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Age, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular Dystrophy.
Coratti, Giorgia; Lenkowicz, Jacopo; Norcia, Giulia; Lucibello, Simona; Ferraroli, Elisabetta; d'Amico, Adele; Bello, Luca; Pegoraro, Elena; Messina, Sonia; Ricci, Federica; Mongini, Tiziana; Berardinelli, Angela; Masson, Riccardo; Previtali, Stefano C; D'angelo, Grazia; Magri, Francesca; Comi, Giacomo P; Politano, Luisa; Passamano, Luigia; Vita, Gianluca; Sansone, Valeria A; Albamonte, Emilio; Panicucci, Chiara; Bruno, Claudio; Pini, Antonella; Bertini, Enrico; Patarnello, Stefano; Pane, Marika; Mercuri, Eugenio.
Afiliação
  • Coratti G; Pediatric Neurology, Department of Woman and Child Health and Public Health, Child Health Area, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Lenkowicz J; Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
  • Norcia G; Fondazione Policlinico Universitario A.Gemelli IRCCS, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Lucibello S; Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
  • Ferraroli E; Pediatric Neurology, Department of Woman and Child Health and Public Health, Child Health Area, Università Cattolica del Sacro Cuore, Rome, Italy.
  • d'Amico A; Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
  • Bello L; Pediatric Neurology, Department of Woman and Child Health and Public Health, Child Health Area, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Pegoraro E; Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
  • Messina S; Department of Neurosciences, Unit of Neuromuscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, Rome, Italy.
  • Ricci F; Department of Neurosciences, University of Padua, Padua, Italy.
  • Mongini T; Department of Neurosciences, University of Padua, Padua, Italy.
  • Berardinelli A; Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
  • Masson R; Neuromuscular Center, AOU Città della Salute e della Scienza, University of Turin, Torino, Italy.
  • Previtali SC; Neuromuscular Center, AOU Città della Salute e della Scienza, University of Turin, Torino, Italy.
  • D'angelo G; IRCCS Mondino Foundation, Pavia, Italy.
  • Magri F; Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Comi GP; Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
  • Politano L; Scientific Institute IRCCS E. Medea, Bosisio Parini, Italy.
  • Passamano L; Dino Ferrari Centre, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
  • Vita G; Dino Ferrari Centre, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
  • Sansone VA; Cardiomyology and Medical Genetics, University of Campania Luigi Vanvitelli, Naples, Italy.
  • Albamonte E; Cardiomyology and Medical Genetics, University of Campania Luigi Vanvitelli, Naples, Italy.
  • Panicucci C; Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
  • Bruno C; The NEMO Center in Milan, Neurorehabilitation Unit, ASST Niguarda Hospital, University of Milan, Milan, Italy.
  • Pini A; The NEMO Center in Milan, Neurorehabilitation Unit, ASST Niguarda Hospital, University of Milan, Milan, Italy.
  • Bertini E; Center 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.
  • Patarnello S; Center 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.
  • Pane M; Neuromuscular Pediatric Unit, UOC di Neuropsichiatria dell'età pediatrica, IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
  • Mercuri E; Department of Neurosciences, Unit of Neuromuscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, Rome, Italy.
PLoS One ; 17(7): e0271681, 2022.
Article em En | MEDLINE | ID: mdl-35905042
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofina / Distrofia Muscular de Duchenne Tipo de estudo: Prognostic_studies Limite: Child / Child, preschool / Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofina / Distrofia Muscular de Duchenne Tipo de estudo: Prognostic_studies Limite: Child / Child, preschool / Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article