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Effect of a high-protein diet with β-cryptoxanthin supplementation on metabolic risk factors, oxidative and inflammatory biomarkers in non-alcoholic fatty liver disease (NAFLD): study protocol for a randomized controlled clinical trial

机译:补充β-隐黄质的高蛋白饮食对非酒精性脂肪肝疾病(NAFLD)代谢危险因素,氧化和炎症生物标志物的影响:一项随机对照临床试验的研究方案

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Excessive hepatic fat is associated with increased metabolic risk factors, production of inflammatory factors, and oxidative stress. High protein intake might trigger an increased hepatic lipid oxidation through an increase in hepatic energy expenditure. Furthermore, the majority of randomized controlled trials (RCT) in humans have failed to show whether carotenoids can be used to prevent and treat non-alcoholic fatty liver disease (NAFLD). However, it is notable and contradictory that NAFLD is rapidly escalating in Iran and other countries with lower intakes of fruit and vegetables (as sources of β-cryptoxanthin [β-CX] and carbohydrates) and higher intake of carbohydrates (as an agent of NAFLD); and the effects of β-CX and a high protein diet (HPD) on NAFLD need to be investigated further. This study will be conducted as a randomized, double-blind, placebo-controlled clinical trial for 12 weeks to receive daily β-CX 6?mg supplementation combined with a HPD on levels of metabolic factors, β-CX, glycemic and lipid profiles, inflammatory factors, adipocytokines, and body composition. Ninety-two eligible patients, aged 18–60?years, of both genders, who are obese and overweight (body mass index [BMI] 25–40 kg/m2) will be randomly assigned to four groups as follow: HPD?+?placebo; normal protein diet + β-CX (NPD?+?β-CX); HPD?+?β-CX; and NPD?+?placebo (control group). Two populations will be analyzed in this work. The intention-to-treat (ITT) population includes all patients who will be randomized, while the per-protocol (PP) population includes all individuals who complete the 12- week intervention (i.e. study completers). Our findings from this trial will contribute to the knowledge of the relationship between β-CX supplementation and a HPD on NAFLD patients and determination of optimal macronutrient ratios without energy restriction. Iran clinical trials registry, IRCT2017060210181N10 . Registered on 20 June 2017.
机译:肝脂肪过多与代谢危险因素增加,炎性因子的产生和氧化应激有关。高蛋白摄入可能会通过增加肝能量消耗来触发肝脂质氧化增加。此外,大多数人类随机对照试验(RCT)未能显示类胡萝卜素是否可用于预防和治疗非酒精性脂肪肝疾病(NAFLD)。然而,值得注意的是,NAFLD在伊朗和其他国家中的水果和蔬菜摄入量较低(作为β-隐黄质[β-CX]和碳水化合物的来源)和碳水化合物的摄入量较高(作为NAFLD的代理商)正在迅速升级); β-CX和高蛋白饮食(HPD)对NAFLD的影响有待进一步研究。这项研究将作为一项随机,双盲,安慰剂对照的临床试验进行,为期12周,每天接受6 mg的β-CX补充剂和HPD的代谢因子,β-CX,血糖和血脂水平的补充,炎症因子,脂肪细胞因子和身体成分。肥胖和超重(体重指数[BMI] 25-40 kg / m2)的九十二名年龄在18-60岁之间的男女患者,将被随机分为以下四组:HPD?+?安慰剂;正常蛋白质饮食+β-CX(NPDβ+ββ-CX); HPD + +β-CX;和NPD +安慰剂(对照组)。这项工作将分析两个人群。意向治疗(ITT)人群包括将被随机分组​​的所有患者,而按方案(PP)人群包括完成12周干预的所有个体(即研究完成者)。我们从该试验中获得的结果将有助于了解NAFLD患者补充β-CX与HPD之间的关系,并确定无能量限制的最佳常量营养素比率。伊朗临床试验注册中心IRCT2017060210181N10。 2017年6月20日注册。

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