Liver and Bile

Hepatology. 2022;76(2):469–82

Zhang X, Wong GLH, Yip TCF, Tse YK, Liang LY, Hui VWK, Lin H, Li GL, Lai JC, Chan HL, Wong VWS

Angiotensin-converting enzyme inhibitors prevent liver-related events in non-alcoholic fatty liver disease


Background and aims: Angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) can inhibit liver fibrogenesis in animal models. The authors aimed to evaluate the impact of ACEI/ARB use on the risk of liver cancer and cirrhosis complications in patients with non-alcoholic fatty liver disease (NAFLD).
Approach and results: They conducted a retrospective, territory-wide cohort study of adult patients with NAFLD diagnosed between January 2000 and December 2014 to allow for at least 5 years of follow-up. ACEI or ARB users were defined as patients who had received ACEI or ARB treatment for at least 6 months. The primary end point was liver-related events (LREs), defined as a composite end point of liver cancer and cirrhosis complications. Data from 12,327 NAFLD patients (mean age, 54.2 ± 14.7 years; 6163 men [50%]) were analyzed; 6805 received ACEIs, and 2877 received ARBs. After propensity score weighting, ACEI treatment was associated with a lower risk of LREs (weighted subdistribution hazard ratio [SHR] = 0.48, 95% confidence interval [CI]: 0.35–0.66; p < 0.001), liver cancer (weighted SHR = 0.46, 95% CI: 0.28–0.75; p = 0.002), and cirrhosis complications (weighted SHR = 0.42, 95% CI: 0.27–0.66; p < 0.001), but ARB was not. In subgroup analysis, ACEI treatment was associated with greater reduction in LREs in patients with chronic kidney diseases (CKDs) than those without (CKD-weighted SHR = 0.74, 95% CI: 0.52–0.96; p = 0.036; non-CKD-weighted SHR = 0.15, 95% CI: 0.07–0.33; p < 0.001).

Conclusions: Angiotensin-converting enzyme inhibitor, rather than angiotensin receptor blocker, treatment is associated with a lower risk of liver-related events in non-alcoholic fatty liver disease patients, especially among those with chronic kidney disease.

Prof. Dr. V.W.S. Wong, Department of Medicine and Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong,
E-Mail: wongv@cuhk.edu.hk

DOI: 10.1002/hep.32294

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