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The effects of gonadotropin-releasing hormone agonist on androstenedione production and follicular development during controlled ovarian hyperstimulation.

作者信息

Akaboshi K, Oda T, Yoshida J, Kohriyama S, Miyazaki T, Yoshimura Y

机构信息

Department of Obstetrics and Gynecology, Tokyo Dental College, Chiba, Japan.

出版信息

J Assist Reprod Genet. 1998 Sep;15(8):478-84. doi: 10.1023/a:1022530420110.

Abstract

PURPOSE

We performed a prospective randomized study to assess the effects of a GnRH agonist (GnRH-a) on follicular development and steroidogenesis during controlled ovarian hyperstimulation (COH).

METHODS

Patients undergoing in vitro fertilization (IVF) for tubal infertility received human menopausal gonadotropin (hMG) stimulation with or without the GnRH-a, buserelin, beginning in the midluteal phase of the prior cycle. We analyzed serum hormone levels, follicular development, and outcome of IVF.

RESULTS

The mean number of retrieved oocytes was significantly greater, and the implantation rate per embryo was significantly higher, in the GnRH-a/hMG group (n = 101) than in the hMG-only group (n = 97). The concentration of androstenedione (A) and the A/estradiol ratio in the serum were significantly lower in the GnRH-a treatment group throughout the follicular phase.

CONCLUSIONS

The concomitant use of GnRH-a during COH prevents atretic change of the follicles and enhances follicular development by reducing androgen accumulation, resulting in a higher developmental competence of the oocytes.

摘要

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本文引用的文献

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Modulation of the steroidogenesis of cultured human granulosa-lutein cells by gonadotropin-releasing hormone analogs.
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J Clin Endocrinol Metab. 1984 Apr;58(4):755-7. doi: 10.1210/jcem-58-4-755.
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