胎儿
非整倍体
胎龄
胎儿游离DNA
怀孕
产科
医学
妊娠期
分数(化学)
产前诊断
男科
生理学
生物
遗传学
化学
染色体
基因
有机化学
作者
Sarah Kinnings,Jennifer A. Geis,Eyad Almasri,Huiquan Wang,Xiaojun Guan,Ron McCullough,Allan T. Bombard,Juan‐Sebastian Saldivar,Paul Oeth,Cosmin Deciu
摘要
Objective Sufficient fetal DNA in a maternal plasma sample is required for accurate aneuploidy detection via noninvasive prenatal testing, thus highlighting a need to understand the factors affecting fetal fraction. Method The MaterniT21™ PLUS test uses massively parallel sequencing to analyze cell-free fetal DNA in maternal plasma and detect chromosomal abnormalities. We assess the impact of a variety of factors, both maternal and fetal, on the fetal fraction across a large number of samples processed by Sequenom Laboratories. Results The rate of increase in fetal fraction with increasing gestational age varies across the duration of the testing period and is also influenced by fetal aneuploidy status. Maternal weight trends inversely with fetal fraction, and we find no added benefit from analyzing body mass index or blood volume instead of weight. Strong correlations exist between fetal fractions from aliquots taken from the same patient at the same blood draw and also at different blood draws. Conclusion While a number of factors trend with fetal fraction across the cohort as a whole, they are not the sole determinants of fetal fraction. In this study, the variability for any one patient does not appear large enough to justify postponing testing to a later gestational age. © 2015 John Wiley & Sons, Ltd.
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