Abstract
Contemporary natural history data in Duchenne muscular dystrophy (DMD) is needed to assess care recommendations and aid in planning future trials. Methods: The Cooperative International Neuromuscular Research Group (CINRG) DMD Natural History Study (DMD-NHS) enrolled 340 individuals, aged 2-28 years, with DMD in a longitudinal, observational study at 20 centers. Assessments obtained every 3 months for 1 year, at 18 months, and annually thereafter included: clinical history; anthropometrics; goniometry; manual muscle testing; quantitative muscle strength; timed function tests; pulmonary function; and patient-reported outcomes/health-related quality-of-life instruments. Results: Glucocorticoid (GC) use at baseline was 62% present, 14% past, and 24% GC-naive. In those ≥6 years of age, 16% lost ambulation over the first 12 months (mean age 10.8 years). Conclusions: Detailed information on the study methodology of the CINRG DMD-NHS lays the groundwork for future analyses of prospective longitudinal natural history data. These data will assist investigators in designing clinical trials of novel therapeutics.
Original language | English (US) |
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Pages (from-to) | 32-54 |
Number of pages | 23 |
Journal | Muscle and Nerve |
Volume | 48 |
Issue number | 1 |
DOIs | |
State | Published - Jul 1 2013 |
Keywords
- Adolescent
- Adult
- Child/preschool
- Follow-up study
- Health status
- Human
- Locomotion
- Male
- Muscle strength/physiology
- Muscular dystrophies/Duchenne/physiopathology
- Muscular dystrophies/classification
- Muscular dystrophies/therapy
- Phenotype
- Quality of life/psychology
- Respiratory function test
ASJC Scopus subject areas
- Clinical Neurology
- Physiology (medical)
- Cellular and Molecular Neuroscience
- Physiology