Skip to main content
Top
Published in: Cardiovascular Toxicology 2/2017

01-04-2017

The Correlation Between 9p21 Chromosome rs4977574 Polymorphism Genotypes and the Development of Coronary Artery Heart Disease

Authors: Oushan Tang, Jin Lv, Yinhong Cheng, Fengming Qin

Published in: Cardiovascular Toxicology | Issue 2/2017

Login to get access

Abstract

Our aim is to investigate the correlation between 9p21 chromosome rs4977574 polymorphism genotypes and the development of coronary artery heart disease (CHD). Two hundred and eighty-nine patients with angiography-confirmed CHD were recruited as the CHD group, while 338 subjects without CHD symptoms were enrolled as the control group. For all participating subjects, the genotypes of rs4977574 polymorphism were examined by the real-time PCR analysis. Analyses acquired from single-locus technique showed that genotype distribution of rs4977574 polymorphism was significantly different (p = 0.041) between CHD group and the control group. Logistic regression analysis demonstrated that rs4977574 polymorphism in a dominant mode significantly increased (p = 0.038) the risk of CHD, where odds ratio (OR) was 0.71 and the 95 % confidence interval (CI) 0.58–0.97 was applied. 9p21 chromosome rs4977574 polymorphism genotypes are associated with the incidence and development of CHD. The presence of C allele may reduce the risk of CHD.
Literature
1.
go back to reference Sathyamurthy, I., & Jayanthi, K. (2014). Dual antiplatelet therapy in acute coronary syndromes and coronary artery interventions. Journal of the Association of Physicians of India, 62, 596–601.PubMed Sathyamurthy, I., & Jayanthi, K. (2014). Dual antiplatelet therapy in acute coronary syndromes and coronary artery interventions. Journal of the Association of Physicians of India, 62, 596–601.PubMed
2.
go back to reference Ducrocq, G., & Steg, P. G. (2015). Treating coronary artery disease in patients with a history of cerebrovascular disease. Archives of Cardiovascular Diseases, 108(11), 606–611.CrossRefPubMed Ducrocq, G., & Steg, P. G. (2015). Treating coronary artery disease in patients with a history of cerebrovascular disease. Archives of Cardiovascular Diseases, 108(11), 606–611.CrossRefPubMed
3.
go back to reference Neelankavil, J., Rau, C. D., & Wang, Y. (2015). The genetic basis of coronary artery disease and atrial fibrillation: A search for disease mechanisms and therapeutic targets. Journal of Cardiothoracic and Vascular Anesthesia, 29, 1328–1332.CrossRefPubMedPubMedCentral Neelankavil, J., Rau, C. D., & Wang, Y. (2015). The genetic basis of coronary artery disease and atrial fibrillation: A search for disease mechanisms and therapeutic targets. Journal of Cardiothoracic and Vascular Anesthesia, 29, 1328–1332.CrossRefPubMedPubMedCentral
4.
5.
go back to reference Munir, M. S., Wang, Z., Alahdab, F., et al. (2014). The association of 9p21-3 locus with coronary atherosclerosis: A systematic review and meta-analysis. BMC Medical Genetics, 15, 66.CrossRefPubMedPubMedCentral Munir, M. S., Wang, Z., Alahdab, F., et al. (2014). The association of 9p21-3 locus with coronary atherosclerosis: A systematic review and meta-analysis. BMC Medical Genetics, 15, 66.CrossRefPubMedPubMedCentral
6.
go back to reference Rivera, N. V., Carreras-Torres, R., Roncarati, R., et al. (2013). Assessment of the 9p21.3 locus in severity of coronary artery disease in the presence and absence of type 2 diabetes. BMC Medical Genetics, 14, 11.CrossRefPubMedPubMedCentral Rivera, N. V., Carreras-Torres, R., Roncarati, R., et al. (2013). Assessment of the 9p21.3 locus in severity of coronary artery disease in the presence and absence of type 2 diabetes. BMC Medical Genetics, 14, 11.CrossRefPubMedPubMedCentral
7.
go back to reference Assimes, T. L., Knowles, J. W., Basu, A., et al. (2008). Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study. Human Molecular Genetics, 17, 2320–2328.CrossRefPubMedPubMedCentral Assimes, T. L., Knowles, J. W., Basu, A., et al. (2008). Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study. Human Molecular Genetics, 17, 2320–2328.CrossRefPubMedPubMedCentral
8.
