Serum levels of stem cell factor for predicting embryo quality

We evaluated whether serum stem cell factor (s-SCF) levels just prior to ovulation induction could indicate the ability to develop a top-quality (TQ) blastocyst by day 5. We investigated patients with normal ovarian reserve (NOR), polycystic ovary syndrome (PCOS), diminished ovarian reserve (DOR), or mild endometriosis. Our pilot research suggests a correlation between s-SCF levels and the ability to form TQ blastocysts in patients with mild endometriosis. This significant statistical difference (p < 0.05) was noted between mild endometriosis patients for whom a TQ blastocyst was obtained and those for whom it was not possible, as measured on the 8th day of stimulation and the day of oocyte retrieval. The mean SCF levels in the serum of these women on the 8th day were at 28.07 (± 2.67) pg/ml for the TQ subgroup and 53.32 (± 16.02) pg/ml for the non-TQ subgroup (p < 0.05). On oocyte retrieval day it was 33.47 (± 3.93) pg/ml and 52.23 (± 9.72) pg/ml (p < 0.05), respectively.

oocyte proliferation, differentiation, growth, and survival 12 .The cross-talk between GCs and oocytes involving the interaction of SCF and c-Kit receptor is relevant to the process of follicular development, from the recruitment of the primordial follicle to ovulation, and even the development of the early embryo 18 .
Salmassi et al. investigated the variability in serum concentrations of SCF (s-SCF) during the menstrual cycle in the process of follicular maturation, ovulation, implantation, and pregnancy, and in response to ovarian stimulation with recombinant follicle-stimulating hormone 15 .The authors demonstrated that SCF is produced during the follicular phase, immediately before the ovulatory phase, and may play an important role in folliculogenesis and ovulation.In addition, they demonstrated that serum s-SCF levels may be an indicator of successful ovarian stimulation, suggesting the possible role of SCF as a predictor of in vitro fertilization (IVF) outcomes 15 .
However, there is no consensus on how serum SCF levels could influence the ovarian response and therefore the outcome of controlled ovarian hyperstimulation (COH) in patients with different ovarian reserves [19][20][21][22] .More recently, the changes and correlations between AMH and SCF during COH have become a subject of study 23 .Furthermore, it is well known that AMH "suppresses" SCF levels, and the concentration of the latter positively correlates with oocyte maturation, embryo quality, and clinical pregnancy 22 .
Successful COH remains a challenge for clinicians because of various causes of infertility.It is unclear e.g.whether endometriosis primarily affects in vitro fertilization outcomes via oocyte quality.Patients with a low ovarian reserve had a significantly reduced number of follicles containing oocytes.Polycystic ovary syndrome (PCOS) contributes to the formation of immature follicles.In each of these cases, there may be abnormalities in the activation and maturation of the primary follicles in which SCF may be involved.
The limited scope of the study above indicates that there is still a need to identify a biomarker that would predict the qualitative success of a COH cycle, understood as the chance of proper embryo development before oocyte retrieval.Thus, in our study, we evaluated whether the SCF serum level just before the induction of ovulation could be a tool that would allow for the prediction of the qualitative success rate of COH.

