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. 2022 Dec 28;29(Suppl):S5–S16. doi: 10.3350/cmh.2022.0424

Table 2.

The definition and subtypes of non-alcoholic fatty liver disease

Classification Definition Prevalence Clinical implications
Traditional classification
NAFL 5% of steatosis in hepatocytes Without any cause of fatty change 5–30% of general populations 30–40% of patients with NAFL seem to experience progression of fibrosis
NASH NAFLD+hepatocyte ballooning degeneration and hepatic lobular inflammation 2–30% of NAFLD Fibrosis is a major prognostic predictor of liver-related and overall mortality
3–6% of the general population
NASH-Cirrhosis NAFLD+necroinflammatory reactions may disappear, and cirrhosis without other specific causes may be present. 20% of patients with NASH Cryptogenic cirrhosis is presumed to be an advanced form of NASH
0.18% of the general population
Variants of NAFLD
Lean NAFLD NAFLD in people with normal body weight (BMI <23 for Asians or <25 for Westerners) 23.5% of the general population Compared with non-lean NAFLD, lean NAFLD had a stronger correlation with metabolic deterioration
More prevalent in Asia The risk of fibrosis is increased
Metabolically healthy Steatosis above 5% 6.2% of NAFLD Diagnosed with NAFLD at a younger age
NAFLD Does not meet any metabolic syndrome criteria The disease progression from metabolically healthy to unhealthy is higher in obesity group than normal weight group
MAFLD Steatosis above 5% 50.7% of the general population; varies across countries and regions Paradigm shift from NAFLD to MAFLD
The presence of one of the following three criteria: overweight/obesity, type 2 diabetes mellitus, and evidence of metabolic dysregulation
Genetics
PNPLA3 Common in Asians with lean NAFLD
Associated with cryptogenic cirrhosis
TM6SF2 Increased risk for progressive NASH
HSD17B13 Loss-of-function variant was associated with progression of NAFLD

NAFL, non-alcoholic fatty liver; NAFLD, non-alcoholic fatty liver disease; NASH, non-alcoholic steatohepatitis; BMI, body mass index; MAFLD, metabolic (dysfunction)-associated fatty liver disease; PNPLA3, patatin-like phospholipase domain-containing protein 3; HSD17B13, hydroxysteroid 17β-dehydrogenase 13; TM6SF2, transmembrane 6 superfamily member 2.