Tao Feng , Yanfeng Yang , Yihe Wang , Xiaotong Fan , Tianren Wang , Sichang Chen , Penghu Wei , Yongzhi Shan , Guoguang Zhao
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引用次数: 0
Abstract
Background
Mesial temporal lobe epilepsy (MTLE) is the most common medically refractory focal epilepsy, classified into seizure-onset patterns (SOPs) such as hypersynchronous (HYP) and low-voltage fast (LVF) rhythms. However, the morphological and network differences underlying these SOPs and their prognostic implications remain unclear.
Methods
Using voxel-based morphometry (VBM) and individualized structural covariance networks (IDSCNs), we analyzed 55 MTLE patients and 37 healthy controls with high-resolution MRI and stereotactic EEG recordings. VBM identified grey matter volume (GMV) abnormalities, and IDSCNs evaluated patient-specific network disruptions. Hierarchical clustering explored network subtypes, and ROC analysis assessed the predictive value of VBM and IDSCN measures for surgical outcomes.
Results
HYP-onset patients exhibited ipsilateral mesial temporal atrophy and widespread bilateral network disruptions centered on the hippocampus and supramarginal gyrus, along with significant interhemispheric connectivity abnormalities. LVF-onset patients showed subcortical abnormalities and hemispheric network disruptions centered on the fusiform gyrus, with limited interhemispheric propagation. Both SOPs displayed basal ganglia abnormalities. Hierarchical clustering revealed SOP-specific network subtypes. IDSCN outperformed VBM in predicting surgical outcomes.
Conclusion
This study identifies distinct SOP-related morphological and network abnormalities in MTLE and suggests that IDSCN may offer valuable insights into personalized treatment planning and prognostic evaluation, supporting further exploration of network-based biomarkers.
期刊介绍:
Neurobiology of Disease is a major international journal at the interface between basic and clinical neuroscience. The journal provides a forum for the publication of top quality research papers on: molecular and cellular definitions of disease mechanisms, the neural systems and underpinning behavioral disorders, the genetics of inherited neurological and psychiatric diseases, nervous system aging, and findings relevant to the development of new therapies.