Commentary
Video
The chief scientific officer of the Parkinson’s Foundation talked about how broad genetic testing through PD GENEration is uncovering valuable prognostic and diagnostic insights in Parkinson disease. [WATCH TIME: 4 minutes]
WATCH TIME: 4 minutes
"We’re talking to clinicians who discover anecdotally that the person they were sure had a genetic form of Parkinson doesn’t and then someone they never suspected turns out to have a genetic link. That really underscores the broad nature of what we’re trying to do with PD GENEration, which is to offer genetic testing to everyone in a clinic."
Parkinson’s Awareness Month, held each April, is a time dedicated to increasing public understanding of Parkinson disease (PD), a progressive movement disorder affecting nearly 1 million patients in the United States. Recently, the Parkinson’s Foundation launched a campaign to educate the public during the month on key aspects of PD, from symptoms to treatment options.1 The animated, digital guide to Parkinson’s Awareness Month (PAM) campaign each week shared videos, tips and resources as answers to the most frequently asked questions about PD in both English and Spanish. The Foundation noted that PD awareness month is also a period for patients to share their stories and build a sense of community to not feel alone in their journey living with the condition.
In addition to the PAM campaign, the Foundation’s PD GENEration study, in partnership with Global Parkinson’s Genetics Program, offers whole genome sequencing (WGS) and genetic counseling to patients with PD across more than 8 countries. Presented at the 2025 American Academy of Neurology (AAN) Annual Meeting, held April 5-9, in San Diego, California, by lead author James Beck, PhD, the program includes a panel of 7 core PD genes and 21 additional genes linked to parkinsonisms, with materials adapted for regional languages and healthcare systems. Using a decentralized, “train the trainer” model, the initiative has enrolled over 18,000 participants since 2019, with more than 1800 undergoing WGS. Notably, a 12.2% positivity rate for PD-related variants has been reported, and all genetic data will be shared via the AMP-PD platform.2
At the AAN Annual Meeting, Beck, chief scientific officer at the Foundation, sat down with NeurologyLive® to highlight the evolving role of genetics in PD, emphasizing how WGS through PD GENEration could be revealing unexpected findings that challenge clinical assumptions. Although current treatment approaches remain symptom-focused, Beck noted that genetic data, such as mutations in GBA1 or LRRK2, may inform prognostic conversations and future clinical trial inclusion. He explained that initiative also includes optional secondary findings panels, identifying not only Parkinsonism-related variants but also CDC Tier 1 actionable genes tied to hereditary cancer and cardiovascular conditions. Beck emphasized that these insights may support broader decision-making in neurology and underscore the potential of precision medicine in PD.
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Editor’s Note: Beck has disclosed that he has received personal compensation for serving as an employee of Parkinson's Foundation and that the institution of Beck has received research support from NIH, MJFF.