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Exercise Challenge in Gulf War Illness Reveals Two Subgroups with Altered Brain Structure and Function
Nearly 30% of the approximately 700,000 military personnel who served in Operation Desert Storm (1990–1991) have developed Gulf War Illness, a condition that presents with symptoms such as cognitive impairment, autonomic dysfunction, debilitating fatigue and chronic widespread pain that implicate th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3683000/ https://www.ncbi.nlm.nih.gov/pubmed/23798990 http://dx.doi.org/10.1371/journal.pone.0063903 |
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author | Rayhan, Rakib U. Stevens, Benson W. Raksit, Megna P. Ripple, Joshua A. Timbol, Christian R. Adewuyi, Oluwatoyin VanMeter, John W. Baraniuk, James N. |
author_facet | Rayhan, Rakib U. Stevens, Benson W. Raksit, Megna P. Ripple, Joshua A. Timbol, Christian R. Adewuyi, Oluwatoyin VanMeter, John W. Baraniuk, James N. |
author_sort | Rayhan, Rakib U. |
collection | PubMed |
description | Nearly 30% of the approximately 700,000 military personnel who served in Operation Desert Storm (1990–1991) have developed Gulf War Illness, a condition that presents with symptoms such as cognitive impairment, autonomic dysfunction, debilitating fatigue and chronic widespread pain that implicate the central nervous system. A hallmark complaint of subjects with Gulf War Illness is post-exertional malaise; defined as an exacerbation of symptoms following physical and/or mental effort. To study the causal relationship between exercise, the brain, and changes in symptoms, 28 Gulf War veterans and 10 controls completed an fMRI scan before and after two exercise stress tests to investigate serial changes in pain, autonomic function, and working memory. Exercise induced two clinical Gulf War Illness subgroups. One subgroup presented with orthostatic tachycardia (n = 10). This phenotype correlated with brainstem atrophy, baseline working memory compensation in the cerebellar vermis, and subsequent loss of compensation after exercise. The other subgroup developed exercise induced hyperalgesia (n = 18) that was associated with cortical atrophy and baseline working memory compensation in the basal ganglia. Alterations in cognition, brain structure, and symptoms were absent in controls. Our novel findings may provide an understanding of the relationship between the brain and post-exertional malaise in Gulf War Illness. |
format | Online Article Text |
id | pubmed-3683000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36830002013-06-24 Exercise Challenge in Gulf War Illness Reveals Two Subgroups with Altered Brain Structure and Function Rayhan, Rakib U. Stevens, Benson W. Raksit, Megna P. Ripple, Joshua A. Timbol, Christian R. Adewuyi, Oluwatoyin VanMeter, John W. Baraniuk, James N. PLoS One Research Article Nearly 30% of the approximately 700,000 military personnel who served in Operation Desert Storm (1990–1991) have developed Gulf War Illness, a condition that presents with symptoms such as cognitive impairment, autonomic dysfunction, debilitating fatigue and chronic widespread pain that implicate the central nervous system. A hallmark complaint of subjects with Gulf War Illness is post-exertional malaise; defined as an exacerbation of symptoms following physical and/or mental effort. To study the causal relationship between exercise, the brain, and changes in symptoms, 28 Gulf War veterans and 10 controls completed an fMRI scan before and after two exercise stress tests to investigate serial changes in pain, autonomic function, and working memory. Exercise induced two clinical Gulf War Illness subgroups. One subgroup presented with orthostatic tachycardia (n = 10). This phenotype correlated with brainstem atrophy, baseline working memory compensation in the cerebellar vermis, and subsequent loss of compensation after exercise. The other subgroup developed exercise induced hyperalgesia (n = 18) that was associated with cortical atrophy and baseline working memory compensation in the basal ganglia. Alterations in cognition, brain structure, and symptoms were absent in controls. Our novel findings may provide an understanding of the relationship between the brain and post-exertional malaise in Gulf War Illness. Public Library of Science 2013-06-14 /pmc/articles/PMC3683000/ /pubmed/23798990 http://dx.doi.org/10.1371/journal.pone.0063903 Text en © 2013 Rayhan et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Rayhan, Rakib U. Stevens, Benson W. Raksit, Megna P. Ripple, Joshua A. Timbol, Christian R. Adewuyi, Oluwatoyin VanMeter, John W. Baraniuk, James N. Exercise Challenge in Gulf War Illness Reveals Two Subgroups with Altered Brain Structure and Function |
title | Exercise Challenge in Gulf War Illness Reveals Two Subgroups with Altered Brain Structure and Function |
title_full | Exercise Challenge in Gulf War Illness Reveals Two Subgroups with Altered Brain Structure and Function |
title_fullStr | Exercise Challenge in Gulf War Illness Reveals Two Subgroups with Altered Brain Structure and Function |
title_full_unstemmed | Exercise Challenge in Gulf War Illness Reveals Two Subgroups with Altered Brain Structure and Function |
title_short | Exercise Challenge in Gulf War Illness Reveals Two Subgroups with Altered Brain Structure and Function |
title_sort | exercise challenge in gulf war illness reveals two subgroups with altered brain structure and function |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3683000/ https://www.ncbi.nlm.nih.gov/pubmed/23798990 http://dx.doi.org/10.1371/journal.pone.0063903 |
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