Cargando…

Factor VIII companion diagnostic for haemophilia

Haemophilia is predominantly an inherited disorder that impairs the body’s ability to make blood clots, a process needed to stop bleeding. The condition of this disease is complex to manage, but many patients do so through home therapy and often only see their core multidisciplinary healthcare team...

Descripción completa

Detalles Bibliográficos
Autores principales: Hu, Chunxiao, Annese, Valerio F., Giagkoulovits, Christos, Barrett, Michael P., Cumming, David R. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9579283/
https://www.ncbi.nlm.nih.gov/pubmed/36277382
http://dx.doi.org/10.3389/fbioe.2022.1006600
_version_ 1784812146098438144
author Hu, Chunxiao
Annese, Valerio F.
Giagkoulovits, Christos
Barrett, Michael P.
Cumming, David R. S.
author_facet Hu, Chunxiao
Annese, Valerio F.
Giagkoulovits, Christos
Barrett, Michael P.
Cumming, David R. S.
author_sort Hu, Chunxiao
collection PubMed
description Haemophilia is predominantly an inherited disorder that impairs the body’s ability to make blood clots, a process needed to stop bleeding. The condition of this disease is complex to manage, but many patients do so through home therapy and often only see their core multidisciplinary healthcare team annually. There is an increasing need for patients to be able to monitor their condition efficiently at home while staying connected with their healthcare team. As a consequence, a low-cost handheld self-monitoring solution for clotting factor is required. Here we have demonstrated a suitable one-step Factor VIII companion diagnostic sensing approach based on a chromogenic assay for haemophilia A. The results show comparable performance to the gold standard method. Our approach is able to deliver accurate cost-effective results in under 5 min from undiluted human plasma. It has the potential to be able to reduce the human and monetary costs of over- or under-medication for haemophiliacs.
format Online
Article
Text
id pubmed-9579283
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-95792832022-10-20 Factor VIII companion diagnostic for haemophilia Hu, Chunxiao Annese, Valerio F. Giagkoulovits, Christos Barrett, Michael P. Cumming, David R. S. Front Bioeng Biotechnol Bioengineering and Biotechnology Haemophilia is predominantly an inherited disorder that impairs the body’s ability to make blood clots, a process needed to stop bleeding. The condition of this disease is complex to manage, but many patients do so through home therapy and often only see their core multidisciplinary healthcare team annually. There is an increasing need for patients to be able to monitor their condition efficiently at home while staying connected with their healthcare team. As a consequence, a low-cost handheld self-monitoring solution for clotting factor is required. Here we have demonstrated a suitable one-step Factor VIII companion diagnostic sensing approach based on a chromogenic assay for haemophilia A. The results show comparable performance to the gold standard method. Our approach is able to deliver accurate cost-effective results in under 5 min from undiluted human plasma. It has the potential to be able to reduce the human and monetary costs of over- or under-medication for haemophiliacs. Frontiers Media S.A. 2022-10-05 /pmc/articles/PMC9579283/ /pubmed/36277382 http://dx.doi.org/10.3389/fbioe.2022.1006600 Text en Copyright © 2022 Hu, Annese, Giagkoulovits, Barrett and Cumming. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Hu, Chunxiao
Annese, Valerio F.
Giagkoulovits, Christos
Barrett, Michael P.
Cumming, David R. S.
Factor VIII companion diagnostic for haemophilia
title Factor VIII companion diagnostic for haemophilia
title_full Factor VIII companion diagnostic for haemophilia
title_fullStr Factor VIII companion diagnostic for haemophilia
title_full_unstemmed Factor VIII companion diagnostic for haemophilia
title_short Factor VIII companion diagnostic for haemophilia
title_sort factor viii companion diagnostic for haemophilia
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9579283/
https://www.ncbi.nlm.nih.gov/pubmed/36277382
http://dx.doi.org/10.3389/fbioe.2022.1006600
work_keys_str_mv AT huchunxiao factorviiicompaniondiagnosticforhaemophilia
AT annesevaleriof factorviiicompaniondiagnosticforhaemophilia
AT giagkoulovitschristos factorviiicompaniondiagnosticforhaemophilia
AT barrettmichaelp factorviiicompaniondiagnosticforhaemophilia
AT cummingdavidrs factorviiicompaniondiagnosticforhaemophilia