James Emma R, Tasnim Maliha, Riera-Escamilla Antoni, Vigh-Conrad Katinka, Emery Benjamin R, Conrad Donald F, Aston Kenneth I
Department of Surgery, Division of Urology, University of Utah School of Medicine, Salt Lake City, UT, USA.
Division of Genetics, ONPRC & Oregon Health & Science University, 505 N.W. 185th Avenue, Beaverton, OR, USA.
Trends Genet. 2025 Aug 21. doi: 10.1016/j.tig.2025.07.007.
Male infertility is a global health problem, affecting up to 6% of reproductive age men worldwide. It has an enormous personal and societal burden, along with public health implications beyond the inability to reproduce, including reduced future health and longevity. While the impact of infertility has long been appreciated, the molecular architecture of the disease is largely unknown. Nevertheless, the past decade has witnessed significant advances in our understanding of the molecular basis of male infertility. Here, we describe the contributions of genetic and epigenetic mechanisms to infertility-associated phenotypes and their impact beyond reproduction. This review focuses on progress in understanding defects in sperm production and function, and the potential impact of these advances on diagnosis, treatments, and improved health.
男性不育是一个全球性的健康问题,影响着全球多达6%的育龄男性。它带来了巨大的个人和社会负担,除了无法生育之外,还对公共健康产生影响,包括未来健康状况下降和寿命缩短。虽然不育症的影响早已为人所知,但其疾病的分子结构在很大程度上仍不明确。然而,在过去十年中,我们对男性不育症分子基础的理解取得了重大进展。在此,我们描述遗传和表观遗传机制对不育相关表型的作用及其在生殖之外的影响。这篇综述重点关注在理解精子生成和功能缺陷方面取得的进展,以及这些进展对诊断、治疗和改善健康状况的潜在影响。