4.6 Article

Genetic Modifiers of Age at Onset for Parkinson's Disease in Asians: A Genome-Wide Association Study

期刊

MOVEMENT DISORDERS
卷 36, 期 9, 页码 2077-2084

出版社

WILEY
DOI: 10.1002/mds.28621

关键词

age at onset; Parkinson's disease; genome-wide association study; genetic modifiers

资金

  1. National Key Research and Development Program of China [2016YFC0901504]
  2. 1.3.5 Project for Disciplines of Excellence, West China Hospital, Sichuan University [ZYJC18038, ZY2016203]
  3. Science Foundation of Chengdu Science and Technology Bureau [2019-YF05-00307-SN]

向作者/读者索取更多资源

This study identified a novel significant intergenic locus that could delay the onset age of Parkinson's disease and suggested a positive selection in the East Asian population. Cross-ethnic meta-analysis also identified a significant locus related to the age at onset of PD in different ethnic groups. These findings contribute to a better understanding of the genetic etiology of AAO of PD and provide new targets for further research and potential therapeutic options.
Background: Age at onset (AAO) is an essential feature of Parkinson's disease (PD) and can help predict disease progression and mortality. Identification of genetic variants influencing AAO of PD could lead to a better understanding of the disease's biological mechanism and provide clinical guidance. However, genetic determinants for AAO of PD remain mostly unknown, especially in the Asian population. Objectives: To identify genetic determinants for AAO of PD in the Asian population. Methods: We performed a genome-wide association meta-analysis on AAO of PD in 5166 Chinese patients with PD (N-discovery = 3628, N-replication = 1538). We then conducted a further cross-ethnic meta-analysis using our results and summary statistics for the AAO of PD from the European population. Results: The total heritability of AAO of PD was around 0.10 similar to 0.14, similar to that (similar to 0.11) estimated in populations of European ancestry. One novel significant intergenic locus rs9783733 (NDN; PWRN4) was identified (P = 3.14E-09, beta = 2.30, SE = 0.39). Remarkably, this variant could delay AAO of PD by similar to 2.43 years, with a more considerable effect on males (similar to 3.18 years) than females (similar to 1.45 years). The variant was suggestively significant in the cross-ethnic meta-analysis and suggested a positive selection in the East Asian population. Additionally, cross-ethnic meta-analysis identified a significant locus rs356203 in SNCA (P = 2.35E-11, beta = -0.71, SE = 0.01). Conclusions: These findings improve the current understanding of the genetic etiology of AAO of PD in different ethnic groups, and provide a new target for further research on PD pathogenesis and potential therapeutic options. (c) 2021 International Parkinson and Movement Disorder Society

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