Published Research from the Parkinson’s Foundation Shows Genetic Variants Are More Common in People with Parkinson’s Disease Than Originally Thought
Published Research from the Parkinson’s Foundation Shows Genetic Variants Are More Common in People with Parkinson’s Disease Than Originally Thought
The PD GENEration study, which tests for clinically relevant Parkinson’s genetic variants and offers genetic counseling, reached a milestone of 15,000 participants in spring 2024 and highlights the importance of sharing genetic data with participants
NEW YORK & MIAMI (July 30, 2024) – New research has found that genetic variants associated with Parkinson’s disease (PD) are more common than researchers previously believed. Investigators in the Parkinson’s Foundation-backed PD GENEration study – which reached its goal of 15,000 participants ahead of schedule this spring – found that 13% of participants have a genetic form of PD, which is a significant observation compared to long-standing estimates. Results from the first 3.5 years of the study, which examined a broad North American cohort, was published in the peer-reviewed scientific journal Brain.
PD GENEration, which tests for clinically relevant Parkinson’s-related genes, has been offered by the Parkinson’s Foundation since 2019 to any person with a confirmed PD diagnosis. The study is the first of its kind to return results at scale via live genetic counseling in English or Spanish. This enables participants and physicians to make more informed decisions about their care, including enrollment in gene-specific clinical trials.
Additional key findings from the PD GENEration study published in Brain include:
- 7.7% of participants carried a GBA1 genetic mutation, 2.1% of participants carried a PRKN genetic mutation, and 2.4% of participants carried a LRRK2 genetic mutation. All participants were informed about their genetic status through the genetic counseling component of the program.
- The positivity rate for a genetic variant is significantly higher for individuals with high risk. Those with early-onset PD, high-risk ancestry (such as Ashkenazi Jewish, Spanish Basque, or North African Berber), or a first-degree relative affected with the disease had an 18% positivity rate. The positivity rate for individuals without one of those risk factors was nearly 10%.
- Many of these participants may qualify for precision medicine trials, showing the feasibility and importance of broadly offering genetic testing.
“We did not anticipate the high positivity rate for genetic mutations, specifically the nearly 10% having a positive result even without any known genetic risk factors,” said Roy Alcalay, MD, MS, Tel Aviv Medical Center, Israel, and the Department of Neurology, Columbia University Irving Medical Center, and lead principal investigator for PD GENEration. “Further, the speed at which participants enrolled in PD GENEration is a testament to the interest of people with PD to obtain data on their genetic status. Taken together, the positivity rate and the high interest in getting genotyped will hopefully translate to increased participation in observational studies and clinical trials toward therapies targeting these genes, simplifying precision medicine clinical trials in PD.”
“PD GENEration stands at the forefront of precision medicine and the potential for tailored treatments. In large part, this is because the Parkinson’s Foundation has recognized the importance of including genetic counseling in a research study that discloses genetic results,” said Lola Cook, MS, CGC, Department of Medical and Molecular Genetics at Indiana University, who is first author of the Brain article and one of six genetic counselors involved in the study to date. “As we’ve seen from the study’s enrollment numbers and survey results, there is a strong interest among people with PD to push the research effort forward. This includes understanding the disease’s genetics, generally and individually. It’s the idea that we are all doing our part to move toward improved treatments and a cure.”
PD GENEration is continuing into its next phase with support from the Global Parkinson’s Genetics Program (GP2), a program of the Aligning Science Across Parkinson’s (ASAP) initiative. ASAP’s funding allows the Parkinson’s Foundation to accelerate the study’s impact by focusing on those who have been historically underrepresented in research. Such enhanced wide-scale recruitment is reaching a larger and more diverse community in the United States, Canada and Latin America. The Parkinson’s Foundation aims to enroll an additional 8,000 participants, including 2,400 in Latin America, during the next phase of the study.
“PD GENEration is designed to be inclusive and accessible to all populations, with the goal of improving clinical outcomes for everyone. We are proud that the data we have collected through PD GENEration reflects the largest and most diverse North American cohort ever tested – and even though we reached our initial recruitment goal of 15,000 this spring, bigger things are on the horizon,” said James Beck, PhD, senior vice president and chief scientific officer of the Parkinson’s Foundation. “Our partnership with ASAP and GP2 allows us to reach significantly more people, further increasing the diversity of participants. Being able to understand the genetics that people with PD have in common across different populations could reveal biological secrets of the disease, with the potential to lead to new treatments.”
