopersistence of the
25 other two kinds of asbestos in the lungs of these
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962
2 MR. GERSON: Published data?
3 MR. BROWNSON: Right.
4 A The other two, either Coalinga and DICC/B?
5 Q Right.
6 A Yea.
7
8A
Q Where would we find that? For Coalinga, it's the Muhle data and for
9 UICC/B it would be references in table 5 as they are
10 expressed in silica content, ashing and there may be
11 some other studies of UICC/B that I haven't come
12 across.
13 Q Well, there may be but -
14 A I'm not aware of.
15 Q So interms of published data concerning
16 the biopersistence of Coalinga asbestos, as I
17 understand it, this Dr. Muhle published about that
18 and you talk about that in your paper, correct?
19 A Right.
20 Q Because he also did a rat inhalation
21 experiment over in Germany, right?
22 A Right.
23 Q Again, I'm trying to get my arms around
24 the published data, if you will, showing
25 biopersistence of Coalinga asbestos in the lungs of
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963
2 A Right.
3 Q You have attempted to make some
4 calculations of your own, which we will get to in a
5 moment, in your paper number 3; and Dr. Muhle had
6 published some results from his rat inhalation study?
7 A Right.
8 Q Is there any others?
9 A To my knowledge, no.
10 Q Then with respect to UICC/B chrysotile
11 asbestos, which is another of the three types that
12 Dr. Pinkerton exposed his rats to, you reference some
13 studies of silica lung content in your table number 5
14 that other people had done, right?
15 A Right.
16 Q We will get to that in a minute; but does
17 that then constitute the published data concerning
18 biopersistence of Coalinga asbestos or UICC/B
19 asbestos in the lungs of rats that you are aware of?
20 A Yes -- wait. I reference another study by
21 Bellmann and I could never get those data. It's
22 referred to on page 105 column 2 paragraph 1 in the
23 -- starting the tenth line. That was an
24 intratracheal injection study, I believe.
25 Q So page 105 of your paper, column 2, the
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1 first paragraph, you make a reference to a study by
2 Bellmann, at which is your reference number 23, and
3 this involved UICC/B chrysotile not Coalinga, right?
4A
No, I believe he looked at both. I would have
5 to get the paper out and look at that again, the
6 Bellmann paper; but that was an intratracheal study.
7 Q That was an injection study where they
8 injected asbestos into the rats? The rats didn't
9 breathe it?
10 A No.
1
11 Q I don't want to get into this issue again
12 about injection versus inhalation studies. We talked
13 about that before.
14 A We did.
15 Q You are not a big proponent of injection
16 studies, I take it. You prefer the inhalation
17 studies?
18 A
Well, to some extent it's all related; but I
19 obviously like to look at the inhalation studies.
20 Q Let me go back and try to summarize. If
21 we can get around the published data concerning
22 inhalation studies of Coalinga asbestos and UICC/B
23 chrysotile asbestos, those would be the ones that we
24 talked about a minute ago?
25 A
Right.
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1 Q Which would be Dr. Pinkerton's work and
2 Dr. Mulhe's work, right?
3A
As I recall.
4 Q And also those things you talked about in
5 your table 5 that we will get to?
6 A Right.
7 Q Now, table 1 of your paper, which is at
8 page 100, let's go to that. I hope to be brief here.
9 Would it be fair to say that in table 1
10 you are attempting to present some of Dr. Pinkerton's
11 data about the lung silica changes over time with
12 respect to the three types of asbestos?
13 A That's correct.
14 Q And you also presented his data
15 concerning the control rats, too, correct?
16 A That's right.
17 Q Now, if we look at the data of Dr.
18 Pinkerton's that you presented in table 1 with
19 respect to the Coalinga, or for that matter, with
20 respect to either of the other two fiber types, I
21 don't see any data concerning the lung silica content
22 twenty-four months.
23 A They didn't do it.
24 Q With respect to the silica lung content,
25 are you aware of any data that exists where that
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1 could be examined in the lungs of those now long dead
2 rats at twenty-four months?
3A
For Pinkerton's study?
4 Q Right, or is that just something that is
5 not available?
6A
It could be buried in the archives.
7 Q But you didn't find it, right?
8 Well, let me ask a different question.
9 You didn't present it in table 1, we know that. Does
10 that indicate you didn't find it?
11 A
Are you asking me whether I looked for
12 twenty-four month data and I didn't find it or I made
13 an attempt to get tissues to do a twenty-four month
14 digestion to fill in the blank?
15 What are you asking?
16 Q Well, actually both are good questions.
17 Let's start with the easy part first.
18 We know that these rats, the lungs of
19 these rats, were examined at twenty-four months,
20 because, for example, we see that in table 2 with
21 respect to the fiber volume changes, right?
22 A
Right.
23 MR. WILL: Some rats were examined.
24 Q The lungs of some rats were examined
25 twenty-four months after they first began exposure to
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1 the asbestos, right?
2 A Right.
3 Q But with respect to the lung and silica
4 content, you don't present any data on that in your
5 paper, right?
6A
Right. Pinkerton sent me, in 1991, a
7 histogram; and the histogram only had three and
8 twelve-month data; and I asked Kent did he have any
9 twenty-four month data and he said no. I didn't ask
10 him why.
11 I might have, but I don't recall why there
12 were no twenty-four month data sent to me; but there
13 were no twenty-four month data sent to me. So I went
14 back, and when I was in the archive, I found the raw
15 data and this is the presentation of the raw data,
16 which underlie the data that he sent me in histogram
17 form.
18 Q But even looking at that, you were unable
19 to present in this paper any twenty-four month data
20 concerning lung silica content?
21 A
I didn't find it. I looked for it.
22 Q Now, would you agree with me that going
23 back these twenty years when this Pinkerton study was
24 designed, this was not designed to be a biopersistent
25 study?
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968
No, that's not true at all. No, he had -- I
2 mean, case in point, per the 1984 paper, fiber
3 localization, and the 1986 paper, which is -- per his
4 1986 paper, they were looking at the manner in which
5 the fiber density and the fiber volume change over
6 time.
7 In Pinkerton's thesis, he talks, as I
8 recall, about the accumulation, the clearance, the
9 retention of three fiber types and the differences
10 between them. I mean, I think it was part and parcel
11 of the whole aim of the effort to look at persistence
12 and clearance.
13 Q Well, if that was part and parcel of the
14 whole aim and effort, would you agree with me that
15 there was no paper actually published by the studies'
16 designers which set forth the biopersistence of the
17 three types of asbestos in the lungs of these rats?
18 A
Well, he sent me two manuscripts, which they
19 sent to some journal. I don't remember the name. It
20 was initially rejected, the data in that.
21 So there is nothing published, to my
22 knowledge, of fiber volume density change data in a
23 presently scientific peer reviewed paper, aside from
24 this one; but I wouldn't say that it wasn't their aim
25 from the outset to present data, not only on fibrosis
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1 and tumora, but also on this particular aspect of the
2 work. So I wouldn't agree with that.
3 Q Do you know for a fact that there was an
4 intent of the study, back when it was originally
5 designed, to measure biopersistence?
6A
Well, that presumes knowledge that I wouldn't
7 necessarily have, because I wasn't there in the
8 beginning of the study; but on the basis of the data
9 Kent sent me and the manuscripts he sent me and the
10 raw data, it would seem to be that that was part of
11 the aim of the work.
12 Q So you are drawing that conclusion,
13 correct?
14 A
Right.
15 Q Now, if we look at your table 1, which is
16 the silica content changes in the rat and lungs over
17 time, what we see, if we focus on the Coalinga, what
18 we see is that the overall average goes from 610
19 micrograms per lung after three months of breathing
20 the Coalinga to 574 after twelve months, correct?
21 A Correct.
22 Q I don't have my calculator with me; but
23 would you agree that with respect to the
24 biopersistence of the Coalinga, it decreases between
25 three and twelve months about ten percent or less?
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1A
Ilgren I don't think you can say that.
970 I think you
2 can just look at this and say, there is some trends
3 here. You get the first -- I mean, trying to perhaps
4 move this along, I mean, you can say that you have
5 got clear deposition of fiber for all three fiber
6 types in the three months.
7 Secondly, at twelve months, there is
8 clearly much more Jeffrey deposited than the other
9 two. Beyond that, on the basis of the data that's
10 presented, I don't think you can say much. At the
11 twelve-month follow-up, with the one day exposure,
12 you get clearance; and that's something that X put in
13 as a kind of control; but beyond -- I mean, beyond
14 that, what I have just said, I don't think you can
15 say too much more.
16 Q Well, the fact of the matter is, from the
17 lung silica content data presented in your table 1,
18 we don't see much clearance of the asbestos from the
19 lungs of these rats by up to twelve months, do we?
20 A
No, but if you look -- the text of the paper
21 directs the reader's attention to table 5; and the
22 discussion text also indicates that these are -- I
23 don't know if I would use the words crude
24 measurements, but crude measurements. If you look at
25 table 5 --
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Q I will get to table 5 in a minute and I
don't mean to cut you off.
MR. WILL: You are.
Q I'm trying to limit my question to table
1. I'm trying to do this table by table.
With respect to silica, table 1, which is
silica content over time, you will agree with me that
that data does not show much clearance up to twelve
months of the asbestos types, does it?
A I don't think you can tell. I mean, it could
be an equilibrium, as Pinkerton suggests. So there
could be significant clearance and significant
deposition.
I think with respect to Jeffrey, we are
comparing three to twelve months. You can have a
deposition with much lower clearance; and I think
that's what you see when you look at the 750 circa at
three months and then you look at twelve months and
you get a thousand.
Q Let me ask you, with respect to the
Coalinga asbestos, your table 1 indicates that after
twelve months the rats had almost as much Coalinga
asbestos in their lungs, as measured by lung silica
content, as they did at three months, correct?
A Right.
.
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1 MR. WILL: Well, I object to the question.
2 It measures silica micrograms per lung. As
3 you pointed out before, that is not an exact
4 measurement of asbestos fibers.
5 MR. BROWNSON: I was attempting to say
6 that.
7 Q Table 1, presumably, is presented in your
8 paper to show something, correct?
9A
Right.
10 Q It does not support your hypothesis that
11 most of the Coalinga is cleared at least by -- over
12 time, does it?
13 A
Well, there is a twelve-month time point. You
14 start the inhalation exposure at zero and you keep it
15 on to twelve months; and I believe what I said in the
16 paper, which is what basically Pinkerton says in his
17 papers and thesis, is that from the zero to three to
18 twelve months, during which these animals were being
19 exposed to very high doses of Coalinga, a steady
20 state has been established between the deposition of
21 the lungs and the clearance of the lungs. So the
22 clearance is very efficient.
23 If you look at the Jeffrey, and again,
24 Pinkerton points this out, it has a much higher
25 concentration of fiber and you have a significant
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1 increase between 734 and 753 at three months up to a
2 thousand at twelve months; and all that is simply-
3 reflected in the other data. It's consistent with
4 what others have seen, such as Muhle, and it's
5 consistent with the fiber volume changes in table 2.
6 Q These rats were exposed to asbestos for
7 twelve months, correct?
8 A Right.
9 Q Then they were allowed to wander about in
10 their cages for another twelve months; and at
11 twenty-four months, their lungs were getting
12 examined, right?
13 A Right.
14 Q But we don't have that particular data
15 with respect to the lung content of silica expressed
16 in table 1. We will get to that in other tables,
17 right?
18 A Right.
19 Q So at least during the time they were
20 breathing the asbestos up to twelve months, what we
21 see is that they breathed, presumably, asbestos into
22 their lungs by three months and it pretty much stayed
23 that level through twelve months for the Coalinga and
24 the UICC/B and it increased by about twenty-five
25 percent for the Jeffrey; is that fair to say?
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974
2 Q We glean that from table 1?
3 A Right.
4 Q What we can't glean from table 1 is what
5 happened over the next twelve months when they
6 weren't breathing asbestos. We have to look at other
7 things to findthat, correct?
8A
Right, andI point
that out in the paper.
9 MR. GERSON: This may be a good time to
10 take a five-minute break.
11 (A short recess is taken.)
12 Q With respect to the lung silica content,
13 do you know what the percentage of silica is in the
14 Coalinga fiber?
15 A No.
16 Q Is it different than in the Canadian
17 chrysotile?
