# New Treatment Options for MASLD Patients with Type 2 Diabetes

**Authors:** Andrea Mega, Chiara Turri, Luca Marzi, Marco Dauriz, Rodolfo Sacco, Annarosa Floreani, Cristina Stasi

PMC · DOI: 10.3390/life16020254 · 2026-02-02

## TL;DR

This paper reviews the connection between liver disease and type 2 diabetes, focusing on new treatments that improve liver health and metabolic outcomes.

## Contribution

The paper provides a comprehensive overview of novel glucose-lowering therapies for MASLD patients with T2DM and their impact on liver fibrosis and inflammation.

## Key findings

- GLP-1RAs and SGLT2is show benefits in MASLD patients with T2DM by improving insulin signaling and reducing inflammation.
- Resmetirom is recommended for non-cirrhotic MASH patients with significant fibrosis, if locally approved.
- MASLD and T2DM share pathophysiological mechanisms that are reversible with treatment.

## Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is defined by hepatic steatosis in individuals with at least one cardiometabolic risk factor, most commonly type 2 diabetes mellitus (T2DM). People with non-alcoholic fatty liver disease, even without other metabolic factors, have a higher risk of T2DM. MASLD includes isolated liver steatosis, metabolic dysfunction-associated steatohepatitis, fibrosis, cirrhosis, and MASH-related hepatocellular carcinoma. MASLD patients are also at a higher risk of developing T2DM than the general population. International guidelines recommend a stepwise approach for identifying those at high risk of fibrotic progression, using the FIB-4 index for initial screening, followed by transient elastography. The link between MASLD and T2DM is notable due to shared pathophysiological mechanisms, some of which are reversible with treatment used in T2DM. Many new glucose-lowering drugs have also proven effective in improving anthropometric and metabolic parameters, as well as the stage of hepatic steatosis and fibrosis. Recent evidence suggests that GLP-1RAs and SGLT2is have beneficial effects in MASLD patients with T2DM. Specifically, GLP-1RAs improve hepatic insulin signaling, modulate lipid metabolism, reduce inflammation, and decrease hepatocyte oxidative stress. European guidelines recommend resmetirom as a MASH-targeted therapy, if locally approved, for adults with non-cirrhotic MASH and significant liver fibrosis (stage ≥ 2) and GLP-1RAs in MASH, including compensated cirrhosis, but they should be used for their respective indications, such as T2DM and obesity. Given the post-COVID burden of MASLD and its high risk of liver fibrosis progression among T2DM patients, this review specifically provides an overview of the complex relationship between MASLD and T2DM. Additionally, it examines current understanding of liver fibrosis evaluation and the effects of novel treatment options, with a particular focus on glucose-lowering therapies and their effects on necroinflammation, hepatic fat accumulation, and fibrosis progression in patients with MASLD and T2DM.

## Linked entities

- **Chemicals:** resmetirom (PubChem CID 15981237)
- **Diseases:** metabolic dysfunction-associated steatotic liver disease (MONDO:0013209), type 2 diabetes mellitus (MONDO:0005148), metabolic dysfunction-associated steatohepatitis (MONDO:0007027), cirrhosis (MONDO:0005155), hepatocellular carcinoma (MONDO:0007256)

