Possible Action of Resveratrol in Improving the Outcomes of IVF/ICSI in Couples With Unexplained Infertility

Overview

Based on available evidence and given the potential beneficial effects of resveratrol in folliculogenesis and in oocyte development, the investigators designed a randomized, controlled, double-blind, single-center trial, whose objective will be the comparison of biological and clinical outcomes of resveratrol supplement in women undergoing IVF/ICSI cycles for unexplained infertility. To the knowledge of the investigators, no study has been published on the potential effect of resveratrol on IVF/ICSI outcomes considering couples with this infertility diagnosis, which may be the natural target of this integrative treatment because the process of folliculogenesis and oocyte maturation cannot be routinely investigated. An alteration of these biological mechanisms could be the unrecognized cause of part of the unexplained infertility and treatment with resveratrol could result in significant clinical improvement for the patients enrolled in the study. In more details, the main objective of this randomized, placebo-controlled, double-blind, single-center trial will be the evaluation of the possible effect of resveratrol in determining a better follicle development in patients with unexplained infertility undergoing controlled ovarian stimulation (COS) for IVF/ICSI. Infertile female patients with normal ovarian reserve will be treated according to clinical practice and the difference between expected (through AFC) and retrieved oocytes will be assessed in relation to use of resveratrol.

On the basis of the last estimates, the global lifetime prevalence of infertility is 17.5%, which means that approximately one in six people have experienced infertility at some stage in their lives. Despite an improvement in conventional diagnostic investigations, still today, around 25% of the causes of couple infertility remain unexplained. In fact, several crucial moments of the human reproductive process cannot be studied and, therefore, specific reproductive alterations remain undiagnosed. Just thinking of the process of ovarian folliculogenesis, oocyte development, embryonic implantation, all ones real "biological mysteries". Among these different biological aspects, it is known that the oocyte quality is the main predictor of clinical pregnancy after IVF/ICSI. Indeed, oocyte maturation process influences the embryo development and, consequently, the embryo viability. Although the mechanisms that determine a good quality oocyte are not known, nevertheless energy-dependent processes are supposed to play a major role in oocyte development. These processes are mediated by mitochondria, whose concentration in oocytes is the highest among the other cells of human body. The oocyte nuclear and cytoplasmic maturation is strictly connected with the growth of granulosa cells (GCs). These cells surround the oocyte and establish a functional bidirectional cross-talk with the oocyte itself through gap junctions and paracrine factors. During folliculogenesis, GCs increase the consumption of glucose and metabolize glucose into pyruvate which passes to the oocyte. All this determines an increase in the energy supply to the oocyte itself, demonstrated by the increase in ATP production, which allows the latter cell to prepare for fertilization and the first stages of embryonic development which, as known, is totally oocyte dependent . Resveratrol seems to be able to fit into this area of cellular functioning. It is a natural polyphenol, widespread in foods, plants, drinks and it seems to induce GCs proliferation through an anti-apoptotic effect in a SIRT1-dependent manner. Furthermore, in GCs, resveratrol reduces the oxidative stress, increases the mitochondria biogenesis and the intracellular ATP levels, determining a high energy availability which favours the oocyte growth. Resveratrol seems to reduce in rat granulosa cells the expression of Vascular Endothelial Growth Factor (VEGF), implicated in angiogenesis and vascular permeability, potentially showing a protective effect on the risk of Ovarian Hyperstimulation Syndrome (OHSS), a life-threatening condition associated with ovarian stimulation, whose VEGF is the main mediator. A recent clinical randomized trial showed that a pre-treatment of 3 months with resveratrol, in women affected by couple infertility and undergoing ICSI, was associated with a higher number of retrieved and mature oocytes, a higher fertilization rate, a higher number of blastocysts per patient and a higher number of surplus cryopreserved embryos per patient, even if no significant effect was observed in clinical pregnancies and live birth rates. Based on this last evidence and given the potential beneficial effects of resveratrol in folliculogenesis and in oocyte development, the investigators designed a randomized, controlled, double-blind, single-center trial, whose objective will be the comparison of biological and clinical outcomes of resveratrol supplement in women undergoing IVF/ICSI cycles for unexplained infertility. To the knowledge of the investigators, no study has been published on the potential effect of resveratrol on IVF/ICSI outcomes considering couples with this infertility diagnosis, which