Genetic landscape of Parkinson’s disease in the Personalized Parkinson Project cohort

Abstract Background Parkinson’s disease (PD) is a multifactorial neurodegenerative disorder shaped by, amongst others, high-impact variants and common polygenic factors. The Personalized Parkinson Project (PPP) offers deep phenotyping and longitudinal follow-up of Dutch people with PD. Here, we characterize the genetic landscape and its interaction with lifestyle factors within PPP. Methods We utilized three complementary approaches in N=507 persons with PD: 1) short-read PD gene panel sequencing of eight PD genes, 2) genome-wide genotyping array, and 3) targeted long-read sequencing of the GBA1 gene. Additionally, we calculated the mitochondrial-function polygenic score (MGS). Associations between genetic factors, smoking status, and age at onset (AAO) were assessed using non-parametric tests, correlation analyses, and multiple regression models. Results Genetic screening of the participants revealed N=79 GBA1 (∼15%), N=3 LRRK2 , N=1 CHCHD2 , N=1 SNCA variant carrier, and N=9 heterozygous PRKN/PINK1 variants. We also observed an interaction between MGS and smoking: MGS was associated with earlier AAO in non-smokers in persons with iPD (N=414, β=-1.87, p=0.038). Conclusion Our findings corroborate previously reported frequencies of variants in PD-associated genes in European populations, and suggest a potential association between smoking and a mitochondrial dysfunction signature in PD. Thus, even in persons without rare variants (iPD subgroup), complex genetic contributions remained relevant. Our study supports future downstream stratification and personalized medicine approaches with high-impact variants and polygenic risk scores.

Authors

Institutions

Publication Details

Journal
medRxiv
Published
2026-03-23
DOI
https://doi.org/10.64898/2026.03.16.26348127
Primary Topic
Parkinson's Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Genetic landscape of Parkinson’s disease in the Personalized Parkinson Project cohort

Sara Beatriz Gomes Fernandes, Marcel M. Verbeek, Theresa Lüth, Kenan Steidel et al.
medRxiv
Parkinson's Disease Mechanisms and Treatments
article

Genetic landscape of Parkinson’s disease in the Personalized Parkinson Project cohort

Sara Beatriz Gomes Fernandes, Marcel M. Verbeek, Theresa Lüth, Kenan Steidel, Susen Schaake, Christoph Much, Zied Landoulsi, Vyron Gorgogietas, Jannik Prasuhn, Sana Hrir, R. Helmich, Patrick May, Tiago F. Outeiro, Norbert Brüggemann, Bart P. van de Warrenburg, Christine Klein, Joanne Trinh, Bastiaan R. Bloem, Rejko Krüger, H. Bea Kuiperij, Teresa Kleinz
article en

Abstract

Abstract Background Parkinson’s disease (PD) is a multifactorial neurodegenerative disorder shaped by, amongst others, high-impact variants and common polygenic factors. The Personalized Parkinson Project (PPP) offers deep phenotyping and longitudinal follow-up of Dutch people with PD. Here, we characterize the genetic landscape and its interaction with lifestyle factors within PPP. Methods We utilized three complementary approaches in N=507 persons with PD: 1) short-read PD gene panel sequencing of eight PD genes, 2) genome-wide genotyping array, and 3) targeted long-read sequencing of the GBA1 gene. Additionally, we calculated the mitochondrial-function polygenic score (MGS). Associations between genetic factors, smoking status, and age at onset (AAO) were assessed using non-parametric tests, correlation analyses, and multiple regression models. Results Genetic screening of the participants revealed N=79 GBA1 (∼15%), N=3 LRRK2 , N=1 CHCHD2 , N=1 SNCA variant carrier, and N=9 heterozygous PRKN/PINK1 variants. We also observed an interaction between MGS and smoking: MGS was associated with earlier AAO in non-smokers in persons with iPD (N=414, β=-1.87, p=0.038). Conclusion Our findings corroborate previously reported frequencies of variants in PD-associated genes in European populations, and suggest a potential association between smoking and a mitochondrial dysfunction signature in PD. Thus, even in persons without rare variants (iPD subgroup), complex genetic contributions remained relevant. Our study supports future downstream stratification and personalized medicine approaches with high-impact variants and polygenic risk scores.

medRxiv
Radboud University Nijmegen (NL), Philipps University of Marburg (DE), Centre Hospitalier de Luxembourg (LU), University of Luxembourg (LU), Radboud University Medical Center (NL), Universitätsmedizin Göttingen (DE), University of Lübeck (DE)
Good health and well-being
Openalex Percentile: Top 16%
Parkinson's Disease Mechanisms and Treatments
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.