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Research on the Nature, Diagnosis, and Treatment of Obesity and Diabetes

FOXA2 Expression in Adipose Tissue of Human Subjects With Obesity/Insulin-Resistance

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00229268
Enrollment
14
Registered
2005-09-29
Start date
2005-09-30
Completion date
2010-04-30
Last updated
2012-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Insulin Resistance, Obesity

Keywords

Healthy Volunteers

Brief summary

The purpose of this study is to determine whether the level of FOXA2 expression in fat tissue is a biomarker of insulin resistance. To test this hypothesis, we will perform euglycemic-hyperinsulinemic clamps in normal and obese human subjects to calculate insulin sensitivity, and see if insulin sensitivity correlates with the FOXA2 expression in subcutaneous fat.

Detailed description

The investigators at Rockefeller University Hospital are engaged in research on the nature, diagnosis and treatment of obesity and diabetes. The investigators are trying to find out why insulin, a blood sugar lowering hormone that is released by the pancreas following a meal, does not work effectively in individuals with obesity or type 2 diabetes. The investigators have recently discovered a protein in fat cells of obese mice that helps fat cells to take up and break down sugar from the blood. This protein (called FOXA2) also prevents the generation of more fat cells. FOXA2 is only present in obese mice, but absent from fat stores of lean animals. Insulin can stimulate the production of FOXA2 in fat cells. Furthermore, the levels of FOXA2 protein correlate with the degree of blood insulin levels. In this study, we are would like to determine whether FOXA2 is also produced in fat cells of humans, and if its level correlates with the degree of obesity and insulin resistance.

Interventions

None listed

Sponsors

Rockefeller University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

1. Healthy individuals 2. Age 21-45 years old 3. BMI: either \< 25, or 30-35, or \> 40 4. All patients must be willing and able to sign an informed consent form -

Exclusion criteria

1. Chronic illnesses other the than mild forms of illnesses related to obesity, such as hypertension, hyperlipidemia, and others, that do not require medical treatment 2. Diabetes mellitus previously diagnosed as per subject report or an abnormal 2 hour OGTT at screening 3. Chronic drug treatment for any medical condition 4. Active weight reduction of more than 7 pounds in the last 3 months 5. History of bleeding or blood clotting disorders 6. Subjects with hemoglobin \<8.5 gm/dl 7. Changes in smoking habits for the last 6 months 8. Current pregnancy or current breast-feeding in women 9. Allergic reaction to local anesthetics 10. History of anaphylaxis or anaphylactic-like reactions 11. Tendency to form scars (keloids) easily 12. Irregular menses 13. HIV and hepatitis B or C positive subjects -

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026