Chinmay Prabhakar, Hongwei Li, J. Paetzold, T. Loehr, Chen Niu, M. Muhlau, D. Rueckert, B. Wiestler, Bjoern H Menze
{"title":"Self-pruning Graph Neural Network for Predicting Inflammatory Disease Activity in Multiple Sclerosis from Brain MR Images","authors":"Chinmay Prabhakar, Hongwei Li, J. Paetzold, T. Loehr, Chen Niu, M. Muhlau, D. Rueckert, B. Wiestler, Bjoern H Menze","doi":"10.48550/arXiv.2308.16863","DOIUrl":null,"url":null,"abstract":"Multiple Sclerosis (MS) is a severe neurological disease characterized by inflammatory lesions in the central nervous system. Hence, predicting inflammatory disease activity is crucial for disease assessment and treatment. However, MS lesions can occur throughout the brain and vary in shape, size and total count among patients. The high variance in lesion load and locations makes it challenging for machine learning methods to learn a globally effective representation of whole-brain MRI scans to assess and predict disease. Technically it is non-trivial to incorporate essential biomarkers such as lesion load or spatial proximity. Our work represents the first attempt to utilize graph neural networks (GNN) to aggregate these biomarkers for a novel global representation. We propose a two-stage MS inflammatory disease activity prediction approach. First, a 3D segmentation network detects lesions, and a self-supervised algorithm extracts their image features. Second, the detected lesions are used to build a patient graph. The lesions act as nodes in the graph and are initialized with image features extracted in the first stage. Finally, the lesions are connected based on their spatial proximity and the inflammatory disease activity prediction is formulated as a graph classification task. Furthermore, we propose a self-pruning strategy to auto-select the most critical lesions for prediction. Our proposed method outperforms the existing baseline by a large margin (AUCs of 0.67 vs. 0.61 and 0.66 vs. 0.60 for one-year and two-year inflammatory disease activity, respectively). Finally, our proposed method enjoys inherent explainability by assigning an importance score to each lesion for the overall prediction. Code is available at https://github.com/chinmay5/ms_ida.git","PeriodicalId":18289,"journal":{"name":"Medical image computing and computer-assisted intervention : MICCAI ... International Conference on Medical Image Computing and Computer-Assisted Intervention","volume":"1 1","pages":"226-236"},"PeriodicalIF":0.0000,"publicationDate":"2023-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical image computing and computer-assisted intervention : MICCAI ... International Conference on Medical Image Computing and Computer-Assisted Intervention","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.48550/arXiv.2308.16863","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Multiple Sclerosis (MS) is a severe neurological disease characterized by inflammatory lesions in the central nervous system. Hence, predicting inflammatory disease activity is crucial for disease assessment and treatment. However, MS lesions can occur throughout the brain and vary in shape, size and total count among patients. The high variance in lesion load and locations makes it challenging for machine learning methods to learn a globally effective representation of whole-brain MRI scans to assess and predict disease. Technically it is non-trivial to incorporate essential biomarkers such as lesion load or spatial proximity. Our work represents the first attempt to utilize graph neural networks (GNN) to aggregate these biomarkers for a novel global representation. We propose a two-stage MS inflammatory disease activity prediction approach. First, a 3D segmentation network detects lesions, and a self-supervised algorithm extracts their image features. Second, the detected lesions are used to build a patient graph. The lesions act as nodes in the graph and are initialized with image features extracted in the first stage. Finally, the lesions are connected based on their spatial proximity and the inflammatory disease activity prediction is formulated as a graph classification task. Furthermore, we propose a self-pruning strategy to auto-select the most critical lesions for prediction. Our proposed method outperforms the existing baseline by a large margin (AUCs of 0.67 vs. 0.61 and 0.66 vs. 0.60 for one-year and two-year inflammatory disease activity, respectively). Finally, our proposed method enjoys inherent explainability by assigning an importance score to each lesion for the overall prediction. Code is available at https://github.com/chinmay5/ms_ida.git
多发性硬化症(MS)是一种以中枢神经系统炎症病变为特征的严重神经系统疾病。因此,预测炎症性疾病的活动性对疾病评估和治疗至关重要。然而,多发性硬化症病变可以发生在整个大脑中,并且在形状、大小和总数上各不相同。病变负荷和位置的高度差异使得机器学习方法难以学习全脑MRI扫描的全局有效表示来评估和预测疾病。从技术上讲,将必要的生物标志物(如损伤负荷或空间接近度)纳入其中是非常重要的。我们的工作代表了首次尝试利用图神经网络(GNN)来聚合这些生物标志物以获得新的全局表示。我们提出了一种两阶段MS炎症性疾病活动性预测方法。首先,用三维分割网络检测病灶,用自监督算法提取病灶的图像特征。其次,使用检测到的病变构建患者图。病灶作为图中的节点,用第一阶段提取的图像特征初始化。最后,根据病灶的空间接近性将其连接起来,并将炎症疾病活动预测制定为一个图分类任务。此外,我们提出了一种自修剪策略来自动选择最关键的病变进行预测。我们提出的方法在很大程度上优于现有基线(1年和2年炎症疾病活动性的auc分别为0.67 vs 0.61和0.66 vs 0.60)。最后,我们提出的方法具有固有的可解释性,通过为每个病变分配一个重要分数来进行整体预测。代码可从https://github.com/chinmay5/ms_ida.git获得