Intrinsic brain activity as a diagnostic biomarker in children with benign epilepsy with centrotemporal spikes

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Abstract

Benign epilepsy with centrotemporal spikes (BECTS) is often associated with neural circuit dysfunction, particularly during the transient active state characterized by interictal epileptiform discharges (IEDs). Little is known, however, about the functional neural circuit abnormalities in BECTS without IEDs, or if such abnormalities could be used to differentiate BECTS patients without IEDs from healthy controls (HCs) for early diagnosis. To this end, we conducted resting-state functional magnetic resonance imaging (RS-fMRI) and simultaneous Electroencephalogram (EEG) in children with BECTS (n=43) and age-matched HC (n=28). The simultaneous EEG recordings distinguished BECTS with IEDs (n=20) from without IEDs (n=23). Intrinsic brain activity was measured in all three groups using the amplitude of low frequency fluctuation at rest. Compared to HC, BECTS patients with IEDs exhibited an intrinsic activity abnormality in the thalamus, suggesting that thalamic dysfunction could contribute to IED emergence while patients without IEDs exhibited intrinsic activity abnormalities in middle frontal gyrus and superior parietal gyrus. Using multivariate pattern classification analysis, we were able to differentiate BECTS without IEDs from HCs with 88.23% accuracy. BECTS without epileptic transients can be distinguished from HC and BECTS with IEDs by unique regional abnormalities in resting brain activity. Both transient abnormalities as reflected by IEDs and chronic abnormalities as reflected by RS-fMRI may contribute to BECTS development and expression. Intrinsic brain activity and multivariate pattern classification techniques are promising tools to diagnose and differentiate BECTS syndromes.

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Zhu, Y., Yu, Y., Shinkareva, S. V., Ji, G. J., Wang, J., Wang, Z. J., … Tang, Y. L. (2015). Intrinsic brain activity as a diagnostic biomarker in children with benign epilepsy with centrotemporal spikes. Human Brain Mapping, 36(10), 3878–3889. https://doi.org/10.1002/hbm.22884

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