Suppr超能文献

[中国重度子痫前期患者雌激素受体α基因的Pvu II和Xba I多态性]

[The Pvu II and Xba I polymorphisms in the estrogen receptor alpha gene in Chinese patients with severe preeclampsia].

作者信息

Zhang Juan, Bai Huai, Liu Xing-hui, Fan Ping, Liu Rui, He Guo-lin

机构信息

Unit of Laboratory Medicine, West China Second Hospital, Sichuan University, Chengdu, Sichuan, 610041 PR China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Feb;26(1):40-4. doi: 10.3760/cma.j.issn.1003-9406.2009.01.009.

Abstract

OBJECTIVE

To assess the allele and genotype frequencies of the estrogen receptor alpha ( ESR alpha) Pvu II and Xba I polymorphisms in patients with severe preeclampsia and compare them with those of normal pregnant women.

METHODS

Blood samples from 131 patients with severe preeclampsia and 223 normal pregnant women from Chinese Han in Chengdu area were analyzed, using PCR-RFLP method. Pregnant patients with blood pressure exceeding 140/90 mmHg (or 18.7/12 kPa) were recruited with a strict definition of preeclampsia. Genotyping was performed using PCR-RFLP for Pvu II and Xba I polymorphisms in the ESR alpha gene.

RESULTS

The T and C allele frequencies for Pvu II site were 0.580 and 0.420 in the patient group, and 0.576 and 0.424 in the controls, respectively. The A and G allele frequencies for Xba I site were 0.763 and 0.237 in the patient group, and 0.807 and 0.193 in control group, respectively. No significant difference in the allele frequencies of either site was observed between the two groups. However, the CC homozygotes or CT heterozygotes in the control pregnant women had higher systolic blood pressure levels than TT homozygotes for Pvu II site after the data was adjusted for age and BMI (114.00+/-21.44 mmHg or 114.33+/-1.21 mmHg vs. 108.62+/-1.91 mmHg, P<0.05). No genotype effect on the blood pressures was found for Pvu II site in the case group, nor for Xba I site in either group.

CONCLUSION

Our work has excluded the association of the ESRalpha Pvu II and Xb I polymorphism with severe preeclampsia in a Southwest Chinese population, although this polymorphism may be associated with the systolic blood pressure level in the normal pregnant women.

摘要

目的

评估重度子痫前期患者雌激素受体α(ESRα)Pvu II和Xba I基因多态性的等位基因及基因型频率,并与正常孕妇进行比较。

方法

采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,分析成都地区131例重度子痫前期患者和223例汉族正常孕妇的血样。严格按照子痫前期的定义招募血压超过140/90 mmHg(或18.7/12 kPa)的孕妇。采用PCR-RFLP对ESRα基因的Pvu II和Xba I多态性进行基因分型。

结果

Pvu II位点的T和C等位基因频率在患者组分别为0.580和0.420,在对照组分别为0.576和0.424。Xba I位点的A和G等位基因频率在患者组分别为0.763和0.237,在对照组分别为0.807和0.193。两组间任一多态性位点的等位基因频率均无显著差异。然而,在校正年龄和体重指数后,对照组孕妇中Pvu II位点的CC纯合子或CT杂合子的收缩压水平高于TT纯合子(114.00±21.44 mmHg或114.33±1.21 mmHg比108.62±1.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验