Pulse Brain · Growing Health Evidence Index
Tier 3 — Observational / field trialPeer-reviewed

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

Mengqin Yuan, Jian He, Xue Hu, Lichao Yao, Ping Chen, Zheng Wang, Pingji Liu, Zhiyu Xiong, Yingan Jiang, Lanjuan Li

Chinese Medical Journal · 2023

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Summary

This study examined the bidirectional relationship between hypertension and non-alcoholic fatty liver disease (NAFLD) using data from NHANES 2017–2018 and genome-wide association summary statistics. Weighted logistic regression of 3,144 participants found hypertension was positively associated with NAFLD risk (OR=1.677), whilst Mendelian randomisation analysis provided evidence for a causal relationship (OR=7.203). Both systolic and diastolic blood pressure elevation showed independent associations with NAFLD, with findings confirmed by sensitivity analyses.

UK applicability

The findings are relevant to UK clinical practice and public health policy regarding hypertension management and NAFLD screening, as both conditions are prevalent in the UK adult population. However, the study used US NHANES data; applicability requires consideration of differences in UK population genetics, healthcare systems, and dietary patterns.

Key measures

Odds ratios for NAFLD risk; systolic blood pressure (SBP) and diastolic blood pressure (DBP) thresholds (≥130 mmHg and ≥80 mmHg); liver steatosis (β coefficient); inverse variance weighted (IVW) analysis

Outcomes reported

The study measured the association between hypertension (and blood pressure measures) and NAFLD risk using observational data, and investigated causal relationships using Mendelian randomization. Primary outcomes included odds ratios for NAFLD risk and liver steatosis severity.

Theme
Nutrition & health
Subject
Dietary patterns & chronic disease
Study type
Research
Study design
Observational cohort analysis with two-sample Mendelian randomization
Source type
Peer-reviewed study
Status
Published
Geography
United States
System type
Human clinical
DOI
10.1097/cm9.0000000000002753
Catalogue ID
SNmoj1y0b7-qe8ngj

Topic tags

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