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Six-Minute Activity-95th Centile, a Novel Wearable-Derived Clinical Outcome Assessment for Duchenne Muscular Dystrophy

  • DMDCCC Investigators
  • Vanderbilt University
  • Children's National Medical Center
  • Northwestern University
  • University of Washington
  • Virginia Commonwealth University
  • Ohio State University
  • Indiana University Bloomington

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Background: The six-minute walk test and quantitative muscle testing (QMT) are commonly used skeletal muscle assessments in Duchenne muscular dystrophy; however, they present challenges in nonambulatory patients. Our objective was to evaluate whether 6-min activity-95th centile, a novel accelerometry metric capturing a participant's greatest amount of movement in six consecutive minutes, distinguished between ambulatory and nonambulatory individuals and correlated with QMT data. Methods: Participants (N = 139) in an observational, longitudinal natural history study with median age of 12.0 years [interquartile range 10.0, 15.0] completed muscle testing and were instructed to wear an accelerometer on dominant wrist for 7 days and nights (a “wear”) at each of three annual study visits. One hundred two male participants were analyzed with a total of 184 valid wear periods. Results: Six-minute activity centiles declined over 2 years (n = 28, P < 0.001). No significant declines in centiles were detected immediately following loss of ambulation (n = 11). Significant correlations were observed between 6-min activity centiles and indexed QMT, with strongest at 95th centile (rs = 0.647, P < 0.001). There was a relationship between 6-min centiles and time since loss of ambulation. Conclusions: Ambulatory and nonambulatory patients with Duchenne muscular dystrophy were differentiated by 6-min activity and declined over time, modeling progression of skeletal myopathy. Six-minute activity-95th centile has potential for future use as an effort-independent outcome of skeletal muscle progression and functional decline for both ambulatory and nonambulatory individuals.

Original languageEnglish
Pages (from-to)187-195
Number of pages9
JournalPediatric Neurology
Volume175
DOIs
StatePublished - Feb 2026
Externally publishedYes

Keywords

  • Accelerometry
  • Ambulation
  • Clinical outcome assessment
  • Duchenne muscular dystrophy
  • Accelerometry/methods
  • Humans
  • Wearable Electronic Devices
  • Male
  • Muscular Dystrophy, Duchenne/physiopathology
  • Adolescent
  • Outcome Assessment, Health Care/methods
  • Walk Test
  • Child
  • Longitudinal Studies

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