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用于胎儿非整倍体无创产前诊断的生物标志物的开发:预测可靠性和潜在临床应用。

Biomarker development for non-invasive prenatal diagnosis of fetal aneuploidies: predictive reliability and potential clinical application.

机构信息

Department of Medical Genetics, Aghia Sofia Children's Hospital, Athens University School of Medicine, Thivon & Levadias, 115 27 Athens, Greece.

出版信息

EPMA J. 2011 Jun;2(2):157-61. doi: 10.1007/s13167-011-0084-z. Epub 2011 May 18.

Abstract

Current non-invasive prenatal diagnosis for fetal aneuploidies is based on biochemical and ultrasound markers and needs to be improved in order to reduce the number of pregnant women subjected to invasive diagnostic procedures. Proteomic technologies allow for new strategies for discovering biomarkers in complex biological fluids in a high-throughput and sensitive manner. Application of advance proteomic tools to profile pathology-specific proteins in maternal plasma obtained from pregnancies with aneuploid fetuses revealed biomarker-candidates that can potentially revolutionize the diagnostic and treatment procedure in favor of better prediction and improved individual outcomes. The current review focuses on studies of maternal peripheral blood using proteomic technologies, describes alterations noted in the presence of fetal aneuploidies and discuss their potential use as biomarkers for non-invasive prenatal diagnosis.

摘要

目前,针对胎儿非整倍体的非侵入性产前诊断基于生化和超声标志物,需要加以改进,以减少需要接受侵入性诊断程序的孕妇数量。蛋白质组学技术允许以高通量和敏感的方式在复杂的生物流体中发现生物标志物的新策略。将先进的蛋白质组学工具应用于分析来自患有非整倍体胎儿的孕妇的母体血浆中的特定病理蛋白,揭示了潜在的生物标志物候选物,这有可能彻底改变诊断和治疗程序,从而更好地预测和改善个体结果。本综述重点介绍了使用蛋白质组学技术研究母体外周血,描述了在存在胎儿非整倍体时观察到的变化,并讨论了它们作为非侵入性产前诊断生物标志物的潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09fd/3405383/4cadf2376fa9/13167_2011_84_Fig1_HTML.jpg

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