Zhao Haifeng, Zhang Yizhuo, Xiao Gangfeng, Wu Ningning, Xu Jianfen, Fang Zhi
Key Laboratory of Cancer Prevention and Therapy, Department of Hematology and Oncology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer , Tianjin , PR China and.
Autoimmunity. 2014 Nov;47(7):478-81. doi: 10.3109/08916934.2014.921812. Epub 2014 Jun 4.
Interleukin-18 (IL-18) is a T helper 1 cytokine, which is postulated to play a role in immune thrombocytopenia (ITP). The aim of this study was to determine whether IL-18 promoter gene -607 A/C polymorphism was associated with ITP. Three-hundred and fifty-four Chinese ITP patients and 300 Chinese healthy individuals were enrolled. Genomic DNA was extracted from the peripheral blood. Polymerase chain reaction-restriction fragment length polymorphism (RFLP) was used to genotype the DNA samples for single nucleotide polymorphism (SNP)-607. Allelic and genotypic frequencies were compared between the case-control groups by the chi-square test. The results showed that the frequencies of the CC, CA and AA genotypes and C and A allele were 32.4, 47.8, 19.8, 56.4 and 43.6% in ITP patients and 32.3, 50.4, 17.3, 57.5 and 42.5% in the controls, respectively. There was no significant difference in either genotypes or allelic distribution between ITP patients and the controls. Furthermore, stratified analysis by the platelet count, age and disease course including ITP with severe thrombocytopenia (sITP), non-sITP, acute adult, chronic adult, acute childhood and chronic childhood revealed no significant difference in genotype and alleles distribution. In conclusion, this polymorphism was almost equally distributed between ITP patients and the controls. These data showed that this SNP may not be used as a stratification marker to predict the susceptibility to Chinese ITP.
白细胞介素-18(IL-18)是一种辅助性T细胞1细胞因子,据推测在免疫性血小板减少症(ITP)中发挥作用。本研究的目的是确定IL-18启动子基因-607 A/C多态性是否与ITP相关。纳入了354例中国ITP患者和300例中国健康个体。从外周血中提取基因组DNA。采用聚合酶链反应-限制性片段长度多态性(RFLP)对DNA样本进行单核苷酸多态性(SNP)-607基因分型。通过卡方检验比较病例对照组之间的等位基因和基因型频率。结果显示,ITP患者中CC、CA和AA基因型以及C和A等位基因的频率分别为32.4%、47.8%、19.8%、56.4%和43.6%,对照组中分别为32.3%、50.4%、17.3%、57.5%和42.5%。ITP患者与对照组在基因型或等位基因分布上均无显著差异。此外,按血小板计数、年龄和病程进行分层分析,包括重度血小板减少性ITP(sITP)、非sITP、成人急性、成人慢性、儿童急性和儿童慢性,结果显示基因型和等位基因分布无显著差异。总之,这种多态性在ITP患者和对照组之间分布几乎相同。这些数据表明,该SNP可能不能用作预测中国ITP易感性的分层标志物。