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游离胎儿DNA检测在子痫前期筛查中是否有未来?

Is there a future for cell-free fetal dna tests in screening for preeclampsia?

作者信息

Sarzynska-Nowacka Urszula, Kosinski Przemyslaw, Wielgos Miroslaw

机构信息

First Department of Obstetrics and Gynaecology, Medical University of Warsaw, Poland.

出版信息

Ginekol Pol. 2019;90(1):55-60. doi: 10.5603/GP.2019.0009.

Abstract

CffDNA screening is a powerful diagnostic tool in the prenatal diagnosis algorithm for chromosomal abnormalities. With detailed ultrasound examination as the mainstay of first-trimester risk assessment, cffDNA has been shown to be superior to first-trimester combined screening (FTCS) in false-positive rates for trisomy 21 detection. In light of the growing interest in cffDNA testing and the possibility of it replacing first-trimester biochemistry, we decided to investigate the usefulness of cffDNA tests in early-pregnancy risk assessment for preeclampsia (PE). The aim of this review paper was to evaluate clinical application of first-trimester cfDNA in predicting PE, as well as to investigate its possible use in first-trimester PE screening enhancement, also in cases where biochemistry is not performed.

摘要

游离胎儿DNA(cffDNA)筛查是染色体异常产前诊断算法中的一项强大诊断工具。以详细超声检查作为孕早期风险评估的主要手段,cffDNA在21三体检测的假阳性率方面已被证明优于孕早期联合筛查(FTCS)。鉴于对cffDNA检测的兴趣日益增加以及其取代孕早期生化检查的可能性,我们决定研究cffDNA检测在子痫前期(PE)早期妊娠风险评估中的有用性。这篇综述文章的目的是评估孕早期cfDNA在预测PE中的临床应用,以及研究其在增强孕早期PE筛查中的可能用途,即使在未进行生化检查的情况下也是如此。

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