Significant Serum Progesterone Variations on the Day of Final Oocyte Maturation in Stimulated IVF Cycles.

The serum level of progesterone (P4) during the follicular phase and especially on the day of final oocyte maturation in stimulated IVF/ICSI cycles has been widely studied since the initial studies in 1991 ( 1 ). Evidence suggests that elevated progesterone levels during late follicular phase adversely affect implantation and pregnancy rates ( 2 , 3 ). According to literature, the critical value above which an adverse impact on pregnancy rate occurs has been defined at 1.5 ng/ml ( 2 ). Hence, serum progesterone values during the late follicular phase of ovarian stimulation attract significant interest and the etiology of the progesterone elevation is a matter of ongoing research. Despite the common belief that progesterone is present only during the luteal phase, a small increase in P4 levels is observed prior to the LH surge. In contrast to a natural cycle with the development of typically a single dominant follicle, the aim of ovarian stimulation for IVF is to maximize the chances of pregnancy by recruiting an adequate number of oocytes. In order to achieve this goal and following the FSH threshold concept ( 4 ), ovarian stimulation prior to IVF requires the administration of relatively high doses of exogenous gonadotropins to support multi-follicular growth ( 5 ). To prevent serum gonadotropin levels from dropping below the threshold with the consequence of follicular growth arrest, daily gonadotropin injections are required to maintain continuous stimulation of the follicles until final oocyte maturation. This results in supraphysiological serum steroid levels creating a completely different endocrine environment as compared to a natural cycle and progesterone elevation at the end of the follicular phase is documented in up to 30% of the stimulated ART cycles ( 6 , 7 ). The progesterone level on the day of final oocyte maturation is a crucial parameter regarding the decision whether to perform a fresh embryo transfer or cryopreserve the embryos. Whereas, in a natural cycle, mean levels of progesterone decline rapidly during the daytime and increase again in the early morning ( 8 , 9 ), there is a lack of knowledge regarding the secretory-pattern of progesterone during the day of final oocyte maturation in stimulated cycles. A recently published study ( 10 ) found a significant decline of progesterone levels on the day of trigger in a population of young oocyte donors, undergoing ovarian stimulation for oocyte retrieval. Contrary to a population of oocyte donors, in the “real life scenario” of an infertility clinic, the progesterone level on the day of final oocyte maturation is of utmost importance for patients who are planned to undergo a fresh embryo transfer. Therefore, this study was designed to analyse the variation of progesterone levels on the day of final oocyte maturation by measuring progesterone at four different times in a “real” infertile population.

US substantial contribution to concept, design, acquisition, analysis, interpretation of data, manuscript preparation. BL substantial contribution to concept, design, analysis and interpretation of data, manuscript preparation, and critical revision of the article and final approval. LB contribution to concept and design of study, critical revision of the article. LD contribution to SAS programming, analysis, and interpretation of data. FR contribution to acquisition of data. CC contribution to linguistic revision of study. HF contribution to critical revision of data and final approval. The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

This study was approved by the ethics committee of IVIRMA Middle East Fertility Clinic, Abu Dhabi, UAE (REFA016/2018) and the Ministry of Health, Oman. This study was registered at the clinicaltrials.gov under the number: NCT03519776 . The patients/participants provided their written informed consent to participate in this study.

