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Chronic
fatigue syndrome finally gains official respect
By David Tuller
Published: July 18, 2007
http://www.iht.com/articles/2007/07/17/healthscience/snfatigue.php
NEW YORK: For decades, people suffering from
chronic fatigue syndrome have struggled to convince doctors,
employers, friends and even family members that they were not
imagining their debilitating symptoms.
Skeptics called the illness "yuppie flu" and
"shirker syndrome."
But the syndrome is now finally gaining some
official respect. The U.S. Centers for Disease Control and
Prevention, which in 1999 acknowledged that it had diverted millions
of dollars allocated by Congress for chronic fatigue syndrome
research to other programs, has released studies that linked the
condition to genetic mutations and abnormalities in gene expression
involved in key physiological processes. The centers have also
sponsored a $6 million public awareness campaign about the illness.
And last month, the CDC released survey data suggesting that the
prevalence of the syndrome is far higher than previously thought,
although these findings have stirred controversy among patients and
scientists. Some scientists and many patients remain highly critical
of the CDC's record on chronic fatigue syndrome, or CFS. But nearly
everyone now agrees that the syndrome is real.
"People with CFS are as sick and as
functionally impaired as someone with AIDS, with breast cancer, with
chronic obstructive pulmonary disease," said William Reeves, the
lead expert on the illness at the CDC, who helped expose the
centers' misuse of chronic fatigue financing.
Chronic fatigue syndrome was first identified
as a distinct entity in the 1980s. (A virtually identical illness
had been identified in Britain three decades earlier and called
myalgic encephalomyelitis.) The illness causes overwhelming fatigue,
sleep disorders and other severe symptoms and afflicts more women
than men. No consistent biomarkers have been identified and no
treatments have been approved for addressing the underlying causes,
although some medications provide symptomatic relief.
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Patients say the word "fatigue" does not begin
to describe their condition. Donna Flowers of Los Gatos, California,
a physical therapist and former professional figure skater, said the
profound exhaustion was unlike anything she had ever experienced. "I
slept for 12 to 14 hours a day but still felt sleep-deprived," said
Flowers, 51, who fell ill several years ago after a bout of
mononucleosis. "I had what we call 'brain fog.' I couldn't think
straight, and I could barely read. I couldn't get the energy to go
out of the door. I thought I was doomed. I wanted to die."
Studies have shown that people with the
syndrome experience abnormalities in the central and autonomic
nervous systems, the immune system, cognitive functions, the stress
response pathways and other major biological functions. Researchers
believe the illness will ultimately prove to have multiple causes,
including genetic predisposition and exposure to microbial agents,
toxins and other physical and emotional traumas. Studies have linked
the onset of chronic fatigue syndrome with an acute bout of Lyme
disease, Q fever, Ross River virus, parvovirus, mononucleosis and
other infectious diseases.
"It's unlikely that this big cluster of people
who fit the symptoms all have the same triggers," said Kimberly
McCleary, president of the Chronic Fatigue and Immune Dysfunction
Syndrome Association of America, the advocacy group in charge of the
CDC-sponsored awareness campaign.
Under the most widely used case definition, a
diagnosis of chronic fatigue syndrome requires six months of
unexplained fatigue as well as four of eight other persistent
symptoms: impaired memory and concentration, sore throat, tender
lymph nodes, muscle pain, joint pain, headaches, disturbed sleeping
patterns and post-exercise malaise.
The broadness of the definition has led to
varying estimates of the syndrome's prevalence. Based on previous
surveys, the CDC has estimated that more than a million Americans
have the illness.
Last month, however, the disease control
centers reported that a randomized telephone survey in Georgia,
using a less restrictive methodology to identify cases, found that
about 1 in 40 adults ages 18 to 59 met the diagnostic criteria - an
estimate 6 to 10 times higher than previously reported rates.
However, many patients and researchers fear
that the expanded prevalence rate could complicate the search for
consistent findings across patient cohorts. These critics say the
new figures are greatly inflated and include many people who are
likely to be suffering not from chronic fatigue syndrome but from
psychiatric illnesses.
"There are many, many conditions that are
psychological in nature that share symptoms with this illness but do
not share much of the underlying biology," said John Herd, 55, a
former medical illustrator and a CFS patient for two decades.
Researchers and patient advocates have faulted
other aspects of the CDC's research. Jonathan Kerr, a microbiologist
and chronic fatigue expert at St. George's University of London,
said the CDC's gene expression findings last year were "rather
meaningless" because they were not confirmed through more advanced
laboratory techniques
Kristin Loomis, executive director of the HHV-6
Foundation, a research advocacy group for a form of herpes virus
that has been linked to CFS, said studying subsets of patients with
similar profiles was more likely to generate useful findings than
Reeves's population-based approach.
In response, Reeves said understanding of the
disease and of some newer research technologies is still in its
infancy, so methodological disagreements were to be expected. He
defended the population-based approach as necessary for obtaining a
broad picture and replicable results.
Joseph Montoya, a Stanford infectious disease
specialist pursuing the kind of research favored by Loomis, caused a
buzz last December when he reported remarkable improvement in 9 out
of 12 patients given a powerful antiviral medication, valganciclovir.
Montoya has just begun a randomized controlled trial of the drug,
which is approved for other uses.
Montoya said some cases of the syndrome were
caused when an acute infection set off a recurrence of latent
infections of Epstein Barr virus and HHV-6, two pathogens that most
people are exposed to in childhood.
Flowers had high levels of antibodies to both
viruses and was one of Montoya's initial CFS patients. Six months
after starting treatment, Flowers said, she was able to go
snowboarding and take yoga and ballet classes. "Now I pace myself,
but I'm probably 75 percent of normal," she said.
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