Altered physiological brain variation in drug-resistant epilepsy

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Dokumenter

Janne Kananen, Timo Tuovinen, Hanna Ansakorpi, Seppo Rytky, Heta Helakari, Niko Huotari, Lauri Raitamaa, Ville Raatikainen, Aleksi Rasila, Viola Borchardt, Vesa Korhonen, Pierre LeVan, Maiken Nedergaard, Vesa Kiviniemi

INTRODUCTION: Functional magnetic resonance imaging (fMRI) combined with simultaneous electroencephalography (EEG-fMRI) has become a major tool in mapping epilepsy sources. In the absence of detectable epileptiform activity, the resting state fMRI may still detect changes in the blood oxygen level-dependent signal, suggesting intrinsic alterations in the underlying brain physiology.

METHODS: In this study, we used coefficient of variation (CV) of critically sampled 10 Hz ultra-fast fMRI (magnetoencephalography, MREG) signal to compare physiological variance between healthy controls (n = 10) and patients (n = 10) with drug-resistant epilepsy (DRE).

RESULTS: We showed highly significant voxel-level (p < 0.01, TFCE-corrected) increase in the physiological variance in DRE patients. At individual level, the elevations range over three standard deviations (σ) above the control mean (μ) CVMREG values solely in DRE patients, enabling patient-specific mapping of elevated physiological variance. The most apparent differences in group-level analysis are found on white matter, brainstem, and cerebellum. Respiratory (0.12-0.4 Hz) and very-low-frequency (VLF = 0.009-0.1 Hz) signal variances were most affected.

CONCLUSIONS: The CVMREG increase was not explained by head motion or physiological cardiorespiratory activity, that is, it seems to be linked to intrinsic physiological pulsations. We suggest that intrinsic brain pulsations play a role in DRE and that critically sampled fMRI may provide a powerful tool for their identification.

OriginalsprogEngelsk
Artikelnummere01090
TidsskriftBrain and Behavior
Vol/bind8
Udgave nummer9
Sider (fra-til)1-17
Antal sider17
ISSN2162-3279
DOI
StatusUdgivet - 2018

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