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Association of Mycoplasma pneumoniae infection with increased risk of asthma in children
The present study was conducted to investigate the relationship between Mycoplasma pneumoniae (MP) infection and the risk of asthma among children by detecting the rate of MP immunoglobulin M (MP-IgM) and the eosinophil (EOS) count. A total of 139 asthmatic children were enrolled as the case group a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443219/ https://www.ncbi.nlm.nih.gov/pubmed/28565772 http://dx.doi.org/10.3892/etm.2017.4219 |
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author | Yin, Sha-Sha Ma, Feng-Lian Gao, Xing |
author_facet | Yin, Sha-Sha Ma, Feng-Lian Gao, Xing |
author_sort | Yin, Sha-Sha |
collection | PubMed |
description | The present study was conducted to investigate the relationship between Mycoplasma pneumoniae (MP) infection and the risk of asthma among children by detecting the rate of MP immunoglobulin M (MP-IgM) and the eosinophil (EOS) count. A total of 139 asthmatic children were enrolled as the case group and assigned into three groups: Group A (aged <3 years, n=42), group B (aged 3–8 years, n=45) and group C (aged >8 years, n=52). Additionally, 115 healthy children were enrolled in the control group. Enzyme-linked immunosorbent assay was used to measure the MP-IgM-positive rate. EOS count was detected in the experimental and control groups by using a hemocytometer analyzer. A meta-analysis was performed by using the Comprehensive Meta-Analysis version 2.0 software. The positive rates of the MP-IgM and EOS count in the experimental group were significantly higher than those in control group (both P<0.001). Furthermore, the asthmatic children in group C had a higher MP-IgM-positive rate and EOS count as compared to those in groups A and B, respectively (all P<0.05). Results from groups A and B were not statistically significant (all P>0.05). The meta-analysis further confirmed that asthmatic children had a higher MP-IgM-positive rate as compared to the healthy controls (P<0.001). Age-stratified analysis revealed that the MP-IgM-positive rate in asthmatic children aged ≥8 and <8 years was significantly higher than that in the healthy controls (P=0.003 and P<0.001). Asthmatic children had a higher MP-IgM-positive rate and EOS count as compared with controls, suggesting that the MP infection may be closely associated with the risk of asthma. Additionally, the positive rate of MP-IgM may indicate an important biological marker in predicting the development of asthma. |
format | Online Article Text |
id | pubmed-5443219 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-54432192017-05-30 Association of Mycoplasma pneumoniae infection with increased risk of asthma in children Yin, Sha-Sha Ma, Feng-Lian Gao, Xing Exp Ther Med Articles The present study was conducted to investigate the relationship between Mycoplasma pneumoniae (MP) infection and the risk of asthma among children by detecting the rate of MP immunoglobulin M (MP-IgM) and the eosinophil (EOS) count. A total of 139 asthmatic children were enrolled as the case group and assigned into three groups: Group A (aged <3 years, n=42), group B (aged 3–8 years, n=45) and group C (aged >8 years, n=52). Additionally, 115 healthy children were enrolled in the control group. Enzyme-linked immunosorbent assay was used to measure the MP-IgM-positive rate. EOS count was detected in the experimental and control groups by using a hemocytometer analyzer. A meta-analysis was performed by using the Comprehensive Meta-Analysis version 2.0 software. The positive rates of the MP-IgM and EOS count in the experimental group were significantly higher than those in control group (both P<0.001). Furthermore, the asthmatic children in group C had a higher MP-IgM-positive rate and EOS count as compared to those in groups A and B, respectively (all P<0.05). Results from groups A and B were not statistically significant (all P>0.05). The meta-analysis further confirmed that asthmatic children had a higher MP-IgM-positive rate as compared to the healthy controls (P<0.001). Age-stratified analysis revealed that the MP-IgM-positive rate in asthmatic children aged ≥8 and <8 years was significantly higher than that in the healthy controls (P=0.003 and P<0.001). Asthmatic children had a higher MP-IgM-positive rate and EOS count as compared with controls, suggesting that the MP infection may be closely associated with the risk of asthma. Additionally, the positive rate of MP-IgM may indicate an important biological marker in predicting the development of asthma. D.A. Spandidos 2017-05 2017-03-10 /pmc/articles/PMC5443219/ /pubmed/28565772 http://dx.doi.org/10.3892/etm.2017.4219 Text en Copyright: © Yin et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Yin, Sha-Sha Ma, Feng-Lian Gao, Xing Association of Mycoplasma pneumoniae infection with increased risk of asthma in children |
title | Association of Mycoplasma pneumoniae infection with increased risk of asthma in children |
title_full | Association of Mycoplasma pneumoniae infection with increased risk of asthma in children |
title_fullStr | Association of Mycoplasma pneumoniae infection with increased risk of asthma in children |
title_full_unstemmed | Association of Mycoplasma pneumoniae infection with increased risk of asthma in children |
title_short | Association of Mycoplasma pneumoniae infection with increased risk of asthma in children |
title_sort | association of mycoplasma pneumoniae infection with increased risk of asthma in children |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443219/ https://www.ncbi.nlm.nih.gov/pubmed/28565772 http://dx.doi.org/10.3892/etm.2017.4219 |
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