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Association between Recent Acetaminophen Use and Asthma: Modification by Polymorphism at TLR4

The risk of asthma has been increasing in parallel with use of acetaminophen, which is a potential source of oxidative stress. Toll-like receptor 4 (TLR4) plays a critical role not only in innate immunity, but also in mediating reactive oxygen species induced inflammation. Therefore, we investigated...

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Autores principales: Lee, Seung-Hwa, Kang, Mi-Jin, Yu, Ho-Sung, Hong, Kyungmo, Jung, Young-Ho, Kim, Hyung-Young, Seo, Ju-Hee, Kwon, Ji-Won, Kim, Byoung-Ju, Kim, Ha-Jung, Kim, Young-Joon, Kim, Hee-Suk, Kim, Hyo Bin, Park, Kang Seo, Lee, So-Yeon, Hong, Soo-Jong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4024959/
https://www.ncbi.nlm.nih.gov/pubmed/24851022
http://dx.doi.org/10.3346/jkms.2014.29.5.662
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author Lee, Seung-Hwa
Kang, Mi-Jin
Yu, Ho-Sung
Hong, Kyungmo
Jung, Young-Ho
Kim, Hyung-Young
Seo, Ju-Hee
Kwon, Ji-Won
Kim, Byoung-Ju
Kim, Ha-Jung
Kim, Young-Joon
Kim, Hee-Suk
Kim, Hyo Bin
Park, Kang Seo
Lee, So-Yeon
Hong, Soo-Jong
author_facet Lee, Seung-Hwa
Kang, Mi-Jin
Yu, Ho-Sung
Hong, Kyungmo
Jung, Young-Ho
Kim, Hyung-Young
Seo, Ju-Hee
Kwon, Ji-Won
Kim, Byoung-Ju
Kim, Ha-Jung
Kim, Young-Joon
Kim, Hee-Suk
Kim, Hyo Bin
Park, Kang Seo
Lee, So-Yeon
Hong, Soo-Jong
author_sort Lee, Seung-Hwa
collection PubMed
description The risk of asthma has been increasing in parallel with use of acetaminophen, which is a potential source of oxidative stress. Toll-like receptor 4 (TLR4) plays a critical role not only in innate immunity, but also in mediating reactive oxygen species induced inflammation. Therefore, we investigated associations between acetaminophen usage and TLR4 polymorphism on asthma and bronchial hyperresponsiveness (BHR). The number of 2,428 elementary school children in Seoul and Jeongeup cities was recruited. Subjects who used acetaminophen with a family history of asthma had an increased risk of both asthma diagnosis ever and current asthma. Individuals with CT+TT genotypes at the TLR4 polymorphism, in combination with acetaminophen usage, also demonstrated an increased risk of asthma diagnosis ever (aOR, 2.08; 95% confidence interval [CI], 1.10-3.92). Family history of asthma and acetaminophen usage were risk factors for BHR. Although TLR4 was not an independent risk factor for BHR, individuals with CT+TT genotypes at the TLR4 polymorphism had an increased risk of BHR when combined with acetaminophen usage (aOR, 1.74; 95% CI, 1.03-2.94). In conclusion, acetaminophen usage may be associated with asthma and BHR in genetically susceptible subjects. This effect may be modified by polymorphism at TLR4. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-40249592014-05-21 Association between Recent Acetaminophen Use and Asthma: Modification by Polymorphism at TLR4 Lee, Seung-Hwa Kang, Mi-Jin Yu, Ho-Sung Hong, Kyungmo Jung, Young-Ho Kim, Hyung-Young Seo, Ju-Hee Kwon, Ji-Won Kim, Byoung-Ju Kim, Ha-Jung Kim, Young-Joon Kim, Hee-Suk Kim, Hyo Bin Park, Kang Seo Lee, So-Yeon Hong, Soo-Jong J Korean Med Sci Original Article The risk of asthma has been increasing in parallel with use of acetaminophen, which is a potential source of oxidative stress. Toll-like receptor 4 (TLR4) plays a critical role not only in innate immunity, but also in mediating reactive oxygen species induced inflammation. Therefore, we investigated associations between acetaminophen usage and TLR4 polymorphism on asthma and bronchial hyperresponsiveness (BHR). The number of 2,428 elementary school children in Seoul and Jeongeup cities was recruited. Subjects who used acetaminophen with a family history of asthma had an increased risk of both asthma diagnosis ever and current asthma. Individuals with CT+TT genotypes at the TLR4 polymorphism, in combination with acetaminophen usage, also demonstrated an increased risk of asthma diagnosis ever (aOR, 2.08; 95% confidence interval [CI], 1.10-3.92). Family history of asthma and acetaminophen usage were risk factors for BHR. Although TLR4 was not an independent risk factor for BHR, individuals with CT+TT genotypes at the TLR4 polymorphism had an increased risk of BHR when combined with acetaminophen usage (aOR, 1.74; 95% CI, 1.03-2.94). In conclusion, acetaminophen usage may be associated with asthma and BHR in genetically susceptible subjects. This effect may be modified by polymorphism at TLR4. GRAPHICAL ABSTRACT: [Image: see text] The Korean Academy of Medical Sciences 2014-05 2014-04-25 /pmc/articles/PMC4024959/ /pubmed/24851022 http://dx.doi.org/10.3346/jkms.2014.29.5.662 Text en © 2014 The Korean Academy of Medical Sciences. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Seung-Hwa
Kang, Mi-Jin
Yu, Ho-Sung
Hong, Kyungmo
Jung, Young-Ho
Kim, Hyung-Young
Seo, Ju-Hee
Kwon, Ji-Won
Kim, Byoung-Ju
Kim, Ha-Jung
Kim, Young-Joon
Kim, Hee-Suk
Kim, Hyo Bin
Park, Kang Seo
Lee, So-Yeon
Hong, Soo-Jong
Association between Recent Acetaminophen Use and Asthma: Modification by Polymorphism at TLR4
title Association between Recent Acetaminophen Use and Asthma: Modification by Polymorphism at TLR4
title_full Association between Recent Acetaminophen Use and Asthma: Modification by Polymorphism at TLR4
title_fullStr Association between Recent Acetaminophen Use and Asthma: Modification by Polymorphism at TLR4
title_full_unstemmed Association between Recent Acetaminophen Use and Asthma: Modification by Polymorphism at TLR4
title_short Association between Recent Acetaminophen Use and Asthma: Modification by Polymorphism at TLR4
title_sort association between recent acetaminophen use and asthma: modification by polymorphism at tlr4
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4024959/
https://www.ncbi.nlm.nih.gov/pubmed/24851022
http://dx.doi.org/10.3346/jkms.2014.29.5.662
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