To learn more about PD GENEration, visit Parkinson.org/PDGENEration or call 1-800-4PD-INFO (473-4636). For questions about enrollment, email Genetics@Parkinson.org.
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About the Parkinson’s Foundation
The Parkinson’s Foundation makes life better for people with Parkinson’s disease by improving care and advancing research toward a cure. In everything we do, we build on the energy, experience and passion of our global Parkinson’s community. Since 1957, the Parkinson’s Foundation has invested more than $449 million in Parkinson’s research and clinical care. Connect with us on Parkinson.org, Facebook, Twitter, Instagram or call 1-800-4PD-INFO (1-800-473-4636).
About Parkinson’s Disease
Affecting an estimated one million Americans, Parkinson’s disease is the second-most common neurodegenerative disease after Alzheimer’s and is the 14th-leading cause of death in the U.S. It is associated with a progressive loss of motor control (e.g., shaking or tremor at rest and lack of facial expression), as well as non-motor symptoms (e.g., depression and anxiety). There is no cure for Parkinson’s and nearly 90,000 new cases are diagnosed each year in the U.S.
Journal
Brain
Method of Research
Observational study
Subject of Research
People
Article Title
Parkinson’s disease variant detection and disclosure: PD GENEration, a North American study
Article Publication Date
29-Jul-2024
COI Statement
L.C. and J.S. received partial funding of salaries from the Michael J. Fox Foundation (MJFF) and the Parkinson’s Foundation; J.V. received partial funding of salaries from MJFF and the Parkinson’s Foundation and received travel funding for the Movement
Disorders Society International Congress, Madrid, Spain, September
2022, abstract and poster presentation ‘PD GENEration Clinical
Phase: Genetic Diagnostic Yield and Clinical Characteristics’ from
the Parkinson’s Foundation and paid to Indiana University School
of Medicine; T.F. received funding of grants from Parkinson’s
Foundation for acting as a Steering Committee Member and received
funding for grants/contracts from Parkinson’s Foundation; A.H. is a
research advocate and received funding of grants from Parkinson’s
Foundation for acting as a Steering Committee Member; K.S.M. received
funding of grants from Parkinson’s Foundation for acting as
a Steering Committee Member, receives funding of grants from
NIH, MJFF, CHDI, HSG, HDSA, Prilenia, Novartis, Roche and Springer
and receives consulting fees from Novartis and funding for leadership
on the Enroll HD Oversight Committee (CHDI) and HSG steering
committee; I.F.M. received funding of grants from the
Parkinson’s Foundation for acting as a Steering Committee
Member and receives funding of grants/conference support from
MJFF, ASAP, NIH and Cleveland Clinic Foundation; N.E.M. received
funding of grants from the Parkinson’s Foundation for acting as a
Steering Committee Member, receives funding of grants from GP2
Monogenic Network, receives payment/honoraria for MDS lectures
and received support for attending the MDS congress in Madrid,
September 2022; M.A.N. received compensation for work as a
Steering Committee member for studies conducted by Bial and
Neurocrine, for consulting work from Roche, Novartis and
Uniqure, grant funding from CHDI and HDSA and received funding
of grants from the Parkinson’s Foundation for acting as a Steering
Committee Member, received payment for presentation at
Parkinson’s Foundation and Parkinson Study Group conferences,
received support for attending Parkinson Study Group conference
and is the Chair of Genetics and environment Working Group for
the Parkinson Study Group; M.A.S. received funding of grants
from the Parkinson’s Foundation for acting as a Steering
Committee Member, receives funding of grants or conference support
from NIH, MJFF, Farmer Family Foundation, Sergey Brin Family
Foundation, American Parkinson’s Disease Association, Cure
Parkinson’s, Parkinson’s Foundation, Harvard School of Public
Health (NIH, DoD), GSK and GE Healthcare, receives consulting
fees through the Parkinson Study Group for PSG advisory services
[including to Bial, Biogen (LUMA/LIGHTHOUSE trials global SC),
UCB (ORHCESTRA trial PSG SC)] and through Sutter Health (NIA),
Northwestern University (NINDS), Cure Parkinson’s for Steering
Committee services (for TOPAZ and SPARX3), International
Linked Clinical Trial Committee (CP), participates on an
Alzheimer’s drug trial Data Monitoring Committee, provides services
for Eli Lilly & Co. and is Chair, Executive Committee for
