Department of Physical Therapy, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv 69978, Israel.
Brain. 2012 Feb;135(Pt 2):418-30. doi: 10.1093/brain/awr270. Epub 2011 Nov 16.
Central pain below the injury level after spinal cord injury is excruciating, chronic and resistive to treatment. Animal studies suggest that pretreatment may prevent central pain, but to date there are no measures to predict its development. Our aim was to monitor changes in the sensory profile below the lesion prior to the development of below-level central pain in order to search for a parameter that could predict its risk and to further explore its pathophysiology. Thirty patients with spinal cord injury and 27 healthy controls underwent measurement of warm, cold, heat-pain and touch thresholds as well as graphaesthesia, allodynia, hyperpathia and wind-up pain in intact region and in the shin and feet (below level). Patients were tested at 2-4 weeks, 1-2.5 months and 2.5-6 months after the injury or until central pain had developed. At the end of the follow-up, 46% of patients developed below-level central pain. During the testing periods, individuals who eventually developed central pain had higher thermal thresholds than those who did not and displayed high rates of abnormal sensations (allodynia and hyperpathia), which gradually increased with time until central pain developed. Logistic regressions revealed that the best predictor for the risk of below-level central pain was allodynia in the foot in the second testing session with a 77% probability (90.9% confidence). The results suggest that neuronal hyperexcitability, which may develop consequent to damage to spinothalamic tracts, precedes central pain. Furthermore, it appears that below-level central pain develops after a substantial build-up of hyperexcitability. To the best of our knowledge, this is the first systematic report establishing that neuronal hyperexcitability precedes central pain. Predicting the risk for central pain can be utilized to initiate early treatment in order to prevent its development.
脊髓损伤后损伤水平以下的中枢性疼痛是剧烈的、慢性的且对治疗有抵抗力。动物研究表明,预处理可能预防中枢性疼痛,但迄今为止尚无预测其发展的措施。我们的目的是在损伤水平以下的中枢性疼痛发展之前监测损伤以下感觉特征的变化,以寻找可预测其风险的参数,并进一步探讨其病理生理学。30 名脊髓损伤患者和 27 名健康对照者接受了完整区域和小腿及足部(损伤以下)的温热、冷、热痛和触觉阈值以及绘图觉、感觉过敏、超敏和上冲痛的测量。患者在损伤后 2-4 周、1-2.5 个月和 2.5-6 个月以及发生中枢性疼痛之前进行测试。在随访结束时,46%的患者出现了损伤以下的中枢性疼痛。在测试期间,最终发生中枢性疼痛的个体的热阈值高于未发生的个体,并且表现出较高的异常感觉(感觉过敏和超敏),这些感觉逐渐随时间增加,直到发生中枢性疼痛。逻辑回归显示,对损伤以下中枢性疼痛风险的最佳预测因子是第二次测试中足部的感觉过敏,其概率为 77%(90.9%置信区间)。结果表明,可能由于脊髓丘脑束损伤而发展的神经元兴奋性过高,先于中枢性疼痛。此外,似乎是在神经元兴奋性过高的大量蓄积之后,才发生损伤以下的中枢性疼痛。据我们所知,这是首次系统报告确立神经元兴奋性过高先于中枢性疼痛。预测中枢性疼痛的风险可以用于早期治疗以预防其发展。