## Full-text entities

- **Genes:** SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, THRB (thyroid hormone receptor beta) [NCBI Gene 7068] {aka C-ERBA-2, C-ERBA-BETA, ERBA2, GRTH, NR1A2, PRTH}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, PRKAA2 (protein kinase AMP-activated catalytic subunit alpha 2) [NCBI Gene 5563] {aka AMPK, AMPK2, AMPKa2, PRKAA}, PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468] {aka CIMT1, FPLD3, GLM1, NR1C3, PPARG1, PPARG2}, UGT1A9 (UDP glucuronosyltransferase family 1 member A9) [NCBI Gene 54600] {aka HLUGP4, LUGP4, UDPGT, UDPGT 1-9, UGT-1I, UGT1-09}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, INSR (insulin receptor) [NCBI Gene 3643] {aka CD220, HHF5}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, ARRB1 (arrestin beta 1) [NCBI Gene 408] {aka ARB1, ARR1}, GIP (gastric inhibitory polypeptide) [NCBI Gene 2695]
- **Diseases:** hyperinsulinemia (MESH:D006946), hyperglycemic (MESH:D006944), hypertension (MESH:D006973), stiffness (MESH:C566112), atherosclerosis (MESH:D050197), viral hepatitis (MESH:D014777), endotoxemia (MESH:D019446), Weight loss (MESH:D015431), polydipsia (MESH:D059606), alpha-1-antitrypsin deficiency (MESH:D019896), insulin deficiency (MESH:D007333), hypoglycemia (MESH:D007003), congestive hepatopathy (MESH:D002311), cardiovascular disease (MESH:D002318), chronic viral hepatitis (MESH:D006525), cholestasis (MESH:D002779), COVID (MESH:D000086382), hepatic necroinflammation (MESH:D056486), Liver stiffness (MESH:D017093), associated (MESH:D018886), alcohol-related liver disease (MESH:D008108), inflammatory cytokines (MESH:D000080424), T2DM (MESH:D003924), adipose tissue dysfunction (MESH:D018205), renal impairment (MESH:D007674), cardiovascular, renal, or heart failure (MESH:D006333), VCTE (MESH:D053421), neuropathy (MESH:D009422), CAP (MESH:C538265), post-COVID (MESH:D000094024), HCC (MESH:D006528), blurred vision (MESH:D014786), dyslipidemia (MESH:D050171), Mitochondrial dysfunction (MESH:D028361), cirrhotic (MESH:D000094724), alcohol abuse (MESH:D000437), MASLD (MESH:D008107), chronic hepatitis (MESH:D006521), fibro-inflammation (MESH:D007249), fatty (MESH:D008067), injury to (MESH:D014947), metabolic syndrome (MESH:D024821), fasting hyperglycemia (MESH:D006943), Fibrosis (MESH:D005355), Hepatic Fibrosis (MESH:D008103), polyuria (MESH:D011141), chronic kidney disease (MESH:D051436), swelling (MESH:D004487), NAFLD (MESH:D065626), kidney failure (MESH:D051437), lactic acidosis (MESH:D000140), -diabetic (MESH:D003920), endothelial dysfunction (MESH:D014652), dysbiosis (MESH:D064806), fatigue (MESH:D005221), overweight (MESH:D050177), retinopathy (MESH:D058437), MASH (MESH:D005234), non-alcoholic steatohepatitis (MESH:D005235), Obesity (MESH:D009765)
- **Chemicals:** GLP-1RAs (-), bile acids (MESH:D001647), fatty acid (MESH:D005227), dapagliflozin (MESH:C529054), lipid (MESH:D008055), resmetirom (MESH:C588408), LPS (MESH:D008070), Pioglitazone (MESH:D000077205), RA (MESH:D011883), fructose (MESH:D005632), amiodarone (MESH:D000638), thiazolidinediones (MESH:D045162), Glucose (MESH:D005947), ROS (MESH:D017382), short-chain fatty acids (MESH:D005232), alcohol (MESH:D000438), diacylglycerols (MESH:D004075), sugars (MESH:D000073893), tamoxifen (MESH:D013629), vitamin E (MESH:D014810), LEAN (MESH:D003061), iron (MESH:D007501), free fatty acids (MESH:D005230), sulfonylureas (MESH:D013453), Empagliflozin (MESH:C570240), Metformin (MESH:D008687), methotrexate (MESH:D008727), ethanol (MESH:D000431), ceramides (MESH:D002518), blood glucose (MESH:D001786)
- **Species:** Homo sapiens (human, species) [taxon 9606], Hepatitis C virus [taxon 11103], Hepatitis B virus (no rank) [taxon 10407]
- **Mutations:** rs6923761, rs9934336, rs140226575

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942142/full.md

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Source: https://tomesphere.com/paper/PMC12942142