Department of Genomic Medicine, D.O. Ott Research Institute for Obstetrics, Gynecology, and Reproduction, St. Petersburg 199034, Russia.
Resource Center "Biobank", St. Petersburg State University, St. Petersburg 199034, Russia.
Genes (Basel). 2022 Nov 3;13(11):2018. doi: 10.3390/genes13112018.
In recent years evidence has been accumulated showing that miRNAs can act as potential biomarkers or targets for therapy of preterm birth, one of the most important problems in modern obstetrics. We have performed a prospective study of the miRNA profile in the plasma during the first and second trimesters in pregnant women with high risk of preterm birth ( = 13 cases and = 11 controls). For the study group plasma blood samples at 9-13 weeks before diagnosis and at 22-24 weeks after start of therapy were selected. Using high-throughput sequencing technology we detected differences in the levels of 15 miRNAs (3 upregulated-hsa-miR-122-5p, hsa-miR-34a-5p, hsa-miR-34c-5p; 12 downregulated-hsa-miR-487b-3p, hsa-miR-493-3p, hsa-miR-432-5p, hsa-miR-323b-3p, hsa-miR-369-3p, hsa-miR-134-5p, hsa-miR-431-5p, hsa-miR-485-5p, hsa-miR-382-5p, hsa-miR-369-5p, hsa-miR-485-3p, hsa-miR-127-3p) (log(FC) ≥ 1.5; FDR ≤ 0.05) during the first trimester compared with the control (non-high-risk of preterm birth pregnant women). All downregulated miRNAs in the first trimester from the placenta-specific C14MC cluster. During the second trimester no differentially expressed miRNAs were found. Our results suggest that the miRNA profile in plasma during early pregnancy may predict a high risk of preterm birth, which is important in preventing gestational problems as early as possible.
近年来,已有大量证据表明,miRNA 可以作为预测早产(一种现代产科最重要的问题之一)的潜在生物标志物或治疗靶点。我们对高危早产孕妇(病例组=13 例,对照组=11 例)在妊娠第一和第二孕期血浆中的 miRNA 谱进行了前瞻性研究。病例组选择在诊断前 9-13 周和治疗开始后 22-24 周采集血浆血样。使用高通量测序技术,我们检测到 15 个 miRNA 的水平存在差异(3 个上调-hsa-miR-122-5p、hsa-miR-34a-5p、hsa-miR-34c-5p;12 个下调-hsa-miR-487b-3p、hsa-miR-493-3p、hsa-miR-432-5p、hsa-miR-323b-3p、hsa-miR-369-3p、hsa-miR-134-5p、hsa-miR-431-5p、hsa-miR-485-5p、hsa-miR-382-5p、hsa-miR-369-5p、hsa-miR-485-3p、hsa-miR-127-3p)(log(FC)≥1.5;FDR≤0.05),与对照组(非高危早产孕妇)相比,在第一孕期。所有在第一孕期下调的 miRNA 均来自胎盘特异性 C14MC 簇。在第二孕期没有发现差异表达的 miRNA。我们的结果表明,妊娠早期血浆中的 miRNA 谱可能预测早产的高风险,这对于尽早预防妊娠问题非常重要。