Results
The s-SCF level was measured in 195 serum samples collected during ovarian stimulation on days 1 and 8 and on the day of oocyte retrieval.SCF levels were juxtaposed with the formation of at least one top-quality (TQ) blastocyst and whether a clinical pregnancy was achieved.No significant differences in the Mann-Whitney U test (MWU test, p > 0.05) were observed in the mean s-SCF levels measured on the 1 st and 8 th day of stimulation and on the day of oocyte retrieval and the formation of non-top-quality (NTQ) and TQ blastocysts in all patients.
Next, the study group was divided into subgroups to assess the level of s-SCF depending on the cause of infertility.The subgroups distinguished were as follows: PCOS group (n = 24), diagnosed based on the Rotterdam criteria 24 , diminished ovarian reserve group (DOR) (n = 11), diagnosed according to biochemical and sonographic features collected during ovarian reserve testing, as suggested by the Bologna criteria 25 , mild endometriosis group (n = 10), confirmed by laparoscopy with histopathological verification 26 , and the normal ovarian reserve group (NOR) (n = 20) with "normal" body mass index (BMI) of 18.5-24.9kg/m 2 , no more than two previous miscarriages and a serum basal anti-Müllerian hormone (AMH) level of 1.2-4.0ng/ml.
The subgroups did not differ with respect to age (Table 1).The highest number of antral follicles was obtained in patients with PCOS (23.6 ± 11.40), while the lowest was in the endometriosis group (7 ± 4.5).The length of ovarian stimulation did not differ between the subgroups.In the PCOS group, a greater number of follicles on the oocyte retrieval day was observed (19.2 ± 10.1), while the number of mature MII oocytes and fertilized oocytes (9.3 ± 4.2 and 4.3 ± 3.0, respectively) was comparable to that in the normal ovarian reserve subgroup.The lowest number of TQ blastocysts on day 5 was observed in the endometriosis group (0.62 ± 1.1) and the highest in the NOR group (2.6 ± 1.9).To verify whether the s-SCF level varied depending on the cause of the patient's infertility, we compared the s-SCF values determined on days 1 and 8 and on the oocyte retrieval day in the investigated subgroups (Fig. 1).No significant differences (MWU, p > 0.05) were observed between subgroups.
However, comparing the s-SCF levels on days 1 and 8 and the oocyte retrieval day with the chance to form top-quality blastocysts revealed an interesting relationship (Fig. 2).In the case of patients in the mild endometriosis group, the mean level of s-SCF was significantly lower on the 8th day of stimulation (28.1 pg/ml vs. 49.1 pg/ml; MWU test, p < 0.05) and on the oocyte retrieval day (33.4 pg/ml vs. 50.4pg/ml; MWU test, p < 0.005) in samples from patients who had at least one TQ blastocyst on day 5 of culture (Fig. 2B and C).
There were no significant differences (MWU test, p > 0.05) in the s-SCF levels on day 1 (Fig. 2A) of stimulation between NTQ and TQ patients in PCOS, NOR, and DOR groups (41.1 pg/ml vs. 40.9pg/ml; 34.8 pg/ml vs. 38.9pg/ml and 32.3 pg/ml vs. 28.7 pg/ml respectively).The mean level of s-SCF in the endometriosis group patients was higher in the NTQ than the TQ subgroup and was 41.1 pg/ml and 29.1 pg/ml respectively.There were also no significant differences observed in the mean level of s-SCF in the NTQ and TQ subgroups on the 8th day of stimulation (Fig. 2B) and oocyte retrieval day (Fig. 2C) in PCOS, NOR, and DOR patients.
Our study suggests that a serum SCF level of less than 30 pg/ml during ovarian stimulation, especially on day 8th and on oocyte retrieval day in patients with mild endometriosis, may potentially suggest that there is a chance of obtaining at least one top-quality blastocyst and thus a chance of treatment success.More data, particularly considering the type of test used to assess SCF levels, are needed to confirm this relationship.

