Back to Search Start Over

Cognitive phenotype of juvenile absence epilepsy: An investigation of patients and unaffected siblings.

Authors :
Caciagli L
Ratcliffe C
Xiao F
van Graan LA
Trimmel K
Vollmar C
Centeno M
Duncan JS
Thompson PJ
Baxendale S
Koepp MJ
Wandschneider B
Source :
Epilepsia [Epilepsia] 2023 Oct; Vol. 64 (10), pp. 2792-2805. Date of Electronic Publication: 2023 Aug 10.
Publication Year :
2023

Abstract

Objective: The cognitive profile of juvenile absence epilepsy (JAE) remains largely uncharacterized. This study aimed to: (1) elucidate the neuropsychological profile of JAE; (2) identify familial cognitive traits by investigating unaffected JAE siblings; (3) establish the clinical meaningfulness of JAE-associated cognitive traits; (4) determine whether cognitive traits across the idiopathic generalized epilepsy (IGE) spectrum are shared or syndrome-specific, by comparing JAE to juvenile myoclonic epilepsy (JME); and (5) identify relationships between cognitive abilities and clinical characteristics.<br />Methods: We investigated 123 participants-23 patients with JAE, 16 unaffected siblings of JAE patients, 45 healthy controls, and 39 patients with JME-who underwent a comprehensive neuropsychological test battery including measures within four cognitive domains: attention/psychomotor speed, language, memory, and executive function. We correlated clinical measures with cognitive performance data to decode effects of age at onset and duration of epilepsy.<br />Results: Cognitive performance in individuals with JAE was reduced compared to controls across attention/psychomotor speed, language, and executive function domains; those with ongoing seizures additionally showed lower memory scores. Patients with JAE and their unaffected siblings had similar language impairment compared to controls. Individuals with JME had worse response inhibition than those with JAE. Across all patients, those with older age at onset had better attention/psychomotor speed performance.<br />Significance: JAE is associated with wide-ranging cognitive difficulties that encompass domains reliant on frontal lobe processing, including language, attention, and executive function. JAE siblings share impairment with patients on linguistic measures, indicative of a familial trait. Executive function subdomains may be differentially affected across the IGE spectrum. Cognitive abilities are detrimentally modulated by an early age at seizure onset.<br /> (© 2023 The Authors. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.)

Details

Language :
English
ISSN :
1528-1167
Volume :
64
Issue :
10
Database :
MEDLINE
Journal :
Epilepsia
Publication Type :
Academic Journal
Accession number :
37475704
Full Text :
https://doi.org/10.1111/epi.17719