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Association between SP‐A rs1965708 gene polymorphism and allergic rhinitis risk in Chinese population

BACKGROUND: Pulmonary surfactant protein A (SP‐A) in the respiratory tract plays an important role in host. In the present, we assessed the association between SP‐A gene polymorphism and allergic rhinitis. METHODS: Using a case–control design, we compared the genotype frequencies of SP‐A rs1965708 b...

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Autores principales: Yin, Xinghong, Wang, Bo, Yan, Zhiqiang, Hu, Lulu, Zhang, Xinhai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8274983/
https://www.ncbi.nlm.nih.gov/pubmed/34028080
http://dx.doi.org/10.1002/jcla.23828
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author Yin, Xinghong
Wang, Bo
Yan, Zhiqiang
Hu, Lulu
Zhang, Xinhai
author_facet Yin, Xinghong
Wang, Bo
Yan, Zhiqiang
Hu, Lulu
Zhang, Xinhai
author_sort Yin, Xinghong
collection PubMed
description BACKGROUND: Pulmonary surfactant protein A (SP‐A) in the respiratory tract plays an important role in host. In the present, we assessed the association between SP‐A gene polymorphism and allergic rhinitis. METHODS: Using a case–control design, we compared the genotype frequencies of SP‐A rs1965708 between allergic rhinitis patients and healthy control group. Genotyping was performed using real‐time quantitative PCR‐based molecular identification methods. Univariate and multivariate logistic regression were performed to quantitatively assess the association between rs1965708 polymorphism and allergic rhinitis, and the odds ratio (OR) and 95% confidence interval (CI) were also calculated. RESULTS: 500 patients with allergic rhinitis and 500 healthy controls were included in the study. Compared with the CC genotype, we found that AA genotype of rs1965708 could increase the allergic rhinitis risk in the univariate analysis (OR = 2.63, 95% CI: 1.56–4.54, p = 0.000). For dominant model, we found no significant difference in the dominant model (OR = 1.14, 95% CI: 0.86–1.52, p = 0.367). In the recessive model, the CC genotype could elevate the risk of allergic rhinitis compared with CC + AA genotype (OR = 2.70, 95% CI: 1.61–4.54, p = 0.000). Similar results were also found in the allele model (OR = 1.28, 95% CI: 1.07–1.54, p = 0.008). Interactions between rs1965708 AA or AC and smoking increased the allergic rhinitis risk. CONCLUSIONS: The rs1965708 variants of SP‐A gene polymorphism are associated with allergic rhinitis, and the A allele could increase the allergic rhinitis risk. The AA SNP variants that interact with smoking may alter the susceptibility to allergic rhinitis.
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spelling pubmed-82749832021-07-15 Association between SP‐A rs1965708 gene polymorphism and allergic rhinitis risk in Chinese population Yin, Xinghong Wang, Bo Yan, Zhiqiang Hu, Lulu Zhang, Xinhai J Clin Lab Anal Research Articles BACKGROUND: Pulmonary surfactant protein A (SP‐A) in the respiratory tract plays an important role in host. In the present, we assessed the association between SP‐A gene polymorphism and allergic rhinitis. METHODS: Using a case–control design, we compared the genotype frequencies of SP‐A rs1965708 between allergic rhinitis patients and healthy control group. Genotyping was performed using real‐time quantitative PCR‐based molecular identification methods. Univariate and multivariate logistic regression were performed to quantitatively assess the association between rs1965708 polymorphism and allergic rhinitis, and the odds ratio (OR) and 95% confidence interval (CI) were also calculated. RESULTS: 500 patients with allergic rhinitis and 500 healthy controls were included in the study. Compared with the CC genotype, we found that AA genotype of rs1965708 could increase the allergic rhinitis risk in the univariate analysis (OR = 2.63, 95% CI: 1.56–4.54, p = 0.000). For dominant model, we found no significant difference in the dominant model (OR = 1.14, 95% CI: 0.86–1.52, p = 0.367). In the recessive model, the CC genotype could elevate the risk of allergic rhinitis compared with CC + AA genotype (OR = 2.70, 95% CI: 1.61–4.54, p = 0.000). Similar results were also found in the allele model (OR = 1.28, 95% CI: 1.07–1.54, p = 0.008). Interactions between rs1965708 AA or AC and smoking increased the allergic rhinitis risk. CONCLUSIONS: The rs1965708 variants of SP‐A gene polymorphism are associated with allergic rhinitis, and the A allele could increase the allergic rhinitis risk. The AA SNP variants that interact with smoking may alter the susceptibility to allergic rhinitis. John Wiley and Sons Inc. 2021-05-24 /pmc/articles/PMC8274983/ /pubmed/34028080 http://dx.doi.org/10.1002/jcla.23828 Text en © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Yin, Xinghong
Wang, Bo
Yan, Zhiqiang
Hu, Lulu
Zhang, Xinhai
Association between SP‐A rs1965708 gene polymorphism and allergic rhinitis risk in Chinese population
title Association between SP‐A rs1965708 gene polymorphism and allergic rhinitis risk in Chinese population
title_full Association between SP‐A rs1965708 gene polymorphism and allergic rhinitis risk in Chinese population
title_fullStr Association between SP‐A rs1965708 gene polymorphism and allergic rhinitis risk in Chinese population
title_full_unstemmed Association between SP‐A rs1965708 gene polymorphism and allergic rhinitis risk in Chinese population
title_short Association between SP‐A rs1965708 gene polymorphism and allergic rhinitis risk in Chinese population
title_sort association between sp‐a rs1965708 gene polymorphism and allergic rhinitis risk in chinese population
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8274983/
https://www.ncbi.nlm.nih.gov/pubmed/34028080
http://dx.doi.org/10.1002/jcla.23828
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