...
首页> 外文期刊>Hematology >The association of cytokine genes polymorphisms and susceptibility to aplastic anemia in Egyptian patients
【24h】

The association of cytokine genes polymorphisms and susceptibility to aplastic anemia in Egyptian patients

机译:埃及患者细胞因子基因多态性与再生障碍性贫血易感性的关系

获取原文
           

摘要

Background and objective : Aplastic anemia (AA) remains a rare disease, with very interesting pathophysiology that is being investigated for years now. The present study aimed to determine the association between cytokine gene polymorphisms (TGF-β1 ?509 C/T, TNF-α ?308 G/A, IFN-γ +874 A/T) and susceptibility to AA in Egyptian patients. Methods : The study included 80 participants subjected to determination of gene polymorphisms on genomic DNA using polymerase chain reaction-restriction fragment length polymorphism assay. Results : It was found that IFN-γ +874 A/T gene polymorphism is associated with three-fold increased risk of development of AA (odds ratio (OR) 3.116, P?=?0.019), while TNF-α ?308 G/A gene polymorphism is associated with decreased risk (OR 0.318, P?=?0.026). TGF-β1 ?509 C/T gene polymorphism showed comparable risk between patients and controls (P?=?0.263). Conclusion : IFN-γ +874 A/T gene polymorphism is associated with the etiology of AA in Egyptian patients.
机译:背景与目的:再生障碍性贫血(AA)仍然是一种罕见的疾病,其病理生理学非常有趣,并且已经进行了多年研究。本研究旨在确定埃及患者中细胞因子基因多态性(TGF-β1≤509C / T,TNF-α≤308G / A,IFN-γ+874 A / T)与AA易感性之间的关联。方法:该研究纳入了80位参与者,他们使用聚合酶链反应-限制性片段长度多态性分析法测定了基因组DNA的基因多态性。结果:发现IFN-γ+874 A / T基因多态性与AA患病风险增加三倍有关(比值比(OR)3.116,P?=?0.019),而TNF-α?308 G / A基因多态性与降低的风险有关(OR 0.318,P≥0.026)。 TGF-β1〜509 C / T基因多态性显示患者和对照组之间具有可比的风险(P == 0.263)。结论:埃及患者的IFN-γ+ 874A / T基因多态性与AA的病因有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号