TY - JOUR
T1 - Apolipoprotein a2 isoforms in relation to the risk of myocardial infarction
T2 - A nested case-control analysis in the jphc study
AU - Kihara, Tomomi
AU - Yamagishi, Kazumasa
AU - Honda, Kazufumi
AU - Ikeda, Ai
AU - Yatsuya, Hiroshi
AU - Saito, Isao
AU - Kokubo, Yoshihiro
AU - Yamaji, Taiki
AU - Shimazu, Taichi
AU - Sawada, Norie
AU - Iwasaki, Motoki
AU - Iso, Hiroyasu
AU - Tsugane, Shoichiro
N1 - Publisher Copyright:
© 2021 Japan Atherosclerosis Society.
PY - 2021
Y1 - 2021
N2 - Aim: The fact that low concentrations of high-density lipoprotein cholesterol are associated with the risk of car-diovascular disease is well known, but high-density lipoprotein metabolism has not been fully understood. Apoli-poprotein 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% Cl, 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% Cl, 0.91-4.97) or drinking only (OR=2.11; 0.91-4.89), and the multivariable OR was 1.20 (95% Cl, 0.41-3.57). Neither ApoA2-ATQ/ATQ nor ApoA2-ATQ/AT was associ-ated 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.
AB - Aim: The fact that low concentrations of high-density lipoprotein cholesterol are associated with the risk of car-diovascular disease is well known, but high-density lipoprotein metabolism has not been fully understood. Apoli-poprotein 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% Cl, 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% Cl, 0.91-4.97) or drinking only (OR=2.11; 0.91-4.89), and the multivariable OR was 1.20 (95% Cl, 0.41-3.57). Neither ApoA2-ATQ/ATQ nor ApoA2-ATQ/AT was associ-ated 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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U2 - 10.5551/jat.56218
DO - 10.5551/jat.56218
M3 - Article
C2 - 32863295
AN - SCOPUS:85105628400
SN - 1340-3478
VL - 28
SP - 483
EP - 490
JO - Journal of atherosclerosis and thrombosis
JF - Journal of atherosclerosis and thrombosis
IS - 5
ER -