Genetic and Phenotypic Characteristics of Mitral Valve Prolapse
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Mitral Valve Prolapse
- Sponsor
- Nantes University Hospital
- Enrollment
- 1000
- Locations
- 3
- Primary Endpoint
- MVP defined by a superior displacement of at least 2 mm
- Last Updated
- 4 years ago
Overview
Brief Summary
Phenotypic characterisation of MVP by echocardiography in families. Identification of genes involved in MVP.
Detailed Description
After clinical identification of patients with MVP, doctors organize 1st degree relative familial screening. A comprehensive echocardiography was carried out along with clinical examination. All echo data were stored for off-line analysis by a sonographer in our Core-lab. Blood was sample at the time of echocardiography in adult patients for DNA analyses. Follow-up for mitral valve changes will be performed after 5 years.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients of any age
- •with typical mitral valve prolapse
- •relatives examined during familial screening
Exclusion Criteria
- •Refusal of the patient
Outcomes
Primary Outcomes
MVP defined by a superior displacement of at least 2 mm
Time Frame: At Day 0
MVP defined by a superior displacement of at least 2 mm
Secondary Outcomes
- Comprehensive mitral valve apparatus characterization per size of items (leaflets, chordae, annulus)(At Day 0)
- Comprehensive mitral valve apparatus characterization per other items (papillary muscle, ventricles)(At Day 0)
- Comprehensive mitral valve apparatus characterization per size of items (ventricle and atrium sizes)(At Day 0)
- Comprehensive mitral valve apparatus characterization per size of items(At Day 0)