may be the natural target of this integrative treatment because the process of folliculogenesis and oocyte maturation cannot be routinely investigated. An alteration of these biological mechanisms could be the unrecognized cause of part of the unexplained infertility and treatment with resveratrol could result in significant clinical improvement for the patients enrolled in the study. In more details, the main objective of this randomized, placebo-controlled, double-blind, single-center trial will be the evaluation of the possible effect of resveratrol in determining a better follicle development in patients with unexplained infertility undergoing controlled ovarian stimulation (COS) for IVF/ICSI. Infertile female patients with normal ovarian reserve will be treated according to clinical practice and the difference between expected (through AFC) and retrieved oocytes will be assessed in relation to use of resveratrol. DESIGN AND METHODOLOGY: Couples affected by unexplained infertility will be enrolled. The definition of unexplained infertility is the following: infertility in couples with apparently normal ovarian function, fallopian tubes, uterus, cervix and pelvis, age ≤ 40 years and with adequate coital frequency; and apparently normal testicular function, genito-urinary anatomy and a normal ejaculate. All patients will be randomized for no treatment (placebo Group - only folic acid) and for treatment of resveratrol (Study group) with a 1:1 ratio. The randomization list, generated by a software, will be managed by a nurse not directly involved in the study and will give the patients the drugs for all duration of treatment. Neither the physicians/embryologists neither the patients will be aware of the content of the boxes of drugs (folic acid or resveratrol) (Double blind design). The duration of treatment will be at least 65 days before the starting of stimulation (from the stage of pre-antral follicles) and until the day of oocyte pick up. All the AFC determinations will be performed by the same two physicians from 2nd to 6th day of the cycle, in one of the last three months before the starting of stimulation. All the follicles ranging from 2 to 10 mm will be recorded (distinguishing between the follicles ranging from 2 to 5 mm and those ranging from 6 to 10 mm). COS will be carried out by daily injections of rFSH (Gonal F; Merck Serono, Italy) and will be started on the 2nd/3rd day of the cycle and continued until the day of induction of oocyte maturation. The pituitary suppression will be obtained by the administration of the GnRH antagonist ganirelix (0.25 mg per day, Fyremadel, Ferring S.p.A.), which will be started from the 6th day of the ovarian stimulation until the day of induction of oocyte maturation. Follicular development will be monitored after 5 days of treatment and thereafter at least every 2 days. Monitoring will consist of: a) transvaginal ultrasound scan to evaluate the number and maximum diameter of ovarian follicles and the endometrial thickness; b) the dosage of 17β-oestradiol, LH and progesterone only on the day of induction of oocyte maturation. The transvaginal ultrasound for monitoring will be performed by the same two physicians. Highly purified urinary hCG (Gonasi HP, IBSA Farmaceutici, Italy) 10.000 IU, subcutaneously or intramuscularly, will be used to induce final oocyte maturation when two or more follicles of ≥16 mm in diameter will be observed and will be administered 35.5-36 h before planned oocyte retrieval. In case of OHSS risk, the final oocyte maturation will be obtained by using a GnRH agonist (Triptorelin, Decapeptyl 0.1 mg, Ipsen S.p.A., Italy) 0.3 mg subcutaneously, and the oocyte retrieval will be planned with the same modalities described above; in this case, all the embryos obtained will be cryopreserved. No difference in the number of oocytes retrieved was shown comparing these two different modalities of triggering the final oocyte maturation (Haahr et al., 2017). The trigger of oocyte maturation will not be achieved in case of inability to reach at least 2 follicles ≥16 mm. The oocyte pick ups will be performed by the two physicians with the highest level of expertise. Fresh transfer of embryos will be performed on the second, third or fifth day after retrieving the oocytes. In case of OHSS risk and/or in case of progesterone rise on the day of hCG administration (≥1.5 ng/ml), all the embryos will be cryopreserved. The couples with all frozen embryos will be considered for the analysis of the endpoints. SAMPLE SIZE CALCULATION: To pursuit the aims of the present study protocol, a priori sample size calculation was conducted to determine the minimal number of participants required. Data available in the literature indicate in average a difference of 1.5 in the no. of pre-ovulatory follicles (≥16mm) between the group treated with resveratrol and the control group, with an average increase of 15% in favour of the study group. Thus, considering a conservative difference of 10%, which is equivalent to a large effect size of d=0.80, a power (1- β) of 95%, an alpha of 0.05, a two-tails t-test, and a ratio of 1:1 between the two groups, a total of 90 subjects (45 for each group) would be needed to verify a significant difference in primary outcome between the two groups.