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阿尔茨海默病与骨质疏松症之间无遗传因果关联:一项双向双样本孟德尔随机化研究。

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

作者信息

Hu Hongxin, Mei Jian, Cai Yuanqing, Ding Haiqi, Niu Susheng, Zhang Wenming, Fang Xinyu

机构信息

Department of Orthopedic Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.

Department of Orthopaedic Surgery, National Regional Medical Center, Binhai Campus of the First Affiliated Hospital, Fujian Medical University, Fuzhou, China.

出版信息

Front Aging Neurosci. 2023 Jan 25;15:1090223. doi: 10.3389/fnagi.2023.1090223. eCollection 2023.

Abstract

OBJECTIVE

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.

METHODS

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 ( < 5 × 10) and independent (  < 0.001) were selected, and SNPs with  ≥ 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 test, pleiotropy was tested using the MR-Egger intercept, and leave-one-out sensitivity analysis was performed to assess the robustness of the results.

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.

CONCLUSION

This study found that there is no bidirectional causal relationship between osteoporosis and AD. However, they share similar pathogenesis and pathways.

摘要

目的

许多观察性研究发现阿尔茨海默病(AD)与骨质疏松症之间存在关联。然而,尚不清楚骨质疏松症与AD之间是否存在因果遗传关系。

方法

采用两样本孟德尔随机化(MR)研究来调查骨质疏松症与AD之间是否存在因果关系。骨质疏松症和AD的基因来自已发表的全基因组关联研究(GWAS)。选择具有显著全基因组差异(<5×10)且独立(<0.001)的单核苷酸多态性(SNP),并对≥10的SNP进行进一步分析。采用逆方差加权(IVW)评估因果关系,结果以优势比(OR)表示。随后,使用 Cochr an检验测试异质性,使用MR-Egger截距测试多效性,并进行留一法敏感性分析以评估结果的稳健性。

结果

使用IVW方法、MR Egger方法和中位数加权方法,我们发现无论是否去除潜在的多效性SNP,不同部位和不同年龄的骨质疏松症对AD均无显著因果效应。因果关系相反方向的结果相似。敏感性分析证实这些结果可靠且稳定。

结论

本研究发现骨质疏松症与AD之间不存在双向因果关系。然而,它们具有相似的发病机制和途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ed2/9905740/8b6d36695cbb/fnagi-15-1090223-g001.jpg

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