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Non-invasive preimplantation genetic testing for conventional IVF blastocysts

BACKGROUND: Previous studies suggested that non-invasive preimplantation genetic testing (niPGT) for intracytoplasmic sperm injection (ICSI) blastocysts can be used to identify chromosomal ploidy and chromosomal abnormalities. Here, we report the feasibility and performance of niPGT for conventional...

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Autores principales: Xie, Pingyuan, Zhang, Shuoping, Gu, Yifang, Jiang, Bo, Hu, Liang, Tan, Yue-qiu, Yao, Yaxin, Tang, Yi, Wan, Anqi, Cai, Sufen, Zou, Yangyun, Lu, Guangxiu, Wan, Cheng, Gong, Fei, Lu, Sijia, Lin, Ge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441092/
https://www.ncbi.nlm.nih.gov/pubmed/36058949
http://dx.doi.org/10.1186/s12967-022-03596-0
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author Xie, Pingyuan
Zhang, Shuoping
Gu, Yifang
Jiang, Bo
Hu, Liang
Tan, Yue-qiu
Yao, Yaxin
Tang, Yi
Wan, Anqi
Cai, Sufen
Zou, Yangyun
Lu, Guangxiu
Wan, Cheng
Gong, Fei
Lu, Sijia
Lin, Ge
author_facet Xie, Pingyuan
Zhang, Shuoping
Gu, Yifang
Jiang, Bo
Hu, Liang
Tan, Yue-qiu
Yao, Yaxin
Tang, Yi
Wan, Anqi
Cai, Sufen
Zou, Yangyun
Lu, Guangxiu
Wan, Cheng
Gong, Fei
Lu, Sijia
Lin, Ge
author_sort Xie, Pingyuan
collection PubMed
description BACKGROUND: Previous studies suggested that non-invasive preimplantation genetic testing (niPGT) for intracytoplasmic sperm injection (ICSI) blastocysts can be used to identify chromosomal ploidy and chromosomal abnormalities. Here, we report the feasibility and performance of niPGT for conventional in vitro fertilization (IVF) blastocysts. METHODS: This was a prospective observational study. In the preclinical stage, whole genome amplification and NGS were performed using the sperm spent culture medium (SCM). Then, trophectoderm (TE) biopsies and corresponding SCM derived from 27 conventional IVF monopronuclear embryos were collected. In the clinical stage, samples from 25 conventional IVF cycles and 37 ICSI cycles from April 2020–August 2021 were collected for performance evaluation. RESULTS: Preclinically, we confirmed failed sperm DNA amplification under the current amplification system. Subsequent niPGT from the 27 monopronuclear blastocysts showed 69.2% concordance with PGT results of corresponding TE biopsies. In the clinical stage, no paternal contamination was observed in any of the 161 SCM samples from conventional IVF. While maternal contamination was observed in 29.8% (48/161) SCM samples, only 2.5% (4/161) samples had a contamination ratio ≥ 50%. Compared with that of TE biopsy, the performances of NiPGT from 161 conventional IVF embryos and 122 ICSI embryos were not significantly different (P > 0.05), with ploidy concordance rates of 75% and 74.6% for IVF and ICSI methods, respectively. Finally, evaluation of the euploid probability of embryos with different types of niPGT results showed prediction probabilities of 82.8%, 77.8%, 62.5%, 50.0%, 40.9% and 18.4% for euploidy, sex-chromosome mosaics only, low-level mosaics, multiple abnormal chromosomes, high-level mosaics and aneuploidy, respectively. CONCLUSIONS: Our research results preliminarily confirm that the niPGT approach using SCM from conventional IVF has comparable performance with ICSI and might broadening the application scope of niPGT. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-022-03596-0.
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spelling pubmed-94410922022-09-05 Non-invasive preimplantation genetic testing for conventional IVF blastocysts Xie, Pingyuan Zhang, Shuoping Gu, Yifang Jiang, Bo Hu, Liang Tan, Yue-qiu Yao, Yaxin Tang, Yi Wan, Anqi Cai, Sufen Zou, Yangyun Lu, Guangxiu Wan, Cheng Gong, Fei Lu, Sijia Lin, Ge J Transl Med Research BACKGROUND: Previous studies suggested that non-invasive preimplantation genetic testing (niPGT) for intracytoplasmic sperm injection (ICSI) blastocysts can be used to identify chromosomal ploidy and chromosomal abnormalities. Here, we report the feasibility and performance of niPGT for conventional in vitro fertilization (IVF) blastocysts. METHODS: This was a prospective observational study. In the preclinical stage, whole genome amplification and NGS were performed using the sperm spent culture medium (SCM). Then, trophectoderm (TE) biopsies and corresponding SCM derived from 27 conventional IVF monopronuclear embryos were collected. In the clinical stage, samples from 25 conventional IVF cycles and 37 ICSI cycles from April 2020–August 2021 were collected for performance evaluation. RESULTS: Preclinically, we confirmed failed sperm DNA amplification under the current amplification system. Subsequent niPGT from the 27 monopronuclear blastocysts showed 69.2% concordance with PGT results of corresponding TE biopsies. In the clinical stage, no paternal contamination was observed in any of the 161 SCM samples from conventional IVF. While maternal contamination was observed in 29.8% (48/161) SCM samples, only 2.5% (4/161) samples had a contamination ratio ≥ 50%. Compared with that of TE biopsy, the performances of NiPGT from 161 conventional IVF embryos and 122 ICSI embryos were not significantly different (P > 0.05), with ploidy concordance rates of 75% and 74.6% for IVF and ICSI methods, respectively. Finally, evaluation of the euploid probability of embryos with different types of niPGT results showed prediction probabilities of 82.8%, 77.8%, 62.5%, 50.0%, 40.9% and 18.4% for euploidy, sex-chromosome mosaics only, low-level mosaics, multiple abnormal chromosomes, high-level mosaics and aneuploidy, respectively. CONCLUSIONS: Our research results preliminarily confirm that the niPGT approach using SCM from conventional IVF has comparable performance with ICSI and might broadening the application scope of niPGT. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-022-03596-0. BioMed Central 2022-09-04 /pmc/articles/PMC9441092/ /pubmed/36058949 http://dx.doi.org/10.1186/s12967-022-03596-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Xie, Pingyuan
Zhang, Shuoping
Gu, Yifang
Jiang, Bo
Hu, Liang
Tan, Yue-qiu
Yao, Yaxin
Tang, Yi
Wan, Anqi
Cai, Sufen
Zou, Yangyun
Lu, Guangxiu
Wan, Cheng
Gong, Fei
Lu, Sijia
Lin, Ge
Non-invasive preimplantation genetic testing for conventional IVF blastocysts
title Non-invasive preimplantation genetic testing for conventional IVF blastocysts
title_full Non-invasive preimplantation genetic testing for conventional IVF blastocysts
title_fullStr Non-invasive preimplantation genetic testing for conventional IVF blastocysts
title_full_unstemmed Non-invasive preimplantation genetic testing for conventional IVF blastocysts
title_short Non-invasive preimplantation genetic testing for conventional IVF blastocysts
title_sort non-invasive preimplantation genetic testing for conventional ivf blastocysts
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441092/
https://www.ncbi.nlm.nih.gov/pubmed/36058949
http://dx.doi.org/10.1186/s12967-022-03596-0
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