18 A I don't know.
19 Q So I take it that you don't know what the
20 percentage of the silica is in the UICC/B or Jeffrey
21 Canadian fibers?
22 A No. These are in the standard tables; but I
23 don't have the numbers offhand.
24 You mean, the part per million per silica?
25 Q Whatever percentage or part silica is of
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the asbestos.
A -I don't know.
Q So now the second thing you do after
examining the lung silica content changes over time
in table 1 is you then move to table 2 and examine the
fiber volume changes over time, correct?
A Right.
Q Now, in reviewing table 2, I don't see
reference to the control rats. Is that in here
somewhere?
A There were nocontrol data.
Q For the lung volume changes?
A Right, nor for thedensity.
Q Which was table 3?
A Right.
Q Now, are there any other published
asbestos biopersistence studies that use fiber volume
changes, such as we see in table 2, that you can
refer us to? A Well, there is Pinkerton '84, '86, and I think
in Pinkerton '90, they certainly do that. I think
there are some papers by Chang and Crapo, his group;
and there may be other people who have also done
other determinations of fiber volume and density,
which I haven't read.
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1 Q With respect to those Pinkerton papers,
2 that's this same study you are talking about in table
3 2, right?
4 A . Yes, though Crapo may not be.
5 Q But do you know what it is that Crapo did
6 or didn't examine concerning fiber volume changes?
1 A His specific study?
8 Q Right.
9 A No, I don't know.
10 MR. BROWNSON: Off the record.
11 (A discussion is held off the record.)
12 MR. BROWNSON: ` Why don't we mark as
13 Exhibit 40 this document. It is a copy of
14 Lung Reaction to Chronic Inhalation of Three
15 Types of Chrysotile Asbestos During the
16 Lifespan of the Fischer 344 Rat, University
17 Microfilms International, copyright 1982 by
18 Pinkerton, Kent Ed.
19 (A copy of Dr. Pinkerton's 1982 thesis is
20 marked as Plaintiff's Exhibit 40 for
21 identification, as of this date.)
22 Q Dr. Ilgren, we marked as Exhibit 40 a
23 copy of the thesis by Dr. Kent Pinkerton for his Ph. D.
24 in 1982; and this is something that you have read, I
25 take it?
.
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Yes.
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977
2 Q At page 103 of the thesis, Dr. Pinkerton
3 writes: "Compared to the control value, the
4 interstitial matrix volume was 60 percent greater in
5 male rats exposed to Coalinga chrysotile, 54 percent
6 greater in males exposed to UICC/B chrysotile and 143
7 percent greater in male rats exposed to Jeffrey
8 chrysotile."
9 He is talking now about twelve months.
10 Do you recall seeing those data?
11 A
Yes. You said 143 percent.
12 Q Yes.
13 A Yes.
14 Q Then he continues at page 103 and writes:
15 "The total volume of the interstitial matrix continued
16 to increase during the postexposure period in control
17 and treatment groups of both sexes."
18 Do you recall that reference?
19 A I believe so.
20 Q Do you want to see it?
21 A No, that's okay.
22 Q What I'm kind of leading into is the lung
23 volume measurements which you -
24 A That doesn't talk about fiber. It's just the
25 matrix. Can you read it again? I don't think -
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1 MR. WILL: Why don't you show it to the
2
3A
witness? It's the interstitial matrix volume. That's
4 not fiber volume.
5 Q What is that?
6A
That's the matrix within the interstitial,
7 which is collagen or precollagen. That's not fiber.
8 Q What causes the matrix in the
9 interstitial?
10 A
There is an aging effect, because you see it
11 in the controls and it could also be and/or due to
12 fiber and/or due to non-specific things. The animals
13 get viruses -- you want me to show you the section?
14 Q You are correct. It's interstitial
15 matrix volume. So that's different than fiber
16 volume.
17 A
Right. We address IMV in paper number 1.
18 Q Now, at page 104 of your paper, now, I'm
19 in the discussion section.
20 A
Right.
21 Q At this point, what you have done is you
22 have set out in your tables the silica lung content
23 data from Dr. Pinkerton and the lung volume data from
24 Dr. Pinkerton that we have just looked at; and you
25 are now discussing what that means, correct?
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Ilgren I guess so, right.
979
2 Q One thing you say on page 104, and I'm
3 looking under the discussion section in the second
4 column about a third of the way down.
5 You describe how the three-month and
6 twelve-month lung data of these rats exposed to
7 Coalinga and UICC/B asbestos are consistent with, and
8 I'm quoting from you, "were consistent with other
9 studies of these two same fibre types that made
10 silica content measurements in investigations
11 conducted under nearly identical exposure intensity
12 and duration conditions"; right?
13 A
Right.
14 Q So what you are doing here, I take it, is
15 finding support or corroboration from these other
16 studies with respect to the Coalinga and the UICC/B,
17 right?
18 A
Right.
19 Q And we talked earlier in the deposition
20 that these are other published data concerning
21 biopersistence of the Coalinga and the UICC/B
22 asbestos, right?
23 A
Right.
24 Q Now, with respect to the other published
25 data concerning biopersistence of Coalinga, you told
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1 us earlier that you found that in this rat inhalation
2 study by Dr. Muhle from Germany, right?
3 A Right.
4 Q And that's what you are now talking about
5 in page 104 of your paper we are looking at, right?
6 A Right.
7 Q And I will show you a photocopy of a
8 paper, which I believe is the paper by Dr. Muhle that
9 you are talking about. 10 Let me show it to you and I will ask you,
11 is this the Dr. Muhle page that shows the Coalinga
12 data that you reference in your paper as reference
13 number 15?
14 A Yes.
15 MR. BROWNSON: Why don't we mark that as
16 41.
17 {A copy of "The Annals of Occupational
18 Hygiene" is marked as Plaintiff's Exhibit 41
19 for identification, as of this date.)
20 Q I will show you, Dr. Ilgren, what's been
21 marked as Exhibit 41. Just for the record, is this
22 the copy of the paper by Dr. Muhle referenced by
23 number 15 in your paper?
24 A Yes.
25 Q To try to move this along, this paper is
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1 entitled, "Inhalation and Injection Experiments in
2 Rats to Test the Carcinogenicity of MMMF."
3 That means man-made mineral fibers,
4 correct?
5 A Yes.
6 Q And they are examining whether some
7 certain man-made mineral fibers can cause cancer in
8 rats; and they are comparing them, if you will, to
9 crocidolite asbestos from South Africa and chrysotile
10 asbestos, which is the Cali'dria asbestos, right?
11 A Right.
12 Q Now, in your paper at the bottom of the
13 second column of page 104 you state that: "The short
14 fibre Coalinga sample used by Muhle et al. were
15 cleared more than any other type of chrysotile and to
16 the same extent (about 90 percent)."
17 Did I read that right?
18 A
"And the short fibre Coalinga sample used by
19 Muhle et al. were cleared more than any other type of
20 chrysotile and to the same extent (about 90
21 percent)."
22 Q Is that right?
23 A
Yes.
24 Q And when you say "any other type of
25 chrysotile," I didn't see any other type of
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1 chrysotile in Muhle's study.
982
2 Is there another type of chrysotile?
3A
I think I was referring to my table 5. I have
4 to read it again.
5 Q And your table 5 references some other
6 studies?
7A
Yes, a whole bunch of other studies.
8 Q So when you say it was cleared more than
9 any other type of chrysotile, you mean as compared to
10 these other types in the other studies in table 5?
11 A 12
Yes. Q Let's go back and look at Muhle's study
13 where you say the Calidria was cleared to about 90
14 percent. I want to look at that, okay?
15 A Okay.
16 Q If you would turn to page 759 of Muhle's
17 paper at table 4. This table is entitled "Fibers
18 (SEM) Retained in Lungs at Various Times From the
19 Start of the Inhalation Study (a) Number of Fibers
20 Per Lung, all sizes, and in Parenthesis, Fibers
21 Longer than Five Microns.n
22 A Okay.
23 Q I'm now looking at table 4 and they are
24 showing the clearance of four different things -
25 what table 4 shows is how much stuff is retained in
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1 the lungs of the rats at different periods of time,
2 right?
3 A Right.
4
Q
Andtheyare talking about
four different
5 things. It's two man-made mineral fibers, which are
6 the glass fibers; and then the chrysotile asbestos
7 and then the crocidolite, right?
8 A Right.
9 Q Now, if you look at this, I'm focusing
10 now on the chrysotile, which is the Calidria. It
11 shows that at six months these rats retained 398,
12 which I assume, means 398 million fibers or does it
13 mean something else?
14
A
No, that's whatit says,
if you look at the
15 top header.
16 Q So with respect to the Calidria
17 chrysotile, these rats that breathed in Dr. Muhle's
18 study after six months retained 398 million fibers in
19 their lungs and at twelve months retained 347 million
20 and at twenty-four months retained 223 million fibers
21 in their lungs?
22 A
Of all sizes.
23 Q I didn't bring my calculator along, but
24 the difference between 398 million fibers at six
25 months and 223 million at twenty-four months is about
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1 forty percent, correct?
984
2 A But you didn't read my paper very carefully.
3 We address the issue of why that's not really so. He
4 analyzes the six and twelve months at SEM and
5 twenty-four months at TEM. So he is finding probably
6 ten to one hundred times more using a higher powered
7 methodology at twenty-four months.
8 Plus, for all sizes, I don't really know
9 what the lower end is; but I think if you actually
10 look at the fibers greater than five at six, twelve
11 and twenty-four months, it's going 39, 33 and then
12 11. If you adjust the 11 for the TEM, the first two
13 are done by SEM, the third one is done by TEM, you
14 are going to find ten to one hundred times more.
15 So, in fact, I would say you are probably
16 going from 39 to 33 to one or less than one and
17 that's a very substantial drop; and it comports well
18 with table 5 data.
19 Q Now, you say and you talk about that in
20 your paper, but I'm now examining table 4 of Dr.
21 Muhle's paper and Dr. Muhle does not say that, does
22 he?
23 He just presents these data. He didn't
24 say that in this paper that the twenty-four month
25 data ought to be reduced by one hundred times, does
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1 he?
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2A
That's just common knowledge.
3 Q Does he say that anywhere in his paper?
4A
He actually does talk about the unreliability
5 of the measurements done with Calidria, I believe,
6 with TEM. So he alludes to that. Hang on a second.
7 I can find that.
8 Well, he is referring to injection study,
9 but that was with TEM and he says that sizing of the
10 fibers is very difficult resulting in numbers and
11 fiber dimensions. They are not very reliable.
12 Q Well, table 4 in this study, that's his
13 inhalation study where the rats are breathing, right?
14 A Right.
15 Q If we look at Dr. Muhle's published data
16 presented in table 4, what we see is that, from six
17 months to twelve months, there is less than a ten
18 percent reduction in the chrysotile, correct?
19 Those were using the same technique,
20 which is SEM, right?
21 A Right.
22 Q And then from six months to twenty-four
23 months, there is about a forty percent reduction.
24 You say, no, it should really be more
25 than that because he is using TEM?
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1A
It's obvious.
Ilgren
986
2 Q That's what you say.
3A
No, that's what the literature would say. Dr.
4 Langor would totally agree, if you are using SEM and
5 then you go to TEM.
6 Q Dr. Muhle does not say that anywhere in
7 this paper, does he?
8A
No, he doesn't actually explicitly say that in
9 his paper.
10 Q Now, the only table that Dr. Muhle
11 presents, as I read it, which actually says there is
12 a significant reduction of the Calidria chrysotile
13 is, in fact, table 5.
14 Would you agree with me in that?
15 A It may also be reflected in table 6 where
16 Bellmann et al. '87 is cited.
17 Q But, again, I'm talking about Dr. Muhle's
18 rat inhalation study.
19 A Okay, that's right.
20 Q Table 5, unlike the first two tables in
21 table 4, rather than actual observed fibers, is a
22 calculated fiber mass per lung, right?
23 A Right.
24 Q And Dr. Muhle calculates the fiber mass
25 per lung using the technique in the King paper?
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1A
Just say that again.
2 Q Dr. Muhle calculates the fiber mass per
3 lung using the technique in King, by Dr. King,
4 correct?
5A
King '55?
6 Q Right.
7A
I have to check. I thought Pinkerton was the
8 one who -- I don't recall.
9 Q Well, if I represent to you -
10 A
You want to show me where Muhle says how he
11 analyzed, through what method he used, because I
12 don't recall seeing that from Muhle.
