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肝脏疾病患者血浆中组织因子途径抑制物与抗凝血酶的表达
引用本文:刘敏涓,周立红,刘卉,董临江. 肝脏疾病患者血浆中组织因子途径抑制物与抗凝血酶的表达[J]. 血栓与止血学, 2005, 11(4): 159-161
作者姓名:刘敏涓  周立红  刘卉  董临江
作者单位:1. 广州医学院附属二院,广州,510260
2. 深圳宝安医院,深圳,518101
基金项目:广东省医学科研课题(A2003317)
摘    要:目的研究肝脏疾病患者血浆中组织因子途径抑制物(TFPI)与抗凝血酶(AT)的改变及其临床意义。方法TFPI抗原(TFPI:Ag)采用双夹心ELISA抗原测定法。TFPI活性(TFPI:A)采用发色底物法。AT:Ag采用免疫浊度法。AT:A采用发色底物法。结果急性中毒性肝炎14例,急性病毒性肝炎20例,慢性乙型肝炎48例,肝硬化50例,共132例肝病患者:TFPI:Ag与TFPI:A均高于正常值(P〈0.05,P〈0.01),仅失代偿期肝硬化TFPI:Ag降低(P〈0.05)。AT:Ag除失代偿期肝硬化外,均接正常值。AT:A除慢性乙肝与肝硬化低于正常值外,其他组接近正常值。结论肝病患者TFPI上调,表明组织受损与炎症存在,而AT正常或降低,表明肝细胞合成AT减少。而失代偿期肝硬化除TFPI:A保持高水平外,其余多项指标均降低,表明肝组织毁损严重,抗凝蛋白合成功能减退。

关 键 词:肝脏疾病 组织因子途径抑制物 抗凝血酶
文章编号:1009-6213(2005)04-0159-03
收稿时间:2005-03-20
修稿时间:2005-03-20

Expression of Tissue Factor Pathway Inhibitor and Antithrombin in Patients with Hepatic Disease
LIN Min-juan,ZHOU Li-hong,LIU Hui,DONG Lin-Jiang. Expression of Tissue Factor Pathway Inhibitor and Antithrombin in Patients with Hepatic Disease[J]. Chinese Journal of Thrombosis and Hemostasis, 2005, 11(4): 159-161
Authors:LIN Min-juan  ZHOU Li-hong  LIU Hui  DONG Lin-Jiang
Abstract:Objective To investigate the chang of tissue factor pathway inhibitor (TFPI) and antithrombin (AT) in the plasma of patients with hepatic disease. Methods TFPI:Ag by ELISA assay. TFPI:A by colored substrate method. AT:Ag by immune furbidimetry. AT:A by colored substrate method. Results The plasma level of TFPI : Ag (except for decompensatory phase of cirrhosis) and TFPI: A all increased than control group. The level of AT: Ag(except for decompensatory phase of cirrhosis) all consistent with normol value. AT: A except for chronic hepaitis B and hepatocirrhosis lower than normol value,other groups close to control group. Conclusion The elevation of TFPI in hepatic inflammatory disease indication of tissue injury and inflammation . The lower level of AT are expression decreased of symtheic proteins in liver. Hepatocirrhosis on the part of syntheic proteins lower preforable to other hepatic disease.
Keywords:Hepatic disease   Tissue factor pathway inhibitor    Anfilhrombin
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