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Gene–Toxicant Interactions in Gulf War Illness: Differential Effects of the PON1 Genotype

About 25–35% of United States veterans who fought in the 1990–1991 Gulf War report several moderate or severe chronic systemic symptoms, defined as Gulf War illness (GWI). Thirty years later, there is little consensus on the causes or biological underpinnings of GWI. The Gulf War Era Cohort and Bior...

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Autores principales: Vahey, Jacqueline, Gifford, Elizabeth J., Sims, Kellie J., Chesnut, Blair, Boyle, Stephen H., Stafford, Crystal, Upchurch, Julie, Stone, Annjanette, Pyarajan, Saiju, Efird, Jimmy T., Williams, Christina D., Hauser, Elizabeth R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699623/
https://www.ncbi.nlm.nih.gov/pubmed/34942860
http://dx.doi.org/10.3390/brainsci11121558
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author Vahey, Jacqueline
Gifford, Elizabeth J.
Sims, Kellie J.
Chesnut, Blair
Boyle, Stephen H.
Stafford, Crystal
Upchurch, Julie
Stone, Annjanette
Pyarajan, Saiju
Efird, Jimmy T.
Williams, Christina D.
Hauser, Elizabeth R.
author_facet Vahey, Jacqueline
Gifford, Elizabeth J.
Sims, Kellie J.
Chesnut, Blair
Boyle, Stephen H.
Stafford, Crystal
Upchurch, Julie
Stone, Annjanette
Pyarajan, Saiju
Efird, Jimmy T.
Williams, Christina D.
Hauser, Elizabeth R.
author_sort Vahey, Jacqueline
collection PubMed
description About 25–35% of United States veterans who fought in the 1990–1991 Gulf War report several moderate or severe chronic systemic symptoms, defined as Gulf War illness (GWI). Thirty years later, there is little consensus on the causes or biological underpinnings of GWI. The Gulf War Era Cohort and Biorepository (GWECB) was designed to investigate genetic and environmental associations with GWI and consists of 1343 veterans. We investigate candidate gene–toxicant interactions that may be associated with GWI based on prior associations found in human and animal model studies, focusing on SNPs in or near ACHE, BCHE, and PON1 genes to replicate results from prior studies. SOD1 was also considered as a candidate gene. CDC Severe GWI, the primary outcome, was observed in 26% of the 810 deployed veterans included in this study. The interaction between the candidate SNP rs662 and pyridostigmine bromide (PB) pills was found to be associated with CDC Severe GWI. Interactions between PB pill exposure and rs3917545, rs3917550, and rs2299255, all in high linkage disequilibrium in PON1, were also associated with respiratory symptoms. These SNPs could point toward biological pathways through which GWI may develop, which could lead to biomarkers to detect GWI or to better treatment options for veterans with GWI.
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spelling pubmed-86996232021-12-24 Gene–Toxicant Interactions in Gulf War Illness: Differential Effects of the PON1 Genotype Vahey, Jacqueline Gifford, Elizabeth J. Sims, Kellie J. Chesnut, Blair Boyle, Stephen H. Stafford, Crystal Upchurch, Julie Stone, Annjanette Pyarajan, Saiju Efird, Jimmy T. Williams, Christina D. Hauser, Elizabeth R. Brain Sci Article About 25–35% of United States veterans who fought in the 1990–1991 Gulf War report several moderate or severe chronic systemic symptoms, defined as Gulf War illness (GWI). Thirty years later, there is little consensus on the causes or biological underpinnings of GWI. The Gulf War Era Cohort and Biorepository (GWECB) was designed to investigate genetic and environmental associations with GWI and consists of 1343 veterans. We investigate candidate gene–toxicant interactions that may be associated with GWI based on prior associations found in human and animal model studies, focusing on SNPs in or near ACHE, BCHE, and PON1 genes to replicate results from prior studies. SOD1 was also considered as a candidate gene. CDC Severe GWI, the primary outcome, was observed in 26% of the 810 deployed veterans included in this study. The interaction between the candidate SNP rs662 and pyridostigmine bromide (PB) pills was found to be associated with CDC Severe GWI. Interactions between PB pill exposure and rs3917545, rs3917550, and rs2299255, all in high linkage disequilibrium in PON1, were also associated with respiratory symptoms. These SNPs could point toward biological pathways through which GWI may develop, which could lead to biomarkers to detect GWI or to better treatment options for veterans with GWI. MDPI 2021-11-25 /pmc/articles/PMC8699623/ /pubmed/34942860 http://dx.doi.org/10.3390/brainsci11121558 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vahey, Jacqueline
Gifford, Elizabeth J.
Sims, Kellie J.
Chesnut, Blair
Boyle, Stephen H.
Stafford, Crystal
Upchurch, Julie
Stone, Annjanette
Pyarajan, Saiju
Efird, Jimmy T.
Williams, Christina D.
Hauser, Elizabeth R.
Gene–Toxicant Interactions in Gulf War Illness: Differential Effects of the PON1 Genotype
title Gene–Toxicant Interactions in Gulf War Illness: Differential Effects of the PON1 Genotype
title_full Gene–Toxicant Interactions in Gulf War Illness: Differential Effects of the PON1 Genotype
title_fullStr Gene–Toxicant Interactions in Gulf War Illness: Differential Effects of the PON1 Genotype
title_full_unstemmed Gene–Toxicant Interactions in Gulf War Illness: Differential Effects of the PON1 Genotype
title_short Gene–Toxicant Interactions in Gulf War Illness: Differential Effects of the PON1 Genotype
title_sort gene–toxicant interactions in gulf war illness: differential effects of the pon1 genotype
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699623/
https://www.ncbi.nlm.nih.gov/pubmed/34942860
http://dx.doi.org/10.3390/brainsci11121558
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