Wang Lei, Lin Ziyan, Lin Yuzuo, Wu Qingtong, Zhong Guodong, Chen Liangwan
Department of Cardiovascular Surgery, Fujian Medical University Union Hospital, 350000 Fuzhou, Fujian, China.
Key Laboratory of Cardio-Thoracic Surgery (Fujian Medical University), Fujian Province University, 350000 Fuzhou, Fujian, China.
Rev Cardiovasc Med. 2025 Apr 27;26(4):27734. doi: 10.31083/RCM27734. eCollection 2025 Apr.
Previous research has suggested that metformin may inhibit the dilation of an abdominal aortic aneurysm (AAA); however, these findings are controversial. Additionally, limited reporting exists on the relationships between metformin and thoracic aortic aneurysm (TAA) and aortic dissection (AD). Therefore, this study aimed to assess the potential relationship between metformin and the risk of aortic aneurysm (AA)/AD using the Mendelian randomization (MR) analysis.
Genome-wide association studies and FinnGen summary data were utilized for the MR analysis. The causal relationship between metformin and AA/AD was primarily assessed using the inverse-variance weighted (IVW) method. Sensitivity analyses were conducted to detect heterogeneity and pleiotropy.
The results indicated a negative correlation between metformin treatment and the risk of both AA and AD, with odds ratios(ORs) reported as follows: OR = 0.010, 95% confidence interval (CI):0.000-0.212, = 0.003 for AA, OR = 0.004, 95% CI: 0.000-0.220, = 0.007 for abdominal aortic aneurysm (AAA); OR = 0.017, 95% CI: 0.000-0.815, = 0.039 for thoracic aortic aneurysm (TAA); and OR = 0.001, 95% CI: 0.000-0.531, = 0.032 for AD using the IVW method. These findings suggested that metformin might act as a protective factor against the occurrence of AA/AD. Furthermore, sensitivity analyses validated the robustness of these findings.
This MR analysis identified a potential genetic causal relationship between metformin use and the risks of AA/AD, suggesting that metformin could serve as a protective agent in decreasing the incidences of these conditions.
先前的研究表明二甲双胍可能抑制腹主动脉瘤(AAA)的扩张;然而,这些发现存在争议。此外,关于二甲双胍与胸主动脉瘤(TAA)和主动脉夹层(AD)之间关系的报道有限。因此,本研究旨在使用孟德尔随机化(MR)分析评估二甲双胍与主动脉瘤(AA)/AD风险之间的潜在关系。
全基因组关联研究和芬兰基因组汇总数据用于MR分析。主要使用逆方差加权(IVW)方法评估二甲双胍与AA/AD之间的因果关系。进行敏感性分析以检测异质性和多效性。
结果表明二甲双胍治疗与AA和AD风险之间呈负相关,优势比(OR)如下:AA的OR = 0.010,95%置信区间(CI):0.000 - 0.212,P = 0.003;腹主动脉瘤(AAA)的OR = 0.004,95%CI:0.000 - 0.220,P = 0.007;胸主动脉瘤(TAA)的OR = 0.017,95%CI:0.000 - 0.815,P = 0.039;使用IVW方法得出AD的OR = 0.001,95%CI:0.000 - 0.531,P = 0.032。这些发现表明二甲双胍可能是预防AA/AD发生的保护因素。此外,敏感性分析验证了这些发现的稳健性。
这项MR分析确定了二甲双胍使用与AA/AD风险之间潜在的遗传因果关系,表明二甲双胍可作为降低这些疾病发病率的保护剂。