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Genetic Association Between CD143 rs4340 Polymorphism and Pneumonia risk: A Meta Analysis
rs4340 polymorphism at intron 16 of the angiotensin-converting enzyme (CD143) gene was reported to repress cough reflex by reducing bradykinin and substance P levels, thus increasing the likelihood to develop pneumonia. There have been different reports regarding the correlation of CD143 rs4340 geno...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554131/ https://www.ncbi.nlm.nih.gov/pubmed/26222869 http://dx.doi.org/10.1097/MD.0000000000000883 |
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author | Wang, Hong Zhang, Kun Qin, Haifeng Yang, Lin Zhang, Liyu Cao, Yanyan |
author_facet | Wang, Hong Zhang, Kun Qin, Haifeng Yang, Lin Zhang, Liyu Cao, Yanyan |
author_sort | Wang, Hong |
collection | PubMed |
description | rs4340 polymorphism at intron 16 of the angiotensin-converting enzyme (CD143) gene was reported to repress cough reflex by reducing bradykinin and substance P levels, thus increasing the likelihood to develop pneumonia. There have been different reports regarding the correlation of CD143 rs4340 genotypes with pneumonia risk, which prompted us to perform a meta-analysis to determine the elusive association. We combined multiple keywords to identify the studies addressing the association between CD143 rs4340 genotypes and pneumonia risk covered in the EMBASE, Google Scholar, PubMed, and CNKI databases. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to assess the risk of pneumonia. The fixed-effects model (FEM) was used. A total of 10 studies were analyzed in this quantitative analysis. We found a strong association between rs4340 single nucleotide polymorphism (SNP) and pneumonia risk using the recessive model (FEM: OR 1.33, 95% CI 1.13–1.57). A significantly increased risk was also indicated under the recessive model in Asian populations (FEM: OR 1.57, 95% CI 1.19–2.07), community-acquired pneumonia (CAP) (FEM: OR 1.31, 95% CI 1.08–1.60), and nosocomial pneumonia (NP) (FEM: OR 1.52, 95% CI 1.06–2.19). Our meta-analysis demonstrates that CD143 rs4340 polymorphism may represent a risk factor for pneumonia. |
format | Online Article Text |
id | pubmed-4554131 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-45541312015-10-27 Genetic Association Between CD143 rs4340 Polymorphism and Pneumonia risk: A Meta Analysis Wang, Hong Zhang, Kun Qin, Haifeng Yang, Lin Zhang, Liyu Cao, Yanyan Medicine (Baltimore) 5700 rs4340 polymorphism at intron 16 of the angiotensin-converting enzyme (CD143) gene was reported to repress cough reflex by reducing bradykinin and substance P levels, thus increasing the likelihood to develop pneumonia. There have been different reports regarding the correlation of CD143 rs4340 genotypes with pneumonia risk, which prompted us to perform a meta-analysis to determine the elusive association. We combined multiple keywords to identify the studies addressing the association between CD143 rs4340 genotypes and pneumonia risk covered in the EMBASE, Google Scholar, PubMed, and CNKI databases. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to assess the risk of pneumonia. The fixed-effects model (FEM) was used. A total of 10 studies were analyzed in this quantitative analysis. We found a strong association between rs4340 single nucleotide polymorphism (SNP) and pneumonia risk using the recessive model (FEM: OR 1.33, 95% CI 1.13–1.57). A significantly increased risk was also indicated under the recessive model in Asian populations (FEM: OR 1.57, 95% CI 1.19–2.07), community-acquired pneumonia (CAP) (FEM: OR 1.31, 95% CI 1.08–1.60), and nosocomial pneumonia (NP) (FEM: OR 1.52, 95% CI 1.06–2.19). Our meta-analysis demonstrates that CD143 rs4340 polymorphism may represent a risk factor for pneumonia. Wolters Kluwer Health 2015-07-31 /pmc/articles/PMC4554131/ /pubmed/26222869 http://dx.doi.org/10.1097/MD.0000000000000883 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 5700 Wang, Hong Zhang, Kun Qin, Haifeng Yang, Lin Zhang, Liyu Cao, Yanyan Genetic Association Between CD143 rs4340 Polymorphism and Pneumonia risk: A Meta Analysis |
title | Genetic Association Between CD143 rs4340 Polymorphism and Pneumonia risk: A Meta Analysis |
title_full | Genetic Association Between CD143 rs4340 Polymorphism and Pneumonia risk: A Meta Analysis |
title_fullStr | Genetic Association Between CD143 rs4340 Polymorphism and Pneumonia risk: A Meta Analysis |
title_full_unstemmed | Genetic Association Between CD143 rs4340 Polymorphism and Pneumonia risk: A Meta Analysis |
title_short | Genetic Association Between CD143 rs4340 Polymorphism and Pneumonia risk: A Meta Analysis |
title_sort | genetic association between cd143 rs4340 polymorphism and pneumonia risk: a meta analysis |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554131/ https://www.ncbi.nlm.nih.gov/pubmed/26222869 http://dx.doi.org/10.1097/MD.0000000000000883 |
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