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妊娠中期母体血浆中的循环 mRNA:心脏圆锥动脉干和左心室流出道异常的一种可能的筛查工具。

Circulating mRNA in Maternal Plasma at the Second Trimester of Pregnancy: A Possible Screening Tool for Cardiac Conotruncal and Left Ventricular Outflow Tract Abnormalities.

机构信息

Division of Obstetrics and Prenatal Medicine, Department of Medicine and Surgery (DIMEC) Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.

Synlab Italia Srl, Castenedolo, Brescia, Italy.

出版信息

Mol Diagn Ther. 2017 Dec;21(6):653-661. doi: 10.1007/s40291-017-0295-7.

DOI:10.1007/s40291-017-0295-7
PMID:28744745
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.

摘要

目的

母体血浆是循环胎盘核酸的来源。本研究旨在检测妊娠中期胎儿圆锥动脉干异常(CNTRA)和左心室流出道(LVOT)梗阻孕妇母体血浆中循环的异常表达胎盘 mRNA 基因。

方法

这是一项回顾性单中心研究,于 2016 年 1 月 1 日至 12 月 31 日进行。采用 NanoString 技术比较 36 名妊娠中晚期(19-24 周)携带胎儿 CNTRA 或 LVOT 梗阻的孕妇和 42 名对照者,鉴定差异表达基因。随后使用实时聚合酶链反应(PCR)检测差异表达基因。使用线性判别分析(LDA)将具有判别能力的所有 mRNA 物种结合起来,用于 CNTRA 和 LVOT 梗阻。生成两个受影响组与对照组的估计判别评分作为解释变量的多变量受试者工作特征(ROC)曲线。

结果

发现三个差异表达的基因,即 MAPK1、IQGAP1 和 Visfatin。ROC 曲线在假阳性率为 5%时,CNTRA 和 LVOT 的检出率分别为 60%和 62.5%。

结论

这些数据表明,在妊娠中期对 CNTRA 和 LVOT 梗阻进行分子筛查是可行的。需要前瞻性研究来测试这些基因的判别能力,并计算在一般人群中的预测阳性值。

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本文引用的文献

1
What Is New in Genetics of Congenital Heart Defects?先天性心脏病遗传学的新进展有哪些?
Front Pediatr. 2016 Dec 1;4:120. doi: 10.3389/fped.2016.00120. eCollection 2016.
2
Measuring circulating placental RNAs to non-invasively assess the placental transcriptome and to predict pregnancy complications.测量循环胎盘RNA以无创评估胎盘转录组并预测妊娠并发症。
Prenat Diagn. 2016 Nov;36(11):997-1008. doi: 10.1002/pd.4934. Epub 2016 Oct 26.
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Maternal plasma mRNA species in fetal heart defects: a potential for molecular screening.
在真空压力下使用不混溶液体的无离心提取循环核酸。
Sci Rep. 2018 Apr 3;8(1):5467. doi: 10.1038/s41598-018-23766-9.
4
Levels of Circulating mRNA for the Tenascin-X (TNXB) Gene in Maternal Plasma at the Second Trimester in Pregnancies with Isolated Congenital Ventricular Septal Defects.母体血浆中存在的第十凝血素 X(TNXB)基因在妊娠中期的孤立性先天性室间隔缺损中的循环 mRNA 水平。
Mol Diagn Ther. 2018 Apr;22(2):235-240. doi: 10.1007/s40291-018-0321-4.
胎儿心脏缺陷中的母体血浆信使核糖核酸种类:分子筛查的潜力
Prenat Diagn. 2016 Aug;36(8):738-43. doi: 10.1002/pd.4853. Epub 2016 Jul 4.
4
Detection of 22q11.2 microduplication by cell-free DNA screening and chromosomal microarray in fetus with multiple anomalies.通过游离DNA筛查和染色体微阵列检测患有多种异常的胎儿中的22q11.2微重复。
Ultrasound Obstet Gynecol. 2016 Oct;48(4):530-532. doi: 10.1002/uog.15965. Epub 2016 Sep 13.
5
Association of Nicotinamide Phosphoribosyltransferase (NAMPT) Gene Polymorphisms and of Serum NAMPT Levels with Dilated Cardiomyopathy in a Chinese Population.中国人群中烟酰胺磷酸核糖转移酶(NAMPT)基因多态性及血清NAMPT水平与扩张型心肌病的关联
Int J Mol Sci. 2015 Sep 15;16(9):22299-318. doi: 10.3390/ijms160922299.
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Nicotinamide phosphoribosyltransferase/pre-B-cell colony enhancing factor/visfatin plasma levels and clinical outcome in patients with dilated cardiomyopathy.烟酰胺磷酸核糖基转移酶/前 B 细胞集落增强因子/内脂素在扩张型心肌病患者中的血浆水平与临床结局。
J Card Fail. 2015 Apr;21(4):330-8. doi: 10.1016/j.cardfail.2014.12.001. Epub 2014 Dec 9.
7
Microdeletion and microduplication analysis of chinese conotruncal defects patients with targeted array comparative genomic hybridization.运用靶向微阵列比较基因组杂交技术对中国圆锥动脉干缺陷患者进行微缺失和微重复分析。
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8
Identification of maternal serum microRNAs as novel non-invasive biomarkers for prenatal detection of fetal congenital heart defects.鉴定母血清 microRNAs 作为胎儿先天性心脏缺陷产前检测的新型无创生物标志物。
Clin Chim Acta. 2013 Sep 23;424:66-72. doi: 10.1016/j.cca.2013.05.010. Epub 2013 May 21.
9
Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: rare association with pulmonary valve stenosis.复发性相互性1q21.1缺失和重复综合征中的先天性心脏缺陷:与肺动脉瓣狭窄的罕见关联。
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Pre-B cell colony enhancing factor (PBEF/NAMPT/Visfatin) and vascular endothelial growth factor (VEGF) cooperate to increase the permeability of the human placental amnion.前 B 细胞集落增强因子(PBEF/NAMPT/Visfatin)和血管内皮生长因子(VEGF)协同作用增加人胎盘羊膜的通透性。
Placenta. 2013 Jan;34(1):42-9. doi: 10.1016/j.placenta.2012.10.008. Epub 2012 Nov 12.