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No genetic causal association between Alzheimer’s disease and osteoporosis: A bidirectional two-sample Mendelian randomization study

孟德尔随机化 单核苷酸多态性 全基因组关联研究 骨质疏松症 多效性 遗传关联 医学 疾病 生物信息学 遗传学 肿瘤科 生物 内科学 基因 基因型 遗传变异 表型
作者
Hongxin Hu,Jian Mei,Yuanqing Cai,Haiqi Ding,Susheng Niu,Wenming Zhang,Xinyu Fang
出处
期刊:Frontiers in Aging Neuroscience [Frontiers Media]
卷期号:15 被引量:3
标识
DOI:10.3389/fnagi.2023.1090223
摘要

Many observational studies have found an association between Alzheimer's disease (AD) and osteoporosis. However, it is unclear whether there is causal genetic between osteoporosis and AD.A two-sample Mendelian randomization (MR) study was used to investigate whether there is a causal relationship between osteoporosis and AD. Genes for osteoporosis and AD were obtained from published the genome-wide association studies (GWAS). Single nucleotide polymorphisms (SNPs) with significant genome-wide differences (p < 5 × 10-8) and independent (r2 < 0.001) were selected, and SNPs with F ≥ 10 were further analyzed. Inverse variance weighted (IVW) was used to assess causality, and the results were reported as odds ratios (ORs). Subsequently, heterogeneity was tested using Cochran's Q test, pleiotropy was tested using the MR-Egger intercept, and leave-one-out sensitivity analysis was performed to assess the robustness of the results.Using the IVW method, MR Egger method, and median-weighted method, we found that the results showed no significant causal effect of osteoporosis at different sites and at different ages on AD, regardless of the removal of potentially pleiotropic SNPs. The results were similar for the opposite direction of causality. These results were confirmed to be reliable and stable by sensitivity analysis.This study found that there is no bidirectional causal relationship between osteoporosis and AD. However, they share similar pathogenesis and pathways.

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