首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Medicine >Association of susceptibility to septic shock with platelet endothelial cell adhesion molecule-1 gene Leu125Val polymorphism and serum sPECAM-1 levels in sepsis patients
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Association of susceptibility to septic shock with platelet endothelial cell adhesion molecule-1 gene Leu125Val polymorphism and serum sPECAM-1 levels in sepsis patients

机译:脓毒症患者感染性休克的易感性与血小板内皮细胞粘附分子-1基因Leu125Val多态性与血清sPECAM-1水平的关系

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摘要

Sepsis is a systemic inflammatory response to infection and includes severe sepsis, septic shock and death. Platelet endothelial cell adhesion molecule-1 (PECAM-1) is one cell adhesion molecule expressed on platelets and leukocytes. It regulates platelet activation and mediates transendothelial migration of leukocytes, thus maintaining the integrity of the vasculature. There are some animal experiments associated with the protective role of PECAM-1 against septic shock. However few host genetic risk factors have been identified for sepsis severity and susceptibility to septic shock. A case-control study was conducted, which included 217 patients with sepsis and 90 control subjects recruited from our hospital. One single nucleotide polymorphisms (SNP) of PECAM-1 gene Leu125Val (C373G) was analyzed by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis. Serum soluble PECAM-1 (sPECAM-1) levels were determined by enzyme-linked immunosorbent assay (ELISA). Our results showed that the CG and GG genotypes of SNP in Leu125Val of PECAM-1 (rs668: C>G) was significantly associated with increased susceptibility to septic shock compared with CC genotype in sepsis patients (CG genotype, OR: 2.493, 95% CI: 1.175~5.287, P = 0.016; GG genotype: OR: 3.328, 95% CI: 1.445~7.666, P = 0.004). The serum levels of sPECAM-1 in the sepsis patients (47.1 ± 17.5 ng/ml) were significantly higher than those in the healthy controls (61.3 ± 20.9 ng/ml, P<0.01). Among sepsis patients, the serum levels of sPECAM-1 were significantly higher in CG and GG genotype than in CC genotype. In septic shock patients, nonsurvivors (83.7 ± 12.6 ng/ml, n = 69) had a significantly higher serum sPECAM-1 level than the survivors (76.9 ± 12.7 ng/ml, n = 53) (P<0.01). In conclusion, PECAM-1 Leu125Val polymorphism and its sPECAM-1 levels are associated with sepsis severity and susceptibility to septic shock.
机译:败血症是对感染的全身性炎症反应,包括严重的败血症,败血性休克和死亡。血小板内皮细胞粘附分子-1(PECAM-1)是在血小板和白细胞上表达的一种细胞粘附分子。它调节血小板活化并介导白细胞的跨内皮迁移,从而维持脉管系统的完整性。有一些动物实验与PECAM-1对败血性休克的保护作用有关。然而,几乎没有宿主遗传危险因素被鉴定为败血症的严重性和对败血性休克的敏感性。进行了一项病例对照研究,其中包括来自我们医院的217名败血症患者和90名对照受试者。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析来分析PECAM-1基因Leu125Val(C373G)的一个单核苷酸多态性(SNP)。血清可溶性PECAM-1(sPECAM-1)水平通过酶联免疫吸附测定(ELISA)确定。我们的结果表明,与败血症患者的CC基因型相比,PECAM-1 Leu125Val(rs668:C> G)中SNP的CG和GG基因型与脓毒症易感性的增加显着相关(CG基因型,OR:2.493,95% CI:1.175〜5.287,P = 0.016; GG基因型:OR:3.328,95%CI:1.445〜7.666,P = 0.004)。脓毒症患者的血清sPECAM-1水平(47.1±17.5 ng / ml)显着高于健康对照组(61.3±20.9 ng / ml,P <0.01)。在败血症患者中,CG和GG基因型的血清sPECAM-1水平显着高于CC基因型。在败血性休克患者中,非存活者(83.7±12.6 ng / ml,n = 69)的血清sPECAM-1水平显着高于存活者(76.9±12.7 ng / ml,n = 53)(P <0.01)。总之,PECAM-1 Leu125Val多态性及其sPECAM-1水平与败血症的严重程度和对感染性休克的敏感性有关。

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