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Non-alcoholic Fatty Liver Disease (NAFLD) or "Fatty Liver" corresponds to the presence of macrovesicular changes without inflammation (steatosis) and lobular inflammation in the absence of significant alcohol use. It can be divided into two subgroups: NAFL (Non-Alcoholic Fatty Liver) or simply Steatosis and NASH (Non-Alcoholic Steatohepatitis). NAFL is defined as hepatic steatosis with no evidence of hepatocellular injury in the form of ballooning the hepatocytes. This activity reviews the cause of fatty liver and highlights the role of the interprofessional team in its management. Objectives: Identify the causes of fatty liver. Assess the pathophysiology of fatty liver. Evaluate the treatment of fatty liver. Communicate the importance of improving care coordination among interprofessional team members to improve outcomes for patients affected by fatty liver. Access free multiple choice questions on this topic.

Non-alcoholic Fatty Liver Disease (NAFLD) or "Fatty Liver" corresponds to the presence of macrovesicular changes without inflammation (steatosis) and lobular inflammation in the absence of significant alcohol use. It can be divided into 2 subgroups: Non-Alcoholic Fatty Liver (NAFL) or simply Steatosis and Non-Alcoholic Steatohepatitis (NASH). NAFL is defined as hepatic steatosis with no evidence of hepatocellular injury in the form of ballooning the hepatocytes. NASH is defined as hepatic steatosis and inflammation with hepatocyte injury (ballooning), Malloryhyaline, and mixed lymphocytic and neutrophilic inflammatory infiltrate in perivenular areas with or without fibrosis.[1] It is important to note that NAFL is a spectrum, with NAFL being the mildest form and NASH and cirrhosis being at the other end. NAFL or Steatosis and NASH could only be distinguished with histology and liver biopsy.[2]. NAFLD is commonly associated with Metabolic Syndrome, obesity, diabetes, and hyperlipidemia. Nearly 80% of patients with Metabolic Syndrome have NAFLD.[3][4][5]

Fat accumulates in the liver for several reasons. It most commonly involves increased delivery of free fatty acids to the liver, increased synthesis of fatty acids in the liver, decreased oxidation of FFA, or decreased synthesis or secretion of very-low-density lipoprotein.[6][7] Oxidative stress in the hepatocytes can activate stellate cells and lead to the production of collagen and inflammation. Other factors that may contribute to fatty liver include: The use of medications (eg, tamoxifen, amiodarone, methotrexate) Metabolic abnormalities (eg, glycogen storage disorders, homocystinuria) Alcohol Nutritional status (eg, total parenteral nutrition, severe malnutrition, overnutrition, or a starvation diet) Other health issues like Wilson disease and celiac sprue.

The prevalence of NAFLD varies dramatically depending on the population being studied. It is estimated that the prevalence of NAFLD is 20% in the United States population and between 11.5% and 46% in the general population. By contrast, the prevalence of NASH is in the range of 2% and 3%. The prevalence is higher in white men than white women, but there are no differences between Hispanic and African-American people[8]. Mean age at diagnosis is 50 years (range 16-80). It is more common in Hispanics when compared to Whites and more common in Whites than in Blacks. Obesity is a well-known risk factor for NAFLD. In patients with severe obesity undergoing bariatric surgery, up to 90% are found to have NAFLD, and some even have cirrhosis. The same study also concluded that insulin resistance was the main predictor for NASH.[9]

Current concepts point to insulin resistance as the primary metabolic defect leading to NAFLD. Insulin resistance increases the influx of free fatty acids into the liver. This happens due to the failure of insulin to suppress the hormone-sensitive lipase, causing more FFA to be released from the adipose tissue. Also, elevated insulin levels and insulin resistance promote continuous synthesis of triglycerides in the liver. These 2 sources of triglycerides result in the accumulation of lipids in the hepatocytes, causing macrovesicular hepatic steatosis (see Image. Liver Biopsy, Hepatic Steatosis).[6][10] Lipid accumulation in nonadipose tissue is a key factor for progressing insulin resistance, DM(Diabetes mellitus), and cardiovascular disease.[11] The current hypothesis is that NASH evolves from NAFLD caused by a second "hit." The evidence behind this second insult is inconclusive, but the most acceptable theories involve oxidative stress, specific cytokines, and lipopolysaccharides. Free fatty acids and hyperinsulinemia potentiate lipid peroxidation and the release of hydroxy-free radicals, directly injuring the hepatocytes by recruiting neuroinflammatory mediators. Chronic liver injury over time lead to activation of stellate cells, creating a potential for hepatic fibrosis. The diagnosis of NASH can only be established with a liver biopsy. Biopsy findings can reveal the following: Type 1: fatty liver alone; macrovesicular steatosis Type 2: fatty accumulation and lobar inflammation Type 3: fat accumulation and ballooning degeneration Type 4: fat accumulation, ballooning degeneration, and either Mallory hyaline or fibrosis. Type 3 and Type 4 are NASH by definition.

Histologically, the fatty liver reveals fat accumulation in the central (centrilobular) zone. Universally, one notes the presence of macrovesicular steatosis with the liver cells containing several large fat droplets that displace the nucleus. Sometimes, the lipid deposits may be released due to the rupture of the overtly distended liver cells, which produces lipogranulomas composed chiefly of macrophages and occasional lymphocytes.[12] See Image. Fatty Liver Disease.

