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Unsupervised Generation of Pseudo Normal PET from MRI with Diffusion Model for Epileptic Focus Localization

Authors :
Chen, Wentao
Li, Jiwei
Xu, Xichen
Huang, Hui
Yuan, Siyu
Zhang, Miao
Xu, Tianming
Luo, Jie
Zhou, Weimin
Chen, Wentao
Li, Jiwei
Xu, Xichen
Huang, Hui
Yuan, Siyu
Zhang, Miao
Xu, Tianming
Luo, Jie
Zhou, Weimin
Publication Year :
2024

Abstract

[$^{18}$F]fluorodeoxyglucose (FDG) positron emission tomography (PET) has emerged as a crucial tool in identifying the epileptic focus, especially in cases where magnetic resonance imaging (MRI) diagnosis yields indeterminate results. FDG PET can provide the metabolic information of glucose and help identify abnormal areas that are not easily found through MRI. However, the effectiveness of FDG PET-based assessment and diagnosis depends on the selection of a healthy control group. The healthy control group typically consists of healthy individuals similar to epilepsy patients in terms of age, gender, and other aspects for providing normal FDG PET data, which will be used as a reference for enhancing the accuracy and reliability of the epilepsy diagnosis. However, significant challenges arise when a healthy PET control group is unattainable. Yaakub \emph{et al.} have previously introduced a Pix2PixGAN-based method for MRI to PET translation. This method used paired MRI and FDG PET scans from healthy individuals for training, and produced pseudo normal FDG PET images from patient MRIs that are subsequently used for lesion detection. However, this approach requires a large amount of high-quality, paired MRI and PET images from healthy control subjects, which may not always be available. In this study, we investigated unsupervised learning methods for unpaired MRI to PET translation for generating pseudo normal FDG PET for epileptic focus localization. Two deep learning methods, CycleGAN and SynDiff, were employed, and we found that diffusion-based method achieved improved performance in accurately localizing the epileptic focus.<br />Comment: SPIE Medical Imaging 2024

Details

Database :
OAIster
Publication Type :
Electronic Resource
Accession number :
edsoai.on1438521060
Document Type :
Electronic Resource