Rashid Tanweer, Liu Hangfan, Ware Jeffrey B, Li Karl, Romero Jose Rafael, Fadaee Elyas, Nasrallah Ilya M, Hilal Saima, Bryan R Nick, Hughes Timothy M, Davatzikos Christos, Launer Lenore, Seshadri Sudha, Heckbert Susan R, Habes Mohamad
Neuroimage Analytics Laboratory and Biggs Institute Neuroimaging Core, Glenn Biggs Institute for Neurodegenerative Disorders, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Center for Biomedical Image Computing and Analytics, University of Pennsylvania, Philadelphia, PA, USA.
Neuroimage Rep. 2023 Mar;3(1). doi: 10.1016/j.ynirp.2023.100162. Epub 2023 Mar 7.
Deep learning has been demonstrated effective in many neuroimaging applications. However, in many scenarios, the number of imaging sequences capturing information related to small vessel disease lesions is insufficient to support data-driven techniques. Additionally, cohort-based studies may not always have the optimal or essential imaging sequences for accurate lesion detection. Therefore, it is necessary to determine which imaging sequences are crucial for precise detection. This study introduces a deep learning framework to detect enlarged perivascular spaces (ePVS) and aims to find the optimal combination of MRI sequences for deep learning-based quantification. We implemented an effective lightweight U-Net adapted for ePVS detection and comprehensively investigated different combinations of information from SWI, FLAIR, T1-weighted (T1w), and T2-weighted (T2w) MRI sequences. The experimental results showed that T2w MRI is the most important for accurate ePVS detection, and the incorporation of SWI, FLAIR and T1w MRI in the deep neural network had minor improvements in accuracy and resulted in the highest sensitivity and precision (sensitivity =0.82, precision =0.83). The proposed method achieved comparable accuracy at a minimal time cost compared to manual reading. The proposed automated pipeline enables robust and time-efficient readings of ePVS from MR scans and demonstrates the importance of T2w MRI for ePVS detection and the potential benefits of using multimodal images. Furthermore, the model provides whole-brain maps of ePVS, enabling a better understanding of their clinical correlates compared to the clinical rating methods within only a couple of brain regions.
深度学习已在许多神经成像应用中被证明是有效的。然而,在许多情况下,捕获与小血管疾病病变相关信息的成像序列数量不足以支持数据驱动技术。此外,基于队列的研究可能并不总是拥有用于精确病变检测的最佳或必要成像序列。因此,有必要确定哪些成像序列对于精确检测至关重要。本研究引入了一种深度学习框架来检测扩大的血管周围间隙(ePVS),旨在找到用于基于深度学习的量化的MRI序列的最佳组合。我们实现了一种适用于ePVS检测的有效轻量级U-Net,并全面研究了来自SWI、FLAIR、T1加权(T1w)和T2加权(T2w)MRI序列的不同信息组合。实验结果表明,T2w MRI对于准确的ePVS检测最为重要,并且在深度神经网络中纳入SWI、FLAIR和T1w MRI在准确性上有微小提升,并导致了最高的灵敏度和精确率(灵敏度 = 0.82,精确率 = 0.83)。与人工读取相比,所提出的方法在最小的时间成本下实现了相当的准确性。所提出的自动化流程能够对MR扫描中的ePVS进行稳健且高效的读取,并证明了T2w MRI对于ePVS检测的重要性以及使用多模态图像的潜在益处。此外,该模型提供了ePVS的全脑图谱,与仅在几个脑区使用的临床评级方法相比,能够更好地理解它们的临床相关性。