Patients are usually asymptomatic, and "fatty liver" is usually an incidental finding on imaging done for other purposes. When patients do have symptoms, they are usually nonspecific, constitutional or right upper quadrant discomfort. It is important to obtain detailed alcohol use, review past medical history, family history, current and past prescription medications, and use of over-the-counter drugs or supplements. The history should include diet, physical activity, weight change ( weight gain of over 18 kg in 2-3 years), and evaluation for associated conditions like obesity, hyperlipidemia, and diabetes ).[13]

Laboratory studies lack specificity and cannot distinguish NASH from NAFLD; however, initial evaluation should include an assessment of a complete hepatic panel, lipid panel, and iron. Lab tests may be used to evaluate insulin resistance, which includes the Homeostasis Model Assessment (normal value<3.99)[14] and The Quantitative Insulin Sensitivity Check Index [15]. Lab tests to rule out viral hepatitis and Hemochromatosis should be ordered. Suppose the patient has elevated liver enzymes chronically or has a family history of cirrhosis. In that case, additional tests, like an antinuclear antibody, smooth muscle antibody,a1-antitrypsin, ceruloplasmin, and thyroid-stimulating hormone levels, should be considered.[16][13] Patients with alcoholic liver disease may have or have not elevated serum aminotransferase levels. The absolute level of liver enzyme elevation is not related to the severity of alcohol liver disease. Still, the pattern of elevation in liver enzymes helps make a diagnosis of alcoholic liver disease. AST level is typically 2 to 3 times greater than ALT in alcoholic liver injury. Also, these patients have an elevated serum gamma-glutamyltranspeptidase.[17] Imaging studies play a key role in the diagnosis of NAFLD. The mainstay is ultrasonography; it is the least invasive and relatively inexpensive. The sensitivity of an ultrasound to detect NAFLD is in the range of 60% to 90%, with a specificity of around 90%. Unenhanced abdominal computed tomography and magnetic resonance are alternatives but more costly and less significantly superior to ultrasonography.[18][3][19] Diagnosis of NASH requires a liver biopsy; however, not all patients with NAFLD require a liver biopsy. The decision to proceed with histological examination depends on risk factors, laboratory workup, and disease severity. According to the 2012 guidelines from the American Association for the Study of Liver Disease, liver biopsy should be reserved for subjects who benefit, for subjects with potentially competing diagnoses, and for children with either an unclear diagnosis or in whom consideration is being given for medication. Liver biopsy has a moderate risk of complications and is invasive, subject to sampling error, and expensive.[20]

Lifestyle modifications and weight loss are the mainstays of the treatment. Treatment also involves glycemic and lipid control. For patients with significant obesity, gastric bypass or other weight loss surgical modalities should be considered. Weight loss is proven to reduce hepatic steatosis. The evidence suggests that a loss of 3% to 5% of body weight is necessary to notice an improvement in steatosis. Still, a greater loss (up to 10%) is necessary to improve necroinflammation.[21][22][23] Patients should abstain from alcohol or hepatotoxic drugs. Pharmacological options include Metformin, Vitamin E, fish oil, Orlistat (an inhibitor of gastric and pancreatic lipase), and Sibutramine. It is important to notice that the evidence behind these pharmacological modalities is weak. Three Cochrane reviews found insufficient evidence to support using bile acids (ursodeoxycholic acid), antioxidant supplements, metformin, or thiazolidinedione in the absence of diabetes in patients with nonalcoholic fatty liver disease.[24][25]Studies have shown that metformin does not significantly affect liver histology; therefore, its use is only recommended if there is another indication. Vitamin E is currently only recommended for non-diabetic patients with biopsy-proven NASH. Pioglitazone can be used to treat patients with biopsy-proven steatohepatitis, but its long-term effects are not known. A randomized controlled trial of 247 adults with nonalcoholic steatohepatitis found improvement in AST and ALT levels with the use of vitamin E and pioglitazone but no improvement in fibrosis.[26] For patients with advanced disease and cirrhosis, liver transplantation might have to be considered.

Differential diagnosis for fatty liver include the following: Viral Hepatitis Alcoholic hepatitis Alpha1 Antitrypsin Deficiency Primary sclerosing cholangitis Wilson disease Primary biliary cholangitis Cirrhosis

Considerations for deterrence and patient education for fatty liver include: The patient should refrain from alcohol. Malnutrition is common in these patients, so a dietary consult should be obtained. A low-fat diet and weight loss is recommended. Participating in a regular exercise program is highly recommended.

Fatty liver is on the rise in the US primarily because of an increase in obesity, type 2 diabetes, and consumption of alcohol. The condition can be reversed if detected early but requires an interprofessional approach. Education of the patient is vital to ensure that there is complete abstinence from alcohol. For those who do not remain compliant, end-stage liver disease can develop, which carries high morbidity and mortality. The nurse should also emphasize the importance of lifestyle changes and a healthy diet. Exercise and a healthy weight can help reverse the disorder and markedly improve the quality of life. The pharmacist must be closely involved in the management of these patients because several studies show that the use of oral hypoglycemics and lipid-lowering agents may help lower the risk of heart disease. A bariatric surgery consult may be helpful for patients who cannot lose weight with conservative measures. There is evidence showing that appropriate weight loss surgery can significantly lower the risk of diabetes and heart disease.[21][28] Outcomes Several studies show that the prognosis is excellent if there is early intervention before the onset of fibrosis. However, if the treatment is delayed and end-stage liver disease develops, the prognosis is poor. To reduce the morbidity of fatty liver, evidence suggests that one should adopt an aggressive and interprofessional strategy for managing obesity, diabetes, and metabolic syndrome.[29][12][30]