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Functional polymorphism in miR-208 is associated with increased risk for ischemic stroke
BACKGROUND: The miR-208 gene is one of the microRNAs now under active studies, and has been found to play significant roles in an array of cardiovascular diseases. Nevertheless, until now, no studies have examined the relationship between the susceptibility to ischemic stroke (IS) and genetic variat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10391967/ https://www.ncbi.nlm.nih.gov/pubmed/37525251 http://dx.doi.org/10.1186/s12920-023-01610-y |
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author | Liu, Chao Luo, Yan-Ping Chen, Jie Weng, Yin-Hua Lan, Yan Liu, Hong-Bo |
author_facet | Liu, Chao Luo, Yan-Ping Chen, Jie Weng, Yin-Hua Lan, Yan Liu, Hong-Bo |
author_sort | Liu, Chao |
collection | PubMed |
description | BACKGROUND: The miR-208 gene is one of the microRNAs now under active studies, and has been found to play significant roles in an array of cardiovascular diseases. Nevertheless, until now, no studies have examined the relationship between the susceptibility to ischemic stroke (IS) and genetic variations in miR-208. This study explored the association between the miR-208 polymorphisms (rs178642, rs8022522, and rs12894524) and the risk of IS. METHODS: A total of 205 cases of IS and 211 control subjects were included. The SNPscans genotyping test was employed to determine the genotypes of the three polymorphisms. RESULTS: Significant correlation was observed between rs8022522 polymorphism and risk of IS on the basis of analyses of genotypes, models and alleles (GA vs. GG: adjusted OR = 2.159, 95% CI: 1.052–4.430, P = 0. 036; AA vs. GG: adjusted OR = 5.154, 95% CI: 1.123–23.660, P = 0.035; dominant model: adjusted OR = 1.746, 95% CI, 1.075–2.838, P = 0.025; G vs. A: adjusted OR = 2.451, 95% CI: 1.374–4.370, P = 0.002). CONCLUSIONS: The rs8022522 polymorphism of the miR-208 gene is significantly associated with an elevated risk of ischemic stroke in Chinese. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-023-01610-y. |
format | Online Article Text |
id | pubmed-10391967 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103919672023-08-02 Functional polymorphism in miR-208 is associated with increased risk for ischemic stroke Liu, Chao Luo, Yan-Ping Chen, Jie Weng, Yin-Hua Lan, Yan Liu, Hong-Bo BMC Med Genomics Research BACKGROUND: The miR-208 gene is one of the microRNAs now under active studies, and has been found to play significant roles in an array of cardiovascular diseases. Nevertheless, until now, no studies have examined the relationship between the susceptibility to ischemic stroke (IS) and genetic variations in miR-208. This study explored the association between the miR-208 polymorphisms (rs178642, rs8022522, and rs12894524) and the risk of IS. METHODS: A total of 205 cases of IS and 211 control subjects were included. The SNPscans genotyping test was employed to determine the genotypes of the three polymorphisms. RESULTS: Significant correlation was observed between rs8022522 polymorphism and risk of IS on the basis of analyses of genotypes, models and alleles (GA vs. GG: adjusted OR = 2.159, 95% CI: 1.052–4.430, P = 0. 036; AA vs. GG: adjusted OR = 5.154, 95% CI: 1.123–23.660, P = 0.035; dominant model: adjusted OR = 1.746, 95% CI, 1.075–2.838, P = 0.025; G vs. A: adjusted OR = 2.451, 95% CI: 1.374–4.370, P = 0.002). CONCLUSIONS: The rs8022522 polymorphism of the miR-208 gene is significantly associated with an elevated risk of ischemic stroke in Chinese. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-023-01610-y. BioMed Central 2023-07-31 /pmc/articles/PMC10391967/ /pubmed/37525251 http://dx.doi.org/10.1186/s12920-023-01610-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Liu, Chao Luo, Yan-Ping Chen, Jie Weng, Yin-Hua Lan, Yan Liu, Hong-Bo Functional polymorphism in miR-208 is associated with increased risk for ischemic stroke |
title | Functional polymorphism in miR-208 is associated with increased risk for ischemic stroke |
title_full | Functional polymorphism in miR-208 is associated with increased risk for ischemic stroke |
title_fullStr | Functional polymorphism in miR-208 is associated with increased risk for ischemic stroke |
title_full_unstemmed | Functional polymorphism in miR-208 is associated with increased risk for ischemic stroke |
title_short | Functional polymorphism in miR-208 is associated with increased risk for ischemic stroke |
title_sort | functional polymorphism in mir-208 is associated with increased risk for ischemic stroke |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10391967/ https://www.ncbi.nlm.nih.gov/pubmed/37525251 http://dx.doi.org/10.1186/s12920-023-01610-y |
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