Thromb Haemost 1999; 82(04): 1247-1249
DOI: 10.1055/s-0037-1614369
Review Article
Schattauer GmbH

Incidence of Factor IX Inhibitor Development in Severe Haemophilia B Patients Treated with only one Brand of High Purity Plasma Derived Factor IX Concentrate

Armelle Parquet
1   From the Haemophilia Centres of ETS-Lille, France
,
Yves Laurian
2   Haemophilia Centres of Bicêtre, France
,
Chantal Rothschild
3   Haemophilia Centres of Paris-Necker, France
,
Robert Navarro
4   Haemophilia Centres of Montpellier, France
,
Claude Guérois
5   Haemophilia Centres of Tours, France
,
Valérie Gay
6   Haemophilia Centres of Chambéry, France
,
Anne Durin
7   Haemophilia Centres of Lyon, France
,
Jocelyne Peynet
8   Haemophilia Centres of Le Chesnay, France
,
Yvette Sultan
9   Haemophilia Centres of Poitiers, France
› Author Affiliations
Further Information

Publication History

Received 15 May 1998

Accepted after resubmission 21 May 1999

Publication Date:
08 December 2017 (online)

Summary

Fifteen previously untreated patients (Pups) with severe haemophilia B (factor IX activity ≤ 2 U/dl) only treated with one brand of plasma-derived high purity factor IX concentrate (FIX LFB) were studied. Age at first injection varied from 1 to 137 months and follow-up since this first injection from 21 to 86 months (median: 35). Cumulative exposure days (CED) were from 4 to over 100 (median: 26). Among these 15 Pups only one developed an inhibitor. Mutation analysis performed in all patients showed total gene deletion in the patient with inhibitor, partial gene deletion in another one, and missense mutations in 9 families. Mutation was not found in one patient. Actually, according to the data already published, only two patients were at high risk for inhibitor development in our population. Our study, although rather small, confirms the previously reported low incidence of inhibitors in haemophilia B. Large studies on incidence of FIX inhibitors are indeed difficult to perform, due to both the overall small number of severe haemophilia B patients and the low incidence of FIX inhibitors. Consequently, the impact of bias, such as prevalence of different types of gene defects in a given population, is major. Therefore, any study, dealing with incidence of FIX inhibitors in severe haemophilia B should report, for each patient, the type of gene defect.

 
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