The Suppression of Toll Like Receptors by Insulin
Primary Purpose
Insulin Resistance
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
insulin
insulin
insulin
Sponsored by
About this trial
This is an interventional treatment trial for Insulin Resistance
Eligibility Criteria
INCLUSION CRITERIA
Lean Group:
- Age: 20 to 65 years of age inclusive
- Sex: male or female
- Normal fasting plasma glucose (65-100 mg/dl)
- Normal BMI (20-25)
Obese Group:
- Age: 20 to 65 years of age inclusive
- Sex: male or female
- Normal fasting plasma glucose (65-100 mg/dl)
- BMI> 30
DM Group:
- Type 2 Diabetes Mellitus
- Age: 20 to 65 years of age inclusive
- Sex: male or female
- BMI >30
- Hba1c < 8%
- If on statins, angiotensin converting enzyme inhibitor, angiotensin receptor blocker or low dose aspirin, should be on a stable dose for one month.
EXCLUSION CRITERIA
- Pregnancy
- Congestive heart failure
- Heart Rate <50 beats /minute
- Sick Sinus Syndrome
- Second or third degree heart block
- Blood pressure <80 mm systolic or > 160/100 mmHg
- Coronary event or procedure (myocardial infarction, unstable angina, coronary artery bypass surgery or coronary angioplasty) in the previous three months
- Hepatic disease (transaminase > 3 times normal)
- Renal impairment (serum creatinine > 1.5)
- History of drug or alcohol abuse within past one year
- Participation in any other concurrent clinical trial
- Potassium (K+) values <3.5 meq/l to > 5.5 meq/l)
- Any other life-threatening, non-cardiac disease
- Use of an investigational agent or therapeutic regimen within 30 days of study
- Type 2 diabetics on thiazolidinediones and/ or insulin
- Subjects on steroids, NSAIDS or antioxidants
- Patients taking exenatide or sitaglipin or loop diuretics
- Anemia (Hemoglobin level less than 12gm/dl in females and 13gm/dl in males) 19)Allergy to lidocaine
Sites / Locations
- Millard Fillmore Gates Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
Experimental
Arm Label
obese
lean
type 2 diabetes
Arm Description
20 obese subjects
20 lean subjects
20 type 2 diabetes
Outcomes
Primary Outcome Measures
The Suppression of Toll Like receptors by Insulin
Expression of TLR2, TLR4, TLR7 and TLR9 mRNA in mononuclear cells and adipose tissue
Secondary Outcome Measures
TLR expression
Basal TLR expression in obese and type 2 diabetic subjects as compared to lean subjects
Full Information
NCT ID
NCT01151605
First Posted
June 25, 2010
Last Updated
January 3, 2023
Sponsor
University at Buffalo
Collaborators
American Diabetes Association
1. Study Identification
Unique Protocol Identification Number
NCT01151605
Brief Title
The Suppression of Toll Like Receptors by Insulin
Official Title
The Suppression of Toll Like Receptors by Insulin
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Completed
Study Start Date
September 2008 (Actual)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
December 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University at Buffalo
Collaborators
American Diabetes Association
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study will help us understand the possible beneficial effects of insulin in inflammation. Inflamamtion is considered to be the cause of atherosclerosis and heart disease.
Detailed Description
Obesity and type 2 diabetes are major health problems in the United States and the world. Both conditions are characterized by increased inflammation and oxidative stress and are associated with increased risk of cardiovascular disease.
Our previous work shows that insulin exerts a prompt and powerful anti-inflammatory effect, on circulating blood cells and in plasma in healthy subjects and in critically ill patients.
Toll like receptors (TLRs) recognize bacterial and viral products like endotoxin and viruses and are major determinants of the inflammatory response against foreign pathogens. In view of the recent data showing that TLRs recognize a range of molecules and proteins that are not of pathogenic source like saturated lipids and that TLRs are involved in the pathogenesis of atherosclerosis which leads to cardiovascular disease and insulin resistance which leads to type 2 diabetes (DM) we hypothesized that insulin infusion suppresses TLRs expression.
Our preliminary data show that insulin infusion for 4 hours reduces the levels of many TLRs and thus might protect from inflammation induced conditions We therefore propose to investigate, in more detail, the effect of infusing different doses of insulin on TLRs mRNA and protein levels and its activity in obese and DM subjects over a longer infusion period and a larger number of subjects in circulating white blood cells and in fat tissue. Also we will be comparing the baseline levels of TLRs and TLRs related proteins as well as their modulation by insulin between normal, obese and DM subjects.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insulin Resistance
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
obese
Arm Type
Experimental
Arm Description
20 obese subjects
Arm Title
lean
Arm Type
Active Comparator
Arm Description
20 lean subjects
Arm Title
type 2 diabetes
Arm Type
Experimental
Arm Description
20 type 2 diabetes
Intervention Type
Drug
Intervention Name(s)
insulin
Intervention Description
insulin to be infused at three different rates (2, 3.5 and 5 units/hour)
Intervention Type
Drug
Intervention Name(s)
insulin
Intervention Description
insulin to be infused at three different rates (2, 3.5 and 5 units/hour)
Intervention Type
Drug
Intervention Name(s)
insulin
Intervention Description
insulin to be infused at three different rates (2, 3.5 and 5 units/hour)
Primary Outcome Measure Information:
Title
The Suppression of Toll Like receptors by Insulin
Description
Expression of TLR2, TLR4, TLR7 and TLR9 mRNA in mononuclear cells and adipose tissue
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
TLR expression
Description
Basal TLR expression in obese and type 2 diabetic subjects as compared to lean subjects
Time Frame
0 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
INCLUSION CRITERIA
Lean Group:
Age: 20 to 65 years of age inclusive
Sex: male or female
Normal fasting plasma glucose (65-100 mg/dl)
Normal BMI (20-25)
Obese Group:
Age: 20 to 65 years of age inclusive
Sex: male or female
Normal fasting plasma glucose (65-100 mg/dl)
BMI> 30
DM Group:
Type 2 Diabetes Mellitus
Age: 20 to 65 years of age inclusive
Sex: male or female
BMI >30
Hba1c < 8%
If on statins, angiotensin converting enzyme inhibitor, angiotensin receptor blocker or low dose aspirin, should be on a stable dose for one month.
EXCLUSION CRITERIA
Pregnancy
Congestive heart failure
Heart Rate <50 beats /minute
Sick Sinus Syndrome
Second or third degree heart block
Blood pressure <80 mm systolic or > 160/100 mmHg
Coronary event or procedure (myocardial infarction, unstable angina, coronary artery bypass surgery or coronary angioplasty) in the previous three months
Hepatic disease (transaminase > 3 times normal)
Renal impairment (serum creatinine > 1.5)
History of drug or alcohol abuse within past one year
Participation in any other concurrent clinical trial
Potassium (K+) values <3.5 meq/l to > 5.5 meq/l)
Any other life-threatening, non-cardiac disease
Use of an investigational agent or therapeutic regimen within 30 days of study
Type 2 diabetics on thiazolidinediones and/ or insulin
Subjects on steroids, NSAIDS or antioxidants
Patients taking exenatide or sitaglipin or loop diuretics
Anemia (Hemoglobin level less than 12gm/dl in females and 13gm/dl in males) 19)Allergy to lidocaine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paresh Dandona, MBBS
Organizational Affiliation
The Research foundation of SUNY at Buffalo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Millard Fillmore Gates Hospital
City
Buffalo
State/Province
New York
ZIP/Postal Code
14209
Country
United States
12. IPD Sharing Statement
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The Suppression of Toll Like Receptors by Insulin
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