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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...

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Autores principales: Lu, Jun-Ti, Deng, Ai-Ping, Song, Juan, Zhang, Li, Luo, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
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.
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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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