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Study of the Mechanisms of Metabolic Adaptations to Overfeeding (Polynut)

V

Vaud University Hospital Center

Status

Unknown

Conditions

Diabetes
Obesity

Treatments

Other: Hypercaloric diet
Dietary Supplement: placebo (for polyphenols)
Dietary Supplement: polyphenols

Study type

Interventional

Funder types

Other

Identifiers

NCT02225457
SNF 320030_141065 (Other Grant/Funding Number)
391/13

Details and patient eligibility

About

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.

Full description

To achieve these goals, healthy male and female volunteers will be enrolled into a one month longitudinal, prospective study on the influence of hypercaloric overfeeding (+50% of daily caloric needs) on different tissues (adipose tissue, muscle and blood).

They will be separated into two different groups: hypercaloric nutrition and placebo, and hypercaloric nutrition and polyphenols (2g/day), where polyphenols administration will be randomized and administered in a double blind fashion. Whole body and hepatic insulin sensitivity, total energy expenditure, glucose hepatic production, protein and gene expression in muscle, adipose tissue and blood as well as intestinal microbiota will be assessed at base line, and after one month of overfeeding.

Enrollment

52 estimated patients

Sex

All

Ages

20 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • normal healthy male and female volunteer

Exclusion criteria

  • Diabetes mellitus
  • High blood pressure
  • Liver disease
  • Kidney disease

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Quadruple Blind

52 participants in 2 patient groups

Hypercaloric diet and polyphenols
Experimental group
Description:
polyphenols will consist in the administration of 1 gram (5x200 mg) of the compound bid during the entire overfeeding period. Hypercaloric diet will consist in a hypercaloric diet providing an excess of 50% KCal over daily requirements, and will last 30 days.
Treatment:
Dietary Supplement: polyphenols
Other: Hypercaloric diet
Hypercaloric diet and placebo
Active Comparator group
Description:
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. Overfeeding will consist in a hypercaloric diet providing an excess of 50% KCal over daily requirements, and will last 30 days.
Treatment:
Dietary Supplement: placebo (for polyphenols)
Other: Hypercaloric diet

Trial contacts and locations

1

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Central trial contact

François P Pralong, MD

Data sourced from clinicaltrials.gov

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