单倍型
队列
帕金森病
帕金森病
疾病
LRRK2
运动障碍
医学
遗传学
队列研究
等位基因
基因型
单核苷酸多态性
遗传关联
等位基因频率
生物
内科学
基因
作者
Marco Toffoli,Abigail Louise Higgins,Chiao Lee,Sofia Koletsi,Xiao Chen,Michael A. Eberle,Fritz J. Sedlazeck,Stephen Mullin,Christos Proukakis,Anthony H.V. Schapira
摘要
GBA mutations are a common risk factor for Parkinson's disease (PD). A recent study has suggested that GBA haplotypes, identified by intronic variants, can affect age at diagnosis of PD.In this study, we assess this hypothesis using long reads across a large cohort and the publicly available Accelerating Medicines Partnership-Parkinson's Disease (AMP-PD) cohort.We recruited a PD cohort through the Remote Assessment of Parkinsonism Supporting Ongoing Development of Interventions in Gaucher Disease study (RAPSODI) and sequenced GBA using Oxford Nanopore technology. Genetic and clinical data on the full AMP-PD cohort were obtained from the online portal of the consortium.A total of 1417 participants were analyzed. There was no significant difference in age at PD diagnosis between the two main haplotypes of the GBA gene.GBA haplotypes do not affect age at diagnosis of PD in the two independent cohorts studied. © 2021 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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