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Not all low fetal fraction cell‐free DNA screening failures are at increased risk for aneuploidy
OBJECTIVE: To evaluate cell‐free DNA (cfDNA) redraws and pregnancy outcomes following low fetal fraction (FF) cfDNA failures, as it has been suggested that a failed cfDNA screen due to insufficient FF carries increased risk for fetal aneuploidy. METHODS: Here >200,000 consecutive samples were rev...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596865/ https://www.ncbi.nlm.nih.gov/pubmed/33682142 http://dx.doi.org/10.1002/pd.5918 |
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author | Caldwell, Samantha Almasri, Eyad Schmidt, Lindsey Xu, Chen Dyr, Brittany Wardrop, Jenna Cacheris, Philip |
author_facet | Caldwell, Samantha Almasri, Eyad Schmidt, Lindsey Xu, Chen Dyr, Brittany Wardrop, Jenna Cacheris, Philip |
author_sort | Caldwell, Samantha |
collection | PubMed |
description | OBJECTIVE: To evaluate cell‐free DNA (cfDNA) redraws and pregnancy outcomes following low fetal fraction (FF) cfDNA failures, as it has been suggested that a failed cfDNA screen due to insufficient FF carries increased risk for fetal aneuploidy. METHODS: Here >200,000 consecutive samples were reviewed and >1,100 patients were identified with a failed cfDNA due to low FF using genome‐wide massively parallel sequencing. Redraw results following the initial low FF failure were analyzed, as well as pregnancy outcomes for patients with repeated low FF failure on redraw. RESULTS: Upon redraw 84.2% of samples yielded a reportable result with no enrichment of aneuploidy observed (p = 0.332). Higher maternal weights and multifetal pregnancy rates were observed in samples with insufficient FF. In patients with repeated low FF failure on redraw, almost all pregnancies resulted in apparently healthy liveborns. CONCLUSION: Insufficient FF was not an indicator of aneuploidy risk or adverse pregnancy outcomes in this study. Caution should be taken in generalizing aneuploidy risk to all low FF cfDNA failures. Redrawing may be an appropriate next step, as proceeding directly with diagnostic testing for aneuploidy may be unwarranted for most patients. |
format | Online Article Text |
id | pubmed-8596865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85968652021-11-22 Not all low fetal fraction cell‐free DNA screening failures are at increased risk for aneuploidy Caldwell, Samantha Almasri, Eyad Schmidt, Lindsey Xu, Chen Dyr, Brittany Wardrop, Jenna Cacheris, Philip Prenat Diagn Original Articles OBJECTIVE: To evaluate cell‐free DNA (cfDNA) redraws and pregnancy outcomes following low fetal fraction (FF) cfDNA failures, as it has been suggested that a failed cfDNA screen due to insufficient FF carries increased risk for fetal aneuploidy. METHODS: Here >200,000 consecutive samples were reviewed and >1,100 patients were identified with a failed cfDNA due to low FF using genome‐wide massively parallel sequencing. Redraw results following the initial low FF failure were analyzed, as well as pregnancy outcomes for patients with repeated low FF failure on redraw. RESULTS: Upon redraw 84.2% of samples yielded a reportable result with no enrichment of aneuploidy observed (p = 0.332). Higher maternal weights and multifetal pregnancy rates were observed in samples with insufficient FF. In patients with repeated low FF failure on redraw, almost all pregnancies resulted in apparently healthy liveborns. CONCLUSION: Insufficient FF was not an indicator of aneuploidy risk or adverse pregnancy outcomes in this study. Caution should be taken in generalizing aneuploidy risk to all low FF cfDNA failures. Redrawing may be an appropriate next step, as proceeding directly with diagnostic testing for aneuploidy may be unwarranted for most patients. John Wiley and Sons Inc. 2021-03-08 2021-10 /pmc/articles/PMC8596865/ /pubmed/33682142 http://dx.doi.org/10.1002/pd.5918 Text en © 2021 Laboratory operation of America. Prenatal Diagnosis published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Caldwell, Samantha Almasri, Eyad Schmidt, Lindsey Xu, Chen Dyr, Brittany Wardrop, Jenna Cacheris, Philip Not all low fetal fraction cell‐free DNA screening failures are at increased risk for aneuploidy |
title | Not all low fetal fraction cell‐free DNA screening failures are at increased risk for aneuploidy |
title_full | Not all low fetal fraction cell‐free DNA screening failures are at increased risk for aneuploidy |
title_fullStr | Not all low fetal fraction cell‐free DNA screening failures are at increased risk for aneuploidy |
title_full_unstemmed | Not all low fetal fraction cell‐free DNA screening failures are at increased risk for aneuploidy |
title_short | Not all low fetal fraction cell‐free DNA screening failures are at increased risk for aneuploidy |
title_sort | not all low fetal fraction cell‐free dna screening failures are at increased risk for aneuploidy |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596865/ https://www.ncbi.nlm.nih.gov/pubmed/33682142 http://dx.doi.org/10.1002/pd.5918 |
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