13 Q Well, let me ask you a different
14 question. Do you know by which method Dr. Muhle
15 calculated these fiber mass per lung data in table 5?
16 A
I have to read this for a second.
17 I think he just says, after low
18 temperature ashing. He doesn't given any reference.
19 Q So do you know, then, how he calculated
20 that or by what method he calculated it?
21 A
If it's not cited, no.
22 Q Are you aware what you cite in your paper
23 number 3, the studies by Dr. King in 1955?
24 A
I think it's what Pinkerton used. That should
25 be in materials and methods on page 99, column one
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1 paragraph 1, "The silica content in lung tissue was
2 determined after ashing by the method of King et al.
3 1955. "
4 That's what Pinkerton used or whoever was
5 working with Pinkerton.
6 Q So if I could summarize the findings by
7 Dr. Muhle as published in his tables, which you say
8 supports your contention that the Calidria fibers are
9 not biopersistent, Dr. Muhle's data shows that when
10 he measures the fibers, there is about -- there is a
11 relatively small clearance; but when he calculates
12 the fiber mass per lung, that's a larger clearance?
13 A
That's not what I'm saying.
14 Q That's what I'm asking. That's what the
15 table shows.
16 A
Well, you can interpret the table for how you
17 want.
18 Q I'm not asking to interpret it. I'm
19 asking what does it show?
20 A
Per the numbers in table 4, it shows for all
21 fiber sizes a drop at twelve to twenty-four months
22 from 347 to 223, which you gave me a percentage
23 before.
24 Q I said forty but we can calculate it.
25 A
And for all fiber sizes greater than five
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1 microns, it goes from 33 to 11, which is what?
2 Q That's about a two-third reduction?
3A
So then there is almost a seventy percent
4 reduction, even using those numbers for greater than
5 five; but with table 5, if you look at the change in
6 the fiber mass going from six to twelve to
7 twenty-four months, you go from .31 to .29 to .03.
8 So that's the drop from .29 to .03.
9 Q That's a much larger drop?
10 A
Right.
11 Q Again, that's the only one of the three
12 tables using a calculation as opposed to an actual
13 measurement of numbers, right?
14 A
These are actual measurements. This is not a
15 calculated -- they ashed the tissue. They measured
16 the residue and this is what they got, as far as I
17 understand.
18 Q It's described as a calculated fiber mass
19 per lung, right?
20 A
I know calculated is a funny word; but my
21 understanding is, per the methodology, they ashed the
22 tissues, they got the numbers and they are presenting
23 for a certain number of animals. It looks like for
24 three animals at each time point.
25 They have averaged them out and they got
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1 0.31. As far as I can see, they are actual
990
2 measurements.
3 Q In any event, though, you don't know what
4 actual methodology was used for that calculation,
5 right?
A No.
7 Q Now, would you agree with me. Dr. Ilgren,
8 though, if you go back looking at table 4 at
9 twenty-four months, using the TEM technique, which
10 you have told us about, what Dr. Muhle found was that
11 there were 223 million fibers in per lung of these
12 rats of Calidria chrysotile, right?
13 A
Right.
14 Q Regardless of what technique you use or
15 how you measure it, 223 million fibers is a lot of
16 fibers in a rat'slung, isn't it?
17 A Well, on theassumption that they are all -
18 you know, I don't even know if his cut-off is at the
19 standard size, which would exclude things beneath
20 that limit that weren't even considered to be fibers;
21 but on the face of the statement 223 million
22 "fibers," that would seem to be a lot of fibers.
23 Q He doesn't say "fibers." He just says
24 fibers.
25 A Fine.
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1 Q Do you know how much a rat'3 lung weighs?
2 A I can't remember.
3 Q Again, regardless of what technique he
4 uses; and, in fact, in twenty-four months he uses TEM
5 and in six and twelve he uses SEM, he finds Calidria
6 asbestos longer than five microns in the lungs of
7 these rats, doesn't he?
8 A Right.
9 Q So although you haveconsistently
10
stated that Calidria is ashortasbestos,
you would
11 agree that some portion of Calidria asbestos is
12 greater than five microns in length and that some
13 portion of Calidria asbestos greater than five
14 microns in length got into the lungs of Dr. Muhle's
15 rats and stayed in the lungs of Dr. Muhle's rats for
16 twenty-four months?
17 MR. WILL: Objection. That's four
18 questions. State them one at a time.
19 . MR. BROWNSON: Well, let him answer that.
20 MR. WILL: Well, it's four questions.
21 MR. BROWNSON: You can answer.
22 MR. WILL: Read the question back.
23 (The record is read back.)
24 MR. WILL: As to my objection as
25 multiple, it's also argumentative.
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1 Doctor, feel free to ask him to rephrase
2 it.
3A
I'm focusing on two -- the first part of your
4 question says I have consistently said something; and
5 the second part alludes to the presence of claimed
6 fibers greater than five.
7 Not to be a major pain in the ass, but
8 would you like to ask the first part of your
9 question? 10 Q You would agree with me. Dr. Ilgren, that
11 Calidria asbestos has fibers that are greater than
12 five microns in length?
13 A 14
Yes, there is a small percentage. Q Do you know what percentage that is in a
15 sample of Calidria?
16 A
In water, it would be generally less than four
17 or five percent.
18 Q Now, in Dr. Pinkerton's thesis at page 23
19 he describes the Coalinga asbestos, which is the same
20 as the Calidria asbestos, that he looked at as having
21 forty-eight percent fibers greater than five microns.
22 You are familiar with that reference?
23 A Well, in error.
24 Q Well, it's in the air that the rats
25 breathed, right?
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Ilgren Well, that the fibers -
993
2 Q The rat breathes the asbestos out of the
3 air and when that rat breathes it, according to Dr.
4 Pinkerton, forty-eight percent is greater than five
5 microns?
6A
Well, as an aerosol. He assumes he is
7 measuring the fiber and his cut-off for short versus
8 long, which is between thirty and forty microns, as
9 indicated in his thesis.
10 Q Well, Dr. Pinkerton states that
11 forty-eight percent of the Coalinga asbestos his rats
12 breathed was greater than five microns in length,
13 right?
14 A
You are asking if it's correct that Dr.
15 Pinkerton stated that?
16 The structures that he was measuring,
17 yes, that's correct that he stated that.
18 Q Well, I can show you where he stated it.
19 MR. WILL: For the record, what is the
20 reference?
21 MR. BROWNSON: The reference is at page
22 23 of the thesis.
23 MR. WILL: Which is Exhibit 40.
24 Q In fact, in the thesis, Dr. Pinkerton
25 actually presents tables showing the size
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1 distribution of the three asbestos, including the
2 Coalinga, right?
3 A Right.
4 Q And you are familiar with the fact that
5 some portion of the Coalinga chrysotile asbestos from
6 the Union Carbide mine is greater than five microns
7 in length?
8 A Yes.
9 Q If we then look at Dr. Muhle's rats that
10 were made to breathe the Coalinga asbestos, their
11 lungs contain some of those fibers that are greater
12 than five microns in length, right?
13 A
Again, I don't know if he is measuring fibers,
14 pseudo-fibers, which are not really fibers. There is
15 a possibility that there are some long fibers there.
16 Again, it's apples and oranges. He does
17 six and twelve months with SEM and then he goes to
18 twenty-four months and looks at the things using an
19 instrument that is tremendously more powerful.
20 Q Let's just focus on this twenty-four
21 month measurement, which is using this TEM.
22 Using that powerful transmission electron
23 microscope, Dr. Muhle reports at page 759 in his
24 paper, that you cite in your paper, that he is
25 finding in lungs of his rats Coalinga asbestos
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1 greater than five microns in length, right?
995
2A
Right.
3 Q And he doesn't say these might be
pseudo-fibers. He reports them as fibers, right?
MR. GERSON: Well, hold on. I just want
to make it clear for us, as well as the
record. You are asking Dr. Ilgren to state
what Dr. Pinkerton has stated?
MR. WILL: No, Dr. Muhle.
MR. GERSON: Dr. Muhle, rather. You are
just asking him to affirm or deny that's what
is in the report, right?
MR. BROWNSON: Right.
A Right.
Q In short, using the transmission electron
microscope, Dr. Pinkerton reports that his rats that
breathed Coalinga asbestos have Coalinga asbestos in
their lungs greater than five microns, right?
A Because he couldn't see them with SEM.
Q Well, with SEM, he reports them too,
doesn't he? Look at six and twelve months. He finds
that using that technique as well, right?
A Well, that's when the animals are being
continuously exposed to very high doses of Calidria.
Q And Dr. Muhle's rats, after six months of
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1 exposure of Coalinga asbestos, using his SEM
2 technique, had 39 million fibers greater than five
3 microns in length in their lungs?
4A
Right.
5 Q After twelve months, they had 33 million 6 Coalinga fibers greater than five microns in their
7 lungs?
8A
Right,
fibers, as hesays, fibers.
9 Q And at twenty-four months, using a
10 different technique, which is now the TEM, he
11 measures 11 million Coalinga fibers greater than five 12 microns in the lungs of those rats?
13 A
Right.
14 MR. BROWNSON: Let's take a lunch break
15 here.
16 (A lunch recess is taken at 12:35 p.m.)
17 (Afternoon session resumes at 1:45 p.m.)
18 Q If we turn our attention, Dr. Ilgren, to
19 part 3 of your paper, the other study that I
20 understand you relied upon to support your belief of
21 the Coalinga studies that we see at table 5; and I'm 22 now looking at table 5, which is on page 106 of your
23 paper.
24 As I understand, from your text, you find
25 support for the notion of clearance of Calidria in
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1 the Muhle study, which we already talked about, and
2 that's the first part of table 5; and then you also
3 find support in the studies of the short fiber
4 immediately beneath that; is that right?
5 A Yes.
6 Q Now, I'm looking at the category in table
7 5 which you have labeled as short, which is the
8
second category there.
Do you seethat?
9A
You mean this?
10 Q Right.
11 A
Again, from reading the text of your paper, I
12 understand you to say that the studies of the short
13 fiber will lend credence to the idea that the short
14 fiber clears more rapidly.
15 Is that a correct statement?
16 A 17
Where are you reading?
Q Well, I'm paraphrasing from the text. T
18 can go to areference, if you would like?
19 A
Page 104, column two?
20 Q Exactly. So then, going to table 5 on
21 page 106, I'm looking at your column headed clearance
22 percentage. Do you see that one?
23 A Yes.
24 Q You cite Davis et al., which is a
25 published paper in 1988, your reference 33, for a
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1 clearance percentage of 89.2. 2 Do I have that right?
3A
Yes.
.
4 Q Now, in the Berman et al. paper, which is
5 the Berman 1995 paper and your reference 29, you
6 don't put a clearance percentage. Why is that?
7A
That was a study they did where they
8 reanalyzed the dust clouds using TEM; and I think I
9 put that in there just because it reassessed the same
10 studies that Davis had originally done.
11 I think they gave some additional
12 measurements for fibers per CC; but I don't think
13 Berman has clearance. I have to go and double check.
14 Q But at least as far as your paper, you
15 don't report a clearance percentage for that Berman
16 cite?
17 A
Right.
18 Q So in terms of actually getting a number,
19 we need to look at Davis' study for a clearance
20 percentage, right? 21 A Right. 22 MR. BROWNSON: Let's do that. Off the
23 record. 24 {A discussion is held off the record.)
25 Q Your table 5 at page 106 of your paper
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1 talks about a study of Davis et al. published 1988 in 2 the "British Journal of Industrial Medicine." That 3 is your reference 33; and I have just showed you the 4 paper, which is your reference 33, and you are saying
5 that's an error?
6A
Yes. The electrostatic charge pertains to
7 this one at the bottom. You see normal charge, the
8 very last one on that page. It says normal charge
9 and draft 33. That's the one.
10 MR. BROWNSON: Okay, mark that paper.
11 MR. WILL: Is it supposed to be 28? 12 THE WITNESS: Ye3.
13 MR. WILL: Reference 33 in the paper
14 should be reference 28.
15 MR. BROWNSON: Let's mark that. 16 (A copy of "Effects of Electrostatic 17 Charge on the Pathogenicity of Chrysotile 18 Asbestos" is marked as Plaintiff's Exhibit 42
19 for identification, as of this date.)
