The AEP 3-T MRI research protocol is feasible at multisite national scale, and sensitive for detection of subtle lesions when read by neuroradiologists with expertise in epilepsy.
Abstract
Objective
Detection of epilepsy-causing structural brain lesions on magnetic resonance imaging (MRI) is critical for diagnosis, prognosis, and treatment planning in people with epilepsy. We aimed to establish an epilepsy-directed multisite harmonized 3-T MRI acquisition protocol for the Australian Epilepsy Project (AEP) and describe the clinical structural brain findings in the initial participant cohort.
Methods
The AEP MRI protocol was designed to meet clinical diagnostic and research needs. It includes HARNESS-MRI sequences plus targeted views (temporal pole), susceptibility and diffusion imaging, quantitative measurements (T1, T2), and selected functional MRI tasks. A total of 1330 adults were enrolled and completed imaging assessment at seven sites. Diagnoses at referral were 146 people with first unprovoked seizure only (FUS), 325 with newly diagnosed epilepsy (NDE), 468 with drug-resistant focal epilepsy (DRE), and 391 healthy controls. Imaging data were curated via a centralized platform, relevant sequences were clinically reported by subspecialist epilepsy neuroradiologists, and the report findings were classified. Findings were compared to prior reports from standard clinical MRI.
Results
A structural brain lesion considered to be epileptogenic was detected in 12% in FUS, 18% in NDE, and 39% in DRE, compared with 2% in healthy controls. The most common epileptogenic lesions included hippocampal sclerosis, acquired cortical injury, malformations of cortical development, long-term epilepsy associated tumors, and vascular malformations. Potentially epileptogenic lesions included temporal pole encephaloceles, which were detected in 12% of epilepsy participants versus 7% of healthy controls. In 682 participants with an available prior clinical MRI report, 62 (9.1%) had a new epileptogenic lesion detected on the AEP scan, indicating greater sensitivity of the AEP imaging and reporting process for detection of epileptogenic lesions over standard care (p < .001).
Significance
The AEP 3-T MRI research protocol is feasible at multisite national scale, and sensitive for detection of subtle lesions when read by neuroradiologists with expertise in epilepsy. When added to current Australian clinical practice, this strategy yields significantly more epileptogenic findings.
WMH are common in adults with focal epilepsy, and the frontal lobe is the most frequently affected region, and age, seizure duration, interictal epileptiform discharges, and seizure duration are independent risk factors for greater WMH burden.
Xu Zhang, Wenjie Zhang, Chang Ge et al.· Clinical EEG and Neuroscienc...· 0 citations
Introduction
Approximately 20-30% of temporal lobe epilepsy (TLE) cases present with no visible abnormalities on conventional magnetic resonance imaging (MRI). When interictal electroencephalography (EEG) recordings are also persistently normal, the diagnosis and lateralization become major clinical challenges. We aimed to investigate whether automated hippocampal subfield volumetry could detect subtle structural alterations in these "electro-clinically silent" MRI-negative cases and to correlate these findings with seizure semiology.
Methods
We analyzed 24 patients with clinically diagnosed MRI-negative/EEG-negative TLE and 26 age-matched healthy controls. Despite normal visual inspection on 1.5-T MRI, hippocampal subfield volumes were extracted using an automated segmentation pipeline (volBrain). Seizure semiology was systematically categorized to provide clinical-anatomical correlation.
Results
TLE patients exhibited a significant and selective volume reduction in the right CA4-dentate gyrus (CA4-DG) subfield compared to healthy controls (p=0.003), even after adjusting for age, sex, and total intracranial volume (p=0.002). No statistically significant differences were observed in other hippocampal subfields (CA1, CA2/3, or subiculum), indicating a highly localized pattern of structural alteration.
Conclusion
These results imply that selective CA4-DG atrophy is a defining characteristic of the MRI-negative TLE phenotype, thereby corroborating the "dentate gate" failure hypothesis. Quantitative volumetry provides a crucial diagnostic tool in settings with limited resources, where advanced techniques like 3-T MRI or invasive monitoring are not accessible. This objective structural marker, when integrated with comprehensive semiological analysis, improves diagnostic accuracy and facilitates early clinical intervention in difficult non-lesional TLE cases.
