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| Sponsors and Collaborators: |
Emory University National Institutes of Health (NIH) |
|---|---|
| Information provided by: | Emory University |
| ClinicalTrials.gov Identifier: | NCT00228579 |
Purpose
In this study, we propose to determine the effect of weight loss on amount of body fat, and on body fat distribution, in severely obese patients. We also want to determine what measurements (waist, hip or thigh circumference) best show the changes in body fat and fat distribution in this group. Most importantly, we want to relate the changes in body measurements to changes in health indicators (blood cholesterol, blood pressure, blood sugars, liver function). With the findings of this study, clinicians should be able to predict an improvement in health based on a change in waist, hip or thigh size. Because this is a pilot study, we will focus on women, who make up the bulk of our clinic population. We will also focus on racial differences between Caucasians and Blacks.
| Condition |
|---|
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Obesity |
| Study Type: | Observational |
| Study Design: | Cohort, Prospective |
| Official Title: | Assessment of Changes in Abdominal Fat and Metabolic and Tissue Biomarkers During a Bariatric Surgery Weight Loss Intervention Program |
| Estimated Enrollment: | 60 |
| Study Start Date: | June 2003 |
| Estimated Study Completion Date: | September 2010 |
| Groups/Cohorts |
|---|
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Bariatric Surgery
Subjects will be recruited from patients undergoing bariatric surgery at Emory Bariatrics. The cost of surgical procedures will not be provided by the research study.
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Severe obesity affects 4.7% of the U.S. population. A significant number of these individuals suffer from impaired glucose tolerance and type II diabetes due to insulin resistance (IR). Although it is generally accepted that the accumulation of intraabdominal (IA) fat increases the risk of developing IR, the mechanisms responsible for this phenomenon are not yet understood. In addition, the role of subcutaneous (SC) fat towards the etiology of IR - protective, inert or detrimental - is still under debate. This is because SC adipose tissue releases adipocytokines (IL-6, leptin, TNF-a) that have been demonstrated to impair insulin action. In individuals who are severely obese, hyperinsulinemia may induce an exaggerated production of adipocytokines from IA compared to SC fat stores. Our specific aims are: (1) to determine relative contribution of abdominal SC fat versus IA fat to systemic levels of IL-6, leptin and TNF-a in lean and in severely obese individuals; (2) to determine the effects of systemic adipocytokine concentrations on whole body as well as tissue sensitivity to insulin. Hypothesis: (a) In the context of severe obesity, IA fat produces increased quantities of IL-6, leptin and TNF-a compared to SC fat; (b) In severely obese patients undergoing weight loss, whole body and tissue IR can be predicted by changes in systemic adipocytokines. Methods: Adipose tissue content of IL-6, leptin and TNF-a will be determined by ELISA in biopsies obtained from IA and SC fat stores in lean and severely obese patients.
Computer tomography-determined areas of IA and SC fat will be related to changes in systemic adipocytokines at baseline and 6-mo following weight loss therapy. Changes in systemic IL-6, leptin and TNF-a will be assessed from measurements made at baseline and following 6-mo weight loss. For this time period we will also determine changes in whole body (via IVGTT) and tissue sensitivity to insulin (via glucose uptake into muscle and fat).
Relationships between systemic adipocytokines and IR will be assessed using uni- and multivariate correlation analysis. These novel studies will determine whether hypersecretion of adipocytokines by IA versus SC adipose tissue induces IR in patients with severe obesity.
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Severely obese volunteers who are undergoing bariatric surgery. Subjects will be recruited from patients who are undergoing bariatric surgery procedures at Emory Bariatrics. The costs of surgical procedures are not provided by the research study.
Exclusion Criteria:
Contacts and Locations| Contact: Nana Gletsu, Ph.D. | 404-712-2033 | ngletsu@emory.edu |
| Contact: Edward Lin, D.O. | 404-712-2198 | elin@emory.edu |
| United States, Georgia | |
| Emory University Hospital | Recruiting |
| Atlanta, Georgia, United States, 30322 | |
| Contact: Nana Gletsu, Ph.D. 404-712-2033 ngletsu@emory.edu | |
| Principal Investigator: Nana Gletsu, Ph.D. | |
| Principal Investigator: | Nana Gletsu, Ph.D. | Emory University |
More Information
| Responsible Party: | Emory University ( Nana Gletsu Miller, PhD ) |
| Study ID Numbers: | 333-2002, DK-067167 |
| Study First Received: | September 27, 2005 |
| Last Updated: | June 4, 2009 |
| ClinicalTrials.gov Identifier: | NCT00228579 History of Changes |
| Health Authority: | United States: Institutional Review Board |
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diabetes insulin resistance |
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Body Weight Signs and Symptoms Obesity Weight Loss Diabetes Mellitus |
Nutrition Disorders Overweight Overnutrition Insulin Resistance Insulin |
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Body Weight Signs and Symptoms Obesity |
Nutrition Disorders Overweight Overnutrition |
