Haemostatic Parameters in Patients with Behçet’s Disease

Objectives: This study aimed to evaluate the cause of thrombosis in Behçet’s disease (BD) patients, since abnormalities in coagulation and fibrinolytic parameters have shown contradictory results. Methods: Haemostatic parameters were retrospectively evaluated in BD patients treated between January 2...

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Main Authors: Juma K. Alkaabi, David Gravell, Hamood Al-Haddabi, Anil Pathare
Format: Article
Language:English
Published: Sultan Qaboos University 2014-05-01
Series:Sultan Qaboos University Medical Journal
Subjects:
Online Access:https://journals.squ.edu.om/index.php/squmj/article/view/1907
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author Juma K. Alkaabi
David Gravell
Hamood Al-Haddabi
Anil Pathare
author_facet Juma K. Alkaabi
David Gravell
Hamood Al-Haddabi
Anil Pathare
author_sort Juma K. Alkaabi
collection DOAJ
description Objectives: This study aimed to evaluate the cause of thrombosis in Behçet’s disease (BD) patients, since abnormalities in coagulation and fibrinolytic parameters have shown contradictory results. Methods: Haemostatic parameters were retrospectively evaluated in BD patients treated between January 2007 and January 2011 at Sultan Qaboos University Hospital, Oman. The blood samples of 35 Omani BD patients and 30 healthy controls were analysed for factor VIII:C levels, activated protein C resistance (APCR), von Willebrand factor (vWF) antigens (Ag), collagen binding and ristocetin co-factor activity (RiCoF), antithrombin (AT), protein C (chromogenic and clotting), protein S, homocysteine, tissue plasminogen activator, plasminogen activator inhibitor, plasminogen, alpha 2-antiplasmin, lupus anticoagulant and anticardiolipin and beta2-glycoprotein-1 antibodies. Results: The mean values of factor VIII:C, vWF Ag, AT and protein S were significantly higher in the patient group (P = 0.01, 0.006, 0.04 and 0.01, respectively). There was no deficiency in protein C. Screening for APCR, anticardiolipin antibodies, anti-beta2-glycoprotein-1 antibodies and lupus anticoagulant was negative and there were no differences in homocysteine levels, nor were there differences between patients with and without thrombosis. Six patients had elevated factor VIII:C levels (>150 IU/dL, P <0.02) which normalised on repeat measurements after three months. Conclusion: The elevation of factors VIII:C, vWF Ag and AT most likely represent an acute phase phenomenon. In this study, thrombophilic factors did not seem to explain thrombotic tendency. Therefore, further mechanistic studies in a larger group of patients are needed to elucidate the basis for thrombosis in BD. We hypothesise that active BD causes vasculitic endothelial perturbation with dysfunction, leading to the observed increased propensity for thrombosis.
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spelling doaj.art-2448ffdbe12843beb34b95e7fb878c482022-12-22T01:37:54ZengSultan Qaboos UniversitySultan Qaboos University Medical Journal2075-051X2075-05282014-05-011421901961831Haemostatic Parameters in Patients with Behçet’s DiseaseJuma K. Alkaabi0David Gravell1Hamood Al-Haddabi2Anil Pathare3Rheumatology Unit, Department of MedicineDepartment of Haematology, Sultan Qaboos University Hospital, Muscat, OmanDepartment of Haematology, Sultan Qaboos University Hospital, Muscat, OmanDepartment of Haematology, Sultan Qaboos University Hospital, Muscat, OmanObjectives: This study aimed to evaluate the cause of thrombosis in Behçet’s disease (BD) patients, since abnormalities in coagulation and fibrinolytic parameters have shown contradictory results. Methods: Haemostatic parameters were retrospectively evaluated in BD patients treated between January 2007 and January 2011 at Sultan Qaboos University Hospital, Oman. The blood samples of 35 Omani BD patients and 30 healthy controls were analysed for factor VIII:C levels, activated protein C resistance (APCR), von Willebrand factor (vWF) antigens (Ag), collagen binding and ristocetin co-factor activity (RiCoF), antithrombin (AT), protein C (chromogenic and clotting), protein S, homocysteine, tissue plasminogen activator, plasminogen activator inhibitor, plasminogen, alpha 2-antiplasmin, lupus anticoagulant and anticardiolipin and beta2-glycoprotein-1 antibodies. Results: The mean values of factor VIII:C, vWF Ag, AT and protein S were significantly higher in the patient group (P = 0.01, 0.006, 0.04 and 0.01, respectively). There was no deficiency in protein C. Screening for APCR, anticardiolipin antibodies, anti-beta2-glycoprotein-1 antibodies and lupus anticoagulant was negative and there were no differences in homocysteine levels, nor were there differences between patients with and without thrombosis. Six patients had elevated factor VIII:C levels (>150 IU/dL, P <0.02) which normalised on repeat measurements after three months. Conclusion: The elevation of factors VIII:C, vWF Ag and AT most likely represent an acute phase phenomenon. In this study, thrombophilic factors did not seem to explain thrombotic tendency. Therefore, further mechanistic studies in a larger group of patients are needed to elucidate the basis for thrombosis in BD. We hypothesise that active BD causes vasculitic endothelial perturbation with dysfunction, leading to the observed increased propensity for thrombosis.https://journals.squ.edu.om/index.php/squmj/article/view/1907behcet syndromevasculitisblood vesselsthrombosishemostasisoman.
spellingShingle Juma K. Alkaabi
David Gravell
Hamood Al-Haddabi
Anil Pathare
Haemostatic Parameters in Patients with Behçet’s Disease
Sultan Qaboos University Medical Journal
behcet syndrome
vasculitis
blood vessels
thrombosis
hemostasis
oman.
title Haemostatic Parameters in Patients with Behçet’s Disease
title_full Haemostatic Parameters in Patients with Behçet’s Disease
title_fullStr Haemostatic Parameters in Patients with Behçet’s Disease
title_full_unstemmed Haemostatic Parameters in Patients with Behçet’s Disease
title_short Haemostatic Parameters in Patients with Behçet’s Disease
title_sort haemostatic parameters in patients with behcet s disease
topic behcet syndrome
vasculitis
blood vessels
thrombosis
hemostasis
oman.
url https://journals.squ.edu.om/index.php/squmj/article/view/1907
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AT davidgravell haemostaticparametersinpatientswithbehcetsdisease
AT hamoodalhaddabi haemostaticparametersinpatientswithbehcetsdisease
AT anilpathare haemostaticparametersinpatientswithbehcetsdisease