Delineating structural and metabolic abnormalities in amygdala and hippocampal subfields for different seizure‐onset patterns via stereotactic electroencephalography

Author:

Feng Tao12,Yang Yanfeng12,Wang Yihe123,Wei Peng‐hu12ORCID,Fan Xiaotong12,Zhang Huaqiang12,An Yang12,Wang Tianren12,Huang Yuda12,Chen Sichang12,Piao Yueshan24,Xiao Fenglai35,Duncan John S.35,Shan Yongzhi12ORCID,Zhao Guoguang126

Affiliation:

1. Department of Neurosurgery Xuanwu Hospital, Capital Medical University Beijing China

2. China International Neuroscience Institute (CHINA‐INI) Beijing China

3. Department of Clinical & Experimental Epilepsy UCL Queen Square Institute of Neurology London UK

4. Department of Pathology, Xuanwu Hospital Capital Medical University Beijing China

5. MRI Unit, Chalfont Centre for Epilepsy Chalfont Saint Peter UK

6. Institute for Brain Disorder Beijing China

Abstract

AbstractAimsWe aimed to investigate mesial temporal lobe abnormalities in mesial temporal lobe epilepsy (MTLE) patients with hypersynchronous (HYP) and low‐voltage fast rhythms (LVF) onset identified by stereotactic electroencephalography (SEEG) and evaluate their diagnostic and prognostic value.MethodsFifty‐one MTLE patients were categorized as HYP or LVF by SEEG. High‐resolution MRI volume‐based analysis and 18F‐FDG‐PET standard uptake values of hippocampal and amygdala subfields were quantified and compared with 57 matched controls. Further analyses were conducted to delineate the distinct pathological characteristics differentiating the two groups. Diagnostic and prognostic prediction performance of these biomarkers were assessed using receiver operating characteristic curves.ResultsLVF‐onset individuals demonstrated ipsilateral amygdala enlargement (p = 0.048) and contralateral hippocampus hypermetabolism (p = 0.042), pathological results often accompany abnormalities in the temporal lobe cortex, while HYP‐onset subjects had significant atrophy (p < 0.001) and hypometabolism (p = 0.013) in ipsilateral hippocampus and its subfields, as well as amygdala atrophy (p < 0.001), pathological results are highly correlated with hippocampal sclerosis. Severe fimbria atrophy was observed in cases of HYP‐onset MTLE with poor prognosis (AUC = 0.874).ConclusionIndividuals with different seizure‐onset patterns display specific morphological and metabolic abnormalities in the amygdala and hippocampus. Identifying these subfield abnormalities can improve diagnostic and prognostic precision, guiding surgical strategies for MTLE.

Funder

Beijing Municipal Health Commission

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

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