Polyphenols and Insulin Resistance (POLYOXRESIST)

University Hospital Center (CHU)

Status: Completed

Conditions: Type 2 Diabetes (T2D); Healthy Volunteers; Insulin Resistance

Treatments: Drug: placebo; Drug: polyphenol

Study type: Interventional

Funder types: Other

Identifiers

NCT01478841

UF8178

Details and patient eligibility

About

Diet and nutrition play an essential role in the development and the clinical expression of the most common health problems. Overeating and obesity induce oxidative stress, which has been proposed to be a pathogenic mechanism leading to insulin resistance, type 2 diabetes (T2D) and associated cardiovascular complications. The main objective of the proposed research is to evaluate the beneficial effects of polyphenolic compounds derived from red grape marc extracts on the cascade of events leading from overeating to oxidative stress and insulin resistance. For that, we will study free radicals production, inflammatory markers, adipokines, mitochondrial function, insulin sensitivity and energy substrate utilization in healthy volunteers at risk for insulin resistance and T2D (1st degree relatives of T2D patients with associated overweight). These volunteers will be randomized between a placebo and a polyphenol group for 9 weeks. The demonstration of the beneficial effects of polyphenols will be sensitized by high-fructose feeding for the last 6 days of the protocol.

Enrollment: 44 patients

Sex: All

Ages: 30 to 55 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Absence of anti HIV or anti hepatitis C antibodies and of HBS antigen.
• Acceptable biological assessment of the hepatic and renal functions (γGT, ALAT, ASAT < 3 times the normal value and serum creatinine <150 micromol/l).
• Age between 30 and 55 years.
• Fasting plasma glucose <110 mg/dl and absence of any anti-diabetic treatment
• No regular physical activity (Voorips index < 9)
• Absence of any drug treatment in progress and during the last 2 months
• Subjects with at least one 1st degree relative with T2D and with a body mass index between 25 and 35 kg/m² and a waist measurement >94 cm for males, and >80 cm for females.
• Normal ionogram (sodium 135 - 145 mmol/l, potassium 3,5 - 4,5 mmol/l).
• Normal ferritin level (75 - 300 ng/ml)
• hs-CRP <8 mg/l.
• Absence of arterial hypertension (systolic pressure <140 mmHg and diastolic pressure <90 mmHg).
• Non smoker or former smoker (quit smoking >1 year).
• Alcohol consumption <30 g/day.

Exclusion criteria

• Hyperthermia (T°>38°c)
• Subject deprived of freedom by a court or administrative order
• Major protected by the law
• Subject who is in a period of relative exclusion due to his/her participation to another protocol or for whom the annual maximum amount of allowances of 3 811.23 € is reached.
• Subject who has been treated with anti-coagulants, anti-inflammatory drugs, b-blockers or insulin during the last month.
• Subject who cannot be subjected to muscle biopsy.
• Allergy to the anaesthetic
• Woman in age to procreate and not taking any oral or intra-uterine contraception

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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44 participants in 2 patient groups, including a placebo group

Polyphenols

Experimental group

Description:

9 weeks of supplementation with polyphenols(D56) and during the last week supplementation with polyphenols associated with a fructose load during the last 6 days (D63).

Treatment:

Drug: polyphenol

placebo

Placebo Comparator group

Description:

9 weeks of supplementation with placebo (D56) and during the last week supplementation with placebo associated with a fructose load during the last 6 days (D63).

Treatment:

Drug: placebo