A total of 120 samples from 30 patients were included in this prospective study. The mean age of the patients was 32.9 years (CI 95% 31.2–34.6; SD 4.5) and the mean BMI was 26.7 kg/m 2 (CI 95% 25.1–28.3; SD 4.3). The ovarian reserve parameters showed a mean value of AMH of 3.1 ng/ml (CI 95% 2.4–3.9; SD 1.9) and for AFC a mean value of 18.2 (CI 95%14.9–21.5; SD 8.8). Out of the 30 patients included in the study 15 (50%) were cases of male factor infertility, 7 (23.3%) with ovulation disorders, 5 (16.7%) with low ovarian reserve according to Bologna criteria ( 14 ), 1 (3.3%) with endometriosis and 2 (6.7%) with infertility of unknown etiology. The baseline investigations are summarized in Table 1 . Baseline parameters of the patients. AFC, antral follicle count; AMH, anti-mullerian hormone; FSH, follicle stimulating hormone; LH, luteinising hormone; BMI, body mass index . Ovarian stimulation for IVF/ICSI was performed in a GnRH-antagonist protocol in all patients. Stimulation length ranged from 8 to 15 days with a mean of 11.3 days (CI 95%10.7–11.8; SD 1.6). The average value of progesterone for reducing the dose of gonadotropin was 0.6 ng/ml (CI 95% 0.5–0.8; SD 0.3). On the day of final oocyte maturation, a mean follicle number of 17.8 (CI 95% 14.8–20.8; SD 8.0) was seen during the vaginal ultrasound. By means of oocyte pick up (OPU) procedure, a mean of number 15.1 (mean CI 95% 12.5–17.6; SD 6.9) were retrieved, out of which 10.7 (mean CI95%, range 8.8–12.5; SD 4.9) oocytes were mature(MII).The stimulation characteristics are charted in Table 2 . Stimulation characteristics. Gn, gonadotropins; COC, Cumulus oophorus complex; CI, confidence interval . Serum progesterone levels on the day of final oocyte maturation were highest in the morning and declined during the day, with the following mean values: at 8 a.m.:1.0 ng/ml, at 11 a.m.:0.8 ng/ml, at 2 p.m.:0.7 ng/ml and at 5 p.m.:0.6 ng/ml. The coefficient of variation for those values were 44.7, 43.8, 43.0, and 50.1 respectively to each point time. The difference between the first and the last progesterone level was 0.4 ng/ml, reflecting a 37.8% decline of the progesterone level within 9 h. The difference noted in the progesterone levels between 8 a.m. and 11 a.m., 8 a.m. and 2 p.m., 8 a.m. and 5 p.m., 11 a.m. and 5 p.m. showed a highly significant decrease ( p < 0.0001) and a significant decrease from 11 a.m. to 2 p.m. ( p = 0.0002). However, no significant decrease was observed between 2 and 5 p.m.The SD, 95% CI for the progesterone measurements at the different time points are given in Table 3 and the decline in progesterone values over the day is charted in Figure 1 . Relationship between the different parameters and the mean progesterone levels at 8 a.m. and 5 p.m. p = ANOVA. COC, Cumulus oophorus complex; MII, Mature oocytes . Mean and Median progesterone levels (ng/ml) on the day of final oocyte maturation. Highly significant correlations were found between the AFC and the progesterone level at 8 a.m. ( p < 0.001) as well as between the AMH level and progesterone level at 8 a.m. ( p < 0.001). The correlation between number of follicles seen on the day of final oocyte maturation and progesterone level at 8 a.m. was significant whereas no correlation was found to the progesterone level at 5 p.m. The values of progesterone at 8 a.m. and 5 p.m. on day of trigger did not show any significant correlation with BMI, age, values of LH, and FSH on day 2/3 of the cycle, the dose of gonadotropin or GnRH-antagonist, the number of stimulation days or type of medication for ovulation induction used. The correlations between the different parameters and the progesterone levels at 8 a.m. and 5 p.m. are summarized in Figure 2 . The absolute mean difference in progesterone levels on day of final oocyte maturation is charted in Figure 3 . Correlations between the parameters AFC, BMI, female age, stimulation period, AMH, and the mean progesterone levels at 8 a.m. and 5 p.m. ρ = Pearson correlation coefficient. AFC, antral follicle count; BMI, body mass index; AMH, anti-mullerian hormone. Absolute Mean difference in progesterone levels (ng/ml) on the day of final oocyte maturation. Diff1 = P4 2 p.m. – P4 5 p.m.; Diff2 = P4 11 a.m. – P4 5 p.m.; Diff3 = P4 11 a.m. – P4 2 p.m.; Diff4 = P4 8 a.m. – P4 11 a.m.; Diff5 = P4 8 a.m. – P4 2 p.m.; Diff6 = P4 8 a.m. – P4 5PM; NS, not significant. *** p < 0.0001; ** p -value 0.0002.

