Abstract
In this article we aim to summarize the data regarding the incidence of sperm aneuploidy detected by FISH in fertile and infertile men with and without normal karyotype. We analyze and discuss studies relating to FISH analysis in sperm from fertile and infertile men that were published until October 2010. Among the control men, the lowest aneuploidy rate (range: 0.09–0.13% for autosomes; 0.04–0.10% for gonosomes) was detected in the normozoospermic and fertile group. In infertile patients with a normal karyotype, the severity of semen alterations was correlated with the frequency of aneuploidy, particularly of gonosomes. Among patients with abnormal karyotype, the 47,XXY and 47,XYY carriers showed high variability of sperm aneuploidy of gonosomes, while carriers of Robertsonian translocation demonstrated an increased aneuploidy rate, which was mainly related to interchromosomal effect. The reciprocal translocation carriers showed a high percentage of imbalanced spermatozoa (≥50%) and interchromosomal effects were possibly observed. The study of sperm chromosomal constitution is a useful tool that obtains information on the effects of andrological and/or systemic diseases on the chromosomal segregation process, which may aid both fertility specialist counseling and their patients in the decision-making process before offering assisted fertilization techniques for the treatment of male factor infertility.
Financial & competing interests disclosure
The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.
No writing assistance was utilized in the production of this manuscript.