Causal Associations of DNA Methylation and Cardiovascular Disease: A Two-Sample Mendelian Randomization Study

被引:0
|
作者
Gao, Hui [1 ,2 ]
Li, Jiahai [3 ]
Ma, Qiaoli [4 ]
Zhang, Qinghui [5 ]
Li, Man [1 ]
Hu, Xiaoliang [1 ]
机构
[1] First Peoples Hosp Shangqiu, Dept Cardiovasc Med, Shangqiu 476000, Peoples R China
[2] Dalian Med Univ, Grad Sch, Dalian 116044, Peoples R China
[3] First Peoples Hosp Qinzhou, Dept Cardiovasc Med, Qinzhou 535000, Peoples R China
[4] Cent Hosp Zibo, Dept Cardiovasc Med, Zibo 255000, Peoples R China
[5] Henan Prov Peoples Hosp, Dept Hypertens, Zhengzhou 450000, Peoples R China
关键词
Mendelian randomization; methylation; cardiovascular disease; ATRIAL-FIBRILLATION; RISK-FACTORS;
D O I
10.5334/gh.1324
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: There is growing evidence that concentrations of DNA methylation are associated with cardiovascular disease; however, it is unclear whether this association reflects a causal relationship. Methods: We utilized a two-sample Mendelian randomization (MR) approach to investigate whether DNA methylation can affect the risk of developing cardiovascular disease in human life. We primarily performed the inverse variance weighted (IVW) method to analyze the causal effect of DNA methylation on multiple cardiovascular diseases. Additionally, to ensure the robustness of our findings, we conducted several sensitivity analyses using alternative methodologies. These analysis methods included maximum likelihood, MR-Egger regression, weighted median method, and weighted model methods. Results: Inverse variance weighted estimates suggested that an SD increase in DNA methylation Hannum age acceleration exposure increased the risk of cardiac arrhythmias (OR = 1.03, 95% CI 1.00-1.05, p = 0.0290) and atrial fibrillation (OR = 1.03, 95% CI 1.00-1.05, p = 0.0022). We also found that an SD increase in DNA methylation PhenoAge acceleration exposure increased the risk of heart failure (OR = 1.01, 95% CI 1.00-1.03, p = 0.0362). Exposure to DNA methylation-estimated granulocyte proportions was found to increase the risk of hypertension (OR = 1.00, 95% CI 1.00-1.0001, p = 0.0291). Exposure to DNA methylation-estimated plasminogen activator inhibitor-1 levels was found to increase the risk of heart failure (OR = 1.00, 95% CI 1.00-1.00, p = 0.0215). Conclusion: This study reveals a causal relationship between DNA methylation and CVD. Exposed to high levels of DNA methylation Hannum age acceleration inhabitants with an increased risk of cardiac arrhythmias and atrial fibrillation. DNA methylation PhenoAge acceleration levels exposure levels were positively associated with the increased risk of developing heart failure. This has important implications for the prevention of cardiovascular diseases.
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页数:11
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