Maternal plasma cell-free DNA in the prediction of pre-eclampsia

被引:49
作者
Rolnik, D. L. [1 ]
O'Gorman, N. [1 ]
Fiolna, M. [1 ]
van den Boom, D. [2 ]
Nicolaides, K. H. [1 ]
Poon, L. C. [1 ]
机构
[1] Kings Coll Hosp London, Harris Birthright Res Ctr Fetal Med, London SE5 9RS, England
[2] Sequenom Inc, San Diego, CA USA
关键词
cell free; DNA; pre-eclampsia; FREE FETAL DNA; INTRAUTERINE GROWTH RESTRICTION; ANEUPLOIDIES; PREVENTION; ASPIRIN; WOMEN;
D O I
10.1002/uog.14671
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
ObjectivesTo examine whether maternal plasma concentrations of total cell-free (cf)DNA and fetal fraction at 11-13 and 20-24weeks' gestation in pregnancies that subsequently develop pre-eclampsia (PE) are different from those without this complication. MethodsTotal cfDNA and fetal fraction were measured in 20 cases of early PE requiring delivery at<34weeks, in 20 cases of late PE with delivery at34weeks and in 200 normotensive controls, at 11-13 and 20-24weeks' gestation. Total cfDNA and fetal fraction measured at 11-13weeks were converted to multiples of the median (MoM), corrected for maternal characteristics and gestational age. The distributions of total cfDNA and fetal fraction at 20-24weeks were expressed as MoM of values at 11-13weeks. The Mann-Whitney U-test was used to determine the significance of differences in the median values in each outcome group relative to that in the controls. ResultsIn the early-PE group at 11-13weeks, compared with controls, there was a significant increase in median total cfDNA (2104 genome equivalents (GE)/mLvs 1590 GE/mL) and a decrease in median fetal fraction (6.8% vs 8.7%). In the late-PE group at 20-24weeks, compared with controls, there was a significant decrease in median fetal fraction (8.2% vs 9.6%). These significant differences between groups were not observed when the values were converted to MoM. ConclusionMeasurements of total cfDNA and fetal fraction in maternal plasma at 11-13 and 20-24weeks are not predictive of PE. Copyright (c) 2014 ISUOG. Published by John Wiley & Sons Ltd.
引用
收藏
页码:106 / 111
页数:6
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