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Mismatch negativity and P3a in drug-naive adults with attention-deficit hyperactivity disorder

BACKGROUND: Individuals with attention-deficit hyperactivity disorder (ADHD) often display over-response to stimuli that are irrelevant to the ongoing task, and their attentional abilities disproportionately worsen in the presence of competing stimuli. Auditory event-related potentials (ERPs) such a...

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Autores principales: Hsieh, Ming H., Chien, Yi-Ling, Gau, Susan Shur-Fen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772912/
https://www.ncbi.nlm.nih.gov/pubmed/33706818
http://dx.doi.org/10.1017/S0033291720005516
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author Hsieh, Ming H.
Chien, Yi-Ling
Gau, Susan Shur-Fen
author_facet Hsieh, Ming H.
Chien, Yi-Ling
Gau, Susan Shur-Fen
author_sort Hsieh, Ming H.
collection PubMed
description BACKGROUND: Individuals with attention-deficit hyperactivity disorder (ADHD) often display over-response to stimuli that are irrelevant to the ongoing task, and their attentional abilities disproportionately worsen in the presence of competing stimuli. Auditory event-related potentials (ERPs) such as mismatch negativity (MMN) and P3a using the passive oddball paradigm have been studied in children and adolescents with ADHD. Still, there is no such data for adults with ADHD. This study aimed to compare the MMN and P3a and their clinical and neurocognitive correlations between drug-naive adults with ADHD and control adults. METHODS: We recruited 52 adults with ADHD (26.5 ± 6.2 years), and 62 age-matched controls (25.6 ± 5.6 years). They received the psychiatric interviews, auditory ERP, the Conners' continuous performance test (CCPT), and the Cambridge gambling test (CGT). They also completed the questionnaires about ADHD symptoms and real-world executive functions. MMN and P3a were assessed during a passive duration-deviant auditory oddball paradigm from the midline electrodes Cz. RESULTS: Adults with ADHD demonstrated smaller Cz MMN amplitude, more severe ADHD symptoms, poorer attention profiles (CCPT), and a wide range of executive dysfunctions than controls. As for the correlates, Cz peak amplitude of MMN correlated with inattention symptoms, executive dysfunctions, attentional vigilance (CCPT), and decision-making (CGT) in ADHD adults but only with decision-making in controls. CONCLUSIONS: Our findings that smaller amplitude of MMN and its differential associated pattern with inattention, real-world executive dysfunction, and decision-making, in drug-naive adults with ADHD from adult controls, provide evidence to support the potential electrophysiological biomarker for adult ADHD.
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spelling pubmed-97729122022-12-28 Mismatch negativity and P3a in drug-naive adults with attention-deficit hyperactivity disorder Hsieh, Ming H. Chien, Yi-Ling Gau, Susan Shur-Fen Psychol Med Original Article BACKGROUND: Individuals with attention-deficit hyperactivity disorder (ADHD) often display over-response to stimuli that are irrelevant to the ongoing task, and their attentional abilities disproportionately worsen in the presence of competing stimuli. Auditory event-related potentials (ERPs) such as mismatch negativity (MMN) and P3a using the passive oddball paradigm have been studied in children and adolescents with ADHD. Still, there is no such data for adults with ADHD. This study aimed to compare the MMN and P3a and their clinical and neurocognitive correlations between drug-naive adults with ADHD and control adults. METHODS: We recruited 52 adults with ADHD (26.5 ± 6.2 years), and 62 age-matched controls (25.6 ± 5.6 years). They received the psychiatric interviews, auditory ERP, the Conners' continuous performance test (CCPT), and the Cambridge gambling test (CGT). They also completed the questionnaires about ADHD symptoms and real-world executive functions. MMN and P3a were assessed during a passive duration-deviant auditory oddball paradigm from the midline electrodes Cz. RESULTS: Adults with ADHD demonstrated smaller Cz MMN amplitude, more severe ADHD symptoms, poorer attention profiles (CCPT), and a wide range of executive dysfunctions than controls. As for the correlates, Cz peak amplitude of MMN correlated with inattention symptoms, executive dysfunctions, attentional vigilance (CCPT), and decision-making (CGT) in ADHD adults but only with decision-making in controls. CONCLUSIONS: Our findings that smaller amplitude of MMN and its differential associated pattern with inattention, real-world executive dysfunction, and decision-making, in drug-naive adults with ADHD from adult controls, provide evidence to support the potential electrophysiological biomarker for adult ADHD. Cambridge University Press 2022-11 2021-03-12 /pmc/articles/PMC9772912/ /pubmed/33706818 http://dx.doi.org/10.1017/S0033291720005516 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Hsieh, Ming H.
Chien, Yi-Ling
Gau, Susan Shur-Fen
Mismatch negativity and P3a in drug-naive adults with attention-deficit hyperactivity disorder
title Mismatch negativity and P3a in drug-naive adults with attention-deficit hyperactivity disorder
title_full Mismatch negativity and P3a in drug-naive adults with attention-deficit hyperactivity disorder
title_fullStr Mismatch negativity and P3a in drug-naive adults with attention-deficit hyperactivity disorder
title_full_unstemmed Mismatch negativity and P3a in drug-naive adults with attention-deficit hyperactivity disorder
title_short Mismatch negativity and P3a in drug-naive adults with attention-deficit hyperactivity disorder
title_sort mismatch negativity and p3a in drug-naive adults with attention-deficit hyperactivity disorder
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772912/
https://www.ncbi.nlm.nih.gov/pubmed/33706818
http://dx.doi.org/10.1017/S0033291720005516
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