# Underuse of statins in MASLD despite population-based associations with lower liver stiffness

**Authors:** Jesse Pustjens, Laurens A. van Kleef, Jelena Pavlović, Lies Lahousse, Adriaan G. Holleboom, Harry L.A. Janssen, Ibrahim Ayada, Maryam Kavousi, Layal Chaker, Jeanine E. Roeters van Lennep, Robert J. De Knegt, Bettina E. Hansen, Bruno H. Stricker, Maarten J.G. Leening, Willem Pieter Brouwer

PMC · DOI: 10.1016/j.jhepr.2026.101764 · 2026-02-11

## TL;DR

Statin use is lower in people with liver disease despite higher heart risk, and statins are linked to better liver and heart outcomes.

## Contribution

First population-based study showing underuse of statins in MASLD and their protective effects on liver stiffness and MASLD.

## Key findings

- MASLD patients with statin indications were less likely to use statins compared to non-MASLD patients.
- Statin use was associated with lower prevalence of MASLD and elevated liver stiffness.
- Higher statin doses were linked to further reductions in MASLD and liver stiffness.

## Abstract

Statins, used for cardiovascular disease (CVD) prevention, may offer hepatoprotective benefits. However, adherence to treatment indications and the associations between statin use, metabolic dysfunction-associated steatotic liver disease (MASLD), and elevated liver stiffness in the general population remain poorly understood.

This prospective, population-based study included adults aged ≥40 years between 2011 and 2020. We evaluated statin indications for CVD risk using prevailing European Society of Cardiology/European Atherosclerosis Society clinical practice guidelines based on SCORE2 and SCORE2-Older Persons algorithms. We used multivariable regression to examine associations between statins, MASLD, and elevated liver stiffness, adjusting for demographic, socioeconomic and metabolic covariables. We performed dose-response analyses using WHO defined daily dosages.

Of 6,405 eligible individuals, 6,055 participants were included in the analysis (median age 64 years; 56% female); MASLD was present in 32%, elevated liver stiffness in 4.8%, and statin use in 21%. Participants with MASLD had higher predicted 10-year CVD risk compared to participants without MASLD (p <0.001), yet were less likely to use statins: 33% of individuals with MASLD and an indication for statin treatment remained untreated, compared to 19% of those without MASLD (p <0.001). Statin use was associated with lower prevalence of MASLD (adjusted odds ratio 0.76; 95% CI 0.63–0.92) and elevated liver stiffness (adjusted odds ratio 0.65; 95% CI 0.46–0.92) relative to untreated individuals with a statin treatment indication. The highest statin WHO defined daily dosage category was associated with lower prevalence of MASLD (p = 0.033) and elevated liver stiffness (p = 0.035).

Individuals with MASLD are less likely to use statins despite a contemporary guideline-based indication. Statin use is independently associated with lower prevalence of both MASLD and elevated liver stiffness. These findings underscore the need to improve CVD risk management in this population with the potential added benefit of mitigating MASLD.

In this large prospective, population-based study, statins were underutilized in metabolic dysfunction-associated steatotic liver disease (MASLD) compared to non-MASLD individuals, even though they had the highest cardiovascular risk and met guideline-based treatment criteria. Our findings further demonstrate that individuals who used statins had a lower likelihood of MASLD and elevated liver stiffness compared with statin-eligible individuals who were not treated. Taken together, these results highlight a missed opportunity: optimizing statin use in people with MASLD could strengthen cardiovascular disease prevention while also offering potential benefits for liver health.

Image 1

•Statins are disproportionally underused in the MASLD population.•Statin use is associated with a lower risk of both MASLD and elevated liver stiffness in the general population.•These findings highlight an opportunity for clinicians to optimize statin therapy in patients with MASLD.•This has the potential to not only reduce cardiovascular morbidity and mortality, but also to mitigate MASLD progression.

Statins are disproportionally underused in the MASLD population.

Statin use is associated with a lower risk of both MASLD and elevated liver stiffness in the general population.

These findings highlight an opportunity for clinicians to optimize statin therapy in patients with MASLD.

This has the potential to not only reduce cardiovascular morbidity and mortality, but also to mitigate MASLD progression.

## Linked entities

- **Diseases:** metabolic dysfunction-associated steatotic liver disease (MONDO:0013209), cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** metabolic diseases (MESH:D008659), viral hepatitis (MESH:D014777), myocardial infarction (MESH:D009203), cirrhosis (MESH:D005355), benign (MESH:D009369), overweight (MESH:D050177), LSM (MESH:D017093), metabolic syndrome (MESH:D024821), heart failure (MESH:D006333), MASLD (MESH:D008107), hypertension (MESH:D006973), Hepatic steatosis (MESH:D005234), liver fibrosis (MESH:D008103), transient ischemic attack (MESH:D002546), insulin resistance (MESH:D007333), abdominal aortic aneurysm (MESH:D017544), peripheral arterial disease (MESH:D058729), dyslipidemia (MESH:D050171), stroke (MESH:D020521), death (MESH:D003643), associated (MESH:D018886), portal hypertension (MESH:D006975), hepatocellular carcinoma (MESH:D006528), CVD (MESH:D002318), Atherosclerosis (MESH:D050197), Diabetes (MESH:D003920)
- **Chemicals:** glucose (MESH:D005947), cholesterol (MESH:D002784), LDL-C (-), alcohol (MESH:D000438), lipid (MESH:D008055), triglycerides (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13019549/full.md

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Source: https://tomesphere.com/paper/PMC13019549