Cargando…
The embryo mosaicism profile of next-generation sequencing PGT-A in different clinical conditions and their associations
INTRODUCTION: Uniform chromosome abnormalities are commonly seen in early pregnancy loss, with analyses of the product of conception suggesting the presence of mosaic autosomal trisomy in ∼10% of cases. Although chromosomal mosaicism occurs in a minority of embryos, their relative commonality and un...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083245/ https://www.ncbi.nlm.nih.gov/pubmed/37050939 http://dx.doi.org/10.3389/frph.2023.1132662 |
_version_ | 1785021465085607936 |
---|---|
author | Heiser, Hadassa Campos Cagnin, Natalia Fagundes de Souza, Mariane Uehara Ali, Taccyanna Mikulski Estrada, Paula Regina Queiroz de Souza, Camila Cristina Wuaquim Dantas Coprerski, Bruno Rubio, Carmen Riboldi, Marcia |
author_facet | Heiser, Hadassa Campos Cagnin, Natalia Fagundes de Souza, Mariane Uehara Ali, Taccyanna Mikulski Estrada, Paula Regina Queiroz de Souza, Camila Cristina Wuaquim Dantas Coprerski, Bruno Rubio, Carmen Riboldi, Marcia |
author_sort | Heiser, Hadassa Campos |
collection | PubMed |
description | INTRODUCTION: Uniform chromosome abnormalities are commonly seen in early pregnancy loss, with analyses of the product of conception suggesting the presence of mosaic autosomal trisomy in ∼10% of cases. Although chromosomal mosaicism occurs in a minority of embryos, their relative commonality and uncertainty regarding associated transfer outcomes have created discussion at both the clinical and research levels, highlighting the need to understand the clinical conditions associated with the incidence of embryo mosaicism. METHODS: We took advantage of a preimplantation genetic testing for aneuploidy (PGT-A) database created from 2019 to 2022 in more than 160 in vitro fertilization (IVF) clinics in Brazil, the second-largest world market for IVF. We carried out descriptive statistical and associative analyses to assess the proportions of mosaicism associated with clinical conditions and reported incidence by chromosome, clinic origin, and biopsy operator. RESULTS: Chromosomal analysis revealed that most mosaic aneuploidies occurred in the last three chromosomes, with 78.06% of cases having only one chromosome affected. Low mosaicism in trisomy represented the most ordinary form, followed by low mosaicism in monosomy. We identified associations between low (negatively-associated) and high mosaicism (positively-associated) and maternal age, indication (male factor and uterus/ovarian factor negatively associated with low and high mosaic, respectively), day of blastocyst development (day five has an overall better outcome), morphology grade (lower quality increased the chances of low and high mosaicism), origin (vitrified oocyte and embryo increased the rates of low and high mosaicism, respectively), and embryo sex (male embryos negatively associated with low mosaic). DISCUSSION: With these results, we hope to foster an improved understanding of the chromosomal mosaicism linked with distinct clinical conditions and their associations in Brazil. |
format | Online Article Text |
id | pubmed-10083245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100832452023-04-11 The embryo mosaicism profile of next-generation sequencing PGT-A in different clinical conditions and their associations Heiser, Hadassa Campos Cagnin, Natalia Fagundes de Souza, Mariane Uehara Ali, Taccyanna Mikulski Estrada, Paula Regina Queiroz de Souza, Camila Cristina Wuaquim Dantas Coprerski, Bruno Rubio, Carmen Riboldi, Marcia Front Reprod Health Reproductive Health INTRODUCTION: Uniform chromosome abnormalities are commonly seen in early pregnancy loss, with analyses of the product of conception suggesting the presence of mosaic autosomal trisomy in ∼10% of cases. Although chromosomal mosaicism occurs in a minority of embryos, their relative commonality and uncertainty regarding associated transfer outcomes have created discussion at both the clinical and research levels, highlighting the need to understand the clinical conditions associated with the incidence of embryo mosaicism. METHODS: We took advantage of a preimplantation genetic testing for aneuploidy (PGT-A) database created from 2019 to 2022 in more than 160 in vitro fertilization (IVF) clinics in Brazil, the second-largest world market for IVF. We carried out descriptive statistical and associative analyses to assess the proportions of mosaicism associated with clinical conditions and reported incidence by chromosome, clinic origin, and biopsy operator. RESULTS: Chromosomal analysis revealed that most mosaic aneuploidies occurred in the last three chromosomes, with 78.06% of cases having only one chromosome affected. Low mosaicism in trisomy represented the most ordinary form, followed by low mosaicism in monosomy. We identified associations between low (negatively-associated) and high mosaicism (positively-associated) and maternal age, indication (male factor and uterus/ovarian factor negatively associated with low and high mosaic, respectively), day of blastocyst development (day five has an overall better outcome), morphology grade (lower quality increased the chances of low and high mosaicism), origin (vitrified oocyte and embryo increased the rates of low and high mosaicism, respectively), and embryo sex (male embryos negatively associated with low mosaic). DISCUSSION: With these results, we hope to foster an improved understanding of the chromosomal mosaicism linked with distinct clinical conditions and their associations in Brazil. Frontiers Media S.A. 2023-03-27 /pmc/articles/PMC10083245/ /pubmed/37050939 http://dx.doi.org/10.3389/frph.2023.1132662 Text en © 2023 Heiser, Cagnin, de Souza, Ali, Estrada, de Souza, Coprerski, Rubio and Riboldi. 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) (https://creativecommons.org/licenses/by/4.0/) . 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 | Reproductive Health Heiser, Hadassa Campos Cagnin, Natalia Fagundes de Souza, Mariane Uehara Ali, Taccyanna Mikulski Estrada, Paula Regina Queiroz de Souza, Camila Cristina Wuaquim Dantas Coprerski, Bruno Rubio, Carmen Riboldi, Marcia The embryo mosaicism profile of next-generation sequencing PGT-A in different clinical conditions and their associations |
title | The embryo mosaicism profile of next-generation sequencing PGT-A in different clinical conditions and their associations |
title_full | The embryo mosaicism profile of next-generation sequencing PGT-A in different clinical conditions and their associations |
title_fullStr | The embryo mosaicism profile of next-generation sequencing PGT-A in different clinical conditions and their associations |
title_full_unstemmed | The embryo mosaicism profile of next-generation sequencing PGT-A in different clinical conditions and their associations |
title_short | The embryo mosaicism profile of next-generation sequencing PGT-A in different clinical conditions and their associations |
title_sort | embryo mosaicism profile of next-generation sequencing pgt-a in different clinical conditions and their associations |
topic | Reproductive Health |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083245/ https://www.ncbi.nlm.nih.gov/pubmed/37050939 http://dx.doi.org/10.3389/frph.2023.1132662 |
work_keys_str_mv | AT heiserhadassacampos theembryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT cagninnataliafagundes theembryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT desouzamarianeuehara theembryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT alitaccyannamikulski theembryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT estradapaulareginaqueiroz theembryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT desouzacamilacristinawuaquimdantas theembryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT coprerskibruno theembryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT rubiocarmen theembryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT riboldimarcia theembryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT heiserhadassacampos embryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT cagninnataliafagundes embryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT desouzamarianeuehara embryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT alitaccyannamikulski embryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT estradapaulareginaqueiroz embryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT desouzacamilacristinawuaquimdantas embryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT coprerskibruno embryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT rubiocarmen embryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations AT riboldimarcia embryomosaicismprofileofnextgenerationsequencingpgtaindifferentclinicalconditionsandtheirassociations |