This article from NYTimes.com 
has been sent to you by [email protected].


CSers
I'm imagining that in weight loss pills the powers that be have an easy target 
against dietary supliments.  I'm also noting that the New York Times is now 
referring to itself as *the world's* newspaper of record.
Reid

[email protected]

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Studies of Dietary Supplements Come Under Growing Scrutiny

June 23, 2003
By FORD FESSENDEN 




 

When a California judge handed down a $12.5 million
false-advertising judgment against the maker of an
ephedra-based weight-loss pill late last month, he also
issued what amounted to a bill of reproach against the
science of dietary supplements. 

The company, Cytodyne Technologies, maker of Xenadrine
RFA-1, the supplement implicated in the death of a
Baltimore Orioles pitcher, had not just exaggerated the
findings of clinical trials it commissioned, Superior Court
Judge Ronald L. Styn said in ruling on a class-action suit,
but had also cajoled some researchers into fudging results
in published scientific articles. 

The evidence, Judge Styn said, had left him no alternative
but to conclude that the researchers had set out to create
a study that "justified the money being spent" by Cytodyne
and would ensure that they received further work from the
company. 

The Cytodyne case is part of a swelling tide of litigation
that is raising serious questions about the way makers of
ephedra and other dietary supplements use - and often
misuse - the promise of scientific proof to market their
products. 

In the last eight months, three leading manufacturers of
weight-loss pills have been hit with false-advertising
verdicts in the millions of dollars. A fourth has been
rebuked by a federal judge for hiding evidence. The
Missouri attorney general and a group of district attorneys
in California have also brought false-advertising suits
against manufacturers, and Congress has demanded Cytodyne's
research records. 

Under pressure in the courts and from regulators, a number
of manufacturers, including Cytodyne, have refashioned some
of their weight-loss products without ephedra. Just this
month, legislative leaders in Albany agreed to make New
York the second state to ban ephedra, after Illinois, and
the federal government is considering its own ban. 

But experts say a switch in ingredients does nothing to
alter the industry's reliance on questionable science. In
fact, they say, they are especially concerned because there
is so little rigorous research on the new ephedra
substitutes, primarily a substance called synephrine. 

The truth is, supplement makers are not obliged to do any
research. A 1994 law exempts them from having to prove, as
drug manufacturers do, that their products are harmless and
effective. But at a time of concern about the safety and
effectiveness of its products, the $18 billion-a-year
supplement industry has embraced research because, when
carefully aimed, it can be worth money. 

Precisely because the industry is not regulated, though,
its research is sometimes less than strictly scientific,
experts say. 

"There will be 250 to 300 clinical trials on nutraceuticals
this year," said Anthony Almada, a consultant and founder
of EAS, the biggest sports nutrition company, who advocates
scientific research on products but has become a critic of
the way supplement makers conduct it. "The rigor applied in
these studies on the average is somewhat notably less than
that of a drug study." 

Often relying on as few as a dozen subjects, these studies
are scaled-down versions of the double-blind,
placebo-controlled clinical trials required before drugs
can be approved. Some are published in abbreviated form at
meetings of scientific organizations, or in obscure
journals, providing a basis for marketing claims like
"clinically proven." 

An industry spokesman, Steven Dentali, vice president for
science and technical affairs at the American Herbal
Products Association, acknowledged that "whenever there's a
desired outcome, you've got the potential for bias." At the
same time, he argued that supplement science is no worse
than that done for pharmaceuticals. 

"There's an interest in making sure you do good science and
representing it properly because there's a spotlight on the
industry," Mr. Dentali said. 

Ambiguous Findings 

Even the best available science about ephedra is ambiguous.
The Food and Drug Administration has collected reports
linking it to more than 100 deaths. But by and large, the
studies done have been too small and too limited - using
only healthy subjects - to assess the actual danger. In
March, the RAND Corporation issued an analysis combining
the results of the many small studies; the analysis found
evidence that ephedra works for weight loss in the short
term, but can produce numerous cardiac side effects. 

