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Evaluation of the diagnostic accuracy of VWF:Ac and VWF Ristocetin Cofactor Activity in the diagnosis of von Willebrand disease

B. Koc1, S. Durmus2, E. Akkaya2, S. Genc3, O. Zulfikar4

1Istanbul University, Oncology Institute, İstanbul, Istanbul, Turkey, 2Istanbul University, Istanbul Faculty of Medicine, Istanbul, Istanbul, Turkey, 3Acibadem Hospital, Maslak , Istanbul, Istanbul, Turkey, 4Istanbul University Oncology Institute, Istanbul, Istanbul, Turkey

Abstract Number: PB0815

Meeting: ISTH 2022 Congress

Theme: Platelet Disorders, von Willebrand Disease and Thrombotic Microangiopathies » VWF and von Willebrand Factor Disorders - Clinical Conditions

Background: VWF antigen (VWF:Ag) and Ristocetin Cofactor activity(VWF:RCo) are initial laboratory tests used in the diagnosis of von Willebrand disease(VWD). Due to the low reproducibility and sensitivity of the VWF:RCo test, the VWF:Ac test has emerged as an alternative diagnostic method, reflecting the binding of plateletGPIb receptors to VWF in the absence of ristocetin.

Aims: The aim of the study was to evaluate the performance of VWF:Ac Innovance (VWF:Ac) and VWF:RCo tests in measuring VWF activity, and to investigate the accuracy and the sensitivity in the diagnosis of VWD.

Methods: The study consisted 40 patients who have been diagnosed VWD previously and 20 healthy subjects. Plasma VWF:Ag, VWF:RCo, VWF:Ac, FVIII activity, platelet aggregation with 0.6mL/1,2mL ristosetin were measured using SysmexXN 6000 coagulation analyzer, and platelet count was measured by Beckman CoulterLH780 hematology analyzer.

Results: The comparison of VWF:RCo with VWF:Ac assay showed good agreement(y=5.4544 + 0.996x,mean bias:0.6). VWFAg levels of type1, type2 and 3 patients were lower than those of control group( p=0.000) being the lowest in type3 patients. VWF:RCo and VWF:Ac were also lower in all types of VWD compared with controls(p=0.011 for type1 and p=0.000 for type2 and 3),VWF:Ac and VWF:RCo in type3 patients were also different than type1(p=0.016, p0.034). FVIII levels were also significantly different than those of control, also,decreased FVIII was obtained in type3 VWD, compared to type1 and 2(p=0.046,p=0.006). Diagnostic value was evaluated by ROC curves; AUC was 0.662 for VWF:RCo/Ag and 0.548 for VWF:Ac/VWFAg for all group.

Conclusion(s): Our results indicate VWF:AC test showed good concordance and aggrement with VWF:RCo. However, we assumed that the VWF activity to antigen ratio had better diagnostic value for the classification of VWF deficiency.

Table 1: VWF:Ag, VWF:RCo, VWF:Ac , FVIII ve RIPA concentrations in type 1, type 2, and type 3 VWDs and healthy controls

Table 1: VWF:Ag, VWF:RCo, VWF:Ac , FVIII ve RIPA concentrations in type 1, type 2, and type 3 VWDs and healthy controls

Figure 1. Diagnostic sensitivity and specificity of VWF:Ag, VWF:RCo, VWF:Ac, VWF:RCo/Ag and VWF:Ac/Ag in diagnosing VWD disease.

Figure 1. Diagnostic sensitivity and specificity of VWF:Ag, VWF:RCo, VWF:Ac, VWF:RCo/Ag and VWF:Ac/Ag in diagnosing VWD disease.

To cite this abstract in AMA style:

Koc B, Durmus S, Akkaya E, Genc S, Zulfikar O. Evaluation of the diagnostic accuracy of VWF:Ac and VWF Ristocetin Cofactor Activity in the diagnosis of von Willebrand disease [abstract]. https://abstracts.isth.org/abstract/evaluation-of-the-diagnostic-accuracy-of-vwfac-and-vwf-ristocetin-cofactor-activity-in-the-diagnosis-of-von-willebrand-disease/. Accessed September 29, 2023.

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