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L.A.
Times front-page story on St. John's wort
Monday,
August 31, 1998
Remedy's U.S. Sales Zoom, but Quality Control Lags
St. John's wort: Regulatory vacuum leaves doubt about potency, effects
of herb used for depression.
By TERENCE MONMANEY, Times Medical Writer
It is the fastest-growing "alternative" in a nation increasingly
enchanted with unconventional and unproven treatments. A million or
more Americans have lately tried St. John's wort, an herbal remedy
for depression with 1998 retail sales estimated at $400 million--up
3,900% since 1995.
Already the leading antidepressant in Germany, where clinical studies
have suggested it can ease mild or moderate depression, it cannonballed
onto the American self-help scene last year after being hailed as
"nature's Prozac."
But independent laboratory tests commissioned by The Times raise questions
about whether consumers are getting what they pay for. Three of the
10 brands of St. John's wort tested--including a brand from the nation's
leading supplement distributor--had no more than about half the potency
listed on the label. Four more had less than 90% of the indicated
potency, according to the laboratory.
A Cautionary
Perspective
If the basic findings are representative of the dozens of St. John's
wort supplements now on the U.S. market, it would suggest that Americans
are spending millions of dollars on products that do not live up to
their claims, health experts say.
Moreover, a significant number of depressed people may be laying hopes
on products too weak to help them even when taken at the recommended
dosages, medical researchers say.
"How is it possible to appropriately regulate a treatment regimen
if you can't even be sure of the dosage?" said Dr. Norman Rosenthal,
a research psychiatrist at the National Institute of Mental Health
and a strong believer in St. John's wort's mood-elevating properties.
"You're using this [product] for important reasons and you want
to know you're getting what you're supposed to be getting," he
said after reviewing results. "It's quite important that there
should be truth in advertising."
Issues raised by the Times-commissioned study offer a cautionary perspective
on the booming U.S. herbal market. Sales of St. John's wort and other
formerly exotic botanical remedies, including ginseng, ginkgo biloba,
echinacea and saw palmetto, may reach $4.3 billion this year, according
to Nutrition Business Journal.
One source of concern is that, unlike pharmaceutical drugs, herbal
supplements do not undergo government scrutiny before marketing.
The Food and Drug Administration can seize dietary supplements that
turn out to be harmful, fraudulent or improperly promoted. But lax
pre-market government oversight means that consumers have less than
the assurance of product quality they expect of medications, said
Sally Guthrie, a University of Michigan pharmacy professor.
People taking St. John's wort cannot "be assured from batch to
batch and manufacturer to manufacturer that they're getting the same
quality or amount," she said.
The Times commissioned the St. John's wort analysis--among the first
to be published--to check the consistency of retail products. For
the analysis, 10 pills were sampled from each of three containers
of one lot of each product. Each product was identified only with
a code, so the laboratory would not know the brand being tested.
Such a limited sampling is not designed to support broad conclusions
about the quality of any particular product. But experts say it is
sufficient to highlight questions that many researchers and herb industry
officials have raised about the reliability of St. John's wort supplements.
In the test, one of the lowest-scoring products sampled, with about
20% of the labeled potency, was from Sundown Herbals, a division of
Rexall, the nation's No. 1 distributor of dietary supplements.
Informed of the results, Deborah Shur Trinker, Sundown's vice president
of regulatory affairs, said they were "false" and "misleading."
Trinker, in a letter to The Times, argued that the tests involved
too few pills for the findings to be significant. Trinker also argued
that chemical ingredients specific to Sundown's brand might interfere
with the analysis, giving an artificially low reading. Finally, she
stated that an independent lab hired by Sundown had found the product
to be 100% potent.
However, The Times arranged for a second lab to analyze the capsules.
That lab's findings were consistent with The Times' original results.
Two of the other low-scoring companies, Pure Source and Futurebiotics,
declined to comment on the results.
No
Standards Established
The herbal industry currently gauges the potency of St. John's wort
by measuring the concentration of a family of compounds in the herb
known collectively as hypericin. The lab commissioned by The Times,
Flora Research of San Juan Capistrano, used the hypericin-measuring
method adopted by health authorities in Germany, who have extensive
experience analyzing and regulating St. John's wort.
Five independent experts who reviewed The Times' procedures said the
approach was sound. "The analysis method used is the best one
widely available," said John Fitzloff, director of the analytical
chemistry laboratory at the University of Illinois in Chicago and
an authority on botanical testing.
However arcane the controversy over testing methods, it is related
to St. John's wort product consistency--and thus consumer confidence.
There are "no officially established standards of quality"
for the herb in the United States, according to the U.S. Pharmacopeia,
an independent organization that sets drug safety and purity standards.
"Although some companies may test their own products," it
stated this month in a report on the herb, "the quality of other
products that are for sale cannot be guaranteed."