Discussion
Many factors influence the successful development of embryos, with the quality of the mature ovarian oocytes playing a key role.Insufficiently developed cells can affect the success of fertilization and subsequent pregnancy.While assessing the levels of AMH, follicle-stimulating hormone (FSH), and antral follicle count through ultrasound examinations provides insight into the ovarian reserve, these measures do not directly inform us about the oocyte quality.The stem cell factor produced during the follicular phase may be a promising candidate for monitoring the activation, growth, and maturation of ovarian follicles.Its role in the regulation and growth of www.nature.com/scientificreports/ovarian follicular function has been preliminary demonstrated [27][28][29] .The interaction of SCF with its receptor c-Kit appears to be an important pathway for the communication between oocytes and surrounding granulosa cells.
In our preliminary study, we explored s-SCF as a potentially useful marker for assessing the quality of formed embryos rather than as a putative indicator of the expected number of follicles and MII oocytes at the retrieval stage.This is one of the pioneering studies evaluating s-SCF levels as a potential early marker to predict the quality of retrieved oocytes and embryos.Here, we demonstrated a differentiated proportion of s-SCF levels during ovarian stimulation in the context of infertility.Previous studies have highlighted the role of SCF as an indicator of oocyte growth, particularly in patients with PCOS or diminished ovarian reserve 21 or have focused on the level of SCF in follicular fluid 19,22 .Our study is the first to include and assess diverse groups of patients with various types of infertility.
Gizzo et al. showed a strong correlation between serum SCF levels and the number of mature oocytes in patients with diminished ovarian reserve and older than 43 years 19 .Their study concluded that, for these patients, an s-SCF assay could be useful during ovarian stimulation to assess the chances of success.An even more interesting finding of Gizzo et al. is that SCF concentration in both follicular fluid and serum remains stable regardless of the gonadotropin administration protocols used.This study indicated that serum SCF levels could be potentially applied to predict the number of embryos and pregnancy.It has already been proven that unceasing cell proliferation in the secretory phase of eutopic endometriosis is linked to deregulation of the c-Kit/SCF-associated signaling pathway 30 .This study showed that in patients with endometriosis, the expression of c-kit and Akt was elevated, suggesting that an increased number of available receptor binding sites could significantly lower the concentration of s-SCF 17 .This would trigger a cascade of events involving PI3K 12 .However, the assumptions presented here require further comprehensive research to elucidate the relationship between s-SCF levels, blastocyst quality, and clinical outcomes of embryo transfer.
For follicle development and maturation, a certain ratio between AMH and SCF levels is essential 21,31 .These two intraovarian factors play crucial roles in follicle recruitment and growth.However, details regarding the molecular mechanisms of these interactions are scarce.AMH downregulates SCF levels via the cyclic 3′,5′-adenosine monophosphate/protein kinase A (cAMP/PKA) signaling pathway 32 .Binding of AMH to its specific receptors on the surface of oocyte granulosa cells induces phosphorylation of cAMP response element-binding protein (CREB) and activates protein kinase A (PKA).Phosphorylated CREB interacts with the SCF promoter, significantly increasing its transcription 32 .Overexpression of AMH inhibits CREB phosphorylation and SCF expression.AMH also reduces the expression of aromatase, which is stimulated by FSH through the cAMP/PKA signaling pathway.The effect of these interactions is particularly evident in women diagnosed with PCOS who exhibit excessive AMH production but slower follicle growth 31 .
In our study, the PCOS subgroup showed a higher number of grown follicles than the other subgroups, although the numbers of MII cells and fertilized oocytes were comparable to those in patients with a normal ovarian reserve.Significant differences in SCF levels were found in patients with mild endometriosis who obtained top-quality embryos.The mean SCF level in the serum of these women was 30.23 (± 5.42) pg/ml.To date, no reports in the literature have confirmed our observations.Elevated SCF concentration is associated with endometriosis.Osuga et al. noted increased SCF levels in the peritoneal fluid of women at the early, mild stages (I/ II) of endometriosis 33 .Conversely, women at more severe stages (III/IV) of endometriosis displayed SCF levels comparable to those in unaffected women, suggesting that heightened SCF levels may reflect the severity of endometriosis pathology.This may negatively influence IVF outcomes; therefore, further investigation of the relationship between SCF levels and IVF success is required.
It has been discussed that SCF is involved in the pathogenesis of endometriosis, particularly through the activation of mast cells.By binding to its c-Kit receptor, SCF could affect mast cells, leading to morphological changes and altered adhesion.Tryptase secreted by mast cells may presumably be associated with the activation of the protease-activated receptor 2 (PAR2) in endometrial cells 34 .PAR2, a member of the transmembrane G protein-coupled receptors, could act via MAPK, PI3K/Akt, or protein kinase C to promote the proliferation of endometriotic stromal cells 35 .Mast cell tryptase might accelerate endometriosis by increasing the number of endometriotic stromal cells and IL-6 and IL-8 secretion.The postulated molecular cascade is as follows: SCF stimulates mast cells to release tryptase; then, PAR2 is activated in endometriotic cells; these cells proliferate and secrete IL-6 and IL-8.IL-8 is a chemoattractant for neutrophils that migrate to endometriotic lesions 34 .Serine proteases released from neutrophils stimulate continues proliferation of endometrial cells, thereby contributing to disease progression.Chronic inflammation, particularly in the pelvic area, may indirectly affect the quality of oocytes.Patients with advanced endometriosis are characterized by a significantly reduced expression of aromatase 36 , redirecting our attention to cAMP/protein kinase A signaling, a probable point of interaction between AMH, FSH, E2, and SCF.
The strength of our study lies in its novelty: it is the first to assess SCF levels in patients with various types of infertility.Our findings highlight the variability in SCF levels according to infertility cause, particularly in patients with mild endometriosis.However, our findings are preliminary and further in-depth research is required.We are aware that our considerations are purely scientific but suggest a new direction for future studies.Until a direct link is established between SCF levels and both blastocyst quality and clinical outcome of an assisted reproductive procedure, it remains challenging to make key decisions (e.g., discontinuation of hormone stimulation) based on the SCF levels alone.Should our hypothesis be confirmed, serum SCF levels could inform clinical decisions regarding the collected oocytes such as wheather to fertilize or freeze them and wheather to repeat ovarian stimulation to collect oocytes with better prospects for resulting in pregnancy.It is also worth noting that our research contributes to a deeper understanding of the biochemical pathways involved in oocyte recruitment and maturation.
The design of the current study also had limitations.This study included a limited number of participants, with only 65 subjects undergoing in vitro procedures.Future studies should be conducted using larger cohorts.Patients with more advanced endometriosis should also be included, as our study focused on patients in the early stages of the condition.A detailed history of ovarian surgery or inflammatory diseases in the pelvic cavity should also be included to deeply analyze the impact of serum SCF on embryo formation.We also acknowledge that integration of preimplantation genetic testing for aneuploidy (PGT-A) could enrich our understanding of the embryo formation process.In our study, blastocyst classification was based on Gardner's metric.Although this metric is widely used in embryological laboratories as the primary tool for morphological assessment of developing blastocysts and is considered a universal approach for interpreting morphological data, using more advanced techniques to assess blastocyst development (e.g., application of a time-lapse system) could broaden the scope of evaluating data.Such an approach warrants consideration in further studies to explore the relationship between SCF levels and the chance of obtaining top-quality embryos.

