Lo Y M Dennis, Tsui Nancy B Y, Chiu Rossa W K, Lau Tze K, Leung Tse N, Heung Macy M S, Gerovassili Ageliki, Jin Yongjie, Nicolaides Kypros H, Cantor Charles R, Ding Chunming
Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong SAR, China.
Nat Med. 2007 Feb;13(2):218-23. doi: 10.1038/nm1530. Epub 2007 Jan 7.
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.
目前用于产前诊断染色体非整倍体的方法包括通过羊膜穿刺术或绒毛取样等程序对胎儿材料进行侵入性采样,这对胎儿构成一定风险。在此,我们概述了一种胎儿染色体剂量评估策略,该策略可通过分析母体血浆中胎盘表达的mRNA来无创进行。我们通过测定母体血浆中PLAC4 mRNA(由21号染色体转录并由胎盘表达的单核苷酸多态性(SNP)等位基因之间的比率),实现了胎儿21三体的无创产前诊断。母体血浆中的PLAC4 mRNA源自胎儿,分娩后清除。母体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,在96.5%的对照中排除了该疾病。