Predicting post-surgical seizure outcomes in drug-resistant temporal lobe epilepsy using hippocampal radiomics from 18F-FDG hybrid PET/MRI

To develop multivariate hippocampal radiomics models using multimodal 18 F-FDG hybrid PET/MRI and clinical variables to predict post-surgical seizure outcomes in patients with drug-resistant temporal lobe epilepsy (TLE). We retrospectively analyzed 117 drug-resistant TLE patients from Xuanwu Hospital (August 2015–March 2023) who underwent preoperative 18 F-FDG hybrid PET/MRI, surgical intervention, and one-year postoperative follow-up using Engel classification. Structural (3D-T1 and T2-FLAIR) and metabolic ( 18 F-FDG PET) images were obtained. Hippocampal subfields were automatically segmented using FreeSurfer on 3D T1 images, with 18 F-FDG PET and T2-FLAIR images registered accordingly. Radiomics features were extracted from the hippocampal subfields. Feature selection was performed using the minimum redundancy maximum relevance algorithm and the least absolute shrinkage and selection operator regression methods to calculate radscores. Radiomics-clinical and clinical models was constructed and model performance was evaluated using receiver operating characteristic analysis and decision curve analysis. Patients were divided into hippocampal sclerosis (HS) and non-HS groups based on histology and mediation analysis explored relationships among radscore, HS, and Engel classification. The radiomics model combining all three imaging sequences outperformed models using single or dual modalities. In the training set, the combined 18 F-FDG PET/MRI radiomics-clinical model demonstrated higher discrimination than the clinical model alone (AUC = 0.915 vs. 0.716, p = 0.004). In the test set, the combined model showed a numerically higher AUC (0.819 vs. 0.743); however, this difference did not reach statistical significance ( p = 0.661). Decision curve analysis shown that the combined 18 F-FDG PET/MRI radiomics-clinical model provides higher clinical benefits in all risk threshold compared with the clinical model. The radscore was significantly higher in the HS group than in the non-HS group ( t = 2.308, p = 0.023). Mediation analysis shows that radscore is a significant mediator between HS and Engel classification (proportion of indirect effect = 45.8%, p = 0.028). The combined 18 F-FDG PET/MRI radiomics-clinical model enhances the prediction of post-surgical seizure outcomes in drug-resistant TLE patients. Radiomics features may reflect the pathological state of HS, aiding in preoperative prognostication and clinical decision-making.

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Publication Details

Journal
BMC Medical Imaging
Published
2026-08-26
DOI
https://doi.org/10.1186/s12880-026-02708-2
Primary Topic
Glioma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

Predicting post-surgical seizure outcomes in drug-resistant temporal lobe epilepsy using hippocampal radiomics from 18F-FDG hybrid PET/MRI

Jingjuan Wang, Bixiao Cui, Yaqin Hou, Siqi Zhang et al.
BMC Medical Imaging
Glioma Diagnosis and Treatment
article

Predicting post-surgical seizure outcomes in drug-resistant temporal lobe epilepsy using hippocampal radiomics from 18F-FDG hybrid PET/MRI

Jingjuan Wang, Bixiao Cui, Yaqin Hou, Siqi Zhang, Chenyang Yao, Jie Lu, Zhenming Wang, Jie Hu
article en

Abstract

To develop multivariate hippocampal radiomics models using multimodal 18 F-FDG hybrid PET/MRI and clinical variables to predict post-surgical seizure outcomes in patients with drug-resistant temporal lobe epilepsy (TLE). We retrospectively analyzed 117 drug-resistant TLE patients from Xuanwu Hospital (August 2015–March 2023) who underwent preoperative 18 F-FDG hybrid PET/MRI, surgical intervention, and one-year postoperative follow-up using Engel classification. Structural (3D-T1 and T2-FLAIR) and metabolic ( 18 F-FDG PET) images were obtained. Hippocampal subfields were automatically segmented using FreeSurfer on 3D T1 images, with 18 F-FDG PET and T2-FLAIR images registered accordingly. Radiomics features were extracted from the hippocampal subfields. Feature selection was performed using the minimum redundancy maximum relevance algorithm and the least absolute shrinkage and selection operator regression methods to calculate radscores. Radiomics-clinical and clinical models was constructed and model performance was evaluated using receiver operating characteristic analysis and decision curve analysis. Patients were divided into hippocampal sclerosis (HS) and non-HS groups based on histology and mediation analysis explored relationships among radscore, HS, and Engel classification. The radiomics model combining all three imaging sequences outperformed models using single or dual modalities. In the training set, the combined 18 F-FDG PET/MRI radiomics-clinical model demonstrated higher discrimination than the clinical model alone (AUC = 0.915 vs. 0.716, p = 0.004). In the test set, the combined model showed a numerically higher AUC (0.819 vs. 0.743); however, this difference did not reach statistical significance ( p = 0.661). Decision curve analysis shown that the combined 18 F-FDG PET/MRI radiomics-clinical model provides higher clinical benefits in all risk threshold compared with the clinical model. The radscore was significantly higher in the HS group than in the non-HS group ( t = 2.308, p = 0.023). Mediation analysis shows that radscore is a significant mediator between HS and Engel classification (proportion of indirect effect = 45.8%, p = 0.028). The combined 18 F-FDG PET/MRI radiomics-clinical model enhances the prediction of post-surgical seizure outcomes in drug-resistant TLE patients. Radiomics features may reflect the pathological state of HS, aiding in preoperative prognostication and clinical decision-making.

BMC Medical Imaging
Union Hospital (HK), Capital Medical University (CN), Huazhong University of Science and Technology (CN)
China Postdoctoral Science Foundation, National Key Research and Development Program of China Stem Cell and Translational Research
Peace, Justice and strong institutions
Openalex Percentile: Top 11%
Glioma Diagnosis and Treatment
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