4.5 Article

Focal corticarl dysplasia in epilepsy is associated with GABA increase

Journal

NEUROIMAGE-CLINICAL
Volume 31, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.nicl.2021.102763

Keywords

Epilepsy; Focal cortical dysplasia; gamma-Aminobutyric acid (GABA); Glutathione; Glutamate

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Funding

  1. Natural Science Foundation of Shandong [ZR2020QH267]

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This study utilized MRI and HERMES to detect metabolic alterations in patients with FCD-associated epilepsy, revealing a significant increase in GABA levels in FCD foci. This suggests that GABA may play a central role in the pathophysiology of FCD patients with epilepsy.
Purpose: Focal cortical dysplasia (FCD) is a major cause of drug-resistant epilepsy; however the underlying epileptogenic mechanisms of FCD metabolism in epilepsy patients remain unclear. The aim of this study is to detect alterations of gamma-aminobutyric acid (GABA), glutathione (GSH), and the composite of glutamate and glutamine (Glx) in MRI-typical and neuropathologically confirmed FCD-associated epilepsy using Hadamard Encoding and Reconstruction of Mega-Edited Spectroscopy (HERMES). Materials and methods: Fourteen epileptic patients suspected to be caused by FCD and 14 healthy controls were enrolled prospectively in this study; all subjects underwent a 3 T MRI scan, including 3D T1 weighted imaging and HERMES. The GABA signal detected by HERMES also contains signals from macromolecules and homo-carnosine, so it is referred as GABA+. Signals of GABA+, GSH and Glx detected by HERMES from tumor foci, contralateral cerebral regions, and healthy controls were quantified using Gannet. Fitting errors and signal to noise ratios (SNRs) of GABA + signals were also recorded. Differences of GABA+, GSH, Glx, fitting error and SNR of GABA + among three groups were analyzed using linear mixed effects models. Results: Twelve FCD-associated epilepsy patients (7 females, aged 21.9 +/- 9.3 years) and 12 matched healthy controls (7 females, aged 22.8 +/- 9.8 years) were finally enrolled in this study. ANOVA results indicated that GABA levels were significantly increased in FCD foci compared with contralateral regions (p = 0.008) and with healthy controls (p = 0.003), while no difference was found in GSH and Glx levels. No difference of fitting errors or SNR of GABA + was found among FCD foci, contralateral regions and healthy controls. Conclusions: Increased GABA levels were found in FCD foci that indicated GABA may play a central role in the pathophysiology of FCD patients with epilepsy.

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