Health & Rehabilitation Research Institute, Faculty of Health and Environmental Sciences, Auckland University of Technology, Private Bag 92006, Auckland 1142, New Zealand; Department of Physiotherapy, Waitakere Hospital, Auckland 0650, New Zealand.
Health & Rehabilitation Research Institute, Faculty of Health and Environmental Sciences, Auckland University of Technology, Private Bag 92006, Auckland 1142, New Zealand.
Brain Stimul. 2016 Jul-Aug;9(4):488-500. doi: 10.1016/j.brs.2016.03.020. Epub 2016 Apr 4.
Chronic pain is characterised by maladaptive neuroplasticity in many systems, including the motor system. There is evidence that patients with chronic pain demonstrate altered corticospinal and intracortical excitability; however, findings are inconsistent and existing literature in this area has not been systematically reviewed.
To systematically review studies examining corticospinal and intracortical excitability using transcranial magnetic stimulation in people with chronic pain compared to healthy controls and to provide a meta-analysis of study outcomes.
Databases were searched for controlled studies evaluating corticospinal and intracortical excitability in chronic pain conditions. Outcome measure data were entered into separate meta-analyses and effect sizes calculated. A subgroup analysis based on the type of chronic pain population was also performed.
Forty-three studies were included, encompassing a pooled total of 1009 people with chronic pain and 658 control participants. Significant effect sizes (P < 0.05) indicated that in chronic pain populations the duration of the silent period and the extent of short-interval intracortical inhibition were both reduced and short-interval intracortical facilitation was enhanced. The subgroup analysis revealed that only the neuropathic pain group exhibited significant effect sizes for these outcome measures. Effect sizes for the remaining outcome measures were not significant
There is evidence of motor cortex disinhibition in chronic pain populations, suggestive of a disruption in GABA-mediated intracortical inhibition. Disinhibition was more pronounced in populations with neuropathic pain. These findings provide new insights into the relationship between chronic pain and motor cortex excitability, which may have meaningful implications for the future treatment of chronic pain conditions.
慢性疼痛的特征是包括运动系统在内的许多系统出现适应性神经可塑性改变。有证据表明,慢性疼痛患者表现出皮质脊髓和皮质内兴奋性改变;然而,研究结果不一致,该领域的现有文献尚未进行系统综述。
系统综述使用经颅磁刺激检查慢性疼痛患者与健康对照者皮质脊髓和皮质内兴奋性的研究,并对研究结果进行荟萃分析。
检索数据库中评估慢性疼痛情况下皮质脊髓和皮质内兴奋性的对照研究。将结局测量数据输入单独的荟萃分析,并计算效应量。还根据慢性疼痛人群的类型进行了亚组分析。
共纳入 43 项研究,共纳入 1009 名慢性疼痛患者和 658 名对照参与者。显著的效应量(P<0.05)表明,在慢性疼痛人群中,静默期持续时间和短程抑制的程度均降低,而短程抑制的程度增加。亚组分析显示,只有神经病理性疼痛组这些结局测量的效应量具有统计学意义。其余结局测量的效应量没有统计学意义。
慢性疼痛人群存在运动皮层去抑制的证据,提示 GABA 介导的皮质内抑制中断。在神经病理性疼痛人群中,抑制作用更为明显。这些发现为慢性疼痛与运动皮层兴奋性之间的关系提供了新的见解,这可能对未来慢性疼痛疾病的治疗具有重要意义。