Literature DB >> 27779757

Analysis of cell-free fetal DNA in maternal blood for detection of trisomy 21, 18 and 13 in a general pregnant population and in a high risk population - a systematic review and meta-analysis.

Erik Iwarsson1, Bo Jacobsson2,3, Jessica Dagerhamn4, Thomas Davidson4,5, Eduardo Bernabé6, Marianne Heibert Arnlind4,7.   

Abstract

INTRODUCTION: The aim of this study was to review the performance of non-invasive prenatal testing (NIPT) for detection of trisomy 21, 18 and 13 (T21, T18 and T13) in a general pregnant population as well as to update the data on high-risk pregnancies.
MATERIAL AND METHODS: Systematic review and meta-analysis. PubMed, Embase and the Cochrane Library were searched. Methodological quality was rated using QUADAS and scientific evidence using GRADE. Summary measures of diagnostic accuracy were calculated using a bivariate random-effects model.
RESULTS: In a general pregnant population, there is moderate evidence that the pooled sensitivity is 0.993 (95% CI 0.955-0.999) and specificity was 0.999 (95% CI 0.998-0.999) for the analysis of T21. Pooled sensitivity and specificity for T13 and T18 was not calculated in this population due to the low number of studies. In a high-risk pregnant population, there is moderate evidence that the pooled sensitivities for T21 and T18 are 0.998 (95% CI 0.981-0.999) and 0.977 (95% CI 0.958-0.987) respectively, and low evidence that the pooled sensitivity for T13 is 0.975 (95% CI 0.819-0.997). The pooled specificity for all three trisomies is 0.999 (95% CI 0.998-0.999).
CONCLUSIONS: This is the first meta-analysis using GRADE that shows that NIPT performs well as a screen for trisomy 21 in a general pregnant population. Although the false positive rate is low compared with first trimester combined screening, women should still be advised to confirm a positive result by invasive testing if termination of pregnancy is under consideration.
© 2016 Nordic Federation of Societies of Obstetrics and Gynecology.

Entities:  

Keywords:  zzm321990NIPTzzm321990; Trisomy; cell-free DNA; cfDNA; chromosome aberration; fetus; non-invasive prenatal testing; prenatal diagnosis

Mesh:

Substances:

Year:  2016        PMID: 27779757     DOI: 10.1111/aogs.13047

Source DB:  PubMed          Journal:  Acta Obstet Gynecol Scand        ISSN: 0001-6349            Impact factor:   3.636


  23 in total

1.  [Noninvasive prenatal genetic testing in 6804 pregnant women aged less than 35 years with positive results in serum screening].

Authors:  Xingkun Yang; Xiaoling Guo; Jin Zhong; Zhihua Chen; Shuijuan Wu
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2019-11-30

Review 2.  Cost-effectiveness of cell-free DNA in maternal blood testing for prenatal detection of trisomy 21, 18 and 13: a systematic review.

Authors:  Lidia García-Pérez; Renata Linertová; Margarita Álvarez-de-la-Rosa; Juan Carlos Bayón; Iñaki Imaz-Iglesia; Jorge Ferrer-Rodríguez; Pedro Serrano-Aguilar
Journal:  Eur J Health Econ       Date:  2017-12-16

3.  European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases.

Authors:  Arthur A M Wilde; Christopher Semsarian; Manlio F Márquez; Alireza Sepehri Shamloo; Michael J Ackerman; Euan A Ashley; Back Sternick Eduardo; Héctor Barajas-Martinez; Elijah R Behr; Connie R Bezzina; Jeroen Breckpot; Philippe Charron; Priya Chockalingam; Lia Crotti; Michael H Gollob; Steven Lubitz; Naomasa Makita; Seiko Ohno; Martín Ortiz-Genga; Luciana Sacilotto; Eric Schulze-Bahr; Wataru Shimizu; Nona Sotoodehnia; Rafik Tadros; James S Ware; David S Winlaw; Elizabeth S Kaufman; Takeshi Aiba; Andreas Bollmann; Jong-Il Choi; Aarti Dalal; Francisco Darrieux; John Giudicessi; Mariana Guerchicoff; Kui Hong; Andrew D Krahn; Ciorsti Mac Intyre; Judith A Mackall; Lluís Mont; Carlo Napolitano; Pablo Ochoa Juan; Petr Peichl; Alexandre C Pereira; Peter J Schwartz; Jon Skinner; Christoph Stellbrink; Jacob Tfelt-Hansen; Thomas Deneke
Journal:  J Arrhythm       Date:  2022-05-31

4.  Combining Z-Score and Maternal Copy Number Variation Analysis Increases the Positive Rate and Accuracy in Non-Invasive Prenatal Testing.

