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Cognitive phenotypes in patients with drug-resistant temporal lobe epilepsy: Relationships with cortisol and affectivity

Drug-resistant temporal lobe epilepsy (TLE) is a neurological disorder characterized by cognitive deficits. This study examined whether patients with TLE and different cognitive phenotypes differ in cortisol levels and affectivity while controlling for demographic and clinical variables. Method : In...

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Bibliographic Details
Published in:Clinical neuropsychologist 2024-07, p.1-24
Main Authors: Cano-López, Irene, Catalán-Aguilar, Judit, Lozano-García, Alejandro, Hidalgo, Vanesa, Hampel, Kevin G, Tormos-Pons, Paula, Salvador, Alicia, Villanueva, Vicente, González-Bono, Esperanza
Format: Article
Language:English
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Summary:Drug-resistant temporal lobe epilepsy (TLE) is a neurological disorder characterized by cognitive deficits. This study examined whether patients with TLE and different cognitive phenotypes differ in cortisol levels and affectivity while controlling for demographic and clinical variables. Method : In this cross-sectional study, 79 adults with TLE underwent neuropsychological evaluation in which memory, language, attention/processing speed, executive function, and affectivity were assessed. Six saliva samples were collected in the afternoon to examine the ability of the hypothalamic-pituitary-adrenal (HPA) axis to descend according to the circadian rhythm (C1 to C6). The cortisol area under the curve concerning ground (AUC ) was computed to examine global cortisol secretion. Three cognitive phenotypes were identified: memory impairment, generalized impairment, and no impairment. The memory-impairment phenotype showed higher cortisol levels at C4, C5, and C6 than the other groups (  = 0.03, η = 0.06), higher cortisol AUC than the generalized-impairment phenotype (  = 0.004, η = 0.14), and a significant reduction in positive affectivity after the evaluation (  = 0.026, η = 0.11). Higher cortisol AUC and reductions in positive affectivity were significant predictors of the memory-impairment phenotype (  
ISSN:1385-4046
1744-4144
1744-4144
DOI:10.1080/13854046.2024.2375605