Task-specific cortical mechanisms of taVNS-paired task-oriented training for post-stroke upper extremity dysfunction under cognitive load: an fNIRS study.

IF 2.7 3区 医学 Q3 NEUROSCIENCES
Frontiers in Human Neuroscience Pub Date : 2025-09-24 eCollection Date: 2025-01-01 DOI:10.3389/fnhum.2025.1652612
Shi-Yi Li, Ke Xu, Yi-Xiu Wang, Meng-Huan Wang, Shu-Shan Li, Feng Lin, Zhong-Li Jiang
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引用次数: 0

Abstract

Objective: This study aimed to investigate the cortical task-specific response patterns underlying the improvement of upper limb dysfunction in stroke patients using transcutaneous auricular vagus nerve stimulation (taVNS) paired with task-oriented training (TOT) under varying cognitive loads.

Methods: In this randomized, double-blinded, sham-controlled trial, 30 patients with subacute stroke were enrolled and randomly assigned to either the taVNS group or the Sham group. Both groups received 3 weeks of TOT. The taVNS group received concurrent active taVNS, while the Sham group received concurrent sham stimulation. Assessments were performed pre- and post-intervention. Clinical function was evaluated using the Fugl-Meyer Assessment-Upper Extremity (FMA-UE), Montreal Cognitive Assessment (MoCA), Fatigue Severity Scale (FSS), and Modified Barthel Index (MBI). Neurophysiological measures included heart rate variability (HRV) to assess taVNS efficacy and motor-evoked potentials (MEPs) to assess cortical excitability changes. Brain functional imaging was conducted using functional near-infrared spectroscopy (fNIRS) during motor tasks with different cognitive loads (low-load: continuous horizontal movement; high-load: goal-directed movement) to analyze changes in spontaneous neural activity, task-related regional brain activation characteristics, and brain functional network alterations.

Results: (1) Post-intervention, the taVNS group showed significantly greater improvements in all HRV indices compared to the Sham group (P < 0.05). (2) Both groups exhibited significant improvements from baseline in FMA-UE, MoCA, MBI, and FSS scores (P < 0.05), with the taVNS group demonstrating significantly greater improvement than the Sham group (P < 0.05). (3) MEP results indicated significant improvements in the elicitation rate of ipsilesional MEPs within the taVNS group post-intervention (P < 0.05). Furthermore, compared to the Sham group, the taVNS group showed significantly greater improvements in the ipsilesional MEP elicitation rate and a significant reduction in contralesional MEP latency (P < 0.05). (4) Regarding resting-state fNIRS, the taVNS group exhibited higher Amplitude of Low-Frequency Fluctuation (ALFF) values post-intervention in the ipsilesional prefrontal cortex (PFC), dorsolateral prefrontal cortex (DLPFC), and sensorimotor cortex (SMC) compared to the Sham group (P < 0.05), but these differences were not significant after correction. In task-state fNIR under the low-cognitive-load condition, activation levels in the ipsilesionalS primary motor cortex (M1) and premotor and supplementary motor areas (pSMA) were significantly higher in the taVNS group compared to the Sham group post-intervention (P FDR < 0.05). During the high-cognitive-load task, activation levels in the ipsilesional PFC and DLPFC were significantly higher in the taVNS group compared to the Sham group post-intervention (P FDR < 0.05). (5) Functional network analysis using complex network metrics revealed that the taVNS group exhibited significantly increased nodal clustering coefficient and nodal local efficiency in the ipsilesional DLPFC during the high-cognitive-load task post-intervention compared to the Sham group (P FDR < 0.05).

Conclusion: taVNS paired with TOT enhances autonomic homeostasis, increases corticospinal pathway excitability, activates cognition-motor related brain regions, and modulates functional connectivity networks through multi-pathway neuroregulatory mechanisms. This promotes the formation of task-specific cortical activation and network connectivity during motor tasks under varying cognitive demands in stroke patients. These changes contribute to improved executive control performance in complex tasks, thereby enhancing cognitive-motor integration capabilities and facilitating upper limb functional recovery.

Clinical trial registration: https://www.chictr.org.cn/index.html, Unique Identifier/Registration Number: ChiCTR2400085163.

