4.4 Article

Ovarian Hyperresponse Following the Sole Administration of GnRH Agonist

Journal

COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING
Volume 25, Issue 6, Pages 1082-1085

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1386207324666210302095049

Keywords

GnRH agonist; ovarian hyperstimulation; assisted reproductive technology; polycystic ovary syndrome; gonadotropins; GnRHa

Funding

  1. Research Team of Female Reproductive Health and Fertility Preservation [SZSM201612065]

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Ovarian hyperstimulation can occur following the sole administration of GnRHa without gonadotropins. The antagonist protocol may be an alternative strategy, but caution should be taken regarding the risk of poor embryo quality and low pregnancy rates.
Background: The gonadotrophin-releasing hormone agonist (GnRHa) has gained widespread popularity in achieving pituitary suppression before ovarian stimulation with exogenous gonadotropins in assisted reproductive technology protocols. However, a very small part of patients may develop ovarian hyper response after the sole administration of GnRHa without gonadotropins. Case Report: A 32-year-old female diagnosed with polycystic ovary syndrome presented for her second IVF cycle in our reproductive center. Twenty-eight days after 3.75mg triptorelin was administrated on day 2 of her menstrual cycle, bilateral ovaries were significantly enlarged and presented multiple cystic masses. The hormone profile was as follows: E2>4870pg/ml, P 13.19ng/ml, FSH 14IU/L, and LH 10.77IU/L. The patient felt symptoms of mild ovarian hyperstimulation syndrome. In the subsequent IVF treatment cycle, antagonist protocol was performed. It showed that follicles developed slowly and exogenous gonadotropins were used for 13 days. Finally, seven oocytes were obtained, and only one blastocyst graded 4BC formed. Conclusion: Ovarian hyperstimulation following the sole administration of GnRHa can occur, but the mechanism is still not yet clear. Antagonist protocol may be an alternative fertility strategy, but the risk of poor embryo quality and low pregnancy rate of transplantation should be warned.

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