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Resveratrol does not benefit patients with nonalcoholic fatty liver disease

Authors :
Chachay, Veronique S.
Macdonald, Graeme A.
Martin, Jennifer H.
Whitehead, Jonathan P.
O'Moore-Sullivan, Trisha M.
Lee, Paul
Franklin, Michael
Klein, Kerenaftali
Taylor, Paul J.
Ferguson, Maree
Coombes, Jeff S.
Thomas, Gethin P.
Cowin, Gary J.
Kirkpatrick, Carl M. J.
Prins, Johannes B.
Hickman, Ingrid J.
Chachay, Veronique S.
Macdonald, Graeme A.
Martin, Jennifer H.
Whitehead, Jonathan P.
O'Moore-Sullivan, Trisha M.
Lee, Paul
Franklin, Michael
Klein, Kerenaftali
Taylor, Paul J.
Ferguson, Maree
Coombes, Jeff S.
Thomas, Gethin P.
Cowin, Gary J.
Kirkpatrick, Carl M. J.
Prins, Johannes B.
Hickman, Ingrid J.

Abstract

Background & Aims: Nonalcoholic fatty liver disease (NAFLD), characterized by accumulation of hepatic triglycerides (steatosis), is associated with abdominal obesity, insulin resistance, and inflammation. Although weight loss via calorie restriction reduces features of NAFLD, there is no pharmacologic therapy. Resveratrol is a polyphenol that prevents high-energy diet-induced steatosis and insulin resistance in animals by up-regulating pathways that regulate energy metabolism. We performed a placebo-controlled trial to assess the effects of resveratrol in patients with NAFLD. Methods: Overweight or obese men diagnosed with NAFLD were recruited from hepatology outpatient clinics in Brisbane, Australia from 2011 through 2012. They were randomly assigned to groups given 3000 mg resveratrol (n= 10) or placebo (n= 10) daily for 8 weeks. Outcomes included insulin resistance (assessed by the euglycemic-hyperinsulinemic clamp), hepatic steatosis, and abdominal fat distribution (assessed by magnetic resonance spectroscopy and imaging). Plasma markers of inflammation, as well as metabolic, hepatic, and antioxidant function, were measured; transcription of target genes was measured in peripheral blood mononuclear cells. Resveratrol pharmacokinetics and safety were assessed. Results: Eight-week administration of resveratrol did not reduce insulin resistance, steatosis, or abdominal fat distribution when compared with baseline. No change was observed in plasma lipids or antioxidant activity. Levels of alanine and aspartate aminotransferases increased significantly among patients in the resveratrol group until week 6 when compared with the placebo group. Resveratrol did not significantly alter transcription of NQO1, PTP1B, IL6, or HO1 in peripheral blood mononuclear cells. Resveratrol was well-tolerated. Conclusions: Eight weeks administration of resveratrol did not significantly improve any features of NAFLD, compared with placebo, but it increased hepatic stress, based on obser

Details

Database :
OAIster
Notes :
10.1016/j.cgh.2014.02.024
Publication Type :
Electronic Resource
Accession number :
edsoai.on1147254382
Document Type :
Electronic Resource