You can help in the search for Parkinson’s cure
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Guest columnistResearchers can learn from Ashkenazi Jews' unique genetics

You can help in the search for Parkinson’s cure

Ashkenazi Jews' unique ancestry presents a treasure trove of data for genetic researchers and an opportunity to improve the kind of disease mapping that can speed cures.

Dr. Barbara Robinson
The Parkinson’s Progression Markers Initiative (PPMI), a study sponsored by The Michael J. Fox Foundation, is studying data and bio samples to learn more about Parkinson's disease and, most importantly, speed research that may lead to cures. (Photo from public domain)
The Parkinson’s Progression Markers Initiative (PPMI), a study sponsored by The Michael J. Fox Foundation, is studying data and bio samples to learn more about Parkinson's disease and, most importantly, speed research that may lead to cures. (Photo from public domain)

April is Parkinson’s Awareness Month, and — in honor of the 1 million people living with Parkinson’s in the United States — I have some knowledge to share and an ask to make of you.

You may know that Ashkenazi Jews can trace their ancestry to just 350 individuals. This heritage has created genetic similarities so acute that, according to scientists, “everyone is a 30th cousin.”

With gene mutations passed from generation to generation, Ashkenazi Jews are more likely to carry genetic variants that increase risk of certain conditions, including Parkinson’s disease. This unique ancestry presents a treasure trove of data for genetic researchers and a powerful opportunity to improve the kind of disease mapping that can speed cures.

I don’t have Parkinson’s myself, but am a daughter, daughter-in-law and sister to
individuals diagnosed with the disease — and I know too well the difficulty and frustration that Parkinson’s causes millions of people and their loved ones, especially since the disease has no cure.

Given my family history and Ashkenazi Jewish descent, I wanted to know my genetic status. I learned that I carry mutations in both my LRRK2 and GBA1 genes, which are each associated with increased risk for Parkinson’s.

My husband Jay also carries a mutation in the GBA1 gene.

So, we set out to do everything in our power to learn more about Parkinson’s and test therapies to stop its progression. Together, we enrolled in the Parkinson’s Progression Markers Initiative (PPMI), a study sponsored by The Michael J. Fox Foundation, to share our data and bio samples to help scientists learn more about this disease and, most importantly, speed research that may lead to cures.

PPMI is looking for people of Ashkenazi Jewish descent who themselves have either Parkinson’s or Gaucher’s disease (given a GBA1 connection) or have a first-degree relative who does. PPMI is enrolling people with a mutation in the LRRK2 or GBA1 gene and provides free genetic testing and counseling.

Jay and I support the study by participating in imaging tests and clinical exams. We each contribute bio samples of blood and spinal fluid on an annual basis. We’ve made this commitment because we know the only way we’re going to fight this disease is with knowledge, and this kind of data is our best hope for unlocking the key to new therapies.

If we’re not willing to volunteer that data, then nothing is ever going to change. I hope you’ll join us.

To mark Parkinson’s Awareness Month, I invite you to take a short quiz at www.michaeljfox.org/genetics or call 888-830-6299 to learn more about the PPMI study. PJC

Dr. Barbara Robinson is an obstetrician-gynecologist who lives outside Chicago.

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