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dc.contributor.author
Bello, Luca  
dc.contributor.author
Gordish Dressman, Heather  
dc.contributor.author
Morgenroth, Lauren P.  
dc.contributor.author
Henricson, Erik K.  
dc.contributor.author
Duong, Tina  
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Hoffman, Eric P.  
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Cnaan, Avital  
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McDonald, Craig M.  
dc.contributor.author
Dubrovsky, Alberto  
dc.contributor.author
Andreone, Luz  
dc.contributor.author
Cooperative International Neuromuscular Research Group Investigators  
dc.date.available
2018-05-29T20:39:02Z  
dc.date.issued
2015-09  
dc.identifier.citation
Bello, Luca; Gordish Dressman, Heather; Morgenroth, Lauren P.; Henricson, Erik K.; Duong, Tina; et al.; Prednisone/prednisolone and deflazacort regimens in the CINRG Duchenne Natural History Study; Lippincott Williams; Neurology; 85; 12; 9-2015; 1048-1055  
dc.identifier.issn
0028-3878  
dc.identifier.uri
http://hdl.handle.net/11336/46536  
dc.description.abstract
Objective: We aimed to perform an observational study of age at loss of independent ambulation (LoA) and side-effect profiles associated with different glucocorticoid corticosteroid (GC) regimens in Duchenne muscular dystrophy (DMD). Methods: We studied 340 participants in the Cooperative International Neuromuscular Research Group Duchenne Natural History Study (CINRG-DNHS). LoA was defined as continuous wheelchair use. Effects of prednisone or prednisolone (PRED)/deflazacort (DFZ), administration frequency, and dose were analyzed by time-varying Cox regression. Side-effect frequencies were compared using x2 test. Results: Participants treated $1 year while ambulatory (n 5 252/340) showed a 3-year median delay in LoA (p , 0.001). Fourteen different regimens were observed. Nondaily treatment was common for PRED (37%) and rare for DFZ (3%). DFZ was associated with later LoA than PRED (hazard ratio 0.294 6 0.053 vs 0.490 6 0.08, p 5 0.003; 2-year difference in median LoA with daily administration, p , 0.001). Average dose was lower for daily PRED (0.56 mg/kg/d, 75% of recommended) than daily DFZ (0.75 mg/kg/d, 83% of recommended, p , 0.001). DFZ showed higher frequencies of growth delay (p , 0.001), cushingoid appearance (p 5 0.002), and cataracts (p , 0.001), but not weight gain. Conclusions: Use of DFZ was associated with later LoA and increased frequency of side effects. Differences in standards of care and dosing complicate interpretation of this finding, but stratification by PRED/DFZ might be considered in clinical trials. This study emphasizes the necessity of a randomized, blinded trial of GC regimens in DMD. Classification of evidence: This study provides Class IV evidence that GCs are effective in delaying LoA in patients with DMD.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Lippincott Williams  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Duchenne Muscular Dystrophy  
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Glucocorticoid  
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Independent Ambulation  
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Medicina Critica y de Emergencia  
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Medicina Clínica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Prednisone/prednisolone and deflazacort regimens in the CINRG Duchenne Natural History Study  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2018-05-23T16:32:39Z  
dc.identifier.eissn
1526-632X  
dc.journal.volume
85  
dc.journal.number
12  
dc.journal.pagination
1048-1055  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
Filadelfia  
dc.description.fil
Fil: Bello, Luca. Children’s National Medical Center; Estados Unidos  
dc.description.fil
Fil: Gordish Dressman, Heather. Children’s National Medical Center; Estados Unidos  
dc.description.fil
Fil: Morgenroth, Lauren P.. Children’s National Medical Center; Estados Unidos  
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Fil: Henricson, Erik K.. University of California at Davis; Estados Unidos  
dc.description.fil
Fil: Duong, Tina. Children’s National Medical Center; Estados Unidos  
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Fil: Hoffman, Eric P.. Children’s National Medical Center; Estados Unidos. The George Washington University; Estados Unidos  
dc.description.fil
Fil: Cnaan, Avital. Children’s National Medical Center; Estados Unidos. The George Washington University; Estados Unidos  
dc.description.fil
Fil: McDonald, Craig M.. University of California at Davis; Estados Unidos  
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Fil: Dubrovsky, Alberto. Cooperative International Neuromuscular Research Group; Argentina  
dc.description.fil
Fil: Andreone, Luz. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigación en Biomedicina de Buenos Aires - Instituto Partner de la Sociedad Max Planck; Argentina. Cooperative International Neuromuscular Research Group; Argentina  
dc.description.fil
Fil: Cooperative International Neuromuscular Research Group Investigators. No especifica;  
dc.journal.title
Neurology  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1212/WNL.0000000000001950  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://n.neurology.org/content/85/12/1048