Mark Hickey said:Bob said:What struck me about all the replies in the thread was that I didn't
see even one post that acknowledged that the results quoted were from
*validation* tests. IOW, the researchers weren't testing the samples.
They were testing the test itself. I'm no scientist but as I recall the
"scientific method" I was taught years ago until a new scientific test
is proven to produce accurate, verifiable, and repeatable results its
results aren't considered proof of anything. Since the tests performed
are in no way verifiable or repeatable- the B samples were exhausted by
the tests, right?- I have to wonder why the researchers chose to even
perform them. Was there grant money at stake?
And I have to wonder WHY did the "anonymous" sample results get
matched up with other documents. Someone obviously had an axe to
grind.
We can assume their motives and actions were as pure as the driven
snow, or we can look at the record to see if those involved had any
history of trying to pin unsupportable accusations on Lance. Well,
I'll be.... they did!
Given a choice to believe an athlete who has been tested over many
years many, many times - and some clandestine witch hunters, I'd put
my money on Lance's side of the facts. There are just too many
questions that haven't (and probably can't) be answered...
1) Was it actually Lance's sample?
From a sample in the freezer to a number on a result sheet there is
potential for, say writing the info on the wrong line, or pipetting sample
4 into sample 5's cuvette. To do that several times seems unlikely, but
that's why there's and A and B sample.
Quoted message said:2) Is the test accurate (what's the potential for false positives)?
Since we're testing the migration of a protein in a gel, and there are lots
of proteins which may migrate similarly, that proves the need for a control
sample run, and not only that, but run with every plate also. Typically a
plate would have a low, medium and high control run, taking up three slots,
and then the remainder of the slots for unknowns.
Quoted message said:3) How long would aggressive EPO treatment during chemotherapy stay
detectable in the blood with the new test (and with a world class
athlete's peculiar body chemistry)?
I believe the time frame is a matter of weeks, not of months - so this is
not likely, -but- we don't know how long he was taking the medically
prescribed EPO either. If he did the Tour in July 99, one would imagine
that the treatment for his disease would have been completed by July 98, to
allow him to train properly, but no one knows how long he took medically
approved drugs of any kind, even other than EPO.
Quoted message said:4) What was the chain of custody for these samples from SO long ago?
Normally it's very tight while the initial samples are being
taken/tested - but six or seven years of storage? Who knows? It
seems like it would be possible to at least do DNA (or other
appropriate) testing on the samples to verify that they were even
Lance's - or possibly check to see if they'd been altered.
I agree, the chain of custody has to be very weak and they'd be unable to
support it if challenged. If the chain of custody is broken on not
contiguous, then the evidence wouldn't even be admissible, imo.
Quoted message said:5) Are there other "reliable" tests for EPO, and any other samples
from 1999 from Lance around?
Common sense says doubtful any samples from Lance still exist with the
above criteria; proper storage; concurrent storage of standards; chain of
custody..
Quoted message said:6) Is there any indication from Lance's hemocrit history that would
provide any statistical evidence that, everything else being
considered, his hemocrit trend showed some sort of increase during
that period. I know a person's hemocrit level varies (Robert), but
presumably one would only take a banned substance if it would produce
a measurable result. If Lance's 1999 hemocrit levels fall well within
the expected range since then, one can only assume that either he
didn't take EPO, or it had very little effect.
My understanding is that it's common to give saline infusions to make sure
the blood is diluted to under 50 - I've heard that there was some warning.
I don't think they'd be able to test Hcts after a grueling 5-6hr ride when
everyone would be somewhat dehydrated, but dilution with saline isn't a
long-lasting solution - by the next day that saline would be excreted.
There may be solutions that would also dilute the blood which might not be
excreted too quickly, say an albumin/saline mixture.
Good points.
jj
Quoted message said:
Mark Hickey
Habanero Cycles
http://www.habcycles.com
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