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Naslov: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
Avtorji:ID Becker, Mia (Avtor)
ID Vogrin, Bernarda (Avtor)
ID Kafol, Jan (Avtor)
ID Čugalj Kern, Barbara (Avtor)
ID Grošelj, Urh (Avtor)
ID Završnik, Jernej (Sodelavec pri raziskavi)
ID Mlinarič, Matej (Sodelavec pri raziskavi)
ID Drole Torkar, Ana (Sodelavec pri raziskavi)
ID Šikonja, Jaka (Sodelavec pri raziskavi)
ID Kovač, Jernej (Sodelavec pri raziskavi)
ID Battelino, Tadej (Sodelavec pri raziskavi)
ID Fras, Zlatko (Sodelavec pri raziskavi)
ID Cevc, Matija (Sodelavec pri raziskavi)
ID Jug, Borut (Sodelavec pri raziskavi)
ID Krevel, Barbara (Sodelavec pri raziskavi)
ID Gorjanc, Tevž (Sodelavec pri raziskavi)
ID Zabkar, Klara (Sodelavec pri raziskavi)
ID Jamnik, Aljaz (Sodelavec pri raziskavi)
ID Debeljak, Maruša (Sodelavec pri raziskavi)
ID Grom, Ana (Sodelavec pri raziskavi)
ID Grgic, Tamara (Sodelavec pri raziskavi)
ID Švarc, Miha (Sodelavec pri raziskavi)
ID Filipič, Maja (Sodelavec pri raziskavi)
ID Leban, Mineja (Sodelavec pri raziskavi)
ID Kjoseva Bakarova, Marija (Sodelavec pri raziskavi)
ID Šnajder, Mateja (Sodelavec pri raziskavi)
ID Koren, Alenka (Sodelavec pri raziskavi)
ID Mir Toplak, Mojca (Sodelavec pri raziskavi)
ID Ivankovič Kacjan, Mojca (Sodelavec pri raziskavi)
ID Kulaš, Mario (Sodelavec pri raziskavi)
ID Trtnik, Benjamina (Sodelavec pri raziskavi)
ID Korez, Saša (Sodelavec pri raziskavi)
ID Hebar, Nina (Sodelavec pri raziskavi)
ID Vogel, Bernarda (Sodelavec pri raziskavi)
ID Amon Prodnik, Vesna (Sodelavec pri raziskavi)
ID Pretnar, Lidija (Sodelavec pri raziskavi)
ID Schweiger Nemanič, Janja (Sodelavec pri raziskavi)
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (812,38 KB)
MD5: EBE6D55FF0B777EB57E95A99B6081CEF
 
URL URL - Izvorni URL, za dostop obiščite https://www.mdpi.com/2075-4426/15/11/510
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo UKC LJ - Univerzitetni klinični center Ljubljana
Povzetek: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.
Ključne besede:hypercholesterolemia, universal screening, preschoolers, total cholesterol, genetic testing
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Leto izida:2025
Št. strani:Str. 1-13
Številčenje:Vol. 15, iss. 11, [article no.] 510
PID:20.500.12556/DiRROS-24675 Novo okno
UDK:616-053.2
ISSN pri članku:2075-4426
DOI:10.3390/jpm15110510 Novo okno
COBISS.SI-ID:255692291 Novo okno
Opomba:Nasl. z nasl. zaslona; Opis vira z dne 3. 11. 2025;
Datum objave v DiRROS:11.12.2025
Število ogledov:69
Število prenosov:22
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Journal of personalized medicine
Skrajšan naslov:J. pers. med.
Založnik:MDPI
ISSN:2075-4426
COBISS.SI-ID:31207641 Novo okno

Gradivo je financirano iz projekta

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:P3-0343-2022
Naslov:Etiologija, zgodnje odkrivanje in zdravljenje bolezni pri otrocih in mladostnikih

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

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