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Reappraisal of XRCC1 Arg194Trp polymorphism and glioma risk: a cumulative meta-analysis
The association between XRCC1 Arg194Trp polymorphism and glioma risk were inconsistent from published meta-analyses and epidemiological studies. Hence, we performed this updated and cumulative meta-analysis to reappraisal this relationship. PubMed, Embase, CBM (Chinese Biomedical Database), and CNKI...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5400609/ https://www.ncbi.nlm.nih.gov/pubmed/28423490 http://dx.doi.org/10.18632/oncotarget.15376 |
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author | Lu, Jun-Ti Deng, Ai-Ping Song, Juan Zhang, Li Luo, Jie |
author_facet | Lu, Jun-Ti Deng, Ai-Ping Song, Juan Zhang, Li Luo, Jie |
author_sort | Lu, Jun-Ti |
collection | PubMed |
description | The association between XRCC1 Arg194Trp polymorphism and glioma risk were inconsistent from published meta-analyses and epidemiological studies. Hence, we performed this updated and cumulative meta-analysis to reappraisal this relationship. PubMed, Embase, CBM (Chinese Biomedical Database), and CNKI (China National Knowledge Internet) databases were comprehensively searched up to August 13, 2016 (updated on December 22, 2016). After study selection and data extraction from eligible studies, the association was evaluated by odds ratios (ORs) and its 95% confidence intervals (95%CIs) using Comprehensive Meta-Analysis software. Finally 16 case-control studies involving 7011 patients and 9519 healthy controls were yielded. The results indicated that XRCC1 Arg194Trp polymorphism was significantly correlated with the increased risk of glioma [Trp vs. Arg: OR = 1.18(1.05-1.34); TrpTrp vs. ArgArg: OR = 1.66(1.31-2.12); ArgTrp vs. ArgArg: OR = 1.34(1.02-1.77); TrpTrp vs. ArgArg+ArgTrp: OR = 1.47(1.26-1.72); TrpTrp+ArgTrp vs. ArgArg: OR = 1.17(1.01-1.35)]. Cumulative analysis showed the results changed from non-significant to significant when new studies accumulated, and sensitivity analysis indicated the results were stable. Subgroup analysis showed the significant association existed in Asians but not in Caucasians. Current evidence indicated that XRCC1 Arg194Trp polymorphism was associated with increased risk for glioma, especially in Asians; however, relevant studies involving other ethnic groups are required to validate our findings in further. |
format | Online Article Text |
id | pubmed-5400609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-54006092017-05-03 Reappraisal of XRCC1 Arg194Trp polymorphism and glioma risk: a cumulative meta-analysis Lu, Jun-Ti Deng, Ai-Ping Song, Juan Zhang, Li Luo, Jie Oncotarget Research Paper The association between XRCC1 Arg194Trp polymorphism and glioma risk were inconsistent from published meta-analyses and epidemiological studies. Hence, we performed this updated and cumulative meta-analysis to reappraisal this relationship. PubMed, Embase, CBM (Chinese Biomedical Database), and CNKI (China National Knowledge Internet) databases were comprehensively searched up to August 13, 2016 (updated on December 22, 2016). After study selection and data extraction from eligible studies, the association was evaluated by odds ratios (ORs) and its 95% confidence intervals (95%CIs) using Comprehensive Meta-Analysis software. Finally 16 case-control studies involving 7011 patients and 9519 healthy controls were yielded. The results indicated that XRCC1 Arg194Trp polymorphism was significantly correlated with the increased risk of glioma [Trp vs. Arg: OR = 1.18(1.05-1.34); TrpTrp vs. ArgArg: OR = 1.66(1.31-2.12); ArgTrp vs. ArgArg: OR = 1.34(1.02-1.77); TrpTrp vs. ArgArg+ArgTrp: OR = 1.47(1.26-1.72); TrpTrp+ArgTrp vs. ArgArg: OR = 1.17(1.01-1.35)]. Cumulative analysis showed the results changed from non-significant to significant when new studies accumulated, and sensitivity analysis indicated the results were stable. Subgroup analysis showed the significant association existed in Asians but not in Caucasians. Current evidence indicated that XRCC1 Arg194Trp polymorphism was associated with increased risk for glioma, especially in Asians; however, relevant studies involving other ethnic groups are required to validate our findings in further. Impact Journals LLC 2017-02-16 /pmc/articles/PMC5400609/ /pubmed/28423490 http://dx.doi.org/10.18632/oncotarget.15376 Text en Copyright: © 2017 Lu et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Lu, Jun-Ti Deng, Ai-Ping Song, Juan Zhang, Li Luo, Jie Reappraisal of XRCC1 Arg194Trp polymorphism and glioma risk: a cumulative meta-analysis |
title | Reappraisal of XRCC1 Arg194Trp polymorphism and glioma risk: a cumulative meta-analysis |
title_full | Reappraisal of XRCC1 Arg194Trp polymorphism and glioma risk: a cumulative meta-analysis |
title_fullStr | Reappraisal of XRCC1 Arg194Trp polymorphism and glioma risk: a cumulative meta-analysis |
title_full_unstemmed | Reappraisal of XRCC1 Arg194Trp polymorphism and glioma risk: a cumulative meta-analysis |
title_short | Reappraisal of XRCC1 Arg194Trp polymorphism and glioma risk: a cumulative meta-analysis |
title_sort | reappraisal of xrcc1 arg194trp polymorphism and glioma risk: a cumulative meta-analysis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5400609/ https://www.ncbi.nlm.nih.gov/pubmed/28423490 http://dx.doi.org/10.18632/oncotarget.15376 |
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