The Effect of Teratozoospermia on Sex Chromosomes in Human Embryos

• Published in: Application of clinical genetics Vol. 14; pp. 125 - 144
• Main Authors: Mostafa Nayel, Dalia, Salah El Din Mahrous, Hanan, El Din Khalifa, Emad, Kholeif, Soha, Mohamed Elhady, Ghada
• Format: Journal Article
• Language: English
• Published: New Zealand Dove Medical Press Limited 01.01.2021; Taylor & Francis Ltd; Dove; Dove Medical Press
• Subjects: Analysis; Aneuploidy; Biopsy; Chromosomes; Couples; Cytogenetics; Embryonic development; Embryos; Females; Fluorescence in situ hybridization; Genetic analysis; Genetic research; Genetic screening; icsi- teratozoospermia- aneuploidy-fish; In vitro fertilization; Infertility; Karyotypes; Morphology; Original Research; Population studies; Povidone; Sample size; Semen; Sex chromosomes; Sperm; Statistical analysis; Ultrasound; United Kingdom; Egypt; FISH; aneuploidy; ICSI; teratozoospermia
• ISSN: 1178-704X; 1178-704X
• DOI: 10.2147/TACG.S299349

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. 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. 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. 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.