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Validation of low-density lipoprotein cholesterol equations in pediatric population

Several studies have shown a high prevalence of dyslipidemia in children. Since childhood lipid concentrations continue into adulthood, recognition of lipid abnormalities in the early period is crucial to prevent the development of future coronary heart disease (CHD). Low density lipoprotein cholest...

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Autores principales: Ertürk Zararsız, Gözde, Bolat, Serkan, Cephe, Ahu, Kochan, Necla, Yerlitaş, Serra Ilayda, Doğan, Halef Okan, Zararsız, Gökmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826611/
https://www.ncbi.nlm.nih.gov/pubmed/36627923
http://dx.doi.org/10.7717/peerj.14544
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author Ertürk Zararsız, Gözde
Bolat, Serkan
Cephe, Ahu
Kochan, Necla
Yerlitaş, Serra Ilayda
Doğan, Halef Okan
Zararsız, Gökmen
author_facet Ertürk Zararsız, Gözde
Bolat, Serkan
Cephe, Ahu
Kochan, Necla
Yerlitaş, Serra Ilayda
Doğan, Halef Okan
Zararsız, Gökmen
author_sort Ertürk Zararsız, Gözde
collection PubMed
description Several studies have shown a high prevalence of dyslipidemia in children. Since childhood lipid concentrations continue into adulthood, recognition of lipid abnormalities in the early period is crucial to prevent the development of future coronary heart disease (CHD). Low density lipoprotein cholesterol (LDL-C) is one of the most used parameters in the initiation and follow-up of treatment in patients with dyslipidemia. It is a well known fact that LDL-C lowering therapy reduces the risk of future CHD. Therefore, accurate determination of the LDL-C levels is so important for the management of lipid abnormalities. This study aimed to validate different LDL-C estimating equations in the Turkish population, composed of children and adolescents. A total of 3,908 children below 18 years old at Sivas Cumhuriyet University Hospital (Sivas, Turkey) were included in this study. LDL-C was directly measured by direct homogeneous assays, i.e., Roche, Beckman, Siemens and estimated by Friedewald’s, Martin/Hopkins’, extended Martin-Hopkins’ and Sampson’s formulas. The concordances between the estimations obtained by the formulas and the direct measurements were evaluated both overall and separately for the LDL-C, triglycerides (TG) and non-high-density lipoprotein cholesterol (non-HDL-C) sublevels. Linear regression analysis was performed and residual error plots were generated between each estimation and direct measurement method. Coefficient of determination (R(2)) and mean absolute deviations were also evaluated. The overall concordance of Friedewald, Sampson, Martin-Hopkins and the extended Martin-Hopkins formula were 64.6%, 69.9%, 69.4%, and 84.3% for the Roche direct assay, 69.8%, 71.6%, 73.6% and 80.4% for the Siemens direct assay, 66.5%, 68.8%, 68.9% and 82.1% for the Beckman direct assay, respectively. The extended Martin-Hopkins formula had the highest concordance coefficient in both overall and all sublevels of LDL-C, non-HDL-C, and TG. When estimating the LDL-C categories, the highest underestimation degrees were obtained with the Friedewald formula. Our analysis, conducted in a large pediatric population, showed that the extended Martin-Hopkins equation gives more reliable results in estimation of LDL-C compared to other equations.
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spelling pubmed-98266112023-01-09 Validation of low-density lipoprotein cholesterol equations in pediatric population Ertürk Zararsız, Gözde Bolat, Serkan Cephe, Ahu Kochan, Necla Yerlitaş, Serra Ilayda Doğan, Halef Okan Zararsız, Gökmen PeerJ Biochemistry Several studies have shown a high prevalence of dyslipidemia in children. Since childhood lipid concentrations continue into adulthood, recognition of lipid abnormalities in the early period is crucial to prevent the development of future coronary heart disease (CHD). Low density lipoprotein cholesterol (LDL-C) is one of the most used parameters in the initiation and follow-up of treatment in patients with dyslipidemia. It is a well known fact that LDL-C lowering therapy reduces the risk of future CHD. Therefore, accurate determination of the LDL-C levels is so important for the management of lipid abnormalities. This study aimed to validate different LDL-C estimating equations in the Turkish population, composed of children and adolescents. A total of 3,908 children below 18 years old at Sivas Cumhuriyet University Hospital (Sivas, Turkey) were included in this study. LDL-C was directly measured by direct homogeneous assays, i.e., Roche, Beckman, Siemens and estimated by Friedewald’s, Martin/Hopkins’, extended Martin-Hopkins’ and Sampson’s formulas. The concordances between the estimations obtained by the formulas and the direct measurements were evaluated both overall and separately for the LDL-C, triglycerides (TG) and non-high-density lipoprotein cholesterol (non-HDL-C) sublevels. Linear regression analysis was performed and residual error plots were generated between each estimation and direct measurement method. Coefficient of determination (R(2)) and mean absolute deviations were also evaluated. The overall concordance of Friedewald, Sampson, Martin-Hopkins and the extended Martin-Hopkins formula were 64.6%, 69.9%, 69.4%, and 84.3% for the Roche direct assay, 69.8%, 71.6%, 73.6% and 80.4% for the Siemens direct assay, 66.5%, 68.8%, 68.9% and 82.1% for the Beckman direct assay, respectively. The extended Martin-Hopkins formula had the highest concordance coefficient in both overall and all sublevels of LDL-C, non-HDL-C, and TG. When estimating the LDL-C categories, the highest underestimation degrees were obtained with the Friedewald formula. Our analysis, conducted in a large pediatric population, showed that the extended Martin-Hopkins equation gives more reliable results in estimation of LDL-C compared to other equations. PeerJ Inc. 2023-01-05 /pmc/articles/PMC9826611/ /pubmed/36627923 http://dx.doi.org/10.7717/peerj.14544 Text en ©2023 Ertürk Zararsız et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Biochemistry
Ertürk Zararsız, Gözde
Bolat, Serkan
Cephe, Ahu
Kochan, Necla
Yerlitaş, Serra Ilayda
Doğan, Halef Okan
Zararsız, Gökmen
Validation of low-density lipoprotein cholesterol equations in pediatric population
title Validation of low-density lipoprotein cholesterol equations in pediatric population
title_full Validation of low-density lipoprotein cholesterol equations in pediatric population
title_fullStr Validation of low-density lipoprotein cholesterol equations in pediatric population
title_full_unstemmed Validation of low-density lipoprotein cholesterol equations in pediatric population
title_short Validation of low-density lipoprotein cholesterol equations in pediatric population
title_sort validation of low-density lipoprotein cholesterol equations in pediatric population
topic Biochemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826611/
https://www.ncbi.nlm.nih.gov/pubmed/36627923
http://dx.doi.org/10.7717/peerj.14544
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