Patients with Parkinson's disease may be the first group to benefit
from gene therapy, the much-hyped technique that has yet to result in
a single reliable treatment despite nearly two decades of
experimentation. Now researchers report that a gene-bearing virus
injected directly into the brain was able to improve patients' motor
function without causing any adverse side effects.

In the 1990s gene therapy was hailed as an impending revolution in
medicine because of its potential to attack disease at its genetic
roots. The research results did not live up to the hype, however, in
1999 much of the remaining hope for gene therapy was destroyed when an
18-year-old boy suffered an unexpectedly severe immune reaction and
died during an experiment, But small-scale research continued with new
safety rules in place, and studies such as this one may give the
treatment option a second life.

This trial is the first time gene therapy has been tested to fight
Parkinson's, which affects an estimated 500,000 Americans. The
disease, which typically strikes people in their 60s, is characterized
by the tremors, stiffness, loss of speech and difficulty with motor
function. Neuroscientists have tracked its biological cause to the
death of neurons in a midbrain region called the substantia nigra,
which produces the neurotransmitter dopamine. Low levels of dopamine
cause the nearby subthalamic nucleus to overproduce glutamate, the
brain's primary excitatory chemical messenger. The excess glutamate
over stimulates other areas of the brain, disrupting motor control.

The research team used a harmless virus transport a gene coding for
gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter that
counteracts glutamate's excitation, into the nerve cells of the
subthalamic nucleus. By ramping up GABA production, the gene therapy
corrected the chemical imbalance and drastically improved motor
function in all 12 patients. Especially significant, according to
researchers, is that this improvement persisted even when the patients
were taking their Parkinson's drugs-meaning the two treatments could
be combined for extra impact.

"The safety and effectiveness clearly indicate that this is something
worth pursuing," says lead author Michael Kaplitt, a neurological
surgeon at New York-Presbyterian Hospital/Weill Cornell Medical
Center. "But we still need to do a larger, more definitive study to
prove this for sure." Kaplitt hopes to have a large-scale trial under
way by the end of the year.
Happy Learning,


Yovan P. Putra
www.primastudy.com <http://www.primastudy.com/>
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