Barnden Leighton, Crouch Benjamin, Kwiatek Richard, Shan Zack, Thapaliya Kiran, Staines Donald, Bhuta Sandeep, Del Fante Peter, Burnet Richard
National Centre for Neuroimmunology and Emerging Diseases, Menzies Health Institute Queensland, Griffith University, Southport, QLD 4222, Australia.
Nuclear Medicine Department, Royal Adelaide Hospital, Adelaide, SA 5000, Australia.
Brain Sci. 2022 Dec 9;12(12):1693. doi: 10.3390/brainsci12121693.
Differential axonal myelination synchronises signalling over different axon lengths. The consequences of myelination processes described at the cellular level for the regulation of myelination at the macroscopic level are unknown. We analysed multiple cohorts of myelin-sensitive brain MRI. Our aim was to (i) confirm a previous report of anti-correlation between myelination in subcortical and sensorimotor areas in healthy subjects, (ii) and thereby test our hypothesis for a regulatory interaction between them. We analysed nine image-sets across three different human cohorts using six MRI modalities. Each image-set contained healthy controls (HC) and ME/CFS subjects. Subcortical and Sensorimotor regions of interest (ROI) were optimised for the detection of anti-correlations and the same ROIs were used to test the HC in all image-sets. For each cohort, median MRI values were computed in both regions for each subject and their correlation across the cohort was computed. We confirmed correlations in healthy controls between subcortical and sensorimotor regions in six image-sets: three T1wSE ( = 5 × 10, 5 × 10, 0.002), T2wSE ( =2 × 10), MTC ( = 0.01), and WM volume ( = 0.02). T1/T2 was the exception with a correlation ( = 0.01). This myelin regulation study is novel in several aspects: human subjects, cross-sectional design, ROI optimization, spin-echo MRI and reproducible across multiple independent image-sets. In multiple independent image-sets we confirmed an anti-correlation between subcortical and sensorimotor myelination which supports a previously unreported regulatory interaction. The subcortical region contained the brain's primary regulatory nuclei. We suggest a mechanism has evolved whereby relatively low subcortical myelination in an individual is compensated by upregulated sensorimotor myelination to maintain adequate sensorimotor performance.
轴突髓鞘形成差异使不同轴突长度上的信号同步。细胞水平上描述的髓鞘形成过程对宏观水平髓鞘形成调节的影响尚不清楚。我们分析了多组对髓鞘敏感的脑磁共振成像(MRI)。我们的目的是:(i)证实先前关于健康受试者皮质下和感觉运动区髓鞘形成呈反相关的报告,(ii)从而检验我们关于它们之间存在调节相互作用的假设。我们使用六种MRI模态分析了来自三个不同人类队列的九个图像集。每个图像集都包含健康对照(HC)和肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)受试者。为检测反相关性,对皮质下和感觉运动感兴趣区域(ROI)进行了优化,并且在所有图像集中都使用相同的ROI来检测HC。对于每个队列,计算每个受试者在两个区域的MRI中位数,并计算整个队列中它们的相关性。我们在六个图像集中证实了健康对照中皮质下和感觉运动区域之间的相关性:三个T1加权自旋回波序列( = 5 × 10, 5 × 10, 0.002)、T2加权自旋回波序列( =2 × 10)、磁化传递对比(MTC)( = 0.01)和白质体积( = 0.02)。T1/T2是个例外,呈正相关( = 0.01)。这项髓鞘形成调节研究在几个方面具有创新性:人类受试者、横断面设计、ROI优化、自旋回波MRI以及在多个独立图像集中具有可重复性。在多个独立图像集中,我们证实了皮质下和感觉运动髓鞘形成之间的反相关性,这支持了一种先前未报道的调节相互作用。皮质下区域包含大脑的主要调节核团。我们提出了一种进化而来的机制,即个体中相对较低的皮质下髓鞘形成可通过上调的感觉运动髓鞘形成来补偿,以维持足够的感觉运动功能。