Mapping the Effect of Interictal Epileptic Activity Density During Wakefulness on Brain Functioning in Focal Childhood Epilepsies With Centrotemporal Spikes.

BOLD CECTS centrotemporal spikes cognition epileptic discharges frequency language network

Journal

Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899

Informations de publication

Date de publication:
2019
Historique:
received: 22 07 2019
accepted: 27 11 2019
entrez: 11 1 2020
pubmed: 11 1 2020
medline: 11 1 2020
Statut: epublish

Résumé

Childhood epilepsy with centrotemporal spikes (CECTS) is the most common type of "self-limited focal epilepsies." In its typical presentation, CECTS is a condition reflecting non-lesional cortical hyperexcitability of rolandic regions. The benign evolution of this disorder is challenged by the frequent observation of associated neuropsychological deficits and behavioral impairment. The abundance (or frequency) of interictal centrotemporal spikes (CTS) in CECTS is considered a risk factor for deficits in cognition. Herein, we captured the hemodynamic changes triggered by the CTS density measure (i.e., the number of CTS for time bin) obtained in a cohort of CECTS, studied by means of video electroencephalophy/functional MRI during quite wakefulness. We aim to demonstrate a direct influence of the diurnal CTS frequency on epileptogenic and cognitive networks of children with CECTS. A total number of 8,950 CTS (range between 27 and 801) were recorded in 23 CECTS (21 male), with a mean number of 255 CTS/patient and a mean density of CTS/30 s equal to 10,866 ± 11.46. Two independent general linear model models were created for each patient based on the effect of interest: "individual CTS" in model 1 and "CTS density" in model 2. Hemodynamic correlates of CTS density revealed the involvement of a widespread cortical-subcortical network encompassing the sensory-motor cortex, the Broca's area, the premotor cortex, the thalamus, the putamen, and red nucleus, while in the CTS event-related model, changes were limited to blood-oxygen-level-dependent (BOLD) signal increases in the sensory-motor cortices. A linear relationship was observed between the CTS density hemodynamic changes and both disease duration (positive correlation) and age (negative correlation) within the language network and the bilateral insular cortices. Our results strongly support the critical role of the CTS frequency, even during wakefulness, to interfere with the normal functioning of language brain networks.

Identifiants

pubmed: 31920937
doi: 10.3389/fneur.2019.01316
pmc: PMC6930928
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1316

Informations de copyright

Copyright © 2019 Vaudano, Avanzini, Cantalupo, Filippini, Ruggieri, Talami, Caramaschi, Bergonzini, Vignoli, Veggiotti, Guerra, Gessaroli, Santucci, Canevini, Piccolo, Pisani, Gobbi, Dalla Bernardina and Meletti.

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Auteurs

Anna Elisabetta Vaudano (AE)

Neurology Unit, OCB Hospital, AOU Modena, Modena, Italy.
Department of Biomedical, Metabolic, and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.

Pietro Avanzini (P)

Italian National Research Council, Parma Research Unit, Parma, Italy.

Gaetano Cantalupo (G)

Child Neuropsychiatry, University of Verona, Verona, Italy.

Melissa Filippini (M)

Child Neuropsychiatry Unit, IRCCS, Institute of Neurological Sciences, Bellaria Hospital, Bologna, Italy.

Andrea Ruggieri (A)

Department of Biomedical, Metabolic, and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Physical Medicine and Rehabilitation Unit, Sant'Andrea Hospital, University of Rome La Sapienza, Rome, Italy.

Francesca Talami (F)

Department of Biomedical, Metabolic, and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.

Elisa Caramaschi (E)

Pediatric Neurology Unit, AOU Modena, Modena, Italy.

Patrizia Bergonzini (P)

Pediatric Neurology Unit, AOU Modena, Modena, Italy.

Aglaia Vignoli (A)

Department of Health Sciences, University of Milano, Milan, Italy.

Pierangelo Veggiotti (P)

Pediatric Neurology Unit, V. Buzzi Hospital, University of Milan, Milan, Italy.

Azzura Guerra (A)

Physical Medicine and Rehabilitation Unit, Sant'Andrea Hospital, University of Rome La Sapienza, Rome, Italy.

Giuliana Gessaroli (G)

Department of Biomedical, Metabolic, and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.

Margherita Santucci (M)

Child Neuropsychiatry Unit, IRCCS, Institute of Neurological Sciences, Bellaria Hospital, Bologna, Italy.

Maria Paola Canevini (MP)

Pediatric Neurology Unit, AOU Modena, Modena, Italy.

Benedetta Piccolo (B)

Child Neuropsychiatry, Department of Medicine and Surgery, University of Parma, Parma, Italy.

Francesco Pisani (F)

Child Neuropsychiatry, Department of Medicine and Surgery, University of Parma, Parma, Italy.

Giuseppe Gobbi (G)

Child Neuropsychiatry Unit, IRCCS, Institute of Neurological Sciences, Bellaria Hospital, Bologna, Italy.

Bernardo Dalla Bernardina (B)

Child Neuropsychiatry, University of Verona, Verona, Italy.

Stefano Meletti (S)

Neurology Unit, OCB Hospital, AOU Modena, Modena, Italy.
Department of Biomedical, Metabolic, and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.

Classifications MeSH