Parkinson Study Group; T.S. received funding of grants from the
Parkinson’s Foundation for acting as a Steering Committee
Member, receives funding of grants from Amneal, Biogen, Roche,
Neuroderm, Sanofi, Prevail and UCB, is an investigator for NINDS,
MJFF, Parkinson’s Foundation studies, receives consulting fees
from 4D Pharma, Acadia, AcureX, AskBio, Amneal, Blue Rock
Therapeutics, Caraway Therapeutics, Critical Path for Parkinson’s
Consortium (CPP), Denali, MJFF, Neuroderm, Sanofi, Sinopia,
Sunovion, Roche, Takeda, UCB, Vanqua Bio and Voyager and is on
the advisory board for Acadia, AcureX, AskBio, Amneal, Denali,
Sunovion and Roche and the Scientific Advisory Board for 4D
Pharma, Neuroderm, Sanofi and UCB; A.M.W. received funding of
grants from the Parkinson’s Foundation for acting as a Steering
Committee Member and receives funding of grants from NIA/NIH,
Roche/Genentech, Biogen and their institution, participates
on Data Safety Monitoring Board or Advisory Board for Ono
Pharmaceuticals and Amylyx Pharmaceuticals; S.B. receives funding
of a grant through institution for acting as a site principal investigator
for PD GENEration; H.H.F. receives funding of a grant
through institution for acting as a site principal investigator for
PD GENEration, receives funding of grants from Biogen, MJFF,
NINDS and Roche, receives consulting fees for the Parkinson
Study Group, Cerevel, Amneal, AbbVie, receives royalties as a
book author from Springer Publishing, is Co-Chair of the PSG
Executive Committee, is a member of the Scientific Advisory
Board for CCXDP and receives payment as Editor-in-Chief of
Parkinsonism and Related Disorders from Elsevier; I.L. receives
10 | BRAIN 2024: 00; 1–12 L. Cook et al.
funding of a grant through institution for acting as a site principal
investigator for PD GENEration, receives funding from the
National Institutes of Health grants: 2R01AG038791-06A,
U01NS100610, U01NS80818, R25NS098999; U19 AG063911-1 and
1R21NS114764-01A1, MJFF, the Parkinson Foundation, Lewy Body
Association, CurePSP, Roche, Abbvie, Biogen, Centogene.
EIP-Pharma, Biohaven Pharmaceuticals, Novartis and United
Biopharma SRL and UCB and is on the Scientific Advisory Board
for Amydis and on the Scientific Advisory Board of the Rossy PSP
Program at the University of Toronto; H.A.S. receives funding of a
grant through institution for acting as a site principal investigator
for PD GENEration, receives grants from UCB Pharma, Transposon
Therapeutics, Jazz Pharmaceuticals, Barrow Neurological
Foundation, MJFF and NINDS/NIH and receives consulting fees
from Sage/Biogen, AbbVie and Parkinson Study Group/NQ; C.S. receives
funding of a grant through institution for acting as a site
principal investigator for PD GENEration, receives grants from
Pharma Two B, TEVA Pharmaceuticals, Amneal Pharmaceuticals,
Revance Therapeutics and Sunovion Pharmaceuticals; T.F.T. receives
funding of a grant through institution for acting as a site
principal investigator for PD GENEration and receives grants from
MJFF and NIH; N.V.A. receives funding of a grant through institution
for acting as a site principal investigator for PD GENEration and receives
grants from MJFF and NIH; R.C.V. receives funding of a grant
through institution for acting as a site principal investigator for PD
GENEration; L.K. receives funding of a grant through institution for
acting as a site principal investigator for PD GENEration; J.F.Q. receives
funding of a grant through institution for acting as a site
principal investigator for PD GENEration, receives funding for acting
as support to their institution as an LBDA RCOE and serves on
DSMB for NIH and for Travere Pharmaceuticals; P.D.H. received partial
funding of salary from the Parkinson’s Foundation and
receives funding for acting on the PD GENE Latino Advisory
Committee; Y.M. is an employee of Fulgent Genetics; S.P.S. received
support for attending meetings from Illumina, Inc; S.C.R. is employed
by the Parkinson’s Foundation; K.G.G. is employed by the
Parkinson’s Foundation; A.N. is employed by the Parkinson’s
Foundation; J.C.B. is employed by the Parkinson’s Foundation and
receives funding for grants through their institution from NIH;
R.N.A. received grants from the Parkinson’s Foundation for acting
as a Steering Committee Member, receives funding from NIH,
Department of Defense, MJFF and the Silverstein Foundation for
GBA/Parkinson’s disease. He received consulting fees from
Biogen, Biohaven, Capsida, Gain Therapeutics, Sanofi, Servier,
Takeda and Vanqua bio. The other authors report no competing
interests.
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