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

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. We included 101 patients, 34 had deletions amenable to skip exon 44, 25 exon 45, 1...

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Veröffentlicht in:PloS one 2021-06, Vol.16 (6), p.e0253882-e0253882
Hauptverfasser: 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
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container_issue 6
container_start_page e0253882
container_title PloS one
container_volume 16
creator 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
description 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. 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. 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[less than or equal to]0.001). 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. 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.
doi_str_mv 10.1371/journal.pone.0253882
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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. 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[less than or equal to]0.001). 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. 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.</description><subject>Ambulatory assessment</subject><subject>Analysis</subject><subject>Biology and Life Sciences</subject><subject>Biomedical research</subject><subject>Boys</subject><subject>Child</subject><subject>Children &amp; youth</subject><subject>Childrens health</subject><subject>Clinical trials</subject><subject>Consortia</subject><subject>Diagnosis</subject><subject>Disease Progression</subject><subject>Duchenne muscular dystrophy</subject><subject>Duchenne's muscular dystrophy</subject><subject>Dystrophin/genetics</subject><subject>Dystrophy</subject><subject>Exon (Molecular genetics)</subject><subject>Exons</subject><subject>Exons/genetics</subject><subject>Follow-Up Studies</subject><subject>Genetic aspects</subject><subject>Health risks</subject><subject>Hospitals</subject><subject>Human health 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Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up</title><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, 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titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Coratti, Giorgia</au><au>Pane, Marika</au><au>Brogna, Claudia</au><au>Ricotti, Valeria</au><au>Messina, Sonia</au><au>D'Amico, Adele</au><au>Bruno, Claudio</au><au>Vita, Gianluca</au><au>Berardinelli, Angela</au><au>Mazzone, Elena</au><au>Magri, Francesca</au><au>Ricci, Federica</au><au>Mongini, Tiziana</au><au>Battini, Roberta</au><au>Bello, Luca</au><au>Pegoraro, Elena</au><au>Baranello, Giovanni</au><au>Previtali, Stefano C</au><au>Politano, Luisa</au><au>Comi, Giacomo P</au><au>Sansone, Valeria A</au><au>Donati, Alice</au><au>Hogrel, Jean Yves</au><au>Straub, Volker</au><au>De Lucia, Silvana</au><au>Niks, Erik</au><au>Servais, Laurent</au><au>De Groot, Imelda</au><au>Chesshyre, Mary</au><au>Bertini, Enrico</au><au>Goemans, Nathalie</au><au>Muntoni, Francesco</au><au>Mercuri, Eugenio</au><au>Asakura, Atsushi</au><aucorp>on behalf on the International DMD Group and the iMDEX Consortium</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up</atitle><jtitle>PloS one</jtitle><date>2021-06-25</date><risdate>2021</risdate><volume>16</volume><issue>6</issue><spage>e0253882</spage><epage>e0253882</epage><pages>e0253882-e0253882</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>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. 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. 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[less than or equal to]0.001). 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. 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.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>34170974</pmid><doi>10.1371/journal.pone.0253882</doi><tpages>e0253882</tpages><orcidid>https://orcid.org/0000-0003-2546-4357</orcidid><orcidid>https://orcid.org/0000-0001-9046-3540</orcidid><orcidid>https://orcid.org/0000-0001-6666-5628</orcidid><orcidid>https://orcid.org/0000-0001-5892-5143</orcidid><orcidid>https://orcid.org/0000-0003-4190-8042</orcidid><orcidid>https://orcid.org/0000-0002-9851-5365</orcidid><orcidid>https://orcid.org/0000-0002-0925-7158</orcidid><orcidid>https://orcid.org/0000-0002-5157-7155</orcidid><oa>free_for_read</oa></addata></record>
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subjects Ambulatory assessment
Analysis
Biology and Life Sciences
Biomedical research
Boys
Child
Children & youth
Childrens health
Clinical trials
Consortia
Diagnosis
Disease Progression
Duchenne muscular dystrophy
Duchenne's muscular dystrophy
Dystrophin/genetics
Dystrophy
Exon (Molecular genetics)
Exons
Exons/genetics
Follow-Up Studies
Genetic aspects
Health risks
Hospitals
Human health sciences
Humans
Longitudinal Studies
Male
Medicine and Health Sciences
Men
Muscular dystrophy
Muscular Dystrophy, Duchenne/genetics/pathology
Mutation
Mutation/genetics
Neurologie
Neurology
Neurosciences
Pathophysiology
Pediatrics
Physical Sciences
Public health
Pédiatrie
Sciences de la santé humaine
Severity of Illness Index
Subgroups
Walking/physiology
title North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up
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