Short-term multidisciplinary non-pharmacological intervention is effective in reducing liver fat content assessed non-invasively in patients with nonalcoholic fatty liver disease (NAFLD)
Summary Background Non-alcoholic fatty liver disease (NAFLD) ranges from simple steatosis to steatohepatitis, and cirrhosis in patients with alcohol intake less than 20 g/day, and is usually associated with insulin resistance (IR). Aim Given that no drugs are specifically approved for NAFLD, we test...
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Veröffentlicht in: | Clinics and research in hepatology and gastroenterology 2013-09, Vol.37 (4), p.353-358 |
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Sprache: | eng |
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Zusammenfassung: | Summary Background Non-alcoholic fatty liver disease (NAFLD) ranges from simple steatosis to steatohepatitis, and cirrhosis in patients with alcohol intake less than 20 g/day, and is usually associated with insulin resistance (IR). Aim Given that no drugs are specifically approved for NAFLD, we tested the efficacy of a non-pharmacological multidisciplinary intervention based on a personalized diet, physical activity and behavior therapy. Methods In this open non-randomized study, personalized diet, physical exercise and behaviour therapy for 3 months were prescribed in 12 consecutive patients with NAFLD. Lifestyle, including total caloric intake, physical activity and resting energy expenditure was monitored by a SenseWear Armband. Insulin Resistance (IR) was measured by HOMA and oral glucose insulin sensitivity tests (OGIS); fat liver content was estimated by two different semi-quantitative scores and by the Doppler Power Index (DPI). Results Data show that the multidisciplinary intervention produced a significant reduction of total caloric intake, a 8% reduction in body weight, a modest increase in daily physical activity, a significant ( P < 0.001) reduction of aminotransferases and a decrease of total hepatic fat content. Conclusions A 3-month multidisciplinary intervention inducing at least 8% of weight loss, improves liver tests and decreases liver fat content. |
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ISSN: | 2210-7401 2210-741X |
DOI: | 10.1016/j.clinre.2012.10.009 |