Impact of serum and follicular fluid kisspeptin and estradiol on oocyte maturity and endometrial thickness among unexplained infertile females during ICSI.

Regulation of fertility by hypothalamo-pituitary-ovarian (HPO) axis involves the pulsatile release of Gonadotropin-Releasing Hormone (GnRH) from the hypothalamus, stimulating the release of Luteinizing Hormone (LH) and Follicle-Stimulating Hormone (FSH) from the anterior pituitary that in turn acts on the ovaries to control gametogenesis [ 1 ]. Kisspeptin (KP) is a neuropeptide that acts via a G-protein coupled receptor and has been found to be the upstream regulator of GnRH release. Hence it plays important roles in female reproduction such as the onset of puberty, ovulation, implantation, placentation and metabolic regulation of fertility [ 1 – 3 ]. The role of KP in puberty onset is supported by the observations that loss of function due to mutations in KP result in the absence of pubertal development, whereas girls with central precocious puberty are found to have higher KP levels [ 4 ]. Furthermore, expression of genes encoding KP in ovarian tissue and granulosa-lutein cells as well as on the glandular and luminal epithelial cells of the endometrium, signifies the role of KP in the regulation of reproductive functions [ 5 , 6 ]. During the ovarian cycle, KP levels increase from the follicular stage to the luteal stage [ 4 ]. Estrogen released by the ovaries acts through its receptors present on KP secreting neurons and, in turn, contributes as the negative feedback on KP secretion [ 6 ]. Infertility is the inability to conceive after one year of regular unprotected intercourse [ 1 , 7 ], an attribute of the dysfunction of the HPO, genetic factors, hormonal imbalances and environmental influences [ 8 ]. However, in 10–30% of couples seeking infertility treatment, the cause cannot be elucidated, referred to as ‘Unexplained Infertility’ (UI). In UI cases, the tubal patency, anatomy of the uterine cavity, serum progesterone levels in the mid-luteal stage and the semen analysis (male partner) are normal [ 9 ]. Treatment options for unexplained infertile females are superovulation and Artificial reproductive techniques (ART), which In Vitro Fertilization (IVF) and ICSI [ 10 ] Constituents of FF indicate variations in the ovarian follicle cells in response to the gonadotrophin’s administration, by producing various biochemically active substances. These may affect oocytes’ sustainability and growing capability and are also linked to fertilization outcomes and early post-fertilization development [ 11 ]. Literature reveals that follicular fluid (FF) produced by the granulosa cells secrete hormones such as growth hormone, insulin-like growth factor-I, estradiol (E2), and progesterone [ 11 ]. Fluctuations in serum and FF-KP levels have been observed during the preovulatory and luteal stages of the reproductive cycle [ 11 – 14 ]. Furthermore, at ovulation induction (OI) during ART, higher serum KP levels are known to be associated with a better pregnancy outcome [ 6 ]. Low serum KP levels in UI females [ 9 ], and significant correlation of FF-KP with E2 concentrations and follicular maturity in infertile females undergoing ICSI [ 13 ], show a link between serum and FF KP concentrations and estradiol with the success of ICSI. Therefore, we aim to determine the relationship between serum and FF-KP and estradiol concentrations with oocyte maturity and endometrial thickness (determinants of successful conception) among unexplained infertile females during ICSI.

