Study of the Mechanisms of Metabolic Adaptations to Overfeeding
NCT02225457 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52
Last updated 2016-03-08
Summary
Obesity results from complex interactions between genetic and environmental factors, and are strongly associated with metabolic complications such as type 2 diabetes mellitus. Obesity is defined as an excessive fat accumulation that presents a risk to health, a risk that is highly dependent upon the type of adipose tissue accumulation, whether visceral or sub-cutaneous, but also upon the characteristics of the fat tissue, especially inflammatory cells accumulation. Because of the well known sexual difference in fat accretion, this obesity-associated risk may also be very different for men and for women. In addition, recent data indicate that various factors such as the intestinal microbiota, but also the dietary intake of protective nutrients might be important determinants of the metabolic complications of obesity.
Here we propose to: 1) study the metabolic adaptations and the mechanisms of adipose tissue accumulation during a period of controlled caloric over-nutrition, both in men and in women; 2) evaluate the potential protective effects of a supplementation with polyphenols on insulin resistance and other metabolic adaptations.
Conditions
Interventions
- OTHER
-
Hypercaloric diet
Hypercaloric diet will be designed to provide 50% excess in calories compared to daily requirements. It will consist in a "snack" type, high fat and high carbohydrates diet.
- DIETARY_SUPPLEMENT
-
polyphenols
Administration of polyphenols will consist in the administration of 1 gram (5x200 mg) of the compound bid during the entire overfeeding period.
- DIETARY_SUPPLEMENT
-
placebo (for polyphenols)
Placebo will consist in the administration of a number of placebo pills matching that of polyphenols, in a similar way (bid) for the duration of the overfeeding experiment.
Sponsors & Collaborators
-
University of Lyon
collaborator OTHER -
Centre Hospitalier Universitaire Vaudois
lead OTHER
Principal Investigators
-
Francois P Pralong, MD · Centre Hospitalier Universitaire Vaudois
Study Design
- Allocation
- RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- QUADRUPLE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 20 Years
- Max Age
- 30 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2013-12-31
- Primary Completion
- 2016-05-31
- Completion
- 2017-01-31
Countries
- Switzerland
Study Locations
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