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首页> 外文期刊>Nature medicine >Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection.
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Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection.

机译:血浆胎盘RNA等位基因比率允许无创的产前染色体非整倍性检测。

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Current methods for prenatal diagnosis of chromosomal aneuploidies involve the invasive sampling of fetal materials using procedures such as amniocentesis or chorionic villus sampling and constitute a finite risk to the fetus. Here, we outline a strategy for fetal chromosome dosage assessment that can be performed noninvasively through analysis of placental expressed mRNA in maternal plasma. We achieved noninvasive prenatal diagnosis of fetal trisomy 21 by determining the ratio between alleles of a single-nucleotide polymorphism (SNP) in PLAC4 mRNA, which is transcribed from chromosome 21 and expressed by the placenta, in maternal plasma. PLAC4 mRNA in maternal plasma was fetal derived and cleared after delivery. The allelic ratios in maternal plasma correlated with those in the placenta. Fetal trisomy 21 was detected noninvasively in 90% of cases and excluded in 96.5% of controls.
机译:当前用于染色体非整倍体的产前诊断的方法包括使用诸如羊膜穿刺术或绒毛膜绒毛取样的方法对胎儿材料进行侵入性采样,这对胎儿构成了有限的风险。在这里,我们概述了胎儿染色体剂量评估的策略,该策略可以通过分析母体血浆中胎盘表达的mRNA来无创地进行。我们通过确定孕妇血浆中PLAC4 mRNA的单核苷酸多态性(SNP)等位基因之间的比率来实现胎儿21三体性的无创产前诊断,该PLAC4 mRNA是从21号染色体转录并由胎盘表达的。孕妇血浆中的PLAC4 mRNA来源于胎儿,分娩后清除。孕妇血浆中的等位基因比率与胎盘中的等位基因比率相关。在90%的病例中无创检测到胎儿21三体性疾病,在96.5%的对照组中未检出。

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