Evidence map›Paper›PMID 35905042›Full record

ArticlePloS one2022

Age, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular Dystrophy.

Giorgia Coratti, Jacopo Lenkowicz, Giulia Norcia, Simona Lucibello, Elisabetta Ferraroli, Adele d'Amico, Luca Bello, Elena Pegoraro, Sonia Messina, Federica Ricci and 20 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 12 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

30 authors at 13 institutions in 1 country.

Giorgia CorattiPediatric Neurology, Department of Woman and Child Health and Public Health, Child Health Area, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID 0000-0001-6666-5628
Jacopo LenkowiczFondazione Policlinico Universitario A.Gemelli IRCCS, Università Cattolica del Sacro Cuore, Rome, Italy.
Giulia NorciaCentro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Simona LucibelloPediatric Neurology, Department of Woman and Child Health and Public Health, Child Health Area, Università Cattolica del Sacro Cuore, Rome, Italy.
Elisabetta FerraroliPediatric Neurology, Department of Woman and Child Health and Public Health, Child Health Area, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID 0000-0002-2004-8330
Adele d'AmicoDepartment of Neurosciences, Unit of Neuromuscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, Rome, Italy.
Luca BelloDepartment of Neurosciences, University of Padua, Padua, Italy.
Elena PegoraroDepartment of Neurosciences, University of Padua, Padua, Italy.
Sonia MessinaDepartment of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Federica RicciNeuromuscular Center, AOU Città della Salute e della Scienza, University of Turin, Torino, Italy.
Tiziana MonginiNeuromuscular Center, AOU Città della Salute e della Scienza, University of Turin, Torino, Italy.
Angela BerardinelliIRCCS Mondino Foundation, Pavia, Italy.
Riccardo MassonFondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Stefano C PrevitaliDivision of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Grazia D'angeloScientific Institute IRCCS E. Medea, Bosisio Parini, Italy.
Francesca MagriDino Ferrari Centre, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
Giacomo P ComiDino Ferrari Centre, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
Luisa PolitanoCardiomyology and Medical Genetics, University of Campania Luigi Vanvitelli, Naples, Italy.ORCID 0000-0002-0925-7158
Luigia PassamanoCardiomyology and Medical Genetics, University of Campania Luigi Vanvitelli, Naples, Italy.
Gianluca VitaDepartment of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Valeria A SansoneThe NEMO Center in Milan, Neurorehabilitation Unit, ASST Niguarda Hospital, University of Milan, Milan, Italy.
Emilio AlbamonteThe NEMO Center in Milan, Neurorehabilitation Unit, ASST Niguarda Hospital, University of Milan, Milan, Italy.
Chiara PanicucciCenter of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, and Department of Neuroscience, Rehabilitation, Ophtalmology, Genetics, Maternal and Child Health-DINOGMI, University of Genova, Genoa, Italy.ORCID 0000-0003-4571-611X
Claudio BrunoCenter of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, and Department of Neuroscience, Rehabilitation, Ophtalmology, Genetics, Maternal and Child Health-DINOGMI, University of Genova, Genoa, Italy.
Antonella PiniNeuromuscular Pediatric Unit, UOC di Neuropsichiatria dell'età pediatrica, IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
Enrico BertiniDepartment of Neurosciences, Unit of Neuromuscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, Rome, Italy.
Stefano PatarnelloFondazione Policlinico Universitario A.Gemelli IRCCS, Università Cattolica del Sacro Cuore, Rome, Italy.
Marika PanePediatric Neurology, Department of Woman and Child Health and Public Health, Child Health Area, Università Cattolica del Sacro Cuore, Rome, Italy.
Eugenio MercuriPediatric Neurology, Department of Woman and Child Health and Public Health, Child Health Area, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID 0000-0002-9851-5365
italian DMD study group
Università Cattolica del Sacro Cuore · ITUniversity of Milan · ITAzienda Ospedaliera Citta' della Salute e della Scienza di Torino · ITBambino Gesù Children's Hospital · ITIstituto Giannina Gaslini · ITUniversity of Campania "Luigi Vanvitelli" · ITUniversity of Messina · ITUniversity of Padua · ITAgostino Gemelli University Polyclinic · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITIRCCS Eugenio Medea · ITIstituto delle Scienze Neurologiche di Bologna · ITVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to establish the possible effect of age, corticosteroid treatment and brain dystrophin involvement on motor function in young boys affected by Duchenne Muscular Dystrophy who were assessed using the North Star Ambulatory Assessment between the age of 4 and 7 years. The study includes 951 North Star assessments from 226 patients. Patients were subdivided according to age, to the site of mutation and therefore to the involvement of different brain dystrophin isoforms and to corticosteroids duration. There was a difference in the maximum North Star score achieved among patients with different brain dystrophin isoforms (p = 0.007). Patients with the involvement of Dp427, Dp140 and Dp71, had lower maximum NSAA scores when compared to those with involvement of Dp427 and Dp140 or of Dp427 only. The difference in the age when the maximum score was achieved in the different subgroups did not reach statistical significance. Using a linear regression model on all assessments we found that each of the three variables, age, site of mutation and corticosteroid treatment had an influence on the NSAA values and their progression over time. A second analysis, looking at 12-month changes showed that within this time interval the magnitude of changes was related to corticosteroid treatment but not to site of mutation. Our findings suggest that each of the considered variables appear to play a role in the progression of North Star scores in patients between the age of 4 and 7 years and that these should be carefully considered in the trial design of boys in this age range.

Indexed as

DystrophinMuscular Dystrophy, DuchenneAdrenal Cortex HormonesChildChild, PreschoolHumansMaleMutationProtein IsoformsAdrenal Cortex HormonesDystrophinProtein Isoforms

Identifiers

PMID35905042
PMCPMC9337636
OpenAlexW4288713859

What OpenQuestion holds

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LicenceCC BY
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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.