A comparative analysis of different automated von Willebrand factor glycoprotein Ib-binding activity assays in well typed von Willebrand disease patients
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, multicentrická studie
PubMed
29742318
DOI
10.1111/jth.14145
PII: S1538-7836(22)02332-7
Knihovny.cz E-zdroje
- Klíčová slova
- Von Willebrand disease, classification, ristocetin cofactor, subtypes, von Willebrand factor,
- MeSH
- biologické markery krev MeSH
- design vybavení MeSH
- hematologické testy přístrojové vybavení metody MeSH
- laboratorní automatizace MeSH
- lidé MeSH
- prediktivní hodnota testů MeSH
- průřezové studie MeSH
- reprodukovatelnost výsledků MeSH
- trombocytový glykoproteinový komplex Ib-IX metabolismus MeSH
- vazba proteinů MeSH
- von Willebrandova nemoc krev klasifikace diagnóza MeSH
- von Willebrandův faktor metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- srovnávací studie MeSH
- Geografické názvy
- Belgie MeSH
- Česká republika MeSH
- Názvy látek
- biologické markery MeSH
- trombocytový glykoproteinový komplex Ib-IX MeSH
- von Willebrandův faktor MeSH
UNLABELLED: Essentials Von Willebrand ristocetin cofactor activity (VWF:RCo) is not a completely reliable assay. Three automated VWF activity assays were compared within a von Willebrand disease (VWD) cohort. Raw values for all three assays were virtually the same. An overall problem within type 2A/IIE VWD using VWF:GPIb-binding activity/VWF:Ag was observed. SUMMARY: Background von Willebrand disease (VWD) is an inherited bleeding disorder caused by quantitative (type 1 and 3) or qualitative (type 2) von Willebrand factor (VWF) defect. VWD diagnosis and classification require numerous laboratory tests. VWF: glycoprotein Ib (GPIb)-binding activity assays are used to distinguish type 1 from type 2 VWD. Objectives Three different automated VWF:GPIb-binding activity assays were compared. Patients and methods BC-VWF:RCo (Siemens Healthcare Diagnostics), HemosIL® VWF:RCo (Instrumentation Laboratory) and INNOVANCE® VWF:Ac (Siemens Healthcare Diagnostics) were performed in a well typed VWD cohort (n = 142). Results Based on the three most used VWD parameters (FVIII:C, VWF:Ag and VWF:GPIb-binding activity) and using a cut-off of <0.70 for type 2 VWD revealed sensitivity and specificity of, respectively, 92% and 72.4% for VWF:RCo/VWF:Ag, 84% and 89.7% for VWF:GPIbR/VWF:Ag, and 92% and 85.1% for VWF:GPIbM/VWF:Ag, whereas a lowered cut-off of < 0.60 resulted in reduced sensitivity with increased specificity for all assays. Conclusion VWD classification based on FVIII:C, VWF:Ag and VWF:GPIb-binding activity revealed an overall problem with normal VWF:GPIb-binding activity/VWF:Ag within type 2, especially type 2A/IIE. Although all assays were practically identical, BC-VWF:RCo had higher %CV compared with both new assays but comparable lower limit of quantification (LLOQ) ~4 IU dL-1 . No clear improved distinction between type 1 and 2 VWD with new assays was seen. BC-VWF: RCo and HemosIL® are ristocetin dependent, whereas INNOVANCE® does not rely upon ristocetin and is not influenced by VWF polymorphisms increasing VWF:GPIb-binding activity levels. INNOVANCE® seems to be the best choice as a first-line VWF:GPIb-binding activity assay, providing the best balance between sensitivity and specificity for type 2 VWD.
CSL Behring Chair in von Willebrand Disease Antwerp University Antwerp Belgium
Department of Clinical Hematology University Hospital Brno Brno Czech Republic
Department of Laboratory Methods Faculty of Medicine Masaryk University Brno Czech Republic
Department of Paediatric Haematology University Hospital Brno Brno Czech Republic
Diagnostic Haemostasis and Thrombosis Laboratory Viapath Analytics St Thomas' Hospital London UK
Haemostasis Research Unit Antwerp University Antwerp Belgium
Haemostasis Unit Department of Haematology Antwerp University Hospital Edegem Belgium
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