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Updated: May 14, 2026

Mouse Model of Metabolic Dysfunction-Associated Steatotic Liver Disease with Fibrosis
Published on: July 18, 2025
Evidence-based clinical practice guidelines for metabolic dysfunction-associated steatotic liver disease (MASLD)
Norio Akuta1,2, Tomomi Kogiso3,4, Kenichi Ikejima1
1Guidelines Committee for Creating and Evaluating the "Evidence-Based Clinical Practice Guidelines for Metabolic Dysfunction-Associated Steatotic Liver Disease 2026 (3rd Edition)", The Japanese Society of Gastroenterology/The Japan Society of Hepatology, 6 F Shimbashi i-MARK Building, 2-6-2 Shimbashi, Minato-ku, Tokyo, 105-0004, Japan.
Metabolic dysfunction-associated steatotic liver disease (MASLD) requires early risk stratification for advanced fibrosis. Guidelines recommend the FIB-4 index as a first-line tool, followed by elastography for higher-risk patients.
Area of Science:
- Hepatology
- Gastroenterology
- Internal Medicine
Background:
- Metabolic dysfunction-associated steatotic liver disease (MASLD) is the leading cause of chronic liver disease globally.
- MASLD progression to cirrhosis and hepatocellular carcinoma (HCC) is increasing.
- Early identification of advanced fibrosis is crucial for preventing liver-related events.
Purpose of the Study:
- To provide practical recommendations for MASLD diagnosis, risk stratification, and management.
- To summarize current evidence and expert consensus for clinical practice.
- To standardize MASLD management in Japan.
Main Methods:
- Systematic literature evaluation and expert consensus.
- Review of diagnostic approaches including noninvasive fibrosis assessment, imaging, and biochemical testing.
- Assessment of indications for specialist referral.
Main Results:
- Advanced fibrosis is the primary determinant of liver-related morbidity and mortality in MASLD.
- The Fibrosis-4 (FIB-4) index is a reliable first-line noninvasive tool for fibrosis risk stratification.
- Secondary assessment with elastography and specialist referral are recommended for elevated FIB-4 or suggestive clinical features.
Conclusions:
- Liver biopsy is not routinely required for MASLD diagnosis but is essential for diagnosing at-risk metabolic dysfunction-associated steatohepatitis (MASH), assessing inflammation, and resolving discrepancies.
- Lifestyle modification is foundational; pharmacological therapy is considered for high-risk MASH.
- These guidelines aim to standardize clinical practice for evidence-based MASLD management.
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