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Recompensation of decompensated cirrhosis in a spectrum of metabolic-dysfunction-related steatotic liver disease, with PEth-corroborated alcohol abstinence and modification of cardiometabolic risk factors

Journal
Hepatology (Baltimore, Md.) (Q1)
Published
17 July 2026
Study design
Unclassified
Evidence level
Level 5, Expert Opinion (CEBM 5)
Authors
Madhumita Premkumar, Anchal Sandhu, Prerna Sharma, Jasvinder Nain, Harish Bhujade, Pankaj Gupta, et al.
PMID
42467948
DOI
10.1097/HEP.0000000000001822

Why clinicians should know about it

Abstract

BACKGROUND AIMS: Recompensation of decompensated metabolic-dysfunction-associated steatotic liver disease (MASLD) and Metabolic Dysfunction-Associated Steatotic Liver Disease with Alcohol Consumption (MetALD) cirrhosis remains unknown. METHODS: We assessed rates and predictors of recompensation (Baveno VII criteria) and outcomes after modifiable interventions, including alcohol abstinence, dry weight loss, and cardiometabolic risk factor management, in a cohort of patients with decompensated MASLD/MetALD cirrhosis between October 2019 and March 2025. RESULTS: Among 344 patients with steatotic liver disease-related cirrhosis (mean MELD-Na 14.7±3.6; MASLD-158, MetALD-186), 64(18.6%) achieved recompensation; MASLD (17.7%) and MetALD (19.4%), at a median of 15 months(IQR:14.5-15.5) over 3.9 years(IQR:2.8-4) follow-up. Baseline phosphatidylethanol (PEth) was negative in MASLD but positive in 69.4% of MetALD patients (p=0.001). 61 patients (17.7%) died, 11(3.2%) underwent liver transplantation, and 5(1.5%) developed hepatocellular carcinoma. Mortality was lower in MASLD than in MetALD (12.0% vs. 22.6%; p=0.011). In competing risk regression adjusted for baseline MELD-Na, absence of large esophageal varices (sHR 1.97, 95%CI:1.22-3.99; p=0.021), weight loss ≥10% (sHR 7.42, 95%CI:3.15-17.47; p< 0.001), alcohol abstinence (sHR 1.87, 95%CI:1.29-3.32; p=0.003), and glycemic control (sHR 1.43, 95%CI:1.03-2.79; p=0.038) were associated with recompensation. Higher MELD-Na (sHR 1.13, 95%CI:1.06-1.2; p<0.001), MetALD etiology (sHR 1.87,95%CI:1.09-3.22; p=0.023), lack of recompensation(p<0.001), and ongoing alcohol consumption (sHR 5.3, 95% CI:2.85-9.74; p< 0.001) were associated with mortality. CONCLUSIONS: PEth improved the ascertainment of alcohol exposure and phenotyping of MASLD and MetALD. Weight loss ≥10%, achievement of glycemic control, and absence of large varices were independently associated with recompensation, which occurred in 18.6% of patients with decompensated MASLD/MetALD cirrhosis.

Abstract as published, via PubMed.

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