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ApoA-I/A-II-HDL positively associates with apoB-lipoproteins as a potential atherogenic indicator

BACKGROUND: We recently reported distinct nature of high-density lipoproteins (HDL) subgroup particles with apolipoprotein (apo) A-I but not apoA-II (LpAI) and HDL having both (LpAI:AII) based on the data from 314 Japanese. While plasma HDL level almost exclusively depends on concentration of LpAI h...

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Autores principales: Kido, Toshimi, Kondo, Kazuo, Kurata, Hideaki, Fujiwara, Yoko, Urata, Takeyoshi, Itakura, Hiroshige, Yokoyama, Shinji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708092/
https://www.ncbi.nlm.nih.gov/pubmed/29187200
http://dx.doi.org/10.1186/s12944-017-0619-y
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author Kido, Toshimi
Kondo, Kazuo
Kurata, Hideaki
Fujiwara, Yoko
Urata, Takeyoshi
Itakura, Hiroshige
Yokoyama, Shinji
author_facet Kido, Toshimi
Kondo, Kazuo
Kurata, Hideaki
Fujiwara, Yoko
Urata, Takeyoshi
Itakura, Hiroshige
Yokoyama, Shinji
author_sort Kido, Toshimi
collection PubMed
description BACKGROUND: We recently reported distinct nature of high-density lipoproteins (HDL) subgroup particles with apolipoprotein (apo) A-I but not apoA-II (LpAI) and HDL having both (LpAI:AII) based on the data from 314 Japanese. While plasma HDL level almost exclusively depends on concentration of LpAI having 3 to 4 apoA-I molecules, LpAI:AII appeared with almost constant concentration regardless of plasma HDL levels having stable structure with two apoA-I and one disulfide-dimeric apoA-II molecules (Sci. Rep. 6; 31,532, 2016). The aim of this study is further characterization of LpAI:AII with respect to its role in atherogenesis. METHODS: Association of LpAI, LpAI:AII and other HDL parameters with apoB-lipoprotein parameters was analyzed among the cohort data above. RESULTS: ApoA-I in LpAI negatively correlated with the apoB-lipoprotein parameters such as apoB, triglyceride, nonHDL-cholesterol, and nonHDL-cholesterol + triglyceride, which are apparently reflected in the relations of the total HDL parameters to apoB-lipoproteins. In contrast, apoA-I in LpAI:AII and apoA-II positively correlated to the apoB-lipoprotein parameters even within their small range of variation. These relationships are independent of sex, but may slightly be influenced by the activity-related CETP mutations. CONCLUSIONS: The study suggested that LpAI:AII is an atherogenic indicator rather than antiatherogenic. These sub-fractions of HDL are to be evaluated separately for estimating atherogenic risk of the patients.
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spelling pubmed-57080922017-12-06 ApoA-I/A-II-HDL positively associates with apoB-lipoproteins as a potential atherogenic indicator Kido, Toshimi Kondo, Kazuo Kurata, Hideaki Fujiwara, Yoko Urata, Takeyoshi Itakura, Hiroshige Yokoyama, Shinji Lipids Health Dis Short Report BACKGROUND: We recently reported distinct nature of high-density lipoproteins (HDL) subgroup particles with apolipoprotein (apo) A-I but not apoA-II (LpAI) and HDL having both (LpAI:AII) based on the data from 314 Japanese. While plasma HDL level almost exclusively depends on concentration of LpAI having 3 to 4 apoA-I molecules, LpAI:AII appeared with almost constant concentration regardless of plasma HDL levels having stable structure with two apoA-I and one disulfide-dimeric apoA-II molecules (Sci. Rep. 6; 31,532, 2016). The aim of this study is further characterization of LpAI:AII with respect to its role in atherogenesis. METHODS: Association of LpAI, LpAI:AII and other HDL parameters with apoB-lipoprotein parameters was analyzed among the cohort data above. RESULTS: ApoA-I in LpAI negatively correlated with the apoB-lipoprotein parameters such as apoB, triglyceride, nonHDL-cholesterol, and nonHDL-cholesterol + triglyceride, which are apparently reflected in the relations of the total HDL parameters to apoB-lipoproteins. In contrast, apoA-I in LpAI:AII and apoA-II positively correlated to the apoB-lipoprotein parameters even within their small range of variation. These relationships are independent of sex, but may slightly be influenced by the activity-related CETP mutations. CONCLUSIONS: The study suggested that LpAI:AII is an atherogenic indicator rather than antiatherogenic. These sub-fractions of HDL are to be evaluated separately for estimating atherogenic risk of the patients. BioMed Central 2017-11-29 /pmc/articles/PMC5708092/ /pubmed/29187200 http://dx.doi.org/10.1186/s12944-017-0619-y Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Kido, Toshimi
Kondo, Kazuo
Kurata, Hideaki
Fujiwara, Yoko
Urata, Takeyoshi
Itakura, Hiroshige
Yokoyama, Shinji
ApoA-I/A-II-HDL positively associates with apoB-lipoproteins as a potential atherogenic indicator
title ApoA-I/A-II-HDL positively associates with apoB-lipoproteins as a potential atherogenic indicator
title_full ApoA-I/A-II-HDL positively associates with apoB-lipoproteins as a potential atherogenic indicator
title_fullStr ApoA-I/A-II-HDL positively associates with apoB-lipoproteins as a potential atherogenic indicator
title_full_unstemmed ApoA-I/A-II-HDL positively associates with apoB-lipoproteins as a potential atherogenic indicator
title_short ApoA-I/A-II-HDL positively associates with apoB-lipoproteins as a potential atherogenic indicator
title_sort apoa-i/a-ii-hdl positively associates with apob-lipoproteins as a potential atherogenic indicator
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708092/
https://www.ncbi.nlm.nih.gov/pubmed/29187200
http://dx.doi.org/10.1186/s12944-017-0619-y
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