Cell-free fetal DNA analysis in maternal plasma as screening test for trisomies 21, 18 and 13 in twin pregnancy

被引:37
|
作者
Le Conte, G. [1 ,2 ]
Letourneau, A. [1 ,2 ]
Jani, J. [3 ]
Kleinfinger, P. [4 ]
Lohmann, L. [4 ]
Costa, J-M. [4 ]
Benachi, A. [1 ,2 ]
机构
[1] Hop Antoine Beclere, AP HP, Serv Gynecol Obstet & Med Reprod, Clamart, France
[2] Univ Paris Sud, Le Kremlin Bicetre, France
[3] Univ Libre Bruxelles, Univ Hosp Brugmann, Dept Obstet & Gynecol, Brussels, Belgium
[4] Lab CERBA, St Ouen, France
关键词
cell-free DNA; non-invasive prenatal testing; twin pregnancy; 1ST TRIMESTER; DOWN-SYNDROME; ANEUPLOIDY DETECTION; BLOOD; AMNIOCENTESIS; METAANALYSIS; PERFORMANCE; ZYGOSITY; IMPACT; ART;
D O I
10.1002/uog.18838
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
Objectives To evaluate in twin pregnancy the utility of non-invasive prenatal testing using circulating cell-free fetal DNA (cfDNA) in screening for the three main autosomal fetal trisomies. Methods cfDNA testing was offered to 492 patients with a twin pregnancy without ultrasound anomaly as a first-line screening test or after routine serum screening. Data were collected prospectively and a retrospective analysis was performed. cfDNA analysis was performed by massively parallel sequencing. The fetal-fraction threshold used for test evaluation was 8%. Regression analysis was performed to investigate the effect on the test failure rate of maternal and pregnancy characteristics, and the performance of the test was also reported. Results cfDNA analysis was performed as a first-line test (after the first-trimester scan) in 377 patients and following serum screening in 115. Of the 420 pregnancies for which outcome was available and cfDNA screening was assessed, 78.7% were dichorionic-diamniotic. The test failed on the first attempt in 12 (2.9%) pregnancies, and regression analysis demonstrated that only maternal weight was a significant independent predictor of test failure. A result was subsequently achieved in the 10 cases for which a second sample was obtained. cfDNA analysis identified all three cases of trisomy 21 and the only case of trisomy 18. For trisomy 21, the specificity was 99.8% (95% CI, 98.7-100.0%). When considering pregnancies according to whether they were conceived spontaneously or after assisted reproductive technology, there were no significant differences in terms of maternal weight or no-result rate for cfDNA screening between these two groups. Conclusions In twin pregnancy without fetal ultrasound abnormality, cfDNA screening for trisomies 21, 18 and 13 had a high success rate and good performance. Therefore, in routine practice, cfDNA analysis could be considered as a first- or second-line screening test. Copyright (c) 2017 ISUOG. Published by John Wiley & Sons Ltd.
引用
收藏
页码:318 / 324
页数:7
相关论文
共 50 条
  • [2] Cell-free fetal DNA analysis in maternal plasma as a screening test for trisomy 21 in twin pregnancies
    Le Conte, G.
    Letourneau, A.
    Jani, J.
    Kleinfinger, P.
    Lohmann, L.
    Costa, J-M
    Benachi, A.
    GYNECOLOGIE OBSTETRIQUE FERTILITE & SENOLOGIE, 2018, 46 (7-8): : 580 - 586
  • [3] Clinical validation of a novel automated cell-free DNA screening assay for trisomies 21, 13, and 18 in maternal plasma
    Ericsson, Olle
    Ahola, Tarja
    Dahl, Fredrik
    Karlsson, Filip
    Persson, Fredrik
    Karlberg, Olof
    Roos, Fredrik
    Alftren, Ida
    Andersson, Bjorn
    Barkenas, Emelie
    Boghos, Ani
    Brandner, Birgit
    Dahlberg, Jenny
    Forsgren, Per-Ola
    Francois, Niels
    Gousseva, Anna
    Hakamali, Faizan
    Janfalk-Carlsson, Asa
    Johansson, Henrik
    Lundgren, Johanna
    Mohsenchian, Atefeh
    Olausson, Linus
    Olofsson, Simon
    Qureshi, Atif
    Skarpas, Bjorn
    Svahn, Peter
    Savneby, Anna
    Astrom, Eva
    Sahlberg, Anna
    Fianu-Jonasson, Aino
    Gautier, Jeremie
    Costa, Jean-Marc
    Jacobsson, Bo
    Nicolaides, Kypros
    PRENATAL DIAGNOSIS, 2019, 39 (11) : 1011 - 1015
  • [4] Massively Parallel Sequencing (MPS) of Cell-Free Fetal DNA (cffDNA) for Trisomies 21, 18, and 13 in Twin Pregnancies
    Du, Erqiu
    Feng, Chun
    Cao, Yuming
    Yao, Yanru
    Lu, Jing
    Zhang, Yuanzhen
    TWIN RESEARCH AND HUMAN GENETICS, 2017, 20 (03) : 242 - 249
  • [5] Screening for trisomies 21, 18 and 13 by cell-free DNA analysis of maternal blood at 10-11 weeks' gestation and the combined test at 11-13 weeks
    Quezada, M. S.
    Gil, M. M.
    Francisco, C.
    Orosz, G.
    Nicolaides, K. H.
    ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2015, 45 (01) : 36 - 41
  • [6] First-Trimester Contingent Screening for Trisomies 21, 18 and 13 by Biomarkers and Maternal Blood Cell-Free DNA Testing
    Nicolaides, K. H.
    Syngelaki, A.
    Poon, L. C.
    Gil, M. M.
    Wright, D.
    FETAL DIAGNOSIS AND THERAPY, 2014, 35 (03) : 185 - 192
  • [7] Clinical experience of noninvasive prenatal testing with cell-free DNA for fetal trisomies 21, 18, and 13, in a general screening population
    Fairbrother, Genevieve
    Johnson, Shayla
    Musci, Thomas J.
    Song, Ken
    PRENATAL DIAGNOSIS, 2013, 33 (06) : 580 - 583
  • [8] Routine first-trimester screening for fetal trisomies in twin pregnancy: cell-free DNA test contingent on results from combined test
    Galeva, S.
    Konstantinidou, L.
    Gil, M. M.
    Akolekar, R.
    Nicolaides, K. H.
    ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2019, 53 (02) : 208 - 213
  • [9] Routine First-Trimester Screening for Fetal Trisomies in Twin Pregnancy: Cell-free DNA Test Contingent on Results From Combined Test
    Galeva, S.
    Konstantinidou, L.
    Gil, M. M.
    Akolekar, R.
    Nicolaides, K. H.
    OBSTETRICAL & GYNECOLOGICAL SURVEY, 2019, 74 (07) : 396 - 398
  • [10] Prospective first-trimester screening for trisomies by cell-free DNA testing of maternal blood in twin pregnancy
    Sarno, L.
    Revello, R.
    Hanson, E.
    Akolekar, R.
    Nicolaides, K. H.
    ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2016, 47 (06) : 705 - 711