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Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis

From January 1(st) 2013 to August 31(st) 2016, 24408 pregnant women received the first trimester Combined test and contingently offered second trimester maternal serum screening to identify those women who would most benefit from invasive prenatal diagnosis (IPD). The screening was based on first tr...

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Autores principales: Guanciali Franchi, Paolo, Palka, Chiara, Morizio, Elisena, Sabbatinelli, Giulia, Alfonsi, Melissa, Fantasia, Donatella, Sitar, Giammaria, Benn, Peter, Calabrese, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720779/
https://www.ncbi.nlm.nih.gov/pubmed/29216282
http://dx.doi.org/10.1371/journal.pone.0189235
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author Guanciali Franchi, Paolo
Palka, Chiara
Morizio, Elisena
Sabbatinelli, Giulia
Alfonsi, Melissa
Fantasia, Donatella
Sitar, Giammaria
Benn, Peter
Calabrese, Giuseppe
author_facet Guanciali Franchi, Paolo
Palka, Chiara
Morizio, Elisena
Sabbatinelli, Giulia
Alfonsi, Melissa
Fantasia, Donatella
Sitar, Giammaria
Benn, Peter
Calabrese, Giuseppe
author_sort Guanciali Franchi, Paolo
collection PubMed
description From January 1(st) 2013 to August 31(st) 2016, 24408 pregnant women received the first trimester Combined test and contingently offered second trimester maternal serum screening to identify those women who would most benefit from invasive prenatal diagnosis (IPD). The screening was based on first trimester cut-offs of ≥1:30 (IPD indicated), 1:31 to 1:899 (second trimester screening indicated) and ≤1:900 (no further action), and a second trimester cut-off of ≥1:250. From January 2014, analysis of fetal cells from peripheral maternal blood was also offered to women with positive screening results. For fetal Down syndrome, the overall detection rate was 96.8% for a false-positive rate of 2.8% resulting in an odds of being affected given a positive result (OAPR) of 1:11, equivalent to a positive predictive value (PPV) of 8.1%. Additional chromosome abnormalities were also identified resulting in an OAPR for any chromosome abnormality of 1:6.6 (PPV 11.9%). For a sub-set of cases with positive contingent test results, FISH analysis of circulating fetal cells in maternal circulation identified 7 abnormal and 39 as normal cases with 100% specificity and 100% sensitivity. We conclude that contingent screening using conventional Combined and second trimester screening tests is effective but can potentially be considerably enhanced through the addition of fetal cell analysis.
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spelling pubmed-57207792017-12-15 Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis Guanciali Franchi, Paolo Palka, Chiara Morizio, Elisena Sabbatinelli, Giulia Alfonsi, Melissa Fantasia, Donatella Sitar, Giammaria Benn, Peter Calabrese, Giuseppe PLoS One Research Article From January 1(st) 2013 to August 31(st) 2016, 24408 pregnant women received the first trimester Combined test and contingently offered second trimester maternal serum screening to identify those women who would most benefit from invasive prenatal diagnosis (IPD). The screening was based on first trimester cut-offs of ≥1:30 (IPD indicated), 1:31 to 1:899 (second trimester screening indicated) and ≤1:900 (no further action), and a second trimester cut-off of ≥1:250. From January 2014, analysis of fetal cells from peripheral maternal blood was also offered to women with positive screening results. For fetal Down syndrome, the overall detection rate was 96.8% for a false-positive rate of 2.8% resulting in an odds of being affected given a positive result (OAPR) of 1:11, equivalent to a positive predictive value (PPV) of 8.1%. Additional chromosome abnormalities were also identified resulting in an OAPR for any chromosome abnormality of 1:6.6 (PPV 11.9%). For a sub-set of cases with positive contingent test results, FISH analysis of circulating fetal cells in maternal circulation identified 7 abnormal and 39 as normal cases with 100% specificity and 100% sensitivity. We conclude that contingent screening using conventional Combined and second trimester screening tests is effective but can potentially be considerably enhanced through the addition of fetal cell analysis. Public Library of Science 2017-12-07 /pmc/articles/PMC5720779/ /pubmed/29216282 http://dx.doi.org/10.1371/journal.pone.0189235 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Guanciali Franchi, Paolo
Palka, Chiara
Morizio, Elisena
Sabbatinelli, Giulia
Alfonsi, Melissa
Fantasia, Donatella
Sitar, Giammaria
Benn, Peter
Calabrese, Giuseppe
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis
title Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis
title_full Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis
title_fullStr Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis
title_full_unstemmed Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis
title_short Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis
title_sort sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720779/
https://www.ncbi.nlm.nih.gov/pubmed/29216282
http://dx.doi.org/10.1371/journal.pone.0189235
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