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AGA Clinical Practice Update on the Evaluation and Management of Metabolic Dysfunction– and Alcohol-Associated Liver Disease: Expert Review
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AGA Clinical Practice Update on the Evaluation and Management of Metabolic Dysfunction– and Alcohol-Associated Liver Disease: Expert Review

Clinical Gastroenterology and Hepatology·September 23Open Access
Gastroenterology & HepatologyPractice changingAlcohol Use DisorderMetabolic Dysfunction- And Alcohol-Associated Liver DiseaseSteatotic Liver DiseaseExpert Review / Clinical Practice GuidelineAlcohol Use Disorder PharmacotherapyGIP Receptor AgonistGLP-1 Receptor AgonistNoninvasive Fibrosis AssessmentThyroid Hormone Receptor Beta AgonistTransient ElastographyAdultRezdiffraResmetiromSemaglutide

Summary

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What was studied

This AGA Clinical Practice Update provides Best Practice Advice (BPA) on the diagnosis, staging, and treatment of metabolic dysfunction– and alcohol-associated liver disease (MetALD), a newly defined category under the 2023 multisociety consensus nomenclature for steatotic liver disease (SLD).

Key findings

Nine BPA statements were issued, covering: classification of MetALD by alcohol intake thresholds (≈140–350 g/wk in women, 210–420 g/wk in men) plus cardiometabolic risk factors; annual alcohol screening; abstinence counseling; tiered noninvasive fibrosis assessment starting with FIB-4; cautious interpretation of elastography during active drinking; micronutrient repletion and exercise; preliminary GLP-1/GIP receptor agonist data suggesting reduced alcohol cravings; pharmacotherapy for alcohol use disorder; and avoidance of bariatric/endobariatric surgery due to insufficient safety data.

Study limitations

Systematic reviews were not performed, so BPA statements carry no formal evidence quality ratings or strength-of-recommendation grades. FDA-approved MASLD treatments (resmetirom, semaglutide) have not been formally studied in MetALD populations, leaving a key therapeutic gap.

Clinical implications

Classify SLD patients into MetALD using the 140–350 g/wk (women) and 210–420 g/wk (men) alcohol thresholds, screen at least annually with validated tools, and use a tiered FIB-4–first strategy for fibrosis staging. Advise complete alcohol abstinence, replete micronutrients, prescribe aerobic exercise, and offer alcohol use disorder pharmacotherapy for moderate-to-severe AUD; avoid bariatric surgery in MetALD patients.

Caveats

  • FDA-approved MASLD therapies (resmetirom, semaglutide) have not been studied in MetALD-specific trials; the GLP-1/GIP data on alcohol craving reduction is described as preliminary only
  • Liver stiffness measurements by elastography can be transiently elevated by active alcohol use, which may lead to fibrosis overestimation if this context is not accounted for in clinical interpretation
  • These Best Practice Advice statements are based on expert opinion and narrative literature review—not systematic review or meta-analysis—so no formal evidence grading or recommendation strength was assigned

Related Questions

Explore related topics

How do GLP-1 receptor agonists affect alcohol consumption and liver outcomes in MetALD?What are the best noninvasive tools to stage fibrosis in patients with combined metabolic and alcohol-related liver disease?Is bariatric surgery safe in patients with alcohol-associated or metabolic liver disease?

Publication Details

Year
2026
Journal
Clinical Gastroenterology and Hepatology
Source
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