透析患者内脏素与内皮功能的关系。

IF 1.9
Jolanta Malyszko, Jacek S Malyszko, Michal Mysliwiec
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引用次数: 22

摘要

目的:Visfatin是一种最近引起广泛关注的脂肪细胞因子。该研究的目的是评估内脏素与血液透析和腹膜透析患者内皮损伤和炎症标志物的相关性。方法:Visfatin, leptin, apelin和脂联素,凝血标志物(凝血酶-抗凝血酶复合物(TAT),凝血酶原片段1+2 (F1+2)),纤维蛋白溶解(组织纤溶酶原激活剂(tPA),纤溶酶原激活剂抑制剂1型(PAI-1)),内皮功能/损伤(血管性血液病因子(vWF),血栓调节蛋白,细胞内粘附分子(ICAM),血管细胞粘附分子(VCAM), CD146)和炎症(高敏c反应蛋白(hsCRP),评估肿瘤坏死因子- α (tnf - α)和白细胞介素(IL)-6)。结果:透析患者的甘油三酯、hsCRP、肌酐、IL-6、tnf - α、vWF、F1+2、TAT、血栓调节素、ICAM、VCAM、CD146、PAI-1、瘦素、脂联素和visfatin均高于对照组。在单变量分析中,Visfatin与血液透析患者内皮损伤/炎症标志物(CD146、ICAM、IL-6)、其他脂肪细胞因子、Kt/V和透析年龄显著相关,并倾向于与hsCRP相关。在腹膜透析患者中,内脏脂肪素与血红蛋白和内皮损伤标志物显著相关。在健康志愿者中,visfatin与ICAM、肌酐和IL-6显著相关。在HD患者的多元回归分析中,visfatin仅与Kt/V、透析时间和IL-6独立相关。结论:与炎症标志物相关的visfatin升高可能代表了透析患者炎症和脂肪细胞因子之间的新联系。透析时间和透析充分性可能影响透析患者的内脂素清除,因为内脂素清除减少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Visfatin and endothelial function in dialyzed patients.

Aim: Visfatin is an adipocytokine that has recently generated much interest. The aim of the study was to assess visfatin in correlation with markers of endothelial damage and inflammation in haemodialyzed and peritoneally dialyzed patients.

Methods: Visfatin, leptin, apelin and adiponectin, markers of coagulation (thrombin-antithrombin complexes (TAT), prothrombin fragments 1+2 (F1+2)), fibrinolysis (tissue plasminogen activator (tPA), plasminogen activator inhibitor type 1 (PAI-1)), endothelial function/injury (Von Willebrand factor (vWF), thrombomodulin, intracellular adhesion molecule (ICAM), vascular cell adhesion molecule (VCAM), CD146) and inflammation (high-sensitivity C-reactive protein (hsCRP), tumour necrosis factor-alpha (TNF-alpha) and interleukin (IL)-6) were assessed.

Results: Triglycerides, hsCRP, creatinine, IL-6, TNF-alpha, vWF, F1+2, TAT, thrombomodulin, ICAM, VCAM, CD146, PAI-1, leptin, adiponectin and visfatin were elevated in dialyzed patients over controls. Visfatin correlated significantly, in univariate analysis, in haemodialyzed patients with markers of endothelial damage/inflammation (CD146, ICAM, IL-6), other adipocytokines, Kt/V and dialysis vintage, and tended to correlate with hsCRP. In peritoneally dialyzed patients, visfatin correlated significantly with haemoglobin, and markers of endothelial damage. In the healthy volunteers visfatin correlated significantly with ICAM, creatinine and IL-6. In multiple regression analysis in HD patients visfatin was only independently related to Kt/V, dialysis vintage and IL-6.

Conclusion: Elevated visfatin related to markers of inflammation might represent a novel link between inflammation and adipocytokines in dialyzed patients. Time on dialyses and dialysis adequacy may influence visfatin in dialyzed patients due to the decreased clearance of visfatin.

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