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基于肌萎缩侧索硬化症全病程的肌萎缩侧索硬化症患者临床分类——呼吸运动麻痹前驱型的提出及其意义

[Clinical classification of ALS patients based on the total course of ALS--proposal of respiratory motor paralysis-preceded type and its significance].

作者信息

Hayashi H, Kato S, Shimizu T, Kawada A

机构信息

Department of Neurology, Komagome Metropolitan Hospital, Tokyo, Japan.

出版信息

No To Shinkei. 1997 May;49(5):435-41.

PMID:9163756
Abstract

Since the motor paralysis occurs in all motor systems in ALS, the clinicopathological findings and care of the patients living beyond the development of respiratory failure must be considered. We have divided the efferent motor systems into four groups, i.e., limb, bulbar, respiratory, and external ocular. In this study, 37 ALS patients were followed for more than two years with respirator, and the onset of motor paralysis in all four systems was observed in each patient. First, we classified the patients into three groups according to the number of paralyzed motor systems observed within six months from the onset of the first motor paralysis, and we discuss the patient's prognosis after the first motor paralysis. Twenty-one patients with paralysis of the respiratory motor system alone were categorized as respiratory paralysis-preceded type ALS (R-type ALS), four patients with paralysis of the bulbar motor system alone as bulbar paralysis-preceded type ALS (B-type ALS), and 12 patients with simultaneous paralysis of two or more motor systems as combined motor system paralysis type ALS (C-type ALS). The results showed that the prognosis of R-type ALS is slow progression and that of C-type ALS, rapid progression. Next, we investigated the time of occurrence of the first motor paralysis of the four motor systems in 37 patients, and we discuss the most vulnerable motor functions in ALS, i.e., the initial clinical presentations in ALS. The most frequent first motor paralysis was of the respiratory motor system, and the initial clinical manifestations in ALS were impairment of fine discriminating voluntary respiratory and limb motor functions. These findings could be explained by the rule of ALS involvements, according to which onto-genetically newer motor functions are lost earlier than the older ones. Based on the findings in this study, we concluded that ALS initially involves the ontogenetically new motor functions in "the first system" proposed by G. Holstege, whose anatomical structure is composed of pre-motoneurons and motoneurons in the brain stem and spinal cord.

摘要

由于肌萎缩侧索硬化症(ALS)患者的所有运动系统都会出现运动麻痹,因此必须考虑呼吸衰竭发生后仍存活患者的临床病理表现及护理。我们将传出运动系统分为四组,即肢体、延髓、呼吸和眼球外运动系统。在本研究中,37例ALS患者使用呼吸机随访两年以上,观察到每位患者所有四个系统均出现运动麻痹。首先,我们根据首次运动麻痹发作后六个月内观察到的麻痹运动系统数量将患者分为三组,并讨论首次运动麻痹后患者的预后。仅呼吸运动系统麻痹的21例患者被归类为呼吸麻痹先行型ALS(R型ALS),仅延髓运动系统麻痹的4例患者被归类为延髓麻痹先行型ALS(B型ALS),两个或更多运动系统同时麻痹的12例患者被归类为联合运动系统麻痹型ALS(C型ALS)。结果显示,R型ALS的预后进展缓慢,C型ALS的预后进展迅速。接下来,我们调查了37例患者四个运动系统首次运动麻痹的发生时间,并讨论了ALS中最易受损的运动功能,即ALS的初始临床表现。最常见的首次运动麻痹是呼吸运动系统的麻痹,ALS的初始临床表现是精细辨别性自主呼吸和肢体运动功能受损。这些发现可以用ALS的累及规律来解释,根据该规律,个体发育中较新的运动功能比较旧的运动功能更早丧失。基于本研究的结果,我们得出结论,ALS最初累及G. Holstege提出的“第一系统”中个体发育较新的运动功能,其解剖结构由脑干和脊髓中的运动前神经元和运动神经元组成。

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