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机构地区:[1]浙江省温州医学院附属第一医院心血管内科,325027
出 处:《中华医学遗传学杂志》2013年第6期724-728,共5页Chinese Journal of Medical Genetics
基 金:浙江省温州市科技局项目(Y20090239)
摘 要:目的研究白细胞介素10(interleukin10,IL10)基因-592C/A多态性与中国南方汉族人群冠状动脉粥样硬化性心脏病(简称冠心病)发病的相关性。方法采用基质辅助激光解吸电离飞行时间质谱技术对249例冠心病患者与132名无冠心病对照组人群儿加基因-592C/A位点(rs1800872)多态性检测,比较不同基因型和等位基因与冠心病患病风险的关系。结果IL10—592C/A位点基因型及等位基因在两组人群分布差异有统计学意义(P〈O.05),经Logistic回归分析校正-般临床资料差异后,发现A等位基因携带者(AA+CA)患冠心病风险是非A等位基因携带者(CC)的2.449倍(95%CI:1.214~4.940,P=0.012)。结论基因-592C/A位点与冠心病发病的危险性相关,A等位基因可能是中国南方汉族人群冠心病发病的遗传危险因素之-。Objective To assess the association of interleukin 10 (ILIO)gene --592C/A polymorphism with morbidity of coronary heart disease in a southern Chinese Han population. Methods Frequencies of various genotypes and alleles for the 11.10 -- 592C/A polymorphism (rs1800872) were determined by the means of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) in 249 patients and 132 unaffected controls. Results The frequencies of both 11.10 -- 592C/A site and different alleles have reached statistical significance (P 〈 0. 05 ) after correcting the difference in clinical data by logistic regression analysis. The risk of coronary heart disease in the patients with A gene (AAq-CA) was 2. 449 times greater than those without (95%CI:1. 214-4. 940, P=0. 012). Conclusion II.10 gene --592C/A polymorphism is associated with the risk of coronary heart disease. Allele A may be a risk factor for this disease in the studied population.
关 键 词:冠状动脉粥样硬化性心脏病 白细胞介素10 -592C A位点 单核苷酸多态性
分 类 号:R541.4[医药卫生—心血管疾病]
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