Non-alcoholic Fatty Liver Disease (NAFLD) Clinical Trial
Official title:
Exercise Dose and Nonalcoholic Fatty Liver Disease
The purpose of this research is to provide a better understanding of how exercise (walking) affects non-alcoholic fatty liver disease (NAFLD) in overweight people. NAFLD, which is common in obese people, occurs when the liver has too much fat.
Non-alcoholic fatty liver disease (NAFLD) affects about 33% of adults in the United States.
The prevalence of NAFLD is four to five times higher in obese than lean persons and is
associated with insulin resistance and the metabolic syndrome. Decreasing calorie intake and
increasing physical activity has been recommended as primary therapy for NAFLD, but the
independent effect of aerobic exercise is unknown. The current exercise guidelines for
disease prevention and weight management range from 150 min/wk, recommended by the Centers
for Disease Control and the American College of Sports Medicine, to 300 min/wk, recommended
by the Institute of Medicine. However, it is not known whether aerobic exercise alone can
improve NAFLD, and which recommended dose of exercise might have the most beneficial
effects. The purpose of this proposal is to determine the effect of moderate intensity
endurance exercise on: 1) hepatic fat content; 2) hepatic lipoprotein kinetics; and 3)
plasma inflammatory markers. We hypothesize that aerobic exercise will decrease hepatic fat
content, improve VLDL kinetics, and decrease inflammation in a dose-dependent fashion. The
results from this study will help determine exercise guidelines for obese patients with
NAFLD, and lay the groundwork for future studies evaluating the effects of exercise on
metabolic diseases associated with obesity.
This proposal involves conducting a randomized controlled trial that will randomize obese
subjects with NAFLD (> 10% hepatic fat content) to one of two groups: Group 1 (Control, no
exercise) and Group 2 (Moderate Intensity Aerobic Exercise- 150 min/wk to 300 min/wk of
supervised exercise performed at 45-55% of O2 max).
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Basic Science
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