20 Q I show you, doctor, what was marked as 21 Exhibit 42, and this is a study by J.M.G. Davis and
22 other authors and this is the reference described as
23 reference 33 in your paper, right?
24 A
Yes.
25 Q When you state at table 5 that reference
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1 33 in the short fiber type category, you are not 2 telling us that that's an error, there's really a 3 different reference that supports that?
4 A Yes.
5 Q And the different reference that supports
6 it is reference 28 in your paper?
7A 8
Yes. MR. BROWNSON: Let's mark that as Exhibit
9 43 .
10 (A copy of "Comparisons of the
11 Pathogenicity of Long and Short Fibres of 12 Chrysotile Asbestos in Rats" is marked as 13 Plaintiff's Exhibit 43 for identification, as
14 of this date.)
15 Q I show you what's been marked as Exhibit
16 43, and I will ask you if this is the paper which is,
17 in fact, reference 28 in your paper?
18 A
Yes.
19 Q Can you show us where in reference 28 of
20 your paper, which is Exhibit 43, we find data that
21 shows that 89.2 percent of the short asbestos was 22 cleared in the lungs of rats?
23 A
I think I just calculated that from the data.
24 I don't think it's stated, though it might be stated.
25 I don't remember.
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1 Q Well, if it ia stated, are you telling us
2 that it would be found somewhere in that paper,
3 Exhibit 43, your reference 28?
4A
Yes, you saw the lung burden data.
5 MR. WILL: Why don't you state that for
6 the record.
7 THE WITNESS: It looks like 732 table 5. 8 Q So you are saying that the 89.2 clearance
9 percentage that you report on table 5 of your paper 10 for short fiber type is derived from table 5 at page
11 732 of Exhibit 43, which is your reference 28?
12 A I think so.
13 Q Now, one thing I do observe is that it 14 appears as though the inhalation study of asbestos on
15 rats referenced in both Exhibits 42 and 43, which are
16 your references 33 and 28, involve the same group of
17 forty-eight rats; is that right?
18 A
No, I don't think so.
19 Q So these are different groups of
20 forty-eight rats?
21 A
Well, I think we are talking about -- you are
22 saying my reference 28 and reference 33 --
23 Q Is that the same group of rats? That's
24 all I'm asking.
25 A No, I don't think so.
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1 Q So those are two different inhalation
2 studies on two different groups of rats?
3A
Yes, short, long, discharged and
4 non-discharged.
-
5 Q Were both of those studies using the same
6 type of chrysotile asbestos?
7A
I don't remember. I think so, but I don't
8 remember. X have to look. You want me to look?
9 Q Sure.
10 A Both studies meaning the twodifferences?
11 Q Right.
12 A
I don't think so. The materials and methods
13 in the reference 28 said that they used a grade 4T-30
14 sample, whereas in the other electrostatic charge
15 paper they are using, I believe, a UICC/A.
16 Q Would you call that a short chrysotile,
17 an intermediate or a long?
18 A Which?
19 Q The UICC/A.
20 A The UICC/A?
21 Q Right.
22
A
I think the UICC/Aissimilar
to UICC/B; but
23 I'm not entirely sure. I think it's an intermediate
24 to long.
25 Q Well, your reference number 33, which is
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Exhibit 42, is a study by Dr. Davis and others where
they are making rats inhale this UICC/A chrysotile
asbestos, right?
A Right.
Q You don't know, as you sit here, whether
that would be what you would call a short.,
intermediate or long fiber?
A I believe it's intermediate to long. It's not
short. It's just a standard UICC/A sample.
Q Do you know how its size distribution
compares to that of Calidria asbestos?
A I mean, there is more long fibers. I can't
give you the exact percentages in each size category
as I sit here.
Q And what type of chrysotile asbestos are
the rats in Dr. Davis' study, which is your reference
28, Exhibit 43, exposed to?
A I think the 4T-30 is a derivation of Jeffrey,
but I'm not sure.
Q Do you know if that is a short,
intermediate or long?
A That's long.
Q Do you know how its size distribution
compares to that of Calidria?
A I can't remember the percentile break down off
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1 the top of my head. It's clearly termed in page 720.
2 The long fiber dust cloud was generated directly from
3 the 4T-30.
4 Q And just so we are clear now, going back
5 to table 5 of your paper on page 106, the short,
6 what you describe as short chrysotile study, is
7 Berman et al., but that one doesn't have any
8 clearance percentage data, correct?
9A
Right. I think 1 just put that in, the Berman
10 et al. study, for the reader if they wanted to get
11 more information about those particular Davis
12 studies, because Berman et al. really looked at the
13 Davis et al. studies; but you are right, it didn't
14 have any clearance, as I recall.
15 Q So are you now telling us that the Davis
16 study, which is your reference 33 and Exhibit 42,
17 does not, in fact, involve short fiber?
18 A
They didn't involve short fiber.
19 Q So when you place it in the short fiber
20 category in your table 5, that's simply an error?
21 A
No, reference 28 involves short -- the
22 reference 28 is short versus long fiber and the
23 second study I put down in table 5 is the fiber type
24 that I label short; and that should refer not to
25 Davis et al. 1988 (33), but it should refer to Davis
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1 et al. 1988 (28). 2 Q So what you call Davis et al. 1988 (33), 3 a short fiber type study, that is an error? It is
4 not short?
5A
That's right.
6 MR. GERSON: But the error is the 33?
7 THE WITNESS: Right.
8 Q The error is you put the wrong study in
9 the short fiber category, right?
10 A
Right.
11 Q Just so I'm clear here, are you telling
12 us that your reference 28, which is Exhibit 43,
13 that's not short fiber either?
14 A Right. 15 Q So inorder tofix your short fiber
16 category on table 5, you can't just plug in your
17 reference 28, Exhibit 43, because that's not short
18 either?
'
19 A
Sure you can. You just put a 28 here instead
20
of a 33.
`
21 Q And if you do that, though, you just told
22 us that was long to intermediate fiber in that study.
23 A No. We weretalking about --we are mixing, I
24 think, exhibit numbers and reference numbers.
25 Q Then let's clearly go through them. We
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1 have established that Exhibit 42, your reference 33,
2 which your table 5 says is short, is not, in fact,
3 short. We have got that much established, right?
4A
Right.
5 Q Now, I thought you were telling us that
6 what should be in that short fiber category is your
7 reference 28?
8 A Yes, which is Exhibit 43.
9 Q But I thought you told us that that study
10 also was intermediate to long fiber?
11 A
No, we were talking at that point, as far as I
12 was concerned, about reference 33, Exhibit 42.
13 Q So if we looked, then, at your reference
14 28, which is Exhibit 43, that study involves some
15 short chrysotile; is that correct?
16 A
Yes, short compared to long.
17 Q You would put that -
18 A Well, that's just in the title.
19 Q If you were to correct your table 5, you
20 would put that study in the short category, right?
21 A
Yes, I would just put a 28 instead of a 33.
22 MR. GERSON: Does it still accurately
23 describe Davis et al.?
24 THE WITNESS: Yes.
25 MR. WILL: Off the record.
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1 (A discussion is held off the record.)
2 THE WITNESS: Actually, I misspoke. When
3 you said is it still Davis et al., it's
4 actually Davis and Jones.
5 Q You would agree with me, again, that your
6 paper, part 3 of your paper, the purpose is to
1 convince the reader that short, in general, and
8 Calidria asbestos, in particular, is cleared from the
9 lungs of rats more quickly than long?
10 A
Reference 28.
11 Q Would you agree with me that your paper,
12 part three of your paper, the purpose of part three
13 of your paper is to convince the reader that short,
14 in general, and Calidria asbestos, in particular, is
15 cleared more quickly from the lungs of rats or more
16 completely from the lungs of rats than long asbestos?
17 A
Yes.
18 Q Would you agree with me that table 5 in
19 your paper on page 106 is offered in support of that
20 proposition?
21 A Yes,to some extent, yes.
22 Q Now, looking at Exhibit 43, which is your
23 reference 28, this is the study by J.M.G. Davis and
24 A.D. Jones where they made rats inhale both short
25 fiber chrysotile and long fiber chrysotile?
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1 A Right.
2 Q At table 5, which is that table you
3 pointed to us a moment ago, they report on the
4 clearance of both the short fiberand the long fiber,
5 correct?
6 A Right.
7 Q Do you anywhere in your table 5 describe
8 what they reported as theclearance of the long fiber
9 chrysotile?
10 A 11 12 A 13
It's on page 107. Q Where do I find it on page 107? It's the third one down. Q That's in the category entitled long?
14 A
Yes.
15 Q And you report the clearance percentage
16 as 54., 1 percent?
17 A
Yes.
18 Q And you report it as coming from that
19 Davis et al . reference 33?
20 A
Right.
21 Q But really it's the Davis and Jones
22 reference 28?
23 A
Right.
24 Q So that's just an error you made in your
25 ' column of references there?
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A Yes. Q Now, even though this Bertnan et al. paper
does not contain actual clearance percentages, you
still cited it in your short category?
A I have to see it. Do you have a copy there?
Do you have Berman's paper?
Q Yes, I do. A Let me look at that, because I don't remember.
MR. BROWNSON: Off the record.
(A discussion is held off the record.)
Q I have showed you, Dr. Ilgren, my working
copy of the Berman paper. Just for the record, is
that the Berman paper?
A Yes. MR. BROWNSON: Even though I have got
some highlighting on it, why don't we mark it
as an exhibit.
MR. GERSON: If you want, I can make a
copy without the highlights.
MR. BROWNSON: Can we take a moment and
do that?
MR. GERSON: Sure.
MR. BROWNSON: Let's do that.
(A short recess is taken.)
MR. BROWNSON: Mark that as Exhibit 44.
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1 (A copy of "The Sizes, Shapes and
2 Mineralogy of Asbestos Structures that Induce 3 Lung Tumors of Mesothelioma in AF/HAN Rats 4 Following Inhalation" is marked as Plaintiff's 5 Exhibit 44 for identification, as of this
6 date.)
7 Q Before we go to the Berman paper, Dr. 8 Ilgren, I'm going to go back to this Davis and Jones
9 paper, which is your reference 28, Exhibit 43, which 10 is the one that should be in the short chrysotile
11 category of your table 5, okay?
12 A
Yes.
13 Q I was just noticing in that paper at page 14 730 there is a table 3 entitled, "Pulmonary Tumors
15 and Mesotheliomas Found in Animals Treated with Long 16 and Short Fibre Samples of Chrysotile Asbestos and in
17 a Control Group of Rats."
18 Do you see that?
19 A
I have a copy here. What's your question?
20 Q According to that table, it indicates
21 that the forty rats that were exposed to long
22 chrysotile had twenty-three tumors, forty rats
23 exposed to short chrysotile had eight tumors and the
24 forty-seven control rats not exposed to any asbestos
25 had two tumors, right?
.
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1 A Right.
2 Q So even though the short chrysotile had
3 less tumors than the long chrysotile, it had four
4 times as many as the control rats.
5A
Right. Is there a question?
6 Q No. Now, let's move to the -
7 MR. WILL: Just to be clear, that's not
8 Coalinga chrysotile in that experiment, is it?
9 THE WITNESS: No.
10 Q Exhibit 44, this is the paper by Dr. D.
11 Wayne Berman and other authors that you talk about at
12 your table 5, right?
13 A Right.
14 Q I see one of those authors is Eric
15 Chatfield. That is the same guy who is your
16 co-author?
17 A
Right.
18 Q And this paper has studies of the
19 inhalation of nine different types of asbestos by a
20 bunch of rats?
21 A The phraseology ofthequestion, there were
22 thirteen inhalation studies analyzed.
23 Q But different rats were exposed to nine
24 different types of asbestos, right?
25
A
Well, it lookslike four chrysotile
-
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1 Q Well, I'm looking at the first line of
2 the abstract where it says they were exposed to nine
3 different types of asbestos dusts.
4A
Well, I don't know how he gets nine. If you
5 look at table 1, there are four types.
6 MR. GERSON: What page is table 1?
7 THE WITNESS: 183.
8 Q If you look at the description, though,
9 the chrysotile are broken down and so are the amosite
10 and -
11 A
Well, as far as I'm concerned, there are kind
12 of sub-types and sub-variations to a type of
13 asbestos. Not to be semantical, but in column one,
14 table 1, fiber type, asbestos type. So anyway, it's
15 semantical. 16 Q Are you saying this group of authors
17 should not call this nine different types of
18 asbestos, as they do in their abstract?
