PROVIDENCE, R.I. - Researchers at Rhode Island Hospital and The Warren Alpert Medical School of Brown University have discovered a gene that could hold the key to developing new treatments for Parkinson's disease - a progressive and often debilitating movement disorder that affects as many as one million Americans.
According to the findings of the study, published online in the American Journal of Human Genetics, mutations in the gene, known as GIGYF2, appear to be directly linked to the development of Parkinson's in people with a family history of the disease. The gene is one of only a handful linked to Parkinson's and one of just two genes known to be a common contributor to this degenerative disease, which has no known cause or cure.
Although less than a quarter of all cases of Parkinson's are familial, researchers believe genes like GIGYF2 can provide clues to the mechanisms behind Parkinson's and could point to new treatments for the more common and sporadic forms of the disease.
"These findings may ultimately help open the door to the development of new therapeutic - and possibly even preventive - strategies that target the underlying cause of Parkinson's disease, improving the quality of life of the many people worldwide who are affected by this devastating disorder," said senior author Robert J. Smith, M.D., director of the division of endocrinology and the Hallett Center for Diabetes and Endocrinology at Rhode Island Hospital and professor of medicine at Alpert Medical School.
Their research also revealed an intriguing secondary finding -- the possible association between Parkinson's and insulin and the related hormone known as insulin-like growth factor (IGF). This joins a small but growing body of research linking insulin and IGF to Parkinson's disease and other neurodegenerative disorders, such as Alzheimer's.
"A better understanding of the link between insulin or IGF and Parkinson's may lead us to new treatment strategies for Parkinson's and also new insights into the connection between diabetes and nervous system disorders," Smith said.
Parkinson's is one of the most common neurodegenerative disorders, second only to Alzheimer's, affecting between one and two percent of the population above age 60. The disease occurs when certain nerve cells in the part of the brain that controls muscle movement either die or become impaired. Normally, these cells produce a vital chemical known as dopamine, which allows smooth, coordinated function of the body's muscles and movement. When the dopamine-producing cells are damaged, the symptoms of Parkinson's appear - including tremors, slow movements, stiffness, and difficulty with balance or coordination.
Smith, an endocrinologist, and his team at Rhode Island Hospital and Brown typically focus on proteins important to the function of insulin and IGF. They initially identified GIGYF2 nearly five years ago because of its potential involvement in IGF and insulin signaling systems, but did not explore an association with Parkinson's at that time.
In the current study, they examined where GIGYF2 is located on the human genome in hopes of learning more about the gene's function, and discovered that it is right in the center of a chromosomal region linked to Parkinson's. Specifically, it appears GIGYF2 resides on PARK11 - a region that was initially identified through a genetic analysis of families with Parkinson's disease.
Because of the potential links between Parkinson's, IGF and diabetes, Smith and his team decided to investigate the involvement of GIGYF2 in Parkinson's. Colleagues in Milan, Italy and Paris, France provided close to 250 DNA samples from patients who had Parkinson's and at least one first-degree relative (parent, child or sibling) with the disease. This included 123 Italian patients and 126 French patients. For comparison, they also studied DNA from more than 200 unrelated healthy controls from both countries.
Following gene sequencing and mutation analysis, the researchers identified seven different forms of GIGYF2 mutations occurring in 12 different people - approximately five percent of those in the study. Eight of these patients had at least one parent with Parkinson's, one had both parents affected, and three had one sibling affected. When available, relatives with Parkinson's were also sampled and the researchers found they carried the same mutation, which led to single amino acid substitutions in the protein encoded by the GIGYF2 gene. None of the mutations were observed in the healthy controls.
"Our data provides strong support for GIGYF2 as a PARK11 gene with a causal role in familial Parkinson's disease," said Smith. "The next step is to zero in on this gene to learn more about its involvement in triggering Parkinson's. It will also be important to evaluate additional and larger families with Parkinson's and these genetic mutations, as well as the frequency of GIGYF2 mutations in patients with the more common, idiopathic form of the disease."
The study - which will also be published in the April 11th print issue of American Journal of Human Genetics - was supported by grants from the National Institutes of Health, the Hallett Center for Diabetes and Endocrinology at Rhode Island Hospital, the Parkinson Institute in Italy, and several French organizations, including the Fondation Fértilité et Stérilité, the Association Française des Femmes Dîplomeés des Universities, the Association France Parkinson, and the Agence Nationale de la Recherche.
Co-authors of the study include Corinne Lautier, formerly of Rhode Island Hospital and Alpert Medical School and currently affiliated with Pitíe-Salpêtrière Hospital, Paris; Barbara Giovannone and William G. Tsiaras from Rhode Island Hospital and Alpert Medical School; Stefano Goldwurm and Gianni Pezzoli from the Parkinson Institute at the Istituti Clinici di Perfezionamentro, Milan, Italy, and Alexandra Durr and Alexis Brice, from Pitíe-Salpêtrière Hospital, Paris.
Editors: Brown University has a fiber link television studio available for domestic and international live and taped interviews and maintains an ISDN line for radio interviews. For more information, call the Office of Media Relations at (401) 863-2476.
Founded in 1863, Rhode Island Hospital (www.rhodeislandhospital.org) is a private, not-for-profit hospital and is the largest teaching hospital of The Warren Alpert Medical School of Brown University. A major trauma center for southeastern New England, the hospital is dedicated to being on the cutting edge of medicine and research. Rhode Island Hospital ranks among the country's leading independent hospitals that receive funding from the National Institutes of Health, with research awards of nearly $27 million annually. Many of its physicians are recognized as leaders in their respective fields of cancer, cardiology, diabetes, orthopedics, neurology and minimally invasive surgery. The hospital's pediatrics division, Hasbro Children's Hospital, has pioneered numerous procedures and is at the forefront of fetal surgery, orthopedics and pediatric neurosurgery. Rhode Island Hospital is a founding member of the Lifespan health system.
Brown University is an internationally known Ivy League institution with a distinctive undergraduate academic curriculum, outstanding faculty, state-of-the-art research facilities, and a tradition of innovative and rigorous multidisciplinary study. Brown offers nearly 100 programs of study to its approximately 7,190 undergraduate, graduate, and medical students and has a firm commitment to academic excellence and diversity in its student population. The University adheres to a collaborative university-college model in which faculty are as committed to teaching as they are to research, embracing a curriculum that requires students to be architects of their education. In 2004, Brown publicly launched its Plan for Academic Enrichment, which is designed to strengthen educational opportunities and significantly increase the number of faculty, add more courses and research opportunities for undergraduates, improve support for graduate and medical education, and invest in libraries, information technology and new academic space. For more information, visit http://www.