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Insights into cognitive and behavioral comorbidities of SLC6A1-related epilepsy: five new cases and literature review

INTRODUCTION: SLC6A1 pathogenic variants have been associated with epilepsy and neurodevelopmental disorders. The clinical phenotype includes different seizure types, intellectual disability, and psychiatric symptoms affecting mood and behavior. Few data regarding neuropsychological features have be...

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Autores principales: Trivisano, Marina, Butera, Ambra, Quintavalle, Chiara, De Dominicis, Angela, Calabrese, Costanza, Cappelletti, Simona, Vigevano, Federico, Novelli, Antonio, Specchio, Nicola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493279/
https://www.ncbi.nlm.nih.gov/pubmed/37700749
http://dx.doi.org/10.3389/fnins.2023.1215684
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author Trivisano, Marina
Butera, Ambra
Quintavalle, Chiara
De Dominicis, Angela
Calabrese, Costanza
Cappelletti, Simona
Vigevano, Federico
Novelli, Antonio
Specchio, Nicola
author_facet Trivisano, Marina
Butera, Ambra
Quintavalle, Chiara
De Dominicis, Angela
Calabrese, Costanza
Cappelletti, Simona
Vigevano, Federico
Novelli, Antonio
Specchio, Nicola
author_sort Trivisano, Marina
collection PubMed
description INTRODUCTION: SLC6A1 pathogenic variants have been associated with epilepsy and neurodevelopmental disorders. The clinical phenotype includes different seizure types, intellectual disability, and psychiatric symptoms affecting mood and behavior. Few data regarding neuropsychological features have been described, and details on cognitive profiles are often missing due to the lack of standardized tests. METHODS: We retrospectively reviewed the neuropsychological assessments of five subjects carrying heterozygous missense genetic variants in SLC6A1. We also collected data on epileptic features, EEGs, and brain MRIs. Additionally, we reviewed neuropsychological data from 204 previously reported patients with SLC6A1 pathogenic variants. RESULTS: In our series, at the last evaluation (median 12.6 years), three patients had borderline intellectual functioning, one patient had mild cognitive impairment, and one patient presented with a moderate cognitive disability. Three out of five patients underwent at least two neuropsychological evaluations, which revealed a worsening of cognitive functions over time. We detected attention deficits in all patients. In addition, we observed anxiety, disruptive behavior disorder, emotional instability, and hetero aggressiveness. We also performed a literature review that highlighted that most of the patients with SLC6A1 pathogenic variants have mild-to-moderate intellectual disability and that one-third of cases have autistic traits. DISCUSSION: Based on the literature review and the detailed description of our cases, we conclude that patients with SLC6A1-related epilepsy mostly present with mild-to-moderate intellectual disability, often associated with attention disorders. Such symptoms may worsen over time. Periodic standardized neuropsychological tests may be useful tools to follow development over time, and patient-specific rehabilitation programs could be tailored consistently.
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spelling pubmed-104932792023-09-12 Insights into cognitive and behavioral comorbidities of SLC6A1-related epilepsy: five new cases and literature review Trivisano, Marina Butera, Ambra Quintavalle, Chiara De Dominicis, Angela Calabrese, Costanza Cappelletti, Simona Vigevano, Federico Novelli, Antonio Specchio, Nicola Front Neurosci Neuroscience INTRODUCTION: SLC6A1 pathogenic variants have been associated with epilepsy and neurodevelopmental disorders. The clinical phenotype includes different seizure types, intellectual disability, and psychiatric symptoms affecting mood and behavior. Few data regarding neuropsychological features have been described, and details on cognitive profiles are often missing due to the lack of standardized tests. METHODS: We retrospectively reviewed the neuropsychological assessments of five subjects carrying heterozygous missense genetic variants in SLC6A1. We also collected data on epileptic features, EEGs, and brain MRIs. Additionally, we reviewed neuropsychological data from 204 previously reported patients with SLC6A1 pathogenic variants. RESULTS: In our series, at the last evaluation (median 12.6 years), three patients had borderline intellectual functioning, one patient had mild cognitive impairment, and one patient presented with a moderate cognitive disability. Three out of five patients underwent at least two neuropsychological evaluations, which revealed a worsening of cognitive functions over time. We detected attention deficits in all patients. In addition, we observed anxiety, disruptive behavior disorder, emotional instability, and hetero aggressiveness. We also performed a literature review that highlighted that most of the patients with SLC6A1 pathogenic variants have mild-to-moderate intellectual disability and that one-third of cases have autistic traits. DISCUSSION: Based on the literature review and the detailed description of our cases, we conclude that patients with SLC6A1-related epilepsy mostly present with mild-to-moderate intellectual disability, often associated with attention disorders. Such symptoms may worsen over time. Periodic standardized neuropsychological tests may be useful tools to follow development over time, and patient-specific rehabilitation programs could be tailored consistently. Frontiers Media S.A. 2023-08-28 /pmc/articles/PMC10493279/ /pubmed/37700749 http://dx.doi.org/10.3389/fnins.2023.1215684 Text en Copyright © 2023 Trivisano, Butera, Quintavalle, De Dominicis, Calabrese, Cappelletti, Vigevano, Novelli and Specchio. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Trivisano, Marina
Butera, Ambra
Quintavalle, Chiara
De Dominicis, Angela
Calabrese, Costanza
Cappelletti, Simona
Vigevano, Federico
Novelli, Antonio
Specchio, Nicola
Insights into cognitive and behavioral comorbidities of SLC6A1-related epilepsy: five new cases and literature review
title Insights into cognitive and behavioral comorbidities of SLC6A1-related epilepsy: five new cases and literature review
title_full Insights into cognitive and behavioral comorbidities of SLC6A1-related epilepsy: five new cases and literature review
title_fullStr Insights into cognitive and behavioral comorbidities of SLC6A1-related epilepsy: five new cases and literature review
title_full_unstemmed Insights into cognitive and behavioral comorbidities of SLC6A1-related epilepsy: five new cases and literature review
title_short Insights into cognitive and behavioral comorbidities of SLC6A1-related epilepsy: five new cases and literature review
title_sort insights into cognitive and behavioral comorbidities of slc6a1-related epilepsy: five new cases and literature review
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493279/
https://www.ncbi.nlm.nih.gov/pubmed/37700749
http://dx.doi.org/10.3389/fnins.2023.1215684
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