孟德尔随机化
阻塞性睡眠呼吸暂停
帕金森病
疾病
医学
置信区间
全基因组关联研究
单核苷酸多态性
内科学
痴呆
快速眼动睡眠行为障碍
人口
肿瘤科
遗传学
生物
基因型
遗传变异
环境卫生
基因
作者
Jinwei Li,Lanqing Zhao,Xiaoxu Ding,Xiangguo Cui,Qi Li,Yu Chen
标识
DOI:10.1016/j.sleep.2022.06.004
摘要
Previous studies reported that obstructive sleep apnea (OSA) was associated with neurodegenerative diseases. However, whether these associations are causal are still unsettled. In our study, we investigated the causal effects of genetically-predicted OSA on Alzheimer's disease (AD) and Parkinson disease (PD).We implemented two-sample Mendelian randomization to judge causation using summary statistics from three independent and large genome-wide association studies on OSA (cases n = 16,761, controls n = 201,194), AD (cases n = 71,880, controls n = 383,378) and PD (cases n = 33,774, controls n = 449,056). Four single nucleotide polymorphisms (SNPs) with genome-wide significance associated with OSA served as instrumental variables. We prioritized the inverse variance weighted method when generating unconfounded estimates. Besides, MR-Egger regression, weighted mode, and weighted median methods were adopted as a supplement to the inverse variance weighted method.We found no evidence supporting significant causal relationships between OSA and AD or PD among European population. The risk ratio of AD was 0.99 (95% confidence interval (CI) [0.92,1.08]) and that of PD was 0.82 (95%CI [0.47, 1.40]). Results from alternative approaches were generally consistent with that of the inverse variance weighted method.The present study found no evidence for causal associations between OSA and the risk of AD or PD in individuals of European ancestry.
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