Ye Rong, Rua Catarina, O'Callaghan Claire, Jones P Simon, Hezemans Frank H, Kaalund Sanne S, Tsvetanov Kamen A, Rodgers Christopher T, Williams Guy, Passamonti Luca, Rowe James B
Department of Clinical Neurosciences, University of Cambridge and Cambridge University Hospitals NHS Foundation Trust, Herchel Smith Building for Brain and Mind Sciences, Forvie Site, Robinson Way, Cambridge CB2 0SZ, UK.
Department of Clinical Neurosciences, University of Cambridge and Cambridge University Hospitals NHS Foundation Trust, Herchel Smith Building for Brain and Mind Sciences, Forvie Site, Robinson Way, Cambridge CB2 0SZ, UK; Wolfson Brain Imaging Centre, University of Cambridge, Cambridge, UK.
Neuroimage. 2021 Jan 15;225:117487. doi: 10.1016/j.neuroimage.2020.117487. Epub 2020 Oct 24.
Early and profound pathological changes are evident in the locus coeruleus (LC) in dementia and Parkinson's disease, with effects on arousal, attention, cognitive and motor control. The LC can be identified in vivo using non-invasive magnetic resonance imaging techniques which have potential as biomarkers for detecting and monitoring disease progression. Technical limitations of existing imaging protocols have impaired the sensitivity to regional contrast variance or the spatial variability on the rostrocaudal extent of the LC, with spatial mapping consistent with post mortem findings. The current study employs a sensitive magnetisation transfer sequence using ultrahigh field 7T MRI to investigate the LC structure in vivo at high-resolution (0.4 × 0.4 × 0.5 mm). Magnetisation transfer images from 53 healthy older volunteers (52 - 84 years) clearly revealed the spatial features of the LC and were used to create a probabilistic LC atlas for older adults. This atlas may be especially relevant for studying disorders associated with older age. To use the atlas does not require use of the same MT sequence of 7T MRI, provided good co-registration and normalisation is achieved. Consistent rostrocaudal gradients of slice-wise volume, contrast and variance along the LC were observed, mirroring distinctive ex vivo spatial distributions of LC cells in its subregions. The contrast-to-noise ratios were calculated for the peak voxels, and for the averaged signals within the atlas, to accommodate the volumetric differences in estimated contrast. The probabilistic atlas is freely available, and the MRI dataset will be made available for non-commercial research, for replication or to facilitate accurate LC localisation and unbiased contrast extraction in future studies.
在痴呆症和帕金森病中,蓝斑(LC)会出现早期且明显的病理变化,这会影响觉醒、注意力、认知和运动控制。使用非侵入性磁共振成像技术可在活体中识别蓝斑,这些技术有潜力作为检测和监测疾病进展的生物标志物。现有成像方案的技术局限性削弱了对区域对比度差异的敏感性,或蓝斑在头尾方向范围上的空间变异性,而空间映射与尸检结果一致。本研究采用敏感的磁化传递序列,利用超高场7T磁共振成像在高分辨率(0.4×0.4×0.5毫米)下对活体蓝斑结构进行研究。来自53名健康老年志愿者(52 - 84岁)的磁化传递图像清晰地显示了蓝斑的空间特征,并被用于创建老年人的概率性蓝斑图谱。该图谱可能对研究与老年相关的疾病特别有用。使用该图谱不需要使用相同的7T磁共振成像的磁化传递序列,前提是实现了良好的配准和归一化。沿蓝斑观察到切片体积、对比度和方差的一致头尾梯度,反映了其亚区域中蓝斑细胞独特的离体空间分布。计算了峰值体素以及图谱内平均信号的对比噪声比,以适应估计对比度中的体积差异。概率性图谱可免费获取,磁共振成像数据集将提供用于非商业研究、复制,或便于未来研究中准确的蓝斑定位和无偏对比度提取。