OBJECTIVE

Patients with newly diagnosed epilepsy exhibit brain white matter (WM) abnormalities, but the temporal dynamics of these are unknown. The literature suggests these alterations might be present before diagnosis. This study investigates WM microstructural integrity using diffusion imaging in non-lesional (NL), interictal epileptiform discharge (IED)-free, unmedicated patients who experienced a first unprovoked seizure compared to healthy controls. Furthermore, we evaluated whether the patients who developed epilepsy within a 1-year follow-up had a divergent pattern of WM alterations in contrast to those who did not. We also evaluated patients with established epilepsy.

METHODS

We performed a diffusion imaging analysis in a cohort of 82 subjects. Twenty patients recently experienced a first unprovoked seizure (first-seizure group), 32 patients had chronic epilepsy (chronic-epilepsy group), and 30 healthy controls. The first-seizure patients were later classified into patients who developed epilepsy (early-epilepsy) and those who did not (single-seizure). Fractional anisotropy (FA), mean diffusivity (MD), and radial diffusivity (RD) were calculated. Group differences were analyzed using tract-based spatial statistics and permutation analysis of linear models.

RESULTS

Compared to controls, first-seizure patients showed decreased FA (p < .05, d = 1.3) in the corpus callosum and forceps minor, among other tracts. Similar changes were found in the single-seizure group (p < .05, d = 1.3), whereas the early-epilepsy patients showed decreases only in the corpus callosum (p < .05, d = 2.4). We confirmed that patients with chronic epilepsy have widespread FA decreases (p < .05, d = 1).

SIGNIFICANCE

We provide evidence that, as early as after the first unprovoked seizure, patients considered NL by conventional methods harbor marked microstructural abnormalities detectable with diffusion magnetic resonance imaging (MRI). These findings suggest that WM alterations are present very early in the epileptogenic process even before the diagnosis can currently be made. These results have important implications for better understanding the epileptogenic process and preexisting structural difference in patients after a first seizure.