Research Article

Male-specific association of the APC rs383830 T allele with the risk of coronary heart disease

Published: October 02, 2015
Genet. Mol. Res. 14 (4) : 11745-11751 DOI: https://doi.org/10.4238/2015.October.2.8
Cite this Article:
J.Y. Zhong, X.W. Zheng, H.D. Ye, H.B. Cui, W.P. Du, Z.X. Zhang, X.H. Fei, S.Y. Lin, J. Wang, J. Su, X.M. Chen, S.W. Duan (2015). Male-specific association of the APC rs383830 T allele with the risk of coronary heart disease. Genet. Mol. Res. 14(4): 11745-11751. https://doi.org/10.4238/2015.October.2.8
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Abstract

APC is a tumor suppressor gene that is involved in the processes of cell migration and adhesion, transcriptional activation, and apoptosis. The goal of this study was to evaluate the contribution of the APC rs383830 polymorphism to coronary heart disease (CHD) in Han Chinese. A total of 783 patients with CHD and 737 controls were tested in the current association study. Although our study did not identify an association between the APC rs383830 polymorphism and CHD, a breakdown analysis by gender indicated there was a significant contribution of the rs383830 T allele to the risk of CHD in males (P = 0.046, odds ratio = 1.267, 95% confidence interval = 1.004-1.598). In conclusion, our study suggested a male-specific association of the APC rs383830 polymorphism with CHD.

APC is a tumor suppressor gene that is involved in the processes of cell migration and adhesion, transcriptional activation, and apoptosis. The goal of this study was to evaluate the contribution of the APC rs383830 polymorphism to coronary heart disease (CHD) in Han Chinese. A total of 783 patients with CHD and 737 controls were tested in the current association study. Although our study did not identify an association between the APC rs383830 polymorphism and CHD, a breakdown analysis by gender indicated there was a significant contribution of the rs383830 T allele to the risk of CHD in males (P = 0.046, odds ratio = 1.267, 95% confidence interval = 1.004-1.598). In conclusion, our study suggested a male-specific association of the APC rs383830 polymorphism with CHD.