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HEALTH CARE: Pathological Science
By Henry I. Miller
Health scares based on bad data represent a growing problem. By Henry I. Miller.
In a landmark 1953 speech, chemistry Nobel
laureate
Irving Langmuir told of his visit to the laboratory of J. B. Rhine
at Duke
University, where Rhine was claiming that results from his ESP
experiments
could not be predicted by chance and ascribing them to psychic
phenomena.
Langmuir discovered that Rhine was only
selectively counting the data in his experiments,
omitting the scores of those he believed were guessing in
order to
humiliate him. The evidence? Rhine felt
that
some of the scores were too low to have occurred by chance and that it would, therefore, actually be
misleading
to include them.
Langmuir dubbed this deviation from the
principles of
the scientific method “pathological science,” the
“science of things that aren’t so.”
Variations on this sort of chicanery are
increasingly
common among certain self-styled public interest groups, who are
less
devoted to fudging data to get the right answer than to grossly
misrepresenting the results in order to achieve some hidden agenda.
Most
often, that agenda is not protection of public health or the
environment
but intractable opposition to, and obstruction
of, whatever research, product, or technology the activists happen
to dislike. Often, the targets of activists’
opprobrium are socially beneficial and highly cost-effective
products or
processes.
Activists often try to stigmatize whatever
they
dislike via guilt by association with greedy or irresponsible
“corporate interests.” But for several
reasons, including the importance of corporate branding,
avoidance
of liability, and a desire to succeed
in the
marketplace, industrial research most often adheres to high professional and legal standards, including
peer
review. When it doesn’t, the scientific method and market
forces
collaborate to ensure that, ultimately, dishonesty and
deceitfulness are
exposed and punished.
By contrast, activist-funded
“research” is
commonly held to a far lower standard. The activists’ claims
are
invariably promoted by alarmist press releases
and reported by the media, but seldom are they independently
peer-reviewed or published in scientific journals. Sadly,
policymakers, the media, and the public
come to
accept this pathological science as credible,
especially after it is repeated again and again.
Examples have become more frequent as special
interests promote health scares as a way to support litigation. The
distortion of science has given rise to flawed policies and
regulations,
interference with research that offers potential benefits to
society,
increased public health risks, unwarranted scares, frivolous
lawsuits, and
higher costs of R&D.
Some examples follow:
In 1998, British researchers published
a study
that suggested an association—but
not
causation—between the administration of
measles-mumps-rubella vaccine and an increased risk of autism.
That prompted speculation that the culprit
might be
thimerosal, an ethylmercury-containing
preservative in the vaccine. Despite the fact that the initial study was based on only 12 children, its
results
were widely publicized, causing some parents and hospitals to stop
or delay
vaccinations for newborns and children. Subsequent studies of much
larger
groups of children have not confirmed such an association, however;
and the
overwhelming consensus among scientists and physicians is that no
such link
exists.
Nevertheless, this
incident inflicted incalculable damage on the
public’s confidence in
vaccination and
on individual children deprived of protection from
life-threatening diseases.
Food
irradiation—a process in which foods are treated with
ionizing
radiation—applied commercially
was an
historic breakthrough in food processing. First
and foremost, it makes our food both safer and cheaper, by delaying
the
spoilage of highly perishable fresh fish and shellfish and
greatly reducing the numbers of microorganisms in
spices and
of bacteria and parasites in meats and
poultry.
It also prevents potatoes and
onions from sprouting and extends the shelf life of fruits
such as strawberries.
Although more than 50 years of scientific
research
have established that food irradiation
has
little or no effect on flavor and that it is safe and highly
effective, the FDA’s gradual approval of new
applications of irradiation has been
opposed at
every turn by anti-nuclear activists. Contrary to their claims, irradiated foods
contain no
by-products unique to the process and
the process is hazardous neither to workers nor to
the
environs of treatment plants.
In the realm of food
processing, irradiation—the most extensively studied food technology in history—is, along with
pasteurization, the closest thing we
have
to a “free lunch.”
The supposed hazards of electromagnetic
radiation—which is emitted from a
variety
of sources including overhead power lines, electric
blankets, computer terminals, and electric razors—has
excited
the imagination of many. For example,
after a
Florida woman developed a brain tumor behind her right ear—where she had usually placed her
cell
phone—her husband blamed her illness (and subsequent death) on radiation
from the
cell phone and filed suit against the
phone’s manufacturer. After the husband’s 1993
appearance on
CNN’s Larry
King Show, other, similar lawsuits
followed.
None was successful, and within several months the scare was
forgotten.
This kind of health scare is an example of the
post hoc, ergo propter hoc
fallacy (believing that because two events are temporally related,
they must be causally related). Fallacy it might be, but
it lends
itself well to the way that Americans
these
days often learn about safety and risk: “Could your cell phone give you cancer? Details at 11!” In
fact, at
the current rate of occurrence of
brain
cancers, about 3,600 cases would be expected to occur among 60
million
owners of cell phones, whether or not they use them.
