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Sleep is associated with task-negative brain activity in fibromyalgia participants with comorbid chronic insomnia
Patients with chronic pain exhibit altered default mode network (DMN) activity. This preliminary project questioned whether comorbid disease states are associated with further brain alterations. Thirteen women with fibromyalgia (FM) only and 26 women with fibromyalgia with comorbid chronic insomnia...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648619/ https://www.ncbi.nlm.nih.gov/pubmed/26648751 http://dx.doi.org/10.2147/JPR.S87501 |
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author | Vatthauer, Karlyn E Craggs, Jason G Robinson, Michael E Staud, Roland Berry, Richard B Perlstein, William M McCrae, Christina S |
author_facet | Vatthauer, Karlyn E Craggs, Jason G Robinson, Michael E Staud, Roland Berry, Richard B Perlstein, William M McCrae, Christina S |
author_sort | Vatthauer, Karlyn E |
collection | PubMed |
description | Patients with chronic pain exhibit altered default mode network (DMN) activity. This preliminary project questioned whether comorbid disease states are associated with further brain alterations. Thirteen women with fibromyalgia (FM) only and 26 women with fibromyalgia with comorbid chronic insomnia (FMI) underwent a single night of ambulatory polysomnography and completed a sleep diary each morning for 14 days prior to performing a neuroimaging protocol. Novel imaging analyses were utilized to identify regions associated with significantly disordered sleep that were more active in task-negative periods than task-oriented periods in participants with FMI, when compared to participants with FM. It was hypothesized that core DMN areas (ie, cingulate cortex, inferior parietal lobule, medial prefrontal cortex, medial temporal cortex, precuneus) would exhibit increased activity during task-negative periods. Analyses revealed that significantly disordered sleep significantly contributed to group differences in the right cingulate gyrus, left lentiform nucleus, left anterior cingulate, left superior gyrus, medial frontal gyrus, right caudate, and the left inferior parietal lobules. Results suggest that FMI may alter some brain areas of the DMN, above and beyond FM. However, future work will need to investigate these results further by controlling for chronic insomnia only before conclusions can be made regarding the effect of FMI comorbidity on the DMN. |
format | Online Article Text |
id | pubmed-4648619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-46486192015-12-08 Sleep is associated with task-negative brain activity in fibromyalgia participants with comorbid chronic insomnia Vatthauer, Karlyn E Craggs, Jason G Robinson, Michael E Staud, Roland Berry, Richard B Perlstein, William M McCrae, Christina S J Pain Res Original Research Patients with chronic pain exhibit altered default mode network (DMN) activity. This preliminary project questioned whether comorbid disease states are associated with further brain alterations. Thirteen women with fibromyalgia (FM) only and 26 women with fibromyalgia with comorbid chronic insomnia (FMI) underwent a single night of ambulatory polysomnography and completed a sleep diary each morning for 14 days prior to performing a neuroimaging protocol. Novel imaging analyses were utilized to identify regions associated with significantly disordered sleep that were more active in task-negative periods than task-oriented periods in participants with FMI, when compared to participants with FM. It was hypothesized that core DMN areas (ie, cingulate cortex, inferior parietal lobule, medial prefrontal cortex, medial temporal cortex, precuneus) would exhibit increased activity during task-negative periods. Analyses revealed that significantly disordered sleep significantly contributed to group differences in the right cingulate gyrus, left lentiform nucleus, left anterior cingulate, left superior gyrus, medial frontal gyrus, right caudate, and the left inferior parietal lobules. Results suggest that FMI may alter some brain areas of the DMN, above and beyond FM. However, future work will need to investigate these results further by controlling for chronic insomnia only before conclusions can be made regarding the effect of FMI comorbidity on the DMN. Dove Medical Press 2015-11-12 /pmc/articles/PMC4648619/ /pubmed/26648751 http://dx.doi.org/10.2147/JPR.S87501 Text en © 2015 Vatthauer et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Vatthauer, Karlyn E Craggs, Jason G Robinson, Michael E Staud, Roland Berry, Richard B Perlstein, William M McCrae, Christina S Sleep is associated with task-negative brain activity in fibromyalgia participants with comorbid chronic insomnia |
title | Sleep is associated with task-negative brain activity in fibromyalgia participants with comorbid chronic insomnia |
title_full | Sleep is associated with task-negative brain activity in fibromyalgia participants with comorbid chronic insomnia |
title_fullStr | Sleep is associated with task-negative brain activity in fibromyalgia participants with comorbid chronic insomnia |
title_full_unstemmed | Sleep is associated with task-negative brain activity in fibromyalgia participants with comorbid chronic insomnia |
title_short | Sleep is associated with task-negative brain activity in fibromyalgia participants with comorbid chronic insomnia |
title_sort | sleep is associated with task-negative brain activity in fibromyalgia participants with comorbid chronic insomnia |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648619/ https://www.ncbi.nlm.nih.gov/pubmed/26648751 http://dx.doi.org/10.2147/JPR.S87501 |
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