Back to Search Start Over

Rapid discrimination of the phenotypic variants of von Willebrand disease.

Authors :
Roberts, Jonathan C.
Morateck, Patti A.
Christopherson, Pamela A.
Ke Yan
Hoffmann, Raymond G.
Gill, Joan Cox
Montgomery, Robert R.
Source :
Blood. 5/19/2016, Vol. 127 Issue 20, p2472-2480. 9p.
Publication Year :
2016

Abstract

Approximately 20% to 25% of patients with von Willebrand disease (VWD) have a qualitative defect of the von Willebrand factor (VWF) protein activities. Variant VW Dtypically is classified as type 1C, 2A, 2B, 2M, or 2N depending on the VWF activity defect. Traditionally, diagnosis has relied on multiple clinical laboratory assays to assign VWD phenotype. We developed an enzyme-linked immunosorbent assay (ELISA) to measure the various activities of VWF on a single plate and evaluated 160 patient samples enrolled in the Zimmerman Program for the Molecular and Clinical Biology of von Willebrand Disease with type 2 VWD. Using linear discriminate analysis (LDA), this assay was able to identify type 1C, 2A, 2B, 2M, or 2N VWD with an overall accuracy of 92.5% in the patient study cohort. LDA jackknife analysis, a statistical resampling technique, identified variant VWD with an overall accuracy of 88.1%, which predicts the assay's performance in the general population. In addition, this assay demonstrated correlation with traditional clinical laboratory VWF assays. The VWF multiplex activity assay may be useful as a same-day screening assay when considering the diagnosis of variant VWD in an individual patient. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00064971
Volume :
127
Issue :
20
Database :
Academic Search Index
Journal :
Blood
Publication Type :
Academic Journal
Accession number :
115473654
Full Text :
https://doi.org/10.1182/blood-2015-11-664680