Literature DB >> 22507643

Comparison of type I, type III and type VI collagen binding assays in diagnosis of von Willebrand disease.

V H Flood1, J C Gill, P A Christopherson, J S Wren, K D Friedman, S L Haberichter, R G Hoffmann, R R Montgomery.   

Abstract

BACKGROUND: von Willebrand factor (VWF) plays a key role in coagulation by tethering platelets to injured subendothelium through binding sites for collagen and platelet GPIb. Collagen binding assays (VWF:CB), however, are not part of the routine work-up for von Willebrand disease (VWD).
OBJECTIVES: This study presents data on collagen binding for healthy controls and VWD subjects to compare three different collagens. PATIENTS/
METHODS: VWF antigen (VWF:Ag), VWF ristocetin cofactor activity and VWF:CB with types I, III and VI collagen were examined for samples obtained from the Zimmerman Program.
RESULTS: Mean VWF:CB in healthy controls was similar and highly correlated for types I, III and VI collagen. The mean VWF:CB/VWF:Ag ratios for types I, III and VI collagen were 1.31, 1.19 and 1.21, respectively. In type 1 VWD subjects, VWF:CB was similar to VWF:Ag with mean VWF:CB/VWF:Ag ratios for types I, III and VI collagen of 1.32, 1.08 and 1.1, respectively. For type 2A and 2B subjects, VWF:CB was uniformly low, with mean ratios of 0.62 and 0.7 for type I collagen, 0.38 and 0.4 for type III collagen, and 0.5 and 0.47 for type VI collagen.
CONCLUSIONS: Normal ranges for type I, III and VI collagen are correlated, but higher values were obtained with type I collagen as compared with types III and VI. The low VWF:CB in type 2A and 2B subjects suggests that VWF:CB may also supplement analysis of multimer distribution. However, these results reflect only one set of assay conditions per collagen type and therefore may not be generalizable to all collagen assays.
© 2012 International Society on Thrombosis and Haemostasis.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22507643      PMCID: PMC3809762          DOI: 10.1111/j.1538-7836.2012.04747.x

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN: 1538-7836            Impact factor:   5.824


  28 in total

1.  An ELISA test for the binding of von Willebrand antigen to collagen.

Authors:  J E Brown; J O Bosak
Journal:  Thromb Res       Date:  1986-08-01       Impact factor: 3.944

2.  Effect of ABO blood group on the collagen-binding assay for von Willebrand factor.

Authors:  Erin Haley; Nadiya Babar; Cory Ritter; Katharine A Downes; Deana Green; Susan Shurin; Ravindra Sarode
Journal:  Am J Hematol       Date:  2002-11       Impact factor: 10.047

3.  Coating conditions matter to collagen matrix formation regarding von Willebrand factor and platelet binding.

Authors:  Shlomit Mendelboum Raviv; Katalin Szekeres-Csiki; Attila Jenei; Janos Nagy; Boris Shenkman; Naphtali Savion; Jolan Harsfalvi
Journal:  Thromb Res       Date:  2011-11-05       Impact factor: 3.944

4.  150-kD von Willebrand factor binding protein extracted from human vascular subendothelium is type VI collagen.

Authors:  J H Rand; N D Patel; E Schwartz; S L Zhou; B J Potter
Journal:  J Clin Invest       Date:  1991-07       Impact factor: 14.808

Review 5.  Von Willebrand factor collagen-binding (activity) assay in the diagnosis of von Willebrand disease: a 15-year journey.

Authors:  Emmanuel J Favaloro
Journal:  Semin Thromb Hemost       Date:  2002-04       Impact factor: 4.180

6.  Collagen binding assay for von Willebrand factor (VWF:CBA): detection of von Willebrands Disease (VWD), and discrimination of VWD subtypes, depends on collagen source.

Authors:  E J Favaloro
Journal:  Thromb Haemost       Date:  2000-01       Impact factor: 5.249

7.  An influence of ABO blood group on the rate of proteolysis of von Willebrand factor by ADAMTS13.

Authors:  D J Bowen
Journal:  J Thromb Haemost       Date:  2003-01       Impact factor: 5.824

8.  Isolation and characterization of two domains of human von Willebrand factor that interact with fibrillar collagen types I and III.

