Department of Obstetrics and Gynecology, School of Medicine, University of São Paulo (USP), São Paulo, Brazil.
Gynecol Endocrinol. 2013 Mar;29(3):201-4. doi: 10.3109/09513590.2012.736554. Epub 2012 Nov 20.
The aim of this study was to evaluate the effects of bromocriptine on vascular endothelial growth factor (VEGF) levels in serum, kidney function and ovarian hyperstimulation syndrome in women undergoing in vitro fertilization. Twenty-eight women were randomly divided into two groups and were administered daily oral capsules for 14 days, starting on the day of human chorionic gonadotropin (hCG) administration. Group A received 2.0 mg of folic acid, whereas Group B was given 2.5 mg of bromocriptine. Physical exams, pelvic ultrasounds and laboratory evaluations were performed on the day of hCG administration and again 7 days later. No differences in ovarian hyperstimulation syndrome, urine volume, creatinine clearance, urine sodium concentration or serum VEGF levels were found between the two groups. Thus, these results indicate that bromocriptine does not affect blood levels of VEGF, kidney function or the incidence of ovarian hyperstimulation syndrome in high-risk patients subjected to in vitro fertilization.
本研究旨在评估溴隐亭对接受体外受精的妇女血清血管内皮生长因子 (VEGF) 水平、肾功能和卵巢过度刺激综合征的影响。28 名妇女随机分为两组,从人绒毛膜促性腺激素 (hCG) 给药日开始每日口服胶囊,持续 14 天。A 组给予 2.0mg 叶酸,B 组给予 2.5mg 溴隐亭。hCG 给药日和 7 天后进行体格检查、盆腔超声和实验室评估。两组间卵巢过度刺激综合征、尿量、肌酐清除率、尿钠浓度或血清 VEGF 水平无差异。因此,这些结果表明,溴隐亭不会影响接受体外受精的高危患者的血液 VEGF 水平、肾功能或卵巢过度刺激综合征的发生率。