Documents from the lawsuits, including e-mail
correspondence and detailed experiment records, provide an
inside look at how, for the supplement makers, the demands
of marketing have sometimes compromised those of science.
They show how companies and researchers suppressed negative
data; removed product names from abstracts when the
conclusions showed no positive effects; changed statistical
methods to see if results improved; and left out subjects
who complained of troublesome side effects like heart
palpitations and high blood pressure. 

For example, an e-mail message in the Cytodyne lawsuit
shows how the company tried to influence one researcher. 

The researcher, Jeffrey Armstrong of Eastern Michigan
University, had refused to rewrite a journal abstract the
way the company wanted, according to testimony, and Tim
Ziegenfuss, the consultant who commissioned the study on
behalf of the company, said he would try to change Dr.
Armstrong's mind. 

"As far as rewriting the abstract, since I am not
recognized as a co-author on the study I am not allowed to
do it," Dr. Ziegenfuss said on November 2000 in an e-mail
message to a company official. He added, "In this case the
best I can do is try to carefully nudge his
interpretation/writing in Cytodyne's favor." 

Cytodyne was unable to budge Dr. Armstrong - "I will not be
intimidated," he said in an e-mail message after being told
that the company was threatening to sue him. But in another
message, Dr. Ziegenfuss suggested that the study could
still be marketed. 

"Let Jeff do his hum-drum `science' thing," he said.


"This will portray Cytodyne in an objective, favorable
manner to the scientific community," he added. "This is
particularly important now considering the recent bad press
on ephedrine. And then since Jeff has no control over the
use of data in ads, use percentage changes there to impress
consumers." 

The company did, turning a modest 3.1-pound average weight
loss over several weeks into exclamatory copy saying that
Xenadrine users lost 759 percent more weight than nonusers.


Cytodyne's lawyer, Brian Molloy, said the company had not
threatened to sue Dr. Armstrong. E-mail messages to that
effect, he said, were a "poor effort to get Armstrong's
attention." 

Mr. Molloy said that he feared court action would
discourage future research on supplements. "Having more
studies on dietary supplements is generally a good thing,"
he added. 

Before and After 

One company, a Canadian concern called Muscletech Research
and Development, commissioned a number of studies in 2001,
when the ephedra industry was beginning to come under
pressure from regulators. Muscletech, maker of an
ephedra-and-caffeine weight-loss product called Hydroxycut,
was then in the midst of a major advertising campaign. The
splashy advertisements in magazines like Men's Health and
Self needed a flow of copy. Like Cytodyne's, those
advertisements featured personal testimonials and
before-and-after photographs - and, often in big type, the
results of trials. 

Muscletech documents from a federal lawsuit in Oklahoma
show how studies would be massaged for advertising copy.
One study, for instance, found that Hydroxycut users lost
15 pounds of fat mass in 12 weeks, while those taking a
placebo lost 10. In an internal memorandum accompanying the
study, a Muscletech official warned, "None of these results
can be deemed significant," adding that "Hydroxycut can't
be claimed as superior" to the placebo. To get around that,
the official proposed that copy writers simply say, "Lose
15 lbs. of fat in 12 weeks with Hydroxycut and exercise!" 

Another study, by Carlon Colker of Peak Wellness, a
Greenwich, Conn., practice that runs trials on dietary
supplements, found that Hydroxycut had no apparent effect
whatsoever. That study simply went unpublished. 

"We are quite surprised at the lack of positive results
from this study," Dr. Colker wrote to Muscletech after his
trial of a new product that added green tea extract, a
caffeine source, to Hydroxycut's ephedra and caffeine
recipe. 

Dr. Colker declined to comment, other than to say through
his lawyer that he stood behind his work. 

'The Data Are Buried' 

Suppression of study results is a
common practice in the dietary supplement industry, said
Mr. Almada, the consultant. "You wouldn't believe how many
studies are done on products like that and the data are
buried," he said. 

Jeff Bauer of Springfield, Mo., the lawyer who sued
Muscletech in the Oklahoma case, agreed. "They don't have
to turn the data over to anyone," he said. "It's the Wild
West of D.S.H.E.A." - a reference to the 1994 law on
dietary supplements, the Dietary Supplement Health and
Education Act. "If they had people dying, I don't think
they'd have to tell anyone." 

