Fatty liver and the metabolic syndrome : Current Opinion in Gastroenterology (original) (raw)

Nutrition

Division of Gastroenterology and Hepatology, Saint Louis University Liver Center, St. Louis, Missouri, USA

Correspondence to Brent A. Neuschwander-Tetri, MD, FACP, Professor of Internal Medicine, Division of Gastroenterology and Hepatology, Saint Louis University Liver Center, 3635 Vista Ave., St. Louis, MO 63110, USA Tel: +1 314 577 8764; fax: +1 314 577 8125; e-fax: mail: [email protected]

Abstract

Purpose of review

Nonalcoholic fatty liver disease and its subset nonalcoholic steatohepatitis represent the liver manifestations of insulin resistance. This review briefly summarizes advances in our understanding of the pathogenesis of nonalcoholic fatty liver disease and its prevalence, natural history and treatment.

Recent findings

The recognition of the role the renin–angiotensin system in promoting insulin resistance is worth noting because of available drugs. Endoplasmic reticulum stress has also become a recent target of investigation because endoplasmic reticulum stress is common in obesity, diabetes and various forms of liver disease including nonalcoholic fatty liver disease. Endoplasmic reticulum stress may be responsible for activation of c-Jun kinase, a process that may cause the hepatocellular injury in nonalcoholic steatohepatitis. Progress has also been made in estimating the prevalence of nonalcoholic fatty liver disease in adults and children. Patients enrolled in the Dallas Heart Study were found to have a 33% prevalence of nonalcoholic fatty liver disease and children dying of accidental deaths in San Diego were found to have a 13% prevalence of nonalcoholic fatty liver disease. Because about 10% of people with nonalcoholic fatty liver disease are at risk for progressive fibrosis, the burden of this disease is now quite substantial.

Summary

Incremental progress in understanding nonalcoholic fatty liver disease and nonalcoholic steatohepatitis promises to lead to new therapeutic options for this common disease.

© 2007 Lippincott Williams & Wilkins, Inc.

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