McComas A J, Sica R E, Toyonaga K
J Neurol Neurosurg Psychiatry. 1978 Oct;41(10):882-93. doi: 10.1136/jnnp.41.10.882.
The numbers of functioning motor units and the amplitudes of the maximum evoked muscle responses have been measured in 198 muscles of 102 patients with myotonic dystrophy. Losses of units could be demonstrated in most of the extensor digitorum brevis and thenar muscles but less commonly in the hypothenar groups. A more proximal limb muscle, the soleus, was also shown to be involved frequently. Investigation of two premature infants withmyotonic dystrophy also revealed reductions of functiong units; in one infant clinical improvement was associated with increased muscle innervation. Repeated examinations of 10 adult patients disclosed an abnormal decline in neuromuscular function below the age of 60 years. The reduction in functioning units amounted to approximately 3% of the mean control value per annum. Analysis of 19 families showed that the severity of neuromuscular involvement was nearly always greater in members of later generations. If the predicted deterioration was also taken into account, the results strongly suggested that anticipation was a true genetic phenomenon rather than an artefact of selection. The combined results are considered to strengthen the concept of motoneurone dysfunction as the major pathogenetic factor in this form of dystrophy.
对102例强直性肌营养不良患者的198块肌肉测量了功能性运动单位的数量和最大诱发肌肉反应的幅度。在大多数拇短伸肌和鱼际肌中可发现运动单位缺失,但在小鱼际肌群中较少见。更为近端的肢体肌肉比目鱼肌也常受累。对两名患有强直性肌营养不良的早产儿的研究也显示功能性运动单位减少;其中一名婴儿的临床改善与肌肉神经支配增加有关。对10名成年患者的反复检查发现,60岁以下患者的神经肌肉功能出现异常下降。每年功能性运动单位的减少量约为平均对照值的3%。对19个家族的分析表明,后代成员的神经肌肉受累严重程度几乎总是更高。如果将预测的病情恶化也考虑在内,结果强烈表明遗传早现是一种真正的遗传现象,而非选择假象。综合结果被认为强化了运动神经元功能障碍是这种类型肌营养不良主要致病因素的概念。