肌萎缩侧索硬化症患者下延髓和颈脊髓下运动神经元受累的进展模式。

Q3 Medicine
J R Zhao, X Y Pang, J M Bai, J H Zhang, H F Wang, M Li, Z H Chen, H M Cheng, L Ling, X S Huang
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引用次数: 0

摘要

目的:探讨肌萎缩性侧索硬化症(ALS)患者下延髓及颈脊髓的下运动神经元(LMN)受累模式。方法:回顾性分析解放军总医院第一医疗中心神经内科自2022年9月至2023年12月收治的200例非胸源性散发性肌萎缩侧索硬化症患者的针肌电图(EMG)资料。所有的参与者都符合EI的诊断标准。根据起病部位分为延髓下发病组(34例)、脊髓起病组(166例)[包括颈下脊髓起病组(92例)和腰骶脊髓起病组(74例)]。统计下延髓和颈髓支配肌肉的肌电异常,分析LMN受累特征。采用二项分布检验确定LMN累及第二中枢神经系统节段的进展是否随机。结果:200例ALS患者中,男性111例(55.5%),女性89例(44.5%),发病年龄28 ~ 86(56±11)岁。同时累及下延髓和下颈脊髓的LMN患者,20例(10.0%)胸锁乳突肌(SCM)或斜方肌(TRA)肌电图正常,7例(3.5%)SCM-EMG和TRA-EMG结果正常。下颈脊髓发病时的肌电异常率分别为舌肌(GEN)-肌电异常(88.2%,30/34)、tra -肌电异常(70.6%,24/34)和scm -肌电异常(67.6%,23/34)。下颈脊髓起病时的肌电异常率分别为TRA-EMG(72.8%, 67/92)、SCM-EMG(38.0%, 35/92)和GEN-EMG(32.6%, 30/92)。二项分布检验显示,LMN累及中枢神经系统第二节段的进展并非随机的。结论:LMN累及下延髓和颈脊髓的进展主要是连续的,但也有不连续的进展模式。脊髓发病的ALS患者的下延髓相对较少参与疾病进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Progression patterns of lower motor neuron involvement in the lower medulla oblongata and cervical spinal cord of amyotrophic lateral sclerosis patients].

Objective: To investigate the lower motor neuron (LMN) involvement patterns in the lower medulla oblongata and cervical spinal cord in amyotrophic lateral sclerosis (ALS) patients. Methods: The needle electromyography (EMG) data of 200 patients with non-thoracic onset sporadic ALS, hospitalized in the Neurology Department of the First Medical Center of the Chinese PLA General Hospital from September 2022 to December 2023, were retropectively analyzed. All participants met the EI Escorial-Revised diagnostic criteria. According to the onset site, the patients were divided into the lower medulla oblongata onset group(34 cases), the spinal cord onset group(166 cases) [including the lower cervical spinal cord onset group (92 cases) and the lumbosacral spinal cord onset group (74 cases)]. Electromyography (EMG) abnormalities in the muscles innervated by the lower medulla oblongata and cervical cord were counted, and the characteristics of LMN involvement were analyzed. The binomial distribution test was used to determine whether the progression of LMN involvement to the second central nervous system segment was random. Results: Among 200 ALS patients, there were 111 males (55.5%) and 89 females (44.5%), with an age onset of 28-86 (56±11) years. 20 (10.0%) cases with normal sternocleidomastoid (SCM)-EMG or trapezius (TRA)-EMG results, and 7 (3.5%) cases with normal SCM-EMG and TRA-EMG results were observed in patients with LMN involvement in both the lower medulla oblongata and lower cervical spinal cord. The abnormal rates of EMG at the onset of lower cervical spinal cord were tongue muscle (GEN)-EMG (88.2%, 30/34), TRA-EMG (70.6%, 24/34) and SCM-EMG (67.6%, 23/34), respectively. The abnormal rates of EMG at the onset of lower cervical spinal cord were TRA-EMG (72.8%, 67/92), SCM-EMG (38.0%, 35/92) and GEN-EMG (32.6%, 30/92), respectively. The binomial distribution test showed that the progression of LMN involvement to the second segment of the central nervous system was not random (all P<0.05). In low bulbar onset patients, the abnormal rate of LMN involvement was higher in the lower cervical spinal cord segment [100.0% (34/34)], and lower in the lumbosacral spinal cord segment[91.2% (31/34)]. In the lower cervical spinal cord onset group, the abnormal rate of LMN involvement was lower in the the low medulla obliterum[32.6% (30/92)] and high in the lumbosacral spinal cord [96.7% (89/92)].In the lumbosacral spinal cord onset group, the abnormal rate of LMN involvement was low in the low medulla oblata [27.0% (20/74)] and high in the lower cervical spinal cord [94.6% (70/74)]. Conclusions: The progression of LMN involvement in the lower medulla oblongata and cervical spinal cord is primarily continuous, while a discontinuous progression pattern was also observed. The lower medulla oblongata of ALS patients with spinal onset is relatively less involved in disease progression.

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Zhonghua yi xue za zhi
Zhonghua yi xue za zhi Medicine-Medicine (all)
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