Department of Obstetrics and Gynecology, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.
Department of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.
J Cell Biochem. 2019 Mar;120(3):3277-3285. doi: 10.1002/jcb.27595. Epub 2018 Oct 10.
Evidence has shown that pre-eclampsia (PE) is associated with an increased level of catecholamines. Renalase is a catecholamine-metabolizing enzyme, which contributes to the occurrence of hypertension. In the current study, we aimed to assess the relation between two renalase gene ( RNLS) polymorphisms, including rs2576178 at the 5'-flanking region and rs10887800 at intron 6, near the exon/intron border and PE susceptibility. In this case-control study, 179 women with PE and 202 normotensive pregnant women were genotyped for RNLS rs2576178 and rs10887800 polymorphisms by the polymerase chain reaction-restriction fragment length polymorphism method. There was no association between RNLS rs10887800 and rs2576178 polymorphisms and PE, neither in the dominant nor in the recessive model. Although there was no association between RNLS rs10887800 polymorphism and mild PE, this polymorphism was associated with 2.2-fold higher risk of severe PE in the recessive model (odds ratio [OR], 2.2; 95% confidence interval [CI], 1.2-4.4; P = 0.01) but not in the dominant model. The RNLS rs2576178 and rs10887800 polymorphisms were not associated with PE severity. The RNLS rs10887800 and rs2576178 GG/GG combined genotypes were associated with 8.4- and 16.7-fold higher risk of PE and severe PE, respectively (OR, 8.4; 95% CI, 1-71.1; P = 0.048 and OR, 16.7; 95% CI, 1.6-167; P = 0.018). Also, the G-G haplotype was associated with 1.7-fold risk of PE and mild PE (OR, 1.7; 95% CI, 1.1-2.4; P = 0.009 and OR, 1.7; 95% CI, 1.1-2.5; P = 0.02). The RNLS rs10887800 polymorphism was associated with severe PE. The RNLS rs10887800 and rs2576178 GG/GG combined genotypes and G-G haplotype were associated with higher risk of PE.
证据表明,先兆子痫(PE)与儿茶酚胺水平升高有关。肾酶是一种儿茶酚胺代谢酶,有助于高血压的发生。在本研究中,我们旨在评估两个肾酶基因(RNLS)多态性与 PE 易感性之间的关系,包括 5'-侧翼区的 rs2576178 和内含子 6 附近的 rs10887800,靠近外显子/内含子边界。在这项病例对照研究中,通过聚合酶链反应-限制性片段长度多态性方法对 179 名 PE 妇女和 202 名正常血压孕妇的 RNLS rs2576178 和 rs10887800 多态性进行了基因分型。RNLS rs10887800 和 rs2576178 多态性与 PE 无关,无论是显性还是隐性模型。虽然 RNLS rs10887800 多态性与轻度 PE 无关,但该多态性与隐性模型中严重 PE 的风险增加 2.2 倍相关(比值比 [OR],2.2;95%置信区间 [CI],1.2-4.4;P=0.01),但在显性模型中并非如此。RNLS rs2576178 和 rs10887800 多态性与 PE 严重程度无关。RNLS rs10887800 和 rs2576178 GG/GG 组合基因型与 PE 和严重 PE 的风险分别增加 8.4-和 16.7 倍相关(OR,8.4;95%CI,1-71.1;P=0.048 和 OR,16.7;95%CI,1.6-167;P=0.018)。此外,G-G 单倍型与 PE 和轻度 PE 的风险增加 1.7 倍相关(OR,1.7;95%CI,1.1-2.4;P=0.009 和 OR,1.7;95%CI,1.1-2.5;P=0.02)。RNLS rs10887800 多态性与严重 PE 相关。RNLS rs10887800 和 rs2576178 GG/GG 组合基因型和 G-G 单倍型与 PE 风险增加相关。