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Brain arousal regulation and depressive symptomatology in adults with attention-deficit/hyperactivity disorder (ADHD)

BACKGROUND: The aim of the present study was to evaluate the stability of brain arousal in adult attention-deficit/hyperactivity disorder (ADHD) outpatients with and without depressive symptomatology, and its association with depressive symptom severity and absolute electroencephalogram (EEG) power...

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Autores principales: Huang, Jue, Ulke, Christine, Strauss, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701141/
https://www.ncbi.nlm.nih.gov/pubmed/31429702
http://dx.doi.org/10.1186/s12868-019-0526-4
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author Huang, Jue
Ulke, Christine
Strauss, Maria
author_facet Huang, Jue
Ulke, Christine
Strauss, Maria
author_sort Huang, Jue
collection PubMed
description BACKGROUND: The aim of the present study was to evaluate the stability of brain arousal in adult attention-deficit/hyperactivity disorder (ADHD) outpatients with and without depressive symptomatology, and its association with depressive symptom severity and absolute electroencephalogram (EEG) power in different frequency bands. METHODS: We included 31 outpatient adults (45.16% females), who were diagnosed according to DSM-IV and received no medication. Their arousal stability score (index of the steepness of arousal decline during a 15-min EEG under resting conditions), the absolute EEG power and self-reports, including depressive and ADHD-related symptoms, were analyzed. Participants were split into an unstable and stable arousal group based on the median (= 6) of the arousal stability score. RESULTS: ADHD patients in the stable group reported more severe depressive symptoms (p = 0.018) and showed reduced absolute EEG power in the delta (0.002 ≤ p ≤ 0.025) and theta (0.011 ≤ p ≤ 0.034) bands compared to those in the unstable group. There was no correlation between the arousal stability score and self-report-scales concerning ADHD-related symptoms (0.214 ≤ p ≤ 0.989), but a positive association with self-reported depressive severity (p = 0.018) and negative association with powers in the EEG delta and theta bands (0.001 ≤ p ≤ 0.033). CONCLUSIONS: In view of high comorbidity of depression and ADHD in adult patients, these findings support the assumption that brain arousal regulation could be considered as a helpful marker for the clinical differentiation between ADHD and depression.
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spelling pubmed-67011412019-08-26 Brain arousal regulation and depressive symptomatology in adults with attention-deficit/hyperactivity disorder (ADHD) Huang, Jue Ulke, Christine Strauss, Maria BMC Neurosci Research Article BACKGROUND: The aim of the present study was to evaluate the stability of brain arousal in adult attention-deficit/hyperactivity disorder (ADHD) outpatients with and without depressive symptomatology, and its association with depressive symptom severity and absolute electroencephalogram (EEG) power in different frequency bands. METHODS: We included 31 outpatient adults (45.16% females), who were diagnosed according to DSM-IV and received no medication. Their arousal stability score (index of the steepness of arousal decline during a 15-min EEG under resting conditions), the absolute EEG power and self-reports, including depressive and ADHD-related symptoms, were analyzed. Participants were split into an unstable and stable arousal group based on the median (= 6) of the arousal stability score. RESULTS: ADHD patients in the stable group reported more severe depressive symptoms (p = 0.018) and showed reduced absolute EEG power in the delta (0.002 ≤ p ≤ 0.025) and theta (0.011 ≤ p ≤ 0.034) bands compared to those in the unstable group. There was no correlation between the arousal stability score and self-report-scales concerning ADHD-related symptoms (0.214 ≤ p ≤ 0.989), but a positive association with self-reported depressive severity (p = 0.018) and negative association with powers in the EEG delta and theta bands (0.001 ≤ p ≤ 0.033). CONCLUSIONS: In view of high comorbidity of depression and ADHD in adult patients, these findings support the assumption that brain arousal regulation could be considered as a helpful marker for the clinical differentiation between ADHD and depression. BioMed Central 2019-08-20 /pmc/articles/PMC6701141/ /pubmed/31429702 http://dx.doi.org/10.1186/s12868-019-0526-4 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Huang, Jue
Ulke, Christine
Strauss, Maria
Brain arousal regulation and depressive symptomatology in adults with attention-deficit/hyperactivity disorder (ADHD)
title Brain arousal regulation and depressive symptomatology in adults with attention-deficit/hyperactivity disorder (ADHD)
title_full Brain arousal regulation and depressive symptomatology in adults with attention-deficit/hyperactivity disorder (ADHD)
title_fullStr Brain arousal regulation and depressive symptomatology in adults with attention-deficit/hyperactivity disorder (ADHD)
title_full_unstemmed Brain arousal regulation and depressive symptomatology in adults with attention-deficit/hyperactivity disorder (ADHD)
title_short Brain arousal regulation and depressive symptomatology in adults with attention-deficit/hyperactivity disorder (ADHD)
title_sort brain arousal regulation and depressive symptomatology in adults with attention-deficit/hyperactivity disorder (adhd)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701141/
https://www.ncbi.nlm.nih.gov/pubmed/31429702
http://dx.doi.org/10.1186/s12868-019-0526-4
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