Not all companies challenged The Times' tests. Within hours of being
informed of the results, for example, officials of Trader Joe's, the
Southern California market chain, said they would remove the particular
St. John's wort lot tested from store shelves.
"Our customers have an expectation that what is on the label
is inside the bottle," said marketing vice president Pat St.
John.
Another vital issue that surfaced in The Times' product survey pertains
to safety information.
Three of the 10 products sampled provided no safety information on
the label, even though St. John's wort can have side effects.
The most frequently noted possible side effect is light sensitivity.
Ranging cattle that feed on the plant have been known to get blisters
on their hide and die of overexposure to the sun. In some clinical
experiments, fair-skinned people in particular got sunburns after
taking twice the usual amount of St. John's wort.
Anecdotally, World Wide Web bulletin boards discussing the herb are
riddled with messages blaming it for unexpected sunburns. European
health authorities and U.S. scientific bodies have issued clear warnings
about the problem.
Similarly, health authorities have cautioned pregnant women against
taking the product. The European Scientific Cooperative on Phytotherapy
said in a 1996 report that "the product should not be used in
pregnancy and lactation without medical advice."
The U.S. Pharmacopeia says that there have been no reports of adverse
effects on fertility or of birth defects associated with St. John's
wort use, but the herb "should be avoided by pregnant women because
of a lack of published safety data."
Evidence that in ancient times the herb was used to induce abortions
should also give pregnant women pause, according to John Riddle, a
historian at North Carolina State University.
Combing ancient medical texts, Riddle found that the herb has been
part of folk medicine for 3,000 years.
In addition to being a treatment for "melancholia"--first
recorded 1,100 years ago, Riddle found--St. John's wort was also used
for abortions.
Package labels should plainly state that pregnant women should not
take this herbal product "simply out of historical prudence,"
he said at a conference this spring of the American Herbal Products
Assn.
Another labeling issue concerns young children, who are increasingly
being given St. John's wort supplements or tinctures, to judge from
Internet messages by parents seeking dosage advice.
In The Times' test, eight of the 10 brands did not warn parents against
giving the product to young children. And yet, the new U.S. Pharmacopeia
report said, "use of hypericum in children should be avoided
because of the lack of safety data."
Wide-Open
Market in U.S.
Though there are gaps in the evidence for the herb's safety, many
scientists and physicians cite the experience in Germany, where millions
of people have taken the herb over the last decade without apparent
excessive adverse effects.
But Germans and Americans are taking St. John's wort in very different
environments. There, the herb is considered a drug. Manufacturers
must register their products with the government and adhere to strict
premarketing quality standards. Doctors prescribe it and health plans
cover it. And most patients take the herb under a doctor's care.
Here, the herbal market is wide open. Most Americans who use St. John's
wort, experts say, are doing so without their doctors' advice and
in many cases they are hiding their use.
The American Psychiatric Assn. sharply criticized the practice. "No
one who thinks he or she may be depressed should self-medicate with
St. John's wort or any other 'alternative' remedy," it said in
a statement last March.
For one thing, symptoms of depression could actually be a sign of
serious physical disease. Also, proven antidepressant medications
are available.
The appeal of herbal remedies to Americans is obvious. Promoters describe
them as safe, gentle, inexpensive and "natural" alternatives
to pharmaceutical drugs and other harsh medical treatments. Consumers
buy them without a prescription, forgoing the costs and hassles of
doctor visits and managed-care bureaucracies.
A part of the rationale for taking herbal remedies is sound. After
all, many drugs have been derived from plants, whether old-fashioned
opium or modern-day taxol, a compound used to treat breast cancer
that is derived from the Pacific yew tree. As many as 120 drugs currently
used by physicians reportedly have plant origins, according to a University
of Illinois study.
A resurgence of interest in natural remedies is at the core of the
alternative medicine movement, said Dr. Harold Bloomfield, a La Jolla
psychiatrist and an author of two books touting the benefits of St.
John's wort. Bloomfield's appearance on the TV program "20/20"
last year is widely cited as one of the sparks that ignited the current
boom.
Still, he said, "good pharmacological studies are needed so a
physician can feel a sense of confi dence and safety prescribing"
St. John's wort.
The explosion of interest in St. John's wort also testifies to depression's
huge, often hidden toll.
About 17 million adults suffer from serious depression. And tens of
millions more are said by researchers to endure a milder, less persistent
form of the disorder called "subsyndromal" depression or
"dysthymia."
To some mental health professionals, St. John's wort--the first over-the-counter
product said to have antidepressant properties--represents a new opportunity
to ease the suffering of millions. That is especially important because
approximately two out of three depressed people do not seek any help
for the condition, according to government studies.
