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Neuronal correlates of ADHD in adults with evidence for compensation strategies – a functional MRI study with a Go/No-Go paradigm
Objective: Response inhibition impairment is one of the most characteristic symptoms of attention-deficit/hyperactivity disorder (ADHD). Thus functional magnetic resonance imaging (fMRI) during a Go/No-Go task seems to be an ideal tool for examining neuronal correlates of inhibitory control deficits...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
German Medical Science GMS Publishing House
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858877/ https://www.ncbi.nlm.nih.gov/pubmed/20421953 http://dx.doi.org/10.3205/000098 |
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author | Dillo, Wolfgang Göke, Andres Prox-Vagedes, Vanessa Szycik, Gregor R. Roy, Mandy Donnerstag, Frank Emrich, Hinderk M. Ohlmeier, Martin D. |
author_facet | Dillo, Wolfgang Göke, Andres Prox-Vagedes, Vanessa Szycik, Gregor R. Roy, Mandy Donnerstag, Frank Emrich, Hinderk M. Ohlmeier, Martin D. |
author_sort | Dillo, Wolfgang |
collection | PubMed |
description | Objective: Response inhibition impairment is one of the most characteristic symptoms of attention-deficit/hyperactivity disorder (ADHD). Thus functional magnetic resonance imaging (fMRI) during a Go/No-Go task seems to be an ideal tool for examining neuronal correlates of inhibitory control deficits in ADHD. Prior studies have shown frontostriatal abnormalities in children and adolescents. The aim of our study was to investigate whether adults with ADHD would still show abnormal brain activation in prefrontal brain regions during motor response inhibition tasks. Methods: fMRI was used to compare brain activation in 15 untreated adult patients with ADHD and 15 healthy reference volunteers during performance of a Go/No-Go task. Results: In contrast to various other studies with children and adolescents with ADHD, we found no significant difference in the activity of anterior cingulate cortex (ACC) or other frontostriatal structures between ADHD and healthy adults. Significantly enhanced activity was found in the parietal cortex, which is known to play an important role in building up attention. Conclusion: We hypothesize that the enhanced activity is due to the ability of adult ADHD patients to compensate their deficits for a short time, which is demonstrated in our study by equal task performance in both groups. |
format | Text |
id | pubmed-2858877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | German Medical Science GMS Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-28588772010-04-26 Neuronal correlates of ADHD in adults with evidence for compensation strategies – a functional MRI study with a Go/No-Go paradigm Dillo, Wolfgang Göke, Andres Prox-Vagedes, Vanessa Szycik, Gregor R. Roy, Mandy Donnerstag, Frank Emrich, Hinderk M. Ohlmeier, Martin D. Ger Med Sci Article Objective: Response inhibition impairment is one of the most characteristic symptoms of attention-deficit/hyperactivity disorder (ADHD). Thus functional magnetic resonance imaging (fMRI) during a Go/No-Go task seems to be an ideal tool for examining neuronal correlates of inhibitory control deficits in ADHD. Prior studies have shown frontostriatal abnormalities in children and adolescents. The aim of our study was to investigate whether adults with ADHD would still show abnormal brain activation in prefrontal brain regions during motor response inhibition tasks. Methods: fMRI was used to compare brain activation in 15 untreated adult patients with ADHD and 15 healthy reference volunteers during performance of a Go/No-Go task. Results: In contrast to various other studies with children and adolescents with ADHD, we found no significant difference in the activity of anterior cingulate cortex (ACC) or other frontostriatal structures between ADHD and healthy adults. Significantly enhanced activity was found in the parietal cortex, which is known to play an important role in building up attention. Conclusion: We hypothesize that the enhanced activity is due to the ability of adult ADHD patients to compensate their deficits for a short time, which is demonstrated in our study by equal task performance in both groups. German Medical Science GMS Publishing House 2010-04-19 /pmc/articles/PMC2858877/ /pubmed/20421953 http://dx.doi.org/10.3205/000098 Text en Copyright © 2010 Dillo et al. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc-nd/3.0/deed.en). You are free to copy, distribute and transmit the work, provided the original author and source are credited. |
spellingShingle | Article Dillo, Wolfgang Göke, Andres Prox-Vagedes, Vanessa Szycik, Gregor R. Roy, Mandy Donnerstag, Frank Emrich, Hinderk M. Ohlmeier, Martin D. Neuronal correlates of ADHD in adults with evidence for compensation strategies – a functional MRI study with a Go/No-Go paradigm |
title | Neuronal correlates of ADHD in adults with evidence for compensation strategies – a functional MRI study with a Go/No-Go paradigm |
title_full | Neuronal correlates of ADHD in adults with evidence for compensation strategies – a functional MRI study with a Go/No-Go paradigm |
title_fullStr | Neuronal correlates of ADHD in adults with evidence for compensation strategies – a functional MRI study with a Go/No-Go paradigm |
title_full_unstemmed | Neuronal correlates of ADHD in adults with evidence for compensation strategies – a functional MRI study with a Go/No-Go paradigm |
title_short | Neuronal correlates of ADHD in adults with evidence for compensation strategies – a functional MRI study with a Go/No-Go paradigm |
title_sort | neuronal correlates of adhd in adults with evidence for compensation strategies – a functional mri study with a go/no-go paradigm |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858877/ https://www.ncbi.nlm.nih.gov/pubmed/20421953 http://dx.doi.org/10.3205/000098 |
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