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Clinical Trials/NCT05783466
NCT05783466RecruitingNot Applicable

Bioactive Dairy Lipids to Manage Cardiometabolic Risk in Obesity

Hospices Civils de Lyon2 sites in 1 country75 target enrollmentStarted: June 28, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
75
Locations
2
Primary Endpoint
Total plasma apolipoprotein B concentration

Study Overview

Brief Summary

It is a randomized parallel arm intervention study in adults with severe obesity. The objective is to demonstrate that within a dietary handling for weight loss, the daily ingestion during 3 months of whole dairy products enriched with milk polar lipids or whole dairy products decreases to a greater extent fasting plasma apolipoprotein B concentrations than the daily ingestion of low-fat dairy products (control group).

Metabolic parameters will be assessed before and after the 3-month intervention, both at fasting and in postprandial period after the consumption of standardized meals.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Men and women between 18-70 years
  • Body Mass Index (BMI) between 35 and 60 kg/m2 inclusive
  • Stable body weight (weight change +/- 5 % for 3 months prior to screening)
  • Consumption of at least 1 serving/day of dairy products made from cow's milk
  • Informed consent

Exclusion Criteria

  • History of bariatric or digestive surgery or disease interfering with main outcomes
  • Drinking more than 3 glasses of alcohol per day (>30g/day)
  • Pregnancy, parturiency or breastfeeding
  • Food allergies or intolerance to dairy products
  • Dietary restriction (vegetarian or lactovegetarian) or high protein diet
  • Use of dietary supplements
  • Treated with lipid lowering drugs (fibrates, statins, anti-PCSK9, ezetimibe, cholestyramine) within the last 6 weeks before study entry
  • Treated with insulin, GLP-1 analogs, acarbose, corticoids, beta-blockers.
  • Medications interfering with intestinal microbiota (beta-lactamines within 3 months before the study or laxatives)
  • Smoking ≥ 5 cigarettes/day during the past 6 months.

Arms & Interventions

Low-fat dairy products within a dietary handling for weight loss

Other

3 servings/day of low-fat dairy products: 1 serving of low-fat cheese, 1 serving of low-fat yogurt and 1 serving of (semi-)skimmed milk.

Intervention: Low-fat dairy products (Other)

Whole-fat dairy products within a dietary handling for weight loss

Experimental

3 servings/day of whole-fat dairy products: 1 serving of whole cheese, 1 serving of whole yogurt and 1 serving of whole milk.

Intervention: Whole-fat dairy products (Other)

Whole-fat dairy products enriched with milk polar lipids within a dietary handling for weight loss

Experimental

3 servings/day of whole-fat dairy products (1 milk, 1 yogurt, 1 cheese) among which 1 serving/day is enriched with milk polar lipids via butterier.

Intervention: Milk polar lipid enriched whole-fat dairy products (Other)

Outcomes

Primary Outcomes

Total plasma apolipoprotein B concentration

Time Frame: day 0 and day 90

Change in fasting total plasma apolipoprotein B concentration after 3-month intervention, measured by ELISA.

