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微 RNA363 和 149 在子痫前期诊断前的母体循环中表达差异。

MicroRNAs 363 and 149 are differentially expressed in the maternal circulation preceding a diagnosis of preeclampsia.

机构信息

Translational Obstetrics Group, The Department of Obstetrics and Gynaecology, Mercy Hospital for Women, University of Melbourne, 163 Studley Road, Heidelberg, VIC, 3084, Australia.

Mercy Perinatal, Mercy Hospital for Women, Heidelberg, VIC, Australia.

出版信息

Sci Rep. 2020 Oct 22;10(1):18077. doi: 10.1038/s41598-020-73783-w.

DOI:10.1038/s41598-020-73783-w
PMID:33093531
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7583242/
Abstract

Preeclampsia is a pregnancy complication associated with angiogenic dysbalance, maternal endothelial dysfunction and end-organ injury. A predictive test to identify those who will develop preeclampsia could substantially decrease morbidity and mortality. MicroRNAs (miRs) are small RNA molecules involved in post-transcriptional gene regulation. We screened for circulating miRs differentially expressed at 36 weeks' gestation in pregnancies before the development of preeclampsia. We used a case-control group (198 controls, 34 pre-preeclampsia diagnosis) selected from a prospective cohort (n = 2015) and performed a PCR-based microarray to measure the expression of 41 miRs. We found six circulating miRs (miRs 363, 149, 18a, 1283, 16, 424) at 36 weeks' had significantly reduced expression (p < 0.0001-0.04). miR363 was significantly downregulated at 28 weeks' gestation, 10-12 weeks before the onset of clinical disease. In the circulation of another cohort of 34 participants with established preterm preeclampsia (vs 23 controls), we found miRs363, 18a, 149 and 16 were significantly down regulated (p < 0.0001-0.04). Combined expression of miRs149 and 363 in the circulation at 36 weeks' gestation provides a test with 45% sensitivity (at a specificity of 90%) which suggests measuring both miRs may have promise as part of a multi-marker test to predict preeclampsia.

摘要

子痫前期是一种与血管生成失衡、母体血管内皮功能障碍和终末器官损伤相关的妊娠并发症。一种预测性测试,可以识别那些将发展为子痫前期的患者,可以显著降低发病率和死亡率。微小 RNA(miRs)是参与转录后基因调控的小 RNA 分子。我们在未发生子痫前期的妊娠中,筛选了在 36 孕周循环中差异表达的微小 RNA。我们使用了一个前瞻性队列(n=2015)中的病例对照组(198 名对照,34 名子痫前期诊断前),并进行了基于 PCR 的微阵列来测量 41 个微小 RNA 的表达。我们发现,在 36 孕周时,六种循环微小 RNA(miRs363、149、18a、1283、16、424)的表达显著降低(p<0.0001-0.04)。miR363 在 28 孕周时显著下调,在临床疾病发生前 10-12 周。在另一组 34 名已确诊的早产子痫前期患者(与 23 名对照)的循环中,我们发现 miR363、18a、149 和 16 显著下调(p<0.0001-0.04)。在 36 孕周的循环中联合检测 miRs149 和 363 的表达,具有 45%的敏感性(特异性为 90%),这表明测量这两种微小 RNA 可能有希望作为预测子痫前期的多标志物测试的一部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/203d/7583242/ab25d059a4d0/41598_2020_73783_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/203d/7583242/9739b638f63c/41598_2020_73783_Fig1a_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/203d/7583242/966473efd778/41598_2020_73783_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/203d/7583242/84db73f9e55f/41598_2020_73783_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/203d/7583242/84245b6506f6/41598_2020_73783_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/203d/7583242/ab25d059a4d0/41598_2020_73783_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/203d/7583242/9739b638f63c/41598_2020_73783_Fig1a_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/203d/7583242/966473efd778/41598_2020_73783_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/203d/7583242/84db73f9e55f/41598_2020_73783_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/203d/7583242/84245b6506f6/41598_2020_73783_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/203d/7583242/ab25d059a4d0/41598_2020_73783_Fig5_HTML.jpg

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2
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3
ACOG Practice Bulletin No. 202: Gestational Hypertension and Preeclampsia.
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Ir J Med Sci. 2024 Oct;193(5):2363-2374. doi: 10.1007/s11845-024-03732-3. Epub 2024 Jun 7.
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Circulating miRNAs and Preeclampsia: From Implantation to Epigenetics.循环 miRNA 与子痫前期:从着床到表观遗传学。
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