首页> 外文期刊>Hypertension research: Official journal of the Japanese Society of Hypertension >Endothelial nitric oxide synthase, angiotensin-converting enzyme and angiotensinogen gene polymorphisms in hypertensive disorders of pregnancy.
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Endothelial nitric oxide synthase, angiotensin-converting enzyme and angiotensinogen gene polymorphisms in hypertensive disorders of pregnancy.

机译:妊娠高血压疾病中的内皮型一氧化氮合酶,血管紧张素转换酶和血管紧张素原基因多态性。

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We investigated the variations in genes encoding endothelial nitric oxide synthase (NOS3), angiotensin-converting enzyme (ACE) and angiotensinogen (AGT) in hypertensive disorders of pregnancy and the relationship between the polymorphisms and circulating nitric oxide (NO) and ACE levels in pregnant north Indian women. Frequencies of NOS3 G894T, 4b/a and T(-786) --> C, AGT T704C and ACE ins/del polymorphisms were studied in 342 subjects: 120 with preeclampsia (PE), 104 with gestational hypertension and 118 normotensive pregnant women. Variations were evaluated by polymerase chain reaction-restriction fragment length polymorphism. NO and ACE levels were determined using ELISA. There was no difference in the distribution of individual NOS3 and ACE polymorphisms in the study groups. Haplotype analysis showed a global difference in the NOS3 haplotype distribution between the PE and non-PE subjects (P=0.03). The presence of AGT 704C allele was associated with a reduced risk of developing PE (odds ratio: 0.33, 95% CI: 0.19-0.59 in recessive mode). Circulating total NO and ACE levels were similar in three groups. No relationship was found between circulating NO levels and any of the NOS3 polymorphisms, but the circulating ACE levels were higher in those with DD genotype (P<0.05). In conclusion, there was no association between individual NOS3 and the ACE gene polymorphisms and hypertensive disorders of pregnancy in north Indian women. The presence of minor alleles at all the three sites in NOS3 seemed to increase the risk of PE, and AGT 704C allele was associated with a reduced PE risk. The complexity of interaction between these genetic abnormalities requires further studies.
机译:我们调查了妊娠高血压疾病中编码内皮型一氧化氮合酶(NOS3),血管紧张素转换酶(ACE)和血管紧张素原(AGT)的基因的变异以及多态性与妊娠循环一氧化氮(NO)和ACE水平之间的关系北印度妇女。在342位受试者中研究了NOS3 G894T,4b / a和T(-786)-> C,AGT T704C和ACE ins / del多态性的频率:120名先兆子痫(PE),104名妊娠高血压和118名血压正常的孕妇。通过聚合酶链反应-限制性片段长度多态性评估变异。使用ELISA确定NO和ACE水平。在研究组中,个体NOS3和ACE多态性的分布没有差异。单倍型分析显示PE和非PE受试者之间NOS3单倍型分布的总体差异(P = 0.03)。 AGT 704C等位基因的存在与罹患PE的风险降低相关(隐性模式下的赔率:0.33,95%CI:0.19-0.59)。三组的循环总NO和ACE水平相似。没有发现循环NO水平与任何NOS3多态性之间的关系,但DD基因型的循环ACE水平较高(P <0.05)。总之,在印度北部妇女中,个体NOS3与ACE基因多态性和妊娠高血压疾病之间没有关联。在NOS3的所有三个位点均存在次要等位基因似乎增加了PE的风险,而AGT 704C等位基因与降低PE的风险有关。这些遗传异常之间相互作用的复杂性需要进一步研究。

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