子痫前期的早期分子生物标志物研究

Vinaya Vijayan, R. Kannan, B. R. Reddy
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引用次数: 0

摘要

先兆子痫(PE)是一种与妊娠相关的高血压疾病,在妊娠20周后出现,可能是由胎盘发育不良引起的,对母亲和胎儿都有严重的风险。这种疾病只有在症状出现时才能被发现,需要一种生物标志物,这使得早期发现这种疾病成为可能,并且可以在怀孕早期对这种疾病进行适当的管理。尽管在全球范围内进行了许多关于microRNA作为子痫前期分子生物标志物的研究,但没有文献显示microRNA在印度人群中对子痫前期的影响。这项研究的目的是找到一种早期分子标记,可以在症状出现之前就在早期发现这种疾病。采用新一代测序技术对60个子痫前期组(30个早发型、30个晚发型子痫前期)的胎盘microrna进行研究,并选择30个对照组;miRNA分析由Illumina测序完成,定量仪进行下游分析鉴定、定量和表达分析。pl, script, and miRDeep2.pl, script。用TRIzol试剂从胎盘组织和细胞中提取总rna并进行纯化。测定miR-483-5p在组织或细胞中的相对表达:与晚发型和正常胎盘样品相比,早发型子痫前期胎盘样品中微量rna 483-5p的表达量显著。对miR 483-5p进行分析,并利用计算方法找到基因靶点。本研究发现,microRNA 483-5p可作为鉴别子痫前期的早期生物标志物。
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An Early Molecular Biomarker Study in Pre-eclampsia
Preeclampsia (PE), a hypertension condition associated with pregnancy that manifests after 20 weeks of pregnancy,may be brought on by faulty placental development and poses a serious risk to both the mother and the fetus. The disease can bedetected only once the symptoms arise, there is a need for a biomarker, which makes early detection of the disease possible, andproper management of the disease can be done at an early stage of pregnancy. Even though many studies were done globallyregarding the role of microRNAs as molecular biomarkers in pre-eclampsia, no literature showed the effect of microRNA inpreeclampsia in the Indian population. The aim of the study was to find an early molecular marker that can detect the disease atan early stage, even before the symptoms arise. Placental MicroRNAs were studied using Next-generation Sequencing of 60Preeclamptic groups ( 30 Early Onset,30Late onset preeclampsia), and 30 control groups were selected; miRNA profiling wasdone by Illumina sequencing, and the quantifier did downstream analysis for identification, quantification, and expression profiling.pl, script, and miRDeep2.pl, script. Total RNAs were extracted from placental tissues and cells by TRIzol reagent and purified. Therelative expression of miR-483-5p in tissues or cells was determined: micro-RNA 483-5p was expressed in significant quantity inEarly Onset preeclamptic placental samples compared to Late Onset and normal samples. miR 483-5p was analyzed, and the genetargets were found using computational methods. From this study, it was found that microRNA 483-5p can be used as an earlybiomarker for the identification of preeclampsia.
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