期刊文献+

冠心病患者血清炎性因子、黏附分子含量及其对病变程度判断价值的研究 被引量:19

Serum inflammatory cytokine and adhesion molecule content in patients with coronary heart disease and their value for disease severity diagnosis
下载PDF
导出
摘要 目的:分析冠心病患者血清炎性因子、黏附分子含量检测及其对病变严重程度的判断价值。方法:113例冠心病患者及107例健康人被纳入研究,根据冠心病病情严重程度进一步将冠心病组患者分为轻度组患者40例,中度组患者52例,重度组患者21例。检测所有入组患者的血清炎性因子及黏附分子含量,进一步分析炎性因子、黏附分子含量在判断冠心病病变严重程度方面的价值。结果:冠心病组血清C-反应蛋白(CRP)、肿瘤坏死因子-α(TNF-α)、几丁质酶-3样蛋白1(YKL-40)水平高于健康对照组,白介素-35(IL-35)水平低于健康对照组(P<0.05);冠心病组血清E-选择素(E-selectin)、单核细胞黏附分子(ICAM-1)、血管细胞黏附分子-1(VCAM-1)、可溶性细胞间黏附分子(sICAM-1)水平均高于健康对照组(P<0.05);轻度组血清CRP、TNF-α、YKL-40、E-selectin、ICAM-1、VCAM-1、sICAM-1水平低于中度组及重度组,IL-35水平高于中度组及重度组(P<0.05),且随着冠心病病情加重CRP、TNF-α、YKL-40、E-selectin、ICAM-1、VCAM-1、sICAM-1水平上升,IL-35水平下降(P<0.05)。结论:冠心病患者血清炎性因子、黏附分子含量发生显著改变,与冠心病严重程度具有直接相关关系,可以作为评估冠心病患者病情及预后的可靠手段。 Objective: To detect inflammatory cytokine and adhesion molecule content in patients with coronary heart disease and analyze their value for disease severity diagnosis. Methods.. A total of 113 patients with coronary heart disease and 107 healthy subjects were included in the study and further divided into mild group (n = 40), moderate group (n = 52) and se- vere group (n = 21) according to the severity of coronary heart disease. Serum inflammatory cytokine and adhesion molecule content of all subjects were detected, and the value of inflammatory cytokine and adhesion molecule content for judging the se- verity of coronary heart disease was further analyzed. Results: Serum CRP, TNF-α and YKL-40 levels of coronary heart disease group were higher than those of healthy control group while IL-35 level was lower than that of healthy control group (P〈 0.05) ;serum E-selectin, ICAM-1, VCAM-1 and sICAM-1 levels of coronary heart disease group were higher than those of healthy control group (P〈0.05); serum CRP, TNF-α, YKL-40, E-selectin, ICAM-1, VCAM-1 and sICAM-1 levels of mild group were lower than those of moderate group and severe group, IL-35 level was higher than those of moderate group and se-vere group (P 〈0.05), and with the aggravation of coronary heart disease, CRP, TNF-α, YKL-40, E-seleetin, ICAM-1, VCAM-1 and sICAM-1 levels increased while IL-35 level decreased (P〈0.05). Conclusion:= Serum inflammatory cytokine and adhesion molecule content change significantly in patients with coronary heart disease, are directly correlated with the severity of coronary heart disease and can be used as the reliable means to assess the condition and prognosis of patients with coronary heart disease.
出处 《海南医学院学报》 CAS 2016年第24期2947-2950,共4页 Journal of Hainan Medical University
基金 朝阳区科委项目:动脉粥样硬化性心血管疾病防治系统开发及应用研究(CYSF 1516)~~
关键词 冠心病 炎性因子 黏附分子 病变严重程度 Coronary heart disease Inflammatory cytokines Adhesion molecule Disease severity
  • 相关文献

参考文献7

二级参考文献61

  • 1徐远溪,邢燕,赵明中,郑黎强,胡大一.冠状动脉病变程度与冠心病危险因素的关系[J].同济大学学报(医学版),2007,28(1):83-88. 被引量:11
  • 2Zhou C, Shen Q, Xue J, et al. Overexpression of TFRAP inhibits cell growth and induces apoptosis in oseosarcoma cells[J]. BMB Rep, 2013, 46(2) :113-118.
  • 3Lu KH, Yang HW, Su CW, et al. Phyllanthus urinaria suppresses human osteosarcoma cell invasion and migration by transcriptionally inhibiting u-PA via ERK and Akt sig- naling pathways [ J ]. Food Chem Toxicol, 2013, 52 : 193-199.
  • 4Liu ZL, Mao JH, Peng AF, et al. Inhibition of fatty acid synthase suppresses osteosarcoma cell invasion and migra- tion via downregulation of the PI3K/Akt signaling pathway in vitro[J]. Mol Med Rep, 2013, 7(2) :608-612.
  • 5Enomoto A, Ping J, Takahashi M. Girdin, a novel actin- binding protein, and its family of proteins possess versatile functions in the Akt and Wnt signaling pathways [ J ]. Ann N Y Acad Sci, 2006, 1086:169-184.
  • 6Ostman A, Hellberg C, Bohmer FD, et al. Protein-tyro- sine phosphatases and cancer[ J]. Nat Rev Cancer, 2006,6(4) :307-320.
  • 7Addams SJ, Aydin T,Celebi JT. GAB2-a scaffolding pro- tein in cancer[J]. Mol Cancer Res, 2012, 10(10): 1265-1270.
  • 8Xu XL, Wang X, Chen ZL, et al. Overexpression of Gab2-associated binder 2 in human lung cancer[ J]. Int J Biol Sci ,2011,7 (5) :496-504.
  • 9Zhang B, Gu F, She C, et al. Reduction of Akt2 inhibits migration and invasion of glioma cells [ J]. Int J Cancer, 2009, 125 ( 3 ) : 585-595.
  • 10Enomoto A, Murakami H, Asai N, et al. Akt/PKB regu- lates actin organization and cell motility via Girdin/APE [J]. Dev Cell, 2005, 9(3) :389-402.

共引文献51

同被引文献198

引证文献19

二级引证文献139

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部