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Association between Sex-Related ALOX5 Gene Polymorphisms and Lung Atopy Risk

Atopy is an exaggerated IgE-mediated immune response to foreign antigens in which metabolic abnormalities of the leukotrienes (LTs) pathway play a crucial role. Recent studies have described sex as a key variable in LT biosynthesis, partly explaining why treatment with anti-LT drugs in atopic subjec...

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Autores principales: Mirra, Davida, Esposito, Renata, Spaziano, Giuseppe, Rafaniello, Concetta, Iovino, Pasquale, Cione, Erika, Gallelli, Luca, D’Agostino, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10145460/
https://www.ncbi.nlm.nih.gov/pubmed/37109111
http://dx.doi.org/10.3390/jcm12082775
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author Mirra, Davida
Esposito, Renata
Spaziano, Giuseppe
Rafaniello, Concetta
Iovino, Pasquale
Cione, Erika
Gallelli, Luca
D’Agostino, Bruno
author_facet Mirra, Davida
Esposito, Renata
Spaziano, Giuseppe
Rafaniello, Concetta
Iovino, Pasquale
Cione, Erika
Gallelli, Luca
D’Agostino, Bruno
author_sort Mirra, Davida
collection PubMed
description Atopy is an exaggerated IgE-mediated immune response to foreign antigens in which metabolic abnormalities of the leukotrienes (LTs) pathway play a crucial role. Recent studies have described sex as a key variable in LT biosynthesis, partly explaining why treatment with anti-LT drugs in atopic subjects leads to better control of symptoms in women. In addition, variability in LT production is often associated with single nucleotide polymorphisms (SNPs) in the arachidonate 5-lipoxygenase (ALOX5) gene, which encodes the leukotriene-synthesizing enzyme machinery, 5-lipoxygenase (5-LO). This study aimed to investigate whether two SNPs of ALOX5 are implicated in sex differences in allergic diseases in a prospective cohort of 150 age- and sex-matched atopic and healthy subjects. Rs2029253 and rs2115819 were genotyped using allele-specific RT-PCR, and serum levels of 5-LO and LTB4 were measured by ELISA. Both polymorphisms are significantly more common in women than in men, and their influences on LT production vary as a function of sex, leading to a decrease in men’s and an increase in women’s serum levels of 5-LO and LTB4. These data represent a new resource for understanding sex-related differences in lung inflammatory diseases, partly explaining why women are more likely to develop allergic disorders than men.
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spelling pubmed-101454602023-04-29 Association between Sex-Related ALOX5 Gene Polymorphisms and Lung Atopy Risk Mirra, Davida Esposito, Renata Spaziano, Giuseppe Rafaniello, Concetta Iovino, Pasquale Cione, Erika Gallelli, Luca D’Agostino, Bruno J Clin Med Article Atopy is an exaggerated IgE-mediated immune response to foreign antigens in which metabolic abnormalities of the leukotrienes (LTs) pathway play a crucial role. Recent studies have described sex as a key variable in LT biosynthesis, partly explaining why treatment with anti-LT drugs in atopic subjects leads to better control of symptoms in women. In addition, variability in LT production is often associated with single nucleotide polymorphisms (SNPs) in the arachidonate 5-lipoxygenase (ALOX5) gene, which encodes the leukotriene-synthesizing enzyme machinery, 5-lipoxygenase (5-LO). This study aimed to investigate whether two SNPs of ALOX5 are implicated in sex differences in allergic diseases in a prospective cohort of 150 age- and sex-matched atopic and healthy subjects. Rs2029253 and rs2115819 were genotyped using allele-specific RT-PCR, and serum levels of 5-LO and LTB4 were measured by ELISA. Both polymorphisms are significantly more common in women than in men, and their influences on LT production vary as a function of sex, leading to a decrease in men’s and an increase in women’s serum levels of 5-LO and LTB4. These data represent a new resource for understanding sex-related differences in lung inflammatory diseases, partly explaining why women are more likely to develop allergic disorders than men. MDPI 2023-04-08 /pmc/articles/PMC10145460/ /pubmed/37109111 http://dx.doi.org/10.3390/jcm12082775 Text en © 2023 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
Mirra, Davida
Esposito, Renata
Spaziano, Giuseppe
Rafaniello, Concetta
Iovino, Pasquale
Cione, Erika
Gallelli, Luca
D’Agostino, Bruno
Association between Sex-Related ALOX5 Gene Polymorphisms and Lung Atopy Risk
title Association between Sex-Related ALOX5 Gene Polymorphisms and Lung Atopy Risk
title_full Association between Sex-Related ALOX5 Gene Polymorphisms and Lung Atopy Risk
title_fullStr Association between Sex-Related ALOX5 Gene Polymorphisms and Lung Atopy Risk
title_full_unstemmed Association between Sex-Related ALOX5 Gene Polymorphisms and Lung Atopy Risk
title_short Association between Sex-Related ALOX5 Gene Polymorphisms and Lung Atopy Risk
title_sort association between sex-related alox5 gene polymorphisms and lung atopy risk
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10145460/
https://www.ncbi.nlm.nih.gov/pubmed/37109111
http://dx.doi.org/10.3390/jcm12082775
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