19 They should only call it three types with
20 sub-groups?
21 A
I would say they used four different types of
22 asbestos of varying -- prepared in different ways. I
23 would just have said it differently, that's all.
24 MR. GERSON: In fact, there are two
25 columns.
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1 Q Well, whatever the columns are, you agree
2 with me in their abstract they call it nine different
3 types of asbestos?
4A
Right, in their abstract.
5 Q And you don't agree with that
6 terminology? Would you call it something else?
7A
I would have just worded the sentence
8 differently, that's all.
9 Q If you look at their table 1, that's the
10 table where they summarizes the data for animal
11 inhalation experiments conducted by Davis and
12 co-workers, right?
-
13 A Yes.
14 Q If you look at what they describe as the
15 short chrysotile, that's that same short chrysotile
16 that we were just looking at a moment ago in Dr.
17 Davis' paper, which is Exhibit 43 and your reference
18 28; is that right?
19 A
Right.
20 Q If you look at table 1 again under their
21 category of short chrysotile, we see again, just like
22 we saw in Exhibit 43, that that short chrysotile
23 caused seven pulmonary tumors and one mesothelioma,
24 correct?
25 A Right, being seriously contaminated with 1,170
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.1 long fibers per CC, which is discussed in Davis and
2 Jones 1988 on page 733, I think, in adequate detail.
3 Q So you are saying that even though they
4 call it short fiber, Davis calls it short fiber and
5 you call it short fiber, it's seriously contaminated
6 with long fiber?
7A
Well, that's what he says in his paper.
8 Q So it's really not short fiber?
9A
They made an attempt to make it short fiber,
10 but they couldn't get out a lot of long fiber.
11 Q When you say a lot of long fiber, do you
12 speak about fiber greater than five microns in
13 length?
14 A
Yes.
15 Q What percentage of this short fiber is
16 greater than five microns in length?
17 A
Say that again.
18 Q What percentage of that short fiber is
19 greater than five microns in length?
20 A
What they began with as the hand sample or in
21 air.
22 Q What the rats inhaled?
23 A I don't know. I just know that as they
24 indicate there. Despite their attempts to develop a
25 method or to apply a method, that under other
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1 circumstances were smaller amounts of fiber, despite
2 that method to separate out long versus short, it
3 just didn't work here. 4 So they had left over a large number of
5 long fibers. Basically, he says, that while this 6 certainly applies the samples of a few milligrams, it 7 was not practical for the 1.5 kilograms needed for 8 long term inhalation studies.
9 Q So the asbestos fiber Drs. Davis and 10 Jones in Exhibit 43 described as short is, in fact, 11 you are telling us, not all short. Some of it is
12 long?
13 A
Yes.
14 Q Nevertheless, Dr. D Wayne Berman, Kenny 15 S. Crump, Eric J. Chatfield, John M.G. Davis and Alan
16 D. Jones in their paper at page 183 table 1 call it
17 short chrysotile, don't they?
18 A
It's the same paper. They cross reference.
19 In their table 1, they cross reference a reference,
20 which is Davis and Jones 1988.
21 Berman et al. 1995 is merely a
22 re-examination of all the Davis studies. So they are
23 stating their reference 13 in Berman et al. 1995 is 24 Davis and Jones 1988 comparisons of the pathogenicity
25 of long and short fibers.
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1 Q Let me ask it again. Drs. Berman, Crump,
2 Chatfield, Davis and Jones, Davis and Jones being the
3 original authors of Exhibit 43, and Chatfield being
4 your co-author, in their paper. Exhibit 44, they
5 don't make all these distinctions you do in table 1.
6 They call it short chrysotile, correct?
7A
What do you mean?
8 Q What do they call that fiber in table 1
9 of their paper? Please read to me what they call it?
10 A
Short, but they refer to reference 13, which
11 is the paper in which the various distinctions are
12 made by the same authors.
13 Q So a reader reading table 1 of their
14 paper at page 183 would be told that that chrysotile
15 is short; but if the reader bothered to go and read
16 the reference 13, he might learn that some of that
17 chrysotile was, in fact, long; right?
18 A
No, you could see it in the fourth column,
19 fifth column from left to right, it is fiber type,
20 description, abbreviations, mass concentration and
21 PCM. Under PCM is 1,170 fibers per milliliter there.
22 ` The reader, I think, would immediately
23 realize that there was a significant number of long
24 fibers in that short preparation, even if they didn't
25 go back to reference 13 Davis and Jones of 1988.
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1 Q Would that be obvious to the reader from
2 looking at your table 5 as well?
3A
Yes.
4 Q Where does your table 5 show that those 5 1,170 fibers are greater than five microns in length?
6A 7
They are because they are PCM. Q Where does it say that in your table 5?
8A
It says it in the footnote on page 107, two
9 lines down.
10 Q So if a reader goes down to your second
11 footnote, he would learn that some of the chrysotile
12 fibers that you categorized as short are, in fact,
13 long, correct?
14 A
Right.
15 Q And he would also learn that some of the
16 Coalinga fibers, which you were calling short in your
17 paper, are also long?
18 A
Right.
19 Q If a reader read the paper by Drs. Berman
20 Crump, Chatfield, Davis and Jones, they might pick up
21 that what those authors describe as short chrysotile,
22 in fact, contains long chrysotile, even though it
23 doesn't say that, because there is a reference that
24 reads, PCM f/ml, right?
25 A Right.
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1 Q And if a reader then went to Dr. Davis 2 and Jones' paper, which is Exhibit 43, your reference 3 28, and read the paper closely, they would learn that
4 what Dr. Davis and Jones called short chrysotile, in
5 fact, contains some long chrysotile?
6 MR. GERSON: You said "some," right?
7 MR. BROWNSON: Right.
8A
Right.
9 Q And if a reader reading your part three
10 paper went back to Dr. Pinkerton's original thesis,
11 which describes the research upon which your part
12 three paper is written, they would discover that some
13 of that Calidria fiber you described as short is also
14 long, wouldn't they?
15 A
What would they be looking at to get that
16 information?
17 Q Well, they could find that information
18 from Dr. Pinkerton's thesis, couldn't they?
19 A
Just sort of ask the question so it's kind of
20 joined up into one question.
21 Q Well, they could find from Dr.
22 Pinkerton's thesis that some of the Calidria asbestos
23 you describe as short in your series of three papers
24 is, in fact, long?
25 A
And you would be citing what for that?
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1 Q Dr. Pinkerton'3 thesis.
2A
What specific part of the thesis?
3 Q Please answer the question.
4A
I am. I'm just trying to -- you are referring
5 to a thesis, which is a big piece of work; and you
6 are saying somewhere in there he is saying something.
7 Can you just specify where in the thesis?
8 Q Okay, page 23 of the thesis.
9A
Okay, let's see page 23.
10 MR. WILL: It's a deposition exhibit.
11 MR. BROWNSON: It's Exhibit 40.
12 Q Dr. Pinkerton's thesis reads at page 23
13 and I quote -
14 MR. WILL: Why don't you show it to the
15 witness?
16 Q "Combined fiber and fiber cluster length
17 in Coalinga chrysotile shows a distribution with many
18 fibers exceeding thirty microns in length."
19 Dr. Pinkerton reported that, correct?
20 A
Yes, he reported that.
21
Q
And his thesis atpage 23 also
shows that
22 of the Coalinga asbestos thatthe ratsbreathed,
23 forty-eight percent was greater than five microns in
24 length, correct?
25 A Right.
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1 Q Do your series of three papers anywhere
2 make reference to the fact that some of the Calidria 3 Coalinga asbestos is greater than thirty microns in
4 length?
5A
That's part four. I don't recall -- I would
6 have to go through the three papers. To my
7 recollection, it does not mention that; but as we
8 have discussed in the past, the issue of fiber size
9 length, width and purity is addressed in part four of
10 the paper.
11 Q Which may be published in the future?
12 A Yes.
13 Q Are you familiar with abstracts that Dr.
14 Kent Pinkerton, Dr. P. Pratt, A. R. Brody and J.D.
15 Crapo published in the "American Review of
16 Respiratory Disease," April of 1981?
17 A These are the three abstracts we talked about
18 before?
19 Q Right.
20 A
I'm familiar -- well, you have to show them to
21 me again.
22 Q Okay. I'm only showing you the one
23 published which I just described.
24 A Okay.
25 Q Would you agree with me that in that
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1 abstract, those authors say that all three types of
2 chrysotile, including the Calidria caused
3 interstitial lung injuries after three months of
4 exposure by the rats?
5A
Can I read this?
6 7A
Q Can you answer the question? I can't remember the question.
8 MR. BROWNSON: Read it back.
9 MR. WILL: Let him read the abstract
10 first, and then we can have the question read
11 back.
12 A
Yes, I see his statement here. After three
13 months' exposure, all fibers caused injury to the
14 epithelium and interstitium with the increase of the
15 volume of alveolar type II cells. I don't consider
16 those injuries.
17 Q So even though they call them injuries,
18 you don't consider them injuries?
19 A
No, I don't consider them injuries. I don't
20 see any data, either.
21 Q Well, you don't see any data; but this are
22 the same rat inhalation studies that you are talking
23 about in your series of three papers, isn't it?
24 A
Right.
25 Q And you have no reason to believe that
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1 Dr. Pinkerton would make that up, do you?
2A
I'm just saying that he is citing an abstract
3 and there is no, to my knowledge, published data
4 prior to that point to support his contention; and I
5 don't see any intended data in which he is basing his
6 statement. 7 Q So if it is your contention, then, that
8 he if makes that statement, he is simply wrong?
9A
I wouldn't call an increase in epithelium and
10 an increase in interstitium volume necessarily an
11 injury, because we see all that as rats age. That is
12 supported in his thesis, Pinkerton et al. 1982; and
13 Pinkerton's thesis demonstrates the same phenomena.
14 Q So you believe he was wrong?
15 A
Well, I wouldn't use the word injury.
16 Q If he again uses the word "injury" in
17 another of his abstracts, would he be wrong again?
18 A
It depends. Show me the abstract.
19 Q I show you the abstract published in the
20 "American Review of Respiratory Disease" at the
21 annual meeting of the American Lung Association, the
22 Canadian Lung Association, the American Thoracic
23 Society, the Canadian Thoracic Society and the
24 Congress of Lung Association Staff in 1980.
25 I have highlighted the sentences there.
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1A 2
Could we make a copy of this? Q Before we do, can you answer the
3 question? In that abstract, again, Dr. Pinkerton 4 describes what the lungs received from exposure to
5 all three types of asbestos as injury, doesn't he?
6A
Yes, he refers to them again as injury and my
7 response would be the same again. He makes the same
8 statement, volume and thickness of epithelium and 9 interstitium increase, alveolar cell increase. 10 I don't think that's necessarily
11 indicative of injury. 12 (A short recess is taken.)
13 Q Going back to your paper, Dr. Ilgren, 14 part three that we have been talking about today, 15 page 102 in the second column at the bottom of the 16 first paragraph you write, "The average density of
17 Coalinga fibre in interstitial cells at three months 18 appeared to be three times greater than UICC/B and 19 Jeffrey, but this was due to one animal with an 20 anomalously high value, so the difference has 21 probably been significantly overestimated."
22 Do you see that?
23 A
Yes.
24 Q So what you are saying is the references
25 or the data we see on table 3 of your paper showing
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1 that the average density of the Coalinga fiber in the
2 interstitial cells at three months to be greater than
3 the other two was due to one anomalous animal?
4A
Yes. It's 21.8, isn't it?
5 Q If we look at table 3, can you show us
6 where that reference appears?
7A
The reference or the animal?
3 Q The anomalous animal.
9A
I think it's 21.8. I just mentioned it.
10 Q Where do we see that?
11 A
Look here. If you look at table 3, you go to
12 the column Coalinga and go under alveolar
13 macrophages; and then you go to three months and you 14 see 8.52 plus or minus 4.69 then in brackets you have
15 0.5-21.8. 16 So I'm referring to that animal, 21.8.
17 If you look at the individual -- I don't have the raw 18 data here, but the 21.8 seems to be a major outlier,
19 greater than the other points. 20 Q Now, you had told us at an earlier
21 deposition that all of these animals in the raw data
22 from Dr. Pinkerton that you looked at had a number to
23 them.
24 A
Right.
25 Q Can you tell us the number of that
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1 anomalous rat?
