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P-743 Semen samples quality and blastocysts diversity after PGT-A

Title: P-743 Semen samples quality and blastocysts diversity after PGT-A
Authors: Albanese, C; Perruzza, D; Azzena, S; Crippa, A; Graziosi, S; Bilotta, G; Magli, M C; Gianaroli, L
Source: Human Reproduction ; volume 38, issue Supplement_1 ; ISSN 0268-1161 1460-2350
Publisher Information: Oxford University Press (OUP)
Publication Year: 2023
Description: Study question Does semen samples quality contribute to blastocyst diversity by correlating with the presence of DNA in the blastocoelic fluid (BF)? Summary answer Semen samples quality is associated with the detection of DNA in BFs from both euploid and aneuploid blastocysts What is known already DNA was detected by whole genome amplification (WGA) in BFs from expanded blastocysts dependently on the blastocyst chromosome condition (assessed by PGT-A on trophectoderm (TE) cells), being more frequent in aneuploid blastocysts. TE-euploid blastocysts with positive BF-WGA also seem to have less chances to implant compared to those with failed BF-WGA. The extrusion of abnormal cells from the embryo proper was proposed as a mechanism triggered by the mosaic embryo to eliminate abnormal cells. Severe male factor samples are at risk of causing embryo mosaicism. Possible association between semen quality and DNA in BFs has not yet been investigated. Study design, size, duration This retrospective cohort study included 115 patients (maternal age 37.9±4.1), which underwent PGT-A in the last three years. The aim of the study was to evaluate whether the detection of DNA in BFs was correlated with semen samples indices. Both TE-euploid and TE-aneuploid blastocysts were considered for the analysis and stratified according to the semen samples quality as normozoospermic (N), moderate oligoasthenoteratozoospermic (m-OAT) and severe OAT (s-OAT) following the 2021 WHO criteria. Participants/materials, setting, methods BF and trophectoderm (TE) biopsies were collected from high grade expanded blastocysts before vitrification, and submitted to WGA. Amplification after WGA was evaluated by loading an aliquot of the amplified product onto a 1.5% agarose gel. 24-chromosome analysis was performed on TE biopsies. To assess the impact of semen samples quality on the detection of DNA in BFs, a multiple logistic regression analysis was performed correcting for maternal age as a confounding factor. Main results and the role of ...
Document Type: article in journal/newspaper
Language: English
DOI: 10.1093/humrep/dead093.338
Availability: https://doi.org/10.1093/humrep/dead093.338; https://academic.oup.com/humrep/article-pdf/38/Supplement_1/dead093.338/50787298/dead093.338.pdf
Rights: https://academic.oup.com/pages/standard-publication-reuse-rights
Accession Number: edsbas.DE909105
Database: BASE