ZhiFei Sun, XiaoDing Wang, QingHe Zhao, Li Xin, PingPing Zhao, XiaoQing Wang, DaCheng Liu
{"title":"A Causal Association Between Atrial Fibrillation and Depression: Evidence From Mendelian Randomization Analyses.","authors":"ZhiFei Sun, XiaoDing Wang, QingHe Zhao, Li Xin, PingPing Zhao, XiaoQing Wang, DaCheng Liu","doi":"10.1177/00912174251393073","DOIUrl":null,"url":null,"abstract":"<p><p>BackgroundThis research assessed the causal influence of atrial fibrillation (AF) on depression.MethodsA two-sample Mendelian randomization (MR) approach was utilized along with data from additional databases. A genome-wide association study (GWAS) involving 463,010 participants allowed for the exploration of genetic variations associated with AF. Another GWAS with 215,644 individuals offered insights into the relationship between gene variants and depression. Data on the correlation between gene variants and depression were obtained from another GWAS encompassing 449,414 individuals. Effect sizes were assessed utilizing the inverse-variance weighted technique. Sensitivity analysis was conducted by weighted median, outlier, MR pleiotropy residual sum, weighted mode, and MR-Egger. A meta-analysis of the inverse-variance weighted (IVW) results from the two datasets was conducted.ResultsA significant association was found between genetically predicted AF and increased incidence of depression using 15 single nucleotide polymorphisms (SNPs) as markers. No evidence of gene pleiotropy was detected, as indicated by MR-Egger. Sensitivity analyses employing alternative Mendelian randomization techniques consistently yielded robust results. The combined odds ratio for depression was estimated at 29.19 (95% CI = 4.43-192.13, <i>P</i> < 0.001).ConclusionThis study found a causal relationship between genetically predicted AF and a heightened risk of depression.</p>","PeriodicalId":50294,"journal":{"name":"International Journal of Psychiatry in Medicine","volume":" ","pages":"736-751"},"PeriodicalIF":1.9000,"publicationDate":"2026-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Psychiatry in Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/00912174251393073","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/20 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 0
Abstract
BackgroundThis research assessed the causal influence of atrial fibrillation (AF) on depression.MethodsA two-sample Mendelian randomization (MR) approach was utilized along with data from additional databases. A genome-wide association study (GWAS) involving 463,010 participants allowed for the exploration of genetic variations associated with AF. Another GWAS with 215,644 individuals offered insights into the relationship between gene variants and depression. Data on the correlation between gene variants and depression were obtained from another GWAS encompassing 449,414 individuals. Effect sizes were assessed utilizing the inverse-variance weighted technique. Sensitivity analysis was conducted by weighted median, outlier, MR pleiotropy residual sum, weighted mode, and MR-Egger. A meta-analysis of the inverse-variance weighted (IVW) results from the two datasets was conducted.ResultsA significant association was found between genetically predicted AF and increased incidence of depression using 15 single nucleotide polymorphisms (SNPs) as markers. No evidence of gene pleiotropy was detected, as indicated by MR-Egger. Sensitivity analyses employing alternative Mendelian randomization techniques consistently yielded robust results. The combined odds ratio for depression was estimated at 29.19 (95% CI = 4.43-192.13, P < 0.001).ConclusionThis study found a causal relationship between genetically predicted AF and a heightened risk of depression.
背景本研究评估心房颤动(AF)对抑郁症的因果影响。方法采用双样本孟德尔随机化(MR)方法,并结合其他数据库的数据。一项涉及463,010名参与者的全基因组关联研究(GWAS)允许探索与房颤相关的遗传变异。另一项涉及215,644名个体的GWAS提供了基因变异与抑郁症之间关系的见解。基因变异与抑郁症之间的相关性数据来自另一项包含449,414人的GWAS。利用反方差加权技术评估效应量。敏感度分析采用加权中位数、离群值、MR多效性残差和、加权模式和MR- egger进行。对两个数据集的反方差加权(IVW)结果进行meta分析。结果以15个单核苷酸多态性(snp)作为标记,发现AF与抑郁发生率显著相关。正如埃格先生所指出的那样,没有发现基因多效性的证据。灵敏度分析采用替代孟德尔随机化技术一致产生稳健的结果。抑郁症的综合优势比估计为29.19 (95% CI = 4.43-192.13, P < 0.001)。结论:本研究发现基因预测的房颤与抑郁风险增加之间存在因果关系。
期刊介绍:
The International Journal of Psychiatry in Medicine (IJPM) bridges the gap between clinical psychiatry research and primary care clinical research. Providing a forum for addressing: The relevance of psychobiological, psychological, social, familial, religious, and cultural factors in the development and treatment of illness; the relationship of biomarkers to psychiatric symptoms and syndromes in primary care...