In April, more than 30 world leaders in Parkinson’s disease (PD) research gathered in New York City for The Michael J. Fox Foundation’s (MJFF) annual Scientific Advisory Board (SAB) meeting. A top theme throughout the two-day meeting: the genetics of Parkinson’s disease.
Genetic research holds critical potential to help all people living with PD, whether or not they carry mutations in genes linked to the disease. By studying the biological processes underlying inherited forms of Parkinson’s, scientists can better understand all forms of the disease (familial and the more common sporadic), opening new avenues to therapeutic development.
“New understandings of the genetics of Parkinson’s disease are informing PD drug development today,” said MJFF CEO Todd Sherer, PhD. “Our Foundation is building on these discoveries to define this research and ensure its translational focus, in order to speed its practical impact for people living with PD.”
SAB members discussed the growing role of the Foundation in driving forward research into four specific genetic targets relevant to PD: LRRK2, alpha-synuclein, tau, and GBA. MJFF is devoting the lion’s share of its gene-based investments to two of these targets: LRRK2, the most common genetic contributor discovered to date, and alpha-synuclein, whose clumping is seen in every case of PD.
A clear message from the SAB was the impact MJFF could make in bringing together patients and their doctors in the quest to understand PD genetics.
“It’s important that the Foundation, and other stakeholders, try to bring their resources to bear on getting geneticists interested in PD research onto the same page and into the same room as neurologists who see patients,” said SAB member Mark Cookson, PhD, of the National Institute on Aging. “It is critical that these groups talk early and often about the next steps in genetic analysis and, in the longer term, in moving from genetic discoveries to practical treatments for Parkinson’s disease.”
Read on for the latest in how the Foundation is working to bring findings from genetics closer to pharmacy shelves. Continue reading “New Understandings of the Genetics of Parkinson’s Disease Inform Drug Development Today” »