Literature DB >> 29958880

Non-invasive prenatal aneuploidy testing: Critical diagnostic performance parameters predict sample z-score values.

Jonatan Blais1, Sylvie Giroux2, André Caron2, Valérie Clément2, Alexandre Dionne-Laporte3, Loubna Jouan4, Julie Gauthier4, Tina MacLeod5, Richard Moore5, Jeremy Parker5, Lucas Swanson5, Yongjun Zhao5, Guy Rouleau3, Aly Karsan6, Sylvie Langlois7, François Rousseau8.   

Abstract

OBJECTIVES: Non-invasive prenatal aneuploidy testing (NIPT) by next-generation sequencing of circulating cell-free DNA in maternal plasma relies on chromosomal ratio (chrratio) measurements to detect aneuploid values that depart from euploid ratios. Diagnostic performances are known to depend on the fraction of fetal DNA (FF) present in maternal plasma, although how this translates into specific quantitative changes in specificity/positive predictive values and which other variables might also be important is not well understood. DESIGN &
METHODS: To explore this issue, theoretical relationships between FF and various measures of diagnostic performances were assessed for a range of parameter values. Empirical data from three NIPT assays were then used to validate theoretical calculations.
RESULTS: For a given positivity threshold, dramatic changes in specificity and positive predictive values (PPV) as a function of both FF and the coefficient of variation (CV) of the chrratio measurement were observed. Theoretically predicted and observed chrratio z-scores agreed closely, confirming the determinant impact of small changes in both FF and chrratio CV.
CONCLUSIONS: Evaluation of NIPT assay performances therefore requires knowledge of the FF distribution in the population in which the test is intended to be used and, in particular, of the precise value of the assay chrratio CV for each chromosome or genomic region of interest. Laboratories offering NIPT testing should carefully measure these parameters to ensure test reliability and clinical usefulness in interpreting individual patients' results.
Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Down syndrome; Fetal DNA; NIPT; Next-generation sequencing; Non-invasive prenatal testing; cffDNA

Mesh:

Year:  2018        PMID: 29958880     DOI: 10.1016/j.clinbiochem.2018.06.015

Source DB:  PubMed          Journal:  Clin Biochem        ISSN: 0009-9120            Impact factor:   3.281


  1 in total

1.  Prospective head-to-head comparison of accuracy of two sequencing platforms for screening for fetal aneuploidy by cell-free DNA: the PEGASUS study.

Authors:  François Rousseau; Sylvie Langlois; Jo-Ann Johnson; Jean Gekas; Emmanuel Bujold; François Audibert; Mark Walker; Sylvie Giroux; André Caron; Valérie Clément; Jonatan Blais; Tina MacLeod; Richard Moore; Julie Gauthier; Loubna Jouan; Alexandre Laporte; Ousmane Diallo; Jeremy Parker; Lucas Swanson; Yongjun Zhao; Yves Labelle; Yves Giguère; Jean-Claude Forest; Julian Little; Aly Karsan; Guy Rouleau
Journal:  Eur J Hum Genet       Date:  2019-06-23       Impact factor: 4.246

  1 in total

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