Morphometric and radiomics analysis toward the prediction of epilepsy associated with supratentorial low-grade glioma in children.
Authors
Affiliations (9)
Affiliations (9)
- Department of Pediatrics, Taipei Medical University Hospital, Taipei Medical University, Taipei, Taiwan.
- Department of Pediatrics, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
- Taipei Neuroscience Institute, Taipei Medical University Hospital, Taipei, Taiwan.
- Department of Medical Imaging, School of Medicine, Taipei Medical University Hospital, Taipei, Taiwan.
- Department of Radiology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
- Division of Pediatric Neurosurgery, Department of Neurosurgery, Taipei Medical University Hospital, Taipei, Taiwan.
- Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
- In-Service Master Program in Artificial Intelligence in Medicine, College of Medicine, Taipei Medical University, No.250, Wuxing St., Xinyi Dist, Taipei City, 110, Taiwan. [email protected].
- Clinical Big Data Research Center, Taipei Medical University Hospital, Taipei Medical University, Taipei, Taiwan. [email protected].
Abstract
Understanding the impact of epilepsy on pediatric brain tumors is crucial to diagnostic precision and optimal treatment selection. This study investigated MRI radiomics features, tumor location, voxel-based morphometry (VBM) for gray matter density, and tumor volumetry to differentiate between children with low grade glioma (LGG)-associated epilepsies and those without, and further identified key radiomics features for predicting of epilepsy risk in children with supratentorial LGG to construct an epilepsy prediction model. A total of 206 radiomics features of tumors and voxel-based morphometric analysis of tumor location features were extracted from T2-FLAIR images in a primary cohort of 48 children with LGG with epilepsy (N = 23) or without epilepsy (N = 25), prior to surgery. Feature selection was performed using the minimum redundancy maximum relevance algorithm, and leave-one-out cross-validation was applied to assess the predictive performance of radiomics and tumor location signatures in differentiating epilepsy-associated LGG from non-epilepsy cases. Voxel-based morphometric analysis showed significant positive t-scores within bilateral temporal cortex and negative t-scores in basal ganglia between epilepsy and non-epilepsy groups. Eight radiomics features were identified as significant predictors of epilepsy in LGG, encompassing characteristics of 2 locations, 2 shapes, 1 image gray scale intensity, and 3 textures. The most important predictor was temporal lobe involvement, followed by high dependence high grey level emphasis, elongation, area density, information correlation 1, midbrain and intensity range. The Linear Support Vector Machine (SVM) model yielded the best prediction performance, when implemented with a combination of radiomics features and tumor location features, as evidenced by the following metrics: precision (0.955), recall (0.913), specificity (0.960), accuracy (0.938), F-1 score (0.933), and area under curve (AUC) (0.950). Our findings demonstrated the efficacy of machine learning models based on radiomics features and voxel-based anatomical locations in predicting the risk of epilepsy in supratentorial LGG. This model provides a highly accurate tool for distinguishing epilepsy-associated LGG in children, supporting precise treatment planning. Not applicable.