Heilbron Karl, Noyce Alastair J, Fontanillas Pierre, Alipanahi Babak, Nalls Mike A, Cannon Paul
123andMe, Inc., 899W Evelyn Avenue, Mountain View, CA 94041 USA.
2Preventive Neurology Unit, Wolfson Institute of Preventive Medicine, Queen Mary University of London, London, UK.
NPJ Parkinsons Dis. 2019 Mar 27;5:4. doi: 10.1038/s41531-019-0077-5. eCollection 2019.
In order to systematically describe the Parkinson's disease phenome, we performed a series of 832 cross-sectional case-control analyses in a large database. Responses to 832 online survey-based phenotypes including diseases, medications, and environmental exposures were analyzed in 23andMe research participants. For each phenotype, survey respondents were used to construct a cohort of Parkinson's disease cases and age-matched and sex-matched controls, and an association test was performed using logistic regression. Cohorts included a median of 3899 Parkinson's disease cases and 49,808 controls, all of European ancestry. Highly correlated phenotypes were removed and the novelty of each significant association was systematically assessed (assigned to one of four categories: known, likely, unclear, or novel). Parkinson's disease diagnosis was associated with 122 phenotypes. We replicated 27 known associations and found 23 associations with a strong a priori link to a known association. We discovered 42 associations that have not previously been reported. Migraine, obsessive-compulsive disorder, and seasonal allergies were associated with Parkinson's disease and tend to occur decades before the typical age of diagnosis for Parkinson's disease. The phenotypes that currently comprise the Parkinson's disease phenome have mostly been explored in relatively small purpose-built studies. Using a single large dataset, we have successfully reproduced many of these established associations and have extended the Parkinson's disease phenome by discovering novel associations. Our work paves the way for studies of these associated phenotypes that explore shared molecular mechanisms with Parkinson's disease, infer causal relationships, and improve our ability to identify individuals at high-risk of Parkinson's disease.
为了系统地描述帕金森病表型组,我们在一个大型数据库中进行了一系列832项横断面病例对照分析。对23andMe研究参与者对832种基于在线调查的表型(包括疾病、药物和环境暴露)的回答进行了分析。对于每种表型,调查受访者被用于构建一组帕金森病病例以及年龄和性别匹配的对照组,并使用逻辑回归进行关联测试。队列包括中位数为3899例帕金森病病例和49808例对照,均为欧洲血统。去除高度相关的表型,并系统评估每个显著关联的新颖性(分为四类之一:已知、可能、不清楚或新颖)。帕金森病诊断与122种表型相关。我们重复了27个已知关联,并发现23个与已知关联有很强先验联系的关联。我们发现了42个以前未报告的关联。偏头痛、强迫症和季节性过敏与帕金森病相关,且往往在帕金森病典型诊断年龄前数十年就出现。目前构成帕金森病表型组的表型大多在相对较小的专门研究中进行了探索。利用单个大型数据集,我们成功地重现了许多这些已确立的关联,并通过发现新的关联扩展了帕金森病表型组。我们的工作为研究这些相关表型铺平了道路,这些研究可以探索与帕金森病共享的分子机制、推断因果关系,并提高我们识别帕金森病高危个体的能力。