Abstract

PurposeChronic kidney disease (CKD) is an estimated risk factor for increased mortality and morbidity due to fibrinolytic system disturbances. Progressive loss of renal function leads to retention of uremic toxins. Anthranilic acid (AA) is a tryptophan-derived uremic toxin with multidirectional properties that can affect the hemostatic system. The goal of this study was to examine the association between AA and the parameters of fibrinolysis at different stages of CKD.MethodsPatients with CKD were divided into two groups: mild-to-moderate (n = 20) and severe-to-end-stage CKD (n = 28). Seventeen healthy volunteers served as an additional control group. Parameters of fibrinolysis, inflammation, and monocytes activation were determined by ELISA immune-enzymatic kits. AA levels were evaluated using high-performance liquid chromatography.ResultsAA concentration and parameters of fibrinolysis: urokinase-type plasminogen activator (uPA), its soluble receptor (suPAR), tissue plasminogen activator (tPA), tissue plasminogen activator inhibitor-1 (PAI-1) and plasmin-antiplasmin complex (PAP) were significantly elevated in the CKD groups compared with the controls. The markers of inflammation, monocyte activation, and impaired kidney function were also increased in those with CKD. AA was positively correlated with the uPA/suPAR system in the early stages of CKD, whereas during severe-to-end-stage CKD, inverse relationships were observed between AA, tPA and PAI-1. Additionally, AA was an independent variable associated with tPA in patients with CKD overall and with uPA levels in the mild-to-moderate CKD group.ConclusionsObtained results suggest for the first time the association between AA and the fibrinolytic system in CKD patients. The distinct relationship between AA and individual parameters of fibrinolysis appears to be dependent on CKD stage.

Highlights

  • Chronic kidney disease (CKD) is an established risk factor for the occurrence of cardiovascular disease (CVD)

  • This study is the first to examine the association between Anthranilic acid (AA) and fibrinolytic components in patients with CKD on conservative treatment exposed to permanently elevated AA levels

  • Our research demonstrates the following: (1) AA and all analyzed parameters of the fibrinolytic system were elevated in patients with CKD compared with the controls; (2) AA concentrations were associated with levels of urokinase-type plasminogen activator (uPA) and soluble urokinase-type plasminogen activator receptor (suPAR) in the mild-to-moderate CKD subgroup as well as with plasminogen activator inhibitor-1 (PAI-1) and tissue plasminogen activator (tPA) in the severe-to-end-stage CKD subgroup; (3) AA levels are an independent variable for predicting tPA concentrations in the overall CKD group and for uPA levels in the mild-to-moderate CKD subgroup; (4) CKD patients are exposed to chronic inflammation and other conditions specific to progressive deterioration of kidney function, which may affect activation of both the fibrinolytic system and kynurenine pathway (KP)

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Summary

Introduction

Chronic kidney disease (CKD) is an established risk factor for the occurrence of cardiovascular disease (CVD). Patients with CKD suffer from dysfunctions in fibrinolytic activity, manifested by prothrombotic and bleeding tendencies. Increased cardiovascular mortality and morbidity of patients with CKD is considered to be intensified due to increased concentrations of accumulated uremic toxins (UTs) [6, 7]. The initial step that activates the fibrinolytic system is a conversion of plasminogen to plasmin through the influence of plasminogen activators: tissue-type (tPA) or urokinase-type (uPA) [8]. The main inhibitor of fibrinolytic activity is a plasminogen activator inhibitor-1 (PAI-1). The complementary factor of this system, which may regulate procoagulant-hyperfibrinolysis counterbalance, is soluble urokinase-type plasminogen activator receptor (suPAR)—a receptor for uPA in its soluble form [10]

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