Authors:  Liheng Chen; Lihong Wang; Zhipeng Hu; Yilun Tao; Wenxia Song; Yu An; Xiaoze Li
Journal:  Front Genet       Date:  2022-06-02       Impact factor: 4.772

5.  European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases.

Authors:  Arthur A M Wilde; Christopher Semsarian; Manlio F Márquez; Alireza Sepehri Shamloo; Michael J Ackerman; Euan A Ashley; Eduardo Back Sternick; Héctor Barajas-Martinez; Elijah R Behr; Connie R Bezzina; Jeroen Breckpot; Philippe Charron; Priya Chockalingam; Lia Crotti; Michael H Gollob; Steven Lubitz; Naomasa Makita; Seiko Ohno; Martín Ortiz-Genga; Luciana Sacilotto; Eric Schulze-Bahr; Wataru Shimizu; Nona Sotoodehnia; Rafik Tadros; James S Ware; David S Winlaw; Elizabeth S Kaufman; Takeshi Aiba; Andreas Bollmann; Jong Il Choi; Aarti Dalal; Francisco Darrieux; John Giudicessi; Mariana Guerchicoff; Kui Hong; Andrew D Krahn; Ciorsti MacIntyre; Judith A Mackall; Lluís Mont; Carlo Napolitano; Juan Pablo Ochoa; Petr Peichl; Alexandre C Pereira; Peter J Schwartz; Jon Skinner; Christoph Stellbrink; Jacob Tfelt-Hansen; Thomas Deneke
Journal:  Europace       Date:  2022-09-01       Impact factor: 5.486

6.  Cell-Free Fetal DNA Increases Prior to Labor at Term and in a Subset of Preterm Births.

Authors:  Nardhy Gomez-Lopez; Roberto Romero; George Schwenkel; Valeria Garcia-Flores; Bogdan Panaitescu; Aneesha Varrey; Fatime Ayoub; Sonia S Hassan; Mark Phillippe
Journal:  Reprod Sci       Date:  2020-01-01       Impact factor: 3.060

7.  Noninvasive Prenatal Testing for Trisomies 21, 18, and 13, Sex Chromosome Aneuploidies, and Microdeletions: A Health Technology Assessment.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2019-02-19

8.  Increased nuchal translucency before 11 weeks of gestation: Reason for referral?

Authors:  Malou A Lugthart; Bo B Bet; Fleur Elsman; Karline van de Kamp; Bernadette S de Bakker; Ingeborg H Linskens; Merel C van Maarle; Elisabeth van Leeuwen; Eva Pajkrt
Journal:  Prenat Diagn       Date:  2021-10-08       Impact factor: 3.242

9.  Patient Preferences for Prenatal and Postpartum Care Delivery: A Survey of Postpartum Women.

Authors:  Alex Friedman Peahl; Alli Novara; Michele Heisler; Vanessa K Dalton; Michelle H Moniz; Roger D Smith
Journal:  Obstet Gynecol       Date:  2020-05       Impact factor: 7.623

10.  An incidental finding of maternal multiple myeloma by non invasive prenatal testing.

Authors:  Marion Imbert-Bouteille; Jean Chiesa; Jean-Baptiste Gaillard; Véronique Dorvaux; Lucille Altounian; Vincent Gatinois; Eve Mousty; Sanae Finge; Pascal Bourquard; Joris Robert Vermeesch; Eric Legius; Peter Vandenberghe
Journal:  Prenat Diagn       Date:  2017-11-28       Impact factor: 3.050

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