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Gene Therapy for Duchenne Muscular Dystrophy: Unlocking the Opportunities in Countries in the Middle East and Beyond

BACKGROUND: Duchenne muscular dystrophy (DMD) is a severe neuromuscular disorder which leads to progressive muscle degeneration and weakness. Most patients die from cardiac or respiratory failure. Gene transfer therapy offers a promising approach to treating this disorder. OBJECTIVE: Given the genet...

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Autores principales: Elbashir, Haitham, Fathalla, Waseem, Mundada, Vivek, Iqbal, Mehtab, Al Tawari, Asmaa A, Chandratre, Saleel, Bastaki, Laila, Romany, Ingy, Ismayl, Omar, Abou Tayoun, Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9697043/
https://www.ncbi.nlm.nih.gov/pubmed/36245386
http://dx.doi.org/10.3233/JND-221528
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author Elbashir, Haitham
Fathalla, Waseem
Mundada, Vivek
Iqbal, Mehtab
Al Tawari, Asmaa A
Chandratre, Saleel
Bastaki, Laila
Romany, Ingy
Ismayl, Omar
Abou Tayoun, Ahmad
author_facet Elbashir, Haitham
Fathalla, Waseem
Mundada, Vivek
Iqbal, Mehtab
Al Tawari, Asmaa A
Chandratre, Saleel
Bastaki, Laila
Romany, Ingy
Ismayl, Omar
Abou Tayoun, Ahmad
author_sort Elbashir, Haitham
collection PubMed
description BACKGROUND: Duchenne muscular dystrophy (DMD) is a severe neuromuscular disorder which leads to progressive muscle degeneration and weakness. Most patients die from cardiac or respiratory failure. Gene transfer therapy offers a promising approach to treating this disorder. OBJECTIVE: Given the genetic disease burden, family size, and the high consanguinity rates in the Middle East, our objective is to address current practices and challenges of DMD patient care within two countries in this region, namely the United Arab Emirates and Kuwait, and to outline readiness for gene therapy. METHODS: An expert panel meeting was held to discuss the DMD patient journey, disease awareness, current management of DMD, challenges faced and recommendations for improvement. Opportunities and challenges for gene therapy in both countries were also deliberated. A pre-meeting survey was conducted, and the results were used to guide the discussion during the meeting. RESULTS: DMD awareness is poor resulting in a delay in referral and diagnosis of patients. Awareness and education initiatives, along with an interconnected referral system could improve early diagnosis. Genetic testing is available in both countries although coverage varies. Corticosteroid therapy is the standard of care however there is often a delay in treatment initiation. Patients with DMD should be diagnosed and managed by a multi-disciplinary team in centers of excellence for neuromuscular disorders. Key success factors to support the introduction of gene therapy include education and training, timely and accessible genetic testing and resolution of reimbursement and cost issues. CONCLUSION: There are many challenges facing the management of DMD patients in the United Arab Emirates and Kuwait and most likely other countries within the Middle East. Successful introduction of gene therapy to treat DMD will require careful planning, education, capacity building and prioritization of core initiatives.
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spelling pubmed-96970432022-12-08 Gene Therapy for Duchenne Muscular Dystrophy: Unlocking the Opportunities in Countries in the Middle East and Beyond Elbashir, Haitham Fathalla, Waseem Mundada, Vivek Iqbal, Mehtab Al Tawari, Asmaa A Chandratre, Saleel Bastaki, Laila Romany, Ingy Ismayl, Omar Abou Tayoun, Ahmad J Neuromuscul Dis Research Report BACKGROUND: Duchenne muscular dystrophy (DMD) is a severe neuromuscular disorder which leads to progressive muscle degeneration and weakness. Most patients die from cardiac or respiratory failure. Gene transfer therapy offers a promising approach to treating this disorder. OBJECTIVE: Given the genetic disease burden, family size, and the high consanguinity rates in the Middle East, our objective is to address current practices and challenges of DMD patient care within two countries in this region, namely the United Arab Emirates and Kuwait, and to outline readiness for gene therapy. METHODS: An expert panel meeting was held to discuss the DMD patient journey, disease awareness, current management of DMD, challenges faced and recommendations for improvement. Opportunities and challenges for gene therapy in both countries were also deliberated. A pre-meeting survey was conducted, and the results were used to guide the discussion during the meeting. RESULTS: DMD awareness is poor resulting in a delay in referral and diagnosis of patients. Awareness and education initiatives, along with an interconnected referral system could improve early diagnosis. Genetic testing is available in both countries although coverage varies. Corticosteroid therapy is the standard of care however there is often a delay in treatment initiation. Patients with DMD should be diagnosed and managed by a multi-disciplinary team in centers of excellence for neuromuscular disorders. Key success factors to support the introduction of gene therapy include education and training, timely and accessible genetic testing and resolution of reimbursement and cost issues. CONCLUSION: There are many challenges facing the management of DMD patients in the United Arab Emirates and Kuwait and most likely other countries within the Middle East. Successful introduction of gene therapy to treat DMD will require careful planning, education, capacity building and prioritization of core initiatives. IOS Press 2022-11-08 /pmc/articles/PMC9697043/ /pubmed/36245386 http://dx.doi.org/10.3233/JND-221528 Text en © 2022 – The authors. Published by IOS Press https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) License (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Report
Elbashir, Haitham
Fathalla, Waseem
Mundada, Vivek
Iqbal, Mehtab
Al Tawari, Asmaa A
Chandratre, Saleel
Bastaki, Laila
Romany, Ingy
Ismayl, Omar
Abou Tayoun, Ahmad
Gene Therapy for Duchenne Muscular Dystrophy: Unlocking the Opportunities in Countries in the Middle East and Beyond
title Gene Therapy for Duchenne Muscular Dystrophy: Unlocking the Opportunities in Countries in the Middle East and Beyond
title_full Gene Therapy for Duchenne Muscular Dystrophy: Unlocking the Opportunities in Countries in the Middle East and Beyond
title_fullStr Gene Therapy for Duchenne Muscular Dystrophy: Unlocking the Opportunities in Countries in the Middle East and Beyond
title_full_unstemmed Gene Therapy for Duchenne Muscular Dystrophy: Unlocking the Opportunities in Countries in the Middle East and Beyond
title_short Gene Therapy for Duchenne Muscular Dystrophy: Unlocking the Opportunities in Countries in the Middle East and Beyond
title_sort gene therapy for duchenne muscular dystrophy: unlocking the opportunities in countries in the middle east and beyond
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9697043/
https://www.ncbi.nlm.nih.gov/pubmed/36245386
http://dx.doi.org/10.3233/JND-221528
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