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Association between interleukin-10-819T/C polymorphism and risk of ischemic stroke: A meta-analysis
BACKGROUND: The interleukin-10 (IL-10)-819T/C polymorphism has been indicated to be correlated with ischemic stroke susceptibility, but this relationship remains controversial. A meta-analysis was conducted to investigate the potential association between IL-10-819T/C polymorphism and ischemic strok...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7253870/ https://www.ncbi.nlm.nih.gov/pubmed/32443287 http://dx.doi.org/10.1097/MD.0000000000019808 |
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author | Zuo, Shuang Zheng, Tingting Li, Haishan |
author_facet | Zuo, Shuang Zheng, Tingting Li, Haishan |
author_sort | Zuo, Shuang |
collection | PubMed |
description | BACKGROUND: The interleukin-10 (IL-10)-819T/C polymorphism has been indicated to be correlated with ischemic stroke susceptibility, but this relationship remains controversial. A meta-analysis was conducted to investigate the potential association between IL-10-819T/C polymorphism and ischemic stroke risk. METHODS: Databases including Pubmed, Embase, and CNKI were searched. Data were extracted and odds ratios (OR) with 95% confidence intervals (CI) were calculated. RESULTS: Eight case-control studies with 1832 cases and 1520 controls were included in this meta-analysis. IL-10-819T/C polymorphism may decrease the risk of ischemic stroke (C vs T: OR = 1.01, 95% CI: 0.91–1.12; CC vs TT: OR = 0.91, 95% CI: 0.73–1.14; CT vs TT: OR = 1.10, 95% CI: 0.95–1.28; CC + CT vs TT: OR = 1.06, 95% CI: 0.92–1.22; CC vs CT + TT: OR = 0.91, 95% CI: 0.75–1.11). In the stratified analysis by sample size, and case-control matched status, significant associations were still not observed in all genetic models. In the subgroup meta-analysis based on source of controls, IL-10-819T/C polymorphism had decreased ischemic stroke risk for recessive model in population-based controls’ subgroup (CC vs CT + TT: OR = 0.69, 95% CI: 0.50–0.95), but not in the hospital-based controls’ subgroup. In the stratified analysis based on ethnicity, IL-10-819T/C polymorphism had decreased ischemic stroke risk for recessive model in Asian populations (CC vs CT + TT: OR = 0.78, 95% CI: 0.62–0.99), but not in Caucasian populations. CONCLUSIONS: In conclusion, the results suggest that the IL-10-819T/C polymorphism is not associated with ischemic stroke risk. Larger scale studies are needed for confirmation. |
format | Online Article Text |
id | pubmed-7253870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-72538702020-06-15 Association between interleukin-10-819T/C polymorphism and risk of ischemic stroke: A meta-analysis Zuo, Shuang Zheng, Tingting Li, Haishan Medicine (Baltimore) 4400 BACKGROUND: The interleukin-10 (IL-10)-819T/C polymorphism has been indicated to be correlated with ischemic stroke susceptibility, but this relationship remains controversial. A meta-analysis was conducted to investigate the potential association between IL-10-819T/C polymorphism and ischemic stroke risk. METHODS: Databases including Pubmed, Embase, and CNKI were searched. Data were extracted and odds ratios (OR) with 95% confidence intervals (CI) were calculated. RESULTS: Eight case-control studies with 1832 cases and 1520 controls were included in this meta-analysis. IL-10-819T/C polymorphism may decrease the risk of ischemic stroke (C vs T: OR = 1.01, 95% CI: 0.91–1.12; CC vs TT: OR = 0.91, 95% CI: 0.73–1.14; CT vs TT: OR = 1.10, 95% CI: 0.95–1.28; CC + CT vs TT: OR = 1.06, 95% CI: 0.92–1.22; CC vs CT + TT: OR = 0.91, 95% CI: 0.75–1.11). In the stratified analysis by sample size, and case-control matched status, significant associations were still not observed in all genetic models. In the subgroup meta-analysis based on source of controls, IL-10-819T/C polymorphism had decreased ischemic stroke risk for recessive model in population-based controls’ subgroup (CC vs CT + TT: OR = 0.69, 95% CI: 0.50–0.95), but not in the hospital-based controls’ subgroup. In the stratified analysis based on ethnicity, IL-10-819T/C polymorphism had decreased ischemic stroke risk for recessive model in Asian populations (CC vs CT + TT: OR = 0.78, 95% CI: 0.62–0.99), but not in Caucasian populations. CONCLUSIONS: In conclusion, the results suggest that the IL-10-819T/C polymorphism is not associated with ischemic stroke risk. Larger scale studies are needed for confirmation. Wolters Kluwer Health 2020-05-15 /pmc/articles/PMC7253870/ /pubmed/32443287 http://dx.doi.org/10.1097/MD.0000000000019808 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 4400 Zuo, Shuang Zheng, Tingting Li, Haishan Association between interleukin-10-819T/C polymorphism and risk of ischemic stroke: A meta-analysis |
title | Association between interleukin-10-819T/C polymorphism and risk of ischemic stroke: A meta-analysis |
title_full | Association between interleukin-10-819T/C polymorphism and risk of ischemic stroke: A meta-analysis |
title_fullStr | Association between interleukin-10-819T/C polymorphism and risk of ischemic stroke: A meta-analysis |
title_full_unstemmed | Association between interleukin-10-819T/C polymorphism and risk of ischemic stroke: A meta-analysis |
title_short | Association between interleukin-10-819T/C polymorphism and risk of ischemic stroke: A meta-analysis |
title_sort | association between interleukin-10-819t/c polymorphism and risk of ischemic stroke: a meta-analysis |
topic | 4400 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7253870/ https://www.ncbi.nlm.nih.gov/pubmed/32443287 http://dx.doi.org/10.1097/MD.0000000000019808 |
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