Dastgheib Seyed Alireza, Asadian Fatemeh, Farbod Meraj, Karimi-Zarchi Mojgan, Meibodi Bahare, Akbarian Elahe, Neamatzadeh Hossein
Department of Medical Genetics, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Department of Medical Laboratory Sciences, School of Paramedical Science, Shiraz University of Medical Sciences, Shiraz, Iran.
Nucleosides Nucleotides Nucleic Acids. 2021;40(1):117-135. doi: 10.1080/15257770.2020.1826515. Epub 2020 Oct 7.
The objective of this meta-analysis was to estimate the association of and AT1R 1166 A > C polymorphisms with breast cancer (BC) risk. A comprehensive search on databases was conducted to identify all eligible case-control studies. Finally, 35 case-control studies, including 20 studies for , seven studies for , and eight studies for were included. The pooled analysis showed a significant association between polymorphism and BC risk under three genetic models, i.e., heterozygote (ID vs. DD: OR = 0.707, 95% CI 0.528-0.946, p = 0.020), homozygote (II vs. DD: OR = 0.662, 95% CI 0.462-0.947, p = 0.024), and dominant (II + ID vs. DD: OR = 0.691, 95% CI 0.507-0.941, p = 0.019). A significant association was also observed in polymorphism with BC risk among Asians and Caucasians. However, and polymorphisms were not associated with BC. Stratified analyses by ethnicity showed a significant association of and polymorphisms with BC risk in Latinos populations, but not in Asians. This meta-analysis inconsistence with all previous meta-analyses suggests that the might be associated with BC in overall and by ethnicity. However, the and were associated with BC risk only among Latinos populations.
本荟萃分析的目的是评估[基因名称]和AT1R 1166 A > C多态性与乳腺癌(BC)风险之间的关联。我们对多个数据库进行了全面检索,以确定所有符合条件的病例对照研究。最终,纳入了35项病例对照研究,其中包括20项关于[基因名称]的研究、7项关于[另一基因名称]的研究和8项关于[又一基因名称]的研究。汇总分析显示,在三种遗传模型下,[基因名称]多态性与BC风险之间存在显著关联,即杂合子(ID与DD:OR = 0.707,95%CI 0.528 - 0.946,p = 0.020)、纯合子(II与DD:OR = 0.662,95%CI 0.462 - 0.947,p = 0.024)和显性模型(II + ID与DD:OR = 0.691,95%CI 0.507 - 0.941,p = 0.019)。在亚洲人和高加索人中,[另一基因名称]多态性与BC风险之间也观察到显著关联。然而,[又一基因名称]和[再一基因名称]多态性与BC无关。按种族进行的分层分析显示,[基因名称]和[另一基因名称]多态性与拉丁裔人群的BC风险显著相关,但在亚洲人群中并非如此。本荟萃分析与之前所有荟萃分析结果不一致,表明[基因名称]可能在总体上以及按种族与BC相关。然而,[又一基因名称]和[再一基因名称]仅在拉丁裔人群中与BC风险相关。