Schilit Samantha L P
Biological and Biomedical Sciences Program, Graduate School of Arts and Sciences, Harvard University, Cambridge, MA, USA.
Program in Genetics and Genomics, Department of Genetics, Harvard Medical School, Boston, MA, USA.
Curr Sex Health Rep. 2019 Dec;11(4):331-341. doi: 10.1007/s11930-019-00225-8. Epub 2019 Oct 26.
Infertility affects 10-15% of couples, making it one of the most frequent health disorders for individuals of reproductive age. The state of childlessness and efforts to restore fertility cause substantial emotional, social, and financial stress on couples. Male factors contribute to about half of all infertility cases, and yet are understudied relative to female factors. The result is that the majority of men with infertility lack specific causal diagnoses, which serves as a missed opportunity to inform therapies for these couples.
In this review, we describe current standards for diagnosing male infertility and the various interventions offered to men in response to differential diagnoses. We then discuss recent advances in the field of genetics to identify novel etiologies for formerly unexplained infertility.
With a specific genetic diagnosis, male factors can be addressed with appropriate reproductive counseling and with potential access to assisted reproductive technologies to improve chances of a healthy pregnancy.
不孕症影响10%至15%的夫妇,使其成为育龄人群中最常见的健康问题之一。无子女状态以及恢复生育能力的努力给夫妇带来了巨大的情感、社会和经济压力。男性因素约占所有不孕症病例的一半,但相对于女性因素而言,对其研究较少。结果是,大多数不孕男性缺乏明确的病因诊断,这为针对这些夫妇的治疗提供信息带来了错失的机会。
在本综述中,我们描述了诊断男性不育症的当前标准以及针对不同诊断为男性提供的各种干预措施。然后,我们讨论了遗传学领域的最新进展,以确定以前原因不明的不孕症的新病因。
通过特定的基因诊断,男性因素可以通过适当的生殖咨询以及可能获得辅助生殖技术来解决,以提高健康怀孕的几率。