# MetALD: decoding the evolution of steatotic liver disease nomenclature and implications for clinical practice and beyond

**Authors:** Farinaz Ghodrati, Ashley B Zhang, Nadim Mahmud

PMC · DOI: 10.1093/gastro/goag006 · Gastroenterology Report · 2026-02-20

## TL;DR

This review discusses the evolution of steatotic liver disease terminology, focusing on the new MetALD classification and its impact on clinical practice and research.

## Contribution

The paper introduces and emphasizes the clinical significance of the new MetALD subclassification of steatotic liver disease.

## Key findings

- The new nomenclature for steatotic liver disease includes MASLD and MASH, which better reflect underlying risk factors.
- The introduction of MetALD highlights the combined impact of metabolic dysfunction and alcohol use on liver disease.
- Accurate classification of SLD is crucial due to its high global prevalence and implications for patient care.

## Abstract

The steatotic liver disease (SLD) landscape has seen a paradigm shift in recent years with a revitalization of the nomenclature following a multi-society Delphi consensus. The terms metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction-associated steatohepatitis (MASH) were introduced to address several of the challenges and limitations associated with the former terminology. By transitioning away from stigmatizing and ambiguous terms, the nomenclature has adopted inclusionary language that emphasizes the underlying risk factors that drive disease progression and are accompanied by distinct diagnostic criteria. With SLD prevalence steadily increasing over the past few decades, affecting over 30% of the global population, accurate classification of the spectrum of conditions that fall under this overarching term is essential. Most importantly, the introduction of combined metabolic and alcohol-associated liver disease (MetALD) as a novel subclassification of SLD has shifted the diagnostic approach, raised awareness of disease prevalence, and paved the way for therapeutic management and multidisciplinary approaches to patient care. By recognizing the distinct clinical entity that is MetALD and the synergistic interplay between the cardiometabolic risk factors and alcohol use, clinicians are better equipped to effectively care for this patient population. In this review, we aim to discuss the catalysts for the SLD nomenclature changes, the dynamic nature of its subclasses, the natural history and disease burden, and the implications for clinical practice and research, with a particular focus on MetALD.

## Linked entities

- **Diseases:** metabolic dysfunction-associated steatotic liver disease (MONDO:0013209), metabolic dysfunction-associated steatohepatitis (MONDO:0007027)

## Full-text entities

- **Genes:** GIP (gastric inhibitory polypeptide) [NCBI Gene 2695], 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}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, FGF21 (fibroblast growth factor 21) [NCBI Gene 26291]
- **Diseases:** autoimmune hepatitis (MESH:D019693), Wilson disease (MESH:D006527), hereditary hemochromatosis (MESH:D006432), primary sclerosing cholangitis (MESH:D015209), metabolic disease (MESH:D008659), seizure (MESH:D012640), HCC (MESH:D006528), primary biliary cholangitis (MESH:D008105), caloric deficit (MESH:D009461), Diabetes and Digestive and Kidney Diseases (MESH:D003928), opioid use disorder (MESH:D009293), DILI (MESH:D056486), MASL (MESH:D017093), HE (MESH:D006501), ALD (MESH:D008108), MASH (MESH:D005234), adult-onset diabetes (MESH:D003924), inborn errors of metabolism (MESH:D008661), Obesity (MESH:D009765), NASH (MESH:D005235), kidney disease (MESH:D007674), autoimmune disease (MESH:D001327), hepatic decompensation (MESH:D006333), hepatic fibrosis (MESH:D008103), Weight loss (MESH:D015431), traumatic brain injury (MESH:D000070642), pancreatic, gastric, esophageal, and most notably (MESH:D010195), insulin resistance (MESH:D007333), Child-Pugh (MESH:C562515), or B (MESH:D006509), chronic kidney disease (MESH:D051436), hypoglycemia (MESH:D007003), cardiovascular disease (MESH:D002318), NAFL (MESH:D065626), psychiatric illness (MESH:D001523), addiction (MESH:D019966), alcohol hepatitis (MESH:D006519), extrahepatic cancers (MESH:D009369), chronic viral hepatitis (MESH:D006525), diabetes (MESH:D003920), death (MESH:D003643), dyslipidemia (MESH:D050171), nutritional deficiencies (MESH:D044342), hypertension (MESH:D006973), cirrhotic (MESH:D000094724), colorectal cancer (MESH:D015179), AUD (MESH:D000437), MASLD (MESH:D008107), inflammation (MESH:D007249), fatty (MESH:D008067), monogenic diseases (MESH:D004194), CMRFs (MESH:D024821), end-stage liver disease (MESH:D058625), acute-on-chronic liver failure (MESH:D065290), cirrhosis (MESH:D005355)
- **Chemicals:** glucose (MESH:D005947), creatinine (MESH:D003404), Acamprosate (MESH:D000077443), gabapentin (MESH:D000077206), Alcohol (MESH:D000438), Topiramate (MESH:D000077236), lipid (MESH:D008055), Resmetirom (MESH:C588408), Aspirin (MESH:D001241), Naltrexone (MESH:D009271), triglycerides (MESH:D014280), Baclofen (MESH:D001418), carbohydrates (MESH:D002241), PEth (MESH:C051521), ethylglucuronide (MESH:C093924), ACE-Is (-), Disulfiram (MESH:D004221)
- **Species:** Human immunodeficiency virus 1 (no rank) [taxon 11676], Homo sapiens (human, species) [taxon 9606], hepatitis C virus [taxon 11103], Human immunodeficiency virus (species) [taxon 12721]

## Full text

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## Figures

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## References

91 references — full list in the complete paper: https://tomesphere.com/paper/PMC12921712/full.md

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Source: https://tomesphere.com/paper/PMC12921712