Affiliation:
1. Division of Hepatology Department of Upper GI Karolinska University Hospital Stockholm Sweden
2. Department of Medicine Karolinska Institute Stockholm Sweden
3. Department of Gastroenterology, Hepatopancreatology and Digestive Oncology Hôpital Universitaire de Bruxelles Université Libre de Bruxelles Brussels Belgium
4. Faculté de Médecine Laboratory of Experimental Gastroenterology Université Libre de Bruxelles Brussels Belgium
Abstract
AbstractAlcohol‐related liver disease (ALD) and non‐alcoholic fatty liver disease (NAFLD, recently renamed metabolic dysfunction‐associated steatotic liver disease [MASLD]) share many features, including certain pathophysiological mechanisms, susceptibility genes, and histological lesions. However, the natural history of the two diseases, studied separately, is significantly different, with ALD being associated with a higher risk of cirrhosis and liver‐related mortality. Moreover, evidence suggests an interactive effect between ALD and metabolic risk factors that are associated with NAFLD on the risk of progressive fibrosis and development of cirrhosis. Patients with both a high consumption of alcohol and metabolic risk factors, such as obesity or diabetes, should therefore be considered a particularly high‐risk group for cirrhosis. Additional studies regarding the efficacy of screening for advanced liver fibrosis or cirrhosis in these risk groups are needed. The most effective and established method for reducing the risk of progression in ALD is alcohol abstinence, whereas weight loss is effective in NAFLD. In this narrative review, we introduce the reader to the literature of the field and present key studies showing this interactive effect.
Funder
Intercept Pharmaceuticals
Gilead Sciences
Pfizer
Cited by
3 articles.
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