Krishna Vibhor, Andrews Hampton, Varma Abhay, Mintzer Jacobo, Kindy Mark S, Guest James
1 Department of Neurosciences, Medical University of South Carolina , Charleston, South Carolina.
J Neurotrauma. 2014 Feb 1;31(3):215-27. doi: 10.1089/neu.2013.2982.
The preservation of functional neural tissue after spinal cord injury (SCI) is the basis for spontaneous neurological recovery. Some injured patients in the acute phase have more potential for recovery than others. This fact is problematic for the construction of clinical trials because enrollment of subjects with variable recovery potential makes it difficult to detect effects, requires large sample sizes, and risks Type II errors. In addition, the current methods to assess injury and recovery are non-quantitative and not sensitive. It is likely that therapeutic combinations will be necessary to cause substantially improved function after SCI, thus we need highly sensitive techniques to evaluate changes in motor, sensory, autonomic and other functions. We review several emerging neurophysiological techniques with high sensitivity. Quantitative methods to evaluate residual tissue sparing after severe acute SCI have not entered widespread clinical use. This reduces the ability to correlate structural preservation with clinical outcome following SCI resulting in enrollment of subjects with varying patterns of tissue preservation and injury into clinical trials. We propose that the inclusion of additional measures of injury severity, pattern, and individual genetic characteristics may enable stratification in clinical trials to make the testing of therapeutic interventions more effective and efficient. New imaging techniques to assess tract injury and demyelination and methods to quantify tissue injury, inflammatory markers, and neuroglial biochemical changes may improve the evaluation of injury severity, and the correlation with neurological outcome, and measure the effects of treatment more robustly than is currently possible. The ability to test such a multimodality approach will require a high degree of collaboration between clinical and research centers and government research support. When the most informative of these assessments is determined, it may be possible to identify patients with substantial recovery potential, improve selection criteria and conduct more efficient clinical trials.
脊髓损伤(SCI)后功能性神经组织的保存是神经自发恢复的基础。一些急性期受伤的患者比其他患者具有更大的恢复潜力。这一事实给临床试验的开展带来了问题,因为纳入恢复潜力各异的受试者会使检测效果变得困难,需要大样本量,并且存在II类错误的风险。此外,目前评估损伤和恢复情况的方法是非定量的且不敏感。很可能需要多种治疗方法联合使用才能在脊髓损伤后带来功能的显著改善,因此我们需要高度敏感的技术来评估运动、感觉、自主神经及其他功能的变化。我们综述了几种具有高灵敏度的新兴神经生理学技术。评估严重急性脊髓损伤后残余组织保留情况的定量方法尚未广泛应用于临床。这降低了将脊髓损伤后结构保存情况与临床结果相关联的能力,导致在临床试验中纳入了组织保存和损伤模式各异的受试者。我们建议纳入额外的损伤严重程度、模式及个体遗传特征的测量指标,这可能使临床试验能够进行分层,从而使治疗干预的测试更有效率。评估神经束损伤和脱髓鞘的新成像技术以及量化组织损伤、炎症标志物和神经胶质生化变化的方法,可以比目前更有力地改善对损伤严重程度的评估、与神经学结果的相关性以及对治疗效果的测量。测试这种多模态方法的能力将需要临床和研究中心之间高度协作以及政府的研究支持。当确定了这些评估中最具信息价值的方法时,或许就有可能识别出具有显著恢复潜力的患者,改进选择标准并开展更高效的临床试验。