Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783713632957235200 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8232423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT corattigiorgia northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT panemarika northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT brognaclaudia northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT ricottivaleria northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT messinasonia northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT damicoadele northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT brunoclaudio northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT vitagianluca northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT berardinelliangela northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT mazzoneelena northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT magrifrancesca northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT riccifederica northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT monginitiziana northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT battiniroberta northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT belloluca northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT pegoraroelena northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT baranellogiovanni northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT previtalistefanoc northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT politanoluisa northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT comigiacomop northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT sansonevaleriaa northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT donatialice northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT hogreljeanyves northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT straubvolker northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT deluciasilvana northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT nikserik northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT servaislaurent northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT degrootimelda northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT chesshyremary northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT bertinienrico northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT goemansnathalie northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT muntonifrancesco northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT mercurieugenio northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup AT northstarambulatoryassessmentchangesinambulantduchenneboysamenabletoskipexons444551and53a3yearfollowup |