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CAG repeat polymorphisms in the androgen receptor and breast cancer risk in women: a meta-analysis of 17 studies

机译:女性雄激素受体中CAG重复多态性与乳腺癌风险:一项17项研究的荟萃分析

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摘要

The association between polymorphic CAG repeats in the androgen receptor gene in women and breast cancer susceptibility has been studied extensively. However, the conclusions regarding this relationship remain conflicting. The purpose of this meta-analysis was to identify whether androgen receptor CAG repeat lengths were related to breast cancer susceptibility. The MEDLINE, PubMed, and EMBASE databases were searched through to December 2014 to identify eligible studies. Data and study quality were rigorously assessed by two investigators according to the Newcastle-Ottawa Quality Assessment Scale. The publication bias was assessed by the Begg’s test. Seventeen eligible studies were included in this meta-analysis. The overall analysis suggested no association between CAG polymorphisms and breast cancer risk (odds ratio [OR] 1.031, 95% confidence interval [CI] 0.855–1.245). However, in the subgroup analysis, we observed that long CAG repeats significantly increased the risk of breast cancer in the Caucasian population (OR 1.447, 95% CI 1.089–1.992). Additionally, the risk was significantly increased in Caucasian women carrying two alleles with CAG repeats ≥22 units compared with those with two shorter alleles (OR 1.315, 95% CI 1.014–1.707). These findings suggest that long CAG repeats increase the risk of breast cancer in Caucasian women. However, larger scale case-control studies are needed to validate our results.
机译:妇女中雄激素受体基因中的多态性CAG重复与乳腺癌易感性之间的关联已得到广泛研究。但是,关于这种关系的结论仍然存在矛盾。这项荟萃分析的目的是确定雄激素受体CAG重复长度是否与乳腺癌易感性有关。搜索MEDLINE,PubMed和EMBASE数据库直至2014年12月,以鉴定合格的研究。两名研究人员根据纽卡斯尔-渥太华质量评估量表对数据和研究质量进行了严格评估。通过Begg的测试评估了发布偏见。该荟萃分析包括十七项符合条件的研究。总体分析表明,CAG多态性与乳腺癌风险之间没有关联(优势比[OR] 1.031,95%置信区间[CI] 0.855–1.245)。然而,在亚组分析中,我们观察到,长时间重复CAG会显着增加白种人人群患乳腺癌的风险(OR 1.447,95%CI 1.089-1.992)。此外,与携带两个等位基因较短的等位基因相比,携带两个CAG重复≥22个等位基因的白人妇女的风险显着增加(OR 1.315,95%CI 1.014-1.707)。这些发现表明,长时间重复CAG会增加白人女性患乳腺癌的风险。但是,需要更大规模的病例对照研究来验证我们的结果。

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