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Familial Hypercholesterolemia: A Narrative Review on Diagnosis and Management Strategies for Children and Adolescents

Authors :
Tada H
Takamura M
Kawashiri M
Source :
Vascular Health and Risk Management, Vol Volume 17, Pp 59-67 (2021)
Publication Year :
2021
Publisher :
Dove Medical Press, 2021.

Abstract

Hayato Tada, Masayuki Takamura, Masa-aki Kawashiri Department of Cardiology, Kanazawa University Graduate School of Medicine, Kanazawa, JapanCorrespondence: Hayato TadaDepartment of Cardiology, Kanazawa University Graduate School of Medicine, 13-1 Takara-Machi, Kanazawa, 920-8641, JapanTel +81-76-265-2000 (2251)Fax +81-76-234-4251Email ht240z@sa3.so-net.ne.jpAbstract: Familial hypercholesterolemia (FH) is a relatively common inherited disorder caused by deleterious mutation(s) in the low-density lipoprotein (LDL) receptor or its associated genes. Given its nature as a heritable disease, any useful screening scheme, including universal, and cascade screening, allows for the early identification of patients with FH. Another important aspect to note is that early diagnosis associated with appropriate treatment can promote better prognosis. However, most clinical diagnostic criteria for adults have adopted clinical elements, such as physical xanthomas and family history, both of which are usually obscure and/or difficult to obtain in children and adolescents. Moreover, LDL cholesterol levels fluctuating considerably during adolescence, hindering the timely diagnosis of FH. In addition, recent advancements in human genetics have revealed several types of FH, including conventional monogenic FH, polygenic FH caused by common single nucleotide variations (SNV) accumulation associated with elevated LDL cholesterol, and oligogenic FH with multiple deleterious genetic variations leading to substantially elevated LDL cholesterol. The aforementioned findings collectively suggest the need for amassing information related to genetics and imaging, in addition to classical clinical elements, for the accurate diagnosis of FH in this era of personalized medicine. The current narrative review summarizes the current status of the clinical and genetic diagnosis of FH in children and adolescents, as well as provide useful management strategies for FH in children and adolescents based on currently available clinical evidence.Keywords: familial hypercholesterolemia, cardiovascular disease, statin, children, adolescents

Details

Language :
English
ISSN :
11782048
Volume :
ume 17
Database :
Directory of Open Access Journals
Journal :
Vascular Health and Risk Management
Publication Type :
Academic Journal
Accession number :
edsdoj.067b4e2db5764161822c034c85b73027
Document Type :
article