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A Detoxification Intervention for Gulf War Illness: A Pilot Randomized Controlled Trial
Approximately 30% of the 700,000 US veterans of the 1990–1991 Persian Gulf War developed multiple persistent symptoms called Gulf War illness. While the etiology is uncertain, several toxic exposures including pesticides and chemical warfare agents have shown associations. There is no effective medi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6862571/ https://www.ncbi.nlm.nih.gov/pubmed/31661809 http://dx.doi.org/10.3390/ijerph16214143 |
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author | Kerr, Kathleen Morse, Gayle Graves, Donald Zuo, Fei Lipowicz, Alain Carpenter, David O. |
author_facet | Kerr, Kathleen Morse, Gayle Graves, Donald Zuo, Fei Lipowicz, Alain Carpenter, David O. |
author_sort | Kerr, Kathleen |
collection | PubMed |
description | Approximately 30% of the 700,000 US veterans of the 1990–1991 Persian Gulf War developed multiple persistent symptoms called Gulf War illness. While the etiology is uncertain, several toxic exposures including pesticides and chemical warfare agents have shown associations. There is no effective medical treatment. An intervention to enhance detoxification developed by Hubbard has improved quality of life and/or reduced body burdens in other cohorts. We evaluated its feasibility and efficacy in ill Gulf War (GW) veterans in a randomized, waitlist-controlled, pilot study at a community-based rehabilitation facility in the United States. Eligible participants (n = 32) were randomly assigned to the intervention (n = 22) or a four-week waitlist control (n = 10). The daily 4–6 week intervention consisted of exercise, sauna-induced sweating, crystalline nicotinic acid and other supplements. Primary outcomes included recruitment, retention and safety; and efficacy was measured via Veteran’s Short Form-36 (SF-36) quality of life, McGill pain, multidimensional fatigue inventory questionnaires and neuropsychological batteries. Scoring of outcomes was blinded. All 32 completed the trial and 21 completed 3-month follow-up. Mean SF-36 physical component summary score after the intervention was 6.9 (95% CI; −0.3, 14.2) points higher compared to waitlist control and 11 of 16 quality of life, pain and fatigue measures improved, with no serious adverse events. Most improvements were retained after 3 months. The Hubbard regimen was feasible, safe and might offer relief for symptoms of GW illness. |
format | Online Article Text |
id | pubmed-6862571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68625712019-12-05 A Detoxification Intervention for Gulf War Illness: A Pilot Randomized Controlled Trial Kerr, Kathleen Morse, Gayle Graves, Donald Zuo, Fei Lipowicz, Alain Carpenter, David O. Int J Environ Res Public Health Article Approximately 30% of the 700,000 US veterans of the 1990–1991 Persian Gulf War developed multiple persistent symptoms called Gulf War illness. While the etiology is uncertain, several toxic exposures including pesticides and chemical warfare agents have shown associations. There is no effective medical treatment. An intervention to enhance detoxification developed by Hubbard has improved quality of life and/or reduced body burdens in other cohorts. We evaluated its feasibility and efficacy in ill Gulf War (GW) veterans in a randomized, waitlist-controlled, pilot study at a community-based rehabilitation facility in the United States. Eligible participants (n = 32) were randomly assigned to the intervention (n = 22) or a four-week waitlist control (n = 10). The daily 4–6 week intervention consisted of exercise, sauna-induced sweating, crystalline nicotinic acid and other supplements. Primary outcomes included recruitment, retention and safety; and efficacy was measured via Veteran’s Short Form-36 (SF-36) quality of life, McGill pain, multidimensional fatigue inventory questionnaires and neuropsychological batteries. Scoring of outcomes was blinded. All 32 completed the trial and 21 completed 3-month follow-up. Mean SF-36 physical component summary score after the intervention was 6.9 (95% CI; −0.3, 14.2) points higher compared to waitlist control and 11 of 16 quality of life, pain and fatigue measures improved, with no serious adverse events. Most improvements were retained after 3 months. The Hubbard regimen was feasible, safe and might offer relief for symptoms of GW illness. MDPI 2019-10-28 2019-11 /pmc/articles/PMC6862571/ /pubmed/31661809 http://dx.doi.org/10.3390/ijerph16214143 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kerr, Kathleen Morse, Gayle Graves, Donald Zuo, Fei Lipowicz, Alain Carpenter, David O. A Detoxification Intervention for Gulf War Illness: A Pilot Randomized Controlled Trial |
title | A Detoxification Intervention for Gulf War Illness: A Pilot Randomized Controlled Trial |
title_full | A Detoxification Intervention for Gulf War Illness: A Pilot Randomized Controlled Trial |
title_fullStr | A Detoxification Intervention for Gulf War Illness: A Pilot Randomized Controlled Trial |
title_full_unstemmed | A Detoxification Intervention for Gulf War Illness: A Pilot Randomized Controlled Trial |
title_short | A Detoxification Intervention for Gulf War Illness: A Pilot Randomized Controlled Trial |
title_sort | detoxification intervention for gulf war illness: a pilot randomized controlled trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6862571/ https://www.ncbi.nlm.nih.gov/pubmed/31661809 http://dx.doi.org/10.3390/ijerph16214143 |
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