Genetic Research of Monogenic Obesity in a Pediatric Cohort With Severe and Early Onset Obesity
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Monogenic Obesity
- Sponsor
- University Hospital, Bordeaux
- Enrollment
- 100
- Locations
- 1
- Primary Endpoint
- Positivity rate of patients for whom a diagnosis of monogenic obesity will be obtained when all analyses have been performed.
- Last Updated
- 3 years ago
Overview
Brief Summary
Obesity is a frequent disease mainly caused by environmental/polygenic factors and more rarely caused by the alteration of a single gene ("monogenic obesity"). The diagnosis of these rare forms can lead to personalized management (new treatments, prognosis, adapted hygienic and dietary rules) and family screening. The use of a panel covering the known causes of monogenic obesity on a pediatric cohort of severe and early obesity will allow to evaluate the relevance of these analyses to adapt the management of this type of patients.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Recruitment age: 2-17 years
- •Body mass index, greater than the International Obesity Task Force (IOTF) 30 curve before the age of 5
- •Care at the specialized pediatric obesity center (CSO) of the Bordeaux University Hospital
- •Informed consent signed
Exclusion Criteria
- •no informed consent
Outcomes
Primary Outcomes
Positivity rate of patients for whom a diagnosis of monogenic obesity will be obtained when all analyses have been performed.
Time Frame: Inclusion visit
Secondary Outcomes
- Number of patients for whom a genetic finding will have changed management and description of changes.(Inclusion visit)
- Number of Patients eligible for a drug targeting single-gene obesity(Inclusion visit)