The relationships between maternal and placental polymorphisms of miR-196a2 and miRNA-499 genes and preeclampsia.

IF 2.7 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY British Journal of Biomedical Science Pub Date : 2020-10-01 Epub Date: 2020-07-20 DOI:10.1080/09674845.2020.1769331
M Asadi-Tarani, M Saravani, B Teimoori, M Ghasemi, S Salimi
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引用次数: 6

Abstract

Background: miRNAs are small non-coding RNAs with potential roles in the complications of pregnancy. We hypothesised links between polymorphisms in miRNA-196a2 and miRNA-499 in maternal blood and the placentas of patients with preeclampsia. Methods: The blood of 315 women with preeclampsia and 317 controls and the placentas of 103 PE and 133 healthy women were collected. The genotyping of both polymorphisms was performed by PCR-RFLP. Results: The maternal blood rs11614913 was unrelated to preeclampsia in genotype and allele models, but in placental tissue, the CT (odds ratio [95% CI] 0.5 [0.3-0.9, p = 0.018) and TT (0.4 [0.2-0.9] p = 0.033) genotypes alone and together (CT+TT v CC 0.5 [0.3-0.8] p = 0.009), and the T allele (0.6 [0.4-0.9], p = 0.019) were associated with lower risk of preeclampsia. The maternal blood rs3746444 CC genotype was more frequent in preeclampsia (2.2 [1.2-3.8] p = 0.008) and the recessive model (CC v TC+TT) was also significant (1.9 [1.1-3.3], p = 0.018), as was the C allele (1.4 [1.1-1.7] p = 0.014). In placental tissue, the increase in the frequency of the CC genotype was marginally significant (2.4 [1.0-5.8] p = 0.046). The maternal or placental miRNA-196a2 rs11614913 and miRNA-499 rs3746444 polymorphisms were unrelated to the severity of preeclampsia. Conclusion: The placental but not maternal miRNA-196a2 rs11614913 variant could be a protective factor for preeclampsia predisposition in all models except the recessive model. The maternal/placental rs3746444 CC genotype was in association with higher preeclampsia risk.

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母体和胎盘miR-196a2和miRNA-499基因多态性与子痫前期的关系
背景:mirna是一种小的非编码rna,在妊娠并发症中具有潜在的作用。我们假设母体血液中miRNA-196a2和miRNA-499的多态性与子痫前期患者的胎盘之间存在联系。方法:采集315例先兆子痫妇女和317例对照组的血液,103例妊娠前期子痫妇女和133例健康妇女的胎盘。采用PCR-RFLP对两种多态性进行基因分型。结果:在基因型和等位基因模型中,母体血液rs11614913与子痫前期不相关,但在胎盘组织中,CT(优势比[95% CI] 0.5 [0.3-0.9, p = 0.018)和TT(优势比[0.4 [0.2-0.9]p = 0.033)基因型单独和联合(CT+TT v CC 0.5 [0.3-0.8] p = 0.009)和T等位基因(0.6 [0.4-0.9],p = 0.019)与子痫前期风险降低相关。母体血液rs3746444 CC基因型在子痫前期更为常见(2.2 [1.2-3.8]p = 0.008),隐性模式(CC v TC+TT)也显著(1.9 [1.1-3.3],p = 0.018), C等位基因(1.4 [1.1-1.7]p = 0.014)。在胎盘组织中,CC基因型频率的增加具有边际意义(2.4 [1.0-5.8]p = 0.046)。母体或胎盘miRNA-196a2 rs11614913和miRNA-499 rs3746444多态性与先兆子痫的严重程度无关。结论:在除隐性模型外的所有模型中,胎盘miRNA-196a2 rs11614913变异可能是子痫前期易感性的保护因素,而非母体miRNA-196a2 rs11614913变异。母体/胎盘rs3746444 CC基因型与较高的子痫前期风险相关。
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来源期刊
British Journal of Biomedical Science
British Journal of Biomedical Science 医学-医学实验技术
CiteScore
4.40
自引率
15.80%
发文量
29
审稿时长
>12 weeks
期刊介绍: The British Journal of Biomedical Science is committed to publishing high quality original research that represents a clear advance in the practice of biomedical science, and reviews that summarise recent advances in the field of biomedical science. The overall aim of the Journal is to provide a platform for the dissemination of new and innovative information on the diagnosis and management of disease that is valuable to the practicing laboratory scientist.
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