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作 者:张蕊[1] 白峰[2] 许广莉[2] 李菲菲[1] 郭心灵[1] 尤崇革[1,3]
机构地区:[1]兰州大学第二医院检验与实验临床医学中心,兰州730030 [2]兰州大学第二医院心内科,兰州730030 [3]兰州大学第二医院甘肃省消化系肿瘤重点实验室,兰州730030
出 处:《临床检验杂志》2013年第6期415-418,共4页Chinese Journal of Clinical Laboratory Science
基 金:甘肃省技术研究与开发专项(1105TCYA002);兰州大学第二医院院内基金(YJ2010-06)
摘 要:目的通过高分辨率熔解曲线(HRM)技术检测IL-6及其受体基因单核苷酸多态性(single nucleotide polymorphism,SNP),探讨IL-6及其受体基因SNP与冠心病(CHD)的相关性。方法用HRM曲线技术检测231例CHD患者和275例健康人IL-6及其受体基因6个SNP位点(IL-6-572C/G、IL-6-597A/G、IL-6-174C/G、IL-6R-183A/G、IL-6R-exon1C/A和IL-6R-exon2A/T),分析其与CHD的相关性。结果 CHD组和健康人对照组IL-6-572C/G、IL-6-597A/G、IL-6R-exon1C/A和IL-6R-exon2A/T基因频率、基因型频率差异有统计学意义(P均<0.05)。IL-6-572CC、IL-6-597GA和IL-6R-exon2AT基因型能增加发生CHD的风险(OR值分别为1.935、2.651、1.809);IL-6R-exon1CC基因型能降低CHD的发生风险(OR=0.514)。结论IL-6-572C/G、IL-6-597A/G、IL-6R-exon1C/A和IL-6R-exon2A/T与西北地区人群CHD易感性相关。Objective To detect the single nucleotide polymorphisms (SNPs) of IL-6 and IL-6 receptor (IL-6R) genes by high resolution melting (HRM) and explore the correlation of the SNPs with coronary heart disease (CHD). Methods PCR-HRM assay was developed for genotyping of the SNPs of IL-6-572C/G, IL-6-597A/G, IL-6-174C/G, IL-6R-183A/G, IL-6R-exonlC/A and IL-6R-exon2A/T and a case-control study between 231 CHD patients and 275 healthy controls was conducted. Results Significant differences were found in the gene and genotype frequencies of IL-6-572C/G, IL-6-597A/G, IL-6R-exonlC/A and IL-6R-exon2A/T between CHD patients and controls (P 〈 0.05 ). The genotypes of IL-6-572CC, IL-6-597GA and IL-6R-exon2AT may increase the risk of CHD ( OR = 1. 935, 2.651, 1. 809 ), but the genotype of IL-6R-exonl CC may reduce the risk ( OR = 0.514). Conclusion 1L-6-572C/G, IL-6-597A/G, IL-6R-cxonlC/A and 1L-6R-exon2A/T mac associate with CHD susceptibility in population living in northwest China.
关 键 词:冠心病 白细胞介素6 单核苷酸多态性 高分辨熔解技术
分 类 号:R541.4[医药卫生—心血管疾病] R446[医药卫生—内科学]
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