THE 6-MINUTE WALK TEST IN DUCHENNE/BECKER MUSCULAR DYSTROPHY: LONGITUDINAL OBSERVATIONS

被引:126
|
作者
McDonald, Craig M. [1 ]
Henricson, Erik K. [1 ]
Han, Jay J. [1 ]
Abresch, R. Ted [1 ]
Nicorici, Alina [1 ]
Atkinson, Leone [2 ]
Elfring, Gary L. [2 ]
Reha, Allen [2 ]
Miller, Langdon L. [2 ]
机构
[1] Univ Calif Davis, Sch Med, Dept Phys Med & Rehabil, Sacramento, CA 95817 USA
[2] PTC Therapeut, S Plainfield, NJ USA
关键词
case control study; child; disabled children; exercise test; gait disorders; neurologic; ENZYME REPLACEMENT THERAPY; DOUBLE-BLIND; CHILDREN; RELIABILITY; DISEASE; ALPHA; GAIT;
D O I
10.1002/mus.21808
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In this study we used the 6-minute 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 4-12 years, over mean [range] intervals of 58 [39-87] and 69 [52-113] 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 [125-481] to 300 [0-510] meters; Delta 57 meters, -15.9%), but increased in 14 of 22 (64%) healthy subjects (overall mean [range]: 623 [479-754] to 636 [547-717] meters; Delta +13 meters, +2.1%). Two DBMD subjects lost ambulation. Changes in 6MWD depended on stride length and age; improvements usually occurred by 7-8 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 42: 966-974, 2010
引用
收藏
页码:966 / 974
页数:9
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