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Parameters influencing FVIII pharmacokinetics in patients with severe and moderate haemophilia A.
Kepa, S; Horvath, B; Reitter-Pfoertner, S; Schemper, M; Quehenberger, P; Grundbichler, M; Heistinger, M; Neumeister, P; Mannhalter, C; Pabinger, I.
Afiliação
  • Kepa S; Clinical Division of Haematology and Haemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
  • Horvath B; Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
  • Reitter-Pfoertner S; Clinical Division of Haematology and Haemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
  • Schemper M; Center for Medical Statistics, Informatics and Intelligent Systems, Medical University of Vienna, Vienna, Austria.
  • Quehenberger P; Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
  • Grundbichler M; Division of Haematology and Oncology, Department of Internal Medicine III, Medical University of Salzburg, Salzburg, Austria.
  • Heistinger M; Department of Internal Medicine I, Clinical Centre of Klagenfurt am Woerthersee, Klagenfurt am Woerthersee, Austria.
  • Neumeister P; Division of Haematology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
  • Mannhalter C; Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
  • Pabinger I; Clinical Division of Haematology and Haemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Haemophilia ; 21(3): 343-350, 2015 May.
Article em En | MEDLINE | ID: mdl-25582282
In haemophilia A patients factor VIII (FVIII) recovery and half-life can vary substantially. There are parameters known to modulate FVIII pharmacokinetics (PK), but they explain only about 34% of the variability. The aim of this study was to identify new parameters that influence FVIII PK and thus to expand the current knowledge. FVIII PK were determined in 42 haemophilia A patients (37 severe, 5 moderate) without inhibitor. Patients' characteristics and laboratory parameters were evaluated for an association with FVIII PK. We analysed plasma levels of low-density lipoprotein receptor-related protein 1 (LRP1) and protein C (PC) activity, which had been hypothesized to influence FVIII activity. Furthermore, four variations in intron 6 of the LRP1 gene, which had been shown to influence LRP1, were investigated. FVIII half-life differed widely from 6.2 to 20.7 h, with a median of 10.0 h. Patients with blood group O had shorter FVIII half-life compared to patients with non-O blood group (median FVIII half-life 9.0 h vs. 10.4 h, P = 0.018). Age was significantly associated with FVIII half-life (r = 0.32, P = 0.035). Besides age, also VWF antigen (r = 0.52, P < 0.001) and blood group (r = -0.37, P = 0.015) was associated with FVIII half-life. No correlation was found with FVIII- or LRP1-genotype, LRP1 or PC concentrations. Our data showed large differences in FVIII PK between individual patients and revealed age, blood group and VWF levels as important determining factors for FVIII half-life. FVIII genotype or levels of LRP1 or PC had no influence on FVIII PK.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Recombinantes / Fator VIII / Hemofilia A Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Humans / Male Idioma: En Revista: Haemophilia Assunto da revista: HEMATOLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Áustria

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Recombinantes / Fator VIII / Hemofilia A Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Humans / Male Idioma: En Revista: Haemophilia Assunto da revista: HEMATOLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Áustria