4.7 Article

Cortico-striato-thalamo-cerebellar networks of structural covariance underlying different epilepsy syndromes associated with generalized tonic-clonic seizures

Journal

HUMAN BRAIN MAPPING
Volume 42, Issue 4, Pages 1102-1115

Publisher

WILEY
DOI: 10.1002/hbm.25279

Keywords

cortico-striato-thalamo-cerebellar network; epilepsy; generalized tonic-clonic seizures; morhpometric MRI; structural covariance connecvity

Funding

  1. National Natural Scientific Foundation of China [81871345, 81790653, 81790650, 81701680]
  2. Postdoctoral grants of China [2016M603064]
  3. Natural scientific foundation-social development [BE2016751]
  4. Government of Jiangsu Province [1501169B, ZDRCA2016093]
  5. National Key Research & Development Program of Ministry of Science & Technology of PR. China [2017YFC0108805, 2018YFA0701703]

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This study explored the brain network changes in patients with generalized tonic-clonic seizures (GTCS) and focal epilepsy associated with focal to bilateral tonic-clonic seizure (FE-FBTS) using structural covariance analysis, revealing differences between the two syndromes. Patients showed increased connectivity within the striatum and thalamus relative to healthy controls, with connectivity changes increasing as a function of epilepsy duration. FE-FBTS presented more severe network disruption compared to GE-GTCS.
Generalized tonic-clonic seizures (GTCS) are the severest and most remarkable clinical expressions of human epilepsy. Cortical, subcortical, and cerebellar structures, organized with different network patterns, underlying the pathophysiological substrates of genetic associated epilepsy with GTCS (GE-GTCS) and focal epilepsy associated with focal to bilateral tonic-clonic seizure (FE-FBTS). Structural covariance analysis can delineate the features of epilepsy network related with long-term effects from seizure. Morphometric MRI data of 111 patients with GE-GTCS, 111 patients with FE-FBTS and 111 healthy controls were studied. Cortico-striato-thalao-cerebellar networks of structural covariance within the gray matter were constructed using a Winner-take-all strategy with five cortical parcellations. Comparisons of structural covariance networks were conducted using permutation tests, and module effects of disease duration on networks were conducted using GLM model. Both patient groups showed increased connectivity of structural covariance relative to controls, mainly within the striatum and thalamus, and mostly correlated with the frontal, motor, and somatosensory cortices. Connectivity changes increased as a function of epilepsy durations. FE-FBTS showed more intensive and extensive gray matter changes with volumetric loss and connectivity increment than GE-GTCS. Our findings implicated cortico-striato-thalamo-cerebellar network changes at a large temporal scale in GTCS, with FE-FBTS showing more severe network disruption. The study contributed novel imaging evidence for understanding the different epilepsy syndromes associated with generalized seizures.

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