CSP Exam Prep Course: Metabolic Dysfunction-Associated Steatohepatitis (MASH)

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Vocabulary flashcards covering the pathophysiology, non-invasive diagnostic criteria, pharmacologic treatments, dosing, and clinical pipeline for Metabolic Dysfunction-Associated Steatohepatitis (MASH) from the NASP 2025 CSP Exam Prep Course.

20 Terms

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Metabolic Dysfunction-Associated Steatohepatitis (MASH)

The updated medical nomenclature replacing non-alcoholic steatohepatitis (NASH) that emphasizes the critical role of metabolic dysfunction in both metabolic dysfunction-associated steatotic liver disease (MASLD) and its more severe, inflammatory form.

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Histological Hallmarks of MASH

The three diagnostic microscopic features of MASH: hepatic steatosis resulting from microvascular accumulation and storage of triglycerides in hepatocytes, local inflammation, and hepatocyte ballooning.

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Leading Causes of Mortality in MASH

Cardiovascular disease is the primary cause of death in early stages of MASH, whereas liver-related morbidity and mortality become more prevalent once patients advance to fibrosis stages F3 to F4.

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Metabolic Syndrome Diagnostic Thresholds in MASH

Clinical indicators comprising abdominal obesity (waist circumference >40 inches> 40\,\text{inches} in men; >35 inches> 35\,\text{inches} in women), triglycerides ≥150 mg/dL\ge 150\,\text{mg/dL}, HDL-C (<40 mg/dL< 40\,\text{mg/dL} in men; <50 mg/dL< 50\,\text{mg/dL} in women), blood pressure ≥130/85 mm Hg\ge 130/85\,\text{mm Hg}, and fasting glucose ≥100 mg/dL\ge 100\,\text{mg/dL}.

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FIB-4 Score Cutoff Adjustment for Older Adults

An updated diagnostic rule-out threshold raised to FIB-4<2.0\text{FIB-4} < 2.0 specifically for adults aged ≥65 years\ge 65\,\text{years}.

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EASL-EASD-EASO 2024 Referral Thresholds

Clinical guideline cutoffs directing patients with FIB-4≥2.67\text{FIB-4} \ge 2.67 or vibration-controlled transient elastography (VCTE) ≥8 kPa\ge 8\,\text{kPa} to hepatology care for advanced fibrosis assessment.

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Rezdiffra (resmetirom)

A thyroid hormone receptor-beta (THR-beta) agonist granted accelerated approval for use alongside diet and exercise to treat noncirrhotic NASH/MASH in adults with moderate to advanced liver fibrosis (stages F2 to F3).

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Rezdiffra Weight-Based Dosing

An oral once-daily dosing regimen taken with or without food: 80 mg80\,\text{mg} daily for patients weighing <100 kg< 100\,\text{kg}, and 100 mg100\,\text{mg} daily for patients weighing ≥100 kg\ge 100\,\text{kg}.

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Rezdiffra Statin Dose Restrictions

Daily statin caps required when co-administered with resmetirom: rosuvastatin ≤20 mg\le 20\,\text{mg}, simvastatin ≤20 mg\le 20\,\text{mg}, pravastatin ≤40 mg\le 40\,\text{mg}, and atorvastatin ≤40 mg\le 40\,\text{mg}.

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Rezdiffra Hepatic Impairment Precaution

A safety instruction to avoid resmetirom use in patients with moderate to severe hepatic impairment classified as Child-Pugh Class B or C.

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Rezdiffra Monitoring Parameters

Recommended assessments including hepatic function panel, noninvasive liver stiffness measurement, and MRI-PDFF for efficacy tracking, along with thyroid function and lipid panels for safety.

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Wegovy (semaglutide)

A glucagon-like peptide 1 (GLP-1) receptor agonist administered subcutaneously once weekly, indicated for chronic weight management, major adverse cardiovascular event (MACE) risk reduction, and FDA-indicated under accelerated approval for non-cirrhotic MASH with F2–F3 fibrosis.

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Saxenda (liraglutide)

A daily subcutaneous glucagon-like peptide 1 (GLP-1) receptor agonist initiated at 0.6 mg0.6\,\text{mg} daily and titrated weekly to a maintenance dose of 3 mg3\,\text{mg} for chronic weight management; it is strictly contraindicated in pregnancy.

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Zepbound (tirzepatide)

A dual glucose-dependent insulinotropic polypeptide (GIP) receptor and glucagon-like peptide-1 (GLP-1) receptor agonist administered subcutaneously once weekly for chronic weight management and moderate to severe obstructive sleep apnea (OSA) in adults with obesity.

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Incretin-Based Therapy Boxed Warning

A black box warning regarding the risk of thyroid C-cell tumors, making these agents contraindicated in patients with a personal or family history of medullary thyroid carcinoma (MTC) or Multiple Endocrine Neoplasia syndrome type 2 (MEN 2).

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Zepbound Oral Contraceptive Interaction

A clinical recommendation directing females taking oral contraceptives to switch to a non-oral method or add barrier contraception for 4 weeks4\,\text{weeks} after drug initiation and for 4 weeks4\,\text{weeks} following each dose escalation.

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Lanifibranor

A pan-peroxisome proliferator-activated receptor (Pan-PPAR) agonist under evaluation in Phase 3 clinical trials for the treatment of MASH.

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Efruxifermin and Pegozafermin

Fibroblast growth factor 21 receptor agonists (FGF21 RAs) currently in Phase 3 clinical trials for MASH management.

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Denifanstat

A fatty acid synthase (FASN) inhibitor being evaluated in Phase 2 clinical trials for the treatment of MASH.

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Saroglitazar

A dual PPAR α/γ\alpha/\gamma agonist being investigated in Phase 2b clinical trials for MASH therapy.