# Efficacy and Safety of Statins in MASLD and Other Chronic Liver Diseases

**Authors:** I. Commins, D. Clayton-Chubb, N. Janko, A. Majeed, W. Kemp, S. K. Roberts

PMC · DOI: 10.3390/medsci14010084 · Medical Sciences · 2026-02-11

## TL;DR

This paper reviews whether statins, commonly used for heart health, can also help treat MASLD, a common liver disease.

## Contribution

The paper provides a comprehensive review of statin use in MASLD, focusing on both cardiovascular benefits and potential liver disease treatment.

## Key findings

- Statins are under-prescribed in MASLD patients despite their cardiovascular benefits.
- There is growing interest in using statins to treat MASLD and its complications.
- The review explores evidence for statin therapy in MASLD patients for both lipid-lowering and liver disease treatment.

## Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is the most common liver disease worldwide, with an estimated global prevalence of 38% in adults. MASLD confers a significant increase in morbidity and mortality due to its association with cardiovascular disease and progressive liver disease, including cirrhosis and hepatocellular carcinoma. Current treatment paradigms for MASLD are centred around lifestyle modification and weight loss, with a need for pharmacotherapeutic options. Given the strong relationship between MASLD and cardiovascular disease, there is an interest in evaluating the efficacy and safety of cardiovascular medications such as statins in liver disease. Statins are the most commonly prescribed lipid-lowering medication in the world, with an established role in reducing cardiovascular morbidity and mortality. Statins are currently under-prescribed in the MASLD patient population, yet there is growing interest in determining whether statins could be utilised to treat MASLD itself. This comprehensive review aims to explore the evidence regarding the use of statin therapy for conventional, lipid-lowering indications in patients with MASLD and its potential benefits for the treatment of MASLD and its complications.

