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GP KFPs / SAQsmetabolic-and-endocrine-health

GP KFPs / SAQs · metabolic-and-endocrine-health

MASLD — KFP-style written assessment

KFP-style staged scenarios on MASLD: the diabetes annual review screen, the FIB-4 traps, staging and referral, and starting pharmacotherapy for F2-F3 MASH.

30 marks45 min3 min readVerification in progress

Target exams

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Target exams

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Prompt
MASLD in general practice: screening the right patients, reading FIB-4 correctly, and knowing who needs the new drugs

KFP 1 (10 marks)

Your practice is designing the type 2 diabetes annual review. A colleague argues liver enzymes are sufficient screening. The practice has 340 patients with T2D. [12] [11]

  1. Quantify the screening need using the pooled prevalence data. (3) [12]
  2. What does the guideline consensus require for T2D and MASLD screening, and why is it bidirectional? (4) [11]
  3. What is the recommended first screening step and its rule-out threshold? (3) [9]

Model answers

  1. Pooled prevalence of MASLD in diabetic adults is 56.9% (95% CI 39.1-74.8) across 81,364 participants in 18 studies; by FibroScan it was 64.3%. Expect roughly half to two-thirds of your 340 T2D patients to have steatotic liver disease. [12]
  2. Guidelines require assessment of liver fibrosis in all individuals with T2DM and regular dysglycaemia screening in those with MASLD. The relationship is bidirectional: MASLD raises T2DM risk stepwise with fibrosis severity, and T2DM accelerates liver disease progression, worsens insulin resistance and impairs glucose metabolism through shared insulin resistance, inflammation, lipotoxicity, adipose dysfunction and gut-liver axis mechanisms. [11]
  3. FIB-4 as first-line assessment, with a threshold below 1.3 to rule out advanced fibrosis, followed by VCTE or ELF for secondary stratification. [9]
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References10ShowHide
  1. [1]Sung S, Al-Karaghouli M, Tam M et al. Age-dependent differences in FIB-4 predictions of fibrosis in patients with MASLD referred from primary care. Hepatol Commun, 2025.PMID 39670870
  2. [3]Petta S, Kim K, Targher G et al. Focus on Semaglutide 2.4 mg/week for the Treatment of Metabolic Dysfunction-Associated Steatohepatitis. Liver Int, 2025.PMID 41144918
  3. [4]Bansal MB, Patton H, Morgan TR et al. Semaglutide therapy for metabolic dysfunction-associated steatohepatitis: November 2025 updates to AASLD Practice Guidance. Hepatology, 2026.PMID 41201884
  4. [7]Shaheen AA, Baguley E, Swain MG et al. Diabetes and obesity reduce FIB-4 accuracy in MASLD referral pathways. JHEP Rep, 2026.PMID 41810425
  5. [8]Njei B, Al-Ajlouni YA, Tanih DN et al. Semaglutide versus resmetirom for noncirrhotic MASH with moderate to advanced fibrosis: a cost-effectiveness analysis. Cost Eff Resour Alloc, 2026.PMID 41862906
  6. [9]Younossi ZM, Kalligeros M, Wong VW et al. Updated Global Consensus Recommendations for Risk Stratification, Treatment Initiation, and Response Monitoring in Metabolic Dysfunction-Associated Steatotic Liver Disease. Clin Gastroenterol Hepatol, 2026.PMID 41950980
  7. [10]Driessen S, van Son KC, Riemersma TR et al. Two-step care pathways for advanced MASLD in primary and hospital care: A multicenter study. Hepatol Commun, 2026.PMID 42275588
  8. [11]Mantovani A, Morandin R, Rolli N et al. Bidirectional relationship between metabolic dysfunction-associated steatotic liver disease and type 2 diabetes mellitus. EXCLI J, 2026.PMID 42376436
  9. [12]Singhai A, Meena R, Joshi R et al. Prevalence of metabolic dysfunction associated steatotic liver disease in type 2 diabetes mellitus in India: A systematic review and meta-analysis. Indian J Med Res, 2026.PMID 42397829
  10. [16]Adinolfi LE, Marrone A, Izzi A et al. Resmetirom and semaglutide: next-generation therapies for metabolic-associated steatohepatitis. Opportunities, challenges and issues. Expert Rev Endocrinol Metab, 2026.PMID 42552573
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