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首页> 外文期刊>Molecular diagnosis & therapy >Circulating mRNA in Maternal Plasma at the Second Trimester of Pregnancy: A Possible Screening Tool for Cardiac Conotruncal and Left Ventricular Outflow Tract Abnormalities
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Circulating mRNA in Maternal Plasma at the Second Trimester of Pregnancy: A Possible Screening Tool for Cardiac Conotruncal and Left Ventricular Outflow Tract Abnormalities

机译:妊娠第二三个月的母体血浆中循环mRNA:一种用于心肌粥样硬腹和左心室流出道异常的可能的筛查工具

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摘要

Abstract Objective Maternal plasma is a source of circulating placental nucleic acids. This study was designed to detect aberrantly expressed placental mRNA genes circulating in the maternal plasma of pregnancies affected with fetal conotruncal anomalies (CNTRA) and left-ventricular outflow tract (LVOT) obstruction in the second trimester of pregnancy. Methods This was a retrospective monocentric study conducted from 1 Jan 2016 to 31 Dec 2016. NanoString technology was used to identify aberrantly expressed genes, comparing 36 women carrying a fetus with CNTRA or LVOT obstruction to 42 controls at 19–24 weeks of gestation. The genes with differential expression were subsequently tested using real-time polymerase chain reaction. Linear discriminant analysis was used to combine all the mRNA species with discriminant ability for CNTRA and LVOT obstruction. A multivariable receiver operating characteristic (ROC) curve having the estimated discriminant score as an explanatory variable was generated for the two affected groups versus controls. Results Three genes with differential expression, namely MAPK1 , IQGAP1 and Visfatin were found. The ROC curves yielded detection rates of 60 and 62.5% at a false-positive rate of 5% for CNTRA and LVOT, respectively. Conclusions These data suggested that molecular screening of CNTRA and LVOT obstruction in the second trimester is feasible. Prospective studies are needed to test the discriminant ability of these genes and to calculate the predictive positive value in the general population.
机译:摘要目标母体等离子体是循环胎盘核酸的源泉。本研究旨在检测在妊娠期胎儿粥样曲线异常(CNTRA)和妊娠期妊娠期妊娠期妊娠期妊娠的孕产妇血浆中循环的异常表达的胎盘mRNA基因。方法这是从2016年1月1日至2016年12月3日开始的回顾性单眼历。纳米过度技术用于鉴定异常表达的基因,比较36名患有CNTRA或LVOT梗阻的胎儿在妊娠19-24周的42个对照中。随后使用实时聚合酶链式反应进行差异表达的基因。线性判别分析用于将所有mRNA物种与CNTRA和LVOT梗阻的判别能力结合起来。对于两个受影响的组对照,生成具有估计判别评分作为解释性变量的多变量接收器的操作特性(ROC)曲线。结果发现,发现患有差异表达的三种基因,即MAPK1,IQGAP1和类粘酰胺。 ROC曲线分别产生60%和62.5%的检测率,分别为CNTRA和LVOT的假阳性率为5%。结论这些数据表明,第二三个月中CNTRA和LVOT梗阻的分子筛是可行的。需要预期研究来测试这些基因的判别能力,并计算一般人群的预测正值。

著录项

  • 来源
    《Molecular diagnosis & therapy》 |2017年第6期|共9页
  • 作者单位

    Division of Obstetrics and Prenatal Medicine Department of Medicine and Surgery (DIMEC) Sant;

    Synlab Italia Srl;

    Synlab Italia Srl;

    Synlab Italia Srl;

    Division of Obstetrics and Prenatal Medicine Department of Medicine and Surgery (DIMEC) Sant;

    Pediatric Cardiology and Adult Congenital Unit Sant’Orsola-Malpighi Hospital;

    Division of Obstetrics and Prenatal Medicine Department of Medicine and Surgery (DIMEC) Sant;

    Division of Obstetrics and Prenatal Medicine Department of Medicine and Surgery (DIMEC) Sant;

    Division of Obstetrics and Prenatal Medicine Department of Medicine and Surgery (DIMEC) Sant;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 临床医学;
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