首页> 外文期刊>Journal of human hypertension >The C242T-polymorphism of the NADPH/NADH oxidase gene p22phox subunit is not associated with pre-eclampsia.
【24h】

The C242T-polymorphism of the NADPH/NADH oxidase gene p22phox subunit is not associated with pre-eclampsia.

机译:NADPH / NADH氧化酶基因p22phox亚基的C242T多态性与先兆子痫无关。

获取原文
获取原文并翻译 | 示例
           

摘要

Pre-eclampsia is a pregnancy-related multisystem disorder characterised by elevation of blood pressure and proteinuria, in which oxidative stress may play an important role. Blood pressure is partly controlled by O(-)(2) production by NADPH/NADH oxidase and recently it was shown that a C242T substitution in the p22phox gene was associated with coronary artery disease, in which elevated blood pressure and oxidative stress are also important pathophysiologic features. Therefore we studied the prevalence of the C242T polymorphism in the NADPH/NADH oxidase gene in women with pre-eclampsia and/or haemolysis, elevated liver enzymes and low platelets (HELLP) syndrome as compared with women with a normotensive pregnancy. DNA from control women (n = 78), women with pre-eclampsia (n = 40), HELLP syndrome (n = 9) or women with HELLP complicated by pregnancy-induced hypertension or pre-eclampsia (n = 46) were tested for the presence of the C242T polymorphism by polymerase chain reaction followed by restriction fragment-length polymorphism. The prevalence of the homozygous CC-genotype was similar in the patient groups compared with controls. The allele frequency of the T-allele was 31% in both control and patient groups. In conclusion the C242T polymorphism in the p22phox subunit of the NADPH/NADH oxidase gene is not associated with pre-eclampsia. Therefore, oxidative stress generated by NADPH/NADH oxidase probably does not play a role in the development of pre-eclampsia.
机译:子痫前期是一种与妊娠有关的多系统疾病,其特征在于血压升高和蛋白尿,其中氧化应激可能起重要作用。血压部分受NADPH / NADH氧化酶产生O(-)(2)的控制,最近显示p22phox基因中的C242T替代与冠状动脉疾病有关,其中血压升高和氧化应激也很重要病理生理特征。因此,我们研究了先兆子痫和/或溶血,肝酶升高和低血小板(HELLP)综合征妇女与正常血压妊娠妇女相比,其NADPH / NADH氧化酶基因中C242T多态性的患病率。检测来自对照妇女(n = 78),先兆子痫(n = 40),HELLP综合征(n = 9)或HELLP并发妊娠高血压或先兆子痫(n = 46)妇女的DNA。 C242T多态性的存在是通过聚合酶链反应,然后是限制性片段长度多态性。与对照组相比,患者组中纯合CC基因型的患病率相似。在对照组和患者组中,T-等位基因的等位基因频率均为31%。总之,NADPH / NADH氧化酶基因p22phox亚基的C242T多态性与先兆子痫无关。因此,NADPH / NADH氧化酶产生的氧化应激可能在先兆子痫的发展中不起作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号