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Genome-Wide Association Study of Fluorescent Oxidation Products Accounting for Tobacco Smoking Status in Adults from the French EGEA Study

Oxidative stress (OS) is the main pathophysiological mechanism involved in several chronic diseases, including asthma. Fluorescent oxidation products (FlOPs), a global biomarker of damage due to OS, is of growing interest in epidemiological studies. We conducted a genome-wide association study (GWAS...

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Autores principales: Orsi, Laurent, Margaritte-Jeannin, Patricia, Andrianjafimasy, Miora, Dumas, Orianne, Mohamdi, Hamida, Bouzigon, Emmanuelle, Demenais, Florence, Matran, Régis, Zerimech, Farid, Nadif, Rachel, Dizier, Marie-Hélène
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9137810/
https://www.ncbi.nlm.nih.gov/pubmed/35624665
http://dx.doi.org/10.3390/antiox11050802
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author Orsi, Laurent
Margaritte-Jeannin, Patricia
Andrianjafimasy, Miora
Dumas, Orianne
Mohamdi, Hamida
Bouzigon, Emmanuelle
Demenais, Florence
Matran, Régis
Zerimech, Farid
Nadif, Rachel
Dizier, Marie-Hélène
author_facet Orsi, Laurent
Margaritte-Jeannin, Patricia
Andrianjafimasy, Miora
Dumas, Orianne
Mohamdi, Hamida
Bouzigon, Emmanuelle
Demenais, Florence
Matran, Régis
Zerimech, Farid
Nadif, Rachel
Dizier, Marie-Hélène
author_sort Orsi, Laurent
collection PubMed
description Oxidative stress (OS) is the main pathophysiological mechanism involved in several chronic diseases, including asthma. Fluorescent oxidation products (FlOPs), a global biomarker of damage due to OS, is of growing interest in epidemiological studies. We conducted a genome-wide association study (GWAS) of the FlOPs level in 1216 adults from the case-control and family-based EGEA study (mean age 43 years old, 51% women, and 23% current smokers) to identify genetic variants associated with FlOPs. The GWAS was first conducted in the whole sample and then stratified according to smoking status, the main exogenous source of reactive oxygen species. Among the top genetic variants identified by the three GWAS, those located in BMP6 (p = 3 × 10(−6)), near BMPER (p = 9 × 10(−6)), in GABRG3 (p = 4 × 10(−7)), and near ATG5 (p = 2 × 10(−9)) are the most relevant because of both their link to biological pathways related to OS and their association with several chronic diseases for which the role of OS in their pathophysiology has been pointed out. BMP6 and BMPER are of particular interest due to their involvement in the same biological pathways related to OS and their functional interaction. To conclude, this study, which is the first GWAS of FlOPs, provides new insights into the pathophysiology of chronic OS-related diseases.
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spelling pubmed-91378102022-05-28 Genome-Wide Association Study of Fluorescent Oxidation Products Accounting for Tobacco Smoking Status in Adults from the French EGEA Study Orsi, Laurent Margaritte-Jeannin, Patricia Andrianjafimasy, Miora Dumas, Orianne Mohamdi, Hamida Bouzigon, Emmanuelle Demenais, Florence Matran, Régis Zerimech, Farid Nadif, Rachel Dizier, Marie-Hélène Antioxidants (Basel) Article Oxidative stress (OS) is the main pathophysiological mechanism involved in several chronic diseases, including asthma. Fluorescent oxidation products (FlOPs), a global biomarker of damage due to OS, is of growing interest in epidemiological studies. We conducted a genome-wide association study (GWAS) of the FlOPs level in 1216 adults from the case-control and family-based EGEA study (mean age 43 years old, 51% women, and 23% current smokers) to identify genetic variants associated with FlOPs. The GWAS was first conducted in the whole sample and then stratified according to smoking status, the main exogenous source of reactive oxygen species. Among the top genetic variants identified by the three GWAS, those located in BMP6 (p = 3 × 10(−6)), near BMPER (p = 9 × 10(−6)), in GABRG3 (p = 4 × 10(−7)), and near ATG5 (p = 2 × 10(−9)) are the most relevant because of both their link to biological pathways related to OS and their association with several chronic diseases for which the role of OS in their pathophysiology has been pointed out. BMP6 and BMPER are of particular interest due to their involvement in the same biological pathways related to OS and their functional interaction. To conclude, this study, which is the first GWAS of FlOPs, provides new insights into the pathophysiology of chronic OS-related diseases. MDPI 2022-04-20 /pmc/articles/PMC9137810/ /pubmed/35624665 http://dx.doi.org/10.3390/antiox11050802 Text en © 2022 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
Orsi, Laurent
Margaritte-Jeannin, Patricia
Andrianjafimasy, Miora
Dumas, Orianne
Mohamdi, Hamida
Bouzigon, Emmanuelle
Demenais, Florence
Matran, Régis
Zerimech, Farid
Nadif, Rachel
Dizier, Marie-Hélène
Genome-Wide Association Study of Fluorescent Oxidation Products Accounting for Tobacco Smoking Status in Adults from the French EGEA Study
title Genome-Wide Association Study of Fluorescent Oxidation Products Accounting for Tobacco Smoking Status in Adults from the French EGEA Study
title_full Genome-Wide Association Study of Fluorescent Oxidation Products Accounting for Tobacco Smoking Status in Adults from the French EGEA Study
title_fullStr Genome-Wide Association Study of Fluorescent Oxidation Products Accounting for Tobacco Smoking Status in Adults from the French EGEA Study
title_full_unstemmed Genome-Wide Association Study of Fluorescent Oxidation Products Accounting for Tobacco Smoking Status in Adults from the French EGEA Study
title_short Genome-Wide Association Study of Fluorescent Oxidation Products Accounting for Tobacco Smoking Status in Adults from the French EGEA Study
title_sort genome-wide association study of fluorescent oxidation products accounting for tobacco smoking status in adults from the french egea study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9137810/
https://www.ncbi.nlm.nih.gov/pubmed/35624665
http://dx.doi.org/10.3390/antiox11050802
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