Department of Cardiology, West China Hospital of Sichuan University, Chengdu, PR China.
Hum Immunol. 2013 May;74(5):635-9. doi: 10.1016/j.humimm.2013.01.019. Epub 2013 Jan 31.
Cardiomyopathy is one of the major causes of sudden death and/or progressive heart failure. Dilated cardiomyopathy (DCM), comprising 60% of the cases of identified cardiomyopathy, is the most common form of heart muscle disease. Interleukin 17 (IL-17) is a proinflammatory cytokine that has been implicated in the pathogenesis of various diseases. To evaluate the influence of IL-17A and IL-17F gene polymorphisms on the risk of DCM, a case-control study was conducted in a Chinese Han population. The TaqMan® SNP Genotyping Assay was used to genotype the SNP rs2275913 of IL-17A and SNP rs763780 of IL-17F in 288 DCM patients and 421 ethnicity-matched controls. No significant difference in genotypic and allelic frequencies between DCM patients and control subjects was observed. However, Results of stratified analysis revealed that rs763780 was associated with male DCM patients in a dominant genetic model (p=0.031, OR=1.83, 95% CI=1.04-3.22). Our results suggest that the tested two IL-17 SNPs, rs2275913 and rs763780, are not found to be associated with DCM in the Chinese population studied.
扩张型心肌病(DCM)占已明确的心肌病的 60%,是最常见的心肌疾病形式。白细胞介素 17(IL-17)是一种促炎细胞因子,与多种疾病的发病机制有关。为了评估白细胞介素 17A 和白细胞介素 17F 基因多态性对 DCM 风险的影响,在中国汉族人群中进行了一项病例对照研究。采用 TaqMan® SNP 基因分型检测 IL-17A 的 SNP rs2275913 和 IL-17F 的 SNP rs763780。在 288 例 DCM 患者和 421 名种族匹配的对照中进行了基因分型。DCM 患者和对照组之间的基因型和等位基因频率无显著差异。然而,分层分析结果显示,rs763780 在显性遗传模型中与男性 DCM 患者相关(p=0.031,OR=1.83,95%CI=1.04-3.22)。我们的结果表明,在所研究的中国人群中,未发现测试的两个白细胞介素 17 基因多态性(rs2275913 和 rs763780)与 DCM 相关。