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Cognitive phenotypes in frontal lobe epilepsy
OBJECTIVE: Neuropsychological profiles are heterogeneous both across and within epilepsy syndromes, but especially in frontal lobe epilepsy (FLE), which has complex semiology and epileptogenicity. This study aimed to characterize the cognitive heterogeneity within FLE by identifying cognitive phenot...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545860/ https://www.ncbi.nlm.nih.gov/pubmed/35429174 http://dx.doi.org/10.1111/epi.17260 |
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author | Arrotta, Kayela Reyes, Anny Kaestner, Erik McDonald, Carrie R. Hermann, Bruce P. Barr, William B. Sarmey, Nehaw Sundar, Swetha Kondylis, Efstathios Najm, Imad Bingaman, William Busch, Robyn M. |
author_facet | Arrotta, Kayela Reyes, Anny Kaestner, Erik McDonald, Carrie R. Hermann, Bruce P. Barr, William B. Sarmey, Nehaw Sundar, Swetha Kondylis, Efstathios Najm, Imad Bingaman, William Busch, Robyn M. |
author_sort | Arrotta, Kayela |
collection | PubMed |
description | OBJECTIVE: Neuropsychological profiles are heterogeneous both across and within epilepsy syndromes, but especially in frontal lobe epilepsy (FLE), which has complex semiology and epileptogenicity. This study aimed to characterize the cognitive heterogeneity within FLE by identifying cognitive phenotypes and determining their demographic and clinical characteristics. METHOD: One hundred and six patients (age 16–66; 44% female) with FLE completed comprehensive neuropsychological testing, including measures within five cognitive domains: language, attention, executive function, processing speed, and verbal/visual learning. Patients were categorized into one of four phenotypes based on the number of impaired domains. Patterns of domain impairment and clinical and demographic characteristics were examined across phenotypes. RESULTS: Twenty‐five percent of patients met criteria for the Generalized Phenotype (impairment in at least four domains), 20% met criteria for the Tri‐Domain Phenotype (impairment in three domains), 36% met criteria for the Domain‐Specific Phenotype (impairment in one or two domains), and 19% met criteria for the Intact Phenotype (no impairment). Language was the most common domain‐specific impairment, followed by attention, executive function, and processing speed. In contrast, learning was the least impacted cognitive domain. The Generalized Phenotype had fewer years of education compared to the Intact Phenotype, but otherwise, there was no differentiation between phenotypes in demographic and clinical variables. However, qualitative analysis suggested that the Generalized and Tri‐Domain Phenotypes had a more widespread area of epileptogenicity, whereas the Intact Phenotype most frequently had seizures limited to the lateral frontal region. SIGNIFICANCE: This study identified four cognitive phenotypes in FLE that were largely indistinguishable in clinical and demographic features, aside from education and extent of epileptogenic zone. These findings enhance our appreciation of the cognitive heterogeneity within FLE and provide additional support for the development and use of cognitive taxonomies in epilepsy. |
format | Online Article Text |
id | pubmed-9545860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95458602022-10-14 Cognitive phenotypes in frontal lobe epilepsy Arrotta, Kayela Reyes, Anny Kaestner, Erik McDonald, Carrie R. Hermann, Bruce P. Barr, William B. Sarmey, Nehaw Sundar, Swetha Kondylis, Efstathios Najm, Imad Bingaman, William Busch, Robyn M. Epilepsia Research Article OBJECTIVE: Neuropsychological profiles are heterogeneous both across and within epilepsy syndromes, but especially in frontal lobe epilepsy (FLE), which has complex semiology and epileptogenicity. This study aimed to characterize the cognitive heterogeneity within FLE by identifying cognitive phenotypes and determining their demographic and clinical characteristics. METHOD: One hundred and six patients (age 16–66; 44% female) with FLE completed comprehensive neuropsychological testing, including measures within five cognitive domains: language, attention, executive function, processing speed, and verbal/visual learning. Patients were categorized into one of four phenotypes based on the number of impaired domains. Patterns of domain impairment and clinical and demographic characteristics were examined across phenotypes. RESULTS: Twenty‐five percent of patients met criteria for the Generalized Phenotype (impairment in at least four domains), 20% met criteria for the Tri‐Domain Phenotype (impairment in three domains), 36% met criteria for the Domain‐Specific Phenotype (impairment in one or two domains), and 19% met criteria for the Intact Phenotype (no impairment). Language was the most common domain‐specific impairment, followed by attention, executive function, and processing speed. In contrast, learning was the least impacted cognitive domain. The Generalized Phenotype had fewer years of education compared to the Intact Phenotype, but otherwise, there was no differentiation between phenotypes in demographic and clinical variables. However, qualitative analysis suggested that the Generalized and Tri‐Domain Phenotypes had a more widespread area of epileptogenicity, whereas the Intact Phenotype most frequently had seizures limited to the lateral frontal region. SIGNIFICANCE: This study identified four cognitive phenotypes in FLE that were largely indistinguishable in clinical and demographic features, aside from education and extent of epileptogenic zone. These findings enhance our appreciation of the cognitive heterogeneity within FLE and provide additional support for the development and use of cognitive taxonomies in epilepsy. John Wiley and Sons Inc. 2022-05-03 2022-07 /pmc/articles/PMC9545860/ /pubmed/35429174 http://dx.doi.org/10.1111/epi.17260 Text en © 2022 The Authors. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Article Arrotta, Kayela Reyes, Anny Kaestner, Erik McDonald, Carrie R. Hermann, Bruce P. Barr, William B. Sarmey, Nehaw Sundar, Swetha Kondylis, Efstathios Najm, Imad Bingaman, William Busch, Robyn M. Cognitive phenotypes in frontal lobe epilepsy |
title | Cognitive phenotypes in frontal lobe epilepsy |
title_full | Cognitive phenotypes in frontal lobe epilepsy |
title_fullStr | Cognitive phenotypes in frontal lobe epilepsy |
title_full_unstemmed | Cognitive phenotypes in frontal lobe epilepsy |
title_short | Cognitive phenotypes in frontal lobe epilepsy |
title_sort | cognitive phenotypes in frontal lobe epilepsy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545860/ https://www.ncbi.nlm.nih.gov/pubmed/35429174 http://dx.doi.org/10.1111/epi.17260 |
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