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Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
BACKGROUND: Matrix metalloproteinases (MMPs) polymorphisms have been implicated in the pathogenesis of glaucoma risk. However, the results were controversial. We performed a meta-analysis to evaluate the precise associations between MMPs polymorphisms and glaucoma risk. METHODS: Related studies were...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5401566/ https://www.ncbi.nlm.nih.gov/pubmed/28431514 http://dx.doi.org/10.1186/s12886-017-0442-2 |
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author | Wu, Ming-Yue Wu, Yang Zhang, Yong Liu, Cai-Yun Deng, Chun-Yan Peng, Le Zhou, Lan |
author_facet | Wu, Ming-Yue Wu, Yang Zhang, Yong Liu, Cai-Yun Deng, Chun-Yan Peng, Le Zhou, Lan |
author_sort | Wu, Ming-Yue |
collection | PubMed |
description | BACKGROUND: Matrix metalloproteinases (MMPs) polymorphisms have been implicated in the pathogenesis of glaucoma risk. However, the results were controversial. We performed a meta-analysis to evaluate the precise associations between MMPs polymorphisms and glaucoma risk. METHODS: Related studies were reviewed by searching electronic databases within four databases. Odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to assess the association between the most common polymorphisms of MMPs and glaucoma risk. Heterogeneity, publication bias and sensitivity analysis were conducted to guarantee the statistical power. RESULTS: Overall, 11 selected articles involving 2,388 cases and 2,319 controls were included in this meta-analysis. Significant associations were only found between MMP-9 rs17576 G > A polymorphism (GA vs. GG: OR = 0.80, 95%CI = 0.67-0.97, P = 0.02, I(2) = 0%), MMP-9 rs3918249 C > T polymorphism (TT vs. CC + CT: OR = 0.71, 95%CI = 0.51-0.98, P = 0.04, I(2) = 0%) and glaucoma risk in the general population. Subgroup analysis also suggested that MMP-9 rs17576 G > A was related to glaucoma in the Caucasian population (GA vs. GG: OR = 0.67, 95%CI = 0.45-1.00, P = 0.05; GA + AA vs. GG: OR = 0.66, 95%CI = 0.45-0.97, P = 0.03, I(2) = 0%). CONCLUSIONS: Our meta-analysis demonstrates that MMP-9 rs17576 G > A polymorphism might be a protective factor against the development of glaucoma in Caucasian population. |
format | Online Article Text |
id | pubmed-5401566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54015662017-04-24 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis Wu, Ming-Yue Wu, Yang Zhang, Yong Liu, Cai-Yun Deng, Chun-Yan Peng, Le Zhou, Lan BMC Ophthalmol Research Article BACKGROUND: Matrix metalloproteinases (MMPs) polymorphisms have been implicated in the pathogenesis of glaucoma risk. However, the results were controversial. We performed a meta-analysis to evaluate the precise associations between MMPs polymorphisms and glaucoma risk. METHODS: Related studies were reviewed by searching electronic databases within four databases. Odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to assess the association between the most common polymorphisms of MMPs and glaucoma risk. Heterogeneity, publication bias and sensitivity analysis were conducted to guarantee the statistical power. RESULTS: Overall, 11 selected articles involving 2,388 cases and 2,319 controls were included in this meta-analysis. Significant associations were only found between MMP-9 rs17576 G > A polymorphism (GA vs. GG: OR = 0.80, 95%CI = 0.67-0.97, P = 0.02, I(2) = 0%), MMP-9 rs3918249 C > T polymorphism (TT vs. CC + CT: OR = 0.71, 95%CI = 0.51-0.98, P = 0.04, I(2) = 0%) and glaucoma risk in the general population. Subgroup analysis also suggested that MMP-9 rs17576 G > A was related to glaucoma in the Caucasian population (GA vs. GG: OR = 0.67, 95%CI = 0.45-1.00, P = 0.05; GA + AA vs. GG: OR = 0.66, 95%CI = 0.45-0.97, P = 0.03, I(2) = 0%). CONCLUSIONS: Our meta-analysis demonstrates that MMP-9 rs17576 G > A polymorphism might be a protective factor against the development of glaucoma in Caucasian population. BioMed Central 2017-04-21 /pmc/articles/PMC5401566/ /pubmed/28431514 http://dx.doi.org/10.1186/s12886-017-0442-2 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Wu, Ming-Yue Wu, Yang Zhang, Yong Liu, Cai-Yun Deng, Chun-Yan Peng, Le Zhou, Lan Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis |
title | Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis |
title_full | Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis |
title_fullStr | Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis |
title_full_unstemmed | Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis |
title_short | Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis |
title_sort | associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5401566/ https://www.ncbi.nlm.nih.gov/pubmed/28431514 http://dx.doi.org/10.1186/s12886-017-0442-2 |
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