Conclusions
Our preliminary study suggests that serum SCF levels below 30 pg/ml during ovarian stimulation (day 8 th and on oocyte retrieval day) in patients with mild endometriosis could potentially be a predictor of the chance of obtaining at least one top-quality blastocyst on day 5 of growth, and therefore indicate the potential for the treatment success.More data are needed to confirm the link between s-SCF levels and formation of top-quality blastocysts in patients with endometriosis at different stages of the disease.

Patients
The study included 65 female patients with a mean age of 33.7 ± 4.2 years who underwent ovarian stimulation for fresh non-donor intracytoplasmic sperm injection (ICSI) treatment at Invicta Fertility Clinics from August 2019 to March 2020.All patients underwent pretreatment assessment of baseline ovarian reserve between days 2 and 5 of their cycle.The average serum FSH level was recorded at 7.3 ± 3.4 mIU/ml, and the AMH at 3.7 ± 3.2 ng/ ml.The sonographic measurement of the antral follicle count (AFC) was determined to be on average 15.3 ± 9.9.
Patients with abnormal karyotypes or inherited genetic diseases, severe male factor infertility, and cases in which oocyte retrieval was canceled due to an insufficient ovarian response were excluded from the study.Following our internal protocols, all patients upon admission provided written informed consent for the processing of their data in compliance with applicable privacy laws.

