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| Sponsor: | Samsung Medical Center |
|---|---|
| Information provided by: | Samsung Medical Center |
| ClinicalTrials.gov Identifier: | NCT00800852 |
Purpose
The inflammatory process is involved in the pathogenesis of obesity. Prader-Willi syndrome (PWS) is a genetic model of syndromic obesity. Adiponectin is an adipokine with potent anti-inflammatory properties, and its effect is mediated through adiponectin receptors 1 (adipoR1) and 2 (adipoR2).
Objective of this study is to compare the expression of adipoR1, adipoR2, and adiponectin in peripheral blood mononuclear cells (PBMCs) in PWS children and obese control and to correlate receptor expression with insulin sensitivity and obesity-related parameters.
| Condition |
|---|
|
Obesity Prader-Willi Syndrome |
| Study Type: | Observational |
| Official Title: | Increased Expression of Adiponectin Receptor 2 in the Mononuclear Cells in Children With Prader-Willi Syndrome |
Eligibility| Ages Eligible for Study: | up to 18 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Probability Sample |
Fourteen children with PWS and control subjects
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
More Information
| Responsible Party: | Samsung Medical Center ( Dong-Kyu Jin ) |
| Study ID Numbers: | 2008-10-040 |
| Study First Received: | November 30, 2008 |
| Last Updated: | December 1, 2008 |
| ClinicalTrials.gov Identifier: | NCT00800852 History of Changes |
| Health Authority: | Korea: Food and Drug Administration |
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adiponectin adiponectin receptor Prader-Willi syndrome |
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Obesity Disease Nervous System Diseases Chromosome Disorders Overweight Body Weight Mental Retardation Signs and Symptoms Pathologic Processes |
Genetic Diseases, Inborn Syndrome Abnormalities, Multiple Nutrition Disorders Neurologic Manifestations Overnutrition Prader-Willi Syndrome Congenital Abnormalities Neurobehavioral Manifestations |