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Study finds antidepressant doesn't help autistic children Nationwide research finds that citalopram is no more effective than a placebo and that its side effects are twice as bad. About a third of autistic kids take the drug, known as Celexa in the U.S. Source: L.A. Times By Karen Kaplan Date: 06/032009
An antidepressant commonly prescribed to help autistic children control their
repetitive behaviors is actually no better than a placebo, according to a report published today.
Roughly
a third of all children diagnosed with autism in the U.S. now take
Citalopram, the antidepressant examined in the study, or others that
are closely related. The results of the nationwide trial, published in
Archives of General Psychiatry, have some experts reconsidering the
appropriateness of antidepressants and other mind-altering drugs used
to treat children with autism spectrum disorders.
"There
are tons of things being advocated as treatments for autism, some with
appropriate caveats and careful explanations, others without any of
that," said David Mandell, associate director of the Center for Autism
Research at Children's Hospital of Philadelphia, who wasn't involved in
the study.
An
estimated 1.5 million Americans have autism, a group of poorly
understood developmental disorders characterized by problems with
communication and social interaction. One of the hallmarks of the
disorder is obsessive, repetitive behavior such as flapping one's arms
or hands or memorizing car makes and models. When those routines are
interrupted, severe tantrums can result.
Only
one medication -- the antipsychotic drug Risperidone -- has been
approved by the Food and Drug Administration for the treatment of
irritability and aggression in children with autism. But doctors,
frustrated by their limited options, haven't shied away from giving
other pharmaceuticals a chance. Worldwide spending on drugs to treat
autism is estimated to be $2.2 billion to $3.5 billion annually.
Because
very few medications have been tested on autistic children in large,
rigorous studies, doctors have looked to drugs that treat similar
symptoms in other conditions, such as obsessive-compulsive disorder or
attention-deficit hyperactivity disorder.
That's
what led physicians to a class of antidepressants called selective
serotonin reuptake inhibitors, or SSRIs, that help adults with
obsessive-compulsive disorder. Their repetitive rituals, such as
counting, cleaning or hand-washing, are reminiscent of the behaviors
seen in autistic patients.
Doctors were also hopeful about SSRIs because the serotonin system is known to function improperly in people with autism.
But
the medications will work only if the root causes of
obsessive-compulsive disorder and autistic repetitive behavior involve
the same biological pathways in the brain. The new study strongly
suggests they do not.
"It just begs for a more careful understanding of the neurological underpinnings of the disorder," Mandell said.
Dr.
Bryan King, director of psychiatry and behavioral medicine at Seattle
Children's Hospital and leader of the study, said he was shocked to
find that citalopram didn't help patients. Not only was the placebo
slightly more effective, but the drug's side effects -- such as
impulsivity and insomnia -- were at least twice as bad, the study found.
"I
personally would have a healthy dose of skepticism about" prescribing
citalopram or other SSRIs, King said. Citalopram is sold in the United
States under the brand name Celexa.
In
the study, King and his colleagues from six academic medical centers,
including UCLA, enrolled 149 autistic children ages 5 to 17 whose
compulsive behaviors were classified as moderate or worse. After 12
weeks, 33% of the 73 patients who took citalopram had improvements in
repetitive behaviors as measured by clinicians and parents, versus 34%
of the 76 patients who took a placebo.
If
there hadn't been a control group for comparison, King said he would
have been impressed by the improvement seen in the children who took
the drug. "The decision would most definitely have been made to
continue them," he said.
The
study underscores the value of evaluating drugs in randomized,
double-blind, placebo-controlled studies, which are considered the gold
standard of medical research, Dr. Fred R. Volkmar, director of the Yale
Child Study Center in New Haven, Conn., wrote in a commentary that
accompanied the study. In such studies, neither patient nor doctor
knows who is getting the drug and who is getting the placebo until all
the results are in.
"We need more studies of this kind to advance research and guide clinical practice," Volkmar wrote.
Placebo-controlled
studies are especially important in evaluating medications to treat
behavior and mood because patients are typically in a crisis state when
they enroll in a clinical trial and could improve on their own in time,
Mandell said.
What's
more, the attention focused on children when they are in a trial tends
to improve their behavior all by itself, Volkmar said in an interview.
The
study was funded by the National Institutes of Health. King and several
of his colleagues have received research grants and other funding from
pharmaceutical firms, including Forest Laboratories Inc. of New York,
the maker of Celexa.
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