Literature DB >> 20704648

In non-severe hemophilia A the risk of inhibitor after intensive factor treatment is greater in older patients: a case-control study.

C L Kempton1, J M Soucie, C H Miller, C Hooper, M A Escobar, A J Cohen, N S Key, A R Thompson, T C Abshire.   

Abstract

BACKGROUND: Twenty-five percent of new anti-factor VIII (FVIII) antibodies (inhibitors) that complicate hemophilia A occur in those with mild and moderate disease. Although intensive FVIII treatment has long been considered a risk factor for inhibitor development in those with non-severe disease, its strength of association and the influence of other factors have remained undefined.
OBJECTIVE: To evaluate risk factors for inhibitor development in patients with non-severe hemophilia A.
METHODS: Information on clinical and demographic variables and FVIII genotype was collected on 36 subjects with mild or moderate hemophilia A and an inhibitor and 62 controls also with mild or moderate hemophilia A but without an inhibitor.
RESULTS: Treatment with FVIII for six or more consecutive days during the prior year was more strongly associated with inhibitor development in those ≥30years of age compared with those <30years of age [adjusted odds ratio (OR) 12.62; 95% confidence interval (CI), 2.76-57.81 vs. OR 2.54; 95% CI, 0.61-10.68]. Having previously received <50days of FVIII was also not statistically associated with inhibitor development on univariate or multivariate analysis.
CONCLUSIONS: These findings suggest that inhibitor development in mild and moderate hemophilia A varies with age, but does not vary significantly with lifetime FVIII exposure days: two features distinct from severe hemophilia A.
© 2010 International Society on Thrombosis and Haemostasis.

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Year:  2010        PMID: 20704648      PMCID: PMC3612936          DOI: 10.1111/j.1538-7836.2010.04013.x

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


  16 in total

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2.  Factor VIII inhibitors in mild and moderate-severity haemophilia A. UK Haemophilia Centre Directors Organisation.

Authors:  C R Hay; C A Ludlam; B T Colvin; F G Hill; F E Preston; N Wasseem; R Bagnall; I R Peake; E Berntorp; E P Mauser Bunschoten; K Fijnvandraat; C K Kasper; G White; E Santagostino
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Review 3.  Mild hemophilia A.

Authors:  M Franchini; E J Favaloro; G Lippi
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4.  Factor VIII inhibitors in two families with mild haemophilia A: structural analysis of the mutations.

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Journal:  Haemostasis       Date:  2000 Sep-Oct

5.  The factor VIII Structure and Mutation Resource Site: HAMSTeRS version 4.

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Review 6.  Intensive exposure to factor VIII is a risk factor for inhibitor development in mild hemophilia A.

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Review 7.  Environmental and genetic factors influencing inhibitor development.

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Authors:  J Michael Soucie; Christy Cianfrini; Robert L Janco; Roshni Kulkarni; Julie Hambleton; Bruce Evatt; Angela Forsyth; Sue Geraghty; Keith Hoots; Tom Abshire; Randall Curtis; Ann Forsberg; Heather Huszti; Margaret Wagner; Gilbert C White
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10.  The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977-99.

Authors:  S C Darby; D M Keeling; R J D Spooner; S Wan Kan; P L F Giangrande; P W Collins; F G H Hill; C R M Hay
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2.  Factor VIII gene variants and inhibitor risk in African American hemophilia A patients.

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Review 5.  Genotypes, phenotypes and whole genome sequence: Approaches from the My Life Our Future haemophilia project.

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6.  Factor VIII A3 domain substitution N1922S results in hemophilia A due to domain-specific misfolding and hyposecretion of functional protein.

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7.  HLA-DRB1-factor VIII binding is a risk factor for inhibitor development in nonsevere hemophilia: a case-control study.

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8.  Factor VIII inhibitors in hemophilia A: rationale and latest evidence.

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9.  Low-dose continuous infusion of factor VIII in patients with haemophilia A.

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10.  Navigating Speed Bumps on the Innovation Highway in Hemophilia Therapeutics.

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