Hypertension and NAFLD risk: Insights from the NHANES 2017–2018 and Mendelian randomization analyses

医学 孟德尔随机化 内科学 全国健康与营养检查调查 优势比 血压 置信区间 脂肪肝 代谢综合征 逻辑回归 疾病 人口 环境卫生 肥胖 基因型 生物化学 化学 遗传变异 基因
作者
Mengqin Yuan,Jian He,Xue Hu,Lichao Yao,Ping Chen,Zheng Wang,Pingji Liu,Zhiyu Xiong,Yingan Jiang,Lanjuan Li
出处
期刊:Chinese Medical Journal [Lippincott Williams & Wilkins]
卷期号:137 (4): 457-464 被引量:39
标识
DOI:10.1097/cm9.0000000000002753
摘要

Abstract Background: Hypertension and non-alcoholic fatty liver disease (NAFLD) share several pathophysiologic risk factors, and the exact relationship between the two remains unclear. Our study aims to provide evidence concerning the relationship between hypertension and NAFLD by analyzing data from the National Health and Nutrition Examination Survey (NHANES) 2017–2018 and Mendelian randomization (MR) analyses. Methods: Weighted multivariable-adjusted logistic regression was applied to assess the relationship between hypertension and NAFLD risk by using data from the NHANES 2017–2018. Subsequently, a two-sample MR study was performed using the genome-wide association study (GWAS) summary statistics to identify the causal association between hypertension, systolic blood pressure (SBP), diastolic blood pressure (DBP), and NAFLD. The primary inverse variance weighted (IVW) and other supplementary MR approaches were conducted to verify the causal association between hypertension and NAFLD. Sensitivity analyses were adopted to confirm the robustness of the results. Results: A total of 3144 participants were enrolled for our observational study in NHANES. Weighted multivariable-adjusted logistic regression analysis suggested that hypertension was positively related to NAFLD risk (odds ratio [OR] = 1.677; 95% confidence interval [CI], 1.159–2.423). SBP ≥130 mmHg and DBP ≥80 mmHg were also significantly positively correlated with NAFLD. Moreover, hypertension was independently connected with liver steatosis ( β = 7.836 [95% CI, 2.334–13.338]). The results of MR analysis also supported a causal association between hypertension (OR = 7.203 [95% CI, 2.297–22.587]) and NAFLD. Similar results were observed for the causal exploration between SBP (OR = 1.024 [95% CI, 1.003–1.046]), DBP (OR = 1.047 [95% CI, 1.005–1.090]), and NAFLD. The sensitive analysis further confirmed the robustness and reliability of these findings (all P >0.05). Conclusion: Hypertension was associated with an increased risk of NAFLD.
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