Illarionov Roman A, Maltseva Anastasia R, Pachuliia Olga V, Postnikova Tatiana B, Vashukova Elena S, Popova Anastasiia K, Nasykhova Yulia A, Bespalova Olesya N, Glotov Andrey S
Department of Genomic Medicine, D.O. Ott Research Institute for Obstetrics, Gynecology, and Reproduction, St. Petersburg 199034, Russia.
Department of Genetics and Biotechnology, St. Petersburg State University, St. Petersburg 199034, Russia.
Noncoding RNA. 2024 Dec 2;10(6):61. doi: 10.3390/ncrna10060061.
Pre-eclampsia (PE) is a serious condition affecting 2-8% of pregnancies worldwide, leading to high maternal and fetal morbidity and mortality. MicroRNAs (miRNAs), small non-coding RNA molecules, have emerged as potential biomarkers for various pregnancy-related pathologies, including PE. MiRNAs in plasma and serum have been extensively studied, but urinary miRNAs remain underexplored, especially during early pregnancy. This study aimed to investigate the urinary miRNA expression profiles in women with pre-eclampsia during the first and second trimesters. A prospective study was conducted using 48 urine samples from 24 pregnant women (n = 12 pre-eclampsia and n = 12 controls). Urine samples were collected in the first (9-13 weeks) and second (22-24 weeks) trimesters. MiRNA isolation, library preparation, and high-throughput sequencing were performed, followed by differential expression and enrichment analyses. In the first trimester, five miRNAs were dysregulated in PE in comparison with the control group (hsa-miR-184, hsa-miR-203a-3p, hsa-miR-205-5p, hsa-miR-223-3p-downregulated; hsa-miR-1-3p-upregulated). In the second trimester, hsa-miR-205-5p and hsa-miR-223-3p were downregulated, and hsa-miR-9-5p, hsa-miR-1-3p, and hsa-miR-206 were upregulated. Our study identified differentially expressed miRNAs in the urine of pre-eclamptic patients during early pregnancy. These findings suggest that specific urinary miRNAs could serve as non-invasive biomarkers for the early detection and risk assessment of pre-eclampsia. The changes in the level of differential expression of miRNAs during gestation highlight their role in the progression of PE. Further research and validation with a larger cohort are needed to explore their clinical potential for improving maternal and fetal outcomes through early intervention.
子痫前期(PE)是一种严重病症,影响着全球2%至8%的孕妇,会导致孕产妇和胎儿的高发病率和死亡率。微小RNA(miRNA)是一类小的非编码RNA分子,已成为包括PE在内的各种妊娠相关病症的潜在生物标志物。血浆和血清中的miRNA已得到广泛研究,但尿液中的miRNA仍未得到充分探索,尤其是在妊娠早期。本研究旨在调查子痫前期女性在妊娠第一和第二阶段的尿液miRNA表达谱。使用来自24名孕妇的48份尿液样本进行了一项前瞻性研究(n = 12例子痫前期患者和n = 12例对照)。在妊娠第一阶段(9至13周)和第二阶段(22至24周)收集尿液样本。进行了miRNA分离、文库制备和高通量测序,随后进行差异表达和富集分析。在妊娠第一阶段,与对照组相比,PE中有5种miRNA表达失调(hsa-miR-184、hsa-miR-203a-3p、hsa-miR-205-5p、hsa-miR-223-3p下调;hsa-miR-1-3p上调)。在妊娠第二阶段,hsa-miR-205-5p和hsa-miR-223-3p下调,hsa-miR-9-5p、hsa-miR-1-3p和hsa-miR-206上调。我们的研究确定了子痫前期患者妊娠早期尿液中差异表达的miRNA。这些发现表明,特定的尿液miRNA可作为子痫前期早期检测和风险评估的非侵入性生物标志物。miRNA差异表达水平在妊娠期的变化突出了它们在PE进展中的作用。需要进一步开展研究并在更大的队列中进行验证,以探索它们通过早期干预改善母婴结局的临床潜力。