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Influence of blood group, von Willebrand factor levels, and age on factor VIII levels in non‐severe haemophilia A
- Source :
- Journal of Thrombosis and Haemostasis
- Publication Year :
- 2020
- Publisher :
- Elsevier BV, 2020.
-
Abstract
- Background Data on the effect of ABO blood group (ABO), von Willebrand factor (VWF) levels, and age on factor VIII (FVIII) in non-severe haemophilia A (HA) is scarce. Objective To investigate if ABO, VWF levels, and age have an influence on the variability of FVIII levels and consequently on the assessment of severity in non-severe HA. Patients/methods Eighty-nine patients with non-severe HA and 82 healthy controls were included. Data on ABO was collected and FVIII clotting activity (FVIII:C) with one-stage clotting assay (FVIII:C OSA) and chromogenic substrate assay (FVIII:C CSA), FVIII antigen (FVIII:Ag) and VWF antigen (VWF:Ag) and activity (VWF:Act) were determined. Results In HA, FVIII:C OSA and CSA and FVIII:Ag were not different between non-O (n = 42, median 15.5, interquartile range 10.4-24.0; 10.0, 6.8-26.0 and 15.2, 10.7-24.9) and O (n = 47, 14.1, 9.0-23.0; 10.0, 5.0-23.0 and 15.2, 9.3-35.5), whereas in healthy controls, non-O individuals had significantly higher FVIII levels. Fviii C showed no relevant correlation with VWF levels in HA, but we observed strong correlations in healthy controls. Age had only a minor influence in HA, but had a considerable impact on FVIII:C in healthy controls. In multivariable regression analysis ABO, VWF:Ag and age were not associated with FVIII:C in HA, whereas this model explained 61.3% of the FVIII:C variance in healthy controls. Conclusions We conclude that in non-severe HA ABO and VWF levels do not substantially influence the variability of FVIII levels and age has only minor effects on it, which is important information for diagnostic procedures.
- Subjects :
- congenital, hereditary, and neonatal diseases and abnormalities
medicine.medical_specialty
animal diseases
Haemophilia A
haemophilia A
030204 cardiovascular system & hematology
Hemophilia A
ABO Blood-Group System
diagnostic techniques and procedures
03 medical and health sciences
0302 clinical medicine
Von Willebrand factor
Antigen
Interquartile range
hemic and lymphatic diseases
ABO blood group system
Internal medicine
von Willebrand Factor
medicine
Humans
Factor VIII
biology
business.industry
Brief Report
HAEMOSTASIS
Background data
Chromogenic substrate assay
Hematology
medicine.disease
von Willebrand Diseases
Endocrinology
Blood Grouping and Crossmatching
ABO blood‐group system
biology.protein
Brief Reports
Severe haemophilia A
business
Subjects
Details
- ISSN :
- 15387836
- Volume :
- 18
- Database :
- OpenAIRE
- Journal :
- Journal of Thrombosis and Haemostasis
- Accession number :
- edsair.doi.dedup.....6ce8cf2c05bfc23f53bd0a000bb63710