Katalog Plus
Bibliothek der Frankfurt UAS
Bald neuer Katalog: sichern Sie sich schon vorab Ihre persönlichen Merklisten im Nutzerkonto: Anleitung.
Dieses Ergebnis aus BASE kann Gästen nicht angezeigt werden.  Login für vollen Zugriff.

Does COMT Play a Role in Parkinson's Disease Susceptibility across Diverse Ancestral Populations?

Title: Does COMT Play a Role in Parkinson's Disease Susceptibility across Diverse Ancestral Populations?
Authors: Martín‐Bórnez, Miguel; Shar, Nisar; Nour, Mohamed Ahmed; Murphy, David; Elsayed, Inas; Nanjundaswamy, Megha Shri; Nwaokorie, Francisca; Olusanya, Adedunni; Kuznetsov, Nicole; Bandres‐Ciga, Sara; Noyce, Alastair J.; Iwaki, Hirotaka; Jones, Lietsel; Gómez‐Garre, Pilar; Mir, Pablo; Periñán, María Teresa
Contributors: Council of Scientific and Industrial Research, India; Instituto de Salud Carlos III; Aligning Science Across Parkinson's
Source: Movement Disorders ; ISSN 0885-3185 1531-8257
Publisher Information: Wiley
Publication Year: 2025
Collection: Wiley Online Library (Open Access Articles via Crossref)
Description: Background The catechol‐ O ‐methyltransferase ( COMT ) gene is involved in brain catecholamine metabolism, but its association with Parkinson's disease (PD) risk remains unclear. Objective Our aim was to investigate the relationship between COMT genetic variants and PD risk across diverse ancestries. Methods We analyzed COMT variants in 2251 PD patients and 2835 controls of European descent using whole‐genome sequencing from the Accelerating Medicines Partnership‐Parkinson Disease (AMP‐PD), along with 20,427 PD patients and 11,837 controls from 10 ancestries using genotyping data from the Global Parkinson's Genetics Program (GP2). Results Using the largest case–control datasets to date, no significant enrichment of COMT risk alleles in PD patients was observed across any ancestry group after correcting for multiple testing. Among Europeans, no correlations with cognitive decline, motor function, motor complications, or time to levodopa‐induced dyskinesia onset were observed. Conclusions This study highlights the need for increased representation of diverse ancestries to better understand the role of COMT variants in PD. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1002/mds.70040
Availability: https://doi.org/10.1002/mds.70040; https://movementdisorders.onlinelibrary.wiley.com/doi/pdf/10.1002/mds.70040
Rights: http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.205E713B
Database: BASE