Update on genetics of familial hypercholesterolemia
| Autoři | |
|---|---|
| Rok publikování | 2026 |
| Druh | Článek v odborném periodiku |
| Časopis / Zdroj | CURRENT OPINION IN LIPIDOLOGY |
| Fakulta / Pracoviště MU | |
| Citace | |
| www | https://journals.lww.com/co-lipidology/fulltext/2026/04000/update_on_genetics_of_familial.4.aspx |
| Doi | https://doi.org/10.1097/MOL.0000000000001027 |
| Klíčová slova | familial hypercholesterolemia; functional studies; lipoprotein(a); monogenic; polygenic risk score |
| Přiložené soubory | |
| Popis | Purpose of reviewFamilial hypercholesterolemia is a monogenic Mendelian disorder characterized by elevated LDL cholesterol and premature atherosclerotic cardiovascular disease. It is caused by pathogenic variants in LDLR, APOB, and PCSK9, with rarer involvement of LDLRAP1 and APOE. Despite advances in molecular diagnostics, no causative variant is identified in approximately 25-75% of clinically diagnosed cases.Recent findingsFamilial hypercholesterolemia is currently defined as an autosomal semi-dominant disorder with a gene-dosage effect, whereby biallelic pathogenic variants result in markedly more severe phenotypes than heterozygous variants. Terminology for homozygous familial hypercholesterolemia has been refined. Former terms such as 'true homozygote', 'compound heterozygote', and 'double heterozygotes' have been replaced by monogenic biallelic forms, with identical or different variants, and digenic biallelic forms involving two familial hypercholesterolemia-associated genes. Polygenic risk score (PRS) and lipoprotein(a) measurement help explain familial hypercholesterolemia-like phenotypes in patients without a monogenic cause and enable determination of polygenic severe hypercholesterolemia and/or hyperlipoproteinemia(a). Although advances in molecular genetics have improved variant detection, interpretation remains challenging. Integration of case-level data and functional studies, including high-throughput LDLR assays and APOB structural analyses, has enhanced variant pathogenicity classification.SummaryCombining monogenic variant detection, PRS determination and lipoprotein(a) assessment enables comprehensive diagnosis, tailored risk stratification, and personalized familial hypercholesterolemia management. |
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