McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, 3801 Rue University, Montreal, QC, H3A 2B4, Canada.
McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, 3801 Rue University, Montreal, QC, H3A 2B4, Canada; Department of Neurology, Perelman Center for Advanced Medicine, University of Pennsylvania, 3400 Civic Center Drive, Philadelphia, PA, USA, 19104.
Neuroimage. 2020 Mar;208:116442. doi: 10.1016/j.neuroimage.2019.116442. Epub 2019 Dec 9.
In conventional non-quantitative magnetic resonance imaging, image contrast is consistent within images, but absolute intensity can vary arbitrarily between scans. For quantitative analysis of intensity data, images are typically normalized to a consistent reference. The most convenient reference is a tissue that is always present in the image, and is unlikely to be affected by pathological processes. In multiple sclerosis neuroimaging, both the white and gray matter are affected, so normalization techniques that depend on brain tissue may introduce bias or remove biological changes of interest. We introduce a complementary procedure, image "calibration," the goal of which is to remove technical intensity artifacts while preserving biological differences. We demonstrate a deep learning approach to segmenting fat from within the orbit of the eyes on T-weighted images at 1.5 and 3 T to use as a reference tissue, and use it to calibrate 1018 scans from 256 participants in a study of pediatric-onset multiple sclerosis. The machine segmentations agreed with the adjudicating expert (DF) segmentations better than did those of other expert humans, and calibration resulted in better agreement with semi-quantitative magnetization transfer ratio imaging than did normalization with the WhiteStripe algorithm. We suggest that our method addresses two key priorities in the field: (1) it provides a robust option for serial calibration of conventional scans, allowing comparison of disease change in persons imaged at multiple time points in their disease; and (ii) the technique is fast, as the deep learning segmentation takes only 0.5 s/scan, which is feasible for both large and small datasets.
在常规的非定量磁共振成像中,图像内的对比度是一致的,但绝对强度在扫描之间可以任意变化。为了对强度数据进行定量分析,通常将图像归一化为一致的参考值。最方便的参考值是始终存在于图像中的组织,并且不太可能受到病理过程的影响。在多发性硬化症神经影像学中,白质和灰质都受到影响,因此依赖于脑组织的归一化技术可能会引入偏差或消除感兴趣的生物学变化。我们引入了一种补充程序,即图像“校准”,其目的是在保留生物学差异的同时去除技术强度伪影。我们展示了一种基于深度学习的方法,用于从 1.5 和 3T 的 T 加权图像中分割眼睛眼眶内的脂肪,作为参考组织,并使用它来校准 256 名儿科多发性硬化症患者研究中的 1018 次扫描。机器分割与裁决专家(DF)的分割比其他专家人类的分割更吻合,并且校准后的结果与半定量磁化传递比成像的一致性优于 WhiteStripe 算法的归一化结果。我们建议我们的方法解决了该领域的两个关键优先事项:(1)它为常规扫描的连续校准提供了一个可靠的选择,允许在疾病的多个时间点对成像的个体进行疾病变化的比较;(ii)该技术速度很快,因为深度学习分割仅需 0.5 秒/扫描,对于大数据集和小数据集都是可行的。