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临床试验/NCT06322940
NCT06322940撤回不适用

Effect of Dairy Product Matrices on Insulin Resistance in People with Overweight and Obesity and Prediabetes

McGill University Health Centre/Research Institute of the McGill University Health Centre2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
发起方
入组人数
60
试验地点
2
主要终点
Change in whole-body insulin sensitivity

研究概览

简要总结

The objective of the study is to determine the effect of dairy product matrices on insulin sensitivity in overweight and obese adults with prediabetes. Females and males (30-65 y) will be recruited from the greater Montreal area. Upon screening, those with prediabetes will complete a 2-wk run-in period in which participants will consume 1 serving/d of regular-fat dairy products (milk, yogurt, or cheese). Adherent participants will be randomized by sex into 1 of 3 groups: ≤1 serving/d of dairy (limited dairy) or 2-3 servings/d of reduced-fat or regular-fat dairy for 12 weeks. Participants will be instructed on how to incorporate foods into their diet to prevent changes in their body weight. The hyperinsulinemic-euglycemic clamp will be used before and after the intervention to document potential changes in insulin sensitivity as the primary outcome. In addition, glycemic variables, body composition, and cardiometabolic risk factors will be assessed as secondary outcomes. Adherence to intervention will be assessed at each visit by food diaries and a record of consumed dairy products.

详细描述

The randomized controlled trial will be preceded by a 2-week run-in period in which participants will consume 1 serving/day of regular-fat dairy. Following the run-in period, adherent participants will be randomly assigned to one of the three treatment groups (n=20 per group) in a 1:1:1 allocation ratio. Stratified permuted block randomization will ensure adequate balance among groups using a computer-generated list of random numbers. Due to the nature of the test products, participants cannot be blinded to the diet intervention. However, outcome assessors will be blinded to treatment allocation.

During the screening visit, and after obtaining informed consent, weight, height, waist circumference, blood pressure, and pulse will be measured. Standard blood and urine tests, an oral glucose tolerance test, chest X-ray, and an electrocardiogram will be performed. In addition, volunteers will be interviewed regarding demographic information, medical and family history, dietary habits, and physical activity using questionnaires.

At the run-in visit, participants will retrieve their dairy products and a dietitian will instruct them on how to incorporate 1 daily serving of regular-fat dairy products into their habitual diet. A physical exam will be performed. Participants will be asked to record their food intake for 3 consecutive days (including one weekend day). They will also receive an accelerometer and instructions for use on the same 3-days they record their food intake. Participants will maintain a daily record of consumed dairy products during the run-in periods and throughout the study.

At the baseline and 12-week intervention visits, participants will undergo a hyperinsulinemic-euglycemic clamp to assess systemic insulin sensitivity. In addition, body composition will be measured by dual-energy X-ray absorptiometry and resting energy expenditure by indirect calorimetry.

During the 12-week intervention, participants will be provided with the study products and instructed to consume 2-3 servings/day of regular fat milk, yogurt or cheese. Serving sizes will be 250 mL milk, 175 g yogurt, and 50 g cheese. The dietitian will instruct participants individually on how to incorporate the dairy products into their habitual diets by reducing the intake of other foods of equivalent caloric content and complementary nutrient density to maintain stable body weight. No additional dietary changes will be recommended.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Investigator, Outcomes Assessor)

盲法说明

Participant's study group will be coded.

入排标准

年龄范围
30 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged between 30 and 65 years,
  • Able to provide informed consent,
  • Stable weight and dietary habits over a period of 3 months (assessed though questions included in the screening questionnaire regarding changes in weight and dietary habits over the past three months from the date of the screening visit),
  • Body mass index of 25-40 kg/m2,
  • Waist circumference will follow the International Diabetes Federation ethnic-specific definition (≥94 cm for Europid males, ≥90 cm for Asian males, ≥80 cm for females),
  • One or more indicators of prediabetes:
  • 5.7-6.4% HbA1c
  • fasting 5.6-6.9 mmol/L glucose, or
  • 7.8-11.0 mmol/L glucose at 2-hour oral glucose tolerance test (OGTT)

排除标准

  • Current smokers,
  • Pregnant or planning to become pregnant in the next 6 months,
  • Breastfeeding,
  • Participation in a weight loss program in the past 3 months,
  • Dairy allergy or lactose intolerance,
  • Any diagnosed eating disorders,
  • Substance abuse (drugs or alcohol >3 drinks/day),
  • Diagnosed medical conditions such as cardiovascular disease, anemia, kidney disease, liver disease and any cancer, other than skin, within 5 years.
  • Diabetes diagnosis,
  • Abnormal electrocardiogram or chest X-Ray,
  • Treatment with diuretics, certain β-blockers, bronchodilators, daily nonsteroidal anti-inflammatory drugs, anticoagulants or antiplatelet agents (except prophylactic aspirin 81 mg/d), antianginals, antiarrhythmics, oral steroids, or other medications known to affect glucose metabolism,
  • Refusal to temporarily stop taking supplements (minerals, micronutrients, herbal remedies),
  • Serum creatinine > 120 µmol/L,
  • Hemoglobin < 120 g/L,
  • Liver function tests ≥ 3× upper limit,
  • Positive viral serology,
  • Inaccessible veins.

研究组 & 干预措施

2-3 servings of regular-fat milk

Experimental

Milk

干预措施: 250 mL serving size, 3.25% fat content (Other)

2-3 servings of regular-fat yogurt

Experimental

Yogurt

干预措施: 175 g serving size, ≥2% fat content (Other)

2-3 servings of regular-fat cheese

Experimental

Cheese

干预措施: 50 g serving size, ≥28% fat content (Other)

结局指标

主要结局

Change in whole-body insulin sensitivity

时间窗: 12 weeks

Change in whole-body insulin sensitivity as measured by glucose infusion rate during the last 30 min of a hyperinsulinemic-euglycemic clamp divided by serum insulin concentration at the same period (M/I)

次要结局

  • Change in Homeostatic Model Assessment for Insulin Resistance(13 weeks)
  • Change in glycated hemoglobin(13 weeks)
  • Change in oral disposition index(13 weeks)
  • Change in total fat mass(12 weeks)
  • Change in visceral fat mass(12 weeks)
  • Change in systolic blood pressure(12 weeks)
  • Change in diastolic blood pressure(12 weeks)
  • Change in Matsuda index(13 weeks)
  • Change in total lean body mass(12 weeks)
  • Change in glucose tolerance(13 weeks)
  • Change in Insulinogenic index(13 weeks)
  • Change in lipid profile(12 weeks)

研究者

发起方
McGill University Health Centre/Research Institute of the McGill University Health Centre
申办方类型
Other
责任方
Principal Investigator
主要研究者

Sergio Burgos

Associate Professor

McGill University Health Centre/Research Institute of the McGill University Health Centre

研究点 (2)

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