Moghimi Mansour, Kargar Saeed, Jafari Mohammad Ali, Ahrar Hossein, Jarahzadeh Mohammad Hossein, Neamatzadeh Hossein, Sadeghizadeh- Yazdi Jalal
Department of Pathology, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. Email:
Asian Pac J Cancer Prev. 2018 Nov 29;19(11):3225-3231. doi: 10.31557/APJCP.2018.19.11.3225.
Background: A number of case-control studies were conducted to investigate the association of angiotensin converting enzyme insertion/deletion (ACE I/D) polymorphism with breast cancer. But the results remain controversial. This meta-analysis aims to comprehensively evaluate the association of ACE I/D polymorphism with breast cancer. Method: A comprehensive literature search on PubMed, Google Scholar, SCOPUS and ISI Web of Knowledge databases for studies published up to June 01, 2018 was performed. Summary odds ratios (ORs) and 95% confidence intervals (CI) were estimated. Publication bias of literatures was evaluated using funnel plots and Egger’s test. Results: A total of 20 studies including 2846 breast cancer cases 9,299 controls meeting the predefined criteria were involved in the meta-analysis. Overall, the ACE I/D polymorphisms was significantly associated with breast cancer under the allele model (I vs. D: OR= 0.803, 95% CI 0.647-0.996, p=0.046), the homozygote model (II vs. DD: OR= 0.662, 95% CI 0.462-0.947, p=0.024), the heterozygote model (ID vs. DD: OR= 0.707, 95% CI 0.528-0.946, p=0.020), the dominant model (II+ID vs. DD: OR= 0.691, 95% CI 0.507-0.941, p=0.019). In the subgroup analysis by ethnicity, a significant association was found among Asian and Caucasian populations, but not among mixed populations. Conclusions: This meta-analysis suggests that ACE I/D polymorphism may be associated with increased risk of breast cancer, especially among Asian and Caucasians. However, well-designed studies with larger sample size and more ethnic groups are needed to further validate the results.
开展了多项病例对照研究以调查血管紧张素转换酶插入/缺失(ACE I/D)多态性与乳腺癌之间的关联。但结果仍存在争议。本荟萃分析旨在全面评估ACE I/D多态性与乳腺癌之间的关联。方法:对PubMed、谷歌学术、SCOPUS和ISI Web of Knowledge数据库进行全面文献检索,以查找截至2018年6月1日发表的研究。估计汇总比值比(OR)和95%置信区间(CI)。使用漏斗图和Egger检验评估文献的发表偏倚。结果:共有20项研究纳入荟萃分析,包括2846例乳腺癌病例和9299例符合预定标准的对照。总体而言,在等位基因模型(I vs. D:OR = 0.803,95% CI 0.647 - 0.996,p = 0.046)、纯合子模型(II vs. DD:OR = 0.662,95% CI 0.462 - 0.947,p = 0.024)、杂合子模型(ID vs. DD:OR = 0.707,95% CI 0.528 - 0.946,p = 0.020)、显性模型(II + ID vs. DD:OR = 0.691,95% CI 0.507 - 0.941,p = 0.019)下,ACE I/D多态性与乳腺癌显著相关。在按种族进行的亚组分析中,亚洲人和高加索人群中发现了显著关联,但在混合人群中未发现。结论:本荟萃分析表明,ACE I/D多态性可能与乳腺癌风险增加有关,尤其是在亚洲人和高加索人中。然而,需要设计更完善、样本量更大且涉及更多种族群体的研究来进一步验证结果。