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土耳其人群中血管紧张素转换酶和谷胱甘肽S-转移酶基因多态性与先兆子痫风险

Polymorphisms in angiotensin-converting enzyme and glutathione s-transferase genes in Turkish population and risk for preeclampsia.

作者信息

Atalay M A, Ozerkan K, Karkucak M, Yakut T, Atik Y, Develioglu O H

机构信息

Department of Obstetrics and Gynecology, Uludag University, Bursa, Turkey.

出版信息

Clin Exp Obstet Gynecol. 2012;39(4):466-9.

Abstract

AIMS

This study was conducted to investigate whether insertion/deletion (I/D) polymorphism of angiotensin-converting enzyme (ACE) gene and polymorphisms in glutathione S-transferase (GST) M1 and T1 genes are associated with increased risk for preeclampsia.

MATERIALS AND METHODS

Sixty-three patients with hypertensive disorder of pregnancy and 85 controls were evaluated in a prospective case-control study. All subjects were genotyped by polymerase chain reaction (PCR) followed by agarose gel electrophoresis.

RESULTS

Allele frequencies of ACE gene I/D polymorphism were found significantly different between preeclampsia and the control groups (p = 0.001). Differences in genotype frequencies of ACE gene I/D polymorphism between the two groups were statistically significant (p = 0.004). Individuals homozygous for D allele were more likely to develop preeclampsia (OR = 2.29; 95% CI, 1.39-3.79), whereas heterozygous individuals were not at increased risk (OR = 0.92; 95% CI, 0.56-1.49), compared to individuals homozygous for I allele. The differences in frequencies of functional and null alleles of GSTM1 and GSTT1 genes between the two groups were not significant (p = 0.46 and p = 0.44, respectively).

CONCLUSION

ACE gene DD genotype was found to be associated with increased risk of preeclampsia development, whereas the authors did not find any significant relationship with polymorphisms of the GSTM1 and GSTT1 genes and preeclampsia.

摘要

目的

本研究旨在调查血管紧张素转换酶(ACE)基因的插入/缺失(I/D)多态性以及谷胱甘肽S-转移酶(GST)M1和T1基因的多态性是否与子痫前期风险增加相关。

材料与方法

在一项前瞻性病例对照研究中评估了63例妊娠高血压疾病患者和85例对照。所有受试者均通过聚合酶链反应(PCR)进行基因分型,随后进行琼脂糖凝胶电泳。

结果

子痫前期组和对照组之间ACE基因I/D多态性的等位基因频率存在显著差异(p = 0.001)。两组之间ACE基因I/D多态性的基因型频率差异具有统计学意义(p = 0.004)。与I等位基因纯合个体相比,D等位基因纯合个体患子痫前期的可能性更高(OR = 2.29;95% CI,1.39 - 3.79),而异合子个体风险未增加(OR = 0.92;95% CI,0.56 - 1.49)。两组之间GSTM1和GSTT1基因的功能等位基因和无效等位基因频率差异不显著(分别为p = 0.46和p = 0.44)。

结论

发现ACE基因DD基因型与子痫前期发生风险增加相关,而作者未发现GSTM1和GSTT1基因多态性与子痫前期之间存在任何显著关系。

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