Low fetal fraction of cell-free DNA predicts placental dysfunction and hypertensive disease in pregnancy

被引:51
作者
Gerson, Kristin D. [1 ,2 ,3 ]
Truong, Samantha [4 ]
Haviland, Miriam J. [1 ,2 ]
O'Brien, Barbara M. [1 ,2 ]
Hacker, Michele R. [1 ,2 ]
Spiel, Melissa H. [1 ,2 ]
机构
[1] Beth Israel Deaconess Med Ctr, Dept Obstet & Gynecol, Boston, MA 02215 USA
[2] Harvard Med Sch, Dept Obstet Gynecol & Reprod Biol, Boston, MA 02115 USA
[3] Univ Penn, Dept Obstet & Gynecol, Perelman Sch Med, Maternal & Child Hlth Res Ctr, Philadelphia, PA 19104 USA
[4] Harvard Med Sch, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
Cell-free DNA; Fetal fraction; Placental dysfunction; Hypertensive disease in pregnancy; MATERNAL PLASMA; SIZE DISTRIBUTIONS; ORIGIN;
D O I
10.1016/j.preghy.2019.04.002
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To examine the association of low fetal fraction of cell-free DNA (cfDNA) with placental compromise and adverse perinatal outcomes. Materials and methods: This was a retrospective cohort utilizing a sample of convenience including 639 women undergoing cfDNA screening at our institution from January 2013 to January 2017. Low fetal fraction was defined as less than the 25th percentile. Indicators of placental compromise were examined individually and as a composite outcome, including hypertensive disease of pregnancy, intrauterine growth restriction, abruption, and oligohydramnios. Neonatal outcomes, including preterm delivery, low Apgar scores, and small for gestational age, also were examined. We calculated risk ratios (RR) and 95% confidence intervals (CI). Results: Low fetal fraction was associated with placental compromise (RR 1.6 [CI 1.1-2.2]), hypertensive disease of pregnancy (RR 1.6 [CI 1.003-2.6]), and preeclampsia with severe features (RR 3.3 [CI 1.2-8.9]). Low fetal faction was not associated with preterm delivery, low Apgar scores, or small for gestational age. Conclusions: Low fetal fraction of cfDNA among asymptomatic women may serve as a predictor of subsequent placental dysfunction and hypertensive disease.
引用
收藏
页码:148 / 153
页数:6
相关论文
共 47 条
[1]  
Al Nakib M., 2009, FETAL DIAGN THER
[2]   Free fetal DNA in maternal plasma in anembryonic pregnancies: confirmation that the origin is the trophoblast [J].
Alberry, M. ;
Maddocks, D. ;
Jones, M. ;
Hadi, M. Abdel ;
Abdel-Fattah, S. ;
Avent, N. ;
Soothill, P. W. .
PRENATAL DIAGNOSIS, 2007, 27 (05) :415-418
[3]   Quantification of cell free fetal DNA in maternal plasma in normal pregnancies and in pregnancies with placental dysfunction [J].
Alberry, Medhat S. ;
Maddocks, Deborah G. ;
Hadi, Medhat A. ;
Metawi, Helmi ;
Hunt, Linda P. ;
Abdel-Fattah, Sherif A. ;
Avent, Neil D. ;
Soothill, Peter W. .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2009, 200 (01) :98.e1-98.e6
[4]  
[Anonymous], 2015, OBSTET GYNECOL, V126, pE31, DOI 10.1097/01.AOG.0000471172.63927.b6
[5]   Fetal fraction in maternal plasma cell-free DNA at 11-13 weeks' gestation: relation to maternal and fetal characteristics [J].
Ashoor, G. ;
Syngelaki, A. ;
Poon, L. C. Y. ;
Rezende, J. C. ;
Nicolaides, K. H. .
ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2013, 41 (01) :26-32
[6]  
Bender W., 2018, AM J PERINATOL
[7]   Aneuploidy screening: a position statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, January 2011 [J].
Benn, Peter ;
Borrell, Antoni ;
Crossley, Jenny ;
Cuckle, Howard ;
Dugoff, Lorraine ;
Gross, Susan ;
Johnson, Jo-ann ;
Maymon, Ron ;
Odibo, Anthony ;
Schielen, Peter ;
Spencer, Kevin ;
Wright, Dave ;
Yaron, Yuval .
PRENATAL DIAGNOSIS, 2011, 31 (06) :519-522
[8]  
Bianchi D. W., 2014, OBSTET GYNECOL SURV
[9]  
Brown MA., 2018, HYPERTENSION
[10]  
Burns W, 2017, PRENAT DIAGN