The progesterone level on the day of final oocyte maturation plays a crucial role in the decision to perform either a fresh embryo transfer or, in the event of progesterone elevation, to vitrify the embryos and perform cycle segmentation. However, the published and commonly accepted cut-off value of 1.5 ng/ml ( 2 ) is not only based on different assays used for progesterone measurement, which may impact the progesterone result ( 12 ), furthermore, it is also based on a progesterone level, taken on an arbitrary time on the trigger day. Recently, the group of González-Foruria et al. ( 10 ) published a 44.0% decline of progesterone levels over the day of final oocyte maturation in a group of 20 oocyte donors. In the herein presented study, we evaluated the course of progesterone levels on the day of final oocyte maturation in a group of 30 patients with primary/secondary infertility and an indication for ovarian stimulation for IVF/ICSI treatment. The findings of our study confirmed the findings of González-Foruria et al. ( 10 ) demonstrating a significant decline of the P4 level from the morning to the afternoon in patients who are stimulated in a GnRH-antagonist protocol, taking the stimulation medication in the evening, 12 h prior to the first P4 measurement. As afore mentioned, the event of P4 elevation on day of final oocyte maturation occurs in up to 30.0% of the stimulated ART cycles ( 6 , 7 ). Elevated progesterone levels adversely affect endometrial receptivity and pregnancy rates through endometrial advancement, leading to asynchrony between endometrial development and embryo stage ( 15 ). Moreover, as per latest studies, elevated progesterone values on trigger day can negatively impact oocyte and embryo quality ( 16 – 18 ). The current study, as well as the study of González-Foruria et al. ( 10 ), demonstrate clearly significant variations in daily progesterone levels on the day of final oocyte maturation. These findings question the accuracy of the single result and raise doubts, whether the reproductive medicine specialist is able to draw solid conclusions when depending on this blood test result to decide on a possible adverse impact on endometrial receptivity and embryo quality. The clear decline of the progesterone levels over the day of final oocyte maturation, which was shown in the blood tests 12, 15, 18, and 21 h after the last gonadotropin administration in both studies confirm the theory, that elevated progesterone levels are a result of enhanced stimulation pressure on the follicles toward the end of stimulation ( 19 , 20 ). Compared to our data, the study of González-Foruria ( 10 ) found a more pronounced decrease of progesterone levels over the day of final oocyte maturation (37.8 vs. 44%), most probably due to a longer duration between the first and the last progesterone measurement (9 vs. 12 h). Ovarian stimulation for IVF requires daily administration of exogenous gonadotropins to result in multifollicular growth and each of these follicles contribute to the amount of progesterone in circulation ( 21 ). The significant correlation in our study between the number of follicles seen on the day of final oocyte maturation and the progesterone level at 8 a.m. confirm the findings of Kyrou et al. ( 21 ). Furthermore, the highly significant correlation between AMH / AFC and the progesterone level at 8 a.m. underlines the risk of patients with a good ovarian reserve to develop elevated progesterone levels on the day of final oocyte maturation. Estradiol and progesterone are products of the steroidogenesis and the concentrations of both hormones increase with growing follicle diameter ( 22 ). The enzyme CYP17 metabolizes progesterone further on, however due to low lyase activity progesterone concentration increases particularly toward the end of ovarian stimulation, causing elevated progesterone levels in stimulated IVF cycles ( 23 ). Reduction of the FSH stimulation dosage will prevent an overload of the capacity of the CYP17 enzyme activity which has been corroborated by our study, finding of a significant decline in serial progesterone levels in parallel with the subsiding effect of the stimulation medication. The inclusion of 30 “real life” infertility patients, the use of different exogenous gonadotropins for ovarian stimulation and the measurement of all progesterone values with the same reagents, starting 12 h after the last gonadotropin injection, are the strengths of our study. A limitation may be seen in the restriction of the study to patients, being stimulated in a GnRH-antagonist protocol, as well as in the administration scheme with the gonadotropin injections taken in the evening. Therefore, these findings may not apply to the course of progesterone levels on the day of final oocyte maturation in other stimulation protocols and with a different timing of the gonadotropin injections. Further on, progesterone levels were not correlated with the reproductive outcomes as the number of participants were only 30 and due to the fact that a “freeze-all” strategy for all cycles was applied. Based on our previous publications on the etiology of progesterone serum levels during ovarian stimulation for ART ( 12 , 19 ) and the knowledge gained from the current study, it maybe speculated that the diurnal serum progesterone levels would be opposite of the current findings (higher in the morning and lower in the evening), if gonadotropins would be administered in the morning. Future studies with different timing of gonadotropin administration should be performed to evaluate and possibly confirm this theory.

The herein described findings of our study have an important impact on the daily work of a reproductive medicine specialist. The findings of a significant decline in progesterone levels from 12 to 21 h after the evening gonadotropin administration, on the day of final oocyte maturation underlines firstly the importance of a critical evaluation of the progesterone measurement, as this progesterone level is a crucial parameter which has a significant impact on the decision for or against a fresh embryo transfer or the need to vitrify embryos. This finding is important as it will raise the awareness of the reproductive medicine specialist that there is a fluctuation of the progesterone levels over the day of the final oocyte maturation and that in the herein described setting with the administration of the gonadotropin in the evening, progesterone levels will decline over the day. Therefore, performing the blood sample for progesterone measurement in the evening will result in a lower progesterone level compared to when the blood sample would have been taken in the morning. Secondly, it confirms the theory of enhanced stimulation pressure on the follicle being a cause of progesterone elevation and the possibility to avoid this event by reducing the stimulation dosage.

All datasets generated for this study are included in the article/supplementary material.

