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Abnormal HDL lipid and protein composition following pediatric cancer treatment: an associative study

BACKGROUND: Long-term childhood cancer survivors (CCS) are at high risk of having dyslipidemia including low high density lipoprotein cholesterol (HDL-C). However, little is known about the prevalence of low HDL-C and the impact of therapy exposure on HDL composition early after treatment is termina...

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Autores principales: Bélanger, Véronique, Morel, Sophia, Napartuk, Mélanie, Bouchard, Isabelle, Meloche, Caroline, Curnier, Daniel, Sultan, Serge, Laverdière, Caroline, Sinnett, Daniel, Marcil, Valérie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257312/
https://www.ncbi.nlm.nih.gov/pubmed/37301877
http://dx.doi.org/10.1186/s12944-023-01822-2
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author Bélanger, Véronique
Morel, Sophia
Napartuk, Mélanie
Bouchard, Isabelle
Meloche, Caroline
Curnier, Daniel
Sultan, Serge
Laverdière, Caroline
Sinnett, Daniel
Marcil, Valérie
author_facet Bélanger, Véronique
Morel, Sophia
Napartuk, Mélanie
Bouchard, Isabelle
Meloche, Caroline
Curnier, Daniel
Sultan, Serge
Laverdière, Caroline
Sinnett, Daniel
Marcil, Valérie
author_sort Bélanger, Véronique
collection PubMed
description BACKGROUND: Long-term childhood cancer survivors (CCS) are at high risk of having dyslipidemia including low high density lipoprotein cholesterol (HDL-C). However, little is known about the prevalence of low HDL-C and the impact of therapy exposure on HDL composition early after treatment is terminated. METHODS: This associative study included 50 children and adolescents who had completed their cancer treatments (< 4 years). Clinical characteristics (demographic, diagnosis, treatment, anthropometric parameters), fasting plasma lipids, apoliporoteins (Apo) A-I and composition of HDL fractions (HDL2 and HDL3) were assessed. Data were stratified according to the presence of dyslipidemia and median doses of therapeutic agents and compared using Fisher exact or Mann–Whitney tests. Univariate binary logistic regression analyses were carried out to evaluate the associations between the clinical and biochemical characteristics and having low HDL-C. Composition of HDL2 and HDL3 particles was assessed in a sub-group of 15 patients and compared to 15 age- and sex-matched healthy controls using Wilcoxon paired test. RESULTS: Of the 50 pediatric cancer patients included in this study (mean age: 11.30 ± 0.72 y; mean time since end of treatment: 1.47 ± 0.12 y; male: 38%), 8 had low HDL-C (16%), all of which were adolescent at diagnosis. Higher doses of doxorubicin were associated with lower HDL-C and Apo A-I levels. In hypertriglyceridemic patients and compared to normolipidemics, triglycerides (TG) content was greater in HDL2 and HDL3 fractions whereas esterified cholesterol (EC) content was lower in HDL2. Enrich TG content of HDL3 and lower EC of HDL2 was found in patients exposed to ≥ 90 mg/m(2) doxorubicin. Factors positively associated with the risk of having low HDL-C were age, being overweight or obese and exposure to doxorubicin ≥ 90 mg/m(2). Compared to healthy controls, a sub-group of 15 patients showed higher TG and free cholesterol (FC) content of HDL2 and HDL3 and lower EC content in HDL3. CONCLUSIONS: Overall, we found abnormalities in HDL-C and Apo A-I levels and in HDL composition early after pediatric cancer treatment that are influenced by age, overweight or obesity status and exposure to doxorubicin. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-023-01822-2.
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spelling pubmed-102573122023-06-11 Abnormal HDL lipid and protein composition following pediatric cancer treatment: an associative study Bélanger, Véronique Morel, Sophia Napartuk, Mélanie Bouchard, Isabelle Meloche, Caroline Curnier, Daniel Sultan, Serge Laverdière, Caroline Sinnett, Daniel Marcil, Valérie Lipids Health Dis Research BACKGROUND: Long-term childhood cancer survivors (CCS) are at high risk of having dyslipidemia including low high density lipoprotein cholesterol (HDL-C). However, little is known about the prevalence of low HDL-C and the impact of therapy exposure on HDL composition early after treatment is terminated. METHODS: This associative study included 50 children and adolescents who had completed their cancer treatments (< 4 years). Clinical characteristics (demographic, diagnosis, treatment, anthropometric parameters), fasting plasma lipids, apoliporoteins (Apo) A-I and composition of HDL fractions (HDL2 and HDL3) were assessed. Data were stratified according to the presence of dyslipidemia and median doses of therapeutic agents and compared using Fisher exact or Mann–Whitney tests. Univariate binary logistic regression analyses were carried out to evaluate the associations between the clinical and biochemical characteristics and having low HDL-C. Composition of HDL2 and HDL3 particles was assessed in a sub-group of 15 patients and compared to 15 age- and sex-matched healthy controls using Wilcoxon paired test. RESULTS: Of the 50 pediatric cancer patients included in this study (mean age: 11.30 ± 0.72 y; mean time since end of treatment: 1.47 ± 0.12 y; male: 38%), 8 had low HDL-C (16%), all of which were adolescent at diagnosis. Higher doses of doxorubicin were associated with lower HDL-C and Apo A-I levels. In hypertriglyceridemic patients and compared to normolipidemics, triglycerides (TG) content was greater in HDL2 and HDL3 fractions whereas esterified cholesterol (EC) content was lower in HDL2. Enrich TG content of HDL3 and lower EC of HDL2 was found in patients exposed to ≥ 90 mg/m(2) doxorubicin. Factors positively associated with the risk of having low HDL-C were age, being overweight or obese and exposure to doxorubicin ≥ 90 mg/m(2). Compared to healthy controls, a sub-group of 15 patients showed higher TG and free cholesterol (FC) content of HDL2 and HDL3 and lower EC content in HDL3. CONCLUSIONS: Overall, we found abnormalities in HDL-C and Apo A-I levels and in HDL composition early after pediatric cancer treatment that are influenced by age, overweight or obesity status and exposure to doxorubicin. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-023-01822-2. BioMed Central 2023-06-10 /pmc/articles/PMC10257312/ /pubmed/37301877 http://dx.doi.org/10.1186/s12944-023-01822-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Bélanger, Véronique
Morel, Sophia
Napartuk, Mélanie
Bouchard, Isabelle
Meloche, Caroline
Curnier, Daniel
Sultan, Serge
Laverdière, Caroline
Sinnett, Daniel
Marcil, Valérie
Abnormal HDL lipid and protein composition following pediatric cancer treatment: an associative study
title Abnormal HDL lipid and protein composition following pediatric cancer treatment: an associative study
title_full Abnormal HDL lipid and protein composition following pediatric cancer treatment: an associative study
title_fullStr Abnormal HDL lipid and protein composition following pediatric cancer treatment: an associative study
title_full_unstemmed Abnormal HDL lipid and protein composition following pediatric cancer treatment: an associative study
title_short Abnormal HDL lipid and protein composition following pediatric cancer treatment: an associative study
title_sort abnormal hdl lipid and protein composition following pediatric cancer treatment: an associative study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257312/
https://www.ncbi.nlm.nih.gov/pubmed/37301877
http://dx.doi.org/10.1186/s12944-023-01822-2
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