Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI study.
DigiMed Bayern
VRONI
atherosclerosis
familial hypercholesterolemia
hyperlipidemia
screening
Journal
Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V
ISSN: 1863-5490
Titre abrégé: Med Genet
Pays: Germany
ID NLM: 9440651
Informations de publication
Date de publication:
Apr 2022
Apr 2022
Historique:
received:
01
11
2021
accepted:
10
03
2022
medline:
7
5
2022
pubmed:
7
5
2022
entrez:
5
6
2024
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 38836010
doi: 10.1515/medgen-2022-2115
pii: medgen-2022-2115
pmc: PMC11006262
doi:
Types de publication
Journal Article
Langues
eng
Pagination
41-51Informations de copyright
© 2022 Sanin et al., published by De Gruyter.
Déclaration de conflit d'intérêts
Competing interests: Authors state no conflict of interest.