Analysis of rare Parkinson’s disease variants in millions of people

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作者
Vanessa Pitz
Mary B. Makarious
Sara Bandres-Ciga
Hirotaka Iwaki
Andrew B. Singleton
Mike Nalls
Karl Heilbron
Cornelis Blauwendraat
机构
[1] National Institutes of Health,Integrative Neurogenomics Unit, Laboratory of Neurogenetics, National Institute on Aging
[2] National Institutes of Health,Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging
[3] UCL Queen Square Institute of Neurology,Department of Clinical and Movement Neurosciences
[4] University College London,UCL Movement Disorders Centre
[5] National Institutes of Health,Center for Alzheimer’s and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke
[6] Data Tecnica International,undefined
[7] 23andMe,undefined
[8] Inc.,undefined
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摘要
Although many rare variants have been reportedly associated with Parkinson’s disease (PD), many have not been replicated or have failed to replicate. Here, we conduct a large-scale replication of rare PD variants. We assessed a total of 27,590 PD cases, 6701 PD proxies, and 3,106,080 controls from three data sets: 23andMe, Inc., UK Biobank, and AMP-PD. Based on well-known PD genes, 834 variants of interest were selected from the ClinVar annotated 23andMe dataset. We performed a meta-analysis using summary statistics of all three studies. The meta-analysis resulted in five significant variants after Bonferroni correction, including variants in GBA1 and LRRK2. Another eight variants are strong candidate variants for their association with PD. Here, we provide the largest rare variant meta-analysis to date, providing information on confirmed and newly identified variants for their association with PD using several large databases. Additionally we also show the complexities of studying rare variants in large-scale cohorts.
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