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首页> 外文期刊>Breast Cancer Research and Treatment >Association between polymorphisms of the ataxia telangiectasia mutated gene and breast cancer risk: evidence from the current studies
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Association between polymorphisms of the ataxia telangiectasia mutated gene and breast cancer risk: evidence from the current studies

机译:共济失调毛细血管扩张突变基因多态性与乳腺癌风险之间的关联:来自当前研究的证据

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Epidemiological studies have evaluated the association between ataxia telangiectasia mutated (ATM) gene polymorphisms and breast cancer risk. However, published data are still inconclusive. We performed a meta-analysis for the first time, based on currently available evidence, by searching PubMed, ISI Web of Knowledge, and Embase databases to derive a more precise assessment of the relationship. Following the inclusion and exclusion criteria, nine publications were included in this meta-analysis. Of these studies, one had a deviation from the Hardy–Weinberg equilibrium (HWE) at a statistical significance level of 0.01 in controls, and another two had no available data for HWE. We observed that the ATM 5557G>A polymorphism was significantly correlated with breast cancer risk when all studies were pooled into the meta-analysis (recessive model: odds ratio, OR = 0.67; 95% confidence interval (CI) 0.51–0.89). For the ATM IVS38-8T>C polymorphism, no significant association was found in the allele contrast, heterozygote codominant, and dominant models. There were no available data to perform this meta-analysis in the homozygote codominant and recessive models. For the ATM IVS1+19A>T polymorphism, a significant association with breast cancer risk was found in the allele contrast model (C vs. T: OR = 1.60; 95% CI 1.02–2.52). For the IVS34+60G>A polymorphism, no significant association was found in the allele contrast, codominant, dominant, and recessive models. Egger’s test did not suggest any evidence of publication bias (P = 0.47 for the recessive model). In conclusion, there is limited evidence to indicate that ATM polymorphisms are associated with increased risk of breast cancer.
机译:流行病学研究评估了共济失调毛细血管扩张突变(ATM)基因多态性与乳腺癌风险之间的关系。但是,发布的数据仍不确定。我们通过搜索PubMed,ISI Web of Knowledge和Embase数据库,基于当前可用的证据,首次进行了荟萃分析,以得出对该关系的更精确评估。根据纳入和排除标准,该荟萃分析纳入了九份出版物。在这些研究中,一项在对照组中的统计显着性水平为0.01,与Hardy-Weinberg平衡(HWE)偏离,另外两项没有HWE的可用数据。我们观察到,当将所有研究汇总到荟萃分析中时,ATM 5557G> A多态性与乳腺癌风险显着相关(隐性模型:优势比,OR = 0.67; 95%置信区间(CI)0.51-0.89)。对于ATM IVS38-8T> C多态性,在等位基因对比,杂合子显性和显性模型中未发现显着关联。没有可用数据在纯合子显性和隐性模型中进行这种荟萃分析。对于ATM IVS1 + 19A> T多态性,在等位基因对比模型中发现与乳腺癌风险显着相关(C vs. T:OR = 1.60; 95%CI 1.02-2.52)。对于IVS34 + 60G> A多态性,在等位基因对比,共显性,显性和隐性模型中未发现显着关联。 Egger的检验没有发现任何发表偏倚的证据(对于隐性模型,P = 0.47)。总之,仅有有限的证据表明ATM多态性与乳腺癌风险增加有关。

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