The association of single nucleotide polymorphism rs189037C>T in ATM gene with coronary artery disease in Chinese Han populations: A case control study. Issue 4 (January 2018)
- Record Type:
- Journal Article
- Title:
- The association of single nucleotide polymorphism rs189037C>T in ATM gene with coronary artery disease in Chinese Han populations: A case control study. Issue 4 (January 2018)
- Main Title:
- The association of single nucleotide polymorphism rs189037C>T in ATM gene with coronary artery disease in Chinese Han populations
- Authors:
- Ding, Xiang
He, Yong
Hao, Qiukui
Chen, Shanping
Yang, Ming
Leng, Sean X.
Yue, Jirong
Dong, Birong - Other Names:
- Li. Sheyu section editor.
- Abstract:
- Abstract : Abstract: Accumulated evidence has indicated that ataxia telangiectasia mutated (ATM) is closely related to atherosclerosis and cardiovascular diseases. So we aimed to examine potential association between a gene variant [single nucleotide polymorphisms (SNPs), i.e., rs189037C>T] in the promoter of ATM gene and coronary artery disease (CAD) in Chinese Han populations. In this hospital-based case–control study, a total of 1308 participants were divided into CAD group (652 patients) and control group (656 subjects) after performing coronary angiography. The SNP rs189037 was genotyped by using polymerase chain reaction-restriction fragment length polymorphism. The distribution of rs189037 genotypes and alleles showed a significant difference between CAD and control subjects (genotypes: P = .032; alleles: P = .028). The percentage of the TT genotype is much higher in control group than that in CAD group (22.0% vs 16.3%, P = .009). After adjustment of the major confounding factors, such difference remained significant (OR = 0.62, 95% CI = 0.43–0.89, P = .010). After analyzing data from different groups divided by genders and smoking status respectively, we found that the protective effect of TT genotype on CAD was significant in males ( P = .007) and smokers ( P = .031). The difference remained statistically significant after multivariate adjustment (adjusted in males: OR = 0.60, 95% CI = 0.38–0.93, P = .022; adjusted in smokers: OR = 0.47, 95% CI = 0.27–0.81, PAbstract : Abstract: Accumulated evidence has indicated that ataxia telangiectasia mutated (ATM) is closely related to atherosclerosis and cardiovascular diseases. So we aimed to examine potential association between a gene variant [single nucleotide polymorphisms (SNPs), i.e., rs189037C>T] in the promoter of ATM gene and coronary artery disease (CAD) in Chinese Han populations. In this hospital-based case–control study, a total of 1308 participants were divided into CAD group (652 patients) and control group (656 subjects) after performing coronary angiography. The SNP rs189037 was genotyped by using polymerase chain reaction-restriction fragment length polymorphism. The distribution of rs189037 genotypes and alleles showed a significant difference between CAD and control subjects (genotypes: P = .032; alleles: P = .028). The percentage of the TT genotype is much higher in control group than that in CAD group (22.0% vs 16.3%, P = .009). After adjustment of the major confounding factors, such difference remained significant (OR = 0.62, 95% CI = 0.43–0.89, P = .010). After analyzing data from different groups divided by genders and smoking status respectively, we found that the protective effect of TT genotype on CAD was significant in males ( P = .007) and smokers ( P = .031). The difference remained statistically significant after multivariate adjustment (adjusted in males: OR = 0.60, 95% CI = 0.38–0.93, P = .022; adjusted in smokers: OR = 0.47, 95% CI = 0.27–0.81, P = .006). Our study suggests that ATM rs189037 polymorphism is associated with CAD in Chinese Han populations. The TT genotype of rs189037 seems to be associated with a lower risk of CAD and a protective genetic marker of CAD, especially in males and smokers. Abstract : Supplemental Digital Content is available in the text … (more)
- Is Part Of:
- Medicine. Volume 97:Issue 4(2018)
- Journal:
- Medicine
- Issue:
- Volume 97:Issue 4(2018)
- Issue Display:
- Volume 97, Issue 4 (2018)
- Year:
- 2018
- Volume:
- 97
- Issue:
- 4
- Issue Sort Value:
- 2018-0097-0004-0000
- Page Start:
- Page End:
- Publication Date:
- 2018-01
- Subjects:
- ataxia telangiectasia mutated -- coronary artery disease -- rs189037 -- single nucleotide polymorphism
Medicine -- Periodicals
Medicine -- Periodicals
Médecine -- Périodiques
Geneeskunde
Medicine
Periodicals
Periodicals
610.5 - Journal URLs:
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http://journals.lww.com ↗ - DOI:
- 10.1097/MD.0000000000009747 ↗
- Languages:
- English
- ISSNs:
- 0025-7974
- Deposit Type:
- Legaldeposit
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