Evidence map›Paper›PMID 42772677›Full record

ArticleClinics and research in hepatology and gastroenterology2026

Association between statins and chronic liver disease progression: A retrospective cohort study.

Nicholas P Smith, Andrew D Schreiner, Jingwen Zhang, Justin Marsden, Mulugeta Gebregziabher, David G Koch

Abstract read
In one paragraph

Article in Clinics and research in hepatology and gastroenterology, 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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Nicholas P SmithDepartment of Medicine, Medical University of South Carolina, Charleston, SC, 29425, USA. Electronic address: smitnich@musc.edu.
Andrew D SchreinerDepartment of Medicine, Medical University of South Carolina, Charleston, SC, 29425, USA.
Jingwen ZhangDepartment of Medicine, Medical University of South Carolina, Charleston, SC, 29425, USA.
Justin MarsdenDepartment of Medicine, Medical University of South Carolina, Charleston, SC, 29425, USA.
Mulugeta GebregziabherDepartment of Public Health Services, Medical University of South Carolina, Charleston, SC, 29425, USA.
David G KochDivision of Gastroenterology and Hepatology, Department of Medicine, Medical University of South Carolina, Charleston, SC, 29425, USA.

Funding

South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
Advanced Fibrosis Detection and a Predictive Diagnostic Model for Metabolic Dysfunction-associated Steatotic Liver Disease (MASLD) in Primary CareR01DK139087 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SCHREINER, ANDREW DAVID · 2025 to 2025
$2.7M
Improving the Diagnosis of Liver Disease in Primary Care Patients with Abnormal Liver FunctionK23DK118200 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SCHREINER, ANDREW DAVID · 2018 to 2022
$866k
Improving the Diagnosis and Fibrosis Risk Assessment of Nonalcoholic Fatty Liver Disease in Primary Care Patients with Abnormal Liver ChemistriesR03DK129558 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SCHREINER, ANDREW DAVID · 2022 to 2023
$226k
NCATS NIH HHS UL1 TR001450NIDDK NIH HHS K23 DK118200NIDDK NIH HHS R01 DK139087NIDDK NIH HHS R03 DK129558
6 · The paper itself

Abstract

BACKGROUND AND

objectivesStatins improve portal hypertension and may reduce mortality in cirrhosis, though their impact on chronic liver disease (CLD) progression before developing advanced fibrosis or cirrhosis remains unclear. We aimed to assess the association of statin use with severe liver disease (SLD) outcomes (cirrhosis or HCC) and fibrosis progression in CLD patients.

methodsWe performed a retrospective cohort study of primary care electronic health record data from 2012-2021. Included were patients with CLD, lab inputs for a Fibrosis-4 (FIB-4) calculation and no prior SLD. Analysis 1 assessed the association of statin prescriptions with time to SLD in all patients. Analysis 2 evaluated the association of statin prescriptions with time to high-risk FIB-4 (≥3.25) in patients with baseline FIB-4 <3.25. Unadjusted and adjusted Cox and Weibull regression models were used.

resultsThe cohort included 2,872 CLD patients (median index FIB-4 1.2 IQR: 0.7-1.9) followed for a mean of 5.7 (±2.6) years. 884 (31%) patients received statins and 378 (13%) experienced an SLD outcome. Statin prescription was associated with a lower risk of SLD (adjusted HR 0.51; 95% CI 0.39-0.66). Analysis 2 included 2,547 patients with an index FIB-4 <3.25 followed for a mean of 5.4 (±2.6) years. 855 (34%) patients received statins and 600 (24%) progressed to a FIB-4 ≥3.25. Statin prescription was associated with a lower hazard of progressing to high-risk FIB-4 (adjusted HR 0.36; 95% CI 0.32-0.42).

conclusionIn a primary care population, statin prescriptions were associated with a lower risk of fibrosis progression and SLD.

Indexed as

CirrhosisFibrosisHepatocellular carcinomaPrimary care

Identifiers

PMID42772677
PMCPMC13690171

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