Authors:  F I Pareti; K Niiya; J M McPherson; Z M Ruggeri
Journal:  J Biol Chem       Date:  1987-10-05       Impact factor: 5.157

9.  A variant of von Willebrand's disease with abnormal expression of factor VIII procoagulant activity.

Authors:  R R Montgomery; W E Hathaway; J Johnson; L Jacobson; W Muntean
Journal:  Blood       Date:  1982-07       Impact factor: 22.113

10.  Measurement of von Willebrand factor activity: relative effects of ABO blood type and race.

Authors:  C H Miller; E Haff; S J Platt; P Rawlins; C D Drews; A B Dilley; B Evatt
Journal:  J Thromb Haemost       Date:  2003-10       Impact factor: 5.824

View more
  19 in total

1.  Crucial role for the VWF A1 domain in binding to type IV collagen.

Authors:  Veronica H Flood; Abraham C Schlauderaff; Sandra L Haberichter; Tricia L Slobodianuk; Paula M Jacobi; Daniel B Bellissimo; Pamela A Christopherson; Kenneth D Friedman; Joan Cox Gill; Raymond G Hoffmann; Robert R Montgomery
Journal:  Blood       Date:  2015-02-06       Impact factor: 22.113

2.  Translational medicine advances in von Willebrand disease.

Authors:  D Lillicrap
Journal:  J Thromb Haemost       Date:  2013-06       Impact factor: 5.824

3.  Rapid discrimination of the phenotypic variants of von Willebrand disease.

Authors:  Jonathan C Roberts; Patti A Morateck; Pamela A Christopherson; Ke Yan; Raymond G Hoffmann; Joan Cox Gill; Robert R Montgomery
Journal:  Blood       Date:  2016-02-25       Impact factor: 22.113

Review 4.  Diagnostic approach to von Willebrand disease.

Authors:  Christopher Ng; David G Motto; Jorge Di Paola
Journal:  Blood       Date:  2015-02-23       Impact factor: 22.113

Review 5.  Perils, problems, and progress in laboratory diagnosis of von Willebrand disease.

Authors:  Veronica H Flood
Journal:  Semin Thromb Hemost       Date:  2013-12-12       Impact factor: 4.180

6.  The Von Willebrand Factor A1-Collagen III Interaction Is Independent of Conformation and Type 2 Von Willebrand Disease Phenotype.

Authors:  Venkata R Machha; Alexander Tischer; Laurie Moon-Tasson; Matthew Auton
Journal:  J Mol Biol       Date:  2016-11-24       Impact factor: 5.469

7.  Third Åland islands conference on von Willebrand disease, 26-28 September 2012: meeting report.

Authors:  E Berntorp; B Fuchs; M Makris; R Montgomery; V Flood; J S O'Donnell; A B Federici; D Lillicrap; P James; U Budde; M Morfini; P Petrini; S Austin; C Kannicht; V Jiménez-Yuste; C Lee
Journal:  Haemophilia       Date:  2013-03       Impact factor: 4.287

8.  Variability in platelet- and collagen-binding defects in type 2M von Willebrand disease.

Authors:  D M Larsen; S L Haberichter; J C Gill; A D Shapiro; V H Flood
Journal:  Haemophilia       Date:  2013-03-18       Impact factor: 4.287

9.  No increase in bleeding identified in type 1 VWD subjects with D1472H sequence variation.

Authors:  Veronica H Flood; Kenneth D Friedman; Joan Cox Gill; Sandra L Haberichter; Pamela A Christopherson; Brian R Branchford; Raymond G Hoffmann; Thomas C Abshire; Amy L Dunn; Jorge A Di Paola; W Keith Hoots; Deborah L Brown; Cindy Leissinger; Jeanne M Lusher; Margaret V Ragni; Amy D Shapiro; Robert R Montgomery
Journal:  Blood       Date:  2013-03-21       Impact factor: 22.113

10.  Analysis of the role of von Willebrand factor, platelet glycoprotein VI-, and α2β1-mediated collagen binding in thrombus formation.

Authors:  Yasuaki Shida; Natalia Rydz; David Stegner; Christine Brown; Jeffrey Mewburn; Kate Sponagle; Ozge Danisment; Bredon Crawford; Barbara Vidal; Carol A Hegadorn; Cynthia M Pruss; Bernhard Nieswandt; David Lillicrap
Journal:  Blood       Date:  2014-07-22       Impact factor: 22.113

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.