Zhong W G, Wang Y, Zhu H, Zhao X
Shanghai Putuo Maternity and Infant Health Hospital, Shanghai, China.
Genet Mol Res. 2012 Aug 13;11(3):2268-76. doi: 10.4238/2012.May.21.1.
Preeclampsia affects 3-8% of pregnancies and is a major cause of maternal and perinatal morbidity and mortality worldwide. Inappropriate activation of the renin-angiotensin system may play a role in the development of preeclampsia. An insertion/deletion polymorphism in the angiotensin-converting enzyme gene (ACE-I/D) has been associated with differences in ACE activity. However, there are controversies in reports on the association of ACE-I/D with preeclampsia. Data were analyzed using Review Manager Version 5.0 and a random effects model was applied irrespective of between studies heterogeneity, which was evaluated via sensitivity and subgroup analyses. Publication bias was evaluated using the fail-safe number. A systematic search was performed based on published case control studies up to October 1, 2011, and 11 studies were included, involving 800 patients and 949 controls. Significant association of the ACE D allele with increase risk of preeclampsia was found (odds ratio = 1.93, 95% confidence interval = 1.19-3.12; P = 0.008). Sensitivity analysis showed that no individual study had an undue influence on the summary odds ratios for all contrasts. An analysis stratified by study size showed an attenuated odds ratio towards a null effect as study size increased. Based on our meta-analysis, we suggest that the D allele of the ACE gene is related with increased risk for preeclampsia in the Chinese population. Considering the potential existence of small study bias, further research should be performed with a larger dataset.
子痫前期影响3%-8%的妊娠,是全球孕产妇和围产儿发病及死亡的主要原因。肾素-血管紧张素系统的不适当激活可能在子痫前期的发生中起作用。血管紧张素转换酶基因插入/缺失多态性(ACE-I/D)与ACE活性差异有关。然而,关于ACE-I/D与子痫前期关联的报道存在争议。使用Review Manager 5.0软件进行数据分析,无论研究间的异质性如何,均采用随机效应模型,并通过敏感性分析和亚组分析进行评估。使用失效安全数评估发表偏倚。基于截至2011年10月1日发表的病例对照研究进行系统检索,纳入11项研究,涉及800例患者和949例对照。发现ACE D等位基因与子痫前期风险增加显著相关(优势比=1.93,95%置信区间=1.19-3.12;P=0.008)。敏感性分析表明,没有任何一项单独研究对所有对比的汇总优势比有过度影响。按研究规模分层分析显示,随着研究规模的增加,优势比趋向于无效而减弱。基于我们的荟萃分析,我们认为ACE基因的D等位基因与中国人群子痫前期风险增加有关。考虑到可能存在小研究偏倚,应使用更大的数据集进行进一步研究。