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Reduced Frontal P3a Amplitude in Migraine Patients during the Pain-Free Period
BACKGROUND AND PURPOSE: Neuropsychological and neuroimaging studies both suggest that frontal lobe dysfunction is present in migraineurs. Since P3a abnormalities manifest in other diseases associated with attention problems, such as attention deficit hyperactivity disorder, we hypothesized that migr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Neurological Association
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3543909/ https://www.ncbi.nlm.nih.gov/pubmed/23346160 http://dx.doi.org/10.3988/jcn.2013.9.1.43 |
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author | Koo, Yong Seo Ko, Deokwon Lee, Gwan-Taek Oh, Kyungmi Kim, Myung-Sun Kim, Kyung Hwan Im, Chang-Hwan Jung, Ki-Young |
author_facet | Koo, Yong Seo Ko, Deokwon Lee, Gwan-Taek Oh, Kyungmi Kim, Myung-Sun Kim, Kyung Hwan Im, Chang-Hwan Jung, Ki-Young |
author_sort | Koo, Yong Seo |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Neuropsychological and neuroimaging studies both suggest that frontal lobe dysfunction is present in migraineurs. Since P3a abnormalities manifest in other diseases associated with attention problems, such as attention deficit hyperactivity disorder, we hypothesized that migraine patients have P3a abnormalities, particularly in the frontal region. METHODS: Event-related potentials were measured using a passive auditory oddball paradigm in 16 female migraineurs (aged 22.9±2.0 years, mean±SD) during the interictal period and in 16 age-matched healthy females (22.6±2.0 years). The amplitudes and latencies were analyzed independently using repeated-measures analysis of variance. Nonparametric statistical testing using a cluster-level randomization method was performed to localize the abnormalities. RESULTS: The mean P3a amplitude at frontal areas during the third trials was significantly lower in migraineurs (1.06 µV) than in controls (1.69 µV, p=0.026). P3a amplitudes were negatively correlated with the duration of the migraine history (r=-0.618, p=0.014). Cluster-based nonparametric statistical analysis showed that the amplitudes over left frontal areas were significantly lower in migraine patients than in controls. CONCLUSIONS: A reduced P3a amplitude of migraineurs reflects attentional deficits and frontal dysfunction. The negative correlation between P3a amplitude and the duration of the migraine history suggests that attentional deficits and frontal dysfunction are either the cause or the result of headache. |
format | Online Article Text |
id | pubmed-3543909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Korean Neurological Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-35439092013-01-23 Reduced Frontal P3a Amplitude in Migraine Patients during the Pain-Free Period Koo, Yong Seo Ko, Deokwon Lee, Gwan-Taek Oh, Kyungmi Kim, Myung-Sun Kim, Kyung Hwan Im, Chang-Hwan Jung, Ki-Young J Clin Neurol Original Article BACKGROUND AND PURPOSE: Neuropsychological and neuroimaging studies both suggest that frontal lobe dysfunction is present in migraineurs. Since P3a abnormalities manifest in other diseases associated with attention problems, such as attention deficit hyperactivity disorder, we hypothesized that migraine patients have P3a abnormalities, particularly in the frontal region. METHODS: Event-related potentials were measured using a passive auditory oddball paradigm in 16 female migraineurs (aged 22.9±2.0 years, mean±SD) during the interictal period and in 16 age-matched healthy females (22.6±2.0 years). The amplitudes and latencies were analyzed independently using repeated-measures analysis of variance. Nonparametric statistical testing using a cluster-level randomization method was performed to localize the abnormalities. RESULTS: The mean P3a amplitude at frontal areas during the third trials was significantly lower in migraineurs (1.06 µV) than in controls (1.69 µV, p=0.026). P3a amplitudes were negatively correlated with the duration of the migraine history (r=-0.618, p=0.014). Cluster-based nonparametric statistical analysis showed that the amplitudes over left frontal areas were significantly lower in migraine patients than in controls. CONCLUSIONS: A reduced P3a amplitude of migraineurs reflects attentional deficits and frontal dysfunction. The negative correlation between P3a amplitude and the duration of the migraine history suggests that attentional deficits and frontal dysfunction are either the cause or the result of headache. Korean Neurological Association 2013-01 2013-01-03 /pmc/articles/PMC3543909/ /pubmed/23346160 http://dx.doi.org/10.3988/jcn.2013.9.1.43 Text en Copyright © 2013 Korean Neurological Association http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Koo, Yong Seo Ko, Deokwon Lee, Gwan-Taek Oh, Kyungmi Kim, Myung-Sun Kim, Kyung Hwan Im, Chang-Hwan Jung, Ki-Young Reduced Frontal P3a Amplitude in Migraine Patients during the Pain-Free Period |
title | Reduced Frontal P3a Amplitude in Migraine Patients during the Pain-Free Period |
title_full | Reduced Frontal P3a Amplitude in Migraine Patients during the Pain-Free Period |
title_fullStr | Reduced Frontal P3a Amplitude in Migraine Patients during the Pain-Free Period |
title_full_unstemmed | Reduced Frontal P3a Amplitude in Migraine Patients during the Pain-Free Period |
title_short | Reduced Frontal P3a Amplitude in Migraine Patients during the Pain-Free Period |
title_sort | reduced frontal p3a amplitude in migraine patients during the pain-free period |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3543909/ https://www.ncbi.nlm.nih.gov/pubmed/23346160 http://dx.doi.org/10.3988/jcn.2013.9.1.43 |
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