Collection of Human Metabolic Tissues (COMET)

University Hospital Center (CHU)

Status: Enrolling

Conditions: Insulin Resistance; Obesity; Diabetes Mellitus, Type 2

Treatments: Other: Collection of blood samples and tissues

Study type: Observational

Funder types: Other

Identifiers

NCT02861781

RECHMPL15_0271

2015-A01193-46 (Other Identifier)

UF 9605 (Other Identifier)

Details and patient eligibility

About

This project aims at identifying new determinants of type 2 diabetes in severe obesity. To do so, a biological collection, including tissues of interest in the field of metabolism, will be collected during bariatric surgery in obese patients. Three different groups of metabolic status of patients, corresponding to different stages of evolution of the disease, will be constituted: type 2 diabetes, insulin resistance, insulin sensitivity.

The main objective is to compare, between these 3 groups of patients, several biological processes that may be involved in the pathophysiology of type 2 diabetes and disorders associated with obesity, including:

• Abnormalities of the transcriptome, proteome, metabolome in all target tissues (plasma, serum, muscle, subcutaneous and visceral adipose tissue, omental artery, liver)
• Identification of metabolic signatures, protein and miRNA in plasma
• Immunoinflammatory response in adipose tissue
• Polymorphisms SNP from whole blood
• Histological analysis of tissue sections This main objective will be studied on samples taken at the time of surgery Secondary objectives will be to study the changes in metabolites, proteins and miRNA in plasma level 3 and 12 months after the completion of surgery, according to the initial metabolic state.

Enrollment: 270 estimated patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

1. Written informed consent

2. Age 18 - 65 years inclusive at surgery

3. IMC > 35

4. Subject qualified for bariatric surgery (sleeve gastrectomy or gastric bypass)

5. Specific criteria :

   • Type 2 diabetes group (D) (90 patients) : type 2 diabetes according to ADA criteria
   • Insulin resistance non diabetes group (IR) (80 patients) : HOMA-IR criteria ≥ 3
   • Insulin Sensitivity non diabetes group (N) (100 patients) : N1.HOMA-IR criteria < 3

Non inclusion Criteria:

1. Vulnerability according to article L1121-6 of the Public Health Code
2. Protected adult or unability to give consent according to article L1121-8 of the Public Health Code
3. Unability to understand the design and aims of the study or to communicate with the investigator
4. Non affiliation to a social security system
5. Prior bariatric surgery (except lap-band procedure)
6. Serologic profile indicating hepatitis B, hepatitis C or HIV infection
7. Inflammatory, infectious or autoimmune disease (current or in the previous 3 month)
8. Malignancies within 5 years prior to inclusion or not considered as treated curatively
9. Concomitant use of steroids or NSAI or use in the 8 days before surgery
10. alcohol abuse/addiction
11. Anticipated poor compliance to study procedures
12. Other type of diabetes than type 2

Exclusion Criteria :

1. Cancelled bariatric surgery
2. Tissue collection not possible during the bariatric surgery

Trial design

270 participants in 3 patient groups

Type 2 diabetes

Description:

Type 2 diabetes according to ADA criteria

Treatment:

Other: Collection of blood samples and tissues

Insulin resistance non diabetes

Description:

HOMA-IR criteria ≥ 3

Treatment:

Other: Collection of blood samples and tissues

Insulin sensitivity non diabetes

Description:

HOMA-IR criteria \< 3

Treatment:

Other: Collection of blood samples and tissues