Chen Jia-Le, Lu Xin-Yi, Chen Dao-Zhen, Chen Yu
Hospital Infection Management Section, Wujin Affiliated Hospital of Nanjing University of Traditional Chinese Medicine, Changzhou, Jiangsu, China.
Wuxi Maternal and Child Health Hospital, Wuxi School of Medicine, Jiangnan University, Wuxi, Jiangsu, China.
Front Cardiovasc Med. 2025 Mar 28;12:1445732. doi: 10.3389/fcvm.2025.1445732. eCollection 2025.
There is a growing body of evidence indicating that metabolites are associated with an increased risk of cardiovascular diseases (CVDs), the underlying causality of these associations remains largely unchallenged. Given the inherent difficulty in establishing causality using epidemiological data, we employed the technique of Mendelian randomization to investigate the potential role of plasma metabolite factors in influencing the risk of CVDs.
The exposure was based on 1,400 plasma metabolites, and outcomes involved four CVD datasets from public databases. Initial causality was assessed by inverse variance weighting (IVW), followed by sensitivity analyses using MR-Egger regression, weighted median, and Multiple Effectiveness Residual Sums and Outliers (MR-PRESSO) method. Potential heterogeneity and multivalence were assessed using the MR-Egger intercept and Cochran's Q statistic. After Bonferroni correction, causal associations were found to be significant with -values less than 0.05. All statistical analyses were rigorously executed in R software.
Our findings identified causal relationships between 15 metabolites and cardiovascular disease. Of these, 4 were associated with AA (aortic aneurysm), 7 with atrial fibrillation and flutter, 2 with HF (heart failure), and 3 with stroke.
This is the first systematic mendelian randomization analysis using genome-wide data to assess the causal relationship between serum metabolites and different cardiovascular diseases, providing preliminary evidence for the impact of lipid metabolism disorders on cardiovascular disease risk.
越来越多的证据表明,代谢物与心血管疾病(CVD)风险增加有关,这些关联的潜在因果关系在很大程度上仍未受到质疑。鉴于使用流行病学数据确定因果关系存在固有困难,我们采用孟德尔随机化技术来研究血浆代谢物因素在影响CVD风险中的潜在作用。
暴露因素基于1400种血浆代谢物,结局涉及来自公共数据库的四个CVD数据集。首先通过逆方差加权(IVW)评估初始因果关系,然后使用MR-Egger回归、加权中位数和多重效应残差总和及异常值(MR-PRESSO)方法进行敏感性分析。使用MR-Egger截距和 Cochr an's Q统计量评估潜在的异质性和多效性。经过 Bonferroni 校正后,发现因果关联在p值小于0.05时具有显著性。所有统计分析均在R软件中严格执行。
我们的研究结果确定了15种代谢物与心血管疾病之间的因果关系。其中,4种与AA(主动脉瘤)相关,7种与心房颤动和扑动相关,2种与HF(心力衰竭)相关,3种与中风相关。
这是首次使用全基因组数据进行的系统孟德尔随机化分析,以评估血清代谢物与不同心血管疾病之间的因果关系,为脂质代谢紊乱对心血管疾病风险的影响提供了初步证据。