The Rostock International Parkinson's Disease (ROPAD) Study: Protocol and Initial Findings

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • ROPAD Study Group - (Author)
  • Centogene
  • University of Lübeck
  • Gertrudis Klinik Biskirchen – Parkinson Zentrum

Abstract

BACKGROUND: Genetic stratification of Parkinson's disease (PD) patients facilitates gene-tailored research studies and clinical trials. The objective of this study was to describe the design of and the initial data from the Rostock International Parkinson's Disease (ROPAD) study, an epidemiological observational study aiming to genetically characterize ~10,000 participants.

METHODS: Recruitment criteria included (1) clinical diagnosis of PD, (2) relative of participant with a reportable LRRK2 variant, or (3) North African Berber or Ashkenazi Jew. DNA analysis involved up to 3 successive steps: (1) variant (LRRK2) and gene (GBA) screening, (2) panel sequencing of 68 PD-linked genes, and (3) genome sequencing.

RESULTS: Initial data based on the first 1360 participants indicated that the ROPAD enrollment strategy revealed a genetic diagnostic yield of ~14% among a PD cohort from tertiary referral centers.

CONCLUSIONS: The ROPAD screening protocol is feasible for high-throughput genetic characterization of PD participants and subsequent prioritization for gene-focused research efforts and clinical trials. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Details

Original languageEnglish
Pages (from-to)1005-1010
Number of pages6
JournalMovement Disorders
Volume36
Issue number4
Publication statusPublished - Apr 2021
Peer-reviewedYes
Externally publishedYes

External IDs

PubMedCentral PMC8246975
Scopus 85104275746

Keywords

Keywords

  • Cohort Studies, Glucosylceramidase/genetics, Humans, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2/genetics, Mutation, Observational Studies as Topic, Parkinson Disease/diagnosis