Metabolic syndrome (type 2 diabetes / insulin resistance, obesity) |
Alcohol consumption |
Hepatitis C (genotype 3), hepatitis B |
Drugs (methotrexate, glucocorticoids, tamoxifen, amiodarone, oestrogens, anti-retroviral medication) |
Rare causes: autoimmune diseases, haemochromatosis, psoriasis, Wilson's disease, apoprotein B deficiency, hypothyroidism, starvation, parenteral nutrition, excessive intake of medium-chain triglycerides (MCT; coconut fat and oil, tube feeding formulas with MCT), HIV |
Causes of microvesicular steatosis, such as drugs (valproate, tetracycline), pregnancy |
Detection of metabolic syndrome (BMI, lipids, blood pressure, fasting glucose, HbA1c) |
Detection of high-risk alcohol consumption (see Detecting substance abuse Recognition of Alcohol and Drug Abuse) |
History: family history of cirrhosis, use of alcohol (AUDIT calculator Audit), drugs, hormonal or natural products |
Clinical examination to exclude advanced liver disease: spider naevi, palmar erythema, yellow skin and sclerae, ascites, muscular wasting |
Upper abdominal ultrasonography |
Elastography, if available |
Laboratory tests, as far as applicable:
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The aetiology of fatty liver should be confirmed by additional workup, as necessary
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If liver biopsy shows NASH and fibrosis F2-F3
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NAFLD cirrhosis
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The PNPLA3 gene http://medlineplus.gov/genetics/gene/pnpla3/ test can be considered in specialized care for patients whose fatty liver is not explained by metabolic syndrome. |