2A
I could. I can't sitting here, but I could do
3 that.
4 Q That data is available to you?
5A
Yes.
6 INSERT: 7 Q You described that as an anomalously high 8 value; but however you described it, that is an
9 actual value in a rat, right?
10 A
Right.
11 Q In other words, what that indicates is
12 that there is one rat that breathed a lot of Coalinga
13 fiber and for some reason a lot of it -- or there was
14 a lot of fiber density change in that particular rat.
15 MR. WILL: Object to the form of the
16 question. Why don't we just stick with the
17 fiber density change?
18 Q One rat had a large fiber density change
19 following exposure to Coalinga?
20
A
It had a fiber density,
yes.
21
.Q
And although you describe that as an
22 anomalous rat, that is a piece of real data?
23 In other words, that rat had a lot of
24 Coalinga fiber in its lungs, didn't it?
25 A
Right.
.
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1 Q I take it you don't know why that
2 particular rat had so much Coalinga in its lungs?
3 A No.
4 Q Could it be particularly susceptible or
5 the fact that it was so stupid it kept its mouth
6 opened when it breathed? It could be any number of
7 things, right?
8 A I imagine so. I don't know why.
9 Q Now, if you look at page 103 of your 10 paper in the second column about the bottom third you
11 again speak about an extremely high fiber density in
12 one Coalinga animal.
13 Is that the same one? That's the same
14 one that we were talking about on page 102 or a
15 different one?
16 A
Let me check here. That's the same one, I
17 think.
18 Q Because now we are talking about fiber
19 density in the alveolar macrophages.
20 A
I beg your pardon, I made a mistake. When we
21 were talking about the anomalous value on page 102,
22 that had to do with cellular interstitium and that
23 would be cellular interstitium; and that would be,
24 again, if you look at the table 2 on page 101 under
25 interstitial cells.
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1 Q Now, is this table 3 or table 2?
2A
Wait a minute, hang on. I'm sorry.
3 Q Take your time, because I'm trying to
4 figure out who these anomalous rats are?
5A
With reference to page 102 and our discussion
6 just a minute ago where you were reading the average 7 density of Coalinga fiber in interstitial cells in
8 three months appeared to be three times greater than
9 UICC/B and Jeffrey, but this was due to one animal
10 with an anomalously high value. So the difference
11 has probably been significantly overestimated, I 12 should have been referring to the portion of page 101
13 in table 3 under interstitial cells for a three-month
14 value of 1.98.
15 Q So is the anomalous rat described at page
16 102 of your paper seen in table 3 under interstitial
17 cells at 1.98?
18 A
Yes.
19 Q And what is the anomalous rat described
20 at page 103 of your paper?
21 A
That is the one that I formerly described as
22 under alveolar macrophages at three months referring
23 to 21.8.
24 Q So if we can summarize, the average
25 density of Coalinga fibers in the interstitial cells
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1 at three months is much higher in the Coalinga; but
2 you attribute that to an anomalous rat, right?
3 A Yes.
4 Q At least in part?
5 A Yes.
6 Q The fiber density leading to an increase
7 in the number of alveolar macrophages is, again,
8 higher than the Coalinga; but you attribute that to
9 another anomalous rat?
10 A Maybe.
11 Q It might be one reason forit?
12 A
Might be.
`
13 Q Whatever the reason for it is, however,
14 the fact remains that the number of alveolar
15 macrophages is increased more in the Coalinga than
16 the UICC/B at three months?
17 A
Right.. It'snot the number it's -
18 MR. GERSON: Off the record.
19 (A discussion is held off the record.)
20 A
Are you referring to number of macrophages or
21 are you referring to fiber density in macrophages?
22 Q I don't know. You are calling it number
23 of macrophages in your paper?
24 A
No, in table 3 it is not the number. The
25 number of macrophages is table 7. Table 3 refers to
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1 the density of fiber in macrophages, the number of
2 macrophages.
3 Q That's not what I'm talking about. 4 MR. WILL: The answer to your question is
5 no. That's what we are getting at.
6 MR. BROWNSON: Let's go back and start
7 over.
8 Q I'm reading at page 103 of your paper.
9 Under the heading of alveolar macrophages, that says
10 there was an increased number of alveolar macrophages 11 in the Coalinga versus the UICC/B; does it not say
12 that?
13 A
Show me exactly where you are reading from.
14 Q Let me quote -
15 A
No, just tell me in regards to where you are.
16 Q Right here.
17 A
Inhalation of Jeffrey and Coalinga fiber for
18 three months led to a greater than 84 percent
19 increase in the number of alveolar macrophages,
20 compared with age-matched control animals, citing
21 table 4.
22 MR. WILL: But you were talking about
23 table 3.
24 MR. BROWNSON: We were talking about
25 something else then. Please, we need to
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1 listen closely to the questions.
2 MR. WILL: Let's go off the record for a
3 second.
4 (A discussion is held off the record.)
5 MR. WILL: Dr. Ilgren, let me ask you to
6 clarify. Does table 3 refer to the number of
7 macrophages?
8 THE WITNESS: No.
9 MR. BROWNSON: I never said it did.
10 Please listen to the question.
11 12 A
Q What does table 3 refer to? Fiber density.
13 MR. WILL: In the macrophages?
14 THE WITNESS: Yes.
15 MR. BROWNSON: Now we have to start over.
16 Q The first anomalous rat described in your
17 paper is at page 102, correct?
18 A
Right.
19 Q Andthat anomalous rat, in your view,
20 contributes or causes the increase in the average
21 density of Coalinga fiber in interstitial cells at
22 three months?
23 A Yes.
24 Q As shown in table 2?
25 A No, table 3.
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1 Q Table 3?
2 MR. WILL: Because table 2 is volume
3 changes.
4 Q Table 3 of your paper at page 101, right?
5A
Right, and the anomalous animal there is 1.98
6 at three months and table 3 on page 101 under
7 interstitial cells.
8 Q Now, the second anomalous animal you
9 describe in your paper, you describe at page 103,
10 right?
11 A
Right.
12 Q And that second anomalous rat caused the
13 difference in the number of alveolar macrophages at
14 three months of exposure?
15 A
No. The anomalous value referred to on page
16 103, as far as I can see, refers to fiber density, not
17 cell number.
18 If you look on column two, page 103, five
19 lines up from the bottom it reads, "However, much of
20 the difference between UICC/B and Coalinga was due to
21 an extremely high fiber density reading of one
22 Coalinga animal."
23 Q Now, I will ask again, is that the same
24 anomalous rat as we were just talking about described
25 on page 102 or is that a different one?
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1A
That, I don't know.
2 Q You will agree with me, at least, that 3 the anomalous rat described on page 103 is extremely4 confusing, because it's under the heading of alveolar 5 macrophages when you are talking about the increase 6 in number of them; but then when you get to this 7 anomalous rat, now we are suddenly talking about
8 fiber density. 9 MR. WILL: I object to the question. 10 It's argumentative. It's speculative and it's
11 multiple.
12 A
I don't understand the question.
13 Q Under your heading of alveolar
14 macrophages on page 103 the first sentence reads, and
15 I quote, "Inhalation of Jeffrey and Coalinga fiber for
16 three months led to a greater than 84 percent
17 increase in the number of alveolar macrophages,
18 compared with age-matched control animals (table 4). 19 However, exposure to UICC/B did not increase 20 macrophage numbers significantly by this time." 21 Then you continue and down later in that
22 column we get to this anomalous rat.
23 A
But it's apples and oranges again. The
24 beginning of the discussion on page 103 about
25 alveolar macrophages talks about cellular number and
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1 cellular volume changes. Later on page 103 we are
2 talking about fiber density.
3 Q Is that the same anomalous rat as you
4 were talking about on page 102?
5 MR. WILL: He told you twice now. He
6 doesn't know. Asked and answered.
7A
The only way I can tell is if you put out the
8 raw data for all four or five animals.
9 Q And your paper doesn't tell you which
10 anomalous rat this is?
11 A
No, just the raw data.
12 Q Is it fair to say, Dr. Ilgren, that all
13 three fiber types, including the Coalinga, caused
14 increased macrophage cell volume after three months,
15 as described in table 4?
16 A
That's what I have said in my paper.
17 Q However, the density of the asbestos in
18 macrophages was higher for the Coalinga than the
19 UICC/B, correct?
20 A
I just want to be sure I get your question.
21 Ask it again. 22 Q The density of Coalinga fiber in the rat 23 macrophages was more than twice the amount than after 24 the exposure to the UICC/B fiber, correct? 25 MR. WILL: The Coalinga was more than
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twice the UICC/B?
MR. BROWNSON: That'3 what I said. MR. WILL: You didn't say which one.
MR. BROWNSON: Stop. Let me ask a
question. Listen carefully to the question.
MR. WILL: I was. That's why I
interrupted. Q Listen carefully to the question. The
density of the Coalinga fiber in the macrophages was more than twice that of the UICC/B fiber in the
macrophages?
A Yes. MR. WILL: At three months?
MR. BROWNSON: At three months.
Q And you attribute that density difference
or much of it to one anomalous Coalinga rat?
A Yes. Q Again, we don't know which Coalinga rat
that was?
A Right.
Q But that is a real piece of data?
A Sure, it's a real piece of data.
Q Now, then turn to page 104 of your paper. In the first column at the last sentence of the first
full paragraph, you again are describing anomalously
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1 high fiber density in a Coalinga rat.
2 Do you see that? '
3A 4 5A
Yes. Q Now, which rat is that one? Again, it's the same, unless I have the raw
6 data, I can't really identify which one it is. 7 Q Well, let me point out that here you are
8 talking about the density of Coalinga fiber after
9 twelve months'exposure.
10 A
Right.
11 Q So can you tell from that if this is that
12 same anomalous rat we had seen earlier or if this is
13 a different one?
14 A
No, we can't tell.
15 Q At twelve months' exposure, this
16 particular anomalous rat described on page 104 had
17 density of Coalinga fiber in its lungs more than six
18 times greater than that found in the Jeffrey treated
19 macrophages, right?
20 A Right.
21 Q Let me ask you this question. Dr. Ilgren.
22 Your paper at page 104 says that the density of
23 Coalinga fiber after twelve months' exposure appeared
24 to be more than six times greater than that found in
25 the Jeffrey-treated macrophages, right?
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1A
Are you talking about the average of the
2 Jeffrey? 3 Q I'm quoting directly from your paper. I 4 quote, "Although the density of Coalinga fiber after
5 twelve months' exposure appeared to be more than six
6 times greater than that found in the Jeffrey-treated
7 macrophages, this was largely due to one exceedingly
8 high, anomalous fiber density reading in a 9 Coalinga-treated animal (table 3)."
10 Do you see that?
11 A 12
I see it. Q Can you show us which animal that is in
13 table 3?
14 A
You want me to tell you which is the anomalous
15 reading that I'm referring to?
16 Q Yes.
17 A
Well, I would say it's the 23.8reading.
18 Q And that isunder the heading Coalinga in
19 the first section at twelve months under alveolar
20 macrophages?
21 A Right.
22 Q So if I could summarize, Dr. Ilgren,
23 because I circled them as you gave your answers,
24 there appear to be three anomalous rats here. The
25 first is --
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1A
You can't say that.
2 Q Well, let me just finish. The first is
3 that under alveolar macrophages three months' exposure
4 in your table 3 at 21.8; the second one is at twelve
5 months' exposure at 23.8 and the third is three months'
6 exposure under interstitial cells at 1.98.
7 MR. WILL: Objection. He said there is
8 three anomalous readings, not three anomalous
9 rats.
10 He told you he couldn't answer the
11 question. Don't answer it. Let him fix it.
12 Q There are three anomalous readings. They
13 may or may not be one rat, two rats or three rats; is
14 that correct?
15 A
That's correct, but that's not what you asked
16 me.
17 Q And you don't know if it was one rat, two
18 rats or three rats?
19 A
That's correct.
20 Q Nor do you set forth any data information
21 or rat number in any of your three papers to tell the
22 reader this is one anomalous rat, two anomalous rats
23 or three anomalous rats?
24 A That's correct.
25 Q Nevertheless, it is upon this one, two or
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1 three anomalous rats that you report that the
2 Coalinga results are higher both at the three-month
3 alveolar macrophages, the twelve-month alveolar 4 macrophages and the three-month interstitial cells?
