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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

Maternal plasma mRNA species in fetal heart defects: a potential for molecular screening.

作者信息

Curti Alessandra, Lapucci Cristina, Berto Silvia, Prandstraller Daniela, Perolo Antonella, Rizzo Nicola, Farina Antonio

机构信息

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

Geneticlab, Noventa Vicentina, Italy.

出版信息

Prenat Diagn. 2016 Aug;36(8):738-43. doi: 10.1002/pd.4853. Epub 2016 Jul 4.

Abstract

OBJECTIVE

To verify the hypothesis that aberrant placental mRNA genes related to cardiogenesis can be detected in maternal plasma at the second trimester of pregnancy.

METHODS

NanoString technology was used to identify aberrant genes, comparing 39 women carrying a fetus with a congenital heart defect (CHD) to 31 controls at 19-24 weeks of gestation. The genes with differential expression were subsequently tested using real time polymerase chain reaction. Linear discriminant analysis (LDA) was used to combine all the mRNA species with discriminant ability for CHD. A multivariable receiver operating characteristic (ROC) curve having the estimated discriminant score as an explanatory variable was generated.

RESULTS

Six genes with differential expression, namely FALZ, PAPP-A, PRKACB, SAV1, STK4 and TNXB2, were found. The ROC curve yielded a detection rate of 66.7% at a false positive rate of 10%. A higher discriminant score (>75(th) centile) was reached for 14 CHD cases (82.4%) and only 1 control (5.8%). Two cases (11.8%) of heart rhythm disorders also yielded a discriminant score value >75(th) centile.

CONCLUSION

These data represent a step forward in the screening of CHDs. Additional studies are needed to detect more mRNAs with discriminant ability and to move the first trimester screening.

摘要

目的

验证在妊娠中期孕妇血浆中可检测到与心脏发生相关的胎盘异常mRNA基因这一假说。

方法

使用纳米孔技术鉴定异常基因,将39名怀有先天性心脏病(CHD)胎儿的女性与31名妊娠19 - 24周的对照组进行比较。随后使用实时聚合酶链反应对差异表达的基因进行检测。使用线性判别分析(LDA)将所有具有CHD判别能力的mRNA种类进行合并。生成以估计判别分数作为解释变量的多变量受试者工作特征(ROC)曲线。

结果

发现6个差异表达基因,即FALZ、PAPP - A、PRKACB、SAV1、STK4和TNXB2。ROC曲线在假阳性率为10%时的检测率为66.7%。14例CHD病例(82.4%)的判别分数较高(>第75百分位数),而只有1例对照(5.8%)。2例(11.8%)心律失常病例的判别分数值也>第75百分位数。

结论

这些数据代表了先天性心脏病筛查的一个进步。需要进一步研究以检测更多具有判别能力的mRNA,并推进孕早期筛查。

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