Iqbal Mehir Un Nisa, Khan Taseer Ahmed
Department of Physiology, University of Karachi, Karachi, Pakistan.
Tumour Biol. 2017 Oct;39(10):1010428317731280. doi: 10.1177/1010428317731280.
The purpose of this systemic review and meta-analysis was to examine the relationship between VDR gene polymorphisms and breast cancer. Literature was searched through PubMed database, Google scholar, and the web of knowledge from December 2015 to January 2017 and consists of 34 studies (26,372 cases and 32,883 controls). All statistical measures were done using STATA version 11.2. The heterogeneity among studies was tested using I statistics. Mantel-Haenszel method and DerSimonian-Laird method were used to combine data from studies using both random-effect model and fixed-effect model, respectively. Potential publication bias was evaluated by Egger's test. Sensitivity analysis was also performed to evaluate the quality and consistency in results. The results of this meta-analysis revealed that VDR gene polymorphisms (Bsm1 bb vs BB; SOR = 1.18, 95% CI = 1.054-1.322, Apa1 aa vs AA; SOR = 1.18, 95% CI = 0.87-1.59, Poly (A) LL vs SS; SOR = 1.41, 95% CI = 1.06-1.88, Fok1 ff + Ff vs FF; SOR = 1.25, 95% CI = 0.896-1.759, Apa1 aa+Aa vs AA; SOR = 1.13, 95% CI = 0.95-1.35, Poly (A) LL + LS vs SS; SOR = 1.19, 95% CI = 1.00-1.43, Poly (A) L vs S; SOR = 1.18, 95% CI = 1.03-1.35) are associated with the breast cancer. Cdx2, Bgl1, and Taq1 do not show association with breast cancer. Thus, the finding of this meta-analysis concluded that VDR Bsm1, Apa1, Fok1, and Poly (A) gene polymorphisms may be susceptible for breast cancer development.
本系统评价和荟萃分析的目的是研究维生素D受体(VDR)基因多态性与乳腺癌之间的关系。通过PubMed数据库、谷歌学术以及2015年12月至2017年1月的Web of Knowledge进行文献检索,共纳入34项研究(26372例病例和32883例对照)。所有统计分析均使用STATA 11.2版本完成。采用I统计量检验研究间的异质性。分别使用Mantel-Haenszel法和DerSimonian-Laird法,采用随机效应模型和固定效应模型合并研究数据。通过Egger检验评估潜在的发表偏倚。还进行了敏感性分析以评估结果的质量和一致性。该荟萃分析的结果显示,VDR基因多态性(Bsm1 bb与BB相比;优势比[SOR]=1.18,95%置信区间[CI]=1.054 - 1.322;Apa1 aa与AA相比;SOR = 1.18,95% CI = 0.87 - 1.59;Poly (A) LL与SS相比;SOR = 1.41,95% CI = 1.06 - 1.88;Fok1 ff + Ff与FF相比;SOR = 1.25,95% CI = 0.896 - 1.759;Apa1 aa + Aa与AA相比;SOR = 1.13,95% CI = 0.95 - 1.35;Poly (A) LL + LS与SS相比;SOR = 1.19,95% CI = 1.00 - 1.43;Poly (A) L与S相比;SOR = 1.18,95% CI = 1.03 - 1.35)与乳腺癌相关。Cdx2、Bgl1和Taq1与乳腺癌无关联。因此,该荟萃分析的结果得出结论,VDR Bsm1、Apa1、Fok1和Poly (A)基因多态性可能易导致乳腺癌的发生。