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. 2015:2015:232048.
doi: 10.1155/2015/232048. Epub 2015 Sep 30.

The Relation between eNOS -786 C/T, 4 a/b, MMP-13 rs640198 G/T, Eotaxin 426 C/T, -384 A/G, and 67 G/A Polymorphisms and Long-Term Outcome in Patients with Coronary Artery Disease

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The Relation between eNOS -786 C/T, 4 a/b, MMP-13 rs640198 G/T, Eotaxin 426 C/T, -384 A/G, and 67 G/A Polymorphisms and Long-Term Outcome in Patients with Coronary Artery Disease

Vladimír Kincl et al. Dis Markers. 2015.

Abstract

Aim: The purpose of this study is to determine the association between eotaxin 426 C/T, -384 A/G, 67 G/A, eNOS -786 T/C, 4 a/b, and MMP-13 rs640198 G/T and prognosis of patients with known CAD.

Methods: From total of 1161 patients referred to coronary angiography, 532 patients with angiographically confirmed CAD were selected. Their long-term outcome was followed up using hospital database. Subsequent events were assessed in this study: death or combined endpoint-myocardial infarction, unstable angina pectoris, revascularization, heart failure hospitalization, and cardioverter-defibrillator implantation.

Results: The multivariate Cox regression model identified age, smoking, and 3-vessel disease as significant predictors of all-cause death. Further analysis showed that eotaxin 67 G/A (GA + AA versus GG) and eotaxin -384 A/G (GG versus GA + AA) were significant independent prognostic factors when added into the model: HR (95% CI) 2.81 (1.35-5.85), p = 0.006; HR (95% CI) 2.63 (1.19-5.83), p = 0.017; eotaxin -384 A/G was significantly associated with the event-free survival, but it did not provide the prognostic information above the effect of two- or three-vessel disease.

Conclusion: The A allele in eotaxin 67 G/A polymorphism is associated with worse survival in CAD patients.

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Figures

Figure 1
Figure 1
Kaplan-Meier analysis of survival in patients cohort.
Figure 2
Figure 2
Kaplan-Meier analysis of event-free survival in patients cohort.
Figure 3
Figure 3
Kaplan-Meier analysis of survival by 67 G/A genotype.

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References

    1. Abraham G., Bhalala O. G., de Bakker P. I. W., Ripatti S., Inouye M. Towards a molecular systems model of coronary artery disease. Current Cardiology Reports. 2014;16, article 488 doi: 10.1007/s11886-014-0488-1. - DOI - PMC - PubMed
    1. Prins B. P., Lagou V., Asselbergs F. W., Snieder H., Fu J. Genetics of coronary artery disease: genome-wide association studies and beyond. Atherosclerosis. 2012;225(1):1–10. doi: 10.1016/j.atherosclerosis.2012.05.015. - DOI - PubMed
    1. Koch W., Mehilli J., Pfeufer A., Schömig A., Kastrati A. Apolipoprotein E gene polymorphisms and thrombosis and restenosis after coronary artery stenting. Journal of Lipid Research. 2004;45(12):2221–2226. doi: 10.1194/jlr.M400148-JLR200. - DOI - PubMed
    1. Blankenberg S., Rupprecht H. J., Bickel C., et al. Common genetic variation of the cholesteryl ester transfer protein gene strongly predicts future cardiovascular death in patients with coronary artery disease. Journal of the American College of Cardiology. 2003;41(11):1983–1989. doi: 10.1016/s0735-1097(03)00408-x. - DOI - PubMed
    1. Szpakowicz A., Pepinski W., Waszkiewicz E., et al. The influence of renal function on the association of rs854560 polymorphism of paraoxonase 1 gene with long-term prognosis in patients after myocardial infarction. Heart and Vessels. 2014 doi: 10.1007/s00380-014-0574-8. - DOI - PMC - PubMed

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