Management of Fibrofatty Liver (NAFLD) Diagnosed on CT Scan
CT scan findings of fibrofatty liver require immediate risk stratification using FIB-4 score or other non-invasive tests to determine fibrosis stage, as CT cannot reliably assess steatohepatitis or fibrosis severity, and management depends entirely on whether advanced fibrosis is present. 1
Limitations of CT for NAFLD Assessment
- CT scan can detect moderate to severe steatosis but has poor sensitivity (53.8%) and suboptimal performance for mild steatosis. 1
- Unenhanced CT showing hepatic attenuation <48 HU has 100% specificity but only 53.8% sensitivity for moderate to severe steatosis. 1
- CT cannot reliably assess steatohepatitis or fibrosis—the critical determinants of prognosis and treatment decisions. 1
- CT raises radiation concerns and is affected by iron, copper, glycogen, or amiodarone deposition, limiting its utility for serial monitoring. 1
Immediate Next Steps: Risk Stratification for Fibrosis
Calculate FIB-4 score immediately using age, AST, ALT, and platelet count to stratify fibrosis risk. 1
FIB-4 Score Interpretation:
- FIB-4 <1.3: Low risk (NPV 92.7%)—manage in primary care with lifestyle interventions 1
- FIB-4 1.3-2.67: Indeterminate risk—proceed to elastography or refer to hepatology 1
- FIB-4 >2.67: High risk—refer to hepatology for further evaluation including possible liver biopsy 1
Alternative validated scores include NAFLD Fibrosis Score (cutoffs: <-1.455 excludes advanced fibrosis; >0.676 suggests advanced fibrosis). 1
Management Based on Risk Stratification
Low-Risk Patients (FIB-4 <1.3, No Advanced Fibrosis)
Lifestyle modification is the cornerstone—no pharmacotherapy is indicated for simple steatosis without fibrosis. 1, 2, 3
Weight Loss Targets:
- Target 7-10% total body weight reduction through hypocaloric diet (500-1000 kcal deficit). 1, 2, 3
- Weight loss of 3-5% improves steatosis; 7-10% is needed to improve inflammation and potentially fibrosis. 3
- Critical: Gradual weight loss only (<1 kg/week)—rapid weight loss can precipitate acute hepatic failure in advanced disease. 4, 3
Dietary Recommendations:
- Implement Mediterranean diet: vegetables, fruits, whole grains, legumes, olive oil as principal fat, moderate fish, minimal red meat. 1, 4
- Avoid fructose-containing beverages and foods. 3
- Restrict alcohol consumption: <30g/day for men, <20g/day for women, or consider complete abstinence. 2, 3
Exercise Prescription:
- Vigorous-intensity exercise (≥6 METs) for at least 150 minutes weekly—moderate-intensity exercise does NOT improve NASH severity or fibrosis. 1, 2, 4
Monitoring:
Intermediate/High-Risk Patients (FIB-4 ≥1.3 or Indeterminate)
Refer to hepatology for vibration-controlled transient elastography (VCTE) or consider liver biopsy. 1
Elastography Interpretation:
- LSM <8.0 kPa: Low risk—manage as above with 6-month follow-up 1
- LSM 8.0-12.0 kPa: Indeterminate—consider MRE or liver biopsy 1
- LSM >12.0 kPa: High risk of advanced fibrosis—liver biopsy recommended 1
- LSM ≥20 kPa or thrombocytopenia: Cirrhosis likely—variceal screening required 1
When Liver Biopsy is Indicated:
- Biopsy-proven NASH with fibrosis is required before initiating pharmacotherapy, as patients without steatohepatitis or fibrosis have excellent prognosis. 4, 3
- Consider biopsy when non-invasive tests are discordant or when other liver diseases cannot be excluded. 1, 3
Pharmacological Treatment (Only for Biopsy-Proven NASH with Fibrosis)
Pharmacological treatment should be limited to patients with biopsy-confirmed NASH and significant fibrosis (≥F2). 4, 3
First-Line Pharmacotherapy Options:
- Vitamin E 800 IU daily: Consider in patients with biopsy-confirmed NASH without diabetes or cirrhosis. 2, 4
- Pioglitazone 30 mg daily: Consider in patients with biopsy-confirmed NASH without cirrhosis, with or without diabetes. 2, 4
Management of Metabolic Comorbidities:
- GLP-1 receptor agonists (liraglutide, semaglutide): Preferred for patients with type 2 diabetes and NASH/fibrosis. 2, 3
- Metformin: NOT recommended as specific treatment for NAFLD—has no significant effect on liver histology despite metabolic benefits. 4, 3
- Statins: Safe and should be used to treat dyslipidemia despite liver disease; may reduce HCC risk by 37%. 2, 3
Monitoring for Treated Patients:
- Follow-up every 6 months with liver function tests and non-invasive fibrosis markers. 2
Management of Cirrhosis (If Present)
LSM ≥20 kPa or clinical/laboratory evidence of cirrhosis requires immediate hepatology referral. 1
- HCC surveillance: Right upper quadrant ultrasound ± AFP every 6 months lifelong. 2, 4
- Variceal screening: Perform esophagogastroduodenoscopy (EGD) in all patients with known cirrhosis. 1, 4
- Liver transplantation evaluation: Refer when first major complication occurs or hepatic dysfunction develops. 4
Critical Pitfalls to Avoid
- Never pursue rapid weight loss in NAFLD patients—this can precipitate acute hepatic failure, especially with advanced disease. 4, 3
- Do not start pharmacotherapy without biopsy confirmation of NASH with fibrosis—no drugs are approved specifically for NAFLD, and simple steatosis has excellent prognosis. 4, 3
- Do not rely on CT alone for disease severity assessment—it cannot detect inflammation, hepatocyte injury, or fibrosis stage. 1
- Do not use moderate-intensity exercise as primary intervention—only vigorous-intensity exercise (≥6 METs) improves NASH. 1, 2, 4
- Avoid aggressive glycemic targets (A1C <7%) in advanced liver disease due to elevated hypoglycemia risk from impaired gluconeogenesis. 4
Exclude Other Liver Diseases
Before confirming NAFLD diagnosis, exclude competing etiologies: 1
- Excessive alcohol use (detailed quantification required)
- Viral hepatitis (HBV, HCV serology)
- Hemochromatosis (ferritin, transferrin saturation, consider HFE gene testing if elevated)
- Autoimmune hepatitis (ANA >1:160, ASMA >1:40 warrant further workup if very high aminotransferases or globulin)
- Wilson's disease (in younger patients)
- Hepatotoxic medications (review all medications)