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血管紧张素原基因M235T多态性与子痫前期/子痫的发生:观察性研究的荟萃分析和荟萃回归

The angiotensinogen gene M235T polymorphism and development of preeclampsia/eclampsia: a meta-analysis and meta-regression of observational studies.

作者信息

Zafarmand Mohammad Hadi, Nijdam Marie-Elise, Franx Arie, Grobbee Diederick E, Bots Michiel L

机构信息

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

J Hypertens. 2008 Sep;26(9):1726-34. doi: 10.1097/HJH.0b013e3283009ca5.

Abstract

OBJECTIVE

The angiotensinogen gene M235T polymorphism is related to an increased risk of hypertension. Hypertension and pregnancy-induced hypertension have been suggested to share common etiologic factors. We examined whether this mutation also increases the risk of preeclampsia/eclampsia.

METHODS

Pubmed/Medline, Web of Science and EMBASE were searched and a hand search of bibliographies was conducted. In all, 17 studies (including 1446 cases and 3829 controls) published in English between 1993 and October 2006 on the association of angiotensinogen gene M235T polymorphism with preeclampsia/eclampsia were selected.

RESULTS

The overall odds ratio (OR) under a random effects model revealed that individuals homozygous for the T allele were 1.62 times more likely to develop preeclampsia/eclampsia [95% confidence interval (CI), 1.12 to 2.33; P = 0.01) compared to individuals homozygous for the M allele. The relation in Caucasians (OR = 1.99; 95% CI, 1.18-3.36; P = 0.01) was similar to that in East Asian populations (OR = 1.74; 95% CI, 0.92-3.28; P = 0.09), although the latter was not statistically significant due to lower numbers of studies. Under additive, recessive and dominant genetic models positive associations were also found. A meta-regression analysis showed that ethnic background was a significant source of between-study heterogeneity (P = 0.04) but design of the study, study size and Hardy-Weinberg equilibrium deviation were not. There was a low probability of publication bias.

CONCLUSION

Our meta-analysis expands the findings on hypertension by showing that the presence of the T allele of the angiotensinogen gene is associated with an increased risk to develop preeclampsia/eclampsia.

摘要

目的

血管紧张素原基因M235T多态性与高血压风险增加相关。高血压和妊娠高血压被认为有共同的病因。我们研究了这种突变是否也会增加子痫前期/子痫的风险。

方法

检索了PubMed/Medline、科学网和EMBASE,并对手头文献进行了检索。共选择了1993年至2006年10月间以英文发表的17项研究(包括1446例病例和3829例对照),这些研究探讨了血管紧张素原基因M235T多态性与子痫前期/子痫的关联。

结果

随机效应模型下的总体比值比(OR)显示,与M等位基因纯合子个体相比,T等位基因纯合子个体发生子痫前期/子痫的可能性高1.62倍[95%置信区间(CI),1.12至2.33;P = 0.01]。白种人(OR = 1.99;95%CI,1.18 - 3.36;P = 0.01)中的关系与东亚人群(OR = 1.74;95%CI,0.92 - 3.28;P = 0.09)相似,尽管由于研究数量较少,后者无统计学意义。在加性、隐性和显性遗传模型下也发现了正相关。荟萃回归分析表明,种族背景是研究间异质性的一个重要来源(P = 0.04),但研究设计、研究规模和哈迪 - 温伯格平衡偏差不是。发表偏倚的可能性较低。

结论

我们的荟萃分析扩展了关于高血压的研究结果,表明血管紧张素原基因T等位基因的存在与子痫前期/子痫发病风险增加相关。

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