Investigating the significance of segmental aneuploidy findings in preimplantation embryos.


Journal

F&S science
ISSN: 2666-335X
Titre abrégé: F S Sci
Pays: United States
ID NLM: 101765857

Informations de publication

Date de publication:
05 2023
Historique:
received: 25 01 2023
revised: 07 03 2023
accepted: 13 03 2023
medline: 22 5 2023
pubmed: 23 3 2023
entrez: 22 3 2023
Statut: ppublish

Résumé

Segmental aneuploidies (SAs) are structural imbalances, namely, gains or losses, involving a chromosomal segment. Most preimplantation genetic testing platforms can detect segmental imbalances greater than 5-10 Mb, either full or mosaic; however, questions remain about clinical significance. An in-depth review was performed to determine the accuracy, frequency, and types of SAs detected in preimplantation embryos. A comprehensive search of the literature revealed an incidence of approximately 8.15% in preimplantation embryos, compared with a prevalence of 3.55% in prenatal diagnosis samples. Several studies have used rebiopsy analysis to validate the accuracy and reproducibility of such findings in blastocyst-stage embryos. A comparison of these studies yielded a mean confirmation rate of SAs slightly higher than 30%. This result could be attributed to their mitotic origin as well as to the technical limitations of preimplantation genetic testing. In addition, the few available studies in which embryos with a segmental finding were transferred in utero are analyzed to discuss the reproductive competence of such embryos. Except for 1 study, all outcomes were described for segmental embryos in a mosaic state. As a result, there is still insufficient evidence to provide accurate information about the effect of segmental imbalances on embryonic reproductive competence and to determine gestational and newborn risks.

Identifiants

pubmed: 36948460
pii: S2666-335X(23)00015-0
doi: 10.1016/j.xfss.2023.03.004
pii:
doi:

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

17-26

Informations de copyright

Copyright © 2023 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

Auteurs

Ludovica Picchetta (L)

JUNO Genetics, Reproductive Genetics, Rome, Italy.

Christian S Ottolini (CS)

Department of Maternal and Fetal Medicine, UCL Institute for Women's Health, University College London, London, United Kingdom.

Helen C O'Neill (HC)

Department of Maternal and Fetal Medicine, UCL Institute for Women's Health, University College London, London, United Kingdom.

Antonio Capalbo (A)

JUNO Genetics, Reproductive Genetics, Rome, Italy. Electronic address: Antonio.capalbo@junogenetics.com.

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Classifications MeSH