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血栓前状态分子标志物在2型糖尿病微血管病变中的变化 被引量:5

The changes of markers to prethrombotics tate in patients with type 2 diabetes microangiopathy
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摘要 目的:探讨凝血与纤溶功能变化在2型糖尿病微血管病变中的临床意义。方法:采用发色底物法测定正常对照组(30例)、无微血管病变组(62例)、微血管病变组(65例)纤溶酶原激活物抑制物-1(PAI-1)活性,采用免疫浊度法测定分组纤维蛋白原(FIB)水平,比较3组PAI-1及FIB水平。结果:糖尿病微血管病变组血浆PAI-1和FIB水平明显高于无微血管病变组及正常对照组(P<0.01),且糖尿病无微血管病变组血浆PAI-1和FIB水平高于正常对照组(P<0.05)。结论:2型糖尿病患者存在血液的高凝及低纤溶状态,在发生2型糖尿病微血管病变后更为明显,检测2型糖尿病患者血浆中PAI-1和FIB水平对糖尿病微血管病变的预防和治疗具有一定的临床意义。 Objective: To investigate the changes of plasma coagulation and fibrinolysis parameters in type 2 diabetic microangiopathy. Methods: The plasminogen activator inhibitor-1 (PAI-1) and plasma fibrinogen (FIB) in type 2 diabetes were measured. Results: In diabetic group, the levels of PAI 1 and FIB were signifiantly higher in patients with microangiopathy than those without diabetic microangiopathy (P 〈0.01). The levels of PAI-1 and FIB were signifiantly increased in both groups of patients with microangiopathy and withoutmicroangiopathy compared with controls (P 〈0.05). Conclusion: The condition of high coagulation and low fibrinolytic base was in type 2 diabetes mellitus, and even more serious in diabetic microangiopathy It's critical to measure the levels of prethrombotic state PAI-1 and FIB for prevention and treatment in type 2 diabetic microangiopathy.
出处 《新疆医科大学学报》 CAS 2009年第4期406-407,411,共3页 Journal of Xinjiang Medical University
基金 国家自然科学基金项目(编号:0608216)
关键词 糖尿病微血管病 血栓前状态 纤溶酶原激活物抑制物-1 纤维蛋白原 diabetic microangiopathy prethrombotic state plasminogen activator inhibitor-l plasma fibrinogen
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  • 1应淑琴,徐耕,单江.冠心病介入治疗前后患者血浆P-选择素、血栓调节蛋白、纤溶酶原激活剂抑制剂-1的变化[J].中国介入心脏病学杂志,2001,9(3):135-137. 被引量:3
  • 2徐秀英,杜凤和,张剑峰,叶珏,惠汝太.血管紧张素转化酶基因多态性与内皮功能的研究[J].临床荟萃,2001,16(1). 被引量:1
  • 3马西.缺血性心脑血管病的纤维蛋白原分子反应性的观察[J].中华血液学杂志,1996,17(3):135-137. 被引量:46
  • 4[2]Salomaa V,Stinson V,Kark JD,et al.Association of fibrinolytic parameters with early atherosclerosis:the ARIS study[J].Circulation,1995,91 (2):284-290.
  • 5[3]Colwell JA,Nesto RW.The platelet in diabetes:focus on prevention of ischemic events[J].Diabetes Care,2003,26(7):2181-2188.
  • 6[4]Biondi-Zoccai GG,Abbate A,Liuzzo G,et al.Atherosclerosis,inflammation and diabetes[J].Am Coll Cardiol,2003,41 (6):1071-1077.
  • 7[5]Galatius SS,Wroblewski H,Vibeke BS,et al.Endothelin and Von will ebrand Factor as parameters of endothelial function in idiopathic dilated cardiomyopathy:different stimuli for release before and after heart transplantation[J].Am Heart J,1999,137(1):549-554.
  • 8Zygment P M, Plane F , Paulsson M, et al. Interactions between endothelium-derived relaxing factors in the rat hepatic artery on regulation of EDHF[J].Br J Pharmacol , 1998, 124: 992..
  • 9Warner TD, Allcock GK, Corder R,et al. Use of the endothelin antagonists BD-123 and PD142893 to reveal three endothelin receptors mediating smooth nmscle contraction and the release of EDRF[J]. Br J Pharmacol,1993,110:777.
  • 10Moncada S, Higgs EA. The L-Arginine-nitric oxide and cell-cell signaling in the nervous systym[J]. Trends Neurosci, 1991,14: 60.

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