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精子发生障碍:常规诊断20年未变后的新型基因诊断前景

Disorders of spermatogenesis: Perspectives for novel genetic diagnostics after 20 years of unchanged routine.

作者信息

Tüttelmann Frank, Ruckert Christian, Röpke Albrecht

机构信息

Institute of Human Genetics, University of Münster, Vesaliusweg 12-14, 48149 Münster, Germany.

出版信息

Med Genet. 2018;30(1):12-20. doi: 10.1007/s11825-018-0181-7. Epub 2018 Feb 26.

Abstract

Infertility is a common condition estimated to affect 10-15% of couples. The clinical causes are attributed in equal parts to the male and female partners. Diagnosing male infertility mostly relies on semen (and hormone) analysis, which results in classification into the two major phenotypes of oligo- and azoospermia. The clinical routine analyses have not changed over the last 20 years and comprise screening for chromosomal aberrations and Y‑chromosomal azoospermia factor deletions. These tests establish a causal genetic diagnosis in about 4% of unselected men in infertile couples and 20% of azoospermic men. Gene sequencing is currently only performed in very rare cases of hypogonadotropic hypogonadism and the gene is routinely analysed in men with obstructive azoospermia. Still, a large number of genes have been proposed to be associated with male infertility by, for example, knock-out mouse models. In particular, those that are exclusively expressed in the testes are potential candidates for further analyses. However, the genome-wide analyses (a few array-CGH, six GWAS, and some small exome sequencing studies) performed so far have not lead to improved clinical diagnostic testing. In 2017, we started to routinely analyse the three validated male infertility genes: , and . Preliminary analyses demonstrated highly likely pathogenic mutations in these genes as a cause of azoospermia in 4 men, equalling 5% of the 80 patients analysed so far, and increasing the diagnostic yield in this group to 25%. Over the past few years, we have observed a steep increase in publications on novel candidate genes for male infertility, especially in men with azoospermia. In addition, concerted efforts to achieve progress in elucidating genetic causes of male infertility and to introduce novel testing strategies into clinical routine have been made recently. Thus, we are confident that major breakthroughs concerning the genetics of male infertility will be achieved in the near future and will translate into clinical routine to improve patient/couple care.

摘要

不孕症是一种常见病症,据估计影响10% - 15%的夫妇。临床病因在男性和女性伴侣中各占一半。男性不育症的诊断主要依赖于精液(和激素)分析,据此可分为少精子症和无精子症这两种主要表型。过去20年临床常规分析没有变化,包括染色体畸变筛查和Y染色体无精子症因子缺失检测。这些检测在未选择的不育夫妇男性中约4%以及无精子症男性中20%能做出因果性基因诊断。基因测序目前仅在极罕见的低促性腺激素性性腺功能减退病例中进行,并且该基因在梗阻性无精子症男性中常规检测。尽管如此,例如通过基因敲除小鼠模型,已有大量基因被提出与男性不育症相关。特别是那些仅在睾丸中表达的基因是进一步分析的潜在候选基因。然而,迄今为止进行的全基因组分析(一些比较基因组杂交、六项全基因组关联研究以及一些小的外显子测序研究)并未带来临床诊断检测的改进。2017年,我们开始常规分析三个已验证的男性不育基因: 、 和 。初步分析表明,这些基因中高度可能的致病突变是4名男性无精子症的病因,占目前已分析的80名患者的5%,并将该组的诊断率提高到25%。在过去几年中,我们观察到关于男性不育症新候选基因的出版物急剧增加,尤其是在无精子症男性中。此外,最近在阐明男性不育症遗传病因方面取得进展并将新检测策略引入临床常规方面已做出协同努力。因此,我们相信在不久的将来,男性不育症遗传学将取得重大突破,并转化为临床常规以改善患者/夫妇护理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d023/5838132/fa0bef3180c1/11825_2018_181_Fig1_HTML.jpg

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