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Parkinson's Strikes Woman With No Family History of the Disease

Defective gene may be to blame

By Randy Dotinga
HealthDay Reporter

TUESDAY, July 1 (HealthDayNews) -- New research suggests a single defective gene caused a young woman to develop
Parkinson's disease -- even though her family had no history of the illness.

The finding could help unravel some of the mystery surrounding the inheritability of the brain disease.

An estimated 1 million to 1.5 million Americans have Parkinson's, which causes tremors, difficulty walking and rigid
muscles. In severe cases, patients can develop dementia and die, but medications have let many lead fairly normal
lives.

The causes of Parkinson's aren't clear, although many experts think environmental contamination, especially from
pesticides, may be at least partially responsible.

In a tiny number of cases, however, Parkinson's appears to be inherited. Researchers have found that the illness runs
in two Dutch and Italian families. A mutated gene appears to cause the disease to appear in some members of the
families, especially the young.

Inherited Parkinson's disease "is considered a scientific curiosity as it is thought to be rare," explains Dr. Paul
Tuite, an assistant professor of neurology at the University of Minnesota.

To better understand the mutated gene, an international team of researchers decided to investigate whether the gene
could cause the disease in other families, including those that had not encountered the illness. The researchers looked
for mutations in the gene, known as DJ-1, in 107 Parkinson's patients who had developed the illness before the age of
50. Only 38 had a family history of the disease.

The researchers -- from Canada, Italy, the Netherlands and the United States -- report their findings in a study that
will appear in an upcoming issue of the journal Annals of Neurology. The journal published the study online June 29.

The researchers found a mutated gene in a single 29-year-old patient, a Hispanic woman, who developed the disease at
the age of 24 and has responded well to medication. Her family had no history of Parkinson's or other brain illnesses.

"As we understand more about genetics and the Human Genome, it's clear that a disease doesn't need to run in families
to be genetic," says study author Andrew Singleton, a researcher at the Molecular Genetics Section of the Laboratory of
Neurogenetics at the U.S. National Institute on Aging. "A recessive disease, which requires one faulty gene from each
parent, can often appear in a patient without any affected relatives."

So far, the full meaning of the defective gene isn't clear. "What remains to be seen is if this mutation is a limited
phenomenon, or does [it] play a more insidious role in other patients throughout the world," Tuite says.

Either way, more understanding of the gene in question could help scientists studying Parkinson's disease, he says.
They could tinker with the genes of animals -- even a fly -- to give them forms of Parkinson's disease and study how
treatments work, he says.

For now, there's no way to prevent Parkinson's. Once people get the disease, it's too late to turn back the brain
damage, although medications can keep it from getting worse, Singleton says.

But determining that a patient is susceptible to the disease in the first place -- perhaps because of a defective gene -
- could let doctors recommend preventative treatments before the disease appears, says Dr. Irene Litvan, director of
the Movement Disorder Program at the University of Louisville. Those may include antioxidants, which have shown promise
in research, or the simple avoidance of pesticides, she says.

More information

Learn about the symptoms of Parkinson's disease from

the Parkinson's Disease Foundation
http://www.pdf.org/AboutPD/symptoms.cfm

or the National Parkinson Foundation.
http://www.parkinson.org/

SOURCE: HealthDayNews / HealthScoutNews
(HealthDay is the new name for HealthScoutNews)
http://drkoop.com/template.asp?page=newsdetail&ap=93&id=513936

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