Circulating Levels of Plasminogen Activator Inhibitor Type-1, Tissue Plasminogen Activator, and Thrombomodulin in Hemodialysis Patients

内科学 血栓调节蛋白 纤溶酶原激活剂 内分泌学 医学 纤维蛋白原 纤溶酶原激活物抑制剂-1 C反应蛋白 血液透析 脂蛋白(a) 组织纤溶酶原激活剂 载脂蛋白B 凝血酶 胆固醇 炎症 血小板
作者
Alfons Segarra,PILAR CHACOCombining Acute AccentN,CRISTINA MARTINEZ-EYARRE,XAVIER ARGELAGUER,Josefa Vila,Pilar Ruíz,Joan Fort,JORGE BARTOLOMECombining Acute Accent,J Camps,ERNESTO MOLINER,ANTONI PELEGRICombining Acute Accent,Fernando Marco,A Olmos,LLUIS PIERA
出处
期刊:Journal of The American Society of Nephrology 卷期号:12 (6): 1255-1263 被引量:102
标识
DOI:10.1681/asn.v1261255
摘要

Abstract. This study investigated the relationship between the circulating levels of the endothelial cell glycoproteins plasminogen activator inhibitor type 1 (PAI-1), tissue plasminogen activator (TPA), and thrombomodulin (TM) and the major vascular risk factors described in dialysis patients. In addition, the role of these endothelial cell products as independent predictors of coronary artery disease (CAD) was analyzed. Levels of TM, TPA antigen (Ag), TPA activity, PAI-1 Ag, PAI-1 activity, TPA/PAI complexes, thrombin-antithrombin complexes, fibrinopeptide A, C-reactive protein (CRP), interleukin-1β and tumor necrosis factor-α, lipids, apoproteins A1 and B, and albumin were measured in a group of 200 nondiabetic dialysis patients and 100 healthy matched volunteers. When compared with healthy controls, dialysis patients showed increased levels of CRP, TM, TPA, and PAI-1 and evidence of increased thrombin-dependent fibrin formation. Increased levels of active PAI-1 were associated to a great extent with major classic vascular risk factors and to a lesser extent with CRP and serum triglycerides. Forty-six patients (23%) had evidence of CAD. Variables associated with CAD in the univariate analysis included age, time on dialysis, male gender, number of packs of cigarettes per year, high BP, fibrinogen, apolipoprotein B, albumin, PAI-1 activity, CRP, thrombin-antithrombin complexes, and fibrinopeptide A. Logistic regression analysis found age, high-density lipoprotein cholesterol, gender, high BP, CRP, time on dialysis, and PAI-1 activity to be independent predictors of CAD. This model classified correctly 85% of patients as having CAD and showed adequate goodness of fit for all risk categories. Our data support a pathogenic link among activated inflammatory response, endothelial injury, and CAD in hemodialysis patients and suggest that assessment of circulating PAI-1 levels could be an additional tool to identify dialysis patients who are at risk for developing atheromatous cardiovascular disease.

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