## Linked entities

- **Diseases:** MASLD (MONDO:0013209), cirrhosis (MONDO:0005155), hepatocellular carcinoma (MONDO:0007256), cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Genes:** CYP4F3 (cytochrome P450 family 4 subfamily F member 3) [NCBI Gene 4051] {aka CPF3, CYP4F, CYPIVF3, LTB4H}, CYP2D6 (cytochrome P450 family 2 subfamily D member 6 (gene/pseudogene)) [NCBI Gene 1565] {aka CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, HMGCR (3-hydroxy-3-methylglutaryl-CoA reductase) [NCBI Gene 3156] {aka LDLCQ3, LGMDR28, MYPLG}, PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 5465] {aka NR1C1, PPAR, PPAR-alpha, PPARalpha, hPPAR}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, PPIG (peptidylprolyl isomerase G) [NCBI Gene 9360] {aka CARS-Cyp, CYP, SCAF10, SRCyp}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, KLF2 (KLF transcription factor 2) [NCBI Gene 10365] {aka LKLF}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, CYP2C19 (cytochrome P450 family 2 subfamily C member 19) [NCBI Gene 1557] {aka CPCJ, CYP2C, CYPIIC17, CYPIIC19, P450C2C, P450IIC19}, CYP2C9 (cytochrome P450 family 2 subfamily C member 9) [NCBI Gene 1559] {aka CPC9, CYP2C, CYP2C10, CYPIIC9, P450-2C9, P450IIC9}, CYP2C8 (cytochrome P450 family 2 subfamily C member 8) [NCBI Gene 1558] {aka CPC8, CYP2C8DM, CYPIIC8, MP-12/MP-20}, GOT1 (glutamic-oxaloacetic transaminase 1) [NCBI Gene 2805] {aka AST, AST1, ASTQTL1, GIG18, SGOT, cAspAT}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, FASTK (Fas activated serine/threonine kinase) [NCBI Gene 10922] {aka FAST}, CYP3A4 (cytochrome P450 family 3 subfamily A member 4) [NCBI Gene 1576] {aka CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4}, PON1 (paraoxonase 1) [NCBI Gene 5444] {aka ESA, MVCD5, PON}, ABCB1 (ATP binding cassette subfamily B member 1) [NCBI Gene 5243] {aka ABC20, CD243, CLCS, ENPAT, GP170, MDR1}, PGP (phosphoglycolate phosphatase) [NCBI Gene 283871] {aka AUM, G3PP, PGPase}, SERPINB9 (serpin family B member 9) [NCBI Gene 5272] {aka CAP-3, CAP3, PI-9, PI9}, NOS3 (nitric oxide synthase 3) [NCBI Gene 4846] {aka EC-NOS, ECNOS, MYMY8, NOSIII, cNOS, eNOS}
- **Diseases:** Child-Pugh C cirrhosis (MESH:D005355), HCV infection (MESH:D006526), Rhabdomyolysis (MESH:D012206), acute-on-chronic liver failure (MESH:D065290), thrombotic (MESH:D013927), ischaemic reperfusion injury (MESH:D015427), variceal bleed (MESH:D014648), injury to (MESH:D014947), ascites (MESH:D001201), inflammation (MESH:D007249), Portal Hypertension (MESH:D006975), Chronic Liver Disease (MESH:D008107), haemorrhagic stroke (MESH:D002543), viral hepatitis (MESH:D014777), muscle (MESH:D019042), cirrhotic (MESH:D000094724), ASCVD (MESH:D050197), C (OMIM:211750), hypertension (MESH:D006973), death (MESH:D003643), endothelial dysfunction (MESH:D014652), Diabetes Mellitus (MESH:D003920), malignancies (MESH:D009369), bacterial peritonitis (MESH:D010538), restlessness (MESH:D011595), NAFLD (MESH:D065626), CVD (MESH:D002318), infections (MESH:D007239), chronic kidney disease (MESH:D051436), hepatitis B- or C (MESH:D006509), Child-Pugh B (MESH:C562515), insulin resistance (MESH:D007333), chronic hepatitis C infection (MESH:D019698), vascular dysfunction (MESH:D002561), weight loss (MESH:D015431), NODM (MESH:C565715), cognitive side effects (MESH:D064420), Child-Pugh A and B cirrhosis (MESH:D008103), myoglobinuria (MESH:D009212), hepatic decompensation (MESH:D006333), renal impairment (MESH:D007674), gynecomastia (MESH:D006177), obesity (MESH:D009765), BD (MESH:D001528), cataracts (MESH:D002386), Hepatic Steatosis (MESH:D005234), Drug (MESH:D000081015), Metabolic and Alcohol Associated Liver Disease (MESH:D008108), Myalgia (MESH:D063806), dementia (MESH:D003704), coronary artery disease (MESH:D003324), associated (MESH:D018886), hepatic encephalopathy (MESH:D006501), liver failure (MESH:D017093), confusion (MESH:D003221), Myositis (MESH:D009220), DILI (MESH:D056486), SAMSs (MESH:D009135), effects (MESH:D065606), proteinuria (MESH:D011507)
- **Chemicals:** prednisolone (MESH:D011239), NO (MESH:D009614), HVPG (-), mevalonate (MESH:D008798), rifaximin (MESH:D000078262), diltiazem (MESH:D004110), Atorvastatin (MESH:D000069059), Carvedilol (MESH:D000077261), Vitamin E (MESH:D014810), Pitavastatin (MESH:C108475), fatty acid (MESH:D005227), Pravastatin (MESH:D017035), triglycerides (MESH:D014280), lovastatin (MESH:D008148), digoxin (MESH:D004077), isoprenoid (MESH:D013729), fluvastatin (MESH:D000077340), lipopolysaccharide (MESH:D008070), fibrates (MESH:D058607), lipid (MESH:D008055), Simvastatin (MESH:D019821), vitamin C (MESH:D001205), verapamil (MESH:D014700), alcohol (MESH:D000438), N-acetyl cysteine (MESH:D000111), ROS (MESH:D017382), ETOH (MESH:D000431), cholesterol (MESH:D002784), nitric oxide (MESH:D009569), Rosuvastatin (MESH:D000068718)
- **Species:** hepatitis C virus [taxon 11103], Homo sapiens (human, species) [taxon 9606], Hepatitis B virus (no rank) [taxon 10407]
- **Cell lines:** LSEC — Homo sapiens (Human), Undefined cell line type (CVCL_QY34)

## Full text

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## Figures

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## References

170 references — full list in the complete paper: https://tomesphere.com/paper/PMC12922148/full.md

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Source: https://tomesphere.com/paper/PMC12922148