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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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><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0253882</identifier><identifier>PMID: 34170974</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>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</subject><ispartof>PloS one, 2021-06, Vol.16 (6), p.e0253882-e0253882</ispartof><rights>COPYRIGHT 2021 Public Library of Science</rights><rights>2021 Coratti et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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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 & 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 sciences</subject><subject>Humans</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Medicine and Health Sciences</subject><subject>Men</subject><subject>Muscular dystrophy</subject><subject>Muscular Dystrophy, Duchenne/genetics/pathology</subject><subject>Mutation</subject><subject>Mutation/genetics</subject><subject>Neurologie</subject><subject>Neurology</subject><subject>Neurosciences</subject><subject>Pathophysiology</subject><subject>Pediatrics</subject><subject>Physical Sciences</subject><subject>Public health</subject><subject>Pédiatrie</subject><subject>Sciences de la santé humaine</subject><subject>Severity of Illness 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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, Eugenio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c713t-e7b6e77d3417650f2d606df602af42278f7067c9ac81109e3b5e224432bed7b43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Ambulatory assessment</topic><topic>Analysis</topic><topic>Biology and Life Sciences</topic><topic>Biomedical research</topic><topic>Boys</topic><topic>Child</topic><topic>Children & youth</topic><topic>Childrens health</topic><topic>Clinical trials</topic><topic>Consortia</topic><topic>Diagnosis</topic><topic>Disease Progression</topic><topic>Duchenne muscular dystrophy</topic><topic>Duchenne's muscular dystrophy</topic><topic>Dystrophin/genetics</topic><topic>Dystrophy</topic><topic>Exon (Molecular genetics)</topic><topic>Exons</topic><topic>Exons/genetics</topic><topic>Follow-Up Studies</topic><topic>Genetic aspects</topic><topic>Health risks</topic><topic>Hospitals</topic><topic>Human health 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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> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2021-06, Vol.16 (6), p.e0253882-e0253882 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_2545226257 |
source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Free Full-Text Journals in Chemistry; Public Library of Science (PLoS) |
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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