Controlled ovarian hyperstimulation (COH)
Menopausal gonadotropins were used in monotherapy as described elsewhere 37 .All women were treated with a long agonist protocol starting with oral contraceptives (OCs) (Rigevidon, Richter Gedeon, Warsaw, Poland) from the 2nd to the 5th day of the cycle.Triptorelin acetate 0.1 mg (Gonapeptyl, Ferring, Saint-Prex, Switzerland) was administered 14 days after the initiation of the OCs.Fourteen days later (7 days after the end of OC administration), urinary gonadotropins (Menopur, Ferring, Saint-Prex, Switzerland) were administered for ovarian stimulation.Follicular growth was monitored on day 8 of COH using transvaginal ultrasound, and assays evaluating serum estradiol (E2), progesterone (P), and luteinizing hormone (LH) levels were performed until pituitary ovarian downregulation was reached (i.e., E2 concentration < 50 pg/ml).Follicular growth was stimulated by administering FSH (Menopur, Ferring, Saint-Prex, Switzerland), considering individual endocrine response as well as ovarian reaction estimated as the presence of at least an 18-mm-diameter follicle.Oocyte retrieval under the guidance of transvaginal ultrasound was performed 36-38 h after ovulation induction with human chorionic gonadotropin (hCG) injection.

Serum sample collection
Serum samples from each patient were collected during routine preprocedural blood checks on the 1st and 8th day of stimulation, and on the day of oocyte retrieval.No additional interventions were performed to obtain samples.Following routine hormone analysis, serum samples were frozen and stored at − 80 °C until SCF level analysis.

ELISA for SCF measurements
The concentration of s-SCF was determined using a commercially available enzyme-linked immunosorbent assay ELISA MAX™ Deluxe Set Human Free SCF kit (BioLegend, San Diego, USA, Cat.No. 442504).The expected minimum detectable concentration of free SCF in this set was 4 pg/ml.The cross-reactivity with mouse SCF was approximately 16% of that with human SCF at sample concentrations of 7.8-500 pg/ml.Recombinant human c-Kit did not cross-react in this assay.No cross-reactivity was observed when this kit was used to analyze the 74 other human/mouse recombinant chemokines and cytokines.All procedures were performed according to the manufacturer's instructions.

Oocyte and embryo assessment
Oocyte retrieval, ICSI procedures, and embryo morphology assessments were performed as previously described 38 .The top-quality (TQ) embryo category, that is, those exhibiting good morphological parameters, included day 2, day 3, and day 4 stage embryos with scoring class 1 or 2 (A or B, equivalent to the Gardner scale).TQ blastocysts were embryos that qualified as TQ and reached min stage 3 of development with additional trophectoderm (TE) and inner cell mass (ICM) scores of min 1 or 2. Embryos not meeting these criteria were described as poor, that is, non-top-quality (NTQ).The NTQ embryos included embryos with different than expected, at specific observation time points, number of blastomeres, and morphological features at a score of 3 39 .

Figure 1 .Figure 2 .
Figure 1.Comparison of s-SCF levels between study groups.Violin plots depict summary statistics and the density of each variable; they were not correlated with any of the clinical variables.The table below describes the mean s-SCF value (pg/ml) ± standard deviation (in parentheses) during controlled ovarian hyperstimulation.No significant differences in s-SCF levels were observed between the subgroups (Mann-Whitney U test, p > 0.05).DOR, diminished ovarian reserve; DS, day of stimulation; NOR, normal ovarian reserve; PCOS, polycystic ovary syndrome; s-SCF, serum stem cell factor; * day of oocyte retrieval (pick-up). https://doi.org/10.1038/s41598-024-61419-2www.nature.com/scientificreports/

Table 1 .
Clinical outcomes after stimulation protocols in various infertility groups.AFC, antral follicle count; AMH, anti-Müllerian hormone; DOR, diminished ovarian reserve; MII, metaphase II; NOR, normal ovarian reserve; PCOS, polycystic ovary syndrome; TQ, top-quality.Data are presented as mean values with standard deviation (SD) in parentheses.The p-values determined by ANOVA are presented.Superscript letters (a, b, c) denote means that have no significant (p > 0.05) differences between groups in Tukey's post-hoc test for multiple comparisons.