In 2003,
something
called the Environmental Working Group (EWG) claimed to have evidence that the farm-raised salmon eaten regularly
by
millions of Americans contain high
levels of
PCBs. PCBs commonly were identified in the
press coverage as a “toxin,” “probable human
carcinogen,” or “cause of cancer and nervous system
damage.”
These reports were grossly misleading. At
levels of
environmental exposure, PCBs have not
been
shown to cause cancer or any other disease in humans. The “study,” which was based
on a
sample of only 10 fish, was condemned
by
experts at a variety of institutions, including the Harvard
School of Public Health, the U.S. Food and Drug
Administration, and the highly respected American Council on Science and Health.
Unfortunately, the criticisms came only
after EWG’s report had generated national media coverage; the
criticism received little attention from the media.
On its website, the EWG
makes no pretense about possessing scientific credentials
or expertise, and its president once admitted to a journalist that
there
was not a single physician or scientist on its staff.
In 1980, a
Canadian
newspaper reported that four women in the classified ad department of another
newspaper
had given birth to children with birth
defects,
including a cleft palate, underdeveloped eye, clubfoot, and heart
problems.
The fact that all the women had worked with video display terminals
(VDTs)
during the early stages of their pregnancies gave rise to
speculation that
radiation from such terminals—most of which are based on
common
television technology—was responsible.
Other such
“clusters” of birth defects came to light, leading to
aggressive anti-VDT activism that in
both North
America and Europe caused management to
be
pitted against workers. In Canada and Sweden, merely the belief that harm could be caused by VDTs was
considered
to be grounds for refusal to use them.
Over the next two
decades, several large studies and repeated analyses concluded that the use of VDTs is not associated with
birth
defects or spontaneous abortions. The Centers for Disease Control
and
Prevention concluded that the clusters were random
occurrences—that
is, the function of probability. (If you flip a coin a million
times,
you’ll likely come close to half a million heads and half a
million
tails, but along the way, there will be occasional long
runs—or
clusters—of heads or tails.)
Environmental activists lately have
taken to
claiming that conventional crops have
been
“contaminated” by the finding of minuscule amounts of
DNA from “genetically modified”—by
which
they mean gene-spliced—varieties. Their methodology is
flawed, but
even if the claims were accurate, they
should
elicit from the public nothing more than a collective
yawn. Genetic modification is not new. Virtually all
of the
200 major crops in the United States have been genetically
improved, or
modified, in some way. Plant breeders—not
“nature”—gave us seedless grapes and watermelons,
the
tangelo (a tangerine-grapefruit hybrid), the “canola”
variety
of rapeseed, and fungus-resistant strawberries. In North American
and
European diets, only fish and wild game, berries and mushrooms may
be said
not to have been genetically engineered in some fashion.
North Americans have consumed more than a
trillion servings of
foods
that contain gene-spliced ingredients, with not a single untoward
reaction.
In fact, when conventional and gene-spliced seed materials are
mixed,
arguably the former should be thought of as contaminating the
latter.
What makes false alarms hard to expose is the
virtual
impossibility of demonstrating the absolute safety of any activity
or
product: There is always the possibility that we haven’t yet
gotten
to the nth
hypothetical risk or to the nth dose or the nth year of exposure, when the risk will finally be
demonstrated. It is logically impossible to prove a
negative, and all activities pose some
nonzero risk of adverse effects.
Pathological science may confuse not only the
public
but also policymakers, who may themselves be scientifically
challenged.
Donald Kennedy, president emeritus of Stanford University and
former FDA
commissioner, chides bureaucrats: “Frequently decision-makers
give up
the difficult task of finding out where the weight of scientific
opinion
lies, and instead attach equal value to each side in an effort to
approximate fairness. In this way extraordinary opinions . . . are
promoted
to a form of respectability that approaches equal
status.”
This kind of undeserved moral equivalence
frequently
compromises governmental decision
making and
has given rise to unscientific and inconsistent regulation
of pesticides, biotechnology applied to agriculture, silicone
breast
implants, herbal dietary supplements, and innumerable other
products and
technologies.
No one should mistake activists’
misdemeanors
for naive exuberance or excessive zeal
in a
good cause. Their motives are self-serving and their
tactics callous—an ongoing example of the sentiments
expressed by Linus Van Pelt in the Peanuts comic strip: “I
love
humanity; it’s people I can’t stand.”
People who understand these issues need to do
a better
job of educating the large segment of the public that is
uninformed—not only about the science but also about the
sophistry of those who would abuse it.
Special to the Hoover Digest.
Available from the Hoover Press is To America’s Health: A Proposal to Reform the Food and Drug Administration, by Henry I. Miller. To order, call 800.935.2882 or visit www.hooverpress.org.
Henry I. Miller, M.S., M.D., is a research fellow at the Hoover Institution, where his research focuses on public policy toward science and technology. It encompasses a number of areas, including pharmaceutical development, the new biotechnology, models for regulatory reform, and the emergence of new viral diseases.
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