The mean age of the study subjects was 32.04 ± 2.29 SD years, with mean BMI of 28.51 ± 4.15 SD kg/m 2 . Clinical characteristics of all participants (n = 50) show mean FSH 7.14 ± 1.55 IU/ml and LH 5.98 ± 1.44 IU/ml. The antral follicle count before COS was 7.91 ± 1.9. The mean dose of puregons (rFSH/day) was 175 ± 24.34 in 44 subjects, OPU of them performed on13 (12–13), median (interquartile range). The mean number of embryos transferred to 27 subjects were 1.63 ± 0.56. Out of these 27 female subjects, 17 remained NP, 4 had PA, and 6 acquired CP. In these subjects, the number and maturity of oocytes were 7.89 ± 1.85 and 6.89 ± 2.01, respectively, and was highest in the CP group. Table 1 describes comparison of study variables in outcome groups; NP, PA, CP). The number of mature follicles and endometrial thickness were significantly more in CP subjects when compared with NP subjects (p<0.01). The FF- KP and estradiol levels were significantly higher in CP subjects compared to NP subjects (p<0.05) ( Table 1 ). Values are mean ± SD. Results compared by Analysis of Variance; post hoc LSD test was applied * Significant with Not pregnant at 0.05 ** Significant with Not pregnant at 0.01 ° Significant with Preclinical abortion at 0.05 °° Significant with Preclinical abortion at 0.01 Fig 2 depicts the mean serum KP concentrations were observed to increase within the subjects as the stimulation preceded; however, the mean dropped after retrieval of the oocytes (stage 3). KP showed an increasing trend from stage 1 to stage 3 and was significantly higher in stages 2 & 3 compared to the first stage (p<0.01). A highly significant correlation of KP1 was observed with KP2 (r = 0.845, p<0.001), KP3 (r = 0.833, p<0.001) and KP4 (r = 0.718, p<0.001) among 27 subjects who reached the end of the stimulation successfully. Comparison of estradiol (a) and kisspeptin (b) in all stages of stimulation. *Significant with stage 1 at 0.05 ** Significant with stage 1 at 0.01. Stage 1, FS: Follicular stimulation, Stage 2, OI: Ovulation Induction, Stage 3, OPU: Oocyte pickup, Stage 4, ET: Embryo transfer. Estradiol also showed an increasing trend from stage 1 to stage 3, and was significantly higher in the latter two when compared with the first stage (p<0.01). E1 demonstrated a moderately significant correlation with E2 (r = 0.445, p = 0.020), E3 (r = 0.501, p = 0.008) and E4 (r = 0.484, p = 0.011) ( Fig 2 ). Serum E2, E3 and E4 were significantly higher in CP compared to PA subjects (p<0.01). Similarly, serum KP2, KP3 and KP4 levels were significantly higher in CP subjects when compared to NP subjects (p<0.05) ( Fig 3 ). Comparison of estradiol (a) and kisspeptin (b) at various stages of stimulation in all three outcome groups. *Significant with stage 1 at 0.05 ** Significant with stage 1 at 0.01. FS: Follicular stimulation, OI: Ovulation Induction, OPU: Oocyte pickup, ET: Embryo transfer. Serum KP and estradiol levels in NP, PA, and CP subjects showed significantly higher concentrations in OI, OPU and ET (stages 2, 3 and 4) as compared to stage 1 (p<0.01), and the highest levels were found in the 3 rd stage. Follicular KP and estradiol levels were highest in the CP females. A moderate association was found between FF-KP and FF estradiol (r = 0.584, p = 0.001) ( Fig 4A ). The FF- KP was observed to correlate with the oocyte maturity (r = 0.511, p = 0.006) ( Fig 4B ) and KP3 (r = 0.930, p = 0.000) ( Fig 4C ). Furthermore, KP3 was positively associated with E3 (r = 0.624, p = 0.001) ( Fig 4D ) and endometrial thickness (r = 0.527, p = 0.005) ( Fig 4E ). a) Correlation of Follicular estradiol and follicular KP b) Correlation of Follicular KP with number of mature oocytes c) Correlation of Follicular KP with Serum KP3 d) Correlation of Serum KP3 with Serum estradiol e) Correlation of Serum KP3 with endometrial thickness.

In ICSI cycles, serum KP and increased from the initiation of stimulation to egg collection (from stages 1 to 3), with a higher concentration depicted in FF. The stimulated granulosa increased the production of estradiol, which was reflected in both serum and FF concentrations, during these stages. Estradiol production reached its maximum in the OI phase. A strong positive correlation of KP3 and E3 with the determinants of successful conception; number of fertilized oocytes and endometrial thickness emphasize on the role of KP and estradiol in successful conceptions. Thus increase in serum and FF of KP and estradiol levels assisted in acquiring an optimum endometrial thickness, and fertilization of oocytes with more chances of clinical pregnancy in ART /ICSI cycles of UI females. We recommend further clinical trials with more UI females to determine the impact of serum and FF -KP and estradiol on UI females’ outcome measures during ICSI. This will help us understand the therapeutic options for KP in treating infertility, especially the unexplained cases.

