Wen Xin, Zeng Wentao, Li Chiyin, Qin Yue, Qiao Yanqiang, Lu Tao, Dun Wanghuan, Zhang Ming, Mu Junya
Department of Medical Imaging, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Xi'an Academy of Fine Arts, Xi'an, Shaanxi, China.
Front Hum Neurosci. 2025 Jul 1;19:1598598. doi: 10.3389/fnhum.2025.1598598. eCollection 2025.
Growing evidence suggests that corticospinal tract (CST) damage and microstructural integrity are key predictors of post-stroke motor impairment. However, their combined clinical utility-particularly in CST sub-pathways originating from non-primary motor cortical areas-remains underexplored. This study aimed to determine whether microstructural integrity and lesion load (LL) of each CST sub-pathway at 2 weeks predict motor outcomes at 2, 6, and 12 weeks post-stroke.
Fifty seven participants completed motor and neuroimaging evaluations at 2 weeks post-stroke and underwent follow-up motor assessments at 6 ( = 37) and 12 weeks ( = 34). The integrity of the CSTs was quantified using diffusion spectrum imaging (DSI), while CST-LL was measured using structural magnetic resonance imaging, both based on the sensorimotor area tract template atlas. Stepwise multiple linear regression models were used to assess the predictive value of CST microstructural integrity and CST-LL in each sub-pathway at 2 weeks for motor function at 2, 6, and 12 weeks post-stroke.
The results indicated CST integrity and CST-LL were both the main determinants of motor deficit at 2 weeks post-stroke. Specifically, the integrity of CSTs from the primary motor cortex (M1), reflected by fractional anisotropy, emerged as a significant predictor of post-stroke motor deficit at 2 weeks, whereas CST integrity from the dorsal premotor cortex (PMd), reflected by generalized fractional anisotropy, quantitative anisotropy, and radial diffusivity. CST-LL originating from non-M1 motor areas, such as primary sensory cortex (S1), were also the main determinants for motor impairment at 2 weeks post-stroke. However, compared to CST integrity, CST-LL from non-M1 motor areas, including both the PMd and S1, were more dominant predictors, explaining 68.3% ( = 0.683, < 0.001) and 79.5% ( = 0.795, < 0.001) of the variance in motor outcomes at 6 and 12 weeks.
The microstructural integrity of the PMd tracts and CST-LL from the non-M1 motor areas may be promising biomarker for post-stroke motor impairment. These findings highlight the pivotal role of non-M1 tracts in post-stroke motor function, particularly the PMd tracts, as a potential intervention target to enhance motor recovery.
越来越多的证据表明,皮质脊髓束(CST)损伤和微观结构完整性是中风后运动功能障碍的关键预测指标。然而,它们的联合临床效用,特别是在源自非初级运动皮层区域的CST子通路中,仍未得到充分探索。本研究旨在确定中风后2周时每个CST子通路的微观结构完整性和病变负荷(LL)是否能预测2周、6周和12周时的运动结果。
57名参与者在中风后2周完成了运动和神经影像学评估,并在6周(n = 37)和12周(n = 34)进行了随访运动评估。基于感觉运动区束模板图谱,使用扩散光谱成像(DSI)对CST的完整性进行量化,同时使用结构磁共振成像测量CST-LL。采用逐步多元线性回归模型评估中风后2周时每个子通路中CST微观结构完整性和CST-LL对2周、6周和12周运动功能的预测价值。
结果表明,CST完整性和CST-LL都是中风后2周时运动功能障碍的主要决定因素。具体而言,由分数各向异性反映的初级运动皮层(M1)的CST完整性,成为中风后2周时运动功能障碍的重要预测指标,而由广义分数各向异性、定量各向异性和径向扩散率反映的背侧运动前皮层(PMd)的CST完整性。源自非M1运动区域(如初级感觉皮层(S1))的CST-LL,也是中风后2周时运动功能障碍的主要决定因素。然而,与CST完整性相比,来自包括PMd和S1在内的非M1运动区域的CST-LL是更主要的预测指标,分别解释了6周和12周时运动结果方差的68.3%(β = 0.683,p < 0.001)和79.5%(β = 0.795,p < 0.001)。
PMd束的微观结构完整性和来自非M1运动区域的CST-LL可能是中风后运动功能障碍的有前景的生物标志物。这些发现突出了非M1束在中风后运动功能中的关键作用,特别是PMd束,作为增强运动恢复的潜在干预靶点。