학술논문

在臺灣族群第9對染色體的基因多型性與冠狀動脈血管攝影的粥狀硬化程度的關係 / Association between Single Nucleotide Polymorphism of Chromosome 9 with the Angiographic Severity of Coronary Atherosclerosis in the Taiwanese Population
Document Type
Dissertation
Author
Source
高雄醫學大學醫學研究所-臨床醫學組學位論文. p1-39. 39 p.
Subject
第九對染色體
9p21
9q22
基因多型性
冠心病
冠狀動脈疾病
基因
動脈粥狀硬化
Chromosome 9p21
Chromosome 9q22
Polymorphism
Coronary artery disease
Gene
Atherosclrosis
Language
繁體中文
Abstract
Background: Coronary artery disease (CAD) is the leading cause of death and disabilities in industrially developed countries. Single nucleotide polymorphism (SNP) of chromosome 9 is associated with the risk of myocardial infarction and carotid atherosclerosis. However, little is known about the association between SNPs of chromosome 9 including rs1333049, rs4977574, rs10757278 and rs1800975 with the angiographic severity of coronary atherosclerosis in the Taiwanese population. Methods: 710 consecutive patients scheduled for diagnostic coronary angiography were enrolled. The significant CAD was defined as diameter stenosis ?d 50%. We used clinical vessel score (CVS, 0-3 vessels) and diffuseness score (DS, 0-11.5) to evaluate the angiographic severity of coronary atherosclerosis. The TaqMan genotyping assay was used for SNPs genotyping. Results:Among 710 enrolled patients, 162 (22.8%) were non-significant CAD, 168 (23.7%) were one-vessel disease, 156 (22.0%) were two-vessel disease, and 224 (31.5%) were three-vessel disease. The frequency of C allele of rs1333049 and T allele of rs1800975 were higher in those with significant CAD [odds ratio (OR) 1.31, 95% CI 1.02-1.68, p = 0.033 and OR 1.33, 95% CI 1.03-1.72, p = 0.028 respectively]. For the rs1333049, the OR of significant CAD for CC to GG genotype was 1.73 (95% CI 1.04-2.87, p = 0.032). For the rs1800975, the OR of significant CAD for TT to CC genotype was1.76 (95% CI 1.05-2.93, p = 0.030). Binary logistic regression analysis found only rs1333049 was still associated with the presence of significant CAD (p = 0.015). Haplotype analysis found GCG of rs4977574, rs1333049 and rs10757278 was associated with the presence of significant CAD (p = 0.037).Univariate and multivariate regression analysis found significant associations between CVS and rs1800975 (p = 0.031 and 0.037, respectively).None of 4 SNPs was associated with DS after multivariate analysis. Conclusion:The SNP rs1333049 on chromosome 9p21 and rs1800975 on chromosome 9q22 were associated with the angiographic severity of coronary atherosclerosis in the Taiwanese population.

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