Universal Screening for Familial Hypercholesterolemia in Preschool Children and Their Families in Slovenia

Mia Becker1,2, Bernarda Vogrin1,3, Jan Kafol4

  • 1Faculty of Medicine, University of Maribor, 2000 Maribor, Slovenia.

PubMed

Insights

Familial hypercholesterolemia (FH), a common genetic disorder, is underdiagnosed globally. Early screening in Slovenian preschoolers aims to identify FH for timely intervention and prevention of cardiovascular disease.

Area of Science:

  • Genetics
  • Pediatrics
  • Cardiology

Background:

  • Familial hypercholesterolemia (FH) is a prevalent metabolic disorder affecting 1:250-1:300 individuals.
  • FH significantly elevates the risk of atherosclerosis and cardiovascular disease (CVD).
  • Early detection and treatment of FH are crucial for preventing premature CVD.

Purpose of the Study:

  • To implement a national, three-staged universal screening program for FH in Slovenian preschoolers.
  • To collect data on 5000 children, representing approximately one-quarter of the 2023 preschool generation.

Main Methods:

  • A non-interventional cohort study with prospective and retrospective components.
  • Prospective data collection via questionnaires completed by pediatricians and school medicine specialists.
  • Retrospective data collection from existing medical records and genetic testing referrals to the Pediatric Lipid Clinic.

Main Results:

  • The study aims to identify children with FH through a systematic screening algorithm.
  • Positive genetic results will trigger cascade genetic testing for parents and siblings.
  • The program follows established protocols for universal cholesterol screening.

Conclusions:

  • Familial hypercholesterolemia remains significantly underdiagnosed worldwide, with less than 10% of cases identified.
  • Effective screening programs are essential for early FH detection.
  • Early identification and treatment can improve patient outcomes and prevent cardiovascular events.

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