Background: Metabolic dysfunction-associated steatotic liver disease (MASLD) is a growing cause of morbidity and mortality, with cardiovascular disease as the leading cause of death. Hypertension is a common comorbidity, yet the impact of antihypertensive medications on MASLD outcomes remains unclear. This study examines the associations between antihypertensive medication use, liver fibrosis, and mortality in MASLD patients. Methods: We analyzed pooled data from NHANES (1999-2018) linked to National Death Index records. MASLD was defined using validated non-invasive indices (US-FLI, FLI, HSI), and liver fibrosis was assessed using FIB-4, APRI, NFS, and BARD scores. Cox proportional hazards models with inverse probability of treatment weighting (IPTW) were used to evaluate the associations between antihypertensive medications (ACEIs, ARBs,β-blockers, CCBs, and diuretics) and clinical outcomes, with multiple sensitivity analyses conducted to assess the robustness of the findings. Results: Among 19,603 participants (mean age 49.5 years, 52.5% female), antihypertensive use was associated with a significantly lower risk of liver fibrosis (FIB-4-defined) in MASLD (aHR, 0.17; 95% CI, 0.04-0.78). ACEIs (aHR, 0.25; 95% CI, 0.08-0.74) and ARBs (aHR, 0.23; 95% CI, 0.06-0.86) were associated with lower all-cause mortality compared to CCBs. Conclusion: ACEIs and ARBs were associated with reduced liver fibrosis and all-cause mortality in MASLD patients. These findings support further investigation into the potential role of renin-angiotensin system inhibition as a therapeutic strategy in MASLD. Key words: Steatotic liver disease; Metabolic dysfunction-associated steatotic liver disease; Liver fibrosis; Antihypertensive medications; Mortality.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis study did not receive any funding
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
https://www.cdc.gov/nchs/nhanes/
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Comments (0)