go back to reference Lee, I. T., Goodarzi, M. O., Lee, W. J., et al. (2014). The chromosome 9p21 variant not predicting long-term cardiovascular mortality in chinese with established coronary artery disease: An eleven-year follow-up study. Biomed Research International, 2014, 626907. doi:10.1155/2014/626907.PubMedPubMedCentral Lee, I. T., Goodarzi, M. O., Lee, W. J., et al. (2014). The chromosome 9p21 variant not predicting long-term cardiovascular mortality in chinese with established coronary artery disease: An eleven-year follow-up study. Biomed Research International, 2014, 626907. doi:10.​1155/​2014/​626907.PubMedPubMedCentral
9.
go back to reference Huang, Yi, Ye, Huadan, Hong, Qingxiao, et al. (2014). Association of CDKN2BAS polymorphism rs4977574 with coronary heart disease: A case-control study and a meta-analysis. International Journal of Molecular Sciences, 15(10), 17478–17492.CrossRefPubMedPubMedCentral Huang, Yi, Ye, Huadan, Hong, Qingxiao, et al. (2014). Association of CDKN2BAS polymorphism rs4977574 with coronary heart disease: A case-control study and a meta-analysis. International Journal of Molecular Sciences, 15(10), 17478–17492.CrossRefPubMedPubMedCentral
10.
go back to reference Saxena, R., Voight, B. F., Lyssenko, V., et al. (2007). Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science, 316, 1331–1336.CrossRefPubMed Saxena, R., Voight, B. F., Lyssenko, V., et al. (2007). Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science, 316, 1331–1336.CrossRefPubMed
11.
go back to reference Scott, L. J., Mohlke, K. L., Bonnycastle, L. L., et al. (2007). A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science, 316, 1341–1345.CrossRefPubMedPubMedCentral Scott, L. J., Mohlke, K. L., Bonnycastle, L. L., et al. (2007). A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science, 316, 1341–1345.CrossRefPubMedPubMedCentral
12.
go back to reference Doria, A., Wojcik, J., Xu, R., et al. (2008). Interaction between poor glycemic control and 9p21 locus on risk of coronary artery disease in type 2 diabetes. JAMA, 300, 2389–2397.CrossRefPubMedPubMedCentral Doria, A., Wojcik, J., Xu, R., et al. (2008). Interaction between poor glycemic control and 9p21 locus on risk of coronary artery disease in type 2 diabetes. JAMA, 300, 2389–2397.CrossRefPubMedPubMedCentral
13.
go back to reference Pipe, A. L., Papadakis, S., & Reid, R. D. (2010). The role of smoking cessation in the prevention of coronary artery disease. Current Atherosclerosis Reports, 12, 145–150.CrossRefPubMed Pipe, A. L., Papadakis, S., & Reid, R. D. (2010). The role of smoking cessation in the prevention of coronary artery disease. Current Atherosclerosis Reports, 12, 145–150.CrossRefPubMed
14.
go back to reference Pechlivanis, S., Muhleisen, T. W., Mohlenkamp, S., et al. (2013). Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf recall study. BMC Medical Genetics, 14, 23.CrossRefPubMedPubMedCentral Pechlivanis, S., Muhleisen, T. W., Mohlenkamp, S., et al. (2013). Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf recall study. BMC Medical Genetics, 14, 23.CrossRefPubMedPubMedCentral
15.
go back to reference Preuss, M., Konig, I. R., Thompson, J. R., et al. (2010). Design of the coronary artery disease genome-wide replication and meta-analysis (CARDIoGRAM) study: A genome-wide association meta-analysis involving more than 22000 cases and 60000 controls. Circulation Cardiovascular Genetics, 3, 475–483.CrossRefPubMedPubMedCentral Preuss, M., Konig, I. R., Thompson, J. R., et al. (2010). Design of the coronary artery disease genome-wide replication and meta-analysis (CARDIoGRAM) study: A genome-wide association meta-analysis involving more than 22000 cases and 60000 controls. Circulation Cardiovascular Genetics, 3, 475–483.CrossRefPubMedPubMedCentral
16.
go back to reference Samani, N. J., Erdmann, J., Hall, A. S., et al. (2007). Genomewide association analysis of coronary artery disease. New England Journal of Medicine, 357, 443–453.CrossRefPubMedPubMedCentral Samani, N. J., Erdmann, J., Hall, A. S., et al. (2007). Genomewide association analysis of coronary artery disease. New England Journal of Medicine, 357, 443–453.CrossRefPubMedPubMedCentral
Metadata
Title
The Correlation Between 9p21 Chromosome rs4977574 Polymorphism Genotypes and the Development of Coronary Artery Heart Disease
Authors
Oushan Tang
Jin Lv
Yinhong Cheng
Fengming Qin
Publication date
01-04-2017
Publisher
Springer US
Published in
Cardiovascular Toxicology / Issue 2/2017
Print ISSN: 1530-7905
Electronic ISSN: 1559-0259
DOI
https://doi.org/10.1007/s12012-016-9372-0

Other articles of this Issue 2/2017

Cardiovascular Toxicology 2/2017 Go to the issue