The national blueprint for pregnancy/birth longitudinal cohorts to study factor VIII immunogenicity: NHLBI State of the Science (SOS) Workshop on factor VIII inhibitors.


Journal

Haemophilia : the official journal of the World Federation of Hemophilia
ISSN: 1365-2516
Titre abrégé: Haemophilia
Pays: England
ID NLM: 9442916

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 29 11 2018
revised: 03 02 2019
accepted: 21 02 2019
entrez: 23 7 2019
pubmed: 23 7 2019
medline: 19 12 2019
Statut: ppublish

Résumé

Patients with haemophilia can develop inhibitors to exogenous coagulation factors. Some patients are tolerant to factor, while those who develop inhibitors do so early in life. Genetics and environmental factors are known to contribute to inhibitor risk. However, it is not yet possible to predict inhibitor formation or treatment responsiveness in individuals. We hypothesize that factors in the antenatal/neonatal period inform inhibitor risk development. To consider the design of longitudinal studies beginning in the antenatal/neonatal period and the use of new technologies to better understand haemophilia inhibitors. A working group was formed for the NHLBI State of the Science Workshop: Factor VIII Inhibitors: Generating a National Blueprint for Future Research to solicit input from the US haemophilia community and international collaborators to consider design of pregnancy/birth longitudinal cohorts that leverage -omics, existing phenotypic data, and in silico modelling to study inhibitors. An antenatal/neonatal longitudinal cohort should begin with enrolment of pregnant genetic carriers of haemophilia and span the at-risk period for inhibitor development in the child. Data and samples from the mother, placenta, neonate and young child can be obtained that are amenable to existing assays, genomics and other -omics studies. Data can inform in silico prediction and mathematical models. A longitudinal study beginning before birth offers the unique opportunity to study factors that influence inhibitor development prior to exposure. Advances in -omics and computational biology can study complex phenotypes in this rare disease. This study could be accomplished through interdisciplinary efforts and patient community engagement.

Identifiants

pubmed: 31329365
doi: 10.1111/hae.13739
doi:

Substances chimiques

Factor VIII 9001-27-8

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

603-609

Subventions

Organisme : Shire Corporation

Informations de copyright

© 2019 John Wiley & Sons Ltd.

Auteurs

Jill M Johnsen (JM)

Bloodworks Northwest Research Institute, Seattle, Washington.
Washington Center for Bleeding Disorders, Seattle, Washington.
Department of Medicine, University of Washington, Seattle, Washington.

Deborah L Brown (DL)

University of Texas Health Science Center, Houston, Texas.
MD Anderson Cancer Center, Houston, Texas.
Gulf States Hemophilia and Thrombophilia Treatment Center, Houston, Texas.

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