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Behavioral disinhibition and antiepileptic treatment in childhood epilepsy: A retrospective cohort study

OBJECTIVE: To test whether specific classes of antiepileptic drugs increase the risk for behavioral disinhibition, a frequent complication of treatment of childhood epilepsy. METHODS: In a sample of children with active epilepsy and antiepileptic drug (AED) treatment (n = 146, age 4–17 years), we pe...

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Autores principales: van Tuijl, Diana C., Groenwold, Rolf H. H., Vlaskamp, Chantal, van Campen, Jolien S., Braun, Kees P. J., Jansen, Floor E., Bruining, Hilgo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5939390/
https://www.ncbi.nlm.nih.gov/pubmed/29750213
http://dx.doi.org/10.1002/epi4.12032
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author van Tuijl, Diana C.
Groenwold, Rolf H. H.
Vlaskamp, Chantal
van Campen, Jolien S.
Braun, Kees P. J.
Jansen, Floor E.
Bruining, Hilgo
author_facet van Tuijl, Diana C.
Groenwold, Rolf H. H.
Vlaskamp, Chantal
van Campen, Jolien S.
Braun, Kees P. J.
Jansen, Floor E.
Bruining, Hilgo
author_sort van Tuijl, Diana C.
collection PubMed
description OBJECTIVE: To test whether specific classes of antiepileptic drugs increase the risk for behavioral disinhibition, a frequent complication of treatment of childhood epilepsy. METHODS: In a sample of children with active epilepsy and antiepileptic drug (AED) treatment (n = 146, age 4–17 years), we performed a retrospective chart analysis of the occurrence of symptoms indicating reduced behavioral disinhibition following AED treatment. We used a risk‐set approach to analyze whether the presence or recent addition of AED categories defined by their mechanism of action were associated with enhanced risk for behavioral disinhibition symptoms. RESULTS: Mean duration of follow‐up was 2,343 days (range 218–6,292, standard deviation [SD] 1,437). Episodes of behavioral disinhibition were reported in 51 (34.9%) children, with variable latencies between latest change and occurrence of behavioral disinhibition symptoms (mean 67 days, range 2–367). Current use of AEDs targeting gamma‐aminobutyric acid (GABA) (odds ratio [OR] 1.8, 95% confidence interval [CI] 1.02–3.29, p = 0.04) and SV2A‐mediated neurotransmitter release (SV2A)‐mediated (2.0, 1.13–3.60, p = 0.02) neurotransmitter release was associated with increased risk for behavioral disinhibition. Restricting the analysis to the 90 days before behavioral disinhibition episode occurrence revealed that only addition of GABAergic AEDs (OR = 26.88, 95% CI = 6.71–107.76, p < 0.001) was associated with behavioral disinhibition. In contrast to our expectations, seizure control was reported to have improved parallel to most behavioral disinhibition episodes. SIGNIFICANCE: This exploration of behavioral disinhibition in relation to antiepileptic drug treatment indicates that GABA potentiating drugs are specifically associated with behavioral problems during treatment of childhood epilepsy. Behavioral disinhibition episodes often occurred while seizure control improved, which may have reduced alertness for the consequences of AEDs on interictal symptoms. Our findings may be related to the increasing evidence for a role for excitatory actions of GABA in childhood epilepsy.
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spelling pubmed-59393902018-05-10 Behavioral disinhibition and antiepileptic treatment in childhood epilepsy: A retrospective cohort study van Tuijl, Diana C. Groenwold, Rolf H. H. Vlaskamp, Chantal van Campen, Jolien S. Braun, Kees P. J. Jansen, Floor E. Bruining, Hilgo Epilepsia Open Full‐length Original Research OBJECTIVE: To test whether specific classes of antiepileptic drugs increase the risk for behavioral disinhibition, a frequent complication of treatment of childhood epilepsy. METHODS: In a sample of children with active epilepsy and antiepileptic drug (AED) treatment (n = 146, age 4–17 years), we performed a retrospective chart analysis of the occurrence of symptoms indicating reduced behavioral disinhibition following AED treatment. We used a risk‐set approach to analyze whether the presence or recent addition of AED categories defined by their mechanism of action were associated with enhanced risk for behavioral disinhibition symptoms. RESULTS: Mean duration of follow‐up was 2,343 days (range 218–6,292, standard deviation [SD] 1,437). Episodes of behavioral disinhibition were reported in 51 (34.9%) children, with variable latencies between latest change and occurrence of behavioral disinhibition symptoms (mean 67 days, range 2–367). Current use of AEDs targeting gamma‐aminobutyric acid (GABA) (odds ratio [OR] 1.8, 95% confidence interval [CI] 1.02–3.29, p = 0.04) and SV2A‐mediated neurotransmitter release (SV2A)‐mediated (2.0, 1.13–3.60, p = 0.02) neurotransmitter release was associated with increased risk for behavioral disinhibition. Restricting the analysis to the 90 days before behavioral disinhibition episode occurrence revealed that only addition of GABAergic AEDs (OR = 26.88, 95% CI = 6.71–107.76, p < 0.001) was associated with behavioral disinhibition. In contrast to our expectations, seizure control was reported to have improved parallel to most behavioral disinhibition episodes. SIGNIFICANCE: This exploration of behavioral disinhibition in relation to antiepileptic drug treatment indicates that GABA potentiating drugs are specifically associated with behavioral problems during treatment of childhood epilepsy. Behavioral disinhibition episodes often occurred while seizure control improved, which may have reduced alertness for the consequences of AEDs on interictal symptoms. Our findings may be related to the increasing evidence for a role for excitatory actions of GABA in childhood epilepsy. John Wiley and Sons Inc. 2017-01-18 /pmc/articles/PMC5939390/ /pubmed/29750213 http://dx.doi.org/10.1002/epi4.12032 Text en © 2016 The Authors. Epilepsia Open published by Wiley Periodicals Inc. on behalf of International League Against Epilepsy. This is an open access article under the terms of the http://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 Full‐length Original Research
van Tuijl, Diana C.
Groenwold, Rolf H. H.
Vlaskamp, Chantal
van Campen, Jolien S.
Braun, Kees P. J.
Jansen, Floor E.
Bruining, Hilgo
Behavioral disinhibition and antiepileptic treatment in childhood epilepsy: A retrospective cohort study
title Behavioral disinhibition and antiepileptic treatment in childhood epilepsy: A retrospective cohort study
title_full Behavioral disinhibition and antiepileptic treatment in childhood epilepsy: A retrospective cohort study
title_fullStr Behavioral disinhibition and antiepileptic treatment in childhood epilepsy: A retrospective cohort study
title_full_unstemmed Behavioral disinhibition and antiepileptic treatment in childhood epilepsy: A retrospective cohort study
title_short Behavioral disinhibition and antiepileptic treatment in childhood epilepsy: A retrospective cohort study
title_sort behavioral disinhibition and antiepileptic treatment in childhood epilepsy: a retrospective cohort study
topic Full‐length Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5939390/
https://www.ncbi.nlm.nih.gov/pubmed/29750213
http://dx.doi.org/10.1002/epi4.12032
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