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Tytuł pozycji:

Walking activity in a large cohort of boys with Duchenne muscular dystrophy.

Tytuł:
Walking activity in a large cohort of boys with Duchenne muscular dystrophy.
Autorzy:
Lott DJ; Department of Physical Therapy, University of Florida, College of Public Health & Health Professions, Gainesville, Florida, USA.
Taivassalo T; Department of Physiology and Functional Genomics, University of Florida, Gainesville, Florida, USA.
Senesac CR; Department of Physical Therapy, University of Florida, College of Public Health & Health Professions, Gainesville, Florida, USA.
Willcocks RJ; Department of Physical Therapy, University of Florida, College of Public Health & Health Professions, Gainesville, Florida, USA.
Harrington AM; Department of Physical Therapy, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Zilke K; Oregon Health & Science University, Shriners Hospitals for Children, Portland, Oregon, USA.
Cunkle H; Department of Physical Therapy, University of Florida, College of Public Health & Health Professions, Gainesville, Florida, USA.
Powers C; Department of Physical Therapy, University of Florida, College of Public Health & Health Professions, Gainesville, Florida, USA.
Finanger EL; Department of Pediatrics, Oregon Health and Science University, Portland, Oregon, USA.
Rooney WD; Advanced Imaging Research Center, Oregon Health and Science University, Portland, Oregon, USA.
Tennekoon GI; Department of Physical Therapy, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Vandenborne K; Department of Physical Therapy, University of Florida, College of Public Health & Health Professions, Gainesville, Florida, USA.
Źródło:
Muscle & nerve [Muscle Nerve] 2021 Feb; Vol. 63 (2), pp. 192-198. Date of Electronic Publication: 2020 Nov 27.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
Język:
English
Imprint Name(s):
Publication: <2005-> : Hoboken, NJ : John Wiley & Sons
Original Publication: New York, NY : John Wiley & Sons
MeSH Terms:
Exercise*
Walking*
Muscular Dystrophy, Duchenne/*physiopathology
Accelerometry ; Activities of Daily Living ; Case-Control Studies ; Child ; Child, Preschool ; Cohort Studies ; Disease Progression ; Functional Status ; Glucocorticoids/therapeutic use ; Humans ; Male ; Mobility Limitation ; Muscular Dystrophy, Duchenne/drug therapy
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Grant Information:
K12 HD055929 United States HD NICHD NIH HHS; R01 AR056973 United States AR NIAMS NIH HHS
Contributed Indexing:
Keywords: accelerometry, daily steps, Duchenne muscular dystrophy, functional ability, physical activity, walking
Substance Nomenclature:
0 (Glucocorticoids)
Entry Date(s):
Date Created: 20201114 Date Completed: 20210315 Latest Revision: 20210729
Update Code:
20240105
PubMed Central ID:
PMC8314165
DOI:
10.1002/mus.27119
PMID:
33188573
Czasopismo naukowe
Introduction: In this study we explored walking activity in a large cohort of boys with Duchenne muscular dystrophy (DMD).
Methods: Step activity (monitored for 7 days), functional ability, and strength were quantified in ambulatory boys (5-12.9 years of age) with DMD and unaffected boys. Ambulatory status was determined 2 years later.
Results: Two to 5 days of activity monitoring predicted weekly step activity (adjusted R 2 = 0.80-0.95). Age comparisons revealed significant declines for step activity with increasing age, and relationships were found between step activity with both function and strength (P < .01). Our regression model predicted 36.5% of the variance in step activity. Those who were still ambulatory after 2 years demonstrated baseline step activity nearly double that of those who were no longer walking 2 years later (P < .01).
Discussion: Step activity for DMD is related to and predictive of functional declines, which may be useful for clinical trials.
(© 2020 Wiley Periodicals LLC.)

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