多模态深度学习模型用于预测中枢神经系统炎症的预后。

IF 4.5 Q1 CLINICAL NEUROLOGY
Brain communications Pub Date : 2025-05-09 eCollection Date: 2025-01-01 DOI:10.1093/braincomms/fcaf179
Bo Kyu Choi, Yoonhyeok Choi, Sooyoung Jang, Woo-Seok Ha, Soomi Cho, Kimoon Chang, Beomseok Sohn, Kyung Min Kim, Yu Rang Park
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引用次数: 0

摘要

中枢神经系统的炎症性疾病造成了巨大的疾病负担,需要及时和适当的预后预测。我们开发了一种整合临床特征和脑MRI数据的多模态深度学习模型,以增强对中枢神经系统炎症的早期预后预测。这项回顾性研究使用薄层t1加权脑MRI扫描和2010年1月至2023年12月期间在三级转诊医院住院的中枢神经系统炎症患者的临床变量。2022年1月以后采集的数据作为外部测试集。首先使用FastSurfer库将3D MRI图像分割成43个大脑区域。然后通过三维卷积神经网络模型对分割后的图像进行特征提取和矢量化处理,然后与临床特征相结合进行预测。每个人工智能模型的性能通过准确性、F1评分、接收者工作特征曲线下面积和精确召回率曲线下面积来评估。内部数据集包括来自291名患者的413张图像(平均年龄:45.5岁±19.3 [SD];男性151例;预后不良者54例)。外部数据集包括来自106名患者的210张图像(平均年龄:45.5岁±18.9 [SD];男性59例;31例预后不良)。在所有病因组中,多模态深度学习模型的表现都优于单模态模型,自身免疫感染的受试者工作特征曲线下面积为0.8048,细菌感染为0.9107,结核病为1.0000,病毒感染为0.9242。此外,与神经科医生、儿科医生和放射科医生相比,人工智能辅助提高了临床医生的预后准确性。我们的研究结果表明,多模态深度学习模型增强了人工智能辅助的中枢神经系统炎症预后预测,提高了模型性能和临床医生的决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multimodal deep learning model for prediction of prognosis in central nervous system inflammation.

Inflammatory diseases of the CNS impose a substantial disease burden, necessitating prompt and appropriate prognosis prediction. We developed a multimodal deep learning model integrating clinical features and brain MRI data to enhance early prognosis prediction of CNS inflammation. This retrospective study used thin-cut T1-weighted brain MRI scans and the clinical variables of patients with CNS inflammation who were admitted to a tertiary referral hospital between January 2010 and December 2023. Data collected after January 2022 served as the external test set. 3D MRI images were first segmented into 43 brain regions using the FastSurfer library. The segmented images were then processed through a 3D convolutional neural network model for feature extraction and vectorization, after which they were integrated with clinical features for prediction. The performance of each artificial intelligence model was assessed using accuracy, F1 score, area under the receiver operating characteristic curve and area under the precision-recall curve. The internal dataset comprised 413 images from 291 patients (mean age, 45.5 years ± 19.3 [SD]; 151 male patients; 54 with poor prognosis). The external dataset comprised 210 images from 106 patients (mean age, 45.5 years ± 18.9 [SD]; 59 male patients; 31 with poor prognosis). The multimodal deep learning model outperformed unimodal models across all aetiological groups, achieving area under the receiver operating characteristic curve values of 0.8048 for autoimmune, 0.9107 for bacterial, 1.0000 for tuberculosis and 0.9242 for viral infections. Furthermore, artificial intelligence assistance improved clinicians' prognostic accuracy, as demonstrated in comparisons with neurologists, paediatricians and radiologists. Our findings demonstrate that the multimodal deep learning model enhances artificial intelligence-assisted prognosis prediction in CNS inflammation, improving both model performance and clinician decision-making.

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