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Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI study.
- Source :
- Medizinische Genetik; 2022, Vol. 34 Issue 1, p41-51, 11p
- Publication Year :
- 2022
-
Abstract
- Familial hypercholesterolemia (FH) is the most frequent monogenic disorder (prevalence 1:250) in the general population. Early diagnosis during childhood enables pre-emptive treatment, thus reducing the risk of severe atherosclerotic manifestations later in life. Nonetheless, FH screening programs are scarce. VRONI offers all children aged 5–14 years in Bavaria a FH screening in the context of regular pediatric visits. LDL-cholesterol (LDL-C) is measured centrally, followed by genetic analysis for FH if exceeding the age-specific 95th percentile (130 mg/dl, 3.34 mmol/l). Children with FH pathogenic variants are treated by specialized pediatricians and offered a FH-focused training course by a qualified training center. Reverse cascade screening is recommended for all first-degree relatives. VRONI aims to prove the feasibility of a population-based FH screening in children and to lay the foundation for a nationwide screening program. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 09365931
- Volume :
- 34
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Medizinische Genetik
- Publication Type :
- Academic Journal
- Accession number :
- 156751668
- Full Text :
- https://doi.org/10.1515/medgen-2022-2115