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认知负荷下tavns配对任务导向训练对脑卒中后上肢功能障碍的任务特异性皮质机制:fNIRS研究。
目的:研究不同认知负荷下经皮耳迷走神经刺激(taVNS)配合任务导向训练(TOT)对脑卒中患者上肢功能障碍改善的皮层任务特异性反应模式。方法:在这项随机、双盲、假对照试验中,30例亚急性脑卒中患者被随机分配到taVNS组和Sham组。两组均接受3周的TOT治疗。taVNS组并发激活taVNS, Sham组并发假手术刺激。评估分别在干预前和干预后进行。临床功能评估采用Fugl-Meyer上肢评估(FMA-UE)、蒙特利尔认知评估(MoCA)、疲劳严重程度量表(FSS)和改良Barthel指数(MBI)。神经生理测量包括心率变异性(HRV)评估taVNS的有效性,运动诱发电位(MEPs)评估皮质兴奋性变化。采用功能近红外光谱(fNIRS)对不同认知负荷(低负荷:连续水平运动;高负荷:目标定向运动)下的运动任务进行脑功能成像,分析自发性神经活动的变化、任务相关脑区域激活特征和脑功能网络的改变。结果:(1)干预后,taVNS组HRV各项指标均较Sham组改善显著(P < 0.05)。(2)两组患者FMA-UE、MoCA、MBI、FSS评分较基线均有显著改善(P < 0.05),其中taVNS组显著高于Sham组(P < 0.05)。(3) MEP结果显示,干预后taVNS组同侧MEP的激发率显著提高(P < 0.05)。此外,与Sham组相比,taVNS组在同侧MEP激发率和对侧MEP潜伏期显著降低方面表现出更大的改善(P < 0.05)。(4)静息状态fNIRS干预后,taVNS组同侧前额叶皮层(PFC)、背外侧前额叶皮层(DLPFC)和感觉运动皮层(SMC)的低频波动幅度(ALFF)值高于Sham组(P < 0.05),但校正后差异不显著。在低认知负荷条件下的任务态fNIR中,干预后,taVNS组的单侧初级运动皮层(M1)和运动前和辅助运动区(pSMA)的激活水平显著高于Sham组(P < 0.05)。在高认知负荷任务中,干预后taVNS组同侧PFC和DLPFC的激活水平显著高于Sham组(P < 0.05)。(5)采用复杂网络指标的功能网络分析显示,干预后高认知负荷任务时,taVNS组同侧DLPFC的节点聚类系数和节点局部效率显著高于Sham组(P < 0.05)。结论:taVNS配合TOT增强自主神经稳态,增加皮质脊髓通路兴奋性,激活认知-运动相关脑区,通过多通路神经调节机制调节功能连接网络。这促进了脑卒中患者在不同认知需求下运动任务中任务特异性皮层激活和网络连接的形成。这些变化有助于改善复杂任务中的执行控制表现,从而增强认知-运动整合能力,促进上肢功能恢复。临床试验注册:https://www.chictr.org.cn/index.html,唯一标识符/注册号:ChiCTR2400085163。
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来源期刊
Frontiers in Human Neuroscience
Frontiers in Human Neuroscience 医学-神经科学
CiteScore
4.70
自引率
6.90%
发文量
830
审稿时长
2-4 weeks
期刊介绍: Frontiers in Human Neuroscience is a first-tier electronic journal devoted to understanding the brain mechanisms supporting cognitive and social behavior in humans, and how these mechanisms might be altered in disease states. The last 25 years have seen an explosive growth in both the methods and the theoretical constructs available to study the human brain. Advances in electrophysiological, neuroimaging, neuropsychological, psychophysical, neuropharmacological and computational approaches have provided key insights into the mechanisms of a broad range of human behaviors in both health and disease. Work in human neuroscience ranges from the cognitive domain, including areas such as memory, attention, language and perception to the social domain, with this last subject addressing topics, such as interpersonal interactions, social discourse and emotional regulation. How these processes unfold during development, mature in adulthood and often decline in aging, and how they are altered in a host of developmental, neurological and psychiatric disorders, has become increasingly amenable to human neuroscience research approaches. Work in human neuroscience has influenced many areas of inquiry ranging from social and cognitive psychology to economics, law and public policy. Accordingly, our journal will provide a forum for human research spanning all areas of human cognitive, social, developmental and translational neuroscience using any research approach.
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