This prospective observational study was conducted from May 2018 to March 2019 in IVIRMA Fertility Clinic Muscat, Oman. Patients with primary/secondary infertility and an indication for IVF/ICSI treatment were included, fulfilling the following inclusion criteria: age 18–40 years, BMI 18–35 kg/m 2 , menstrual cycle length 24–35 days and ovarian stimulation using recombinant Follicle-stimulating-hormone (rec FSH) or human-Menopausal-Gonadotropin (hMG) in an antagonist cycle. At the time of drafting of protocol there was no published data on the fluctuation of the progesterone levels during the day of final oocyte maturation, therefore 30 patients were chosen as this trial was launched as a pilot study. All recruited patients provided written informed consent in accordance with the Declaration of Helsinki. The value of AMH for all patients was measured on day 2/3 of the menstrual cycle using Cobas e 411 analyzer (Roche Diagnostics, Mannheim, Germany). The measuring range is 0.01–23 ng/ml (0.07–164 pmol/L). Values below the limit of detection are reported as 23 ng/ml or up to 46 ng/ml for a two-fold diluted sample. The antral follicle count (AFC) was evaluated on day 2/3 of the cycle at the time of start of ovarian stimulation. Transvaginal scans were performed using a Voluson 6 (GE Healthcare, Milwaukee, WI, USA) ultrasound machine, equipped with a 7–10 MHz two-dimensional transvaginal probe. The patients were asked to empty their bladders and were placed in the lithotomy position. For the determination of the AFC, all follicles in a size from 2 to 10 mm were counted for each ovary and summed up for the AFC result. The samples of estrogen, progesterone, FSH, LH, AMH were collected on the first day of stimulation. The patients were followed up and reevaluated for hormones on day 8/9 of stimulation and thereafter as per individual response to treatment. Ovarian stimulation was performed in a flexible antagonist protocol, using either rec FSH or HMG as stimulation medication and GnRH antagonist Cetrotide 0.25 {European marketing division-Serono, Mfg. date 03/2018}, or Ganirelix Acetate 0.25 mg {Organon, Mfg. date 27/10/2017} for pituitary suppression. Stimulation medication dose was individualized according to the ovarian reserve parameters ( 11 ). A daily dose of 0.25 mg of GnRH antagonist was started depending on follicular size when a dominant follicle was 14 mm in diameter. All patients were administered the gonadotropins for ovarian stimulation at 8 p.m. and GnRH antagonist for pituitary suppression at 8 a.m. If indicated, dose adjustment during ovarian stimulation was individualized according to patient's response. In case a starting progesterone elevation, in combination with a good ovarian response was seen during ovarian stimulation, gonadotropin dosage was reduced as described previously ( 12 ). As soon as three or more leading follicles ≥17 mm in diameter were observed, depending on the ovarian response, final oocyte maturation was induced by administration of either hCG (2,500, 5,000 or 10,000 IU), GnRH agonist (Triptorelin 0.3 mg) in case of risk of OHSS ( 13 ), or dual trigger (hCG and GnRH-analog). Oocyte retrieval was carried out 36 h after administration of medication for final oocyte maturation. Two experienced reproductive medicine specialists performed the oocyte retrieval and a common technique was established for these procedures. The samples of FSH and LH were collected at the time of starting stimulation, which was day 2/3 of patient's menstrual cycle. They were measured by Cobas elecys 2010, modular analytics E170. The detection limits are p 0.1–200 mIU/ml (defined by the lower detection limit and the maximum of the master curve). Values below the detection limit are reported as 200 mIU/ml. Blood samples on the day of final oocyte maturation were drawn from the ante cubital vein by direct puncture. Blood sampling was performed four times during the day at an interval of 3 h: 8 a.m.,11 a.m.,2 p.m., and 5 p.m. before administration of the trigger medicine. The blood samples with a volume of 10 ml were centrifuged for 10 min at 4,000 rpm (revolution per minute) and the supernatant was retrieved and frozen at −21°C. For progesterone measurement, the assay ELECSYS® progesterone generation III was used. The measuring range is 0.159–191 nmol/L or 0.05–60 ng/ml. For detection of analytical specificity, cross-reactivities toward other hormones were used with a maximum cross-reactivity of 3.9% toward 11-Deoxycorticosterone and the minimum cross-reactivity of 0.001% toward Danazol 1 . All samples were thawed at one time and analyzed using the same assay in order to avoid any batch-to-batch variability. Continuous data are summarized according to mean, standard deviation, minimum and maximum. Confidence intervals at 95% are presented for the mean values (95% CI). Progesterone levels are represented as a box plot to describe the variable distribution according to time measurements. The absolute difference between values in P4 based on pair difference for the four measurements were calculated to test mean differences. Since measures are evaluated in a single patient four times but compared two by two a dependent paired T -test was used to test for mean differences. Pearson's correlation coefficient (ρ) was calculated to find the correlation between the continuous parameters and the progesterone levels at the different time points. GLM(General Linear Model) procedure was applied to evaluate the relationship of categorical variables and progesterone levels at different time points. A p < 0.05 is statistically significant. All analyses were performed using SAS studio (SAS® Studio).