Centre for Reproductive Medicine, Universitair Ziekenhuis Brussel, Laarbeeklaan 101, Brussels 1090, Belgium; Department of Obstetrics, Gynecology and Reproductive Medicine, Santa Maria University Hospital, Avenida Professor Egas Moniz, Lisbon 1649-035, Portugal.
Centre for Reproductive Medicine, Universitair Ziekenhuis Brussel, Laarbeeklaan 101, Brussels 1090, Belgium; Academic Unit of Obstetrics and Gynecology, IRCCS AOU San Martino-IST, University of Genoa, Largo Rosanna Benzi 10, Genova 16132, Italy.
Reprod Biomed Online. 2019 Apr;38(4):647-654. doi: 10.1016/j.rbmo.2018.11.016. Epub 2018 Dec 8.
Progesterone overproduction during ovarian stimulation is associated with lower live birth rates (LBR) after fresh embryo transfer. Therefore, circulating P concentrations on the day of HCG administration are frequently measured in clinical practice and followed by an elective cryopreservation strategy whenever late-follicular elevated P (LFEP) occurs. A recent study concluded that the duration of LFEP >1.00 ng/mL prior to HCG administration may also affect clinical pregnancy rates. The objective of this current study was to assess whether this hypothesis was reproducible using LBR as the primary outcome.
Retrospective analysis including women undergoing IVF/ICSI between 2010-2015. LBR were compared among different P elevation duration subgroups (0, 1 or >1 day) using two LFEP thresholds (>1.00 ng/mL and >1.50 ng/mL).
The duration of LFEP >1.00 ng/mL was not associated with a significant decrease in LBR according to whether the patient had LFEP lasting for 0, 1 or >1 days (29.9%, 30.3% and 26.3%, respectively). Conversely, when using >1.50 ng/mL as the LFEP threshold, LBR decreased significantly (30.3% 20.4% and 20.5%, respectively). However, the relative frequency of having LFEP >1.50 ng/mL for >1 day was exceedingly rare (1.9%) and the additional benefit of evaluating LFEP beyond the day of HCG triggering no longer remained statistically significant after confounder-adjustment with multivariable regression analysis.
These results suggest a lack of benefit in measuring serum P in the days preceding HCG administration, since LBR in women with LFEP >1 day do not vary significantly from those with LFEP detected only on the day of HCG administration.
卵巢刺激过程中孕酮过度产生与新鲜胚胎移植后的活产率(LBR)降低有关。因此,在临床实践中,通常会在 HCG 给药日测量循环 P 浓度,并在出现晚卵泡期高 P(LFEP)时,根据情况选择进行选择性冷冻保存策略。最近的一项研究得出结论,HCG 给药前 LFEP 持续时间>1.00ng/ml 也可能影响临床妊娠率。本研究的目的是评估使用 LBR 作为主要结局来验证该假说是否具有重现性。
对 2010-2015 年期间进行 IVF/ICSI 的女性进行回顾性分析。使用两个 LFEP 阈值(>1.00ng/ml 和>1.50ng/ml),根据不同的 P 升高持续时间亚组(0、1 或>1 天)比较 LBR。
根据 LFEP 持续时间为 0、1 或>1 天的患者,LFEP >1.00ng/ml 与 LBR 无显著降低相关(分别为 29.9%、30.3%和 26.3%)。相反,当使用>1.50ng/ml 作为 LFEP 阈值时,LBR 显著降低(分别为 30.3%、20.4%和 20.5%)。然而,LFEP >1.50ng/ml 持续时间>1 天的相对频率非常罕见(1.9%),并且在经过多变量回归分析调整混杂因素后,评估 HCG 触发日之外的 LFEP 不再具有统计学意义。
这些结果表明,在 HCG 给药日前测量血清 P 并无益处,因为 LFEP 持续时间>1 天的女性的 LBR 与仅在 HCG 给药日检测到 LFEP 的女性没有显著差异。