Effect of Angiotensin Receptor Blockade on Insulin Resistance and Adipose Tissue Cytokines in Type 2 Diabetes
Primary Purpose
Insulin Resistance, Type 2 Diabetes
Status
Completed
Phase
Not Applicable
Locations
Czech Republic
Study Type
Interventional
Intervention
Hyperinsulinaemia
Losartan
Saline
Sponsored by
About this trial
This is an interventional basic science trial for Insulin Resistance focused on measuring Adipose tissue, Adipokines
Eligibility Criteria
Inclusion Criteria:
- Type 2 Diabetes treated with oral agents and/or diet
- Healthy volunteers age- and sex-matched to type 2 diabetes, without any concomitant disease
Exclusion Criteria:
Type 2 Diabetes
- treated with insulin
- clinical evidence of atherosclerotic complications
- advanced long-term diabetic complications (manifest nephropathy, proliferative retinopathy)
- other internal disease
- weight change >10% 3 months prior to study
Healthy volunteers
- fulfilling the criteria of metabolic syndrome
- weight change >10% 3 months prior to study
Sites / Locations
- Diabetes Center, Institute of Clinical and Experimental Medicine
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Placebo Comparator
Arm Label
Hyperinsulinaemia
Losartan + hyperinsulinaemia
Saline
Arm Description
Hyperinsulinaemic (1 mIU/kg/min) euglycaemic (5 mmol/l) clamp
Infusion of Saline as a volume control intervention
Outcomes
Primary Outcome Measures
insulin sensitivity measured as glucose disposal during clamp
Secondary Outcome Measures
plasma adipokines and their expressions in SAT
Full Information
NCT ID
NCT01011062
First Posted
November 10, 2009
Last Updated
October 17, 2013
Sponsor
Institute for Clinical and Experimental Medicine
Collaborators
Ministry of Health, Czech Republic
1. Study Identification
Unique Protocol Identification Number
NCT01011062
Brief Title
Effect of Angiotensin Receptor Blockade on Insulin Resistance and Adipose Tissue Cytokines in Type 2 Diabetes
Official Title
Effect of Acute Angiotensin Receptor Blockade on Insulin Resistance and Selected Cytokines in Adipose Tissue in Type 2 Diabetes
Study Type
Interventional
2. Study Status
Record Verification Date
November 2009
Overall Recruitment Status
Completed
Study Start Date
January 2004 (undefined)
Primary Completion Date
October 2007 (Actual)
Study Completion Date
August 2009 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Institute for Clinical and Experimental Medicine
Collaborators
Ministry of Health, Czech Republic
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The study aims to investigate the effect of acute angiotensin receptor blockade on insulin action/insulin resistance and expressions of selected adipocytokines in subcutaneous adipose tissue in insulin-resistant subjects with type 2 diabetes and healthy controls.
Hypothesis: Changes in adipocytokine concentrations and/or expressions and different reactions to acute in vivo induced hyperinsulinemia and angiotensin receptor blockade will be found in patients with type 2 diabetes compared to healthy subjects. A significant relationships between insulin sensitivity and selected adipokines and intracellular fat content and high energy phosphates in soleus muscle will be documented in healthy individuals, while no significant relation will be found in patients with type 2 diabetes.
Detailed Description
10-15 patients with type 2 diabetes and 10-15 healthy control subjects will be examined on an outpatient basis. The following examination will be carried out in each subject after 12 hrs fasting:
Oral glucose tolerance test (75 g of glucose) (in healthy subjects to confirm the normal tolerance of glucose).
Evaluation of insulin secretion after 1 mg of glucagon i.v.
Hyperinsulinaemic (75 milly-international unit(mIU)/l) euglycemic clamp study lasting 4 hours combined with indirect calorimetry and biopsy of subcutaneous adipose tissue.
Hyperinsulinemic (75 mIU/l) euglycemic clamp study lasting 4 hours combined with indirect calorimetry after losartan 100 mg given in the evening and in the morning before the study.
Proton and phosphorus magnetic resonance spectroscopy.
Before (0 min), at 30 min and in the end of studies c) and d) the blood samples will be taken and biopsies of subcutaneous abdominal adipose tissue will be done.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insulin Resistance, Type 2 Diabetes
Keywords
Adipose tissue, Adipokines
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
23 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Hyperinsulinaemia
Arm Type
Experimental
Arm Description
Hyperinsulinaemic (1 mIU/kg/min) euglycaemic (5 mmol/l) clamp
Arm Title
Losartan + hyperinsulinaemia
Arm Type
Experimental
Arm Title
Saline
Arm Type
Placebo Comparator
Arm Description
Infusion of Saline as a volume control intervention
Intervention Type
Procedure
Intervention Name(s)
Hyperinsulinaemia
Intervention Description
Hyperinsulinaemic (1 mIU/kg/min) euglycaemic (5 mmol/l) clamp
Intervention Type
Drug
Intervention Name(s)
Losartan
Intervention Description
Acute administration of losartan 200mg total prior to clamp
Intervention Type
Drug
Intervention Name(s)
Saline
Intervention Description
Infusion of Saline as a volume control intervention
Primary Outcome Measure Information:
Title
insulin sensitivity measured as glucose disposal during clamp
Time Frame
4 hours
Secondary Outcome Measure Information:
Title
plasma adipokines and their expressions in SAT
Time Frame
at 0 and 240 min of the clamp
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Type 2 Diabetes treated with oral agents and/or diet
Healthy volunteers age- and sex-matched to type 2 diabetes, without any concomitant disease
Exclusion Criteria:
Type 2 Diabetes
treated with insulin
clinical evidence of atherosclerotic complications
advanced long-term diabetic complications (manifest nephropathy, proliferative retinopathy)
other internal disease
weight change >10% 3 months prior to study
Healthy volunteers
fulfilling the criteria of metabolic syndrome
weight change >10% 3 months prior to study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Terezie Pelikanova, Prof., MD
Organizational Affiliation
Diabetes Center, Institute of Clinical and Experimental Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Diabetes Center, Institute of Clinical and Experimental Medicine
City
Prague
ZIP/Postal Code
14021
Country
Czech Republic
12. IPD Sharing Statement
Learn more about this trial
Effect of Angiotensin Receptor Blockade on Insulin Resistance and Adipose Tissue Cytokines in Type 2 Diabetes
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