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妊娠高血压疾病中血管紧张素转换酶基因缺失多态性的研究

[Study on a deletion polymorphism of the angiotensin converting enzyme gene in pregnancy induced hypertension].

作者信息

Zhu M, Xia Y, Cheng W

机构信息

Hospital of Obstetrics & Gynecology, Shanghai Medical University.

出版信息

Zhonghua Fu Chan Ke Za Zhi. 1998 Feb;33(2):83-5.

Abstract

OBJECTIVE

To study a polymorphism and allele frequency of the angiotensin converting enzyme (ACE) gene in pregnancy induced hypertension (PIH).

METHODS

Polymerase chain reaction (PCR) for detection of ACE gene polymorphism was performed to show the deletion/insertion (D/I) polymorphism in intron 16 of ACE gene. A 490 bp(I) and 190 bp(D) PCR products were identified, corresponding to the PCR amplification of the the allele with or without the insertion.

RESULTS

Derived allele frequencies for insertion and deletion were the different between 35 PIH and 25 control subjects. Compared the frequency of D allele gene (0.76) and the percentage of the ACE DD genotype (65.7%) in the PIH patients with the frequency (0.28) and the percentage (8.0%) in the control population, they were significant higher in individuals with PIH (P < 0.001).

CONCLUSIONS

There was an excess of DD genotype and the frequency of D allele gene in PIH, confirming the genetic variation in the ACE locus could be involved in the risk of PIH and suggesting the ACE gene may contribute to the pathogenesis of PIH.

摘要

目的

研究血管紧张素转换酶(ACE)基因在妊娠高血压综合征(PIH)中的多态性及等位基因频率。

方法

采用聚合酶链反应(PCR)检测ACE基因多态性,以显示ACE基因第16内含子中的缺失/插入(D/I)多态性。鉴定出490 bp(I)和190 bp(D)的PCR产物,分别对应于插入或未插入等位基因的PCR扩增。

结果

35例PIH患者和25例对照者之间插入和缺失的衍生等位基因频率不同。PIH患者中D等位基因频率(0.76)和ACE DD基因型百分比(65.7%)与对照人群中的频率(0.28)和百分比(8.0%)相比,PIH患者显著更高(P < 0.001)。

结论

PIH中DD基因型和D等位基因频率过高,证实ACE基因座的遗传变异可能与PIH风险有关,并提示ACE基因可能参与PIH的发病机制。

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