5 A Right.
6 Q Now, I would like to turn to page 105 of
7 your paper. On the first column about two-thirds of
8 the way down, you are talking about this 223 million
9 fibers that Dr. Davis found in that study that we
10 talked about earlier?
11 A
Dr. Muhle.
12
Q
Dr. Muhle?
"
13 A Yes.
14 Q And you say that a substantial number of
15 fibers, 223 million, noted twelve months post
16 exposure in Dr. Muhle's inhalation study seems to be
17 at odds with some observation.
18 What observation was that?
19 A Six lines above that I note the very low (0.03
20 plus or minus 0.03 mg) post-ashing fiber mass
21 readings observed by these workers, which is Muhle et
22 al.
23 Q So in Muhle's rat inhalation study, when
24 he did this fiber ashing to come up with the asbestos
25 mass in the lungs, he got a low value; but when he
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15 16 17 18 19 20 21 22 23
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1039
actually counted fibers, he got his 223 million; and
you are saying that there seems to be some odds
between those two things?
A Right.
Q And then you continue and I quote, "The
most likely explanation for these apparently
discordant findings is probably a trivial technical
one," right?
A Right.
Q What do you mean by trivial technical
explanation?
A Well, if youread on --
Q I did read on but I couldn't figure it
out.
A Well, what I'm saying is that the 223 million
all sizes or eleven times ten to the sixth is greater
than five microns. The number is probably -- when
you look at that with TEM, it's actually a relatively
small number.
Stated differently, it may also be that
since long fibers contribute more to mass than short
fibers, then what he is actually measuring as long
fibers may not be long fibers.
Q But when he is measuring them by TEM and
counting fibers, he is actually seeing them. That
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1 was not a mass calculation, was it?
2A
I know but it goes to the question as to what
3 he is actually counting, even by TEM, as a long
4 fiber.
5 Q Well, presumably, he is counting fibers, 6 because that's what people do with TEM, isn't it?
7A
Well, one counts structures and the structure
8 may be a complex structure or it may be a single. I
9 don't think you can tell by this.
10 Q Whatever it was that Dr. Muhle saw under
11 this TEM, he reported it in his paper as fibers, 12 right; and you are now speculating, well, it might
13 have been something else?
14 A
Well, let me read through this for one second
15 and then I will return to your question.
16 I think what's going on is there is a
17 discrepancy between what appears to be a very low
18 mass and a high fiber number; and I think one
19 explanation for that is that, as Muhle points out and 20 he says here, "considerable decrease of fiber
21 diameter observed for the Coalinga fibers in lungs
22 compared with fibers in the inhalation chamber, which 23 occurred because of splitting. The splitting
24 produced fibrils that were, in fact, too fine to
25 count and size reliably."
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1 Q Right, which he documented under his TEM,
2 correct?
3A
Right, but the fibrils have very, very little
4 mass, per se. So I think what's happening is that
5 the very low mass dose does not necessarily reflect
6 the increase or this number of fibrils.
7 Q In the Muhle study the Coalinga fibers
8 seen under the TEM, Muhle thinks, might have been
9 much thinner, which attributes to their smaller mass;
10 is that what you are saying?
11 A
Yes.
12 Q But nevertheless, the 223 million fibers
13 that he points out in his paper are counted fibers,
14 although they are thin?
15 A
Right.
16 Q Going back to the anomalous rats whether
17 it's one, two or three, do you know if any of those
18 rats, rat or rats, were the ones that got tumors, as
19 you read in part 2 of your paper?
20 A I would have to go and check. You mean, of
21 the one or two tumors that came in the Coalinga
22 animals?
23 Q Part 2 of your paper is about the tumors
24 and some of the Coalinga rats had tumors.
25 My question is, do you know if any of the
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1 tumors in the Coalinga exposed rats were in those rat 2 or rats described as the anomalous rats in part 3
3 that got the high Coalinga fiber?
4A
No. You mean just sitting here?
5 Q Can you tell by looking at the papers,
6 because paper 2 does actually list rats by rat
7 number?
8A
I can't because I don't have the correlated
9 data in this paper.
10 Q In the abstract of paper number 3, I'm
11 going now to the abstract on the first page, on the
12 fourth line -- actually, the third and fourth line
13 you write, "A short amphibole-free chrysotile from
14 Coalinga, California failed to induce pathological
15 effects whilst the other two, both long fibers from
16 Canada, were both fibrogenic and tumourigenic."
17 Do you see that?
18 A
Yes.
19 Q And you say you have demonstrated that in
20 papers 1 and 2?
21 A
Yes.
22 Q Again, if you look at paper 2 table 1,
23 the Coalinga induced rats had two tumors and three
24 BAH, right; and wetalked aboutthat before?
25 A
Yes, wehave gonethrough that.
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1 Q Basically, in order for the statement in
2 the abstract part 3 to be correct, there shouldn't be
3 the two tumors and the three BAHs in table 1 of part
4 2.
5A
No, there were two tumors in the controls. I
6 have subsequently added that to-be two carcinomas
7 looking at the raw data. I don't think there is a
8 significant increase in tumors above the controls.
9 I don't think there is any difference
10 between the number of tumors in the controls of the
11 Coalinga-treated animals.
12 Q We have gone through that at length. We
13 will let that stand. We won't get into it again.
14 MR. BROWNSON: That's all I have.
15 MR. WILL: I have a couple questions.
16
17 CROSS-EXAMINATION BY MR. WILL:
18 MR. WILL: Mark these please.
19 (A copy of "American Review of
20 Respiratory Disease" Volume 123 dated April
21 1981 is marked as Plaintiff's Exhibit 45 for
22 identification, as of this date.)
23 (A copy of "American Review of
24 Respiratory Disease" Volume 121 dated April
25 1980 is marked as Plaintiff's Exhibit 46 for
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1 2 3 4 5 6 7 8 9
10
11 12 13 14 15 16 17 18 19 20 21 22 23 24 25
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1044
identification, as of this date.)
Q Dr. Ilgren, the first thing I want to ask
you is, you were asked a question by Mr. Brownson
about whether the anomalous rat at twelve months in
terms of the fiber density and the alveolar
macrophages that had been exposed to the Coalinga
fiber whether that rat more than six times increased
density compared to the Jeffrey; do you remember that
question?
A Yes.
Q When you said six, is that comparing the
averages of the two exposed groups?
MR. BROWNSON: Objection, leading. You
already clarified that.
MR. WILL: That was a different question.
MR. BROWNSON: I will agree with you. It
was not the anomalous rat that had six times
more. It's the Coalinga group which had six
times more, which he attributes largely to
that anomalous rat.
MR. WILL: That's not the question you
asked.
-
Q Let me put it this way. Look at table 3,
alveolar macrophages. If you compare the average for
the group Coalinga versus the average for the Jeffrey
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1 group, ia that where you get the six times difference?
2 A At twelve months?
3 Q Yes.
4 A Yes.
5 Q Obviously if we were comparing the
6 relationship between the value for the anomalous rat,
7 we could get a different number than six?
8A
Yes.
9 Q You were asked whether the three
10 so-called anomalous readings came from the same rat
11 or different rats. 12 What, if anything, can you tell about
13 that question, based on the dates of the readings?
14 A
You meanthree,
twelve or twenty-four months?
15 Q Three or twelve months, yes?
16 A
Well, the correct answer is that it would have
17 to be at least two rats, because you wouldn't have
18 the same rat at three months and twelve months. They
19 are killed at three months.
20 Q And with respect to the two rats that
21 were found to have the tumors, do you know anything
22 about what their sacrifice date was?
23 MR. WILL: I'm going back to page number
24 2, Mr. Brownson.
25 Q Do you know anything about the sacrifice
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1 date of those rats, just based on the fact that they
2 had tumors?
3A
I don't believe any of the rats had tumors at
4 three or twelve months. So it couldn't have been
5 either of those.
6 Q So based upon those assumptions, the
7 anomalous rats would not be the ones that developed
8 tumors?
9A
That's right.
10 Q Let me show you what I have marked as
11 Exhibit 45. Can you tell me briefly what that is?
12 A
This is the abstract by Pinkerton et al., lung
13 injury patterns in rats.
14 Q And what's the date of that one?
15 A April 1981.
16 Q Is that the document Mr. Brownson showed
17 you earlier?
18 A
Yes.
19 Q Let me show you what I had marked as
20 Exhibit 46 and ask you what is that?
21 A
This is morphologic lung changes following
22 exposure to chrysotile asbestos fibers by Pinkerton
23 et al. published April 1980.
24 Q Now, Mr. Brownson asked you some
25 questions about the statements in the abstracts by
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1 Dr. Pinkerton that refer to injury.
2 Do you recall those questions?
3 A Yes.
4 Q Why is it that you would not call the
5 reported changes an injury?
6 A They are not irreversible. There is no
7 evidence that they are irreversible, nor is there
3 clear evidence that they manifest overt fibrosis and
9 tumor formation.
10 Q Are you doubting that Dr. Pinkerton, in
11 fact, observed the characteristics that he reports in
12 the abstracts?
13 A Not at all.
14 Q Have you observed and reviewed the same
15 tissue slides that he is talking about here?
16 A
Yes.
-
17 Q Did you observe the changes or the
18 conditions that he remarks upon?
19 A
Well, let's step back. When you say I
20 observed the same slides and the same conditions, I
21 mean, X understand he is saying there is injury based
22 on an increase in value and number of alveolar type
23 II cells and an increase in interstitial matrix after
24 three months; but I didn't look at any of the
25 materials under a TEM microscope. So I haven't, to
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1 that extent, looked at the material, no.
2 Q Did you look at them under an SEM
3 microscope?
4A
Yes -- no, actually after three months there
5 was no available material.
6 Q Was there after twelve months?
7A
No, there was available for end of life.
8 Q To get back to where I was, are you
9 disputing that Dr. Pinkerton saw the physical
10 characteristics that he reports in the abstract?
11 A
No.
12 Q How would you characterize those physical
13 characteristics?
14 MR. BROWNSON: Well, that's been asked
15 and answered.
16 THE WITNESS: I don't think that's been
17 asked and answered at all.
18 MR. BROWNSON: Well, go ahead and answer
19 it; but I think it has been.
20 A
I think the reactions to the presence of an
21 irritating material administered to animals in very
22 high doses for a long time.
23 Q Is that reaction or response specific to
24 asbestos?
25 A
Not at all.
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1 Q Let me turn your attention to Exhibit 46
2 to the early part of the abstract; and there is a
3 statement in it that says, "Greater than ninety
4 percent of the fibers in both groups are less than
5 five microns in length, but the mean fiber mass in
6 the intermediate range fibers is 45-fold greater due
7 to the presence of a larger number of long fibers in
8 that chrysotile preparation."
9 Did I read that correctly?
10 A Yes.
11 Q What do you understand the intermediate
12 range fibers to be?
13 A Jeffrey. 14 Q What about the UICC/B, what do you
15 understand that to be?
16 A That's not here.
17 Q How does the concept of fiber mass relate
18 to the concept of fiber number, if at all?
19 A
Well, long fibers contribute far more to mass
20 than tiny small fibers.
21 Q Does the fact that an animal got a
22 greater mass of Jeffrey fibers than Coalinga fibers
23 necessarily mean that the animal got more Jeffrey
24 fibers than Coalinga fibers?
25 A
Well, as stated, it suggests that the animals
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got a larger number of long fibers.
Q As you understand it, did the animals
receive a higher mass of Jeffrey asbestos than
Coalinga asbestos?
A No, it's stated right here. They got three
times higher mass dose of Jeffrey than Coalinga.
Q The fact that they got three times higher
mass dose of Jeffrey than Coalinga, does that mean
that they got three times as many fibers of Jeffrey
them Coalinga?
A You mean long fibers or short fibers?
Q All sizes.
A Presumably, yes. Presumably that if they got
a greater mass dose, they would have gotten a greater
number of fibers of all sizes.
Q Does that depend upon the mass of each
particular fiber?
A Yes.
Q So it's possible to have more fibers of
Coalinga if they are smaller in mass, as we were
talking about before?
MR. BROWNSON: Objection to that last
question as leading.
You can't impeach your own witness.
A I think what one has here is -
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1 Q Doctor, I just want you to answer my
2 question. The question is, does the size of the mass
3 necessarily dictate the number of fibers?
4 A No.
5 Q Is it possible to have more fibers in a
6 smaller mass of asbestos than in a larger mass of a
7 different kind of asbestos?
