Evidence map›Paper›PMID 34498054›Full record

ArticleJournal of neuropathology and experimental neurology2021

High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients.

Silvia Torelli, Domenic Scaglioni, Valentina Sardone, Matthew J Ellis, Joana Domingos, Adam Jones, Lucy Feng, Darren Chambers, Deborah M Eastwood, France Leturcq and 15 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of neuropathology and experimental neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

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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

25 authors at 11 institutions in 3 countries.

Silvia TorelliFrom the Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0002-8840-6835
Domenic ScaglioniFrom the Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London, UK.
Valentina SardoneFrom the Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London, UK.
Matthew J EllisFrom the Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London, UK.
Joana DomingosFrom the Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London, UK.
Adam JonesFrom the Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London, UK.
Lucy FengDubowitz Neuromuscular Centre, UCL Queen Square Institute of Neurology & Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Darren ChambersFrom the Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London, UK.
Deborah M EastwoodDepartment of Orthopaedics, Great Ormond Street Hospital, London, UK.
France LeturcqAPHP, Laboratoire de Génétique et Biologie Moléculaire, HUPC Hôpital Cochin, Paris, France.
Rabah Ben YaouAPHP, Laboratoire de Génétique et Biologie Moléculaire, HUPC Hôpital Cochin, Paris, France.
Andoni UrtizbereaAPHP-Hôpital Marin de Hendaye, Hendaye, France.
Pascal SabouraudCHU de Reims-American Memorial Hospital, Reims, France.
Christine BarneriasDepartment of Pediatric Neurology, Necker Enfants Maladies Hospital, Paris, France.
Tanya StojkovicSorbonne Université, Inserm, Institut de Myologie, Center de Recherche en Myologie, Paris, France.
Enzo RicciInstitute of Neurology, Catholic University, Rome, Italy.
Maud BeuvinAPHP-Sorbonne Université, Centre de Référence Maladies Neuromusculaires Nord/Est/Ile de France, Institut de Myologie, GH Pitié-Salpêtrière, Paris, France.
Gisele BonneAPHP-Sorbonne Université, Centre de Référence Maladies Neuromusculaires Nord/Est/Ile de France, Institut de Myologie, GH Pitié-Salpêtrière, Paris, France.
Caroline A SewryWolfson Centre for Inherited Neuromuscular Diseases and Department of Musculoskeletal Histopathology, RJAH Orthopaedic Hospital, Oswestry, UK.
Tracey WillisWolfson Centre for Inherited Neuromuscular Diseases and Department of Musculoskeletal Histopathology, RJAH Orthopaedic Hospital, Oswestry, UK.
Richa KulshresthaWolfson Centre for Inherited Neuromuscular Diseases and Department of Musculoskeletal Histopathology, RJAH Orthopaedic Hospital, Oswestry, UK.
Giorgio TascaUOC di Neurologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Rahul PhadkeDubowitz Neuromuscular Centre, UCL Queen Square Institute of Neurology & Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Jennifer E MorganDepartment of Neurodegenerative Diseases, UCL Queen Square Institute of Neurology, London, UK.
Francesco MuntoniFrom the Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London, UK.
Great Ormond Street Hospital · GBRobert Jones and Agnes Hunt Orthopaedic Hospital · GBGreat Ormond Street Hospital for Children NHS Foundation Trust · GBInserm · FRSorbonne Université · FRAgostino Gemelli University Polyclinic · ITCentre Hospitalier Universitaire de Reims · FRHôpital Cochin · FRHôpital Marin de Hendaye · FRNational Hospital for Neurology and Neurosurgery · GBUniversità Cattolica del Sacro Cuore · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Duchenne muscular dystrophy (DMD) is an incurable disease caused by out-of-frame DMD gene deletions while in frame deletions lead to the milder Becker muscular dystrophy (BMD). In the last decade several antisense oligonucleotides drugs have been developed to induce a partially functional internally deleted dystrophin, similar to that produced in BMD, and expected to ameliorate the disease course. The pattern of dystrophin expression and functionality in dystrophinopathy patients is variable due to multiple factors, such as molecular functionality of the dystrophin and its distribution. To benchmark the success of therapeutic intervention, a clear understanding of dystrophin expression patterns in dystrophinopathy patients is vital. Recently, several groups have used innovative techniques to quantify dystrophin in muscle biopsies of children but not in patients with milder BMD. This study reports on dystrophin expression using both Western blotting and an automated, high-throughput, image analysis platform in DMD, BMD, and intermediate DMD/BMD skeletal muscle biopsies. Our results found a significant correlation between Western blot and immunofluorescent quantification indicating consistency between the different methodologies. However, we identified significant inter- and intradisease heterogeneity of patterns of dystrophin expression in patients irrespective of the amount detected on blot, due to variability in both fluorescence intensity and dystrophin sarcolemmal circumference coverage. Our data highlight the heterogeneity of the pattern of dystrophin expression in BMD, which will assist the assessment of dystrophin restoration therapies.

Indexed as

AdolescentChildChild, PreschoolDystrophinFemaleGene ExpressionHigh-Throughput Screening AssaysHumansMaleMolecular ImagingMuscular Dystrophy, DuchenneDMD protein, humanDystrophinBecker muscular dystrophyDuchenne muscular dystrophyDystrophinHigh–throughput digital analysisMuscle biopsySkeletal muscle

Identifiers

PMID34498054
PMCPMC8557329
OpenAlexW3197426383

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Registered trials

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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.