利用卷积神经网络对动脉粥样硬化性狭窄患者的四维血流磁共振成像数据进行颅内血管自动分割

Patrick Winter, Haben Berhane, Jackson E. Moore, M. Aristova, Teresa Reichl, Julian Wollenberg, Adam Richter, Kelly B. Jarvis, Abhinav Patel, Fan Caprio, Ramez Abdalla, S. Ansari, Michael Markl, Susanne Schnell
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引用次数: 0

摘要

颅内四维血流 MRI 可对颅内动脉粥样硬化性疾病(ICAD)患者的血流动力学进行定量评估。然而,由于血管分割耗时,特别是在血管狭窄的情况下,定量评估仍具有挑战性,这往往会导致用户的差异性。为了提高可重复性和稳健性并加快数据分析,我们利用深度学习开发了一种精确的全自动颅内血管狭窄分割方法。手动分割被用作训练的基本事实。对于自动分割,则使用 3D U-Net 进行深度学习。随机选取的 20 个病例(10 个对照组,10 个患者)被分离出来,单独用于测试。确定了威利斯环(CoW)和静脉窦的横截面积和血流参数。此外,还计算了血流保护误差。为了进行统计比较,以两名独立观察者的手动分割为参考,计算了 Dice 评分(DS)、Hausdorff 距离(HD)、平均对称表面距离(ASSD)、Bland-Altman 分析和类间相关性。最后,通过比较基于四维血流的分割与黑色血管壁成像(VWI)的分割,对三个血管狭窄病例进行了更详细的分析。与两名独立观察者相比,没有观察到明显的分割性能差异。在对照组中,CoW 的平均 DS 为 0.85 ± 0.03,鼻窦的平均 DS 为 0.86 ± 0.06。平均 HD 为 7.2 ± 1.5 毫米(CoW)和 6.6 ± 3.7 毫米(鼻窦)。平均 ASSD 为 0.15 ± 0.04 毫米(CoW)和 0.22 ± 0.17 毫米(鼻窦)。患者的平均 DS 为 0.85 ± 0.04(CoW)和 0.82 ± 0.07(鼻窦),HD 为 8.4 ± 3.1 毫米(CoW)和 5.7 ± 1.9 毫米(鼻窦),平均 ASSD 为 0.22 ± 0.10 毫米(CoW)和 0.22 ± 0.11 毫米(鼻窦)。在两个队列中均观察到血流参数的小偏差和一致性限制。对狭窄血管横截面管腔面积的评估显示,该结果与 VWI 分割结果的一致性非常好(ICC:0.93),但存在一致的高估(偏差 ± LOA:28.1 ± 13.9%)。对分割和血流指标的统计分析表明,CNN 和人工分割之间的一致性非常好,在狭窄血管中表现良好。为了进一步提高性能和通用性,未来将考虑更多的 ICAD 分割以及其他颅内血管病变。
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Automated intracranial vessel segmentation of 4D flow MRI data in patients with atherosclerotic stenosis using a convolutional neural network
Intracranial 4D flow MRI enables quantitative assessment of hemodynamics in patients with intracranial atherosclerotic disease (ICAD). However, quantitative assessments are still challenging due to the time-consuming vessel segmentation, especially in the presence of stenoses, which can often result in user variability. To improve the reproducibility and robustness as well as to accelerate data analysis, we developed an accurate, fully automated segmentation for stenosed intracranial vessels using deep learning.154 dual-VENC 4D flow MRI scans (68 ICAD patients with stenosis, 86 healthy controls) were retrospectively selected. Manual segmentations were used as ground truth for training. For automated segmentation, deep learning was performed using a 3D U-Net. 20 randomly selected cases (10 controls, 10 patients) were separated and solely used for testing. Cross-sectional areas and flow parameters were determined in the Circle of Willis (CoW) and the sinuses. Furthermore, the flow conservation error was calculated. For statistical comparisons, Dice scores (DS), Hausdorff distance (HD), average symmetrical surface distance (ASSD), Bland-Altman analyses, and interclass correlations were computed using the manual segmentations from two independent observers as reference. Finally, three stenosis cases were analyzed in more detail by comparing the 4D flow-based segmentations with segmentations from black blood vessel wall imaging (VWI).Training of the network took approximately 10 h and the average automated segmentation time was 2.2 ± 1.0 s. No significant differences in segmentation performance relative to two independent observers were observed. For the controls, mean DS was 0.85 ± 0.03 for the CoW and 0.86 ± 0.06 for the sinuses. Mean HD was 7.2 ± 1.5 mm (CoW) and 6.6 ± 3.7 mm (sinuses). Mean ASSD was 0.15 ± 0.04 mm (CoW) and 0.22 ± 0.17 mm (sinuses). For the patients, the mean DS was 0.85 ± 0.04 (CoW) and 0.82 ± 0.07 (sinuses), the HD was 8.4 ± 3.1 mm (CoW) and 5.7 ± 1.9 mm (sinuses) and the mean ASSD was 0.22 ± 0.10 mm (CoW) and 0.22 ± 0.11 mm (sinuses). Small bias and limits of agreement were observed in both cohorts for the flow parameters. The assessment of the cross-sectional lumen areas in stenosed vessels revealed very good agreement (ICC: 0.93) with the VWI segmentation but a consistent overestimation (bias ± LOA: 28.1 ± 13.9%).Deep learning was successfully applied for fully automated segmentation of stenosed intracranial vasculatures using 4D flow MRI data. The statistical analysis of segmentation and flow metrics demonstrated very good agreement between the CNN and manual segmentation and good performance in stenosed vessels. To further improve the performance and generalization, more ICAD segmentations as well as other intracranial vascular pathologies will be considered in the future.
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