C. Sayman, Elif Özdemir, Sena Güneş et al.· Nöropsikiyatri arşivi· 0 citations
Magnetic resonance imaging (MRI) has become the gold standard for evaluating brain injury and development in newborn infants, providing structural, metabolic, and functional information without ionizing radiation. This review comprehensively examines the principal MRI modalities used in current neonatal neuroimaging for a novice/intermediate-level reader—including conventional T1- and T2-weighted imaging, diffusion-weighted imaging (DWI) with apparent diffusion coefficient (ADC) mapping, diffusion tensor imaging (DTI), magnetic resonance spectroscopy (MRS), susceptibility-weighted imaging (SWI), volumetric analysis, arterial spin labeling (ASL), and functional connectivity MRI—with particular attention to their applications in preterm and term populations. Additionally, validated MRI scoring systems for quantifying brain injury severity and predicting neurodevelopmental outcomes are reviewed and summarized. Understanding the technical principles, clinical applications, and limitations of these modalities is essential for optimal interpretation of neonatal brain MRI, and for advancing prognostication and therapeutic decision-making in this vulnerable population.
Purpose: This study evaluated the impact of magnetoencephalography-magnetic source imaging (MEG-MSI) on the presurgical evaluation of patients with epilepsy. Methods: We retrospectively analyzed presurgical evaluation reports for 64 patients considered for epilepsy surgery at a single pediatric epilepsy center. Results: Overall, 52 of 64 patients (81%) were considered candidates for resective surgery before MEG-MSI. In 37 of these 52 patients (71%), MEG-MSI findings were concordant with those of other modalities, supporting the clinical decision to proceed with resective surgery. However, in 11 of the 52 cases (21%), resective surgery was no longer considered beneficial after MEG-MSI. Among these 11 patients, five underwent either corpus callosotomy or vagus nerve stimulator insertion. Conclusion: Since MEG was incorporated into routine presurgical evaluation for patients with epilepsy, MEG-MSI findings have influenced clinical decision-making in 11 patients.
Seok-Jin Lee, A. Ko, Se Hee Kim et al.· Annals of Child Neurology· 0 citations
OBJECTIVE
Previous longitudinal neuroimaging studies suggest that epilepsy is a progressive disorder. To date, these findings have relied largely on populations from tertiary centers, resulting in ascertainment bias, as severely affected individuals are more likely to be rescanned. We aimed to determine rates of progressive brain atrophy in a prospective, population-based cohort.
METHODS
We analyzed longitudinal magnetic resonance imaging (MRI) data from 116 individuals with epilepsy and 89 age- and sex-matched healthy controls recruited from a prospective, longitudinal, community-based cohort in the United Kingdom. All participants underwent 2 scans 3.5 years apart, regardless of seizure status. We quantified progressive changes in cortical thickness and subcortical volumes using state-of-the-art longitudinal morphometry.
RESULTS
People with epilepsy exhibited accelerated but modest global grey matter volume (GMV) loss compared with controls (2.7 vs 2.4 ml/year; p = 0.01). This acceleration was associated with specific phenotypes: focal epilepsy, MRI-identifiable lesions, and ongoing seizures. In contrast, generalized epilepsy and seizure-free periods were associated with more stable global trajectories. Cortical regions identified as vulnerable were characterized by markedly accelerated thinning compared to controls (5.3 vs 3.4 μm/year; p < 0.001) and were pervasive across most epilepsy phenotypes.
INTERPRETATION
Epilepsy is associated with progressive structural brain damage that exceeds normal aging, but the trajectory is heterogeneous. These prospective population-based data confirm that vulnerable regions show progressive atrophy, particularly in focal and lesional epilepsy and individuals with ongoing seizures. ANN NEUROL 2026.
M. Galovic, Rebecca S. N. Liu, A. Everitt et al.· Annals of Neurology· 0 citations