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Ploidy Testing of Blastocoel Fluid for Screening May Be Technically Challenging and More Invasive Than That of Spent Cell Culture Media

BACKGROUND: Recent studies have demonstrated that both blastocoel fluid (BF) and spent cell culture media (SCM) have potential as materials for non-invasive or less-invasive pre-implantation genetic analysis. BF may allow more opportunity to obtain cell-free DNA from the inner cell mass (ICM), and i...

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Autores principales: Shi, Wenhao, Zhao, Zhenghao, Xue, Xia, Li, Qian, Yao, Yaxin, Wang, Dongyang, Wang, Jing, Lu, Sijia, Shi, Juanzi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8900197/
https://www.ncbi.nlm.nih.gov/pubmed/35264976
http://dx.doi.org/10.3389/fphys.2022.794210
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author Shi, Wenhao
Zhao, Zhenghao
Xue, Xia
Li, Qian
Yao, Yaxin
Wang, Dongyang
Wang, Jing
Lu, Sijia
Shi, Juanzi
author_facet Shi, Wenhao
Zhao, Zhenghao
Xue, Xia
Li, Qian
Yao, Yaxin
Wang, Dongyang
Wang, Jing
Lu, Sijia
Shi, Juanzi
author_sort Shi, Wenhao
collection PubMed
description BACKGROUND: Recent studies have demonstrated that both blastocoel fluid (BF) and spent cell culture media (SCM) have potential as materials for non-invasive or less-invasive pre-implantation genetic analysis. BF may allow more opportunity to obtain cell-free DNA from the inner cell mass (ICM), and it has a lower risk of containing contaminant DNA from cumulus cells, sperm and culture media. There are no data regarding the ICM as a gold standard to evaluate the chromosome constitution of BF or SCM for embryo liquid biopsy. METHODS: Two hundred eighteen donated human blastocysts were warmed and cultured in blastocyst culture media for 18–24 h. The corresponding SCM was collected, and only clear ICM was biopsied in blastocysts; otherwise, the whole blastocyst (WB) was biopsied. Quantitative PCR was performed to determine the DNA levels in the SCM and BF before and after amplification. ChromInst was used to amplify BF/SCM and blastocyst DNA before sequencing. Chromosomal copy number variation (CNV) was investigated to evaluate the chromosome constitution. RESULTS: In total, 212 blastocysts were available for SCM and BF collection. The technical success rates (next-generation sequencing data) were 100 and 69.8% (148/212) for SCM and BF, respectively. Among the 148 blastocysts with both SCM and BF data, 101 were euploid and 47 were aneuploid based on ICM (n = 89) or WB (n = 59) analysis as the gold standard. Among all blastocysts, SCM was comparable to BF [specificity: 80.2 versus 61.4% (P = 0.005, χ(2) test); sensitivity: 91.5 versus 87.2% (P = 0.738, χ(2) test); negative predictive value (NPV): 95.3 versus 91.2% (P = 0.487, χ(2) test); positive predictive value (PPV): 68.3% versus 51.3% (P = 0.042, χ(2) test)]. The SCM and BF samples were 83.8% (124/148) and 69.6% (103/148) concordant with the corresponding ICM/WB samples when only two categories, euploid or aneuploid/mosaic, were grouped to calculate the concordance. CONCLUSIONS: Compared with BF, SCM has superior diagnostic performance, and it is non-invasive for embryos. CLINICAL TRIAL REGISTRATION: [http://www.chictr.org.cn], identifier [ChiCTR-BPD-17014087].
