## Abstract Walking abnormalities are prominent in Duchenne muscular dystrophy (DMD). We modified the 6βminute walk test (6MWT) for use as an outcome measure in patients with DMD and evaluated its performance in 21 ambulatory boys with DMD and 34 healthy boys, ages 4 to 12 years. Boys with DMD were
The 6-minute walk test in Duchenne/Becker muscular dystrophy: Longitudinal observations
β Scribed by Craig M. MCDonald; Erik K. Henricson; Jay J. Han; R. Ted Abresch; Alina Nicorici; Leone Atkinson; Gary L. Elfring; Allen Reha; Langdon L. Miller
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 532 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0148-639X
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β¦ Synopsis
Abstract
In this study we used the 6βminute walk distance (6MWD) to characterize ambulation over time in Duchenne/Becker muscular dystrophy (DBMD). The 6MWD was assessed in 18 boys with DBMD and 22 healthy boys, ages 4β12 years, over mean [range] intervals of 58 [39β87] and 69 [52β113] weeks, respectively. Height and weight increased similarly in both groups. At 52 weeks, 6MWD decreased in 12 of 18 (67%) DBMD subjects (overall mean [range]: 357 [125β481] to 300 [0β510] meters; Ξ β57 meters, β15.9%), but increased in 14 of 22 (64%) healthy subjects (overall mean [range]: 623 [479β754] to 636 [547β717] meters; Ξ +13 meters, +2.1%). Two DBMD subjects lost ambulation. Changes in 6MWD depended on stride length and age; improvements usually occurred by 7β8 years of age; older DBMD subjects worsened, whereas older healthy subjects were stable. The 6MWD changes at 1 year confirm the validity of this endpoint and emphasize that preserving ambulation must remain a major goal of DBMD therapy. Muscle Nerve, 2010
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