Secondary Outcomes

  • Questionnaires on digestive comfort(day 0 and day 90)
  • Anthropometric measurements 2(day 0 and day 90)
  • Changes in weight(day 0 and day 90)
  • Body mass composition measurements(day 0 and day 90)
  • Plasma lipid concentrations after 3-month intervention, measured using standard laboratory methods 3(day 0 and day 90 for fasting and postprandial measurements. For postprandial measurements: time 360 minutes.)
  • Plasma lipid concentrations after 3-month intervention, measured using standard laboratory methods 4(day 0 and day 90 for fasting and postprandial measurements. For postprandial measurements: time 360 minutes.)
  • Glucose concentrations after 3-month intervention, measured using standard laboratory methods(day 0 and day 90 for fasting and postprandial measurements. For postprandial measurements: times 120 minutes -240 minutes)
  • Glucose concentrations after 3-month intervention, measured using standard laboratory methods 2(day 0 and day 90 for fasting and postprandial measurements. For postprandial measurements: times 120 minutes -240 minutes)
  • Plasma lipid concentrations after 3-month intervention, measured using standard laboratory methods(day 0 and day 90 for fasting and postprandial measurements. • For postprandial measurements: times 60 minutes-120 minutes -180 minutes -240 minutes -270 minutes -300 minutes -360 minutes)
  • Targeted plasma lipidomics after 3-month intervention 4(day 0 and day 90 for fasting and postprandial measurements For postprandial measurements :times 120 minutes -240 minutes -300 minutes -360 minutes.)
  • Targeted chylomicrons of plasma after 3-month intervention(day 0 and day 90 for fasting and postprandial measurements For postprandial measurements :times 120 minutes -240 minutes -300 minutes -360 minutes.)
  • Targeted chylomicrons of plasma after 3-month intervention 2(day 0 and day 90 for fasting and postprandial measurements For postprandial measurements :times 120 minutes -240 minutes -300 minutes -360 minutes.)
  • Targeted chylomicrons of plasma after 3-month intervention 3(day 0 and day 90 for fasting and postprandial measurements For postprandial measurements :times 120 minutes -240 minutes -300 minutes -360 minutes.)
  • Targeted chylomicrons of plasma after 3-month intervention 4(day 0 and day 90 for fasting and postprandial measurements For postprandial measurements :times 120 minutes -240 minutes -300 minutes -360 minutes.)
  • Inflammation markers(day 0 and day 90 for fasting and postprandial measurements.)
  • Inflammation markers 5(day 0 and day 90 for fasting and postprandial measurements.)
  • Inflammation markers 6(day 0 and day 90 for fasting and postprandial measurements.)
  • Plasma lipid concentrations after 3-month intervention, measured using standard laboratory methods 7(day 0 and day 90 for fasting and postprandial measurements. For postprandial measurements:times 360 minutes.)
  • Inflammation markers 4(day 0 and day 90 for fasting and postprandial measurements.)
  • Inflammation markers 7(day 0 and day 90 for fasting and postprandial measurements.)
  • Platelet activation markers(day 0 and day 90 for fasting and postprandial measurements. For postprandial measurements,times 120 minutes-240 minutes-300 minutes -360 minutes.)
  • Oxidative stress marker(day 0 and day 90)
  • Markers of immune cells 2(day 0 and day 90)
  • Intestinal microbiota after 3-month intervention.(day 0 and day 90)
  • Intestinal microbiota after 3-month intervention 2(day 0 and day 90)
  • Plasma lipid concentrations after 3-month intervention, measured using standard laboratory methods 2(day 0 and day 90 for fasting and postprandial measurements. For postprandial measurements: times 120 minutes -180 minutes -240 minutes -270 minutes -300 minutes.)
  • Plasma lipid concentrations after 3-month intervention, measured using standard laboratory methods 5(day 0 and day 90 for fasting and postprandial measurements. For postprandial measurements: times 120 minutes -240 minutes -300 minutes.)
  • Plasma lipid concentrations after 3-month intervention, measured using standard laboratory methods 6(day 0 and day 90 for fasting and postprandial measurements. For postprandial measurements: times 120 minutes -240 minutes -300 minutes - 360 minutes)
  • Plasma lipid concentrations after 3-month intervention, measured using standard laboratory methods 8(day 0 and day 90 for fasting and postprandial measurements. For postprandial measurements: times 120 minutes -240 minutes)
  • Targeted plasma lipidomics after 3-month intervention 2(day 0 and day 90 for fasting and postprandial measurements For postprandial measurements :times 120 minutes -240 minutes -300 minutes -360 minutes.)
  • Targeted plasma lipidomics after 3-month intervention 3(day 0 and day 90 for fasting and postprandial measurements For postprandial measurements :times 120 minutes -240 minutes -300 minutes -360 minutes.)
  • Inflammation markers 3(day 0 and day 90 for fasting and postprandial measurements.)
  • Markers of immune cells(day 0 and day 90)
  • Targeted plasma lipidomics after 3-month intervention(day 0 and day 90 for fasting and postprandial measurements For postprandial measurements :times 120 minutes -240 minutes -300 minutes -360 minutes.)
  • Questionnaires on physical activity(day 0 and day 90)
  • Questionnaires on product satiety(day 0 and day 90)
  • Targeted plasma lipidomics after 3-month intervention 5(day 0 and day 90 for fasting and postprandial measurements For postprandial measurements :times 120 minutes -240 minutes -300 minutes -360 minutes.)
  • Inflammation markers 2(day 0 and day 90 for fasting and postprandial measurements.)
  • Questionnaires on product appreciation(day 0 and day 90)
  • Questionnaires food intake(day 0 and day 90)
  • Dietary intake questionnaire(day 0 and day 90)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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