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首页> 外文期刊>DNA and Cell Biology >The CD40 Gene Polymorphism rs1883832 Is Associated with Risk of Acute Coronary Syndrome in a Chinese Case-Control Study
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The CD40 Gene Polymorphism rs1883832 Is Associated with Risk of Acute Coronary Syndrome in a Chinese Case-Control Study

机译:在中国的病例对照研究中,CD40基因多态性rs1883832与急性冠状动脉综合征的风险相关

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Numerous reports in the past few years have demonstrated that atherosclerosis is a lipid-driven, chronic inflammatory disease of the vessel. Recent studies have indicated that the immune mediator CD40-CD40L (CD40 ligand), which is expressed on several inflammatory cells within human atherosclerotic lesions, has roles in atherogenesis. A functional polymorphism (-1C>T, rs1883832) in the 5' untranslated region of TNFRSF5 gene has been reported to affect CD40 expression and be associated with several chronic inflammatory and autoimmune diseases. The aim of the present study was to validate the potential coronary artery disease susceptibility marker in a Chinese case-control study. A total of 160 patients with acute coronary syndrome (ACS) and 180 control subjects were used to genotype and identify this single-nucleotide polymorphism by polymerase chain reaction-restriction fragment length polymorphism and sequencing, respectively. Peripheral blood mononuclear cells were isolated and incubated with interferon- gamma with or without pretreatment of fluvastatin, followed by measurement of CD40 expression using flow cytometry. In addition, soluble CD40L was determined by ELISA as another biomarker of coronary artery disease. The distribution of the rs1883832 genotypes (CC, CT, and TT) was 33.1%, 54.4%, and 12.5% in the ACS group and 22.8%, 53.3%, and 23.9% in controls, respectively. The frequency of the C allele was significantly higher among ACS patients compared with controls (60.3% vs. 49.4%, odds ratio = 1.554, 95% confidence intervals: 1.146-2.107, p < 0.05). ACS patients showed a significant increase of CD40 and sCD40L coexpression compared with controls (p < 0.05). Cell culture experiments showed that CC carriers presented significantly higher CD40 expression levels than CT and TT subjects (p < 0.05). Additionally, fluvastatin suppressed CD40 expression in all three genotypes. These data suggest that the single-nucleotide polymorphism of CD40 gene is associated with susceptibility to ACS in Chinese population, and the polymorphism may influence the CD40 production. These expand the understanding of inflammatory mechanisms during atherogenesis.
机译:过去几年的大量报道表明,动脉粥样硬化是脂质驱动的血管慢性炎症性疾病。最近的研究表明,免疫介质CD40-CD40L(CD40配体)在人的动脉粥样硬化病变内的几种炎症细胞上表达,在动脉粥样硬化中起作用。据报道,TNFRSF5基因5'非翻译区的功能性多态性(-1C> T,rs1883832)影响CD40表达,并与几种慢性炎症和自身免疫性疾病有关。本研究的目的是在一项中国病例对照研究中验证潜在的冠状动脉疾病易感性标志物。分别使用聚合酶链反应-限制性片段长度多态性和测序方法,分别对160例急性冠脉综合征(ACS)患者和180例对照受试者进行基因分型和鉴定。分离外周血单个核细胞,并在有或没有氟伐他汀预处理的情况下与干扰素-γ一起孵育,然后使用流式细胞仪测量CD40的表达。另外,通过ELISA确定了可溶性CD40L作为冠状动脉疾病的另一生物标记。 rs1883832基因型(CC,CT和TT)在ACS组中的分布分别为33.1%,54.4%和12.5%,在对照组中分别为22.8%,53.3%和23.9%。与对照组相比,ACS患者中C等位基因的频率明显更高(60.3%比49.4%,优势比= 1.554,95%置信区间:1.146-2.107,p <0.05)。与对照组相比,ACS患者显示CD40和sCD40L共表达显着增加(p <0.05)。细胞培养实验表明,CC携带者的CD40表达水平明显高于CT和TT受试者(p <0.05)。此外,氟伐他汀在所有三种基因型中均抑制了CD40的表达。这些数据表明,CD40基因的单核苷酸多态性与中国人群对ACS的易感性有关,并且该多态性可能影响CD40的产生。这些扩展了对动脉粥样硬化形成过程中炎症机制的理解。

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