CClinicalTrials.gg
CompletedNCT00560469Updated Feb 2, 2011

Impaired Adipogenesis in Insulin Resistance: Pilot Clinical and In Vitro Studies

An observational study in Adipocyte Differentiation and Insulin Resistance, sponsored by University of Vermont. Completed at 1 site in United States. Open to participants aged 40 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2011-02-02.

Sponsored by University of Vermont · Observational

Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
20
Ages
40 Years to 65 Years
Sex
All
01

Study summary

Obesity is a strong risk factor for developing type 2 diabetes (T2DM), but the reasons for this are not fully understood. In particular, it is not known why some obese people develop T2DM while other obese individuals do not. This study tests whether differences in fat cells (adipocytes) are to blame. Even in adults, fat cells are constantly being formed to replace old fat cells and to respond to the body's need to store excess energy. The ability to form new fat cells may be diminished in some individuals, leading to larger fat cells. These large fat cells secrete hormones that may increase risk for T2DM. This study tests whether fat cells from obese insulin resistant subjects (who are at risk for developing T2DM) form at a slower rate than those from insulin sensitive subjects (who are at lower risk for developing T2DM).

To address this question we will recruit and study two groups of obese subjects, selected to be similar in age, gender and degree of obesity. One group of subjects will be obese and insulin resistant (the OIR group), while the other will be comparably obese, but insulin sensitive (OIS). Subjects will undergo a series of studies to characterize their metabolism including measurement of body fat by DEXA scanning, oral glucose tolerance (a test used to diagnose diabetes) and measurement of insulin sensitivity in response to an infusion of insulin (a research study used to classify patients into the OIR and OIS groups). Small samples of fat (from just under the skin of the belly and the buttocks) will obtained using a needle on two occasions over 12 weeks. During these 12 weeks, subjects will drink a small amount of water that contains a non-radioactive label. This labeled water will allow us to measure the rate of growth of new fat cells in the body. We will also look at the rate of growth of fat cells obtained from these biopsies in the laboratory.

The results of this study may tell us more about why certain obese people develop diabetes and why others do not. This might lead to new ways to prevent or treat T2DM.

Read the detailed description

Overview of design: To address the specific aims of this study we will recruit and study two groups of obese subjects, selected to be similar in age, gender and BMI. Based on the results of an oral glucose tolerance test (OGTT) and hyperinsulinemic-glucose clamp, one group will be obese and insulin resistant (OIR) and one will be obese and insulin sensitive (OIS). Subjects will undergo measurement of body fat and fat distribution, oral glucose tolerance, in vivo insulin sensitivity, percutaneous needle biopsies of subcutaneous abdominal and gluteal fat and in vivo measurement of SVC and adipocyte turnover using the D2O DNA labeling technique. Adipocyte size and the expression of pro-inflammatory cytokines and adipokines will be compared in the two groups. Primary cultures of preadipocytes will be derived from subjects and proliferation and differentiation measured in vitro and compared to in vivo measures.

Measurement of adipocyte proliferation and differentiation in vivo: The stable isotope technique of Hellerstein et al. for the measurement of slowly dividing cells is based on the incorporation of deuterium oxide (D2O) into DNA. This method has been used to estimate rates of turnover of adipocytes and stromal vascular cells in healthy normal volunteers. It has not, to date, been employed to compare groups of subjects who may differ in their adipogenic propensity. A major objective of the study, therefore, is to evaluate the utility of this approach for quantifying in vivo differences in adipocyte and SVC turnover between groups that vary by insulin sensitivity and to compare the in vivo measures obtained using this technique with in vitro measures of adipogenesis.

02

Conditions studied

  • Adipocyte Differentiation
  • Insulin Resistance

Browse trials for

Keywords

  • Adipokines
  • Inflammation
  • Metabolic syndrome
03

In context

Insulin Resistance

1,959 studies on the registry are indexed under Insulin Resistance; 305 are open to participants now.

This study's enrollment of 20 is below the median of 80 across 339 observational studies indexed under Insulin Resistance.

Browse Insulin Resistance studies →

Lead sponsor

University of Vermont is the lead sponsor of 215 studies on the registry; 28 are open to participants now.

Of its 16 completed or terminated interventional studies of FDA-regulated products, 9 (56%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Community sample

Inclusion criteria

  • Men and women age 40-65 who are obese (BMI>30)and weight stable for 6 months prior to enrollment.

Exclusion criteria

Exclusion Criteria:

  • Acute or chronic medical conditions that would contraindicate participation in the research testing
  • Pregnant or nursing women
  • HbA1c>6.5%
  • Active alcohol or drug abuse
  • Weight >300 pounds.
  • Smoking
05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
20 participants (actual)
Biospecimen retention
Samples with dna

Groups and cohorts

  • 1

    Men and Women over age 40 who are obese (BMI\>30) and insulin-resistant.

    Other: Administration of 70% deuterated water

  • 2

    Men and women over age 40 who are obese (BMI\>30) and insulin-sensitive.

    Other: Administration of 70% deuterated water

Interventions

  • OtherAdministration of 70% deuterated water

    Subjects will drink 70% deuterated water daily for 8 weeks.

06

What researchers measure

Primary outcomes

  1. In vitro rates of adipocyte turnover

    Time frame: 8 weeks

07

Study locations

1 site
  • Fletcher Allen Health Care
    South Burlington, Vermont 05403, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 2, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00560469
Lead sponsor
University of Vermont
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
First posted
Nov 19, 2007
Start date
Jan 2008
Primary completion
Jul 2010
Completion
Jul 2010
Last update
Feb 2, 2011

Study contacts

Richard E Pratley, MD
principal investigator · University of Vermont

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2010. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion