首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Effects of long-term erythropoietin therapy on fibrinolytic system in haemodialyzed patients.
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Effects of long-term erythropoietin therapy on fibrinolytic system in haemodialyzed patients.

机译:长期促红细胞生成素治疗对血液透析患者纤溶系统的影响。

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INTRODUCTION: Recombinant human erythropoietin (rHuEPO) is the cornerstone of anaemia therapy in uraemic patients however the effects of this hormone on fibrinolytic system are difficult to interpret. MATERIALS AND METHODS: Assessment of fibrinolytic parameters: tissue-type plasminogen activator (tPA) antigen, urokinase-type plasminogen activator (uPA) and its soluble receptor (suPAR), plasminogen activator inhibitor 1 (PAI-1) and plasmin/antiplasmin (PAP) complexes were performed in haemodialyzed (HD) patients without rHuEPO therapy: Group I (n=8, Hg<10 g/dl); Group II (n=12, Hg>10 g/dl); and in HD patients treated with rHuEPO for more than 6 months (Group III, n=10) or for more than 12 months (Group IV, n=9) in relation to the healthy controls. RESULTS: Patients of Group I had the significantly lower haematological parameters than those of Groups II, III and IV. All the fibrinolytic parameters studied, except PAI-1, were significantly higher in HD patients without rHuEPO therapy when compared to the controls. There were no significant differences in fibrinolytic system between the Groups I and II. Erythropoietin therapy resulted in progressive decrease in antigenic tPA levels, which reach normal range values after 6 months rHuEPO administration. uPA and PAP concentrations were also decreased and reached normal values after 12 months of rHuEPO therapy. In these patients a significant decrease in uPAR levels was also observed. Therapy with rHuEPO did not alter PAI-1 concentrations in HD patients. CONCLUSIONS: These results suggest that long-term rHuEPO therapy can correct fibrinolytic parameters in patients undergoing regular HD irrespective from haemoglobin levels and in the absence of concomitant iron supplementation.
机译:简介:重组人促红细胞生成素(rHuEPO)是尿毒症患者贫血治疗的基石,但是这种激素对纤溶系统的作用难以解释。材料和方法:纤溶参数的评估:组织型纤溶酶原激活物(tPA)抗原,尿激酶型纤溶酶原激活物(uPA)及其可溶性受体(suPAR),纤溶酶原激活物抑制剂1(PAI-1)和纤溶酶/抗纤溶酶(PAP) )在未经rHuEPO治疗的血液透析(HD)患者中进行复合物:I组(n = 8,Hg <10 g / dl);第二组(n = 12,Hg> 10 g / dl);与健康对照组相比,在接受rHuEPO治疗的HD患者中,超过6个月(III组,n = 10)或超过12个月(IV,n = 9)。结果:第一组患者的血液学参数明显低于第二,第三和第四组。与对照组相比,未经rHuEPO治疗的HD患者,除PAI-1外,所有研究的纤溶参数均显着较高。第一和第二组之间的纤溶系统没有显着差异。促红细胞生成素疗法导致抗原性tPA水平逐渐降低,在给予rHuEPO 6个月后达到正常范围值。 rHuEPO治疗12个月后,uPA和PAP浓度也降低并达到正常值。在这些患者中,还观察到uPAR水平显着下降。用rHuEPO进行的治疗不会改变HD患者的PAI-1浓度。结论:这些结果表明,长期的rHuEPO治疗可以纠正接受定期HD的患者的纤溶参数,而不论其血红蛋白水平如何,并且无需同时补充铁。

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