[肾移植后sp -选择素及其他心血管危险因素:纤维蛋白原、组织纤溶酶原激活物(t-PA Ag)和急性期蛋白升高]。

Sbornik lekarsky Pub Date : 2002-01-01
J Kvasnicka, O Viklický, A Umlaufová, T Kvasnicka, E Teplá, H Homolková, I Malíkova, R Sauerová
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引用次数: 0

摘要

背景:我们的研究旨在监测肾移植后“冠状动脉疾病(CAD)危险因素”的存在。方法:选取26例功能良好(肌酐清除率> 0.8 mL/s)接受环孢素A (CsA)免疫抑制治疗的同种异体肾移植受者和60例年龄匹配的健康对照。作为“冠心病危险因素”,测定外周血血清或血浆中纤维蛋白原、急性期蛋白、类状体和c反应蛋白、t-PA Ag、PAI-1 Ag及可溶性粘附分子e -选择素、p -选择素和ICAM-1的水平。结果:肾移植受者BMI (p < 0.001)、纤维蛋白原(p < 0.001)、t-PA Ag (p = 0.007)、PAI-1 Ag (p < 0.001)、急性期蛋白orosomucoid (p < 0.001)和可溶性p选择素(p = 0.038)水平均较高。与对照组相比,sICAM-1和sE-selectin水平无统计学差异。结论:我们的研究表明,肾功能良好的肾移植受者的“CAD危险因素”纤维蛋白原、急性期反应物orosomucoid、t-PA Ag、PAI-1 Ag和sp -选择素水平明显升高。
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[Increased sP-selectin and other cardiovascular risk factors: fibrinogen, tissue plasminogen activator (t-PA Ag) and acute phase proteins after kidney transplantation].

Background: Our study was designed to monitor the presence of the "coronary artery disease (CAD) risk factors" after kidney transplantation.

Methods: 26 kidneys transplant recipients with well-functioning (creatinine clearance > 0.8 mL/s) renal allografts receiving cyclosporine A (CsA) as the basic component of immunosuppressive therapy and 60 healthy age-matched controls were included into the study. As "CAD risk factors" were determined the levels of fibrinogen, acute phase proteins orosomucoid and C-reactive protein, t-PA Ag, PAI-1 Ag and soluble adhesion molecules E-selectin, P-selectin and ICAM-1 in the peripheral blood serum or plasma.

Results: Renal transplant recipients showed higher BMI (p < 0.001) and levels of fibrinogen (p < 0.001), t-PA Ag (p = 0.007) and PAI-1 Ag (p < 0.001), acute phase protein orosomucoid (p < 0.001) and higher level of soluble P-selectin (p = 0.038). The levels of sICAM-1 and sE-selectin did not differ statistically significantly from those in controls.

Conclusion: Our study has demonstrated renal graft recipients with good kidney function already show significantly raised levels of "CAD risk factors" fibrinogen, acute phase reactant orosomucoid, t-PA Ag, PAI-1 Ag and sP-selectin.

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