Yoganathan Katie, Trubshaw Michael, Kohl Oliver, Gohil Chetan, Echeverria-Altuna Irene, Dharmadasa Thanuja, Northall Alicia, Zokaei Nahid, Lester David, Garcia Gayle, Collins Alexis, Amein Benazir, Nobre Anna C, Talbot Kevin, Thompson Alexander G, Woolrich Mark, Turner Martin R
Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DU, UK.
Oxford Centre for Human Brain Activity, Wellcome Centre for Integrative Neuroimaging, Department of Psychiatry, University of Oxford, Oxford OX3 7JX, UK.
Brain Commun. 2025 Sep 9;7(5):fcaf339. doi: 10.1093/braincomms/fcaf339. eCollection 2025.
Biomarkers of disease activity that holistically capture motor system dysfunction are needed to accelerate drug discovery in amyotrophic lateral sclerosis. Magnetoencephalography is a sensitive, non-invasive measure of cortical neurophysiology. Corticomuscular coherence reflects the functional coupling of cortical oscillations with downstream muscle activity recorded by electromyography. Cortical beta frequency bursting is known to represent a core feature of the neurophysiology underpinning movement. This study aimed to characterize disruption of beta frequency activity in both cortex and muscle to refine the understanding of corticomuscular coherence loss in amyotrophic lateral sclerosis. The study analysed 42 people living with amyotrophic lateral sclerosis and 33 healthy age-matched controls. Participants undertook an isometric hand gripping task during magnetoencephalography. Muscle contraction was measured using bipolar surface electromyography recordings at both forearms. All participants performed 120 trials of the gripper task bilaterally, and 60 trials unilaterally on each side. For each trial type, the mean corticomuscular coherence over trials was calculated for each participant and the groups were compared via cluster-based permutations tests. Beta burst metrics were calculated for the motor cortex (magnetoencephalography) and flexor forearm muscles (surface electromyography) including burst fractional occupancy, burst duration and amplitude. During muscular contraction, beta frequency corticomuscular coherence from the motor cortices contralateral to the gripper task was markedly reduced in amyotrophic lateral sclerosis patients, despite no significant difference in grip strength compared with controls. Source localization analysis showed globally reduced corticomuscular coherence in amyotrophic lateral sclerosis with significant differences in the motor regions contralateral to the engaged hand. There were no significant beta frequency activity changes in the engaged-hand electromyography signal in amyotrophic lateral sclerosis compared with controls. In contrast, analysis of the cortical motor regions revealed reduced rate of beta bursting and higher amplitude during the contraction phase of the task in amyotrophic lateral sclerosis. The corticomuscular coherence disruption in amyotrophic lateral sclerosis appears driven more by cerebral pathology than by muscle denervation. Equal grip strength during the task implies compensatory pathways in disease that are not captured by corticomuscular coherence. Interneuronal dysfunction may underlie the disruption to motor cortex beta bursting. Motor cortical beta frequency metrics have potential as secondary outcome measures in therapeutic trials and need exploration as prodromal markers in asymptomatic individuals genetically predisposed to amyotrophic lateral sclerosis.
为了加速肌萎缩侧索硬化症的药物研发,需要能够全面反映运动系统功能障碍的疾病活动生物标志物。脑磁图是一种对皮质神经生理学敏感的非侵入性测量方法。皮质-肌肉相干性反映了皮质振荡与通过肌电图记录的下游肌肉活动之间的功能耦合。已知皮质β频率爆发代表了支撑运动的神经生理学的核心特征。本研究旨在表征皮质和肌肉中β频率活动的破坏情况,以加深对肌萎缩侧索硬化症中皮质-肌肉相干性丧失的理解。该研究分析了42名肌萎缩侧索硬化症患者和33名年龄匹配的健康对照者。参与者在进行脑磁图检查时执行了等长手部抓握任务。使用双极表面肌电图记录测量双侧前臂的肌肉收缩情况。所有参与者双侧进行120次抓握任务试验,每侧单侧进行60次试验。对于每种试验类型,计算每个参与者试验中的平均皮质-肌肉相干性,并通过基于聚类的置换检验对各组进行比较。计算运动皮质(脑磁图)和前臂屈肌(表面肌电图)的β爆发指标,包括爆发分数占有率、爆发持续时间和幅度。在肌肉收缩期间,与抓握任务对侧的运动皮质的β频率皮质-肌肉相干性在肌萎缩侧索硬化症患者中明显降低,尽管与对照组相比握力没有显著差异。源定位分析显示,肌萎缩侧索硬化症患者的皮质-肌肉相干性整体降低,与被使用手对侧的运动区域存在显著差异。与对照组相比,肌萎缩侧索硬化症患者被使用手的肌电图信号中β频率活动没有显著变化。相反,对皮质运动区域的分析显示,在肌萎缩侧索硬化症患者中,任务收缩期的β爆发率降低,幅度更高。肌萎缩侧索硬化症中的皮质-肌肉相干性破坏似乎更多地是由脑部病变而非肌肉去神经支配驱动的。任务期间握力相等意味着疾病中存在未被皮质-肌肉相干性捕捉到的代偿途径。中间神经元功能障碍可能是运动皮质β爆发破坏的基础。运动皮质β频率指标有潜力作为治疗试验的次要结局指标,并且需要作为无症状个体中肌萎缩侧索硬化症遗传易感性的前驱标志物进行探索。