Nrf2 rs6721961 and Oxidative Stress in Preeclampsia: Association with the Risk of Preeclampsia and Early-Onset Preeclampsia.

IF 1.5 Q3 MEDICINE, RESEARCH & EXPERIMENTAL International Journal of Molecular and Cellular Medicine Pub Date : 2022-01-01 DOI:10.22088/IJMCM.BUMS.11.2.127
Fatemeh Khadir, Zohreh Rahimi, Azita Ghanbarpour, Asad Vaisi-Raygani
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引用次数: 1

Abstract

Preeclampsia as a multifactor hypertensive disorder of pregnancy is associated with enhanced placental oxidative stress. The Keap1-Nrf2 pathway protects cells against oxidative stress. We examined the possible association between the Nrf2 variants in relation to oxidative stress parameters with the risk of preeclampsia. We studied 150 preeclampsia women and 150 women with a normal pregnancy to find the frequency of Nrf2 rs6721961 genotypes using the PCR-RFLP method. Also, an association between the Nrf2 genotypes with the levels of malondialdehyde (MDA) and total antioxidant capacity (TAC) was analyzed. Significantly lower TAC and higher MDA levels were found in preeclampsia patients compared to controls (P<0.0001). For the first time, we report an association between the Nrf2 rs6721961 polymorphism and preeclampsia risk. The present study indicated that the GT genotype and the T allele of the Nrf2 rs6721961 increased the risk of preeclampsia by 2.81 and 2.39 times, respectively. Also, the Nrf2 TT genotype was associated with a 3.9-fold increased risk of early-onset preeclampsia. We detected a positive association between the levels of body mass index, MDA, and the Nrf2 polymorphism with the risk of preeclampsia and a negative correlation between the level of TAC with the preeclampsia risk. Also, an association between the rs6721961 TT genotype with higher serum MDA levels was found. Our study suggests oxidative stress is involved in the pathogenesis of preeclampsia and the Nrf2 rs6721961 polymorphism through alteration in the levels of oxidative stress parameters might increase the risk of preeclampsia and early-onset preeclampsia.

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Nrf2 rs6721961和氧化应激在子痫前期:与子痫前期和早发性子痫前期的风险相关
先兆子痫作为一种多因素妊娠高血压疾病与胎盘氧化应激增强有关。Keap1-Nrf2通路保护细胞免受氧化应激。我们研究了Nrf2变异与氧化应激参数与子痫前期风险之间的可能关联。我们研究了150例子痫前期妇女和150例正常妊娠妇女,采用PCR-RFLP方法寻找Nrf2 rs6721961基因型的频率。此外,还分析了Nrf2基因型与丙二醛(MDA)水平和总抗氧化能力(TAC)之间的关系。与对照组相比,子痫前期患者的TAC显著降低,MDA水平显著升高(PNrf2 rs6721961多态性与子痫前期风险相关)。本研究表明,Nrf2 rs6721961的GT基因型和T等位基因分别使子痫前期风险增加2.81倍和2.39倍。此外,Nrf2 TT基因型与早发性子痫前期风险增加3.9倍相关。我们发现体重指数、MDA和Nrf2多态性水平与子痫前期风险呈正相关,而TAC水平与子痫前期风险呈负相关。此外,rs6721961 TT基因型与较高的血清MDA水平之间存在关联。我们的研究提示氧化应激参与了子痫前期的发病机制,Nrf2 rs6721961多态性通过改变氧化应激参数的水平可能增加子痫前期和早发性子痫前期的风险。
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期刊介绍: The International Journal of Molecular and Cellular Medicine (IJMCM) is a peer-reviewed, quarterly publication of Cellular and Molecular Biology Research Center (CMBRC), Babol University of Medical Sciences, Babol, Iran. The journal covers all cellular & molecular biology and medicine disciplines such as the genetic basis of disease, biomarker discovery in diagnosis and treatment, genomics and proteomics, bioinformatics, computer applications in human biology, stem cells and tissue engineering, medical biotechnology, nanomedicine, cellular processes related to growth, death and survival, clinical biochemistry, molecular & cellular immunology, molecular and cellular aspects of infectious disease and cancer research. IJMCM is a free access journal. All open access articles published in IJMCM are distributed under the terms of the Creative Commons Attribution CC BY. The journal doesn''t have any submission and article processing charges (APCs).
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