"For the depressed person who would previously not have sought
medical help, perhaps for financial reasons or out of feelings of
shame or the fear of stigma, St. John's wort might well be a boon,"
Rosenthal, of the Mental Health Institute, writes in his new book
"St. John's Wort: The Herbal Way to Feeling Good."
Clinical
Evidence of Effectiveness
The clinical evidence on the effectiveness of St. John's wort appears
positive overall, according to independent summaries of the data.
So far, 27 published clinical studies of 2,291 patients have met strict
scientific criteria, such as randomly assigning patients to a treatment
or control group, according to a new overview by Dr. Klaus Linde of
the Technical University in Munich, Germany, and Dr. Cynthia Mulrow
of the Veterans Affairs Medical Center in San Antonio.
Pooling the data from those studies, Linde and Mulrow found that 56%
of the patients felt less depressed a month or longer after taking
St. John's wort, compared with 25% of the patients who were given
a placebo.
But in their analysis--the most comprehensive review of the evidence
so far--the medical researchers described several key weaknesses in
the existing studies, all of which were conducted in Europe or the
United Kingdom.
For instance, most of the trials were too brief, lasting only four
weeks, whereas the usual minimum for studying antidepressant drugs
is six weeks.
Moreover, none of the published studies so far compares St. John's
wort with the newest antidepressant drugs, such as Prozac and Zoloft.
Mulrow also said there was reason to believe that some negative clinical
findings had been suppressed. That could stem from what researchers
call "publication bias"--the tendency of scientists not
to bother reporting unimpressive findings, fearing that medical journals
would not be interested in a "failed" study. A more pernicious
bias occurs when a study's director or sponsor withholds negative
data.
An expert committee of the German government's drug-regulating branch
concluded 14 years ago that St. John's wort could reasonably be prescribed
for "depressive moods, anxiety and/or nervous unrest."
But the U.S. Pharmacopeia, citing a "lack of adequate scientific
evidence" on the effectiveness of St. John's wort, said its expert
panel could not support "a general recommendation for its use."
To bridge the gulf between U.S. questions and European acceptance,
two large U.S. studies are getting underway. One, led by Dr. Richard
Shelton, a research psychiatrist at Vanderbilt University Medical
Center, is funded by Pfizer, which makes the antidepressant drug Zoloft.
The other study, with $4 million from the National Institutes of Health,
is being coordinated by Dr. Jonathan Davidson, a research psychiatrist
at Duke University.
Both studies will involve people with serious depression, to put the
herb to a stricter test than older studies have done. The subjects
will receive St. John's wort, an antidepressant drug or a placebo
for at least eight weeks and as long as six months. Results are expected
in two to three years, the researchers say.
Factors
in Potential Quality Problems
Of course, even if St. John's wort is eventually proved effective,
it would not help consumers who happen to buy a product lacking potency,
health researchers and herb industry officials say.
Several factors contribute to potential quality problems with St.
John's wort extracts, experts say. Greatly increased demand for the
herb, coupled with tight supplies, has quadrupled the wholesale price
of raw plant material in the last three years. Processing and extracting
methods are onerous. Moreover, scientists have not identified all
the active ingredients.
In the face of rocketing demand, unscrupulous manufacturers have reportedly
turned to fraud. Some of the St. John's wort material on the wholesale
market has been identified as coming from a different, perhaps less
active, species of the plant, according to some distributors. And
the most common tests of St. John's wort potency can be fooled by
adding synthetic chemicals to the mixture, making poor extracts appear
up to grade, said Joerg Gruenwald, head of the German herbal medication
company PhytoPharm Consulting.
"We have heard that people are doing that," he said.
None of the products sampled by The Times, however, showed evidence
of fraud, according to an analysis that checked for chemical adulterants
and also verified that the extract came from the correct plant species.
Also contributing to quality control questions is the leeway U.S.
herbal distributors have to copy one another's products, which are
very seldom patented, since herbal remedies are generally based on
centuries of use.
Copycat herbal supplements are a concern because they may not in fact
be identical to the original formulations tested in research studies,
said Mark Blumenthal, director of the American Botanical Council,
an independent scientific and policy group, which receives some funding
from the herb industry.
"Is it possible that some of the herbal supplements out there
are not wearing any clothes?" he said. "Are they just making
claims . . . after borrowing somebody else's research conducted on
a different commercial product that may or may not be similar?"
Industry
Trying to Police Itself
Given the absence of direct government oversight, the herb industry
is taking steps to improve standards and police itself. Industrial
Laboratories, a Denver-based testing firm, has formed the Institute
for Nutraceutical Advancement, an industry-funded group to validate
methods of analyzing botanical products.
The National Nutritional Foods Assn., a trade group, randomly tests
members' herbal supplements to encourage adherence to label claims.
In a recent spot check of 45 retail St. John's wort supplements, the
group found that only four contained less than 100% of labeled potency.
