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Title:Child-parent cascade screening for familial hypercholesterolemia in Slovenia : insights from the pilot program
Authors:ID Šikonja, Jaka (Author)
ID Kobale, Kaja (Author)
ID Kafol, Jan (Author)
ID Čugalj Kern, Barbara (Author)
ID Mlinarič, Matej (Author)
ID Drole Torkar, Ana (Author)
ID Kovač, Jernej (Author)
ID Cevc, Matija (Author)
ID Fras, Zlatko (Author)
ID Battelino, Tadej (Author)
ID Grošelj, Urh (Author)
Files:.pdf PDF - Presentation file, download (926,21 KB)
MD5: F32ABAFDFD918CEA360147BAC4C354E2
 
URL URL - Source URL, visit https://www.sciencedirect.com/science/article/pii/S002191502501439X
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo UKC LJ - Ljubljana University Medical Centre
Abstract:Background and aims: Cascade familial hypercholesterolemia (FH) screening of parents could reduce the burden cardiovascular disease (CVD) in relatives of index cases by enabling timely diagnosis of FH. Here, we present the positive outcomes of the pilot child-parent cascade screening program in Slovenia. Methods: One hundred and thirty-eight parents from 123 families of an index child with genetically confirmed FH were randomly included in the pilot child-parent cascade screening program. Index children were identified through the universal FH screening program in preschool children. Genetic testing using Sanger sequencing was performed for cascade screening to detect (likely) pathogenic variants, previously confirmed in the index child. Results: The success rate of confirming a (likely) pathogenic variant was 77.2 % when the first parent, preferably with higher total cholesterol levels, was tested, and reached 99.1 % when the variant was identified in the first tested parent or when both parents were tested. In the minority of cases (13.8 %), parents had had a clinical diagnosis of FH prior to their child and these had somewhat higher prevalence of CVD compared to parents that were diagnosed after their index child through the pilot program (12.5 % vs. 4.3 %; p = 0.382). Conclusions: In conclusion, the presented pilot child–parent cascade screening program is feasible in clinical practice and shows a high success rate in identifying parents with FH. Parents diagnosed through the program appeared to have a lower prevalence of CVD. However, larger cohorts are needed to confirm these findings.
Keywords:child-parent screening, cascade screening, familial hypercholesterolemia, cardiovascular disease, Slovenia
Publication status:Published
Publication version:Version of Record
Year of publishing:2025
Number of pages:str. 1-6
Numbering:Vol. 411, [article no.] 120541
PID:20.500.12556/DiRROS-24733 New window
UDC:616.4-053.2
ISSN on article:1879-1484
DOI:10.1016/j.atherosclerosis.2025.120541 New window
COBISS.SI-ID:257705475 New window
Note:Nasl. z nasl. zaslona; Opis vira z dne 19. 11. 2025;
Publication date in DiRROS:16.12.2025
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Downloads:7
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Record is a part of a journal

Title:Atherosclerosis
Shortened title:Atherosclerosis
Publisher:Elsevier
ISSN:1879-1484
COBISS.SI-ID:23193093 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

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J3-2536-2020
Name:UGOTAVLJANJE GENETSKIH VZROKOV DISLIPIDEMIJ PRI OTROCIH IN MLADOSTNIKIH TER NJIHOVO ZGODNJE ODKRIVANJE S POPULACIJSKIM PRESEJANJEM

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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.

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