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A meta-analysis of mannose-binding lectin gene polymorphisms with the risk of recurrent vulvovaginal infections

The genetic variants of Mannose-Binding Lectin, a vital component of innate immunity have been studied with acute/recurrent vaginal infections ((R)VVI) and presented inconclusive findings. Therefore, a systematic review and meta-analysis of published data were conducted to assess the possible role o...

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Autores principales: Kalia, Namarta, Singh, Jatinder, Rauniyar, Akash Kumar, Kaur, Manpreet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142065/
https://www.ncbi.nlm.nih.gov/pubmed/32269261
http://dx.doi.org/10.1038/s41598-020-63261-8
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author Kalia, Namarta
Singh, Jatinder
Rauniyar, Akash Kumar
Kaur, Manpreet
author_facet Kalia, Namarta
Singh, Jatinder
Rauniyar, Akash Kumar
Kaur, Manpreet
author_sort Kalia, Namarta
collection PubMed
description The genetic variants of Mannose-Binding Lectin, a vital component of innate immunity have been studied with acute/recurrent vaginal infections ((R)VVI) and presented inconclusive findings. Therefore, a systematic review and meta-analysis of published data were conducted to assess the possible role of these variations in (R)VVI. A comprehensive search was made using PubMed, Web of Science and Google scholar till June 18, 2019. A total of 12 studies met the specified criteria and were included in the analysis. Different comparisons were made on the basis of the outcome of interest that resulted in the filtering of studies for the pooled analysis to find an association using the standard genetic models. Odds ratio (OR) with 95% confidence interval (CI) was chosen as the effect measure for the data synthesis. The trim and fill technique was applied to adjust the publication bias. The meta-analysis revealed the significant association (p < 0.05) of rs1800450 polymorphism with RVVI risk (OR ≥ 3.5) in all the genetic models. The subgroup analysis identified the same association in Caucasian and Mixed ethnicity. Quantitative synthesis based on RVVC showed>3.5 fold risk of disease development accredited to rs1800450. A combined evaluation of Exon1 variants showed no association with (R)VVI. This meta-analysis suggests rs1800450 polymorphism as a genetic predisposing factor for RVVI, but to reinforce, further studies with a larger sample size are warranted.
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spelling pubmed-71420652020-04-11 A meta-analysis of mannose-binding lectin gene polymorphisms with the risk of recurrent vulvovaginal infections Kalia, Namarta Singh, Jatinder Rauniyar, Akash Kumar Kaur, Manpreet Sci Rep Article The genetic variants of Mannose-Binding Lectin, a vital component of innate immunity have been studied with acute/recurrent vaginal infections ((R)VVI) and presented inconclusive findings. Therefore, a systematic review and meta-analysis of published data were conducted to assess the possible role of these variations in (R)VVI. A comprehensive search was made using PubMed, Web of Science and Google scholar till June 18, 2019. A total of 12 studies met the specified criteria and were included in the analysis. Different comparisons were made on the basis of the outcome of interest that resulted in the filtering of studies for the pooled analysis to find an association using the standard genetic models. Odds ratio (OR) with 95% confidence interval (CI) was chosen as the effect measure for the data synthesis. The trim and fill technique was applied to adjust the publication bias. The meta-analysis revealed the significant association (p < 0.05) of rs1800450 polymorphism with RVVI risk (OR ≥ 3.5) in all the genetic models. The subgroup analysis identified the same association in Caucasian and Mixed ethnicity. Quantitative synthesis based on RVVC showed>3.5 fold risk of disease development accredited to rs1800450. A combined evaluation of Exon1 variants showed no association with (R)VVI. This meta-analysis suggests rs1800450 polymorphism as a genetic predisposing factor for RVVI, but to reinforce, further studies with a larger sample size are warranted. Nature Publishing Group UK 2020-04-08 /pmc/articles/PMC7142065/ /pubmed/32269261 http://dx.doi.org/10.1038/s41598-020-63261-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kalia, Namarta
Singh, Jatinder
Rauniyar, Akash Kumar
Kaur, Manpreet
A meta-analysis of mannose-binding lectin gene polymorphisms with the risk of recurrent vulvovaginal infections
title A meta-analysis of mannose-binding lectin gene polymorphisms with the risk of recurrent vulvovaginal infections
title_full A meta-analysis of mannose-binding lectin gene polymorphisms with the risk of recurrent vulvovaginal infections
title_fullStr A meta-analysis of mannose-binding lectin gene polymorphisms with the risk of recurrent vulvovaginal infections
title_full_unstemmed A meta-analysis of mannose-binding lectin gene polymorphisms with the risk of recurrent vulvovaginal infections
title_short A meta-analysis of mannose-binding lectin gene polymorphisms with the risk of recurrent vulvovaginal infections
title_sort meta-analysis of mannose-binding lectin gene polymorphisms with the risk of recurrent vulvovaginal infections
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142065/
https://www.ncbi.nlm.nih.gov/pubmed/32269261
http://dx.doi.org/10.1038/s41598-020-63261-8
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