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Apolipoprotein A2 Isoforms in Relation to the Risk of Myocardial Infarction: A Nested Case-Control Analysis in the JPHC Study

Aim: The fact that low concentrations of high-density lipoprotein cholesterol are associated with the risk of cardiovascular disease is well known, but high-density lipoprotein metabolism has not been fully understood. Apolipoprotein A2 (ApoA2) is the second-most dominant apolipoprotein of high-dens...

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Autores principales: Kihara, Tomomi, Yamagishi, Kazumasa, Honda, Kazufumi, Ikeda, Ai, Yatsuya, Hiroshi, Saito, Isao, Kokubo, Yoshihiro, Yamaji, Taiki, Shimazu, Taichi, Sawada, Norie, Iwasaki, Motoki, Iso, Hiroyasu, Tsugane, Shoichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Atherosclerosis Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8193784/
https://www.ncbi.nlm.nih.gov/pubmed/32863295
http://dx.doi.org/10.5551/jat.56218
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author Kihara, Tomomi
Yamagishi, Kazumasa
Honda, Kazufumi
Ikeda, Ai
Yatsuya, Hiroshi
Saito, Isao
Kokubo, Yoshihiro
Yamaji, Taiki
Shimazu, Taichi
Sawada, Norie
Iwasaki, Motoki
Iso, Hiroyasu
Tsugane, Shoichiro
author_facet Kihara, Tomomi
Yamagishi, Kazumasa
Honda, Kazufumi
Ikeda, Ai
Yatsuya, Hiroshi
Saito, Isao
Kokubo, Yoshihiro
Yamaji, Taiki
Shimazu, Taichi
Sawada, Norie
Iwasaki, Motoki
Iso, Hiroyasu
Tsugane, Shoichiro
author_sort Kihara, Tomomi
collection PubMed
description Aim: The fact that low concentrations of high-density lipoprotein cholesterol are associated with the risk of cardiovascular disease is well known, but high-density lipoprotein metabolism has not been fully understood. Apolipoprotein A2 (ApoA2) is the second-most dominant apolipoprotein of high-density lipoprotein. We tested the hypothesis that ApoA2 isoforms are inversely associated with myocardial infarction. Methods: We measured the plasma levels of three ApoA2 isoforms (ApoA2-ATQ/ATQ, ApoA2-ATQ/AT, ApoA2-AT/AT) in nested case-control study samples of 1:2 from the Japan Public Health-Center-based Study (JPHC Study): 106 myocardial infarction incidence cases and 212 controls. Results: ApoA2-AT/AT was inversely associated with risk of myocardial infarction, in a matched model (OR, 2.78; 95% CI, 1.26–6.09 for lowest compared with the highest quartile), but its association was attenuated after adjustment for smoking only (OR=2.13; 95% CI, 0.91–4.97) or drinking only (OR=2.11; 0.91–4.89), and the multivariable OR was 1.20 (95% CI, 0.41–3.57). Neither ApoA2-ATQ/ATQ nor ApoA2-ATQ/AT was associated with the risk of myocardial infarction. Conclusions: Our nested case-control study did not show a significant association of ApoA2 isoforms with a risk of myocardial infarction.
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spelling pubmed-81937842021-06-22 Apolipoprotein A2 Isoforms in Relation to the Risk of Myocardial Infarction: A Nested Case-Control Analysis in the JPHC Study Kihara, Tomomi Yamagishi, Kazumasa Honda, Kazufumi Ikeda, Ai Yatsuya, Hiroshi Saito, Isao Kokubo, Yoshihiro Yamaji, Taiki Shimazu, Taichi Sawada, Norie Iwasaki, Motoki Iso, Hiroyasu Tsugane, Shoichiro J Atheroscler Thromb Original Article Aim: The fact that low concentrations of high-density lipoprotein cholesterol are associated with the risk of cardiovascular disease is well known, but high-density lipoprotein metabolism has not been fully understood. Apolipoprotein A2 (ApoA2) is the second-most dominant apolipoprotein of high-density lipoprotein. We tested the hypothesis that ApoA2 isoforms are inversely associated with myocardial infarction. Methods: We measured the plasma levels of three ApoA2 isoforms (ApoA2-ATQ/ATQ, ApoA2-ATQ/AT, ApoA2-AT/AT) in nested case-control study samples of 1:2 from the Japan Public Health-Center-based Study (JPHC Study): 106 myocardial infarction incidence cases and 212 controls. Results: ApoA2-AT/AT was inversely associated with risk of myocardial infarction, in a matched model (OR, 2.78; 95% CI, 1.26–6.09 for lowest compared with the highest quartile), but its association was attenuated after adjustment for smoking only (OR=2.13; 95% CI, 0.91–4.97) or drinking only (OR=2.11; 0.91–4.89), and the multivariable OR was 1.20 (95% CI, 0.41–3.57). Neither ApoA2-ATQ/ATQ nor ApoA2-ATQ/AT was associated with the risk of myocardial infarction. Conclusions: Our nested case-control study did not show a significant association of ApoA2 isoforms with a risk of myocardial infarction. Japan Atherosclerosis Society 2021-05-01 2020-08-29 /pmc/articles/PMC8193784/ /pubmed/32863295 http://dx.doi.org/10.5551/jat.56218 Text en 2021 Japan Atherosclerosis Society https://creativecommons.org/licenses/by-nc-sa/3.0/This article is distributed under the terms of the latest version of CC BY-NC-SA defined by the Creative Commons Attribution License.http://creativecommons.org/licenses/by-nc-sa/3.0/ (https://creativecommons.org/licenses/by-nc-sa/3.0/)
spellingShingle Original Article
Kihara, Tomomi
Yamagishi, Kazumasa
Honda, Kazufumi
Ikeda, Ai
Yatsuya, Hiroshi
Saito, Isao
Kokubo, Yoshihiro
Yamaji, Taiki
Shimazu, Taichi
Sawada, Norie
Iwasaki, Motoki
Iso, Hiroyasu
Tsugane, Shoichiro
Apolipoprotein A2 Isoforms in Relation to the Risk of Myocardial Infarction: A Nested Case-Control Analysis in the JPHC Study
title Apolipoprotein A2 Isoforms in Relation to the Risk of Myocardial Infarction: A Nested Case-Control Analysis in the JPHC Study
title_full Apolipoprotein A2 Isoforms in Relation to the Risk of Myocardial Infarction: A Nested Case-Control Analysis in the JPHC Study
title_fullStr Apolipoprotein A2 Isoforms in Relation to the Risk of Myocardial Infarction: A Nested Case-Control Analysis in the JPHC Study
title_full_unstemmed Apolipoprotein A2 Isoforms in Relation to the Risk of Myocardial Infarction: A Nested Case-Control Analysis in the JPHC Study
title_short Apolipoprotein A2 Isoforms in Relation to the Risk of Myocardial Infarction: A Nested Case-Control Analysis in the JPHC Study
title_sort apolipoprotein a2 isoforms in relation to the risk of myocardial infarction: a nested case-control analysis in the jphc study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8193784/
https://www.ncbi.nlm.nih.gov/pubmed/32863295
http://dx.doi.org/10.5551/jat.56218
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