Lipoprotein profile assessed by 1H NMR, BMI and blood pressure are associated with vascular alterations in children with familial hypercholesterolaemia.


Journal

Nutrition, metabolism, and cardiovascular diseases : NMCD
ISSN: 1590-3729
Titre abrégé: Nutr Metab Cardiovasc Dis
Pays: Netherlands
ID NLM: 9111474

Informations de publication

Date de publication:
10 2023
Historique:
received: 08 03 2023
revised: 07 06 2023
accepted: 16 06 2023
medline: 20 9 2023
pubmed: 6 8 2023
entrez: 5 8 2023
Statut: ppublish

Résumé

Children with familial hypercholesterolaemia (FH) have elevated low-density lipoprotein cholesterol (LDL-C) concentrations since birth, which increases the risk of cardiovascular disease in adulthood. Arterial injury and stiffness parameters, including carotid intima media thickness (cIMT), pulse wave velocity (PWV) and distensibility (DIST), can be detected early in childhood. We studied the associations between cIMT, PWV and DIST with the lipoprotein profile assessed by proton nuclear magnetic resonance ( In this cross-sectional study, we included 201 children (96 with FH and 105 non-FH controls). Clinical history, physical examination and standard biochemical studies were performed. FH genetic testing was performed when clinically indicated. Carotid ultrasonography and an advanced lipoprotein profile by Alterations in lipoprotein parameters assessed by are associated with early structural and functional arterial characteristics in children with FH. BMI and BP act as boosting factors. Cardiovascular prevention should start early in children with FH, encompassing all components of a healthy lifestyle.

Sections du résumé

BACKGROUND AND AIMS
Children with familial hypercholesterolaemia (FH) have elevated low-density lipoprotein cholesterol (LDL-C) concentrations since birth, which increases the risk of cardiovascular disease in adulthood. Arterial injury and stiffness parameters, including carotid intima media thickness (cIMT), pulse wave velocity (PWV) and distensibility (DIST), can be detected early in childhood. We studied the associations between cIMT, PWV and DIST with the lipoprotein profile assessed by proton nuclear magnetic resonance (
METHODS AND RESULTS
In this cross-sectional study, we included 201 children (96 with FH and 105 non-FH controls). Clinical history, physical examination and standard biochemical studies were performed. FH genetic testing was performed when clinically indicated. Carotid ultrasonography and an advanced lipoprotein profile by
CONCLUSIONS
Alterations in lipoprotein parameters assessed by are associated with early structural and functional arterial characteristics in children with FH. BMI and BP act as boosting factors. Cardiovascular prevention should start early in children with FH, encompassing all components of a healthy lifestyle.

Identifiants

pubmed: 37543518
pii: S0939-4753(23)00245-4
doi: 10.1016/j.numecd.2023.06.012
pii:
doi:

Substances chimiques

Cholesterol, LDL 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2035-2043

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: LM: fees for lectures/advisory work from AMGEN, AMARIN, AMRYT, SANOFI, NOVARTIS, SERVIER, DAIICHI-SAMKYO. DLL, AF, DI, JE, NP, CBR and JC declare no conflict of interest.

Auteurs

D Llop (D)

Unitat de Recerca de Lípids I Arteriosclerosi, Universitat Rovira I Virgili, Reus, Catalonia, Spain; Institut D'Investigació Sanitària Pere Virgili (IISPV), Reus, Catalonia, Spain; Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Madrid, Spain.

A Feliu (A)

Pediatric Nutrition and Human Development Research Unit, Universitat Rovira I Virgili, IISPV, Reus, Spain.

D Ibarretxe (D)

Unitat de Recerca de Lípids I Arteriosclerosi, Universitat Rovira I Virgili, Reus, Catalonia, Spain; Institut D'Investigació Sanitària Pere Virgili (IISPV), Reus, Catalonia, Spain; Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Madrid, Spain; Servicio de Medicina Interna, Hospital Universitario Sant Joan, Reus, Catalonia, Spain.

J Escribano (J)

Pediatric Nutrition and Human Development Research Unit, Universitat Rovira I Virgili, IISPV, Reus, Spain.

N Plana (N)

Unitat de Recerca de Lípids I Arteriosclerosi, Universitat Rovira I Virgili, Reus, Catalonia, Spain; Institut D'Investigació Sanitària Pere Virgili (IISPV), Reus, Catalonia, Spain; Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Madrid, Spain; Servicio de Medicina Interna, Hospital Universitario Sant Joan, Reus, Catalonia, Spain.

C Borjabad-Rodríguez (C)

Unitat de Recerca de Lípids I Arteriosclerosi, Universitat Rovira I Virgili, Reus, Catalonia, Spain; Institut D'Investigació Sanitària Pere Virgili (IISPV), Reus, Catalonia, Spain; Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Madrid, Spain; Servicio de Medicina Interna, Hospital Universitario Sant Joan, Reus, Catalonia, Spain.

L Masana (L)

Unitat de Recerca de Lípids I Arteriosclerosi, Universitat Rovira I Virgili, Reus, Catalonia, Spain; Institut D'Investigació Sanitària Pere Virgili (IISPV), Reus, Catalonia, Spain; Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Madrid, Spain; Servicio de Medicina Interna, Hospital Universitario Sant Joan, Reus, Catalonia, Spain.

J C Vallvé (JC)

Unitat de Recerca de Lípids I Arteriosclerosi, Universitat Rovira I Virgili, Reus, Catalonia, Spain; Institut D'Investigació Sanitària Pere Virgili (IISPV), Reus, Catalonia, Spain; Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Madrid, Spain. Electronic address: jc.vallve@urv.cat.

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