Elsevier

Fertility and Sterility

Volume 82, Issue 5, November 2004, Pages 1251-1263
Fertility and Sterility

Modern trends
Clinical application of sperm-oocyte interaction tests in in vitro fertilization–embryo transfer and intracytoplasmic sperm injection programs

https://doi.org/10.1016/j.fertnstert.2003.10.057Get rights and content
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Objective

To review the clinical value of sperm-oocyte interaction tests for the diagnosis and management of infertility by standard IVF or intracytoplasmic sperm injection (ICSI).

Design

Review of recent publications on relationships among sperm-oocyte interaction tests, sperm characteristics, and results of IVF and determination of frequency of defective sperm-oocyte interaction in infertile men.

Main outcome measure(s)

Fertilization rates with IVF, sperm characteristics, sperm–zona pellucida (ZP) binding, ZP-induced acrosome reaction (AR), and sperm-ZP penetration.

Result(s)

Sperm defects associated with low sperm-ZP binding or impaired ZP-induced AR and sperm-ZP penetration are the major causes of failure of fertilization when all or most oocytes from a couple do not fertilize in standard IVF. There is a high frequency of defective sperm-ZP interaction in men with oligozoospermia (<20 × 106/mL) and severe teratozoospermia (strict normal sperm morphology ≤5%). Sperm morphology correlates with sperm-ZP binding, and sperm concentration correlates with ZP-induced AR in infertile men with sperm concentrations >20 × 106/mL. Defective ZP-induced AR may cause infertility in up to 25% men with idiopathic infertility. These patients require ICSI despite the normal standard semen analyses.

Conclusion(s)

Sperm-oocyte interaction tests are useful for diagnosis of subtle sperm defects that cause infertility in men without severe abnormalities of semen analysis. Pre-IVF diagnosis of these sperm defects will assist in the clinical assignment of patients to treatment with either standard IVF or ICSI.

Key words

Sperm characteristics
sperm-oocyte interactions
IVF
ICSI

Cited by (0)

Supported by Melbourne IVF, East Melbourne, Victoria, Australia, National Health and Medical Research Council, Canberra, Australia (grant nos. 930628 and 970261), and Royal Women's Hospital Research and Ethics Committee.