Clinical Research Directory

Inclusion Criteria: * Waist circumference \> 94cm * Triglycerides \> 1.5 g/L or HDL cholesterol \< 0.4 g/L * Fasting blood glucose \< 1.26g/L * Biological profile considered compatible with study participation, * Venous status judged satisfactory by the nurses, allowing catheter placement for the study, * Individuals able to sign the informed consent form, * Persons subject to a social security scheme. Exclusion Criteria: * Subjects on special diets (vegetarian, vegan, etc.), * Subject showing a weight loss ≥ 5% in 1 month or ≥ 10% in 6 months compared to usual weight. * Subject refusing to stop taking dietary supplements for the duration of the study, * Subject refusing to consume any of the proposed products, * Subject with food allergy(ies) to one or more components of the products under study, or with a contraindication to the consumption of these products, * Subjects with a pathology or treatment (antidiabetics, hypolipidemics, corticoids, neuroleptics) judged by the investigator to be incompatible with the study, * Subjects with dysthyroidism that has not been stabilized for at least 3 months, * Subject with unstabilized hypertension for at least 3 months, * Subject with a medical and/or surgical history deemed by the investigator to be incompatible with the trial, * Subject having undergone surgery that could interfere with the study objectives (as judged by the investigating physician) in the 3 months preceding the study, * Smoking \> 5 cigarettes/day, * Alcohol \> 3 glasses/day, * Claustrophobic subject, * Person refusing to be registered with the French Ministry of Health's Fichier National des Volontaires Sains, * Major under guardianship or with limited rights, * Subject not affiliated to social security, * Subject in a period of exclusion from a previous study or having received a total amount of compensation exceeding 6000 euros over the 12 months preceding the start of the trial (after verification in the Fichier des Volontaires pour la Recherche Biomédicale).