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[关于使用赛美克斯治疗的运动神经元病患者慢性部分去神经支配与生活质量的研究]

[The study of chronic partial denervation and quality of life in patients with motor neuron disease treated with semax].

作者信息

Serdiuk A V, Levitskiĭ G N, Miasoedov N F, Skvortsova V I

出版信息

Zh Nevrol Psikhiatr Im S S Korsakova. 2007;107(4):29-39.

Abstract

The study of chronic partial denervation (CPD) and quality of life was carried out in 27 patients with definite, probable and possible diagnosis of motor neuron disease (MND) treated with semax (1% solution). The needle electromyography (EMG) was performed thrice with short-term 2 month interval (60 days before enrollment and on day 1 and day 48 of the study) in three muscles on bulbar, cervical and lumbosacral levels on the less affected side. According to Revised El-Escorial Criteria (1998) the needle EMG for diagnostic purposes was also performed in two muscles on the cervical and lumbosacral levels on the more affected side along with stimulation electroneuronmyography of motor and sensory fibers of the peripheral nerves of neck, upper and lower extremities. The open-label clinical trial of Semax (1% solution) was conducted in sequential groups of patients. The drug was administered intranasally in two 10-day-long courses with 2-weeks break in daily dose of 12 mg. Sixty days before enrollment, and on days 1, 10, 24, 34 and 48, patients were assessed by the Norris ALS, the ALS Functioning Rating Scale and the ALSAQ-40 quality of life in the ALS scale. It was shown that CPD on the early as well as on the late stages was characterized by forward-backward, but not unidirectional course, that did not allow to recommend the follow-up needle EMG with short-term interval for evaluation of drug efficacy monitoring. Early CPD stages were characterized by forward-backwards fluctuations reflecting the compensatory reinnervation process (a phenomenon of exchange of muscle fibers, more rational in view of reinnervation, between adjacent motor units) whereas on the late CPD stages these forward-backwards CPD fluctuations reflected the processes of progressive deterioration of muscle fibers and secondary demyelination of large motor axons. Semax (1% solution) does not influence either the course of CPD or the dynamics of clinical estimates, in particular the terms of ensuing marked functional deficits on bulbar, cervical and lumbosacral levels of segmental innervation. However, 1% semax significantly improves the total estimate of life quality due to the improvement of emotional state and motivation in MND patients with the maximal effect on day 10. This finding suggests that it is feasible to administer 1% semax in complex MND palliative therapy.

摘要

对27例确诊、疑似和可能诊断为运动神经元病(MND)且接受赛美克斯(1%溶液)治疗的患者进行了慢性部分去神经支配(CPD)与生活质量的研究。在病情较轻一侧的延髓、颈部和腰骶部的三块肌肉上,每隔2个月(入组前60天以及研究的第1天和第48天)进行三次针极肌电图(EMG)检查。根据修订的埃尔埃斯科里亚尔标准(1998年),为诊断目的,还在病情较重一侧的颈部和腰骶部的两块肌肉上进行了针极肌电图检查,并对颈部、上肢和下肢周围神经的运动和感觉纤维进行了刺激神经电图检查。赛美克斯(1%溶液)的开放标签临床试验在连续的患者组中进行。该药物通过鼻腔给药,分两个为期10天的疗程,每日剂量为12毫克,中间间隔2周。在入组前60天以及第1、10、24、34和48天,通过诺里斯肌萎缩侧索硬化症(ALS)量表、ALS功能评定量表和ALS生活质量量表(ALSAQ - 40)对患者进行评估。结果显示,早期和晚期的CPD特征均为有反复变化,而非单向病程,这使得不建议通过短期间隔的随访针极肌电图来评估药物疗效监测。早期CPD阶段的特征是反复波动,反映了代偿性再支配过程(一种肌肉纤维交换现象,从再支配角度来看,相邻运动单位之间的这种交换更为合理),而在晚期CPD阶段,这些反复的CPD波动反映了肌肉纤维进行性恶化和大型运动轴突继发性脱髓鞘的过程。赛美克斯(1%溶液)既不影响CPD的病程,也不影响临床评估的动态变化,特别是在延髓、颈部和腰骶部节段性神经支配水平上随后出现明显功能缺陷的情况。然而,1%的赛美克斯由于改善了MND患者的情绪状态和动机,显著提高了生活质量的总体评估,在第10天效果最为明显。这一发现表明,在MND综合姑息治疗中给予1%的赛美克斯是可行的。

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