Meanwhile, herb distributors have also uncovered potency problems.
Last year, Botanicals International of Long Beach teamed with a German
firm to test wholesale St. John's wort extracts. Using the same method
employed by the Times-commissioned lab, only one out of the 10 extracts
analyzed was as potent as the wholesalers had maintained, said Chris
Tower, a product manager at the company.
Consumers face a daunting task, he said: "You can walk into a
store and if you're not up to speed it can be darned confusing . .
. trying to make an educated guess about what is quality and what
is not."
T he
analysis of St. John's wort commissioned by The Times examined whether
retail products were as potent as they claimed to be. The analytical
technique, called spectrophotometry, tested each product for a family
of compounds known collectively as hypericin.
Scientists say that hypericin is not the only, and probably not even
the primary, ingredient with antidepressant activity in St. John's
wort. The herb contains several other compounds that also appear to
affect brain chemistry in ways that could lift mood, according to
test-tube studies of nerve cells. Strictly speaking, then, a product
with low hypericin levels is not necessarily an inactive one, researchers
and herbalists say.
However, unusually low hypericin levels are generally accepted in
the industry as a sign of poor quality. Hypericin remains the gauge
of authenticity, purity and strength of St. John's wort extracts.
For the tests, only products that specified the hypericin level were
sampled. Bought in six Los Angeles-area stores in July, they were
labeled as "standardized" or having "certified potency,"
"high potency" or "guaranteed potency."
Overall, seven of the 10 products contained between 75% and 135% of
the labeled hypericin level, and three contained no more than about
half the labeled potency, the lab found.
Cost and potency did not necessarily go together. Two of the three
lowest-scoring brands cost less than the average price of 18 cents
per pill. But two of the three highest-scoring brands also cost somewhat
less than the average. The most expensive brand was among the highest
in potency, but the second-most expensive brand was among the least
potent.
Some of the variation in potency may reflect natural decay of hypericin
in the product after it leaves the factory, several scientists said.
For instance, one of the three packages of Kira--the brand used in
most of the German clinical trials--was found to have pills with 81%
of the labeled hypericin level, whereas the other two packages had
91%. Dick Middleton, technical manager of Lichtwer Pharma in Britain,
said the lower-level package might have suffered in shipping and storage
since leaving Berlin some months before.
Three methods exist for measuring hypericin. The U.S. Pharmacopeia
plans to issue specifications for a new hypericin test this fall.
The method used in the tests for The Times is a spectrophotometric
test--a measurement of color in a solution--called DAC-91.
Officials of several companies objected to the use of that method,
saying it yields results that are slightly lower than an earlier version,
called DAC-86. Some of the companies still use DAC-86 to monitor their
products.
The head of Jarrow Formulas, Jarrow Rogovin, for example, said the
method used in The Times' survey resulted in hypericin readings that
are 20% below those found by the method the company's extract supplier
uses, "which accounts for the difference between our label claim
and the results obtained."
Officials at Enzymatic Therapy and Nature's Resource made a similar
argument.
The method used by The Times is "the accepted industry standard
for testing," said Roy Upton, an herbalist and editor of the
American Herbal Pharmacopoeia. It was adopted several years ago by
the German government for St. John's wort testing, though methods
continue to evolve.
Just how closely herbal supplements should adhere to their labeled
potency is a matter of some debate. FDA regulations state that the
concentration of labeled ingredients in dietary supplements, including
herbal medications, must equal 100% of the amount claimed on the package
throughout the product's shelf life.
In reality, though, holding herbal products to that standard can be
difficult because the chemical composition of a plant varies from
crop to crop, and analytical techniques for measuring key compounds
can yield somewhat different results, an FDA official said.
So some experts argue that herbal products containing 80% to 120%
of the labeled potency are close enough. "That might be reasonable,"
said Sally Guthrie, a University of Michigan clinical pharmacist.
Others narrow the margin to 90% to 110%. "At this point, 90%
of label claim is what I would specify" as a minimum, said V.
Srini Srinivasan, a senior scientist at the U.S. Pharmacopeia.
But Mark Blumenthal, director of the American Botanical Council, an
independent scientific and policy group, disagrees, arguing that a
product really should have 100% of what its label claims.
"If they say they have 0.3% hypericin at 300 milligrams, they
should have that," he said. "As a consumer, I want to know
that I'm getting what I pay for."
Testing St. John's Wort
In a spot check of retail St. John's wort supplements, the potency
varied, according to an independent laboratory test commissioned by
The Times. The potency depends on the milligrams of the compound hypericin
in each capsule or tablet.
The
tested potency represents the average of three samples. The margin
of error is approximately +/- 5%. The testing, using a spectrophotometric
method known officially as DAC-91, was done by Flora Research, an
analytical firm in San Juan Capistrano.
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