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Gene–gene and gene-environment interactions on cord blood total IgE in Chinese Han children

BACKGROUND: IL13, IL4, IL4RA, FCER1B and ADRB2 are susceptible genes of asthma and atopy. Our previous study has found gene–gene interactions on asthma between these genes in Chinese Han children. Whether the interactions begin in fetal stage, and whether these genes interact with prenatal environme...

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Autores principales: Hua, Li, Liu, Quanhua, Li, Jing, Zuo, Xianbo, Chen, Qian, Li, Jingyang, Wang, Yuwei, Liu, Haipei, Shen, Zhaobo, Li, Yi, Ma, Zenan, Dong, Shengdong, Ji, Ruoxu, Fang, Dingzhu, Chen, Yi, Zhong, Wenwei, Zhang, Jun, Zhang, Jianhua, Bao, Yixiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268446/
https://www.ncbi.nlm.nih.gov/pubmed/34243801
http://dx.doi.org/10.1186/s13223-021-00571-0
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author Hua, Li
Liu, Quanhua
Li, Jing
Zuo, Xianbo
Chen, Qian
Li, Jingyang
Wang, Yuwei
Liu, Haipei
Shen, Zhaobo
Li, Yi
Ma, Zenan
Dong, Shengdong
Ji, Ruoxu
Fang, Dingzhu
Chen, Yi
Zhong, Wenwei
Zhang, Jun
Zhang, Jianhua
Bao, Yixiao
author_facet Hua, Li
Liu, Quanhua
Li, Jing
Zuo, Xianbo
Chen, Qian
Li, Jingyang
Wang, Yuwei
Liu, Haipei
Shen, Zhaobo
Li, Yi
Ma, Zenan
Dong, Shengdong
Ji, Ruoxu
Fang, Dingzhu
Chen, Yi
Zhong, Wenwei
Zhang, Jun
Zhang, Jianhua
Bao, Yixiao
author_sort Hua, Li
collection PubMed
description BACKGROUND: IL13, IL4, IL4RA, FCER1B and ADRB2 are susceptible genes of asthma and atopy. Our previous study has found gene–gene interactions on asthma between these genes in Chinese Han children. Whether the interactions begin in fetal stage, and whether these genes interact with prenatal environment to enhance cord blood IgE (CBIgE) levels and then cause subsequent allergic diseases have yet to be determined. This study aimed to determine whether there are gene–gene and gene-environment interactions on CBIgE elevation among the aforementioned five genes and prenatal environmental factors in Chinese Han population. METHODS: 989 cord blood samples from a Chinese birth cohort were genotyped for nine single-nucleotide polymorphisms (SNPs) in the five genes, and measured for CBIgE levels. Prenatal environmental factors were collected using a questionnaire. Gene–gene and gene-environment interactions were analyzed with generalized multifactor dimensionality methods. RESULTS: A four-way gene–gene interaction model (IL13 rs20541, IL13 rs1800925, IL4 rs2243250 and ADRB2 rs1042713) was regarded as the optimal one for CBIgE elevation (testing balanced accuracy = 0.5805, P = 9.03 × 10(–4)). Among the four SNPs, only IL13 rs20541 was identified to have an independent effect on elevated CBIgE (odds ratio (OR) = 1.36, P = 3.57 × 10(–3)), while the other three had small but synergistic effects. Carriers of IL13 rs20541 TT, IL13 rs1800925 CT/TT, IL4 rs2243250 TT and ADRB2 rs1042713 AA were estimated to be at more than fourfold higher risk for CBIgE elevation (OR = 4.14, P = 2.69 × 10(–2)). Gene-environment interaction on elevated CBIgE was found between IL4 rs2243250 and maternal atopy (OR = 1.41, P = 2.65 × 10(–2)). CONCLUSIONS: Gene–gene interaction between IL13 rs20541, IL13 rs1800925, IL4 rs2243250 and ADRB2 rs1042713, and gene-environment interaction between IL4 rs2243250 and maternal atopy begin in prenatal stage to augment IgE production in Chinese Han children.
