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The Effect of Teratozoospermia on Sex Chromosomes in Human Embryos

PURPOSE: The aim of this study is to evaluate the effect of abnormal semen morphology on the frequency of sex chromosomal abnormalities in embryos obtained by ICSI, which represents the first to be studied in Egyptian population. METHODS: Forty-two couples suffering from male infertility due to tera...

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Autores principales: Mostafa Nayel, Dalia, Salah El Din Mahrous, Hanan, El Din Khalifa, Emad, Kholeif, Soha, Mohamed Elhady, Ghada
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7959001/
https://www.ncbi.nlm.nih.gov/pubmed/33732009
http://dx.doi.org/10.2147/TACG.S299349
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author Mostafa Nayel, Dalia
Salah El Din Mahrous, Hanan
El Din Khalifa, Emad
Kholeif, Soha
Mohamed Elhady, Ghada
author_facet Mostafa Nayel, Dalia
Salah El Din Mahrous, Hanan
El Din Khalifa, Emad
Kholeif, Soha
Mohamed Elhady, Ghada
author_sort Mostafa Nayel, Dalia
collection PubMed
description PURPOSE: The aim of this study is to evaluate the effect of abnormal semen morphology on the frequency of sex chromosomal abnormalities in embryos obtained by ICSI, which represents the first to be studied in Egyptian population. METHODS: Forty-two couples suffering from male infertility due to teratozoospermia were divided into two groups: patients with severe and moderate teratozoospermia (group A and B, respectively). All involved couples were subjected to careful history taking and had a normal clinical examination and karyotype. Females were subjected to hormonal assays, pelvic ultrasound, hysterosalpingography and yielded normal results, while male partners were subjected to computerized semen analysis. Preimplantation genetic diagnosis was performed for all suitably developed embryos including embryo biopsy, fixation of biopsied cells and fluorescent in situ hybridization (FISH) analysis. RESULTS: Couples included in the two groups were found to be homogenous in terms of age of both partners and duration of infertility. Interpretation of FISH results was performed by evaluation of embryos’ chromosomal constitution as regards abnormalities in chromosomes X, Y and 18. Twenty-seven embryos (48.2%) were found chromosomally abnormal in group A, while only 14 embryos (25.0%) were found chromosomally abnormal in group B. Aneuploidies involved only sex chromosomes were tripled in group A embryos when compared to their frequency in group B embryos (26.8% and 8.3%, respectively) with statistically significant difference between the two groups (p=0.002). Monosomies were the most common type of aneuploidy and were significantly higher in group A (14.3%) when compared to group B (3.6%) (p=0.047). Embryos with mosaic abnormalities were more common in group A (12.5%) when compared to group B (3.6%), however not statistically significantly different (p= 0.162). A significant difference between the two studied groups as regards the total number of potentially viable chromosomal abnormalities detected and the potentially viable sex chromosomal aneuploidies detected (p<0.001 and p=0.002), respectively. CONCLUSION: The cases with severe teratozoospermia undergoing ICSI treatment can display a higher rate of sex chromosome aneuploidies in their embryos (threefold) than cases with moderate teratozoospermia.
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spelling pubmed-79590012021-03-16 The Effect of Teratozoospermia on Sex Chromosomes in Human Embryos Mostafa Nayel, Dalia Salah El Din Mahrous, Hanan El Din Khalifa, Emad Kholeif, Soha Mohamed Elhady, Ghada Appl Clin Genet Original Research PURPOSE: The aim of this study is to evaluate the effect of abnormal semen morphology on the frequency of sex chromosomal abnormalities in embryos obtained by ICSI, which represents the first to be studied in Egyptian population. METHODS: Forty-two couples suffering from male infertility due to teratozoospermia were divided into two groups: patients with severe and moderate teratozoospermia (group A and B, respectively). All involved couples were subjected to careful history taking and had a normal clinical examination and karyotype. Females were subjected to hormonal assays, pelvic ultrasound, hysterosalpingography and yielded normal results, while male partners were subjected to computerized semen analysis. Preimplantation genetic diagnosis was performed for all suitably developed embryos including embryo biopsy, fixation of biopsied cells and fluorescent in situ hybridization (FISH) analysis. RESULTS: Couples included in the two groups were found to be homogenous in terms of age of both partners and duration of infertility. Interpretation of FISH results was performed by evaluation of embryos’ chromosomal constitution as regards abnormalities in chromosomes X, Y and 18. Twenty-seven embryos (48.2%) were found chromosomally abnormal in group A, while only 14 embryos (25.0%) were found chromosomally abnormal in group B. Aneuploidies involved only sex chromosomes were tripled in group A embryos when compared to their frequency in group B embryos (26.8% and 8.3%, respectively) with statistically significant difference between the two groups (p=0.002). Monosomies were the most common type of aneuploidy and were significantly higher in group A (14.3%) when compared to group B (3.6%) (p=0.047). Embryos with mosaic abnormalities were more common in group A (12.5%) when compared to group B (3.6%), however not statistically significantly different (p= 0.162). A significant difference between the two studied groups as regards the total number of potentially viable chromosomal abnormalities detected and the potentially viable sex chromosomal aneuploidies detected (p<0.001 and p=0.002), respectively. CONCLUSION: The cases with severe teratozoospermia undergoing ICSI treatment can display a higher rate of sex chromosome aneuploidies in their embryos (threefold) than cases with moderate teratozoospermia. Dove 2021-03-11 /pmc/articles/PMC7959001/ /pubmed/33732009 http://dx.doi.org/10.2147/TACG.S299349 Text en © 2021 Mostafa Nayel et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Mostafa Nayel, Dalia
Salah El Din Mahrous, Hanan
El Din Khalifa, Emad
Kholeif, Soha
Mohamed Elhady, Ghada
The Effect of Teratozoospermia on Sex Chromosomes in Human Embryos
title The Effect of Teratozoospermia on Sex Chromosomes in Human Embryos
title_full The Effect of Teratozoospermia on Sex Chromosomes in Human Embryos
title_fullStr The Effect of Teratozoospermia on Sex Chromosomes in Human Embryos
title_full_unstemmed The Effect of Teratozoospermia on Sex Chromosomes in Human Embryos
title_short The Effect of Teratozoospermia on Sex Chromosomes in Human Embryos
title_sort effect of teratozoospermia on sex chromosomes in human embryos
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7959001/
https://www.ncbi.nlm.nih.gov/pubmed/33732009
http://dx.doi.org/10.2147/TACG.S299349
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