AI Article Synopsis

  • The study aimed to investigate the impact of chronic viral hepatitis (PVH) on oxidative stress and the coagulation system in patients undergoing hemodialysis (HD).
  • Markers related to coagulation and fibrinolysis were measured in HD patients with and without PVH, and results showed that those with PVH had significantly higher levels of these markers compared to controls.
  • Overall, the findings suggest that PVH is a key factor contributing to increased oxidative stress and disruptions in the coagulation/fibrinolysis system in HD patients.

Article Abstract

Introduction: The aim of the present study was to establish whether the presence of chronic viral hepatitis (PVH) could be implicated in the elevation of oxidative stress (SOX) and haemostasis system in haemodialysis (HD) patients.

Materials And Methods: In HD patients with and without PVH and in controls we compared the markers of: coagulation pathway- tissue factor (TF) and its inhibitor (TFPI), prothrombin fragment F (1+2) (F (1+2)); fibrinolysis: tissue-type plasminogen activator (tPA), urokinase-type plasminogen activator (uPA) and its soluble receptor (suPAR), plasminogen activator inhibitor 1 (PAI-1), plasmin/antiplasmin complexes (PAP); and a marker of SOX-Cu/Zn superoxide dismutase (Cu/Zn SOD) levels.

Results: Patients, particularly those with PVH, showed a significant increase in the markers of the coagulation, fibrinolysis and oxidative status as compared to controls. All parameters of coagulation/fibrinolysis system were directly associated with the PVH and Cu/Zn SOD levels, and there was a relationship between the PVH and Cu/Zn SOD levels. Multivariable analysis showed that PVH and increased SOX were identified as independent variables significantly associated with the disturbances of coagulation/fibrinolysis system in these patients.

Conclusions: We concluded that PVH is a novel determinant of the increased oxidative stress as well as the disturbances of coagulation/fibrinolysis system in haemodialysis patients.

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Source
http://dx.doi.org/10.1016/j.thromres.2008.02.012DOI Listing

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