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不稳定型心绞痛患者血清细胞因子与基质金属蛋白酶-2的关系 被引量:4

Relation between inflammatory cytokines and matrix metalloproteinase-2 in patients with unstable angina
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摘要 目的:探讨不稳定型心绞痛(UAP)患者血清致炎因子(IL-1、IL-6、TNF-α)、抗炎因子(IL-10)水平与基质金属蛋白酶-2(MMP-2)及其抑制剂(TIMP-2)的关系。方法:选择UAP患者135例(UAP组)、稳定型心绞痛(SAP)患者35例(SAP组)、对照组30例,应用ELISA法检测血清IL-1、IL-6、TNF-α、IL-10、MMP-2、TIMP-2水平。结果:UAP组患者血清IL-1、IL-6、TNF-α、IL-10、(IL-1+IL-6+TNF-α)/IL-10、MMP-2、TIMP-2、MMP-2/TIMP-2水平高于对照组及SAP组(P均<0.05);Spearson相关分析显示,UAP患者血清MMP-2活性与IL-1、IL-6、IL-10、TNF-α水平正相关(P<0.05);多元逐步回归分析显示,UAP患者血清MMP-2与IL-1、(IL-1+IL-6+TNF-α)/IL-10、空腹血糖独立正相关。结论:UAP患者致炎与抗炎细胞因子平衡失调,可能通过影响MMP-2活性介导斑块向不稳定性进展,促进UAP的发生。 Objective: To elucidate the relationship among pro-inflammatory cytokine(IL-1,IL-6,TNF-α),anti-inflammatory cytokine(IL-10) and MMP-2 and their effects on the stability of plaque in unstable angina.Methods: The concentrations of IL-1,IL-6,TNF-α,IL-10,MMP-2 and TIMP-2 were analyzed using ELISA in 170 patients and 30 healthy control subjects.Patients were divided into two groups,stable angina(n=35) and unstable angina(n=135).Results: The serum levels of IL-1,IL-6,TNF-α,IL-10,MMP-2 and TIMP-2 were significantly higher in UAP group and SAP group compared with the healthy control group(P0.05),and so were the ratio of MMP-2/TIMP-2 and(IL-1+IL-6+TNF-α)/IL-10(P0.05).The levels of above mentioned cytokines and ratios in patients with unstable angina were significantly higher than those with stable angina(P0.05).Correlation analysis revealed the level of MMP-2 was positively related to the levels of IL-1,IL-6,IL-10 and TNF-α.In multiple linear regression analysis,significant positive correlations were found between MMP-2 and IL-10,(IL-1+IL-6+TNF-α)/IL-10 and fasting blood glucose separately in patients with unstable angina.Conclusion: The imbalance of proinflammation/anti-inflammation could lead to unstability of the plaque through the regulation of MMP-2,which could trigger unstable angina.
出处 《新医学》 2011年第12期801-804,共4页 Journal of New Medicine
关键词 心绞痛 不稳定型 细胞因子 基质金属蛋白酶-2 Angina unstable Cytokines Matrix metalloproteinase-2
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