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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
Institute for Clinical and Experimental Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Insulin Resistance focused on measuring Adipose tissue, Adipokines

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  1. Type 2 Diabetes treated with oral agents and/or diet
  2. Healthy volunteers age- and sex-matched to type 2 diabetes, without any concomitant disease

Exclusion Criteria:

  1. 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
  2. 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

First Posted
November 10, 2009
Last Updated
October 17, 2013
Sponsor
Institute for Clinical and Experimental Medicine
Collaborators
Ministry of Health, Czech Republic
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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

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Effect of Angiotensin Receptor Blockade on Insulin Resistance and Adipose Tissue Cytokines in Type 2 Diabetes

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