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ArticleHepatology international2026

A real-world multicenter study of statins in compensated advanced chronic liver disease on hepatic decompensation and mortality outcomes.

Cheng Han Ng, N Apoorva Sasikumar, Margaret L P Teng, Vincent L Chen, Jimmy Che-To Lai, Karn Wijarnpreecha, Rahul Kumar, Apichat Kaewdech, Masayuki Ueno, Anand V Kulkarni and 10 more

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Article in Hepatology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

20 authors.

Cheng Han Ng *National University Centre for Digestive Health, National University Hospital, Singapore, Singapore.
N Apoorva Sasikumar *Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Margaret L P TengNational University Centre for Digestive Health, National University Hospital, Singapore, Singapore. tenglpm@gmail.com.ORCID http://orcid.org/0000-0001-7472-9214
Vincent L ChenDivision of Gastroenterology and Hepatology, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA.
Jimmy Che-To LaiMedical Data Analytics Centre, Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong Kong.
Karn WijarnpreechaDepartment of Transplant, Mayo Clinic, Jacksonville, FL, USA.
Rahul KumarDepartment of Gastroenterology and Hepatology, Changi General Hospital, Singapore, Singapore.
Apichat KaewdechGastroenterology and Hepatology Unit, Division of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla, Thailand.
Masayuki UenoDepartment of Gastroenterology and Hepatology, Kurashiki Central Hospital, Kurashiki, Japan.
Anand V KulkarniDepartment of Hepatology and Liver Transplantation, Asian Institute of Gastroenterology, Hyderabad, India.
Ming-Hua ZhengMAFLD Research Centre, Department of Hepatology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Akash RoyDepartment of Gastrosciences and Liver Transplantation, Apollo Multispeciality Hospital, Kolkata, West Bengal, India.
Ken LiuDepartment of Gastroenterology, Royal Prince Alfred Hospital, Sydney, Australia.
Chitchai RattananukromDivision of Gastroenterology and Hepatology, Department of Medicine, Faculty of Medicine, Srinagarind Hospital, Khon Kaen University, Khon Kaen, Thailand.
Mazen NoureddinHouston Methodist Hospital and Houston Research Institute, Houston, TX, USA.
Mohammad Shadab SiddiquiUniversity of Virginia School of Medicine, Charlottesville, VA, USA.
Emmanuel TsochatzisUCL Institute for Liver and Digestive Health, University College London, London, UK.
Mark D Muthiah *National University Centre for Digestive Health, National University Hospital, Singapore, Singapore.
Hirokazu Takahashi *Division of Metabolism and Endocrinology, Saga Medical School Faculty of Medicine, Saga University, 5-1-1 Nabeshima, Saga, 849-8501, Japan. takahas2@cc.saga-u.ac.jp.
CORE Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsStatins exert pleiotropic effects, including antiinflammatory, endothelial, and antifibrotic actions, which may slow the progression of cirrhosis. However, their use in patients with compensated advanced chronic liver disease (cACLD) remains limited due to concerns regarding potential hepatotoxicity, and data specific to this population remains sparse.

methodsWe conducted a retrospective, multinational cohort study of adult cACLD (LSM >10 kPa) patients using data from the Cirrhosis Outcome and Research Endeavor (CORE) consortium, across 13 centers in 8 countries. Baseline statin use was the exposure of interest. Associations with first and second hepatic decompensation, composite liver-related events, and all-cause and cause-specific mortality were assessed using Fine-Gray competing-risks regression across two sequentially adjusted multivariable models and an inverse probability of treatment weighting (IPTW) analysis.

resultsAmong 2267 patients, 786 (34.7%) were statin users. Statin use was independently associated with a lower risk of first decompensation (Model 1: sHR 0.64; Model 2: sHR 0.66; IPTW: sHR 0.56) and composite liver-related events (Model 1: sHR 0.61; Model 2: sHR 0.63; IPTW: sHR 0.50), with benefit most pronounced in the moderate-risk portal hypertension strata and MASLD subgroup. No association was observed with all-cause, liver-related, or cardiovascular mortality. Associations with second decompensation were inconsistent.

conclusionIn this large multinational cohort of cACLD patients, statin use was associated with reduced risk of hepatic decompensation and liver-related events, but not all-cause mortality. These findings support a potential benefit for statins in this population.

Indexed as

CirrhosisHepatic decompensationOutcomesStatins

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.