8 A Yes.
9 Q Can you tell from the data here whether
10 there were necessarily more Jeffrey fibers or more
11 Coalinga fibers?
12 MR. BRQWNSON: That's been asked and
13 answered.
14 A No.
.
15 Q Directing your attention to the last five
16 lines of Exhibit 46. The sentence there beginning on
17 the fifth line says, "In addition, light microscopy
18 revealed a greater degree of fibrosis and
19 hypercellularity in the perivascular and
20 peribronchial interstitium of the animals exposed to
21 intermediate range fibers."
22 Did I read that correctly?
23 A Yes.
24 Q What type of fiber do you understand that
25 to refer to?
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1A
Jeffrey.
2 Q In terms of the reaction, response in
3 this rat tissue that you described earlier, is it
4 possible that some of that is reversible?
5 A Sure. Well, that'swhat the datashowed,
6 resolution. We have evidence of reversibility.
7 Q With which type of exposure?
8
A
With Coalinga, largelywithCoalinga
and there
9 is a certain degree of resolution with all three
10 types; but it's most marked with Coalinga.
11 Q You were asked some questions about your
12 characterization of the Coalinga as a short fiber.
13 Do you recall that?
14 A 15
Yes. Q What do you mean in terms of
16 characterizing asbestos as short?
17 A
The size cut
off.
18 Q I'm asking what you mean when you talk 19 about asbestos as being short. What do you mean? 20 What's your definition?
21 A Less than five to eight microns in length. 22 Q Does that mean that every single fiber in
23 the sample would be less than five to eight microns?
24 A No. 25 Q What does that mean then?
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1A
A predominance, something is predominantly
2 short. 3 Q The fact that there may be some Coalinga
4 fiber longer than five to eight microns, does that
5 suggest to you that your characterization of it as
6 short is an error?
7 MR. BROWNSON: I object as leading.
8 A No. In direct preparation it's clear. There
9 is some there.
10 Q You were asked some questions earlier
11 about this Muhle study that used TEM for the
12 twenty-four month counting while using SEM for the
13 prior count; do you recall that?
14 A
Yes.
15 Q What is the difference in sensitivity or
16 resolvability, if you will, of TEM as opposed to SEM?
17 A
It's my understanding that with SEM you can't
18 resolve things that are less than 0.2 microns in
19 width, whereas with TEM, these can be seen.
20 Q In terms of a comparison of the numbers
21 of fibers that you could observe with TEM versus SEM,
22 is there a standard factor or conversion number?
23 A
My understanding in a very, very general sense
24 would be something like ten to a hundred to one; but
25 again, I would have to check that.
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1 Q It would be ten to one hundred fibers
2 visible under TEM compared to one visible under SEM?
3 MR. BROWNSON: Object to the form of the
4 question as leading. He also said he didn't
5 6 7A
know. Q Is that your understanding? Yes. If Muhle is saying that the splitting is
8 causing most of the Coalinga in the lung to become
9 fibrils, fibrils are going to be less than 0.2
10 microns in width.
11 Q You were asked some questions earlier 12 this morning about the Waggoner case out in 13 California and you were asked about whether policeman
14 Waggoner was alleged to have any asbestos exposure, 15 other than what he got from driving around in his
16
police car.
Do you recall that?
17 A
Yes.
18 Q To your understanding, what were the
19 other asbestos exposures that policeman Waggoner was
20 alleged to have had?
21 A Manipulating or cutting transite pipe, working
22 with drywall and other construction-related exposure,
23 either directly or indirectly. I don't recall
24 exactly.
25 Q Do you have an understanding of whose
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1 transite pipe that was?
2A
I think it was JM, but X can't remember.
3 Q Assuming that it was JM, do you have
4 knowledge about what type of fiber was used in JM
5 transite pipe?
6 MR. BROWNSON: Do you know this, Dr.
7 Ilgren?
8 THE WITNESS: Yes, I do actually.
9 MR. BROWNSON: He doesn't know what
10 exposure this policeman had.
11 THE WITNESS: He didn't ask me what the
12 exposure the policeman had. He asked me about
13 a product composition that is in various
14 Answers to Interrogatories in certain cases.
15 A
Chrysotile is not an uncommon component of JM
16 transite pipe.
17 Q From your own personal knowledge, do you
18 know where that chrysotile came from?
19 A
Not infrequently from Australia.
20 Q From the Wittenoom deposit?
21 MR. BROWNSON: Objection, leading.
22 Q Where in Australia, then?
23 A
The Wittenoom deposit.
24 Q You were asked a question by Mr. Brownson
25 regarding the mineralogical composition of
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1 chrysotile. I know you are not a mineralogist. 2 MR. BROWNSON: You are disqualifying him 3 right from the question.
4 Q I'm not trying to ask you a terribly
5 technical question. 6 What is your understanding about whether 7 all chrysotile are the same mineralogically?
8 MR. BROWNSON: Objection to the form.
9A
10
They are not. Q Is there anyplace in your paper where
11 you, in either of the three papers, where you 12 indicate what length cut off you were using for long
13 versus short?
14 A
Yes.
"
15 Q Where is that?
IS A
I think it's in the beginning of the part 1 or
17 part 2. I think it'sactually in theabstract or
18 perhaps in the fibrosis paper.
19 Q Is that part 1?
20 A
Part 1.
21 Q I'm showing you a copy of part 1, which
22 was previously marked as Exhibit 36.
23 A
Well, I refer to greaterthan
five toeight
24 microns in length.
25 Q As being long?
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1A
Yes.
2 MR. GOLDMAN: What line and what page?
3 THE WITNESS: Line 3, page 265 part 1.
4 Q In the scientific literature, are there
5 papers that characterize Coalinga as being either
6 long or short?
7A 8
Yes. Q What is the characterization in the
9 literature?
10 A
That it's a short preparation.
11 Q Can you identify some authors that have
12 characterized Coalinga as a short fiber?
13 A
Langor et al. 1978; Yaeger, et al. 1983;
14 Campbell et al. 1980; Siegrist and Wyle 1979; Wyle
15 1980, among others.
16 MR. BROWNSON: Name the others. .
17 THE WITNESS: I can't recall at the
18 (noinsnti
19 Q Those are the ones that you can recall 20 off the top of your head?
21 A 22
Yes. Q First of all, we marked as Exhibit 45 and
23 46 two of the Pinkerton abstracts, correct?
24 A
Yes.
25 Q Are there any other Pinkerton abstracts?
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1A
2
There is one other. I think there are three. Q Do those abstracts present the set of
3 data that you do in your three papers?
4 A No.
5 Q Do the abstracts present any data at all
6 between the twelve and twenty-four month period?
7 A I have to look. 8 Q Fine. We won't go back and review that.
9 You don't recall?
10
A
I don't recall.
I think one might, but I
11 don't recall.
12 Q We can look at' them to see, right?
13 A Yes.
14 Q Mr. Brownson asked you with respect to
15 your earlier papers 1 and 2 about the differing
16 numbers of the rats that were on tests; do you recall
17 that?
18 A Yes.
19 MR. BROWNSON: Wasthat today Iasked
20 that?
'
21 MR. WILL: No, you asked him that the 22 last time; but since I never had a chance to
23 ask questions the last time, I'm asking now.
24 Q And the question I have for you is, how
25 many sources of data are there for giving numbers for
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1 rats on. teats?
2A
Half a dozen, at least.
3 Q Are those different sources of data
4 consistent in terms of the number of rats they
5 report?
6 MR. BROWNSON: Who reports? I'm
7 3A
confused. I mean, there is inconsistencies in the
9 reporting.
10 Q Do you have this data somewhere in your
11 files?
12 A
Yes.
13 Q Did you have it with you at the
14 deposition when Mr. Brownson was asking you about
15 whether it was 320 or 330 or 360 rats?
16 A
No.
17 Q When you were answering the questions
18 from Mr. Brownson last time, were you going, then, as
19 best as you could from your memory?
20 A Yes. 21 Q I want to direct your attention to table 22 1 of your paper number 2, which was previously marked
23 as Exhibit 37. This reports animals with tumors; is
24 that correct?
25 A Yes.
.
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1 Q Was this data previously reported in 1984
2 by the NIEHS publication?
3A
It was presented by the NIEHS for the
4 untreated controls and for the UICC-treated animals.
5 Q Not for the Coalinga or the Jeffrey?
6A
Correct.
7 Q As for the controls and the UICC animals,
8 are the same slides and the same animals presented in
9 your table 1 that were presented by the NIEHS in
10 1984?
'
11 A Yes.
12 Q Let me direct your attention to table 8
13 of paper 1, which was Exhibit 36. In terms of the 14 rats that are represented in table 8 of paper 1, is 15 it your understanding that there were eighty rats
16 there?
17 MR. BROWNSON: Where?
18 A Eighty rats where?
19 Q Did you look at the -
20 A I looked at Coalinga COP-25. 21 Q There are ninety rats in that group, 22 correct?
23 A As stated there, yes.
24 Q I know you said earlier you did not look
25 at the slides of the animals that Pinkerton killed or
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1 sacrificed at three, twelve and twenty-four months, 2 correct?
3A 4
They weren't available. Q And those are the rats that were looked
5 at for the morphometric analysis?
6A
Yes, and for morphological analysis, for both.
7 Q To your knowledge, was any tumor reported
8 in any of those animals that were sacrificed at
9 three, twelve or twenty-four months and were exposed
10 to Coalinga?
11 A
12
No. MR. WILL:Give me two
minutes and then I
13 think I'm done. 14 (A short recess is taken.)
15 Q Dr. Ilgren, I want to ask you, putting
16 aside for a moment the question of comparing TEM to
17 SEM counts and just taking the numbers at face value
18 as they are reported in Muhle's paper, in your
19 opinion, what, if anything, does that data show about
20 the clearance of Coalinga chrysotile?
21 A
The mass data shows it'scompletely gone.
22 There is a small residue.
23 MR. BROWNSON: 223 million fibers.
24 THE WITNESS: I don't consider that
25 reflective at the moment.
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1 MR. WILL: He talked about mass not 2 fibers.
3 Q But aside from Mr. Brownson's 4 interruption of your answer, you were talking about
5 mass. Are you finished with that?
6A
Yes.
7 Q And even if we look at number of fibers,
8 again, forgetting about the difference between TEM
9 and SEM, what does Muhle's data show with respect to
10 the number of fibers?
11 A
Well, you have apples and oranges. You look
12 at them using one technique and you will see a
13 radical drop-off between the twelve and twenty-four
14 time point.
15 Q Even using different techniques, do you
16 see any change over that period?
17 A
You do.
18 Q I want to ask you this, Dr. Ilgren, to a
19 reasonable degree of medical certainty, in your
20 opinion, what does all of this data set forth in 21 paper 1, 2 and 3 mean, if anything, about Coalinga
22 fiber?
23 A
It doesn't -- there is near total clearance.
24 So it doesn't biopersist and that accounts for the
25 fact that it doesn't induce fibrosis in tumors.
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MR. GERSON: It being the Coalinga fiber?
THE WITNESS: The Coalinga fiber.
MR. WILL: Subject to anything Mr.
Brownson may have for you on recroas, that's
all I have. Thank you.
MR. BROWNSON: I have nothing further.
(Time noted is 4:35 p.m.)
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CERTIFICATE
1064
I, EVAMARIE WALSH, a Notary Public and Shorthand Reporter, do hereby certify that prior to the commencement of the examination
DR. EDWARD ILGREN
was sworn by me to testify to the truth, the whole truth and nothing but the truth.
I DO FURTHER CERTIFY that the foregoing is a true and accurate transcript of the testimony as taken stenographically by and before me at the time, place and on the date hereinbefore set forth.
I DO FURTHER CERTIFY that I am neither a relative of nor employee nor attorney nor counsel for any of the parties to this action, and that I am neither a relative nor employee of such attorney or counsel, and that I am not financially interested in the action.
Notary Public
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1
CERTIFICATION
OF WITNESS
2
3 I have read the foregoing transcript of my
4 deposition and find it to be true and accurate
5 to the best of my knowledge and belief.
6
7
8
9 DR. EDWARD ILGREN
10
11
12
13 Sworn and subscribed to before me on
14 the
day
15 of
, 1999
16
17
18
19 Notary ______________________
20 My Commission Expires
21 22
23
24
25
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