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The Number of Circulating Fetal Extravillous Trophoblasts Varies from Gestational Week 6 to 20

Cell-based non-invasive prenatal testing (cbNIPT) based on circulating fetal extravillous trophoblasts (fEVTs) has shown to be possible in gestational week (GW) 10–13. Prenatal testing is relevant for a wider time period than GW 10–13, but it is unclear if fEVTs are present in sufficient numbers for...

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Autores principales: Ravn, Katarina, Singh, Ripudaman, Hatt, Lotte, Kølvraa, Mathias, Schelde, Palle, Vogel, Ida, Uldbjerg, Niels, Hindkjær, Johnny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593292/
https://www.ncbi.nlm.nih.gov/pubmed/32602048
http://dx.doi.org/10.1007/s43032-020-00243-1
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author Ravn, Katarina
Singh, Ripudaman
Hatt, Lotte
Kølvraa, Mathias
Schelde, Palle
Vogel, Ida
Uldbjerg, Niels
Hindkjær, Johnny
author_facet Ravn, Katarina
Singh, Ripudaman
Hatt, Lotte
Kølvraa, Mathias
Schelde, Palle
Vogel, Ida
Uldbjerg, Niels
Hindkjær, Johnny
author_sort Ravn, Katarina
collection PubMed
description Cell-based non-invasive prenatal testing (cbNIPT) based on circulating fetal extravillous trophoblasts (fEVTs) has shown to be possible in gestational week (GW) 10–13. Prenatal testing is relevant for a wider time period than GW 10–13, but it is unclear if fEVTs are present in sufficient numbers for cbNIPT at other time points during pregnancy. We present the first longitudinal study where the number of circulating fEVTs was determined from the mid first trimester to the mid second, specifically GW 6–8, 12–13, and 19–20. Blood samples from 13 women opting for assisted reproduction were collected at GW 6–8, 12–13, and 19–20. fEVTs were enriched using a magnetic-activated cell sorting system, stained with anti-cytokeratin antibodies, and fEVTs were identified with the use of a MetaSystem fluorescence microscope scanner. Blood samples drawn at GW 6–8 yielded an average of 5.5 fEVTs per 30 mL of blood. This increased significantly to an average of 11.8 in GW 12–13 (P value: 0.0070, Mann-Whitney test), and decreased significantly to an average of 5.3 in GW 19–20 (P value: 0.0063, Mann-Whitney test). In 9 out of 13 cases, the number of fEVTs peaked in GW 12–13 compared to GW 6–8 and GW 19–20. For the majority of cases, fEVTs can be identified at GW 6–8 and GW 19–20, but the highest number of fEVTs is observed at GW 12–13 indicating this is the optimal time point for cbNIPT.
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spelling pubmed-75932922020-11-10 The Number of Circulating Fetal Extravillous Trophoblasts Varies from Gestational Week 6 to 20 Ravn, Katarina Singh, Ripudaman Hatt, Lotte Kølvraa, Mathias Schelde, Palle Vogel, Ida Uldbjerg, Niels Hindkjær, Johnny Reprod Sci Placenta: Original Article Cell-based non-invasive prenatal testing (cbNIPT) based on circulating fetal extravillous trophoblasts (fEVTs) has shown to be possible in gestational week (GW) 10–13. Prenatal testing is relevant for a wider time period than GW 10–13, but it is unclear if fEVTs are present in sufficient numbers for cbNIPT at other time points during pregnancy. We present the first longitudinal study where the number of circulating fEVTs was determined from the mid first trimester to the mid second, specifically GW 6–8, 12–13, and 19–20. Blood samples from 13 women opting for assisted reproduction were collected at GW 6–8, 12–13, and 19–20. fEVTs were enriched using a magnetic-activated cell sorting system, stained with anti-cytokeratin antibodies, and fEVTs were identified with the use of a MetaSystem fluorescence microscope scanner. Blood samples drawn at GW 6–8 yielded an average of 5.5 fEVTs per 30 mL of blood. This increased significantly to an average of 11.8 in GW 12–13 (P value: 0.0070, Mann-Whitney test), and decreased significantly to an average of 5.3 in GW 19–20 (P value: 0.0063, Mann-Whitney test). In 9 out of 13 cases, the number of fEVTs peaked in GW 12–13 compared to GW 6–8 and GW 19–20. For the majority of cases, fEVTs can be identified at GW 6–8 and GW 19–20, but the highest number of fEVTs is observed at GW 12–13 indicating this is the optimal time point for cbNIPT. Springer International Publishing 2020-06-29 /pmc/articles/PMC7593292/ /pubmed/32602048 http://dx.doi.org/10.1007/s43032-020-00243-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Placenta: Original Article
Ravn, Katarina
Singh, Ripudaman
Hatt, Lotte
Kølvraa, Mathias
Schelde, Palle
Vogel, Ida
Uldbjerg, Niels
Hindkjær, Johnny
The Number of Circulating Fetal Extravillous Trophoblasts Varies from Gestational Week 6 to 20
title The Number of Circulating Fetal Extravillous Trophoblasts Varies from Gestational Week 6 to 20
title_full The Number of Circulating Fetal Extravillous Trophoblasts Varies from Gestational Week 6 to 20
title_fullStr The Number of Circulating Fetal Extravillous Trophoblasts Varies from Gestational Week 6 to 20
title_full_unstemmed The Number of Circulating Fetal Extravillous Trophoblasts Varies from Gestational Week 6 to 20
title_short The Number of Circulating Fetal Extravillous Trophoblasts Varies from Gestational Week 6 to 20
title_sort number of circulating fetal extravillous trophoblasts varies from gestational week 6 to 20
topic Placenta: Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593292/
https://www.ncbi.nlm.nih.gov/pubmed/32602048
http://dx.doi.org/10.1007/s43032-020-00243-1
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