Guttmann University Institute for Neurorehabilitation-UAB , Badalona, Spain.
J Neurotrauma. 2009 Dec;26(12):2185-93. doi: 10.1089/neu.2008.0859.
This study aimed to investigate the cortical motor excitability characteristics in diffuse axonal injury (DAI) due to severe traumatic brain injury (TBI). A variety of excitatory and inhibitory transcranial magnetic stimulation (TMS) paradigms were applied to primary motor cortices of 17 patients and 11 healthy controls. The parameters of testing included resting motor threshold (MT), motor evoked potential (MEP) area under the curve, input-output curves, MEP variability, and silent period (SP) duration. The patient group overall revealed a higher MT, smaller MEP areas, and narrower recruitment curves compared to normal controls (p < 0.05). The alterations in excitability were more pronounced with an increase in DAI severity (p < 0.005) and the presence of motor impairment (p < 0.05), while co-existence of focal lesions did not affect the degree of MEP changes. MEP variability was significantly lower in the group with motor impairment only (p < 0.05). The intracortical inhibition, as revealed by SP duration, did not exhibit any significant differences in any of the patient groups. In conclusion, our findings expand the concept that impairment of the excitatory and inhibitory phenomena in the motor cortex does not proceed in parallel and demonstrate distinct patterns of aberrations in TBI. Furthermore, these data suggest that alterations in the corticospinal excitatory mechanisms are determined predominantly by the severity of DAI, and show a significant relationship with clinical motor dysfunction following severe trauma diffusely affecting the motor cortical connections. In severe TBI, motor and functional recovery might be linked to restitution of normal corticospinal mechanisms, indexed by normalization of the cortical excitability parameters.
本研究旨在探讨严重创伤性脑损伤(TBI)所致弥漫性轴索损伤(DAI)的皮质运动兴奋性特征。我们应用多种兴奋性和抑制性经颅磁刺激(TMS)范式,对 17 名患者和 11 名健康对照者的初级运动皮质进行了检测。测试参数包括静息运动阈值(MT)、运动诱发电位(MEP)曲线下面积、输入-输出曲线、MEP 变异性和静息期(SP)持续时间。与正常对照组相比,患者组整体表现出更高的 MT、更小的 MEP 面积和更窄的募集曲线(p<0.05)。兴奋性改变在 DAI 严重程度增加(p<0.005)和运动功能障碍存在(p<0.05)时更为明显,而局灶性病变的共存并不影响 MEP 变化的程度。仅在存在运动障碍的组中,MEP 变异性显著降低(p<0.05)。作为 SP 持续时间反映的皮质内抑制,在任何患者组中均未显示出任何显著差异。总之,我们的发现扩展了这样一个概念,即运动皮质中兴奋性和抑制性现象的损害并非平行发生,并展示了 TBI 中明显不同的异常模式。此外,这些数据表明,皮质脊髓兴奋性机制的改变主要取决于 DAI 的严重程度,与广泛影响运动皮质连接的严重创伤后运动功能障碍存在显著相关性。在严重 TBI 中,运动和功能恢复可能与正常皮质脊髓机制的恢复有关,这可以通过皮质兴奋性参数的正常化来衡量。