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复发性流产中血管生成与氧化应激相关基因变异

Angiogenesis and oxidative stress-related gene variants in recurrent pregnancy loss.

作者信息

Fortis Marcela Felix, Fraga Lucas Rosa, Boquett Juliano André, Kowalski Thayne Woycinck, Dutra Caroline Gross, Gonçalves Rozana Oliveira, Vianna Fernanda Sales Luiz, Schüler-Faccini Lavinia, Sanseverino Maria Teresa Vieira

机构信息

Postgraduate Program in Genetics and Molecular Biology, Federal University of Rio Grande do Sul (UFRGS), Porto Alegre, 91501-970, Brazil.

Obstetrics, Gynaecology and Human Reproduction Department, Federal University of Bahia, Salvador, 40110-100, Brazil.

出版信息

Reprod Fertil Dev. 2018 Mar;30(3):498-506. doi: 10.1071/RD17117.

Abstract

Recurrent pregnancy loss (RPL) affects ~3-5% of couples attempting to conceive and in around 50% of cases the aetiology remains unknown. Adequate vascularisation and placental circulation are indispensable for the development of a normal pregnancy. Prostaglandin-endoperoxide synthase 2 (PTGS2), vascular endothelial growth factor (VEGF) and the nitric oxide (NO) systems play important roles in reproductive physiology, participating in several steps including implantation and apoptosis of trophoblast cells. In this study we evaluated genetic polymorphisms in the inducible nitric oxide synthase (NOS2), PTGS2 and VEGFA genes as susceptibility factors for RPL. A case-control study was conducted in 149 women having two or more miscarriages and 208 controls. Allele and genotype distributions of the polymorphisms studied in the two groups were not statistically different. However, the dominant model showed that the presence of variant T (TT/GT) of rs2779249 (-1290G>T) of NOS2 was significantly associated with RPL (OR=1.58, CI 95%=1.03-2.44; P=0.037). The increased risk remained significant when adjusted for number of pregnancies, alcohol consumption and ethnicity (OR=1.92, CI95%=1.18-3.11; P=0.008). These results suggest that the variant genotypes of the functional polymorphism rs2779249 in the NOS2 promoter are a potential risk for RPL, possibly due to oxidative stress mechanisms.

摘要

复发性流产(RPL)影响约3%-5%试图受孕的夫妇,约50%的病例病因不明。充足的血管形成和胎盘循环对于正常妊娠的发展不可或缺。前列腺素内过氧化物合酶2(PTGS2)、血管内皮生长因子(VEGF)和一氧化氮(NO)系统在生殖生理学中发挥重要作用,参与包括滋养层细胞着床和凋亡在内的多个步骤。在本研究中,我们评估了诱导型一氧化氮合酶(NOS2)、PTGS2和VEGFA基因中的基因多态性作为RPL的易感因素。对149名有两次或更多次流产的女性和208名对照进行了病例对照研究。两组中所研究多态性的等位基因和基因型分布无统计学差异。然而,显性模型显示,NOS2的rs2779249(-1290G>T)的变异型T(TT/GT)的存在与RPL显著相关(OR=1.58,95%CI=1.03-2.44;P=0.037)。在根据妊娠次数、饮酒情况和种族进行调整后,增加的风险仍然显著(OR=1.92,95%CI=1.18-3.11;P=0.008)。这些结果表明,NOS2启动子中功能性多态性rs2779249的变异基因型是RPL的潜在风险因素,可能是由于氧化应激机制。

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