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首页> 外文期刊>Trials >A double-blind, randomized, crossover trial protocol of whole hemp seed protein and hemp seed protein hydrolysate consumption for hypertension
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A double-blind, randomized, crossover trial protocol of whole hemp seed protein and hemp seed protein hydrolysate consumption for hypertension

机译:全麻蛋白和大麻种子蛋白的双盲,随机,交叉试验协议水解消耗的高血压

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Primary hypertension accounts for almost 95% of all cases of high blood pressure and is a major modifiable risk factor for cardiovascular diseases. Lifestyle interventions have been shown to prevent hypertension. One of the prominent potential therapeutic lifestyle strategies to prevent or manage hypertension is increasing dietary protein as a macronutrient or as bioactive peptides. An emerging plant-based protein source that may have anti-hypertensive properties is hemp seed. A randomized, double-blind, crossover clinical trial will be conducted on 35 hypertensive participants aged 18–75?years, with a BMI between 18.5 and 40?kg/m2, systolic blood pressure (SBP) between 130 and 160?mmHg and diastolic blood pressure?(DBP) ≤?110?mmHg. The trial will be conducted for a period of 22?weeks and will consist of three treatment periods of 6?weeks, separated by 2-week washout periods. The treatments will be consumed twice a day and consist of 25 g casein, hemp seed protein (HSP), or HSP plus HSP hydrolysate (HSP+). The primary outcome of this trial is 24-h SBP, measured on the first day of first phase and the last day of each phase. Office-measured blood pressure, pulse-wave velocity and augmentation index and anthropometrics will be determined at the first and last days of each period. Also, body composition will be assessed by dual x-ray absorptiometry (DXA) scan on the first day of the first phase and within the last 2 days of each treatment period. Blood samples will be collected on the first and last 2 days of each treatment phase whereas urine samples will be collected on the first day of the first phase plus the last day of each phase to be analyzed for specific biomarkers. This trial protocol is designed to evaluate the hypotensive potential of consuming whole HSP, and HSP+, in comparison to casein protein. This study will be the first trial investigating the potential anti-hypertensive benefit of dietary hemp protein plus bioactive peptide consumption in humans. National Clinical Trial (NCT), ID: NCT03508895. Registered on 28 June 2018. Retrospectively registered on the publicly accessible Registry Databank at ClinicalTrials.gov (http://ClinicalTrials.gov).
机译:原发性高血压占所有高血压病例的近95%,是心血管疾病的主要可修改的危险因素。已显示生活方式干预以防止高血压。预防或管理高血压的突出潜在的治疗性生活方式策略之一正在增加膳食蛋白作为Macronurient或生物活性肽。可能具有抗高血压性质的新兴植物的蛋白质来源是大麻种子。随机,双盲的交叉临床临床试验将在18-75岁以下的35岁的高血压参与者进行,BMI在18.5和40℃之间,130至160 kg / m 2之间,收缩压(SBP)在130和160?mmHg和舒张之间血压?(DBP)≤α110?mmhg。该审判将进行22个星期,并将组成6个治疗时间为6?周,分隔2周的洗涤期。治疗将每天消耗两次,由25g酪蛋白,大麻种子蛋白(HSP)或Hsp加HSP水解物(HSP +)组成。该试验的主要结果是24-H SBP,在第一阶段的第一天和每个阶段的最后一天测量。办公室测量的血压,脉搏波速度和增强指数和蒽型测定剂将在每个时期的第一个和最后几天确定。此外,通过双X射线吸收度(DXA)扫描在第一阶段的第一天和每个治疗期的最后2天内评估体组合物。将在每种治疗阶段的第一个和最后2天收集血液样品,而尿液样品将在第一阶段的第一天收集加上每个阶段的最后一天进行特定生物标志物。与酪蛋白蛋白相比,该试验协议旨在评估消费全HSP和HSP +的低脉搏潜力。本研究将是第一次研究膳食大麻蛋白和人类生物活性肽消费的潜在抗高血压益处。国家临床试验(NCT),ID:NCT03508895。 2018年6月28日注册。回顾性地在ClinicalTrials.gov(http://clinicaltrials.gov)的公开访问的注册表数据库上注册。

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