y染色体微缺失:患病率,筛查和临床考虑的回顾。

IF 2.6 Q2 GENETICS & HEREDITY Application of Clinical Genetics Pub Date : 2021-02-12 eCollection Date: 2021-01-01 DOI:10.2147/TACG.S267421
Matthew J Rabinowitz, Phillip J Huffman, Nora M Haney, Taylor P Kohn
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引用次数: 14

摘要

y染色体男性特异性区域的缺失,被称为y染色体微缺失(YCMs),分别存在于5%和10%的严重少精子和无精子男性中。这些微缺失是通过Y染色体的哪个片段缺失来区分的,确定为AZFa(最近段),AZFb(中间)和AZFc(远段)。据报道,在世界不育男性人群中,ycm的患病率显示出巨大的异质性,根据地区和种族,从不到2%到超过24%不等。AZFc是最常见的YCM,其表型表现通过人工生殖技术提供了最高的生育机会。相反,在AZFa、AZFb亚区或包含这些片段的任何区域的组合中发现的缺失与低怀孕概率有关。一种推测的解释这种差异的机制在于常染色体AZFc样基因的表达,这种基因可以“拯救”野生型AZFc基因的表达,从而促进精子发生。然而,最近的报道挑战了这一教条,并强调了在检测到AZFb缺失时进一步分析的重要性。确定哪些少精子和无精子男性接受潜在ycm检测的筛选阈值最近一直存在争议。最近的文献支持将阈值从500万精子/mL降低到100万/mL,因为在精子浓度在100万到500万精子/mL之间的男性中,ycm的频率非常低(约0.8%)。因此,后续指南应建议降低筛查阈值。虽然ycm在全球范围内非常普遍,但对其临床意义的理解仍然分散,没有达成共识。此外,目前对AZFc区域的部分缺失(如b1/b3、b2/b3和gr/gr)知之甚少。因此,本综述旨在总结和讨论与ycm有关的流行病学、筛查指南和临床考虑的现代趋势。
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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 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.

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来源期刊
Application of Clinical Genetics
Application of Clinical Genetics Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
5.40
自引率
0.00%
发文量
20
审稿时长
16 weeks
期刊最新文献
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