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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: | Dong-Kyu Jin, Samsung Medical Center |
| ClinicalTrials.gov Identifier: | NCT00800852 History of Changes |
| Other Study ID Numbers: | 2008-10-040 |
| Study First Received: | November 30, 2008 |
| Last Updated: | December 1, 2008 |
| Health Authority: | Korea: Food and Drug Administration |
|
adiponectin adiponectin receptor Prader-Willi syndrome |
|
Obesity Prader-Willi Syndrome Overnutrition Nutrition Disorders Overweight Body Weight Signs and Symptoms Mental Retardation |
Neurobehavioral Manifestations Neurologic Manifestations Nervous System Diseases Abnormalities, Multiple Congenital Abnormalities Chromosome Disorders Genetic Diseases, Inborn |