microRNA作为妊娠期糖尿病诊断潜在生物标志物的最新进展

Kazi Mahmuda Akter, B. Umar, S. Rahman
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引用次数: 1

摘要

背景/目的:妊娠期糖尿病(GDM)的筛查目前在怀孕24-28周时进行,错过了器官发生的最脆弱时期,从而使临床医生无法在妊娠中期或晚期开始治疗。微小RNA(miR)是一种小的非编码RNA分子,可以通过建立一种新的无创产前检测(NIPT)工具来帮助检测或预测GDM。本研究的目的是总结血浆微小RNA作为GDM诊断生物标志物的最新进展。方法:在2021年4月至6月期间,PubMed进行了文献检索,以回顾最近关于与GDM相关的人血浆miR的文章。动物研究和用英语以外的语言撰写的论文被排除在外。仅使用血浆miRNA来避免凝血偏差。结果:共发现31个miRNA在GDM患者的血浆样本中显著上调。除miR-223和miR-23a在妊娠9-11周上调外,主要在妊娠中期或晚期发现。结论:尽管需要进行广泛的前瞻性队列研究,但miR-223和miR-23a应被认为是开发成功的NIPT工具最有希望的,因为它们被发现最早在妊娠早期上调。
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Recent Updates on microRNA as Potential Biomarkers for Diagnosis of Gestational Diabetes mellitus
Background/Aims: Screening for gestational diabetes mellitus (GDM) are currently done at 24 - 28 weeks of conception, missing out on the most vulnerable period of organogenesis and thus preventing clinicians from starting treatments until the late second or third trimester. MicroRNAs (miR) are small non-coding RNA molecules that could aid in detecting or predicting GDM through establishing a novel non-invasive prenatal testing (NIPT) tool. The objective of this study was to summarize the most recent updates on plasma microRNAs as GDM diagnostic biomarkers. Methods: Between April and June 2021, a PubMed literature search was undertaken to review recent articles on human plasma miR associated with GDM. Animal studies and papers that are written in languages other than English were excluded. Only plasma miRNAs were used to avoid coagulation biases. Results: A total of 31 miRNAs were found significantly upregulated in the plasma samples of patients with GDM. It was found mainly during the 2nd or 3rd trimester except for miR-223 and miR-23a that were upregulated at 9 – 11 weeks of gestation. Conclusion: Though extensive prospective cohort studies are required, miR-223 and miR-23a should be considered the most promising to develop a successful NIPT tool because they were found to be upregulated earliest, during the first trimester.
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