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Sex-Based Differences in Plasma Autoantibodies to Central Nervous System Proteins in Gulf War Veterans versus Healthy and Symptomatic Controls

Veterans from the 1991 Gulf War (GW) have suffered from Gulf War illness (GWI) for nearly 30 years. This illness encompasses multiple body systems, including the central nervous system (CNS). Diagnosis and treatment of GWI is difficult because there has not been an objective diagnostic biomarker. Re...

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Autores principales: Abou-Donia, Mohamed B., Krengel, Maxine H., Lapadula, Elizabeth S., Zundel, Clara G., LeClair, Jessica, Massaro, Joseph, Quinn, Emily, Conboy, Lisa A., Kokkotou, Efi, Nguyen, Daniel D., Abreu, Maria, Klimas, Nancy G., Sullivan, Kimberly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911379/
https://www.ncbi.nlm.nih.gov/pubmed/33498629
http://dx.doi.org/10.3390/brainsci11020148
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author Abou-Donia, Mohamed B.
Krengel, Maxine H.
Lapadula, Elizabeth S.
Zundel, Clara G.
LeClair, Jessica
Massaro, Joseph
Quinn, Emily
Conboy, Lisa A.
Kokkotou, Efi
Nguyen, Daniel D.
Abreu, Maria
Klimas, Nancy G.
Sullivan, Kimberly
author_facet Abou-Donia, Mohamed B.
Krengel, Maxine H.
Lapadula, Elizabeth S.
Zundel, Clara G.
LeClair, Jessica
Massaro, Joseph
Quinn, Emily
Conboy, Lisa A.
Kokkotou, Efi
Nguyen, Daniel D.
Abreu, Maria
Klimas, Nancy G.
Sullivan, Kimberly
author_sort Abou-Donia, Mohamed B.
collection PubMed
description Veterans from the 1991 Gulf War (GW) have suffered from Gulf War illness (GWI) for nearly 30 years. This illness encompasses multiple body systems, including the central nervous system (CNS). Diagnosis and treatment of GWI is difficult because there has not been an objective diagnostic biomarker. Recently, we reported on a newly developed blood biomarker that discriminates GWI from GW healthy controls, and symptomatic controls with irritable bowel syndrome (IBS) and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). The present study was designed to compare levels of these biomarkers between men and women with GWI, as well as sex-specific effects in comparison to healthy GW veterans and symptomatic controls (IBS, ME/CFS). The results showed that men and women with GWI differ in 2 of 10 plasma autoantibodies, with men showing significantly elevated levels. Men and women with GWI showed significantly different levels of autoantibodies in 8 of 10 biomarkers to neuronal and glial proteins in plasma relative to controls. In summary, the present study addressed the utility of the use of plasma autoantibodies for CNS proteins to distinguish among both men and women veterans with GWI and other healthy and symptomatic control groups.
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spelling pubmed-79113792021-02-28 Sex-Based Differences in Plasma Autoantibodies to Central Nervous System Proteins in Gulf War Veterans versus Healthy and Symptomatic Controls Abou-Donia, Mohamed B. Krengel, Maxine H. Lapadula, Elizabeth S. Zundel, Clara G. LeClair, Jessica Massaro, Joseph Quinn, Emily Conboy, Lisa A. Kokkotou, Efi Nguyen, Daniel D. Abreu, Maria Klimas, Nancy G. Sullivan, Kimberly Brain Sci Article Veterans from the 1991 Gulf War (GW) have suffered from Gulf War illness (GWI) for nearly 30 years. This illness encompasses multiple body systems, including the central nervous system (CNS). Diagnosis and treatment of GWI is difficult because there has not been an objective diagnostic biomarker. Recently, we reported on a newly developed blood biomarker that discriminates GWI from GW healthy controls, and symptomatic controls with irritable bowel syndrome (IBS) and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). The present study was designed to compare levels of these biomarkers between men and women with GWI, as well as sex-specific effects in comparison to healthy GW veterans and symptomatic controls (IBS, ME/CFS). The results showed that men and women with GWI differ in 2 of 10 plasma autoantibodies, with men showing significantly elevated levels. Men and women with GWI showed significantly different levels of autoantibodies in 8 of 10 biomarkers to neuronal and glial proteins in plasma relative to controls. In summary, the present study addressed the utility of the use of plasma autoantibodies for CNS proteins to distinguish among both men and women veterans with GWI and other healthy and symptomatic control groups. MDPI 2021-01-23 /pmc/articles/PMC7911379/ /pubmed/33498629 http://dx.doi.org/10.3390/brainsci11020148 Text en © 2021 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
Abou-Donia, Mohamed B.
Krengel, Maxine H.
Lapadula, Elizabeth S.
Zundel, Clara G.
LeClair, Jessica
Massaro, Joseph
Quinn, Emily
Conboy, Lisa A.
Kokkotou, Efi
Nguyen, Daniel D.
Abreu, Maria
Klimas, Nancy G.
Sullivan, Kimberly
Sex-Based Differences in Plasma Autoantibodies to Central Nervous System Proteins in Gulf War Veterans versus Healthy and Symptomatic Controls
title Sex-Based Differences in Plasma Autoantibodies to Central Nervous System Proteins in Gulf War Veterans versus Healthy and Symptomatic Controls
title_full Sex-Based Differences in Plasma Autoantibodies to Central Nervous System Proteins in Gulf War Veterans versus Healthy and Symptomatic Controls
title_fullStr Sex-Based Differences in Plasma Autoantibodies to Central Nervous System Proteins in Gulf War Veterans versus Healthy and Symptomatic Controls
title_full_unstemmed Sex-Based Differences in Plasma Autoantibodies to Central Nervous System Proteins in Gulf War Veterans versus Healthy and Symptomatic Controls
title_short Sex-Based Differences in Plasma Autoantibodies to Central Nervous System Proteins in Gulf War Veterans versus Healthy and Symptomatic Controls
title_sort sex-based differences in plasma autoantibodies to central nervous system proteins in gulf war veterans versus healthy and symptomatic controls
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911379/
https://www.ncbi.nlm.nih.gov/pubmed/33498629
http://dx.doi.org/10.3390/brainsci11020148
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