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临床试验/NCT02907684
NCT02907684已完成不适用

A Randomised, Controlled Parallel Dietary Intervention to Investigate the Effect of Almond Snack Consumption on Cardio-metabolic Disease Risk Markers Compared With Isocaloric Snacks, in Adults at Moderate Risk of Cardiovascular Disease

King's College London2 个研究点 分布在 1 个国家目标入组 108 人开始时间: 2017年3月29日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
108
试验地点
2
主要终点
Endothelium-dependent vasodilation

研究概览

简要总结

The purpose of this study is to investigate the cardio-metabolic health effects of consuming almond nuts in place of habitual (usual) snack products in adults at moderate risk of developing cardiovascular disease

详细描述

Tree nuts are recommended in the prevention and management of cardiovascular disease (CVD) largely based on their LDL (low density lipoprotein) lowering effects, but the CVD risk reduction observed with tree nut consumption is greater than that predicted by their hypocholesterolemic effects alone. Other health benefits have also been noted by our group, such as moderation of postprandial lipemia , as well as by others such as modified postprandial glycemia , decreased blood pressure (BP) , improvement in oxidant status and weight loss. Robust evidence for the protective cardio-metabolic effects of nuts from the PREDIMED study has highlighted the association between nut consumption and decreased risk of cardiovascular events, obesity, metabolic syndrome and type 2 diabetes (T2DM). However, there is a paucity of evidence on the effects of almonds on vascular function in humans (BP and endothelium-dependent vasodilation (EDV)), although there is evidence that almonds promote nitric oxide (NO) release in animals consuming high-fat diets. Fundamental to vascular health is a well-functioning liver and there is increasing evidence to demonstrate that the accumulation of liver fat is a causative factor in the development of cardio-metabolic disorders. Non-alcoholic fatty liver disease (NAFLD) is now considered the hepatic manifestation of the metabolic syndrome (MetS); recent data has shown that it is linked to increased CVD risk via direct effects on vascular function (and EDV) independently of obesity and MetS . NAFLD is thought to affect 30% of the population in developed countries, and up to two-thirds of people with obesity and 50% of people with hyperlipidemia. Development of fatty liver, mainly attributable to obesity and elevated postprandial lipemia, is associated with increased inflammation, oxidative stress, insulin resistance, dyslipidemia and impaired EDV, and predicts risk of CVD and T2DM .

Therefore, the long-term goal of this research is to understand the mechanisms underpinning how dietary change can drive favourable modification of CVD disease risk and to identify patterns in population food choices, specifically almond consumption, that tend to correlate with reduced CVD disease risk. The primary aim of this proposal is to investigate, in a randomised controlled, parallel arm, 6-wk dietary intervention (n=100) whether replacing snacks based on refined carbohydrates and poor in micronutrients/non-nutrient bioactives (NNB) with nutrient/NNB-dense, whole almond snacks can influence liver fat content (a key metabolic driver of insulin resistance and vascular dysfunction, and a hallmark of metabolic syndrome) and EDV (brachial FMD being an independent predictor of CVD events, in addition to related biomarkers of cardio-metabolic disease risk. The snacks products provide participants with 20% of their energy requirements via either whole almonds or as muffins/crackers that have been designed to mimic the average UK snack.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
30 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects will be male or female, aged between 30-70 years who regularly consume ≥2 snack products a day. A principal aim is to identify and recruit subjects with increased risk of CVD, in order to increase the sensitivity of the study subjects to dietary change. Subjects who are at above average risk for developing CVD (relative risk >1.5) will be selected using a metabolic scoring system (scoring ≥2 points), adapted from the Framingham risk score system, as used previously by Chong et al.
  • Subjects will give their own written informed consent.

排除标准

  • Non-snack consumers (assessed as subjects consuming <2 snack products per day by a specific FFQ (food frequency questionnaire) at screening, adapted from the short Health Survey for England (2007) Eating Habits Questionnaire).
  • A reported history of myocardial infarction or cancer.
  • Being fitted with a heart pacemaker.
  • Presence of metal inside the body (implants, devices, shrapnel, metal particles in eyes from welding etc.). History of black-outs/epilepsy.
  • Diabetes mellitus (fasting plasma glucose >7 mmol/L).
  • Chronic coronary, renal or bowel disease or history of cholestatic liver disease or pancreatitis.
  • Presence of gastrointestinal disorder or use of a drug, which is likely to alter gastrointestinal motility or nutrient absorption.
  • History of substance abuse or alcoholism (past history of alcohol intake >60 units/men or 50 units/women).
  • Currently pregnant, planning pregnancy, breastfeeding or having had a baby in the last 12 months.
  • Allergy or intolerance to nuts.
  • Unwilling to follow the protocol and/or give informed consent.
  • Weight change of > 3 kg in preceding 2 months. BMI <18 kg/m2 (underweight) or >40 kg/m2 (morbidly obese due to potential technical difficulties making FMD and ambulatory blood pressure (ABP) measurements).
  • Current smokers or individuals who quit smoking within the last 6 months.
  • Participation in other research trials involving dietary or drug intervention and/ or blood collection in the past 3 months.
  • Unable or unwilling to comply with study protocol.
  • The above criteria will be measured using the screening questionnaires and from physical (blood pressure, weight, height) and biochemical measurements (full lipid count, liver function test, full blood count, glucose and insulin) made during the screening visit. Participant eligibility will be assessed against the inclusion/exclusion criteria and 'fitness' to participate will be assessed and signed off by a clinician.

结局指标

主要结局

Endothelium-dependent vasodilation

时间窗: Week 8 (after 2 week run in)

Measured via flow mediated dilation (FMD)

Liver fat %

时间窗: Week 8 (after 2 week run in)

Via MRI and MRS analysis. Only a subset of 48 participants with aim of 20 per each arm to complete

次要结局

  • Pancreatic fat(Week 8 (after 2 week run in))
  • Abdominal fat(Week 8 (after 2 week run in))
  • Body composition: body weight(Week 8)
  • Plasma triglyceride concentration(Week 8)
  • Plasma resistin(Week 8)
  • Blood pressure(Week 8)
  • Fasting non esterified fatty acids (NEFA)(Week 8)
  • Muscle fat(Week 8 (after 2 week run in))
  • 24 hour ambulatory blood pressure(Week 8)
  • Gut microbiota(Week 8)
  • Fasting insulin(week 8)
  • Homeostasis model assessment estimated insulin resistance (HOMA-IR)(Week 8)
  • Plasma adiponectin(Week 8)
  • Body composition: body mass index(Week 8)
  • Plasma LDL cholesterol(Week 8)
  • Plasma HDL cholesterol(Week 8)
  • Plasma leptin(Week 8)
  • Body composition: Waist circumference(Week 8)
  • Body composition: Hip circumference(Week 8)
  • 24 hour heart rate variability(Week 8)
  • Fecal short chain fatty acids(Week 8)
  • Fasting glucose(Week 8)
  • Plasma Total cholesterol(Week 8)
  • Plasma HDL:LDL ratio(Week 8)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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