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Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI study.

Authors :
Sanin, Veronika
Schmieder, Raphael
Ates, Sara
Schlieben, Lea Dewi
Wiehler, Jens
Sun, Ruoyu
Decker, Manuela
Sander, Michaela
Holdenrieder, Stefan
Kohlmayer, Florian
Friedmann, Anna
Mall, Volker
Feiler, Therese
Dreßler, Arne
Strom, Tim M.
Prokisch, Holger
Meitinger, Thomas
von Scheidt, Moritz
Koenig, Wolfgang
Leipold, Georg
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