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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
dc.contributor.author
Hoffman, Eric P.
dc.contributor.author
Cnaan, Avital
dc.contributor.author
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
dc.subject
Glucocorticoid
dc.subject
Independent Ambulation
dc.subject.classification
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
dc.description.fil
Fil: Henricson, Erik K.. University of California at Davis; Estados Unidos
dc.description.fil
Fil: Duong, Tina. Children’s National Medical Center; Estados Unidos
dc.description.fil
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
dc.description.fil
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
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