GLUCOSTRESS: Role of Endoplasmic Reticulum Stress in the Pathophysiology of Type 2 Diabetes

Sponsor
Assistance Publique - Hôpitaux de Paris (Other)
Overall Status
Unknown status
CT.gov ID
NCT02368704
Collaborator
(none)
40
1
48
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Study Details

Study Description

Brief Summary

The purpose of this study is to investigate whether Endoplasmic Reticulum (ER) stress pathway is activated in peripheral tissues (adipose tissue) in insulin resistant diabetic patients compared to healthy subjects normoglycemic matched for age and sex an to investigate whether ER stress pathway can be activated in response to insulin. Indeed, some preliminar on rates studies shows that ER stress pathway is activated by insulin in liver and adipose tissue showing that hyperinsulinemia might help trigger stress path ER.

For this, we propose a case control study of type 2 diabetic patients vs control subjects in which markers of ER stress will be evaluated from abdominal subcutaneous adipose tissue obtained before and after euglycemic hyperinsulinemic. We chose to consider adipose tissue subcutaneous rather than visceral adipose tissue for obvious reasons of lesser invasiveness.

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

Study Design

Study Type:
Observational
Actual Enrollment :
40 participants
Observational Model:
Case-Control
Time Perspective:
Cross-Sectional
Official Title:
Role of Endoplasmic Reticulum Stress in the Pathophysiology of Type 2 Diabetes
Study Start Date :
Nov 1, 2012
Anticipated Primary Completion Date :
Nov 1, 2016
Anticipated Study Completion Date :
Nov 1, 2016

Arms and Interventions

Arm Intervention/Treatment
control

control subjects with : Nondiabetic subjects (blood glucose <7.0 mmol/l without hypoglycemic treatment). The control subjects should be matched to patients for age (± 5 years), sex, and BMI (± 2 kg/m2).

Other: No intervention

case

Diabetic patients with : Having type 2 diabetes for at least 6 months HbA1c ≤ 8% Treat by lifestyle and dietary rules associated or not to a hypoglycemic therapy (metformin and / or sulfamid) and / or insulin secretors dependent glucose as inhibitors of DPP4 (dipeptidyl peptidase-4): Vildagliptin, Sitagliptin, Saxagliptin No modification of hypoglycemic therapy and / or insulin secretors for at least 3 months

Other: No intervention

Outcome Measures

Primary Outcome Measures

  1. Show an increase in markers of ER stress in fasting patients with type 2 diabetes [2 days]

    Protein expression markers of ER stress pathway BiP / GRP 78, CHOP, ATF4 EDEM and XBP-1

Secondary Outcome Measures

  1. Assess whether insulin induces an increase in markers of ER stress [2 days]

    Insulin sensitivity

  2. Insulin secretion in response to glucose infusion [2 days]

  3. Insulin secretion in response to arginine infusion [2 days]

  4. Lipolysis on insulin [2 days]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Specific criteria for diabetic patients:

  • Having type 2 diabetes for at least 6 months

  • HbA1c ≤ 8%

  • Treated by lifestyle and dietary rules associated or not to a hypoglycemic therapy (metformin and / or sulfamid) and / or insulin secretors dependent glucose as inhibitors of DPP4 (dipeptidyl peptidase-4): Vildagliptin, Sitagliptin, Saxagliptin

  • No modification of hypoglycemic therapy and / or insulin secretors for at least 3 months

Specific criteria for control subjects:
  • Nondiabetic subjects (fasting blood glucose <7.0 mmol / l without hypoglycemic treatment).

  • The control subjects should be matched to patients for age (± 5 years), sex, and BMI (± 2 kg/m2).

Common criteria for patients and control subjects:
  • Aged 18 to 60 years

  • Body Mass Index between 25 and 35 kg/m2

  • Accepting the constraints of the protocol and who signed the informed consent

  • Systolic blood pressure < 160 mmHg, diastolic blood pressure < 90 mm Hg (with or without antihypertensive treatment)

  • Resting heart rate between 55 and 100 beats/min.

  • Normal laboratory tests or not clinically significant abnormality for NFS platelets, PT, aPTT, fibrinogen ALT, AST, GGT, Serum electrolytes, urea, creatinine, Uric acid Triglycerides, total cholesterol, HDL cholesterol

  • HCG negative blood (for female subjects)

  • Affiliated to the Social Security.

Exclusion Criteria:
  • Current infections or recent infections (<10 days)

  • Neoplastic disorders (with the exception of carcinoma in situ of the cervix or cutaneous epithelioma), haematological, cardiovascular, psychiatric, neurological

  • Poisoning smoking (>10 cigarettes per day, what ever the duration of intoxication)

  • Treatment with insulin or glitazones Pregnancy, Breastfeeding

  • Body Mass Index > 35 kg/m2

  • Any drug taken for less than 8 days without the inclusion of minor analgesics (aspirin, paracetamol), anti-hypertensive medications, oral hypoglycemic (metformin and sulphonylureas) and insulin secretors dependent glucose as inhibitors of DPP4 (dipeptidyl peptidase-4) and oral contraceptives.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Saint-Louis Hospital Paris France 75010

Sponsors and Collaborators

  • Assistance Publique - Hôpitaux de Paris

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT02368704
Other Study ID Numbers:
  • GLUCOSTRESS P 08 11 22
First Posted:
Feb 23, 2015
Last Update Posted:
Apr 18, 2016
Last Verified:
Apr 1, 2016
Keywords provided by Assistance Publique - Hôpitaux de Paris
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 18, 2016