Lopes A C S, Macedo A A de, Mendes F S, Costa I M, Dusse L M S, Alpoim P N
Departamento de Análises Clínicas e Toxicológicas, Faculdade de Farmácia, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brasil.
Braz J Med Biol Res. 2025 May 30;58:e13988. doi: 10.1590/1414-431X2025e13988. eCollection 2025.
Preeclampsia (PE) is a disease of pregnancy characterized by the new onset of hypertension accompanied by proteinuria and/or other signs of maternal organ dysfunction that manifests after 20 weeks of gestation. MicroRNAs (miRNAs) are small non-coding RNAs (19-25 nucleotides) that function in the post-transcriptional regulation of gene expression. Many studies have suggested that different microRNA expression profiles may be associated with the development of PE. Hence, this study aims to report differentially expressed microRNAs that may be associated with the pathogenesis of PE and investigate whether different miRNA expression profiles are associated with different PE classifications and different phases of pregnancy. The bibliographic search was conducted from September 2021 to August 2024 and was performed on MEDLINE/PubMed, EMBASE, and Web of Science. This systematic review followed the methodological guidelines of the Cochrane Collaboration Manual for Systematic Intervention Reviews and was written according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). Of the 1362 studies identified, 263 articles were selected as the sample of this study. The most frequently cited upregulated microRNAs were: miR-210, miR-155, miR-518b, miR-181a, miR-125b, miR-183, and miR-16. The most frequently cited downregulated microRNAs were: miR-363, miR-18a, miR-144, miR-149, miR-16, miR-18b, and miR-195. This study will serve as a reference to guide future experimental research. In addition, knowledge of the expression profiles of microRNAs associated with PE can help in the development of new protocols for early prediction of the disease.
子痫前期(PE)是一种妊娠期疾病,其特征为妊娠20周后新出现的高血压,并伴有蛋白尿和/或其他母体器官功能障碍的体征。微小RNA(miRNA)是小的非编码RNA(19 - 25个核苷酸),在基因表达的转录后调控中发挥作用。许多研究表明,不同的微小RNA表达谱可能与子痫前期的发生发展有关。因此,本研究旨在报告可能与子痫前期发病机制相关的差异表达微小RNA,并研究不同的miRNA表达谱是否与子痫前期的不同分类及妊娠的不同阶段相关。文献检索于2021年9月至2024年8月进行,检索数据库为MEDLINE/PubMed、EMBASE和科学网。本系统评价遵循Cochrane协作网系统干预评价手册的方法学指南,并按照系统评价和Meta分析的首选报告项目(PRISMA)撰写。在检索到的1362项研究中,263篇文章被选为该研究的样本。最常被引用的上调微小RNA为:miR - 210、miR - 155、miR - 518b、miR - 181a、miR - 125b、miR - 183和miR - 16。最常被引用的下调微小RNA为:miR - 363、miR - 18a、miR - 144、miR - 149、miR - 16、miR - 18b和miR - 195。本研究将作为指导未来实验研究的参考。此外,了解与子痫前期相关的微小RNA表达谱有助于制定新的疾病早期预测方案。