Nonalcoholic fatty liver disease and cardiovascular diseases: A Mendelian randomization study

孟德尔随机化 医学 非酒精性脂肪肝 内科学 心脏病学 冲程(发动机) 动脉硬化 心力衰竭 冠状动脉疾病 疾病 生物信息学 脂肪肝 血压 基因型 机械工程 生物化学 化学 遗传变异 生物 工程类 基因
作者
Hexiang Peng,Siyue Wang,Mengying Wang,Ying Ye,E C Xue,Xi Chen,Xueheng Wang,Fan Meng,Wenjing Gao,Xueying Qin,Yiqun Wu,Dafang Chen,Jin Li,Yonghua Hu,Li Wang,Tao Wu
出处
期刊:Metabolism-clinical and Experimental [Elsevier BV]
卷期号:133: 155220-155220 被引量:56
标识
DOI:10.1016/j.metabol.2022.155220
摘要

Abstract

Background

Evidence suggests that nonalcoholic fatty liver disease (NAFLD) is associated with cardiovascular diseases (CVDs). However, the results are inconsistent, and the causality remains to be established.

Objective

We aimed to investigate the potential causal relationship between NAFLD and CVDs, including arterial stiffness, coronary artery disease, heart failure, stroke, ischemic stroke and its subtypes using two-sample Mendelian randomization (MR).

Methods

Genetic instruments were used as proxies for NAFLD. Publicly available summary-level data were obtained from the UK Biobank, the CARDIoGRAMplusC4D Consortium, the MEGASTROKE Consortium, and other consortia. Six complementary MR methods were performed, including inverse variance weighted method (IVW), MR-Egger, weighted median, weighted mode, MR-PRESSO, and MR-RAPS.

Results

NAFLD was significantly associated with arterial stiffness (β = 0.04 [95%CI, 0.02–0.06], P = 5.53E-04). Moreover, the results remained consistent and robust in the sensitivity analysis. As for heart failure, the IVW method suggested that NAFLD was significantly associated with heart failure (OR = 1.08, 95%CI: 1.02–1.14, P = 0.005) in the absence of pleiotropy. However, there were no significant associations of NAFLD with coronary artery disease, stroke, ischemic stroke, or any ischemic stroke subtype.

Conclusion

The MR study supported the causal effect of NAFLD on arterial stiffness. However, the study did not provide enough evidence suggesting the causal associations of NAFLD with heart failure, coronary artery disease, and any stroke subtypes.
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