Preisler N, Andersen G, Thøgersen F, Crone C, Jeppesen T D, Wibrand F, Vissing J
Neuromuscular Research Unit 3342, University of Copenhagen, Rigshospitalet, Copenhagen, Denmark.
Neurology. 2009 Jan 27;72(4):317-23. doi: 10.1212/01.wnl.0000341274.61236.02.
We examined the effect of aerobic exercise in patients with spinal and bulbar muscular atrophy (SBMA). SBMA is caused by a defect androgen receptor. This defect causes motor neuron death, but considering the important function of androgens in muscle, it is possible that muscle damage in SBMA also occurs independently of motor neuron damage.
Eight patients with SBMA engaged in regular cycling exercise for 12 weeks. Maximum oxygen uptake (Vo(2max)), maximal work capacity (W(max)), muscle morphology, citrate synthase (CS) activity, body composition, EMG, static strength measurements, lung function, plasma proteins, and hormones were evaluated before and after training. Evaluation of improvements in activities of daily living (ADL) was conducted after training.
W(max) increased by 18%, and CS activity increased by 35%. There was no significant change in Vo(2max) or any of the other variables examined before and after training, and the patients with SBMA did not feel improvements in ADL.
Frequent, moderate-intensity aerobic conditioning is of little beneficial effect in patients with spinal and bulbar muscular atrophy (SBMA). High levels of plasma creatine kinase and muscle regeneration indicate a primary myopathic affection, which, in parallel with the motor neuron deficiency, may attenuate the response to exercise training in patients with SBMA.
我们研究了有氧运动对脊髓延髓肌萎缩症(SBMA)患者的影响。SBMA由雄激素受体缺陷引起。这种缺陷导致运动神经元死亡,但考虑到雄激素在肌肉中的重要功能,SBMA中的肌肉损伤也可能独立于运动神经元损伤而发生。
8名SBMA患者进行了为期12周的定期骑自行车运动。在训练前后评估了最大摄氧量(Vo₂max)、最大工作能力(Wmax)、肌肉形态、柠檬酸合酶(CS)活性、身体成分、肌电图、静态力量测量、肺功能、血浆蛋白和激素。训练后对日常生活活动(ADL)的改善进行了评估。
Wmax增加了18%,CS活性增加了35%。训练前后Vo₂max或任何其他检测变量均无显著变化,SBMA患者在ADL方面也未感到改善。
频繁的中等强度有氧调节对脊髓延髓肌萎缩症(SBMA)患者几乎没有益处。高水平的血浆肌酸激酶和肌肉再生表明存在原发性肌病,这与运动神经元缺陷一起,可能会减弱SBMA患者对运动训练的反应。