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Association of a four‐gene model with allergic diseases: Two‐year follow‐up of a birth cohort study

BACKGROUND: Our previous study has developed a four‐gene model involving IL13 rs20541, IL4 rs2243250, ADRB2 rs1042713, and FCER1B rs569108 associated with asthma and atopy in Chinese Han children. However, whether the gene model is associated with allergies in early life has yet to be determined. Th...

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Autores principales: Hua, Li, Yang, Fen, Chen, Qian, Liu, Quanhua, Ji, Ruoxu, Liu, Haipei, Ye, Jianmin, Zhang, Jun, Zhang, Jianhua, Bao, Yixiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7860525/
https://www.ncbi.nlm.nih.gov/pubmed/33277970
http://dx.doi.org/10.1002/iid3.385
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author Hua, Li
Yang, Fen
Chen, Qian
Liu, Quanhua
Ji, Ruoxu
Liu, Haipei
Ye, Jianmin
Zhang, Jun
Zhang, Jianhua
Bao, Yixiao
author_facet Hua, Li
Yang, Fen
Chen, Qian
Liu, Quanhua
Ji, Ruoxu
Liu, Haipei
Ye, Jianmin
Zhang, Jun
Zhang, Jianhua
Bao, Yixiao
author_sort Hua, Li
collection PubMed
description BACKGROUND: Our previous study has developed a four‐gene model involving IL13 rs20541, IL4 rs2243250, ADRB2 rs1042713, and FCER1B rs569108 associated with asthma and atopy in Chinese Han children. However, whether the gene model is associated with allergies in early life has yet to be determined. This study aimed to apply the gene model in a birth cohort to investigate its associations with the development of allergic diseases in Chinese Han toddlers. METHODS: Five hundred and ninety‐seven children from a birth cohort completing 2‐year follow‐up were included. Epidemiologic information and cord blood were collected. Children were genotyped for the above polymorphisms and divided into high or low genetic risk groups based on the genotypes. Subjects were followed at 6, 12, and 24 months, with information on allergic diseases collected via standard questionnaires and assessed by specialists. RESULTS: Two hundred and eighty‐four children were divided into a high‐risk group and 313 into a low‐risk group. Between the two groups, a significant difference was only found in delivery mode among all the subject characteristics (p = .025). After stratification for delivery mode, children at high risk were more likely to develop eczema (relative risk [RR] = 1.46, p = .040) over 2 years of follow‐up compared with those at low risk. No significant associations were found between genetic risk and food allergy, wheezing and allergic rhinitis (p > .05). CONCLUSION: The gene model was significantly associated with the development of eczema in Chinese Han toddlers. Long‐term follow‐up along with functional and replication studies on the gene model are still needed in future.
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spelling pubmed-78605252021-02-05 Association of a four‐gene model with allergic diseases: Two‐year follow‐up of a birth cohort study Hua, Li Yang, Fen Chen, Qian Liu, Quanhua Ji, Ruoxu Liu, Haipei Ye, Jianmin Zhang, Jun Zhang, Jianhua Bao, Yixiao Immun Inflamm Dis Original Research BACKGROUND: Our previous study has developed a four‐gene model involving IL13 rs20541, IL4 rs2243250, ADRB2 rs1042713, and FCER1B rs569108 associated with asthma and atopy in Chinese Han children. However, whether the gene model is associated with allergies in early life has yet to be determined. This study aimed to apply the gene model in a birth cohort to investigate its associations with the development of allergic diseases in Chinese Han toddlers. METHODS: Five hundred and ninety‐seven children from a birth cohort completing 2‐year follow‐up were included. Epidemiologic information and cord blood were collected. Children were genotyped for the above polymorphisms and divided into high or low genetic risk groups based on the genotypes. Subjects were followed at 6, 12, and 24 months, with information on allergic diseases collected via standard questionnaires and assessed by specialists. RESULTS: Two hundred and eighty‐four children were divided into a high‐risk group and 313 into a low‐risk group. Between the two groups, a significant difference was only found in delivery mode among all the subject characteristics (p = .025). After stratification for delivery mode, children at high risk were more likely to develop eczema (relative risk [RR] = 1.46, p = .040) over 2 years of follow‐up compared with those at low risk. No significant associations were found between genetic risk and food allergy, wheezing and allergic rhinitis (p > .05). CONCLUSION: The gene model was significantly associated with the development of eczema in Chinese Han toddlers. Long‐term follow‐up along with functional and replication studies on the gene model are still needed in future. John Wiley and Sons Inc. 2020-12-05 /pmc/articles/PMC7860525/ /pubmed/33277970 http://dx.doi.org/10.1002/iid3.385 Text en © 2020 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Hua, Li
Yang, Fen
Chen, Qian
Liu, Quanhua
Ji, Ruoxu
Liu, Haipei
Ye, Jianmin
Zhang, Jun
Zhang, Jianhua
Bao, Yixiao
Association of a four‐gene model with allergic diseases: Two‐year follow‐up of a birth cohort study
title Association of a four‐gene model with allergic diseases: Two‐year follow‐up of a birth cohort study
title_full Association of a four‐gene model with allergic diseases: Two‐year follow‐up of a birth cohort study
title_fullStr Association of a four‐gene model with allergic diseases: Two‐year follow‐up of a birth cohort study
title_full_unstemmed Association of a four‐gene model with allergic diseases: Two‐year follow‐up of a birth cohort study
title_short Association of a four‐gene model with allergic diseases: Two‐year follow‐up of a birth cohort study
title_sort association of a four‐gene model with allergic diseases: two‐year follow‐up of a birth cohort study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7860525/
https://www.ncbi.nlm.nih.gov/pubmed/33277970
http://dx.doi.org/10.1002/iid3.385
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