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Percent-Predicted 6-Minute Walk Distance in Duchenne Muscular Dystrophy to Account for Maturational Influences

We recently described a modified version of the 6-minute walk test (6MWT) for Duchenne muscular dystrophy (DMD) based partly on the American Thoracic Society (ATS) guidelines. This measure has shown reliability, validity and utility as a primary outcome measure in DMD clinical trials. Because loss o...

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Detalles Bibliográficos
Autores principales: Henricson, Erik, Abresch, Richard, Han, Jay J., Nicorici, Alina, Goude Keller, Erica, Elfring, Gary, Reha, Allen, Barth, Jay, McDonald, Craig M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269886/
https://www.ncbi.nlm.nih.gov/pubmed/22306689
http://dx.doi.org/10.1371/currents.RRN1297
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author Henricson, Erik
Abresch, Richard
Han, Jay J.
Nicorici, Alina
Goude Keller, Erica
Elfring, Gary
Reha, Allen
Barth, Jay
McDonald, Craig M.
author_facet Henricson, Erik
Abresch, Richard
Han, Jay J.
Nicorici, Alina
Goude Keller, Erica
Elfring, Gary
Reha, Allen
Barth, Jay
McDonald, Craig M.
author_sort Henricson, Erik
collection PubMed
description We recently described a modified version of the 6-minute walk test (6MWT) for Duchenne muscular dystrophy (DMD) based partly on the American Thoracic Society (ATS) guidelines. This measure has shown reliability, validity and utility as a primary outcome measure in DMD clinical trials. Because loss of muscle function in DMD occurs against the background of normal childhood growth and development, younger children with DMD can show increase in distance walked during 6MWT over ~1 year despite progressive muscular impairment. In this study, we compare 6-minute walk distance (6MWD) data from DMD boys (n=17) and typically developing control subjects (n=22) to existing normative data from age- and sex-matched children and adolescents. An age- and height-based equation fitted to normative data by Geiger and colleagues was used to convert 6MWD to a percent-predicted (%-predicted) value in boys with DMD. Analysis of %-predicted 6MWD data represents a method to account for normal growth and development, and shows that gains in function at early ages represents stable rather than improving abilities in boys with DMD. Boys with DMD from 4-7 years of age maintain a stable 6MWD approximately 80% of that of typically developing peers, with the deficit progressing at a variable rate thereafter.
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spelling pubmed-32698862012-02-02 Percent-Predicted 6-Minute Walk Distance in Duchenne Muscular Dystrophy to Account for Maturational Influences Henricson, Erik Abresch, Richard Han, Jay J. Nicorici, Alina Goude Keller, Erica Elfring, Gary Reha, Allen Barth, Jay McDonald, Craig M. PLoS Curr Muscular Dystrophy We recently described a modified version of the 6-minute walk test (6MWT) for Duchenne muscular dystrophy (DMD) based partly on the American Thoracic Society (ATS) guidelines. This measure has shown reliability, validity and utility as a primary outcome measure in DMD clinical trials. Because loss of muscle function in DMD occurs against the background of normal childhood growth and development, younger children with DMD can show increase in distance walked during 6MWT over ~1 year despite progressive muscular impairment. In this study, we compare 6-minute walk distance (6MWD) data from DMD boys (n=17) and typically developing control subjects (n=22) to existing normative data from age- and sex-matched children and adolescents. An age- and height-based equation fitted to normative data by Geiger and colleagues was used to convert 6MWD to a percent-predicted (%-predicted) value in boys with DMD. Analysis of %-predicted 6MWD data represents a method to account for normal growth and development, and shows that gains in function at early ages represents stable rather than improving abilities in boys with DMD. Boys with DMD from 4-7 years of age maintain a stable 6MWD approximately 80% of that of typically developing peers, with the deficit progressing at a variable rate thereafter. Public Library of Science 2012-02-02 /pmc/articles/PMC3269886/ /pubmed/22306689 http://dx.doi.org/10.1371/currents.RRN1297 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Muscular Dystrophy
Henricson, Erik
Abresch, Richard
Han, Jay J.
Nicorici, Alina
Goude Keller, Erica
Elfring, Gary
Reha, Allen
Barth, Jay
McDonald, Craig M.
Percent-Predicted 6-Minute Walk Distance in Duchenne Muscular Dystrophy to Account for Maturational Influences
title Percent-Predicted 6-Minute Walk Distance in Duchenne Muscular Dystrophy to Account for Maturational Influences
title_full Percent-Predicted 6-Minute Walk Distance in Duchenne Muscular Dystrophy to Account for Maturational Influences
title_fullStr Percent-Predicted 6-Minute Walk Distance in Duchenne Muscular Dystrophy to Account for Maturational Influences
title_full_unstemmed Percent-Predicted 6-Minute Walk Distance in Duchenne Muscular Dystrophy to Account for Maturational Influences
title_short Percent-Predicted 6-Minute Walk Distance in Duchenne Muscular Dystrophy to Account for Maturational Influences
title_sort percent-predicted 6-minute walk distance in duchenne muscular dystrophy to account for maturational influences
topic Muscular Dystrophy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269886/
https://www.ncbi.nlm.nih.gov/pubmed/22306689
http://dx.doi.org/10.1371/currents.RRN1297
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