Trait impulsivity correlates with active myoclonic seizures in genetic generalized epilepsy.


Journal

Epilepsy & behavior : E&B
ISSN: 1525-5069
Titre abrégé: Epilepsy Behav
Pays: United States
ID NLM: 100892858

Informations de publication

Date de publication:
11 2020
Historique:
received: 01 04 2020
revised: 12 06 2020
accepted: 12 06 2020
pubmed: 4 8 2020
medline: 15 4 2021
entrez: 4 8 2020
Statut: ppublish

Résumé

Juvenile myoclonic epilepsy (JME) is a common subtype of genetic generalized epilepsy (GGE) arising in adolescence and is often associated with executive function (EF) deficits. Some EF components like response inhibition have been extensively evaluated in JME, but few studies have focused upon trait impulsivity or compared between GGE subtypes. The aim of the present study was to compare the association of trait impulsivity in JME with other GGE subtypes. Patients with GGE aged between 14 and 40 years (n = 137) were divided into those with JME (n = 92) and those with other GGEs (n = 45: 8 childhood absence epilepsy (CAE), 22 juvenile absence epilepsy (JAE), and 15 epilepsy with generalized tonic-clonic seizures only (EGTCS)). The study participants were recruited through medical records of the general population of Buskerud County and the neighboring municipalities, covering 477,000 people or 9.1% of Norway's total population. All participants underwent a clinical interview including the Barratt Impulsiveness Scale (BIS), an established measure of trait impulsivity. We controlled for other potential predictors of BIS score using analysis of covariance (ANCOVA). There were no differences between JME and other types of GGE for BIS scores, but the presence of myoclonic seizures within the last year, irrespective of GGE subtype, was independently associated with significantly increased behavioral impulsivity. This study demonstrates that trait impulsivity in GGE is most strongly related to the recent occurrence of myoclonic seizures rather than GGE subtype.

Sections du résumé

BACKGROUND
Juvenile myoclonic epilepsy (JME) is a common subtype of genetic generalized epilepsy (GGE) arising in adolescence and is often associated with executive function (EF) deficits. Some EF components like response inhibition have been extensively evaluated in JME, but few studies have focused upon trait impulsivity or compared between GGE subtypes. The aim of the present study was to compare the association of trait impulsivity in JME with other GGE subtypes.
METHODS
Patients with GGE aged between 14 and 40 years (n = 137) were divided into those with JME (n = 92) and those with other GGEs (n = 45: 8 childhood absence epilepsy (CAE), 22 juvenile absence epilepsy (JAE), and 15 epilepsy with generalized tonic-clonic seizures only (EGTCS)). The study participants were recruited through medical records of the general population of Buskerud County and the neighboring municipalities, covering 477,000 people or 9.1% of Norway's total population. All participants underwent a clinical interview including the Barratt Impulsiveness Scale (BIS), an established measure of trait impulsivity. We controlled for other potential predictors of BIS score using analysis of covariance (ANCOVA).
RESULTS
There were no differences between JME and other types of GGE for BIS scores, but the presence of myoclonic seizures within the last year, irrespective of GGE subtype, was independently associated with significantly increased behavioral impulsivity.
CONCLUSIONS
This study demonstrates that trait impulsivity in GGE is most strongly related to the recent occurrence of myoclonic seizures rather than GGE subtype.

Identifiants

pubmed: 32745958
pii: S1525-5050(20)30439-X
doi: 10.1016/j.yebeh.2020.107260
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

107260

Subventions

Organisme : Medical Research Council
ID : MR/N026063/1
Pays : United Kingdom
Organisme : Department of Health
ID : RP-PG-0615-20007
Pays : United Kingdom
Organisme : CIHR
ID : 201503MOP-342469
Pays : Canada

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest Marte Syvertsen received speaker honoraria from Eisai, and Kaja Selmer received travel imbursement from UCB. The remaining authors have no conflicts of interest.

Auteurs

Marte Syvertsen (M)

Department of Neurology, Drammen Hospital, Vestre Viken Hospital Trust, Norway; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Jeanette Koht (J)

Department of Neurology, Drammen Hospital, Vestre Viken Hospital Trust, Norway; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Kaja Selmer (K)

Division of Clinical Neuroscience, Department of Research and Innovation, Oslo University Hospital, Oslo, Norway; National Center for Epilepsy, Oslo University Hospital, Sandvika, Norway.

Ulla Enger (U)

Department of Neurology, Drammen Hospital, Vestre Viken Hospital Trust, Norway.

Deb K Pal (DK)

Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom; MRC Centre for Neurodevelopmental Disorders, King's College London, London, United Kingdom; King's College Hospital, London, United Kingdom; Evelina London Children's Hospital, London, United Kingdom. Electronic address: deb.pal@kcl.ac.uk.

Anna Smith (A)

Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom; MRC Centre for Neurodevelopmental Disorders, King's College London, London, United Kingdom; King's College Hospital, London, United Kingdom; Evelina London Children's Hospital, London, United Kingdom.

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