Evidence map›Paper›PMID 36245386›Full record

ArticleJournal of neuromuscular diseases2022

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

Haitham Elbashir, Waseem Fathalla, Vivek Mundada, Mehtab Iqbal, Asmaa A Al Tawari, Saleel Chandratre, Laila Bastaki, Ingy Romany, Omar Ismayl, Ahmad Abou Tayoun

Open access · hybridAbstract read
In one paragraph

Article in Journal of neuromuscular diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 47% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 2 countries.

Haitham ElbashirNeurosciences Center of Excellence, Al Jalila Children's Hospital, Dubai, United Arab Emirates.
Waseem FathallaSheikh Shakhbout Medical City, Abu Dhabi, United Arab Emirates.
Vivek MundadaMedcare Women and Children Hospital, Dubai, United Arab Emirates.
Mehtab IqbalTawam Hospital, Al Ain, Abu Dhabi, United Arab Emirates.
Asmaa A Al TawariAl Sabah Hospital, Kuwait.
Saleel ChandratreSheikh Khalifa Medical City, Ajman, United Arab Emirates.
Laila BastakiKuwait Medical Genetic Centre, Kuwait.
Ingy RomanyPfizer Gulf FZ LLC, Dubai, United Arab Emirates.
Omar IsmaylSheikh Khalifa Medical City, Abu Dhabi, United Arab Emirates.
Ahmad Abou TayounGenomic Center of Excellence, Al Jalila Children's Hospital, Dubai, United Arab Emirates.
Al Jalila Foundation · AEShaikh Khalifa Medical City · AEAl-Sabah Hospital · KWKuwait Institute for Medical Specialization · KWSheikh Shakhbout Medical City · AETawam Hospital · AE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDuchenne 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.

objectiveGiven 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.

methodsAn 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.

resultsDMD 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.

conclusionThere 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.

Indexed as

Muscular Dystrophy, DuchenneGenetic TestingGenetic TherapyHumansMiddle EastDuchenne muscular dystrophygene therapygenetic disordersmultidisciplinary caremuscle degeneration

Identifiers

PMID36245386
PMCPMC9697043
OpenAlexW4306178571

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.