肠道菌群与心房颤动风险的因果关联:基于两样本孟德尔随机化研究OA
Causal associations between gut microbiota and atrial fibrillation risk:a two-sample Mendelian randomization study
目的 探讨特定肠道菌群与心房颤动(简称房颤)风险之间的因果关联,并评估房颤对肠道菌群的潜在反向作用.方法 采用两样本孟德尔随机化方法,基于芬兰基因数据库发布的全基因组关联研究汇总数据,分析19种菌群与房颤的双向关系.正向分析纳入芽孢杆菌C类群、双歧杆菌属、CAG-273未命名菌株sp003534295、蓝菌门、菌毛菌纲、厚壁菌门A类群及姜氏菌科;反向分析纳入CAG-245未命名菌株sp000435175、CAG-245类群、链状粪杆菌、粪芽孢菌属、巨球形菌属、Phocea属菌、费氏丙酸杆菌、琥珀酸弧菌属、热球菌科、热球菌纲及UBA2922未命名菌株sp900313925.采用逆方差加权法、MR-Egger回归及加权中位数法检验稳健性,并以错误发现率(false discovery rate,FDR)<0.05进行多重比较校正.结果 双歧杆菌属、CAG-273未命名菌株sp003534295、蓝菌门、菌毛菌纲及姜氏菌科丰度升高与房颤风险降低相关;芽孢杆菌C类群及厚壁菌门A类群与房颤呈正相关.房颤可导致粪芽孢菌属、链状粪杆菌、Phocea属菌、费氏丙酸杆菌、热球菌科等丰度增加,而CAG-245未命名菌株sp000435175、CAG-245类群、巨球形菌属及琥珀酸弧菌属丰度下降.结论 多种肠道菌群与房颤存在方向不同的遗传因果关联,房颤亦可重塑肠道微生态."肠道-心脏轴"可能参与房颤的发生发展,为微生态干预提供了潜在靶点.
Objective To investigate the causal associations between specific gut microbiota and the risk of atrial fibrillation(AF),and to evaluate the potential reverse effects of AF on gut microbiota.Methods A two-sample Mendelian randomization(MR)approach was employed to analyze bidirectional relationships between 19 gut microbial taxa and AF,based on the Genome-Wide Association Study(GWAS)summary statistics from the FinnGen consortium.Forward analysis included Bacillus group C,Bifidobacterium,unnamed strain sp003534295 of CAG-273,Cyanobacteria,Fimbriimonadia,Firmicutes group A,and Jiangellaceae.Reverse analysis included unnamed strain sp000435175 of CAG-245,CAG-245 group,Coprobacillus cateniformis,Coprobacillus,Megasphaera,Phocea sp.,Propionibacterium freudenreichii,Succinivibrio,Thermococcaceae,Thermococci,and unnamed strain sp900313925 of UBA2922.Robustness was assessed using inverse variance weighted,MR-Egger regression,and weighted median methods,with multiple comparisons corrected using a false discovery rate(FDR)threshold of<0.05.Results Higher abundances of Bifidobacterium,unnamed strain sp003534295 of CAG-273,Cyanobacteria,Fimbriimonadia,and Jiangellaceae were associated with a reduced risk of AF;Bacillus group C and Firmicutes group A showed positive associations with AF.AF led to increased abundances of Coprobacillus,Coprobacillus cateniformis,Phocea sp.,Propionibacterium freudenreichii,and Thermococcaceae,while the abundances of unnamed strain sp000435175 of CAG-245,CAG-245 group,Megasphaera,and Succinivibrio decreased.Conclusion Multiple gut microbial taxa exhibit genetically predicted causal relationships with AF in different directions,and AF itself can reshape the gut microbiome.The"gut-heart axis"may be involved in the pathogenesis and progression of AF,offering potential targets for microbiota-based interventions.
袁关秀;廖丽华
545000 广西柳州,柳州市人民医院门诊部545000 广西柳州,柳州市人民医院门诊部
医药卫生
孟德尔随机化心房颤动肠道菌群因果推断
Mendelian randomizationatrial fibrillationgut microbiotacausal inference
《实用心电与临床诊疗》 2026 (3)
407-413,419,8
评论