Automated segmentation of the dorsal root ganglia in MRI

IF 4.7 2区 医学 Q1 NEUROIMAGING
Aliya C. Nauroth-Kreß , Simon Weiner , Lea Hölzli , Thomas Kampf , György A. Homola , Mirko Pham , Philip Kollmannsberger , Magnus Schindehütte
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引用次数: 0

Abstract

The dorsal root ganglion (DRG) contains all primary sensory neurons, but its functional role in somatosensory and pain processing remains unclear. Recently, MR imaging techniques have been developed for objective in vivo observation of the DRG. In particular, DRG MR imaging endpoints such as DRG volume and DRG T2w signal are emerging as biomarkers with initial evidence of meaningful correlations with biochemical and genetic parameters as well as neuropathic pain as clinically relevant applications. However, the future validation and use of these novel imaging biomarkers critically depends on the development of fully automated methods for DRG image analysis. To date, DRG detection and evaluation on MR images has been limited to expert annotation through manual segmentation. Fast and operator-independent, yet accurate and robust, segmentation methods are required to enable observation of larger patient cohorts and across multiple sites. Thus, fully automated DRG segmentation is a prerequisite for the analysis of more complex microstructural and functional image datasets, such as from DRG diffusion tensor or perfusion metabolic imaging.
Here, we developed a fully automated DRG segmentation workflow based on deep learning. A convolutional neural network (CNN) was trained using the nnU-Net framework on a large dataset of high-resolution 3D T2-weighted MR images of healthy controls (220 DRGs). Automated DRG segmentations generated with this network were on par with expert annotations (dice similarity coefficient of 0.87 for human expert vs. 0.89 for trained CNN) while being faster by a factor of 10. Finally, we validated the method in Fabry disease as a genetic model disorder for DRG pathomorphological injury. The trained CNN was able to reproduce the manually segmented changes known in FD patients as a function of FD genotype and FD pain phenotype.
We developed a fully automated method for DRG MRI segmentation and validated its application as a novel imaging biomarker using the DRG injury example of Fabry disease.
背根神经节的MRI自动分割。
背根神经节(DRG)包含所有初级感觉神经元,但其在体感觉和疼痛加工中的功能作用尚不清楚。近年来,磁共振成像技术已经发展到对DRG进行客观的体内观察。特别是,DRG MR成像终点,如DRG体积和DRG T2w信号正在成为生物标志物,初步证据表明与生化和遗传参数以及神经性疼痛具有临床相关应用的有意义的相关性。然而,这些新型成像生物标志物的未来验证和使用严重依赖于DRG图像分析全自动方法的发展。迄今为止,对MR图像的DRG检测和评价仅限于通过人工分割的专家标注。需要快速且独立于操作人员,但准确且稳健的分割方法,以便能够观察更大的患者队列和跨多个部位。因此,全自动DRG分割是分析更复杂的微观结构和功能图像数据集(如DRG扩散张量或灌注代谢成像)的先决条件。在这里,我们开发了一个基于深度学习的全自动DRG分割工作流程。使用nnU-Net框架在健康对照(220个DRGs)的高分辨率3D t2加权MR图像的大型数据集上训练卷积神经网络(CNN)。使用该网络生成的自动DRG分割与专家注释相当(人类专家的骰子相似系数为0.87,而训练CNN的骰子相似系数为0.89),同时速度提高了10倍。最后,我们在Fabry病中验证了该方法作为DRG病理形态学损伤的遗传模型疾病。经过训练的CNN能够再现FD患者中已知的人工分割的变化,作为FD基因型和FD疼痛表型的功能。我们开发了一种全自动的DRG MRI分割方法,并以Fabry病DRG损伤为例验证了其作为新型成像生物标志物的应用。
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来源期刊
NeuroImage
NeuroImage 医学-核医学
CiteScore
11.30
自引率
10.50%
发文量
809
审稿时长
63 days
期刊介绍: NeuroImage, a Journal of Brain Function provides a vehicle for communicating important advances in acquiring, analyzing, and modelling neuroimaging data and in applying these techniques to the study of structure-function and brain-behavior relationships. Though the emphasis is on the macroscopic level of human brain organization, meso-and microscopic neuroimaging across all species will be considered if informative for understanding the aforementioned relationships.
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