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急性脊髓损伤的非侵入性药物神经保护治疗的系统评价。

A systematic review of non-invasive pharmacologic neuroprotective treatments for acute spinal cord injury.

机构信息

University of British Columbia, Combined Neurosurgical and Orthopaedic Spine Program, Department of Orthopaedics, Vancouver, British Columbia, Canada.

出版信息

J Neurotrauma. 2011 Aug;28(8):1545-88. doi: 10.1089/neu.2009.1149. Epub 2010 Apr 14.

Abstract

An increasing number of therapies for spinal cord injury (SCI) are emerging from the laboratory and seeking translation into human clinical trials. Many of these are administered as soon as possible after injury with the hope of attenuating secondary damage and maximizing the extent of spared neurologic tissue. In this article, we systematically review the available pre-clinical research on such neuroprotective therapies that are administered in a non-invasive manner for acute SCI. Specifically, we review treatments that have a relatively high potential for translation due to the fact that they are already used in human clinical applications, or are available in a form that could be administered to humans. These include: erythropoietin, NSAIDs, anti-CD11d antibodies, minocycline, progesterone, estrogen, magnesium, riluzole, polyethylene glycol, atorvastatin, inosine, and pioglitazone. The literature was systematically reviewed to examine studies in which an in-vivo animal model was utilized to assess the efficacy of the therapy in a traumatic SCI paradigm. Using these criteria, 122 studies were identified and reviewed in detail. Wide variations exist in the animal species, injury models, and experimental designs reported in the pre-clinical literature on the therapies reviewed. The review highlights the extent of investigation that has occurred in these specific therapies, and points out gaps in our knowledge that would be potentially valuable prior to human translation.

摘要

越来越多的脊髓损伤 (SCI) 治疗方法正在从实验室中涌现,并寻求转化为人体临床试验。许多治疗方法在受伤后尽快进行,希望减轻继发性损伤并最大限度地保留神经组织。在本文中,我们系统地回顾了这些非侵入性急性 SCI 神经保护治疗方法的可用临床前研究。具体来说,我们回顾了那些由于已经在人类临床应用中使用,或者可以以可用于人类的形式提供而具有较高转化潜力的治疗方法。这些方法包括:促红细胞生成素、非甾体抗炎药、抗 CD11d 抗体、米诺环素、孕酮、雌激素、镁、利鲁唑、聚乙二醇、阿托伐他汀、肌苷和吡格列酮。系统地审查了文献,以检查在创伤性 SCI 范式中利用体内动物模型评估治疗效果的研究。使用这些标准,确定了 122 项研究,并进行了详细审查。在综述的治疗方法的临床前文献中,动物物种、损伤模型和实验设计存在广泛差异。该综述强调了这些特定疗法的研究程度,并指出了在人类转化之前可能有价值的知识空白。

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