Treatment Options for Hepatic Steatosis
The cornerstone of treatment for hepatic steatosis is lifestyle modification, including weight loss of 5-10% of body weight, adherence to a Mediterranean diet pattern, and regular physical activity of 150-300 minutes per week. 1, 2
Understanding Hepatic Steatosis
Hepatic steatosis, now termed Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) or previously Non-Alcoholic Fatty Liver Disease (NAFLD), is defined as excess fat accumulation in the liver (≥5% of liver weight). It exists on a spectrum from:
- Simple steatosis
- Steatohepatitis (MASH, previously NASH)
- Fibrosis
- Cirrhosis
- Hepatocellular carcinoma
First-Line Treatment: Lifestyle Modifications
Weight Loss Goals
- 5% weight reduction: Improves hepatic steatosis
- 7-10% weight reduction: Improves inflammation (steatohepatitis)
Dietary Recommendations
Mediterranean diet pattern 2, 1:
- Daily consumption of vegetables and fresh fruits
- Fiber-rich whole grains
- Nuts and seeds
- Fish and white meat
- Olive oil as primary fat source
- Limited red and processed meats
- Minimal simple sugars
Specific dietary restrictions 2, 1:
- Avoid ultra-processed foods
- Limit sugar-sweetened beverages
- Replace saturated fats with unsaturated fats
- Limit excess fructose consumption
Physical Activity
- 150-300 minutes/week of moderate-intensity exercise OR
- 75-150 minutes/week of vigorous-intensity exercise 2, 1
- Even without significant weight loss, exercise alone can reduce hepatic steatosis 1, 3
Alcohol Consumption
- Complete abstinence is recommended for patients with advanced fibrosis or cirrhosis
- Significant limitation for all other patients with hepatic steatosis
- Even low alcohol intake (9-20g daily) can double the risk of adverse liver outcomes 2, 1
Pharmacological Therapy
For Non-Cirrhotic MASH with Significant Fibrosis
- Resmetirom may be considered for adults with non-cirrhotic steatohepatitis and significant hepatic fibrosis (stage ≥2) if locally approved 2, 1
For Patients with Comorbidities
- GLP-1 receptor agonists (semaglutide, liraglutide) are not specifically for steatohepatitis but provide indirect hepatic benefits through weight loss in patients with obesity or type 2 diabetes 2, 1
- Pioglitazone is safe in adults with non-cirrhotic steatohepatitis but lacks robust demonstration of histological efficacy 1, 4
- Vitamin E is not recommended due to lack of robust histological efficacy evidence and potential long-term risks 1
- Metformin has no significant effect on liver histology 1
- SGLT2 inhibitors are safe but not specifically recommended for steatohepatitis 1
Bariatric Surgery
Bariatric surgery should be considered for patients with obesity and hepatic steatosis who have not responded adequately to lifestyle interventions 2, 1
Monitoring and Follow-up
Baseline assessment:
- Liver enzymes (ALT, AST, bilirubin, alkaline phosphatase)
- Complete blood count
- Coagulation profile (INR)
- Renal function 2
Follow-up monitoring:
Consider liver biopsy if:
- Patient has risk factors for MASH and advanced fibrosis (diabetes, metabolic syndrome)
- Findings concerning for cirrhosis (thrombocytopenia, AST>ALT, hypoalbuminemia) 2
Common Pitfalls to Avoid
- Focusing only on liver enzymes - normal enzymes don't exclude significant liver disease
- Ignoring cardiovascular risk - cardiovascular disease is the main driver of morbidity and mortality
- Rapid weight loss - can potentially worsen liver inflammation; gradual, sustained weight loss is preferred
- Inadequate follow-up - sustained adherence to lifestyle changes is critical for success 1
- Recommending alcohol consumption - even light-moderate alcohol intake can worsen outcomes in patients with hepatic steatosis 2
Special Considerations
- For patients with sarcopenia or decompensated cirrhosis: high-protein diet and late-evening snack
- For patients with compensated cirrhosis and obesity: moderate weight reduction plus high-protein intake and physical activity 1
By implementing these evidence-based interventions, hepatic steatosis can be effectively managed, reducing the risk of progression to more severe forms of liver disease and associated complications.