rong
family history, could lead to earlier detection of Parkinson's disease.
Further study of how this gene works also might help scientists
identify new treatments."
In addition to Dr. Singleton, the collaborative work was spearheaded by
William C. Nichols, Ph.D., of Cincinnati Children's Hospital, Tatiana
Foroud, Ph.D., of Indiana University Medical Center, Indianapolis, and
Nicholas W. Wood, M.D., of the Institute of Neurology in London. The
NIA and the NINDS are part of the National Institutes of Health (NIH)
at the U.S. Department of Health and Human Services.
Singleton and his colleagues recently discovered LRRK2, a gene that
encodes a protein named dardarin by the researchers from the Basque
word dardara, which means tremor, a major symptom of Parkinson's
disease. It was isolated on a region of chromosome 12 called PARK8 by
investigators who studied five families with a history of Parkinson's
disease who lived in the Basque region of Spain and in England.
In these new studies, the researchers sought to determine the
prevalence of the genetic mutation in other families and individuals
being studied by the Parkinson's Study Group with NINDS support. In an
analysis of 358 families with a history of Parkinson's disease, for
instance, the investigators found that 34 of the 767 people who had
inherited the disease had at least one copy of the mutated gene.
Similarly, the team detected one copy of the mutation in 8 of 482
people with Parkinson's disease, but who didn't report a family history
of the disease. The Parkinson's Study Group is a non-profit,
cooperative group of Parkinson's disease experts from 59 medical
centers in the United States and Canada who are dedicated to improving
treatment for people affected by Parkinson's disease.
"NINDS is pleased to have supported the collection of this large group
of families and sibling pairs, which is proving to be an invaluable
resource for these studies," says Diane Murphy, Ph.D., a program
director at NINDS. "Because
'"/>Source:
Eurekalert
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