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Non-Alcoholic Fatty Liver Disease (MASLD)

GMJ News knowledge hub · last reviewed August 2026 · Georgian Medical Journal

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Non-alcoholic fatty liver disease — now renamed metabolic dysfunction-associated steatotic liver disease (MASLD) in 2023 — affects approximately 25% of the global adult population (approximately 1.9 billion people), making it the most common liver disease globally and a rapidly growing cause of liver cirrhosis, liver failure and hepatocellular carcinoma (WHO). The progressive inflammatory form — metabolic dysfunction-associated steatohepatitis (MASH, formerly NASH) — affects approximately 5% of the global population and progresses to cirrhosis in approximately 20-25% over 10-15 years. Resmetirom (Rezdiffra) — approved by FDA in March 2024 — is the first drug approved specifically for MASH with fibrosis, a landmark therapeutic breakthrough.

Key messages

25% of global population — the new epidemic
MASLD (metabolic dysfunction-associated steatotic liver disease, formerly NAFLD) affects approximately 25% of the global adult population — approximately 1.9 billion people — making it the most common liver disease globally (WHO/Lancet).
New nomenclature — MASLD and MASH
A 2023 international consensus renamed NAFLD → MASLD (metabolic dysfunction-associated steatotic liver disease) and NASH → MASH (metabolic dysfunction-associated steatohepatitis) — recognising the metabolic drivers and reducing stigma.
First approved drug for MASH — resmetirom 2024
Resmetirom (Rezdiffra) — a thyroid hormone receptor beta agonist — received FDA approval in March 2024 for non-cirrhotic MASH with moderate-advanced fibrosis (stages F2-F3). The MAESTRO-NASH trial showed 25-30% histological response, marking the first approved MASH-specific treatment.
Progressive in 20% — cirrhosis and HCC
Approximately 20-25% of MASH patients develop cirrhosis over 10-15 years. MASLD-related hepatocellular carcinoma (HCC) can occur even without cirrhosis. MASLD is now the leading cause of liver transplantation in the US, surpassing hepatitis C.
Driven by the obesity epidemic
MASLD is the hepatic manifestation of metabolic syndrome — driven by obesity, type 2 diabetes, dyslipidaemia and hypertension. Weight loss ≥10% substantially reduces liver fat, inflammation and fibrosis — making lifestyle intervention the cornerstone of management.
Lean MASLD is real
Approximately 10-20% of MASLD occurs in individuals with normal BMI ("lean MASLD") — driven by visceral adiposity, genetic factors (PNPLA3, TM6SF2 variants) and insulin resistance. BMI should not be used to exclude MASLD.

Key statistics

25%
of global adults have MASLD (~1.9 billion)
WHO/Lancet
5%
of global adults have MASH (progressive form)
WHO
20-25%
of MASH patients develop cirrhosis in 10-15 years
EASL/WHO
#1
cause of liver transplantation in the US (overtook HCV)
AASLD
2024
year resmetirom (first MASH drug) FDA-approved
FDA
10%
weight loss substantially reverses MASLD
EASL/WHO

MASLD global prevalence (%) by region — WHO/Lancet Gastroenterology

Source: Lancet Gastroenterology 2023. Middle East and Latin America have highest MASLD prevalence.

Glossary of key terms

MASLD (Metabolic dysfunction-associated steatotic liver disease)
WHO/EASL 2023
Renamed from NAFLD in 2023 by international consensus. Defined as hepatic steatosis (liver fat ≥5%) with at least one cardiometabolic risk factor and no other hepatic cause. The predominant form (approximately 25% of adults).
MASH (Metabolic dysfunction-associated steatohepatitis)
WHO/EASL 2023
Renamed from NASH. The progressive inflammatory form of MASLD — histologically defined by steatohepatitis (fat + inflammation + hepatocyte ballooning ± fibrosis). Affects approximately 5% of adults; progresses to cirrhosis in approximately 20-25%.
Resmetirom (Rezdiffra)
FDA 2024
The first FDA-approved drug for non-cirrhotic MASH — a selective thyroid hormone receptor beta (THR-β) agonist that reduces hepatic fat and inflammation without thyroid systemic effects. MAESTRO-NASH trial: 25-30% histological response vs 10% placebo. Approved March 2024 for MASH with stages F2-F3 fibrosis.
Hepatic steatosis
EASL/WHO
Accumulation of fat (predominantly triglycerides) in >5% of hepatocytes — the defining feature of MASLD. Diagnosed by imaging (ultrasound — sensitive for moderate-severe steatosis; MRI-PDFF — quantitative gold standard) or liver biopsy.
FIB-4 score
EASL/AASLD
A non-invasive fibrosis score — FIB-4 = (age × AST) / (platelet count × √ALT). FIB-4 <1.30 rules out advanced fibrosis with high negative predictive value; FIB-4 >2.67 suggests advanced fibrosis needing specialist evaluation. WHO-recommended as the first-line fibrosis assessment in MASLD.
PNPLA3 variant
Research
A common genetic variant (PNPLA3 rs738409 — I148M) — the strongest single genetic risk factor for MASLD severity, fibrosis and HCC. Present in approximately 40% of European-ancestry and 50% of Hispanic populations; less common in African ancestry.

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