Literature DB >> 20132333

Assessing risk factors: prevention of inhibitors in haemophilia.

H Chambost1.   

Abstract

The formation of antibodies against factor VIII or factor IX that inhibit replacement therapy is currently the most serious treatment-related complication faced by patients with haemophilia. This review highlights non-modifiable and modifiable risk factors that determine the development of these antibodies. The non-modifiable risk factors include patient genotype for haemophilia, immunogenotype, ethnicity and positive family history. Age, intensity of treatment and the type of clotting factor administered are identified as modifiable risk factors. These risk factors are likely to be identified more accurately in forthcoming prospective randomized controlled trials and current patient registries. Through a more complete picture of a patient's overall risk profile, individually tailored treatment schedules might be developed that could minimize the incidence of inhibitor formation and thus maximize therapeutic benefit.

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Year:  2010        PMID: 20132333     DOI: 10.1111/j.1365-2516.2009.02197.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  8 in total

1.  Plasma-derived versus recombinant factor VIII concentrates for the treatment of haemophilia A: plasma-derived is better.

Authors:  Pier Mannuccio Mannucci
Journal:  Blood Transfus       Date:  2010-10       Impact factor: 3.443

2.  Plasma-derived versus recombinant Factor VIII concentrates for the treatment of haemophilia A: recombinant is better.

Authors:  Massimo Franchini
Journal:  Blood Transfus       Date:  2010-10       Impact factor: 3.443

Review 3.  Past, present and future of hemophilia: a narrative review.

Authors:  Massimo Franchini; Pier Mannuccio Mannucci
Journal:  Orphanet J Rare Dis       Date:  2012-05-02       Impact factor: 4.123

4.  Ex Vivo Expanded Autologous Polyclonal Regulatory T Cells Suppress Inhibitor Formation in Hemophilia.

Authors:  Debalina Sarkar; Moanaro Biswas; Gongxian Liao; Howard R Seay; George Q Perrin; David M Markusic; Brad E Hoffman; Todd M Brusko; Cox Terhorst; Roland W Herzog
Journal:  Mol Ther Methods Clin Dev       Date:  2014-07-30       Impact factor: 6.698

Review 5.  Haemophilia and joint disease: pathophysiology, evaluation, and management.

Authors:  Karin Knobe; Erik Berntorp
Journal:  J Comorb       Date:  2011-12-27

6.  Pharmacological modulation of humoral immunity in a nonhuman primate model of AAV gene transfer for hemophilia B.

Authors:  Federico Mingozzi; Yifeng Chen; Samuel L Murphy; Shyrie C Edmonson; Alex Tai; Sandra D Price; Mark E Metzger; Shangzhen Zhou; J Fraser Wright; Robert E Donahue; Cynthia E Dunbar; Katherine A High
Journal:  Mol Ther       Date:  2012-05-08       Impact factor: 11.454

7.  Practice of Iranian Adolescents with Hemophilia in Prevention of Complications of Hemophilia.

Authors:  Leila Valizadeh; Fahimeh Alsadat Hosseini; Vahid Zamanzadeh; Fatemeh Heidarnezhad; Madineh Jasemi; Kamran Bagheri Lankarani
Journal:  Indian J Palliat Care       Date:  2015 Sep-Dec

8.  Polymorphisms in the cytotoxic T lymphocyte-associated protein-4 immune regulatory gene and their impact on inhibitor development in patients with hemophilia A.

Authors:  Aveen M Raouf Abdulqader; Ali Ibrahim Mohammed; Shwan Rachid
Journal:  J Int Med Res       Date:  2019-09-15       Impact factor: 1.671

  8 in total

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