Digital repository of Slovenian research organisations

Show document
A+ | A- | Help | SLO | ENG

Title:Universal screening for familial hypercholesterolemia in preschool children and their families in Slovenia (FH-FAMILIES) : a protocol for a study of four-stage screening program
Authors:ID Becker, Mia (Author)
ID Vogrin, Bernarda (Author)
ID Kafol, Jan (Author)
ID Čugalj Kern, Barbara (Author)
ID Grošelj, Urh (Author)
ID Završnik, Jernej (Research coworker)
ID Mlinarič, Matej (Research coworker)
ID Drole Torkar, Ana (Research coworker)
ID Šikonja, Jaka (Research coworker)
ID Kovač, Jernej (Research coworker)
ID Battelino, Tadej (Research coworker)
ID Fras, Zlatko (Research coworker)
ID Cevc, Matija (Research coworker)
ID Jug, Borut (Research coworker)
ID Krevel, Barbara (Research coworker)
ID Gorjanc, Tevž (Research coworker)
ID Zabkar, Klara (Research coworker)
ID Jamnik, Aljaz (Research coworker)
ID Debeljak, Maruša (Research coworker)
ID Grom, Ana (Research coworker)
ID Grgic, Tamara (Research coworker)
ID Švarc, Miha (Research coworker)
ID Filipič, Maja (Research coworker)
ID Leban, Mineja (Research coworker)
ID Kjoseva Bakarova, Marija (Research coworker)
ID Šnajder, Mateja (Research coworker)
ID Koren, Alenka (Research coworker)
ID Mir Toplak, Mojca (Research coworker)
ID Ivankovič Kacjan, Mojca (Research coworker)
ID Kulaš, Mario (Research coworker)
ID Trtnik, Benjamina (Research coworker)
ID Korez, Saša (Research coworker)
ID Hebar, Nina (Research coworker)
ID Vogel, Bernarda (Research coworker)
ID Amon Prodnik, Vesna (Research coworker)
ID Pretnar, Lidija (Research coworker)
ID Schweiger Nemanič, Janja (Research coworker)
Files:.pdf PDF - Presentation file, download (812,38 KB)
MD5: EBE6D55FF0B777EB57E95A99B6081CEF
 
URL URL - Source URL, visit https://www.mdpi.com/2075-4426/15/11/510
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo UKC LJ - Ljubljana University Medical Centre
Abstract:Familial hypercholesterolemia (FH) is the most common metabolic disease, with prevalence estimated between 1:250 and 1:300. The affected individuals have a significantly higher risk for developing atherosclerosis and cardiovascular disease (CVD) compared to non-affected individuals. Early CVD can be prevented with early detection and treatment of FH. In Slovenia we have been conducting a national three-staged program of universal screening for FH of preschoolers. Goals: Our goal is to collect data for 5000 children, which is approximately one-quarter of one generation of preschoolers for the year 2023 (n = 5000). Methods: Our study includes both prospective and retrospective components and is a non-interventional cohort study. The prospective component began in 2023, when a questionnaire was distributed to multiple community health centers and outpatient practices in Slovenia. Pediatricians or school medicine specialists completed these questionnaires. The retrospective component involves our research team collecting the remaining necessary data from existing medical records. We are going to follow our algorithm for the implementation of the universal cholesterol screening program and seek all children that will be referred to the Pediatric Lipid Clinic at the University Children’s Hospital, University Medical Centre (UCH-UMC), Ljubljana, for further genetic testing. If a child has a positive genetic result, their parents and siblings will undergo genetic testing. Conclusions: Despite being a common genetic disorder, familial hypercholesterolemia (FH) is still largely underdiagnosed globally; fewer than 10% of affected individuals are thought to be identified. Early detection through effective screening is therefore essential to improve outcomes and prevent premature cardiovascular events.
Keywords:hypercholesterolemia, universal screening, preschoolers, total cholesterol, genetic testing
Publication status:Published
Publication version:Version of Record
Year of publishing:2025
Number of pages:Str. 1-13
Numbering:Vol. 15, iss. 11, [article no.] 510
PID:20.500.12556/DiRROS-24675 New window
UDC:616-053.2
ISSN on article:2075-4426
DOI:10.3390/jpm15110510 New window
COBISS.SI-ID:255692291 New window
Note:Nasl. z nasl. zaslona; Opis vira z dne 3. 11. 2025;
Publication date in DiRROS:11.12.2025
Views:77
Downloads:25
Metadata:XML DC-XML DC-RDF
:
Copy citation
  
Share:Bookmark and Share


Hover the mouse pointer over a document title to show the abstract or click on the title to get all document metadata.

Record is a part of a journal

Title:Journal of personalized medicine
Shortened title:J. pers. med.
Publisher:MDPI
ISSN:2075-4426
COBISS.SI-ID:31207641 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P3-0343-2022
Name:Etiologija, zgodnje odkrivanje in zdravljenje bolezni pri otrocih in mladostnikih

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Back