Reed D M, Brody J A, Holden E M
Neurology. 1975 Mar;25(3):277-80. doi: 10.1212/wnl.25.3.277.
During the years of study of amyotrophic lateral sclerosis on Guam we have observed a wide range in clinical signs and rate of progression of the disease. Some patients died within 6 months of onset, while others have lived for 20 years. It was our assumption that some aspects of the early neurologic involvement would be related to length of survival, and hence be of prognostic value. We found that an early age at onset and male sex were associated with longer survival. The detailed analysis of degree of involvement of four major neurologic components of amyotrophic lateral sclerosis (progressive muscular atrophy, lateral sclerosis, bulbar paralysis, and pseudobulbar palsy) showed no meaningful pattern of association with duration of illness that could be useful in predicting the course.
在对关岛肌萎缩侧索硬化症进行研究的这些年里,我们观察到了该疾病临床症状和进展速度的广泛差异。一些患者在发病后6个月内死亡,而另一些患者则存活了20年。我们推测,早期神经受累的某些方面可能与存活时间有关,因此具有预后价值。我们发现,发病年龄早和男性与较长的生存期相关。对肌萎缩侧索硬化症四个主要神经组成部分(进行性肌肉萎缩、侧索硬化、延髓麻痹和假性延髓麻痹)受累程度的详细分析显示,与疾病持续时间没有有意义的关联模式,无法用于预测病程。