Pharmacological Treatment of Degenerative Cervical Myelopathy: A Critical Review of Current Evidence.

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY Neurospine Pub Date : 2024-06-01 Epub Date: 2024-06-30 DOI:10.14245/ns.2448140.070
Jordan J Levett, Miltiadis Georgiopoulos, Simon Martel, Wissam Al Mugheiry, Nikolaos A Stavropoulos, Miguel Vega-Arroyo, Carlo Santaguida, Michael H Weber, Jeff D Golan, Peter Jarzem, Jean A Ouellet, Georgios Klironomos, Andreas K Demetriades
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Abstract

Degenerative cervical myelopathy (DCM) is the leading cause of spinal cord dysfunction in adults, representing substantial morbidity and significant financial and resource burdens. Typically, patients with progressive DCM will eventually receive surgical treatment. Nonetheless, despite advancements in pharmacotherapeutics, evidence for pharmacological therapy remains limited. Health professionals from various fields would find interest in pharmacological agents that could benefit patients with mild DCM or enhance surgical outcomes. This review aims to consolidate all clinical and experimental evidence on the pharmacological treatment of DCM. We conducted a comprehensive narrative review that presents all pharmacological agents that have been investigated for DCM treatment in both humans and animal models. Riluzole exhibits effectiveness solely in rat models, but not in treating mild DCM in humans. Cerebrolysin emerges as a potential neuroprotective agent for myelopathy in animals but had contradictory results in clinical trials. Limaprost alfadex demonstrates motor function improvement in animal models and exhibits promising outcomes in a small clinical trial. Glucocorticoids not only fail to provide clinical benefits but may also lead to adverse events. Cilostazol, anti-Fas ligand antibody, and Jingshu Keli display promise in animal studies, while erythropoietin, granulocyte colony-stimulating factor and limaprost alfadex exhibit potential in both animal and human research. Existing evidence mainly rests on weak clinical data and animal experimentation. Current pharmacological efforts target ion channels, stem cell differentiation, inflammatory, vascular, and apoptotic pathways. The inherent nature and pathogenesis of DCM offer substantial prospects for developing neurodegenerative or neuroprotective therapies capable of altering disease progression, potentially delaying surgical intervention, and optimizing outcomes for those undergoing surgical decompression.

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退行性颈椎病的药物治疗:对当前证据的严格审查
退行性颈椎脊髓病(DCM)是导致成人脊髓功能障碍的主要原因,不仅发病率高,而且会带来巨大的经济和资源负担。通常情况下,进展性 DCM 患者最终会接受手术治疗。然而,尽管药物治疗取得了进步,但药物治疗的证据仍然有限。各领域的医疗专业人员都会对能使轻度 DCM 患者受益或提高手术效果的药理药物感兴趣。本综述旨在整合有关 DCM 药物治疗的所有临床和实验证据。我们进行了全面的叙述性综述,介绍了在人体和动物模型中用于 DCM 治疗的所有药理药物。利鲁唑仅对大鼠模型有效,但对治疗人类轻度 DCM 无效。脑活素是一种潜在的神经保护剂,可治疗动物脊髓病,但在临床试验中的结果却相互矛盾。利马前列素(Limaprost alfadex)可改善动物模型的运动功能,并在一项小型临床试验中显示出良好的疗效。糖皮质激素不仅不能带来临床疗效,还可能导致不良反应。西洛他唑、抗 Fas 配体抗体和京舒克力在动物实验中表现出良好的疗效,而促红细胞生成素、粒细胞集落刺激因子和利马前列素在动物和人体研究中均表现出潜力。现有证据主要依赖于薄弱的临床数据和动物实验。目前的药理学研究主要针对离子通道、干细胞分化、炎症、血管和细胞凋亡途径。DCM 的固有性质和发病机制为开发神经退行性变或神经保护疗法提供了广阔的前景,这些疗法能够改变疾病的进展,有可能推迟手术干预,并优化接受手术减压者的预后。
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来源期刊
Neurospine
Neurospine Multiple-
CiteScore
5.80
自引率
18.80%
发文量
93
审稿时长
10 weeks
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