A Mayo Clinic-led international research collaboration - one of the largest studies of its kind - provides strong evidence that a genetic risk factor may account for 3 percent of the cause of Parkinson's disease.
Parkinson's disease is a debilitating neurological disease that affects about 1 million people in the United States. Little is known about its causes and hence there is no cure.
"This is an important step forward because the contribution of common genetic risk factors to the development of Parkinson's has long been suspected, but the high quality of data needed to make such discoveries has been missing," says Demetrius Maraganore, M.D., Mayo Clinic neurologist and lead study investigator. "This well-designed and large study provides evidence that common genetic variants contribute to the cause of Parkinson's."
The collaboration included researchers from 11 countries. Their findings will be published in the Aug. 9 issue of the Journal of the American Medical Association.
In their study, the researchers analyzed clinical and genetic data from 2,692 Parkinson's disease patients and 2,652 healthy subjects who were matched to the Parkinson's patients for age and gender. Results showed that persons with longer lengths of a DNA segment that promotes the activity of a gene known as alpha-synuclein had a 1.5 times greater risk for Parkinson's disease.