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The effects of Mediterranean diet on hepatic steatosis, oxidative stress, and inflammation in adolescents with non‐alcoholic fatty liver disease: A randomized controlled trial

医学 脂肪变性 内科学 非酒精性脂肪肝 脂肪肝 随机对照试验 氧化应激 内分泌学 胃肠病学 地中海饮食法 炎症 疾病
作者
Gamze Yurtdaş Depboylu,Gamze Akbulut,Maşallah Baran,Canan Yılmaz
出处
期刊:Pediatric obesity [Wiley]
卷期号:17 (4) 被引量:47
标识
DOI:10.1111/ijpo.12872
摘要

Summary Background Non‐alcoholic fatty liver disease (NAFLD) has become the most common liver disease in children and adolescents. The optimal dietary strategy to improve hepatic stetatosis and reduce oxidative stress and inflammation in adolescents is unknown. Objective This study was conducted to evaluate the effect of Mediterranean diet (MD) versus low‐fat diet (LFD) on hepatic steatosis, inflammation, and oxidative stress in adolescents with obesity and NAFLD. Methods Adolescents diagnosed with NAFLD between the ages of 11–18 years were randomized to either a MD or conventional LFD (control diet) for 12 weeks. Dietary status, anthropometry, body composition, and biochemical parameters were evaluated. Hepatic steatosis was determined by ultrasonography. Results A total of 44 participants completed the study. At the end of the study, severity of hepatic steatosis, serum transaminase levels, and insulin resistance decreased significantly in both groups with no significant differences between groups except for aspartate aminotransferase (AST). The amount of decrease in AST levels in the MD group was greater than the LFD group ( p < 0.05). In the MD group, serum total antioxidant capacity, paraoxanase‐1, and glutathione peroxidase levels increased ( p < 0.05); it did not change in the LFD group compared to baseline ( p > 0.05). C‐Reactive Protein (CRP) levels decreased only in the MD group ( p = 0.008), interleukine‐6 decreased only in the LFD group ( p = 0.031). Conclusion Consumption of MD and LFD for 12 weeks in adolescents with obesity and NAFLD reduced BMI, fat mass, hepatic steatosis, and insulin resistance, improved high transaminase levels, and had positive effects on inflammation and oxidative stress. Registered under ClinicalTrials.gov Identifier no. NCT04845373.
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