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North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up

INTRODUCTION: The aim of this study was to report 36-month longitudinal changes using the North Star Ambulatory Assessment (NSAA) in ambulant patients affected by Duchenne muscular dystrophy amenable to skip exons 44, 45, 51 or 53. MATERIALS AND METHODS: We included 101 patients, 34 had deletions am...

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Autores principales: Coratti, Giorgia, Pane, Marika, Brogna, Claudia, Ricotti, Valeria, Messina, Sonia, D’Amico, Adele, Bruno, Claudio, Vita, Gianluca, Berardinelli, Angela, Mazzone, Elena, Magri, Francesca, Ricci, Federica, Mongini, Tiziana, Battini, Roberta, Bello, Luca, Pegoraro, Elena, Baranello, Giovanni, Previtali, Stefano C., Politano, Luisa, Comi, Giacomo P., Sansone, Valeria A., Donati, Alice, Hogrel, Jean Yves, Straub, Volker, De Lucia, Silvana, Niks, Erik, Servais, Laurent, De Groot, Imelda, Chesshyre, Mary, Bertini, Enrico, Goemans, Nathalie, Muntoni, Francesco, Mercuri, Eugenio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232423/
https://www.ncbi.nlm.nih.gov/pubmed/34170974
http://dx.doi.org/10.1371/journal.pone.0253882
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author Coratti, Giorgia
Pane, Marika
Brogna, Claudia
Ricotti, Valeria
Messina, Sonia
D’Amico, Adele
Bruno, Claudio
Vita, Gianluca
Berardinelli, Angela
Mazzone, Elena
Magri, Francesca
Ricci, Federica
Mongini, Tiziana
Battini, Roberta
Bello, Luca
Pegoraro, Elena
Baranello, Giovanni
Previtali, Stefano C.
Politano, Luisa
Comi, Giacomo P.
Sansone, Valeria A.
Donati, Alice
Hogrel, Jean Yves
Straub, Volker
De Lucia, Silvana
Niks, Erik
Servais, Laurent
De Groot, Imelda
Chesshyre, Mary
Bertini, Enrico
Goemans, Nathalie
Muntoni, Francesco
Mercuri, Eugenio
author_facet Coratti, Giorgia
Pane, Marika
Brogna, Claudia
Ricotti, Valeria
Messina, Sonia
D’Amico, Adele
Bruno, Claudio
Vita, Gianluca
Berardinelli, Angela
Mazzone, Elena
Magri, Francesca
Ricci, Federica
Mongini, Tiziana
Battini, Roberta
Bello, Luca
Pegoraro, Elena
Baranello, Giovanni
Previtali, Stefano C.
Politano, Luisa
Comi, Giacomo P.
Sansone, Valeria A.
Donati, Alice
Hogrel, Jean Yves
Straub, Volker
De Lucia, Silvana
Niks, Erik
Servais, Laurent
De Groot, Imelda
Chesshyre, Mary
Bertini, Enrico
Goemans, Nathalie
Muntoni, Francesco
Mercuri, Eugenio
author_sort Coratti, Giorgia
collection PubMed
description INTRODUCTION: The aim of this study was to report 36-month longitudinal changes using the North Star Ambulatory Assessment (NSAA) in ambulant patients affected by Duchenne muscular dystrophy amenable to skip exons 44, 45, 51 or 53. MATERIALS AND METHODS: We included 101 patients, 34 had deletions amenable to skip exon 44, 25 exon 45, 19 exon 51, and 28 exon 53, not recruited in any ongoing clinical trials. Five patients were counted to skip exon 51 and 53 since they had a single deletion of exon 52. RESULTS: The difference between subgroups (skip 44, 45, 51 and 53) was significant at 12 (p = 0.043), 24 (p = 0.005) and 36 months (p≤0.001). DISCUSSION: Mutations amenable to skip exons 53 and 51 had lower baseline values and more negative changes than the other subgroups while those amenable to skip exon 44 had higher scores both at baseline and at follow up. CONCLUSION: Our results confirm different progression of disease in subgroups of patients with deletions amenable to skip different exons. This information is relevant as current long term clinical trials are using the NSAA in these subgroups of mutations.
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spelling pubmed-82324232021-07-07 North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up Coratti, Giorgia Pane, Marika Brogna, Claudia Ricotti, Valeria Messina, Sonia D’Amico, Adele Bruno, Claudio Vita, Gianluca Berardinelli, Angela Mazzone, Elena Magri, Francesca Ricci, Federica Mongini, Tiziana Battini, Roberta Bello, Luca Pegoraro, Elena Baranello, Giovanni Previtali, Stefano C. Politano, Luisa Comi, Giacomo P. Sansone, Valeria A. Donati, Alice Hogrel, Jean Yves Straub, Volker De Lucia, Silvana Niks, Erik Servais, Laurent De Groot, Imelda Chesshyre, Mary Bertini, Enrico Goemans, Nathalie Muntoni, Francesco Mercuri, Eugenio PLoS One Research Article INTRODUCTION: The aim of this study was to report 36-month longitudinal changes using the North Star Ambulatory Assessment (NSAA) in ambulant patients affected by Duchenne muscular dystrophy amenable to skip exons 44, 45, 51 or 53. MATERIALS AND METHODS: We included 101 patients, 34 had deletions amenable to skip exon 44, 25 exon 45, 19 exon 51, and 28 exon 53, not recruited in any ongoing clinical trials. Five patients were counted to skip exon 51 and 53 since they had a single deletion of exon 52. RESULTS: The difference between subgroups (skip 44, 45, 51 and 53) was significant at 12 (p = 0.043), 24 (p = 0.005) and 36 months (p≤0.001). DISCUSSION: Mutations amenable to skip exons 53 and 51 had lower baseline values and more negative changes than the other subgroups while those amenable to skip exon 44 had higher scores both at baseline and at follow up. CONCLUSION: Our results confirm different progression of disease in subgroups of patients with deletions amenable to skip different exons. This information is relevant as current long term clinical trials are using the NSAA in these subgroups of mutations. Public Library of Science 2021-06-25 /pmc/articles/PMC8232423/ /pubmed/34170974 http://dx.doi.org/10.1371/journal.pone.0253882 Text en © 2021 Coratti et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Coratti, Giorgia
Pane, Marika
Brogna, Claudia
Ricotti, Valeria
Messina, Sonia
D’Amico, Adele
Bruno, Claudio
Vita, Gianluca
Berardinelli, Angela
Mazzone, Elena
Magri, Francesca
Ricci, Federica
Mongini, Tiziana
Battini, Roberta
Bello, Luca
Pegoraro, Elena
Baranello, Giovanni
Previtali, Stefano C.
Politano, Luisa
Comi, Giacomo P.
Sansone, Valeria A.
Donati, Alice
Hogrel, Jean Yves
Straub, Volker
De Lucia, Silvana
Niks, Erik
Servais, Laurent
De Groot, Imelda
Chesshyre, Mary
Bertini, Enrico
Goemans, Nathalie
Muntoni, Francesco
Mercuri, Eugenio
North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up
title North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up
title_full North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up
title_fullStr North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up
title_full_unstemmed North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up
title_short North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up
title_sort north star ambulatory assessment changes in ambulant duchenne boys amenable to skip exons 44, 45, 51, and 53: a 3 year follow up
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232423/
https://www.ncbi.nlm.nih.gov/pubmed/34170974
http://dx.doi.org/10.1371/journal.pone.0253882
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