Human brain mapping · 2024
Tractography-Based Automated Identification of Retinogeniculate Visual Pathway With Novel Microstructure-Informed Supervised Contrastive Learning.
СтатьяПоддержка исследования: вне правительства СШАПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
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Li Sipei, Zhang Wei, Yao Shun, He Jianzhong, Gao Jingjing, Xue Tengfei, Xie Guoqiang, Chen Yuqian, Torio Erickson F, Feng Yuanjing, Bastos Dhiego C A, Rathi Yogesh, Makris Nikos, Kikinis Ron, Bi Wenya Linda, Golby Alexandra J, O'Donnell Lauren J, Zhang Fan
Аннотация
The retinogeniculate visual pathway (RGVP) is responsible for carrying visual information from the retina to the lateral geniculate nucleus. Identification and visualization of the RGVP are important in studying the anatomy of the visual system and can inform the treatment of related brain diseases. Diffusion MRI (dMRI) tractography is an advanced imaging method that uniquely enables in vivo mapping of the 3D trajectory of the RGVP. Currently, identification of the RGVP from tractography data relies on expert (manual) selection of tractography streamlines, which is time-consuming, has high clinical and expert labor costs, and is affected by inter-observer variability. In this paper, we present a novel deep learning framework, DeepRGVP, to enable fast and accurate identification of the RGVP from dMRI tractography data. We design a novel microstructure-informed supervised contrastive learning method that leverages both streamline label and tissue microstructure information to determine positive and negative pairs. We propose a new streamline-level data augmentation method to address highly imbalanced training data, where the number of RGVP streamlines is much lower than that of non-RGVP streamlines. In the experiments, we perform comparisons with several state-of-the-art deep learning methods that were designed for tractography parcellation. Furthermore, to assess the generalizability of the proposed RGVP method, we apply our method to dMRI tractography data from neurosurgical patients with pituitary tumors. In comparison with the state-of-the-art methods, we show superior RGVP identification results using DeepRGVP with significantly higher accuracy and F1 scores. In the patient data experiment, we show DeepRGVP can successfully identify RGVPs despite the effect of lesions affecting the RGVPs. Overall, our study shows the high potential of using deep learning to automatically identify the RGVP.