UC Irvine

Objective

A subset of children with febrile status epilepticus (FSE) are at risk for development of temporal lobe epilepsy later in life. We sought a noninvasive predictive marker of those at risk that can be identified soon after FSE, within a clinically realistic timeframe.

Methods

Longitudinal T₂ -weighted magnetic resonance imaging (T₂ WI MRI) of rat pups at several time points after experimental FSE (eFSE) was performed on a high-field scanner followed by long-term continuous electroencephalography. In parallel, T₂ WI MRI scans were performed on a 3.0-T clinical scanner. Finally, chronic T₂ WI MRI signal changes were examined in rats that experienced eFSE and were imaged months later in adulthood.

Results

Epilepsy-predicting T₂ changes, previously observed at 2 hours after eFSE, persisted for at least 6 hours, enabling translation to the clinic. Repeated scans, creating MRI trajectories of T₂ relaxation times following eFSE, provided improved prediction of epileptogenesis compared with a single MRI scan. Predictive signal changes centered on limbic structures, such as the basolateral and medial amygdala. T₂ WI MRI changes, originally described on high-field scanners, can also be measured on clinical MRI scanners. Chronically elevated T₂ relaxation times in hippocampus were observed months after eFSE in rats, as noted for post-FSE changes in children.

Significance

Early T₂ WI MRI changes after eFSE provide a strong predictive measure of epileptogenesis following eFSE, on both high-field and clinical MRI scanners. Importantly, the extension of the acute signal changes to at least 6 hours after the FSE enables its inclusion in clinical studies. Chronic elevations of T₂ relaxation times within the hippocampal formation and related structures are common to human and rodent FSE, suggesting that similar processes are involved across species.