Obesity Clinical Trial
Official title:
Study of the Determinants and Mechanisms of Adaptation of Metabolic Responses to Controlled Overfeeding in Female and Male Healthy Volunteers
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.
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.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Basic Science
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