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spelling pubmed-82684462021-07-09 Gene–gene and gene-environment interactions on cord blood total IgE in Chinese Han children Hua, Li Liu, Quanhua Li, Jing Zuo, Xianbo Chen, Qian Li, Jingyang Wang, Yuwei Liu, Haipei Shen, Zhaobo Li, Yi Ma, Zenan Dong, Shengdong Ji, Ruoxu Fang, Dingzhu Chen, Yi Zhong, Wenwei Zhang, Jun Zhang, Jianhua Bao, Yixiao Allergy Asthma Clin Immunol Research BACKGROUND: IL13, IL4, IL4RA, FCER1B and ADRB2 are susceptible genes of asthma and atopy. Our previous study has found gene–gene interactions on asthma between these genes in Chinese Han children. Whether the interactions begin in fetal stage, and whether these genes interact with prenatal environment to enhance cord blood IgE (CBIgE) levels and then cause subsequent allergic diseases have yet to be determined. This study aimed to determine whether there are gene–gene and gene-environment interactions on CBIgE elevation among the aforementioned five genes and prenatal environmental factors in Chinese Han population. METHODS: 989 cord blood samples from a Chinese birth cohort were genotyped for nine single-nucleotide polymorphisms (SNPs) in the five genes, and measured for CBIgE levels. Prenatal environmental factors were collected using a questionnaire. Gene–gene and gene-environment interactions were analyzed with generalized multifactor dimensionality methods. RESULTS: A four-way gene–gene interaction model (IL13 rs20541, IL13 rs1800925, IL4 rs2243250 and ADRB2 rs1042713) was regarded as the optimal one for CBIgE elevation (testing balanced accuracy = 0.5805, P = 9.03 × 10(–4)). Among the four SNPs, only IL13 rs20541 was identified to have an independent effect on elevated CBIgE (odds ratio (OR) = 1.36, P = 3.57 × 10(–3)), while the other three had small but synergistic effects. Carriers of IL13 rs20541 TT, IL13 rs1800925 CT/TT, IL4 rs2243250 TT and ADRB2 rs1042713 AA were estimated to be at more than fourfold higher risk for CBIgE elevation (OR = 4.14, P = 2.69 × 10(–2)). Gene-environment interaction on elevated CBIgE was found between IL4 rs2243250 and maternal atopy (OR = 1.41, P = 2.65 × 10(–2)). CONCLUSIONS: Gene–gene interaction between IL13 rs20541, IL13 rs1800925, IL4 rs2243250 and ADRB2 rs1042713, and gene-environment interaction between IL4 rs2243250 and maternal atopy begin in prenatal stage to augment IgE production in Chinese Han children. BioMed Central 2021-07-09 /pmc/articles/PMC8268446/ /pubmed/34243801 http://dx.doi.org/10.1186/s13223-021-00571-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Hua, Li
Liu, Quanhua
Li, Jing
Zuo, Xianbo
Chen, Qian
Li, Jingyang
Wang, Yuwei
Liu, Haipei
Shen, Zhaobo
Li, Yi
Ma, Zenan
Dong, Shengdong
Ji, Ruoxu
Fang, Dingzhu
Chen, Yi
Zhong, Wenwei
Zhang, Jun
Zhang, Jianhua
Bao, Yixiao
Gene–gene and gene-environment interactions on cord blood total IgE in Chinese Han children
title Gene–gene and gene-environment interactions on cord blood total IgE in Chinese Han children
title_full Gene–gene and gene-environment interactions on cord blood total IgE in Chinese Han children
title_fullStr Gene–gene and gene-environment interactions on cord blood total IgE in Chinese Han children
title_full_unstemmed Gene–gene and gene-environment interactions on cord blood total IgE in Chinese Han children
title_short Gene–gene and gene-environment interactions on cord blood total IgE in Chinese Han children
title_sort gene–gene and gene-environment interactions on cord blood total ige in chinese han children
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268446/
https://www.ncbi.nlm.nih.gov/pubmed/34243801
http://dx.doi.org/10.1186/s13223-021-00571-0
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