Cargando…
Lack of association between interleukin-1 receptor antagonist gene 86-bp VNTR polymorphism and ischemic stroke: A meta-analysis
OBJECTIVE: The results of published studies which examined the association between variable number tandem repeat (VNTR) polymorphism of interleukin-1 receptor antagonist (IL-1RN) and ischemic stroke (IS) are conflicting. Thus, we performed a meta-analysis to examine the potential association between...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081086/ https://www.ncbi.nlm.nih.gov/pubmed/30075593 http://dx.doi.org/10.1097/MD.0000000000011750 |
_version_ | 1783345597551476736 |
---|---|
author | Yang, Yujiao Wu, Wenhui Wang, Long Ding, Yi |
author_facet | Yang, Yujiao Wu, Wenhui Wang, Long Ding, Yi |
author_sort | Yang, Yujiao |
collection | PubMed |
description | OBJECTIVE: The results of published studies which examined the association between variable number tandem repeat (VNTR) polymorphism of interleukin-1 receptor antagonist (IL-1RN) and ischemic stroke (IS) are conflicting. Thus, we performed a meta-analysis to examine the potential association between IL-1RN VNTR polymorphism and IS risk. METHODS: A systematic literature search of PubMed, Embase, Medline, Web of Science, Cochrane Library, Chinese Biomedical Literature Database, Chinese National Knowledge Infrastructure, CQVIP, and WANFANG Database identified 10 studies with 2331 cases and 3335 controls. The pooled odds ratio (OR) with 95% confidence interval (95% CI) was calculated to evaluate the strength of the association. Subgroup analysis and meta-regression analysis were used to investigate the potential sources of heterogeneity. Begg funnel plots were used to explore the publication bias. RESULTS: In this study, no enough proof was found to prove the association between IL-1RN 86-bp VNTR polymorphism and IS risk with random-effects model in the homozygous model (1/1 vs 2/2, OR = 0.97, 95% CI = 0.50–1.87, P(heterogeneity) = .00), the heterozygous model (1/2 vs 2/2, OR = 0.64, 95% CI = 0.41–1.01, P(heterogeneity) = .10), the dominant model (1/1 + 1/2 vs 2/2, OR = 0.85, 95% CI = 0.51–1.42, P(heterogeneity) = .02), the recessive model (1/1 vs 1/2 + 2/2, OR = 0.69, 95% CI = 0.46–1.03, P(heterogeneity) = .00), and allelic model (1 vs 2, OR = 1.24, 95% CI = 0.89–1.74, P(heterogeneity) = .00). A marginally significant negative association was observed between IL-1RN 86-bp VNTR polymorphism and IS risk in the heterozygous model in the fixed-effects model (1/2 vs 2/2, OR = 0.71, 95% CI = 0.53–0.95, P(heterogeneity) = .10). In subgroup analyses, similar association was found in the group whose control size was lower than 300. CONCLUSION: In conclusion, our results suggested that there was no sufficient evidence to support the association between IL-1RN 86-bp VNTR polymorphism and IS. Further large epidemiologic studies need to be done to confirm these findings. |
format | Online Article Text |
id | pubmed-6081086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-60810862018-08-17 Lack of association between interleukin-1 receptor antagonist gene 86-bp VNTR polymorphism and ischemic stroke: A meta-analysis Yang, Yujiao Wu, Wenhui Wang, Long Ding, Yi Medicine (Baltimore) Research Article OBJECTIVE: The results of published studies which examined the association between variable number tandem repeat (VNTR) polymorphism of interleukin-1 receptor antagonist (IL-1RN) and ischemic stroke (IS) are conflicting. Thus, we performed a meta-analysis to examine the potential association between IL-1RN VNTR polymorphism and IS risk. METHODS: A systematic literature search of PubMed, Embase, Medline, Web of Science, Cochrane Library, Chinese Biomedical Literature Database, Chinese National Knowledge Infrastructure, CQVIP, and WANFANG Database identified 10 studies with 2331 cases and 3335 controls. The pooled odds ratio (OR) with 95% confidence interval (95% CI) was calculated to evaluate the strength of the association. Subgroup analysis and meta-regression analysis were used to investigate the potential sources of heterogeneity. Begg funnel plots were used to explore the publication bias. RESULTS: In this study, no enough proof was found to prove the association between IL-1RN 86-bp VNTR polymorphism and IS risk with random-effects model in the homozygous model (1/1 vs 2/2, OR = 0.97, 95% CI = 0.50–1.87, P(heterogeneity) = .00), the heterozygous model (1/2 vs 2/2, OR = 0.64, 95% CI = 0.41–1.01, P(heterogeneity) = .10), the dominant model (1/1 + 1/2 vs 2/2, OR = 0.85, 95% CI = 0.51–1.42, P(heterogeneity) = .02), the recessive model (1/1 vs 1/2 + 2/2, OR = 0.69, 95% CI = 0.46–1.03, P(heterogeneity) = .00), and allelic model (1 vs 2, OR = 1.24, 95% CI = 0.89–1.74, P(heterogeneity) = .00). A marginally significant negative association was observed between IL-1RN 86-bp VNTR polymorphism and IS risk in the heterozygous model in the fixed-effects model (1/2 vs 2/2, OR = 0.71, 95% CI = 0.53–0.95, P(heterogeneity) = .10). In subgroup analyses, similar association was found in the group whose control size was lower than 300. CONCLUSION: In conclusion, our results suggested that there was no sufficient evidence to support the association between IL-1RN 86-bp VNTR polymorphism and IS. Further large epidemiologic studies need to be done to confirm these findings. Wolters Kluwer Health 2018-08-03 /pmc/articles/PMC6081086/ /pubmed/30075593 http://dx.doi.org/10.1097/MD.0000000000011750 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), 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 | Research Article Yang, Yujiao Wu, Wenhui Wang, Long Ding, Yi Lack of association between interleukin-1 receptor antagonist gene 86-bp VNTR polymorphism and ischemic stroke: A meta-analysis |
title | Lack of association between interleukin-1 receptor antagonist gene 86-bp VNTR polymorphism and ischemic stroke: A meta-analysis |
title_full | Lack of association between interleukin-1 receptor antagonist gene 86-bp VNTR polymorphism and ischemic stroke: A meta-analysis |
title_fullStr | Lack of association between interleukin-1 receptor antagonist gene 86-bp VNTR polymorphism and ischemic stroke: A meta-analysis |
title_full_unstemmed | Lack of association between interleukin-1 receptor antagonist gene 86-bp VNTR polymorphism and ischemic stroke: A meta-analysis |
title_short | Lack of association between interleukin-1 receptor antagonist gene 86-bp VNTR polymorphism and ischemic stroke: A meta-analysis |
title_sort | lack of association between interleukin-1 receptor antagonist gene 86-bp vntr polymorphism and ischemic stroke: a meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081086/ https://www.ncbi.nlm.nih.gov/pubmed/30075593 http://dx.doi.org/10.1097/MD.0000000000011750 |
work_keys_str_mv | AT yangyujiao lackofassociationbetweeninterleukin1receptorantagonistgene86bpvntrpolymorphismandischemicstrokeametaanalysis AT wuwenhui lackofassociationbetweeninterleukin1receptorantagonistgene86bpvntrpolymorphismandischemicstrokeametaanalysis AT wanglong lackofassociationbetweeninterleukin1receptorantagonistgene86bpvntrpolymorphismandischemicstrokeametaanalysis AT dingyi lackofassociationbetweeninterleukin1receptorantagonistgene86bpvntrpolymorphismandischemicstrokeametaanalysis |