Cirstea Carmen M, Lee Phil, Craciunas Sorin C, Choi In-Young, Burris Joseph E, Nudo Randolph J
From the Departments of Neurology (CMC, I-YC), Molecular & Integrative Physiology (PL), Physical Medicine & Rehabilitation (RJN); Hoglund Brain Imaging Center (CMC, PL, SCC, I-YC), Landon Center on Aging (RJN), University of Kansas Medical Center, Kansas City, Kansas; and Department of Physical Medicine and Rehabilitation, University of Missouri, Columbia, Missouri (CMC, JEB).
Am J Phys Med Rehabil. 2018 Jan;97(1):23-33. doi: 10.1097/PHM.0000000000000791.
The aim of the study was to examine whether neural state of spared motor and premotor cortices captured before a therapy predicts therapy-related motor gains in chronic subcortical stroke.
Ten survivors, presenting chronic moderate upper limb impairment, underwent proton magnetic resonance spectroscopy, magnetic resonance imaging, clinical, and kinematics assessments before a 4-wk impairment-oriented training. Clinical/kinematics assessments were repeated after therapy, and motor gain was defined as positive values of clinical upper limb/elbow motion changes and negative values of trunk motion changes. Candidate predictors were N-acetylaspartate-neuronal marker, glutamate-glutamine-indicator of glutamatergic neurotransmission, and myo-inositol-glial marker, measured bilaterally within the upper limb territory in motor and premotor (premotor cortex, supplementary motor area) cortices. Traditional predictors (age, stroke length, pre-therapy upper limb clinical impairment, infarct volume) were also investigated.
Poor motor gain was associated with lower glutamate-glutamine levels in ipsilesional primary motor cortex and premotor cortex (r = 0.77, P = 0.01 and r = 0.78, P = 0.008, respectively), lower N-acetylaspartate in ipsilesional premotor cortex (r = 0.69, P = 0.02), higher glutamate-glutamine in contralesional primary motor cortex (r = -0.68, P = 0.03), and lower glutamate-glutamine in contralesional supplementary motor area (r = 0.64, P = 0.04). These predictors outperformed myo-inositol metrics and traditional predictors (P ≈ 0.05-1.0).
Glutamatergic state of bilateral motor and premotor cortices and neuronal state of ipsilesional premotor cortex may be important for predicting motor outcome in the context of a restorative therapy.
本研究旨在探讨在治疗前获取的保留运动皮质和运动前皮质的神经状态是否能预测慢性皮质下卒中与治疗相关的运动功能改善情况。
10名患有慢性中度上肢功能障碍的幸存者,在进行为期4周的以损伤为导向的训练前,接受了质子磁共振波谱、磁共振成像、临床和运动学评估。治疗后重复进行临床/运动学评估,运动功能改善定义为临床上肢/肘部运动变化的正值和躯干运动变化的负值。候选预测指标包括双侧上肢运动皮质和运动前皮质(运动前皮质、辅助运动区)区域内测量的N-乙酰天门冬氨酸(神经元标志物)、谷氨酸-谷氨酰胺(谷氨酸能神经传递指标)和肌醇(胶质细胞标志物)。还研究了传统预测指标(年龄、卒中时长、治疗前上肢临床损伤、梗死体积)。
运动功能改善不佳与患侧初级运动皮质和运动前皮质中较低的谷氨酸-谷氨酰胺水平相关(分别为r = 0.77,P = 0.01和r = 0.78,P = 0.008),患侧运动前皮质中较低的N-乙酰天门冬氨酸水平(r = 0.69,P = 0.02),健侧初级运动皮质中较高的谷氨酸-谷氨酰胺水平(r = -0.68,P = 0.03),以及健侧辅助运动区中较低的谷氨酸-谷氨酰胺水平(r = 0.64,P = 0.04)。这些预测指标优于肌醇指标和传统预测指标(P≈0.05 - 1.0)。
双侧运动皮质和运动前皮质的谷氨酸能状态以及患侧运动前皮质的神经元状态可能对预测恢复性治疗背景下的运动结果很重要。