The delineation of largely deformed brain midline using regression‐based line detection network

稳健性(进化) 卷积神经网络 人工智能 中线偏移 地标 深度学习 回归 计算机科学 计算机视觉 模式识别(心理学) 计算机断层摄影术 统计 数学 医学 放射科 生物 生物化学 基因
作者
Hao Wei,Xiangyu Tang,Minqing Zhang,Qingfeng Li,Xiaodan Xing,Xiang Zhou,Zhong Xue,Wenzhen Zhu,Zailiang Chen,Feng Shi
出处
期刊:Medical Physics [Wiley]
卷期号:47 (11): 5531-5542 被引量:6
标识
DOI:10.1002/mp.14302
摘要

Purpose The human brain has two cerebral hemispheres that are roughly symmetric and separated by a midline, which is nearly a straight line shown in axial computed tomography (CT) images in healthy subjects. However, brain diseases such as hematoma and tumors often cause midline shift, where the degree of shift can be regarded as a quantitative indication in clinical practice. To facilitate clinical evaluation, we need computer‐aided methods to automate this quantification. Nevertheless, most existing studies focused on the landmark‐ or symmetry‐based methods that provide only the existence of shift or its maximum distance, which could be easily affected by anatomical variability and large brain deformations. Intuitive results such as midline delineation or measurement are lacking. In this study, we focus on developing an automated and robust method based on the fully convolutional neural network for the delineation of midline in largely deformed brains. Methods We propose a novel regression‐based line detection network (RLDN) for the robust midline delineation, especially in largely deformed brains. Specifically, to improve the robustness of delineation in largely deformed brains, we regard the delineation of the midline as the skeleton extraction task and then use the multiscale bidirectional integration module to acquire more representative features. Based on the skeleton extraction, we incorporate the regression task into it to delineate more accurate and continuous midline, especially in largely deformed brains. Our study utilized the public CQ 500 dataset (128 subjects) for training with hold‐out validation on 61 subjects from a private cohort accrued from a local hospital. Results The mean line distance error and F1‐score were 1.17 ± 0.72 mm with 0.78 on CQ 500 test set, and 4.15 ± 3.97 mm with 0.61 on the private dataset. Besides, significant differences ( P < 0.05) were observed between our method and other comparative ones on these two datasets. Conclusions This work provides a novel solution to acquire robust delineation of the midline, especially in largely deformed brains, and achieves state‐of‐the‐art performance on the public and our private dataset, which makes it possible for automated diagnosis of relevant brain diseases in the future.

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