Characterization of Transcriptional Regulators of Ghrelin Hormone Which Causes Genetic Obesity
NCT01404624 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 58
Last updated 2011-07-28
Summary
The problem point of the Prader-Willi Syndrome (PWS) patient is the obesity which is intense and the plasma ghrelin level which increases unusual from the recently PWS patients was discovered. The Ghrelin is endogeneous ligand of growth hormone secretagogue receptor with peptide hormone and the location is 3p26-p25. Becomes the secretion even from nervous system but from dignity X/A cell it is secreted mainly and growth is important even in the vagal control against food and intake and a dignity function even on the action outside which promotes the secretion which drives it operates. It increases food intake specially and in order to accomplish the action which diminishes fat utilization the obesity with the week cause which it does the mortar it is thought. Active the ghrelin of the form is essential in hormonal activity of the ghrelin and appetite and growth hormone it participates to the secretion promotion which drives. Action of the Ghrelin measuring the quantitative change in middle acylated of the PWS patient ghrelin in order to happen after the acylation initially by one interest ghrelin which is attempted the appetite of the PWS patient is is controlled the method it will be able to prove the thing directly, it used the RIA kit and the ELISA it will be able to measure kit it will be able to measure the whole ghrelin to pick the PWS patient and the blood of the normal army and active ghrelin it measured a change.
Conditions
- Prader Willi Syndrome
- Obesity
Sponsors & Collaborators
-
Samsung Medical Center
lead OTHER
Principal Investigators
-
Dong-Kyu Jin, M.D · Samsung Medical Center, Sungkyunkwan University School of Medicine
Eligibility
- Min Age
- 5 Years
- Max Age
- 11 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2005-01-31
- Completion
- 2006-12-31
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