Department of Neurology, Royal Brisbane & Women's Hospital, Queensland, Australia.
Clin Neurophysiol. 2012 Dec;123(12):2446-53. doi: 10.1016/j.clinph.2012.04.022. Epub 2012 May 17.
To evaluate differences among patients with different clinical features of ALS, we used our Bayesian method of motor unit number estimation (MUNE).
We performed serial MUNE studies on 42 subjects who fulfilled the diagnostic criteria for ALS during the course of their illness. Subjects were classified into three subgroups according to whether they had typical ALS (with upper and lower motor neurone signs) or had predominantly upper motor neurone weakness with only minor LMN signs, or predominantly lower motor neurone weakness with only minor UMN signs. In all subjects we calculated the half life of MUs, defined as the expected time for the number of MUs to halve, in one or more of the abductor digiti minimi (ADM), abductor pollicis brevis (APB) and extensor digitorum brevis (EDB) muscles.
The mean half life of MUs was less in subjects who had typical ALS with both upper and lower motor neurone signs than in those with predominantly upper motor neurone weakness or predominantly lower motor neurone weakness. In 18 subjects we analysed the estimated size of the MUs and demonstrated the appearance of large MUs in subjects with upper or lower motor neurone predominant weakness. We found that the appearance of large MUs was correlated with the half life of MUs.
Patients with different clinical features of ALS have different rates of loss and different sizes of MUs.
These findings could indicate differences in disease pathogenesis.
通过我们的运动单位数量估计(MUNE)贝叶斯方法,评估具有不同 ALS 临床特征的患者之间的差异。
我们对 42 名在疾病过程中符合 ALS 诊断标准的患者进行了连续的 MUNE 研究。根据他们是否具有典型的 ALS(上下运动神经元体征)或主要为上运动神经元无力,仅有轻微的 LMN 体征,或主要为下运动神经元无力,仅有轻微的 UMN 体征,将患者分为三组。在所有患者中,我们计算了一个或多个趾短伸肌(ADM)、拇指短展肌(APB)和趾短伸肌(EDB)肌肉中 MU 的半衰期,定义为 MU 数量减半的预期时间。
具有上下运动神经元体征的典型 ALS 患者的 MU 半衰期平均值低于主要为上运动神经元无力或主要为下运动神经元无力的患者。在 18 名患者中,我们分析了估计的 MU 大小,并在具有上下运动神经元无力的患者中观察到了大 MU 的出现。我们发现大 MU 的出现与 MU 的半衰期相关。
具有不同 ALS 临床特征的患者具有不同的 MU 丢失率和不同的 MU 大小。
这些发现可能表明疾病发病机制的差异。