Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data

Marika Pane(Università Cattolica del Sacro Cuore), Giorgia Coratti(Università Cattolica del Sacro Cuore), Claudia Brogna(Università Cattolica del Sacro Cuore), Elena Mazzone(Università Cattolica del Sacro Cuore), Anna Mayhew(Centre for Life), Lavinia Fanelli(Università Cattolica del Sacro Cuore), Sonia Messina(University of Messina), Adele D’Amico(Bambino Gesù Children's Hospital), Michela Catteruccia(Bambino Gesù Children's Hospital), Marianna Scutifero(University of Campania "Luigi Vanvitelli"), Silvia Frosini(Fondazione Stella Maris), Valentina Lanzillotta(Istituto Giannina Gaslini), Giulia Colia(Bambino Gesù Children's Hospital), Filippo Cavallaro(University of Messina), Enrica Rolle(Azienda Ospedaliera Citta' della Salute e della Scienza di Torino), Roberto De Sanctis(Università Cattolica del Sacro Cuore), Nicola Forcina(Università Cattolica del Sacro Cuore), Roberta Petillo(University of Campania "Luigi Vanvitelli"), Andrea Barp(University of Padua), Alice Gardani(Fondazione Istituto Neurologico Nazionale Casimiro Mondino), Antonella Pini(Institute of Neurological Sciences), Giulia Monaco(Institute of Neurological Sciences), Maria Grazia D’Angelo(IRCCS Eugenio Medea), Riccardo Zanin(Fondazione IRCCS Istituto Neurologico Carlo Besta), Gian Luca Vita(University of Messina), Claudio Bruno(Istituto Giannina Gaslini), Tiziana Mongini(Azienda Ospedaliera Citta' della Salute e della Scienza di Torino), Federica Ricci(Azienda Ospedaliera Citta' della Salute e della Scienza di Torino), Elena Pegoraro(University of Padua), Luca Bello(University of Padua), Angela Berardinelli(Fondazione Istituto Neurologico Nazionale Casimiro Mondino), Roberta Battini(Fondazione Stella Maris), Valeria Sansone(Centro Clinico Nemo), Emilio Albamonte(Centro Clinico Nemo), Giovanni Baranello(Fondazione IRCCS Istituto Neurologico Carlo Besta), Enrico Bertini(Bambino Gesù Children's Hospital), Luisa Politano(University of Campania "Luigi Vanvitelli"), Maria Pia Sormani(University of Genoa), Eugenio Mercuri(Università Cattolica del Sacro Cuore)
PLoS ONE
June 20, 2018
Cited by 89Open Access
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Abstract

The aim of the study was to establish 24 month changes in upper limb function using a revised version of the performance of upper limb test (PUL 2.0) in a large cohort of ambulant and non-ambulant boys with Duchenne muscular dystrophy and to identify possible trajectories of progression. Of the 187 patients studied, 87 were ambulant (age range: 7-15.8 years), and 90 non-ambulant (age range: 9.08-24.78). The total scores changed significantly over time (p<0.001). Non-ambulant patients had lower total scores at baseline (mean 19.7) when compared to the ambulant ones (mean 38.4). They also had also a bigger decrease in total scores over 24 months compared to the ambulant boys (4.36 vs 2.07 points). Multivariate model analysis showed that the Performance of Upper Limb changes reflected the entry level and ambulation status, that were independently associated to the slope of Performance of Upper Limb changes. This information will be of help both in clinical practice and at the time of designing clinical trials.


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