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Y-Chromosome Microdeletions: A Review of Prevalence, Screening, and Clinical Considerations
Deletions within the male-specific region of the Y-chromosome, known as Y-Chromosome Microdeletions (YCMs), are present in as many as 5% and 10% of severe oligospermic and azoospermic men, respectively. These microdeletions are distinguished by which segment of the Y chromosome is absent, identified...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886244/ https://www.ncbi.nlm.nih.gov/pubmed/33603438 http://dx.doi.org/10.2147/TACG.S267421 |
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author | Rabinowitz, Matthew J Huffman, Phillip J Haney, Nora M Kohn, Taylor P |
author_facet | Rabinowitz, Matthew J Huffman, Phillip J Haney, Nora M Kohn, Taylor P |
author_sort | Rabinowitz, Matthew J |
collection | PubMed |
description | Deletions within the male-specific region of the Y-chromosome, known as Y-Chromosome Microdeletions (YCMs), are present in as many as 5% and 10% of severe oligospermic and azoospermic men, respectively. These microdeletions are distinguished by which segment of the Y chromosome is absent, identified as AZFa (the most proximal segment), AZFb (middle), and AZFc (distal). The reported prevalence of YCMs within the world’s populations of infertile men displays vast heterogeneity, ranging from less than 2% to over 24% based on region and ethnicity. AZFc is the most commonly identified YCM, and its phenotypic presentation provides for the highest chance for fertility through artificial reproductive techniques. Conversely, deletions identified in the subregions of AZFa, AZFb, or any combination of regions containing these segments, are associated with low probabilities of achieving pregnancy. A putative mechanism explaining this discrepancy lies within the expression of autosomal, DAZ-like genes which could serve to “rescue” wild type AZFc gene expression and hence spermatogenesis. Nevertheless, recent reports challenge this dogma and stress the importance of further analysis when an AZFb deletion is detected. The screening thresholds to determine which oligospermic and azoospermic men are tested for potential YCMs has been recently contested. More recent literature supports lowering the threshold from 5 million sperm/mL of ejaculate to 1 million/mL as the frequency of YCMs in men with sperm concentrations between 1 and 5 million sperm/mL is very low (~0.8%). As such, subsequent guidelines should recommend a lower screening threshold. While YCMs are extremely common globally, the understanding of their clinical significance in the field remains scattered and without consensus. Furthermore, very little is currently known about partial deletions within the AZFc region, such as b1/b3, b2/b3, and gr/gr. Hence, this review aimed to summarize and discuss modern trends in the epidemiology, screening guidelines, and clinical considerations pertaining to YCMs. |
format | Online Article Text |
id | pubmed-7886244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-78862442021-02-17 Y-Chromosome Microdeletions: A Review of Prevalence, Screening, and Clinical Considerations Rabinowitz, Matthew J Huffman, Phillip J Haney, Nora M Kohn, Taylor P Appl Clin Genet Review Deletions within the male-specific region of the Y-chromosome, known as Y-Chromosome Microdeletions (YCMs), are present in as many as 5% and 10% of severe oligospermic and azoospermic men, respectively. These microdeletions are distinguished by which segment of the Y chromosome is absent, identified as AZFa (the most proximal segment), AZFb (middle), and AZFc (distal). The reported prevalence of YCMs within the world’s populations of infertile men displays vast heterogeneity, ranging from less than 2% to over 24% based on region and ethnicity. AZFc is the most commonly identified YCM, and its phenotypic presentation provides for the highest chance for fertility through artificial reproductive techniques. Conversely, deletions identified in the subregions of AZFa, AZFb, or any combination of regions containing these segments, are associated with low probabilities of achieving pregnancy. A putative mechanism explaining this discrepancy lies within the expression of autosomal, DAZ-like genes which could serve to “rescue” wild type AZFc gene expression and hence spermatogenesis. Nevertheless, recent reports challenge this dogma and stress the importance of further analysis when an AZFb deletion is detected. The screening thresholds to determine which oligospermic and azoospermic men are tested for potential YCMs has been recently contested. More recent literature supports lowering the threshold from 5 million sperm/mL of ejaculate to 1 million/mL as the frequency of YCMs in men with sperm concentrations between 1 and 5 million sperm/mL is very low (~0.8%). As such, subsequent guidelines should recommend a lower screening threshold. While YCMs are extremely common globally, the understanding of their clinical significance in the field remains scattered and without consensus. Furthermore, very little is currently known about partial deletions within the AZFc region, such as b1/b3, b2/b3, and gr/gr. Hence, this review aimed to summarize and discuss modern trends in the epidemiology, screening guidelines, and clinical considerations pertaining to YCMs. Dove 2021-02-12 /pmc/articles/PMC7886244/ /pubmed/33603438 http://dx.doi.org/10.2147/TACG.S267421 Text en © 2021 Rabinowitz 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 | Review Rabinowitz, Matthew J Huffman, Phillip J Haney, Nora M Kohn, Taylor P Y-Chromosome Microdeletions: A Review of Prevalence, Screening, and Clinical Considerations |
title | Y-Chromosome Microdeletions: A Review of Prevalence, Screening, and Clinical Considerations |
title_full | Y-Chromosome Microdeletions: A Review of Prevalence, Screening, and Clinical Considerations |
title_fullStr | Y-Chromosome Microdeletions: A Review of Prevalence, Screening, and Clinical Considerations |
title_full_unstemmed | Y-Chromosome Microdeletions: A Review of Prevalence, Screening, and Clinical Considerations |
title_short | Y-Chromosome Microdeletions: A Review of Prevalence, Screening, and Clinical Considerations |
title_sort | y-chromosome microdeletions: a review of prevalence, screening, and clinical considerations |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886244/ https://www.ncbi.nlm.nih.gov/pubmed/33603438 http://dx.doi.org/10.2147/TACG.S267421 |
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