Li Yue, Chen Yunxian, Li Zhe, Li Yanrong, Chen Yicai, Tang Liangqiu
Department of Cardiology, Yue Bei People's Hospital, Shantou University Medical College, 512099 Shaoguan, Guangdong, China.
Department of Rheumatology and Immunology, Shenzhen People's Hospital, The Second Clinical Medical College, Jinan University, 518071 Shenzhen, Guangdong, China.
Rev Cardiovasc Med. 2024 Jan 29;25(2):41. doi: 10.31083/j.rcm2502041. eCollection 2024 Feb.
According to recent studies, atherosclerosis and gut microbiota are related. Nevertheless, it has been discovered that the gut microbiota varies across studies, with its function still being debated, and such relationships not proven to be causal. Thus, our study aimed to identify the key gut microbiota taxa (GM taxa) at different taxonomic levels, namely, the phylum, class, order, family, and genus, to investigate any potential causal links to atherosclerosis.
We employed summary data from the MiBioGen consortium on the gut microbiota to conduct a sophisticated two-sample Mendelian randomization (MR) analysis. Pertinent information regarding atherosclerosis statistics was acquired from the FinnGen Consortium R8 publication. To assess causality, the utilized principal analytical technique was the inverse variance-weighted (IVW) method. Supplementary to IVW, additional MR methodologies were employed, including weighted median, MR-Egger, weighted methods, and simple mode. Sensitivity analyses involved the application of Cochrane's Q-test, MR-Egger intercept test, MR-PRESSO global test, and leave-one-out analysis.
Finally, after performing an MR study on the risk of 211 GM taxa on atherosclerosis, we discovered 20 nominal links and one strong causal link. Firmicutes (phylum ID: 1672) (odds ratio (OR) = 0.852 (0.763, 0.950), = 0.004) continued to be connected with a lower incidence of coronary atherosclerosis, even after Bonferroni correction.
Based on the discovered data, it was established that the phylum Firmicutes exhibits a causal relationship with a reduced occurrence of coronary atherosclerosis. This investigation could potentially provide novel insights into therapeutic objectives for atherosclerosis by focusing on the gut microbiota.
根据最近的研究,动脉粥样硬化与肠道微生物群有关。然而,人们发现不同研究中的肠道微生物群存在差异,其功能仍存在争议,而且这种关系尚未被证明具有因果性。因此,我们的研究旨在确定不同分类水平(即门、纲、目、科和属)上的关键肠道微生物分类群(GM分类群),以研究与动脉粥样硬化的任何潜在因果联系。
我们利用来自MiBioGen联盟的肠道微生物群汇总数据进行了复杂的两样本孟德尔随机化(MR)分析。有关动脉粥样硬化统计的相关信息从FinnGen联盟R8出版物中获取。为了评估因果关系,使用的主要分析技术是逆方差加权(IVW)方法。除IVW外,还采用了其他MR方法,包括加权中位数、MR-Egger、加权方法和简单模式。敏感性分析包括应用Cochrane's Q检验、MR-Egger截距检验、MR-PRESSO全局检验和留一法分析。
最后,在对211个GM分类群对动脉粥样硬化的风险进行MR研究后,我们发现了20个名义联系和1个强因果联系。即使经过Bonferroni校正,厚壁菌门(门ID:1672)(优势比(OR)=0.852(0.763,0.950),P=0.004)仍与冠状动脉粥样硬化的较低发病率相关。
根据发现的数据,确定厚壁菌门与冠状动脉粥样硬化发生率降低之间存在因果关系。这项研究可能通过关注肠道微生物群为动脉粥样硬化的治疗目标提供新的见解。