Muscletech was also unhappy with another study, by the
University of Guelph in Ontario, that found Hydroxycut did
not "burn fat," a claim made by many companies that sell
ephedra. The company was unable to keep Guelph from
publishing the results, but demanded that its product name
be removed from publications. 

The most problematic study came next, court records show.
Four subjects dropped out and were replaced, complaining of
symptoms like heart palpitations and high blood pressure.
Four more had to lower their doses, two under doctors'
orders. 

When this study generated no strong scientific claims -
Hydroxycut users lost more weight, but the numbers were not
statistically significant - the company demanded new data
omitting the dropouts. That kind of analysis is widely
considered scientifically inferior. Although the principal
researcher, Douglas Kalman, at first resisted, he was
eventually persuaded. 

"That's unacceptable," Dr. Marcia Angell, a former editor
of The New England Journal of Medicine, said in a recent
interview. 

"You don't change your protocol as you go along," added Dr.
Angell, who reviewed the court records at the request of
The New York Times. "And you certainly don't do it to
satisfy someone with a commercial interest in the outcome."


In the end, the published abstract ignored the four
dropouts and said the product was safe - precisely because
it had not raised blood pressure or heart rates. 

Those problems with the study were also initially hidden
from the court in documents that, days before trial, were
found to have been altered. The company's obfuscation so
angered Judge Robin Cauthron of district court that she
refused to honor a confidentiality agreement when the suit
was settled in January. 

Muscletech declined to comment on most specific issues, but
said through its lawyer, Thomas Ringe III of Philadelphia,
"Muscletech is proud of its record of providing to its
customers a range of high-quality dietary supplements that
have enabled thousands and perhaps millions to achieve a
better level of fitness." 

Jon Whitcomb, Mr. Kalman's lawyer, defended the process.
"It is common during the course of a study to analyze data
and results in different ways," he said in an e-mail
message, "and in this instance Muscletech requested more
than one evaluation." 

Mr. Kalman and Dr. Colker were also involved in the
Cytodyne study that the California judge said he believed
had been designed to justify the money spent by the
company. In that study, reported in the journal Current
Therapeutic Research in April 2000, Mr. Kalman said
Xenadrine users lost significantly more weight than people
who took placebos. But the statistician's report on which
it was based, produced at the trial, showed that the weight
loss was not significant, or only marginally so. 

Mr. Kalman said at trial that the claims of significance
were typographical errors. He testified that he remembered
sending a correction to the journal, but Mr. Whitcomb said
he later acknowledged he had not. 

More important, several of the more seriously overweight
subjects dropped out during the course of the study. The
statistician left them out of his analysis of average
weight loss, according to testimony. Mr. Kalman, in a table
in the study, used those overweight subjects to calculate
the average weight at the beginning of the study, but not
at the end - serving, the judge said, to exaggerate the
appearance of weight loss among Xenadrine users. 

Mr. Whitcomb said the judge misunderstood the calculations,
and cited another judge's decision in a 1999 lawsuit, which
found the analysis legitimate. But experts said Mr.
Kalman's methods were scientifically indefensible. 

"That's not justifiable on any statistical basis," said Dr.
Stan Heshka, a methodology and statistics specialist at the
New York Obesity Research Center and co-author of a 2000
study on the science of weight-loss alternatives. He added,
"I would say it would be a deceptive analysis." 

Mr. Whitcomb said: "There's no such thing as a perfect
study. Despite any of those perceived deficiencies, the
bottom line is the conclusions still hold up. The product
was safe and effective within the confines of the study." 

The exaggerated - in Judge Styn's estimation, false -
assessment of weight loss made it into dozens of Xenadrine
advertisements, and proved critical to his
false-advertising ruling. 

"The statements of 9 percent decrease in weight are false
and misleading and were known or should have been known by
defendant to be so," Judge Styn said. "It appears that Mr.
Kalman went through and picked and chose the data which
would give the most favorable results."

http://www.nytimes.com/2003/06/23/national/23DIET.html?ex=1057370714&ei=1&en=7e486f6875f0362c


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