Impact of Luteinizing Hormone on IVF/ICSI Assisted Reproduction on the Initiation Day of Gonadotropin-releasing Hormone Antagonist Protocol.

Li-Jia Zhang, Dun Liu, Li-Qing Xu, Jin-Yan Wei, Lin Fan, Xi-Qian Zhang, Feng-Hua Liu
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Abstract

Objective: The aim of the study was to explore the optimal timing of gonadotropin initiation and the reasonable interval of luteinizing hormone (LH) levels in the gonadotropin-releasing hormone antagonist (GnRH-A) protocol.

Methods: A retrospective cohort study was conducted to analyze the data concerning the oocyte retrieval cycles from 1,361 cases with the GnRH-A protocol implemented. The ovarian responses (including AMH, AFC) in these patients were divided into the poor ovarian response group (an antral follicle count [AFC] ≤ 6, n = 394), the normal ovarian response group (an AFC > 6 and < 15, n = 570), and the high ovarian response group (an AFC ≥ 15, n = 397), according to the AFC. The patients were sub-grouped according to LH levels on the protocol initiation day, and the clinical outcomes (including dose of Gn initiation, Gn administration days, GnRH-ant administration days, P levels on the HCG day, E2 levels on the HCG day, LH levels on the HCG day, number of embryos transferred, total fertilization rate, embryo implantation rate(%), proportion of 2PN, proportion of good-quality embryos, endometrial thickness on the hCG injection day(mm), moderate to severe OHSS, AFC on the initiation day, proportion of type A endometrium on the hCG injection day, clinical pregnancy rate, biochemical pregnancy rate, early abortion rate, ectopic pregnancy rate) were compared.

Results: On the GnRH-A protocol initiation day, among all patients with different ovarian responses, the body mass index (BMI) in those with an LH ≥ 5 IU/L was lower. The differences in pregnancy outcomes between the LH < 5 IU/L group and the LH ≥ 5 IU/L group were not statistically significant across the different ovarian response groups, but the LH < 5 IU/L group had a higher proportion of good-quality embryos (80.3±24.9 vs. 74.8±26.9, P =0.035) than the LH≥5IU/Lgroup in those with poor ovarian response. The total fertilization rate (82.2±18.1 vs 85.4±15.1, P =0.021) and proportion of two pronuclei (2PN) (69.0±20.9 vs 72.7±19.9, P =0.035) were higher in the LH ≥ 5 IU/L group than the LH<5 IU/L group for those with normal ovarian responses. The embryo implantation rate (41.4±41.3 vs 52.6±43.4, P =0.012) was higher in the LH ≥ 5 IU/L group than in the LH<5 IU/L group in those with high ovarian response. The results of the multivariate logistic analysis showed that the age of the female partner, number of embryos transferred, proportion of good-quality embryos, endometrial thickness on the hCG injection day, and moderate- to-severe ovarian hyperstimulation syndrome (OHSS) were independent factors correlated with the outcome of live births (P < 0.05).

Conclusion: The LH levels on the gonadotropins (Gn) initiation day in the GnRH-A protocol will not affect pregnancy outcomes.

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促性腺激素释放激素拮抗剂方案启动日促黄体素对试管婴儿/卵胞浆内单精子显微注射辅助生殖的影响。
研究目的该研究旨在探讨促性腺激素释放激素拮抗剂(GnRH-A)方案中促性腺激素启动的最佳时机和黄体生成素(LH)水平的合理间隔:方法: 我们进行了一项回顾性队列研究,分析了 1,361 例实施 GnRH-A 方案的卵母细胞获取周期的相关数据。根据这些患者的卵巢反应(包括AMH、AFC),将其分为卵巢反应差组(前卵泡计数[AFC]≤6,n=394)、卵巢反应正常组(AFC>6且<15,n=570)和卵巢反应高组(AFC≥15,n=397)。根据方案启动日的 LH 水平和临床结果(包括 Gn 启动剂量、Gn 施用天数、GnRH-ant 施用天数、HCG 日的 P 水平、HCG 日的 E2 水平、HCG 日的 LH 水平、胚胎移植数量、总受精率、胚胎着床率(%))对患者进行分组、比较了胚胎移植数量、总受精率、胚胎植入率(%)、2PN 比例、优质胚胎比例、hCG 注射日子宫内膜厚度(毫米)、中重度 OHSS、启动日 AFC、hCG 注射日 A 型子宫内膜比例、临床妊娠率、生化妊娠率、早期流产率、异位妊娠率。结果在 GnRH-A 方案启动日,在所有卵巢反应不同的患者中,LH ≥ 5 IU/L 的患者体重指数(BMI)较低。在不同卵巢反应组中,LH < 5 IU/L 组和 LH≥ 5 IU/L 组的妊娠结局差异无统计学意义,但在卵巢反应差的患者中,LH < 5 IU/L 组的优质胚胎比例(80.3±24.9 vs. 74.8±26.9,P =0.035)高于 LH≥5IU/L 组。LH≥5IU/L组的总受精率(82.2±18.1 vs 85.4±15.1,P =0.021)和双子核(2PN)比例(69.0±20.9 vs 72.7±19.9,P =0.035)均高于LH≥5IU/L组:GnRH-A方案中促性腺激素(Gn)起始日的LH水平不会影响妊娠结局。
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