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spelling pubmed-89001972022-03-08 Ploidy Testing of Blastocoel Fluid for Screening May Be Technically Challenging and More Invasive Than That of Spent Cell Culture Media Shi, Wenhao Zhao, Zhenghao Xue, Xia Li, Qian Yao, Yaxin Wang, Dongyang Wang, Jing Lu, Sijia Shi, Juanzi Front Physiol Physiology BACKGROUND: Recent studies have demonstrated that both blastocoel fluid (BF) and spent cell culture media (SCM) have potential as materials for non-invasive or less-invasive pre-implantation genetic analysis. BF may allow more opportunity to obtain cell-free DNA from the inner cell mass (ICM), and it has a lower risk of containing contaminant DNA from cumulus cells, sperm and culture media. There are no data regarding the ICM as a gold standard to evaluate the chromosome constitution of BF or SCM for embryo liquid biopsy. METHODS: Two hundred eighteen donated human blastocysts were warmed and cultured in blastocyst culture media for 18–24 h. The corresponding SCM was collected, and only clear ICM was biopsied in blastocysts; otherwise, the whole blastocyst (WB) was biopsied. Quantitative PCR was performed to determine the DNA levels in the SCM and BF before and after amplification. ChromInst was used to amplify BF/SCM and blastocyst DNA before sequencing. Chromosomal copy number variation (CNV) was investigated to evaluate the chromosome constitution. RESULTS: In total, 212 blastocysts were available for SCM and BF collection. The technical success rates (next-generation sequencing data) were 100 and 69.8% (148/212) for SCM and BF, respectively. Among the 148 blastocysts with both SCM and BF data, 101 were euploid and 47 were aneuploid based on ICM (n = 89) or WB (n = 59) analysis as the gold standard. Among all blastocysts, SCM was comparable to BF [specificity: 80.2 versus 61.4% (P = 0.005, χ(2) test); sensitivity: 91.5 versus 87.2% (P = 0.738, χ(2) test); negative predictive value (NPV): 95.3 versus 91.2% (P = 0.487, χ(2) test); positive predictive value (PPV): 68.3% versus 51.3% (P = 0.042, χ(2) test)]. The SCM and BF samples were 83.8% (124/148) and 69.6% (103/148) concordant with the corresponding ICM/WB samples when only two categories, euploid or aneuploid/mosaic, were grouped to calculate the concordance. CONCLUSIONS: Compared with BF, SCM has superior diagnostic performance, and it is non-invasive for embryos. CLINICAL TRIAL REGISTRATION: [http://www.chictr.org.cn], identifier [ChiCTR-BPD-17014087]. Frontiers Media S.A. 2022-02-21 /pmc/articles/PMC8900197/ /pubmed/35264976 http://dx.doi.org/10.3389/fphys.2022.794210 Text en Copyright © 2022 Shi, Zhao, Xue, Li, Yao, Wang, Wang, Lu and Shi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Shi, Wenhao
Zhao, Zhenghao
Xue, Xia
Li, Qian
Yao, Yaxin
Wang, Dongyang
Wang, Jing
Lu, Sijia
Shi, Juanzi
Ploidy Testing of Blastocoel Fluid for Screening May Be Technically Challenging and More Invasive Than That of Spent Cell Culture Media
title Ploidy Testing of Blastocoel Fluid for Screening May Be Technically Challenging and More Invasive Than That of Spent Cell Culture Media
title_full Ploidy Testing of Blastocoel Fluid for Screening May Be Technically Challenging and More Invasive Than That of Spent Cell Culture Media
title_fullStr Ploidy Testing of Blastocoel Fluid for Screening May Be Technically Challenging and More Invasive Than That of Spent Cell Culture Media
title_full_unstemmed Ploidy Testing of Blastocoel Fluid for Screening May Be Technically Challenging and More Invasive Than That of Spent Cell Culture Media
title_short Ploidy Testing of Blastocoel Fluid for Screening May Be Technically Challenging and More Invasive Than That of Spent Cell Culture Media
title_sort ploidy testing of blastocoel fluid for screening may be technically challenging and more invasive than that of spent cell culture media
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8900197/
https://www.ncbi.nlm.nih.gov/pubmed/35264976
http://dx.doi.org/10.3389/fphys.2022.794210
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