Behavioral phenotypes of childhood idiopathic epilepsies.


Journal

Epilepsia
ISSN: 1528-1167
Titre abrégé: Epilepsia
Pays: United States
ID NLM: 2983306R

Informations de publication

Date de publication:
07 2020
Historique:
received: 13 03 2020
revised: 11 05 2020
accepted: 11 05 2020
pubmed: 20 6 2020
medline: 1 12 2020
entrez: 20 6 2020
Statut: ppublish

Résumé

To characterize the presence and nature of discrete behavioral phenotypes and their correlates in a cohort of youth with new and recent onset focal and generalized epilepsies. The parents of 290 youth (age = 8-18 years) with epilepsy (n = 183) and typically developing participants (n = 107) completed the Child Behavior Checklist for children aged 6-18 from the Achenbach System of Empirically Based Assessment. The eight behavior problem scales were subjected to hierarchical clustering analytics to identify behavioral subgroups. To characterize the external validity and co-occurring comorbidities of the identified subgroups, we examined demographic features (age, gender, handedness), cognition (language, perception, attention, executive function, speed), academic problems (present/absent), clinical epilepsy characteristics (epilepsy syndrome, medications), familial factors (parental intelligence quotient, education, employment), neuroimaging features (cortical thickness), parent-observed day-to-day executive function, and number of lifetime-to-date Diagnostic and Statistical Manual of Mental Disorders, 4th edition (DSM-IV) diagnoses. Hierarchical clustering identified three behavioral phenotypes, which included no behavioral complications (Cluster 1, 67% of epilepsy cohort [n = 122]), nonexternalizing problems (Cluster 2, 11% of cohort [n = 21]), and combined internalizing and externalizing problems (Cluster 3, 22% of cohort [n = 40]). These behavioral phenotypes were characterized by orderly differences in personal characteristics, neuropsychological status, history of academic problems, parental status, cortical thickness, daily executive function, and number of lifetime-to-date DSM-IV diagnoses. Cluster 1 was most similar to controls across most metrics, whereas Cluster 3 was the most abnormal compared to controls. Epilepsy syndrome was not a predictor of cluster membership. Youth with new and recent onset epilepsy fall into three distinct behavioral phenotypes associated with a variety of co-occurring features and comorbidities. This approach identifies important phenotypes of behavior problem presentations and their accompanying factors that serve to advance clinical and theoretical understanding of the behavioral complications of children with epilepsy and the complex conditions with which they co-occur.

Identifiants

pubmed: 32557544
doi: 10.1111/epi.16569
pmc: PMC7387224
mid: NIHMS1604469
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1427-1437

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS044351
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS111022
Pays : United States
Organisme : NINDS NIH HHS
ID : R56 NS044351
Pays : United States
Organisme : NIH HHS
ID : 2RO1-44351
Pays : United States

Informations de copyright

© 2020 International League Against Epilepsy.

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Auteurs

Bruce P Hermann (BP)

Department of Neurology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.

Aaron F Struck (AF)

Department of Neurology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.

Carl E Stafstrom (CE)

Department of Neurology, Johns Hopkins University, Baltimore, Maryland, USA.

David A Hsu (DA)

Department of Neurology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.

Kevin Dabbs (K)

Department of Neurology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.

Carson Gundlach (C)

Department of Neurology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.

Dace Almane (D)

Department of Neurology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.

Michael Seidenberg (M)

Department of Psychology, Rosalind Franklin University of Medicine and Science, North Chicago, Illinois, USA.

Jana E Jones (JE)

Department of Neurology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.

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