This cross-sectional study was carried out at the Australian Concept Infertility Medical Center (ACIMC) from March 2017 to March 2018. Ethical approval was obtained from the Institute Review Board of the ACIMC and Aga Khan University, Pakistan (ERC#3331-BBS-ERC-14), and all participants signed written consent. Women with unexplained infertility (n = 50); duration of infertility more than two years with regular menstrual cycles (21–35 days), normal endocrine profile (normal levels of FSH (<11 IU/L) in early follicular phase (day 2–5), normal Prolactin levels (<20 mg/L) in serum, normal thyroid levels), pelvic ultrasonography with patent fallopian tubes, intact ovaries and uterus, no prior ovarian surgery with normal semen profile of their husband [ 9 , 15 ] age 24 to 35 years booked for ICSI treatment were included in the study. Females with uterine fibroids, endometriosis, polycystic ovaries, uterine and cervical lesions, metabolic disorders, and those following the short agonist and antagonist protocol for ICSI, were excluded. Male causes of infertility based on low sperm parameters (sperm count/motility/morphology) according to Kruger’s strict criteria were also omitted [ 16 ]. For the downregulation of the hormones, daily injections of Deca-Peptyl (Gonadotropin-releasing hormone agonist) were administered to the patients from Day 21 of the previous cycle. The treatment protocol was carried out in stages (1–4) with sequence of dropouts from the study is given in Fig 1 . Stage 1: Follicular stimulation (FS) (n = 50). Down-regulation was followed by controlled ovarian stimulation (COS) by gonadotrophin injections (Only Inj Puregon) for fourteen days. The dose was titrated with respect to basal FSH and follicular monitoring by Transvaginal Ultrasound (TVS). Out of the 50 females, 44 females reached the ovarian induction stage (stage 2). Cycle of 4 females was cancelled due to inadequate response to stimulation, whereas two did not opt to continue the treatment. Stage 2: Ovulation induction (OI)(n = 44). On the confirmation of the maturity of at least 3 follicles (measuring18 mm in diameter) by TVS, ovulation was induced by injecting human chorionic gonadotrophin (hCG) 36 ± 1 hour before oocyte pick up (OPU). Maturity of follicles was not confirmed in six females, we could not perform OPU of these females. On the same day, endometrial thickness was measured by a Transvaginal Scan (TVS) in the midsagittal plane by two-dimensional ultrasound with a 7.5 MHz vaginal probe (Hitachi E UB 525; Hitachi, Tokyo Japan) at the thickest endometrial segment [ 17 ]. Stage 3: Oocyte Pick Up (OPU) (n = 38). Mature oocytes of females (n = 38) were retrieved 36 hours after hCG injection by vaginal ultrasound probe with 16G adapter and double-lumen oocyte aspiration needle on 14 th , 15 th , or 16 th day of stimulation. All the collected eggs were treated and then transferred to the incubator for about 1–2 hours prior to insemination by ICSI procedures. During this phase, follicular fluid (FF) was acquired from all follicles (measuring 18 mm or more on ultrasound) from each ovary of the patient [ 18 ]. Stage 4: Embryo transfer (ET) (n = 27). After confirmation of fertilization and cleavage (18 to 24 hours after egg collection), embryos were graded from 1–5 [ 19 ]. The embryo transfer of 27 females (blastocysts) was done on Day 5 using Sims-Wallace Embryo Replacement Catheter, under ultrasound guidance. The venous blood samples were collected for estimation of serum KP and estradiol at the beginning of stimulation (stage 1), at the time of hCG administration on OI day (stage 2), on OPU (stage 3) and ET days (stage 4). After collecting blood, the serum fraction and the plasma fraction were separated rapidly by centrifuge and frozen at −80°C until assayed. Serum samples were used to detect the concentration of the hormone, using commercially available ELISA kits, following the manufacturer’s protocol. The ELISA kits used were: serum KP (Cat. No: 95611, Glory BioScience, USA) with analytical sensitivity of 10.16 ng/L and intra and inter assay coefficients of variation of less than 10% and 12%, respectively, serum FSH (Kit Cat. No DKO010; DiaMetra) with the inter assay coefficient of variation, <8% and intra assay coefficient of variation <9.7% and serum LH (Kit Cat. No DKO010; Dia Metra) with inter assay coefficient of variation of <7.91%; intra assay coefficient of variation of <9.21%. Serum estradiol was determined using a commercially available kit for Human estradiol (E2) Enzyme Immunoassay Kit (Catalog # 07BC-1111 by MP BioCheck, Inc.). On the day of oocyte retrieval, two-dimensional mean diameter the follicles, were measured by TVS followed by ultrasound guided aspiration in order to pool FF samples from around one to five follicles of both ovaries, each 18-mm diameter or larger. Samples that appeared blood stained or with oocytes were discarded. For each patient, about 20–40 ml of FF were transferred to sterile conical tubes (BD Falcon, Becton Dickinson, Franklin Lakes, NJ) and centrifuged at 1500 x G for 10 minutes at room temperature. Supernatant was aliquoted in 2ml cryovials and was stored at -80°C refrigerator until further analyzed for hormones [ 18 ]. Luteal support of included females (after egg collection) was maintained by progesterone vaginal pessaries (Cyclogest 400 mg) twice a day. We assessed ß-hCG at the end of the treatment approximately 14 days after ET as the outcome marker. TVS was performed 14 days after receiving positive results of ß-hCG to confirm the presence of gestational sac and cardiac activity. Based on ß-hCG and TVS results, women were grouped as: Non-pregnant (NP) if women had ß-hCG 5–25 mIU/ml, Preclinical Abortion (PA) if women had ß-hCG>25 mIU/ml and no fetal cardiac activity on TVS. Women with ß-hCG >25 mIU/ml and evidence of cardiac activity on TVS were grouped as Clinical pregnancy (CP) [ 20 ]. All of the clinical and hormonal data were entered and statistically analyzed on SPSS IBM Statistical Package for the Social Sciences (IBM, SPSS version 21;IBM Corp Inc., Armonk, NY, USA). Descriptive analysis of continuous variables was expressed as mean ± standard deviation/error and median (interquartile range). For statistical comparison of variables among stages or groups of patients (NP, CA, CP), analysis of variance (ANOVA) was performed, where p value <0.05 and <0.01 was considered statistically significant and highly significant, respectively. Spearmen correlation coefficient was utilized to detect the effect of hormones on the outcome, p value <0.05 and <0.01 was considered statistically significant and highly significant, respectively.

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