WHY SHORT STATURE IS BENEFICIAL IN DUCHENNE MUSCULAR DYSTROPHY

被引:27
作者
Bodor, Marko [1 ,2 ]
Mcdonald, Craig M. [1 ]
机构
[1] Univ Calif Davis, Sch Med, Dept Phys Med & Rehabil, Sacramento, CA 95817 USA
[2] Univ Calif San Francisco, Sch Med, Dept Neurol Surg, San Francisco, CA USA
关键词
Duchenne muscular dystrophy; growth; sarcolemma; stature; stress; 6-MINUTE WALK TEST; GROWTH-HORMONE; MUSCLE-FIBERS; BOYS; MAZINDOL;
D O I
10.1002/mus.23793
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
IntroductionDuchenne muscular dystrophy (DMD) is caused by a genetic defect resulting in absent dystrophin, yet children are able to walk when small and young but lose this ability as they grow. The mdx mouse has absent dystrophin yet does not exhibit significant disability. MethodsAllometric modeling of linearly increasing load per muscle fiber and stress on the sarcolemma with growth and exponential decline associated with loss of muscle fibers correlated with case studies and animal models of DMD. ResultsSmaller species or breeds are predictably less affected than large as follows: mdx mice<small golden retriever muscular dystrophy (GRMD) dogs<large GRMD dogs<humans. Case reports of combined growth hormone and dystrophin deficiency show a relatively benign course of disease. ConclusionsFuture therapeutic trials in DMD might include specific growth inhibitors in combination with standard of care treatments to delay the clinical onset and reduce the severity of disease and disability. Muscle Nerve48: 336-342, 2013
引用
收藏
页码:336 / 342
页数:7
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