Frontiers in Aging Neuroscience | |
Bidirectional Mendelian randomization study of psychiatric disorders and Parkinson’s disease | |
Aging Neuroscience | |
Shulin Liu1  Yaqing Xiang1  Jiabin Liu1  Yige Wang1  Xiurong Huang1  Qi Wu2  Xuxiong Tang2  Qian Xu3  Jifeng Guo3  Xinxiang Yan4  Beisha Tang4  | |
[1] Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China;Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China;Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, Hunan, China;Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China;Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, Hunan, China;Hunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha, China;Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China;Engineering Research Center of Hunan Province in Cognitive Impairment Disorders, Central South University, Changsha, China;National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan, China;Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China;Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, Hunan, China;Hunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha, China;Engineering Research Center of Hunan Province in Cognitive Impairment Disorders, Central South University, Changsha, China;National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan, China; | |
关键词: Parkinson’s disease; psychiatric disorders; Mendelian randomization; genome-wide association studies; causal relationship; | |
DOI : 10.3389/fnagi.2023.1120615 | |
received in 2022-12-10, accepted in 2023-02-21, 发布年份 2023 | |
来源: Frontiers | |
【 摘 要 】
IntroductionAlthough the relationship between psychiatric disorders and Parkinson’s disease (PD) has attracted continuous research attention, the causal linkage between them has not reached a definite conclusion.MethodsTo identify the causal relationship between psychiatric disorders and PD, we used public summary-level data from the most recent and largest genome-wide association studies (GWASs) on psychiatric disorders and PD to conduct a bidirectional two-sample Mendelian randomization (MR). We applied stringent control steps in instrumental variable selection using the Mendelian randomization pleiotropy residual sum and outlier (MR-PRESSO) method to rule out pleiotropy. The inverse-variance weighted (IVW) method was used to identify the causal relationship between psychiatric disorders and PD. Multiple MR analysis methods, including MR-Egger, weighted-median, and leave-one-out analyses, were used for sensitivity analysis, followed by heterogeneity tests. Further validation and reverse MR analyses were conducted to strengthen the results of the forward MR analysis.ResultsThe lack of sufficient estimation results could suggest a causal relationship between psychiatric disorders and PD in the forward MR analysis. However, the subsequent reverse MR analysis detected a causal relationship between PD and bipolar disorder (IVW: odds ratios [OR] =1.053, 95% confidence interval [CI] =1.02–1.09, p = 0.001). Further analysis demonstrated a causal relationship between genetically predicted PD and the risk of bipolar disorder subtype. No pleiotropy or heterogeneity was detected in the analyses.DiscussionOur study suggested that while psychiatric disorders and traits might play various roles in the risk of developing PD, PD might also be involved in the risk of developing psychiatric disorders.
【 授权许可】
Unknown
Copyright © 2023 Wu, Liu, Huang, Liu, Wang, Xiang, Tang, Xu, Yan, Tang and Guo.
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