Surgically retrieved spermatozoa for ICSI cycles in non‐azoospermic males with high sperm DNA fragmentation in semen

Author:

Esteves Sandro C.123,Coimbra Igor4,Hallak Jorge4567

Affiliation:

1. ANDROFERT, Andrology and Human Reproduction Clinic Av. Dr. Heitor Penteado Campinas SP Brazil

2. Department of Surgery (Division of Urology), Faculty of Medical Sciences University of Campinas (UNICAMP) Campinas SP Brazil

3. Department of Clinical Medicine, Faculty of Health Aarhus University Aarhus Denmark

4. Department of Surgery, Division of Urology University of São Paulo Medical School São Paulo SP Brazil

5. Department of Pathology, Reproductive Toxicology Unit University of São Paulo Medical School São Paulo SP Brazil

6. Men's Health Study Group, Institute for Advanced Studies University of São Paulo São Paulo SP Brazil

7. Androscience Science and Innovation Center in Andrology and High‐Complex Clinical and Andrology Research Laboratory São Paulo SP Brazil

Abstract

AbstractIntracytoplasmic sperm injection (ICSI) using surgically retrieved spermatozoa outside the classic context of azoospermia has been increasingly used to overcome infertility. The primary indications include high levels of sperm DNA damage in ejaculated spermatozoa and severe oligozoospermia or cryptozoospermia, particularly in couples with ICSI failure for no apparent reason. Current evidence suggests that surgically retrieved spermatozoa for ICSI in the above context improves  outcomes, mainly concerning pregnancy and miscarriage rates. The reasons are not fully understood but may be related to the lower levels of DNA damage in spermatozoa retrieved from the testis compared with ejaculated counterparts. These findings are consistent with the notion that excessive sperm DNA damage  can be a limiting factor responsible for the failure to conceive. Using testicular in preference of low‐quality ejaculated spermatozoa bypasses post‐testicular sperm DNA damage caused primarily by oxidative stress, thus increasing the likelihood of oocyte fertilization by genomically intact spermatozoa. Despite the overall favorable results, data remain limited, and mainly concern males with confirmed sperm DNA damage in the ejaculate. Additionally, information regarding the health of ICSI offspring resulting from the use of surgically retrieved spermatoa of non‐azoospermic males is still lacking. Efforts should be made to improve the male partner's reproductive health for safer ICSI utilization. A comprehensive andrological evaluation aiming to identify and treat the underlying male infertility factor contributing to sperm DNA damage is essential for achieving this goal.

Publisher

Wiley

Subject

Urology,Endocrinology,Reproductive Medicine,Endocrinology, Diabetes and Metabolism

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