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Melatonin improves fertilization rate in assisted reproduction: Systematic review and meta-analysis

Abstract

Background:

Melatonin is a hormone produced by the pineal gland and it has antioxidant properties.

Aim:

This study aimed to evaluate the effects of melatonin on assisted reproductive technologies through a systematic review and a meta-analysis.

Materials and methods:

Search strategies were used in PubMed and in other databases covering the last 15 years. After screening for eligibility, 17 articles were selected for the systematic review. For the meta-analysis statistics, two groups were formed, the treatment group (with melatonin) and the control group (without melatonin) for various assisted reproduction outcomes.

Results:

The main results were that no statistical differences were found concerning the clinical pregnancy outcome (p = 0.64), but there was a statistical difference with respect to Mature Oocytes (MII) (p = 0.001), antral follicle count (p = 0.0002), and the fertilization rate (p ≤ 0.0001).

Conclusions:

Melatonin had beneficial effects such as the improvement in the fertilization rate, although the authors did not obtain significance in the clinical pregnancy rate.

Keywords:
Melatonin; Ovarian hyperstimulation syndrome; Assisted reproduction outcomes; In vitro fertilization; Human reproduction; Sytematic review

HIGHLIGHTS

Melatonin had beneficial effects on outcomes in assisted reproductive technologies, but it had no influence on pregnancy.

Melatonin had beneficial effects such as the improvement in the fertilization rate.

Melatonin has a beneficial effect on the formation of mature oocytes (MII).

Introduction

Infertility affects millions of women worldwide and is one of the main causes of the unfulfilled dream of having a child.11 Graham ME, Jelin A, Hoon AH, Wilms Floet AM, Levey E, Graham EM. Assisted reproductive technology: short- and long-term outcomes. Dev Med Child Neurol 2023;65 (1):38–49. Assisted reproduction techniques may be accompanied by complications such as Ovarian Hyperstimulation Syndrome (OHSS), which can be fatal.22 Zhang Q, Ma Y, Bu X, Jia C, Liu Y, Wang S. Comparison of bromocriptine and hydroxyethyl starch in the prevention of ovarian hyperstimulation syndrome. Int J Gynecol Obstet 2022;159(3):944–50. As many as 20 % to 33 % of In Vitro Fertilization (IVF) cycles are affected by mild OHSS, whereas moderate to severe OHSS reportedly occurs in 3 % to 8 % of patients.33 Mourad S, Brown J, Farquhar C. Interventions for the prevention of OHSS in ART cycles: an overview of Cochrane reviews. Cochrane Database Syst Rev 2017;1(1): CD012103.

Melatonin is a hormone that is primarily produced by the pineal gland. Two characteristics worth emphasizing are its antioxidant properties and its capacity to improve mitochondrial functions in female germ cells, which can lead to benefits in human reproduction treatments.44 Reiter RJ, Tan DX, Rosales-Corral S, Galano A, Zhou XJ, Xu B. Mitochondria: central organelles for melatonins antioxidant and anti-Aging actions. Molecules 2018;23 (2):509.,55 Tamura H, Jozaki M, Tanabe M, Shirafuta Y, Mihara Y, Shinagawa M, et al. Importance of melatonin in assisted reproductive technology and ovarian aging. Vol. 21, Int J Mol Sci. 2020;21(3):1135.,66 Cheng JC, Fang L, Li Y, Wang S, Li Y, Yan Y, et al. Melatonin stimulates aromatase expression and estradiol production in human granulosa-lutein cells: relevance for high serum estradiol levels in patients with ovarian hyperstimulation syndrome. Exp Mol Med 2020;52(8):1341–50. Melatonin plays a role in sleep and in physiological oocyte maturation.77 Yong W, Ma H, Na M, Gao T, Zhang Y, Hao L, et al. Roles of melatonin in the field of reproductive medicine. Biomed Pharmacother 2021;144:112001. Both in vitro and in vivo studies, in animals and in humans, show the benefits of melatonin as a substance that reduces the oxidative stress of cells related to reproduction, even improving fertilization rates.88 Cosme P, Rodríguez AB, Garrido M, Espino J. Coping with oxidative stress in reproductive pathophysiology and assisted reproduction: melatonin as an emerging therapeutical tool. Antioxidants (Basel) 2023;12(1):86.

Two recent works have demonstrated that melatonin not only alleviates reactive oxygen species, but also improves apoptosis and that it may clinically benefit women who have developed OHSS.99 Li Y, Fang L, Yu Y, Shi H, Wang S, Guo Y, et al. Higher melatonin in the follicle fluid and MT2 expression in the granulosa cells contribute to the OHSS occurrence. Reprod Biol Endocrinol 2019;17(1):37.,1010 Zheng M, Jiao S, Liu M, Zhang C. Melatonin ameliorates ovarian hyperstimulation syndrome (OHSS) through SESN2 regulated antiapoptosis. Obstet Gynecol Int 2023;2023:1121227. Other works discuss the important role, still under study, of melatonin related to steroid sex hormones, in one of these works it was observed that melatonin plays a role in maintaining follicular function through the production of progesterone,1111 Maganhin CC, Fuchs LF, Simoes RS, Oliveira-Filho RM, de Jesus Simões M, Baracat EC, et al. Effects of melatonin on ovarian follicles. Eur J Obstet Gynecol Reprod Biol 2013;166(2):178–84. while in the most recent review, it is considered that melatonin plays a role not only in the production of progesterone but also in estrogen and spermatogenesis.1212 Cipolla-Neto J, Amaral FG, Soares Jr JM, Gallo CC, Furtado A, Cavaco JE, et al. The crosstalk between melatonin and sex steroid hormones. Neuroendocrinology 2022;112(2):115–29. Among the positive results of using melatonin for women on Assisted Reproductive Technology (ART) are increases in the number of mature oocytes, the fertilization rate, the number of high-quality embryos, and, in some cases, increased pregnancy rates.1313 Tamura H, Takasaki A, Miwa I, Taniguchi K, Maekawa R, Asada H, et al. Oxidative stress impairs oocyte quality and melatonin protects oocytes from free radical damage and improves fertilization rate. J Pineal Res 2008;44(3):280–7.,1414 Ge ZJ, Schatten H, Zhang CL, Sun QY. Oocyte ageing and epigenetics. Reproduction 2015;49(3):R103–14.

Given the above, this study aimed to evaluate the effects of melatonin on assisted reproductive technologies through a systematic review and a meta-analysis.

Materials and methods

For the systematic review, the authors drew on several articles and guidelines, including Berstock et al., 2019,1515 Berstock JR, Whitehouse MR. How to prepare and manage a systematic review and meta-analysis of clinical studies Vol. 4 EFORT Open Reviews 2019;4(5):213–20. Hennessey et al., 2019,1616 Hennessy EA, Johnson BT, Keenan C. Best Practice Guidelines and essential methodological steps to conduct rigorous and systematic meta-reviews. Appl Psychol Health Well Being 2019;11(3):353–81. and Page et al., 2021.1717 Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 2021;372:n71. The meta-analysis was conducted in accordance with Higgins et al., 2022.1818(Professor of SR and P Higgins JPT, Thomas J, Chandler J, Cumpston M, Li T, et al. Writer on evidence-based medicine. In: Page MJ, ed. Cochrane Handbook For Systematic Reviews of Interventions; 2023. p. 694.

Search strategy

The studies selected for this review were published between January 2008 and April 2023, and they are indexed in PubMed and Scielo (Fig. 1). The initial search yielded 127 articles. After applying the eligibility criteria, they were narrowed down to the 17 articles included in this systematic review. Fig. 1 shows the selection process in detail.

Fig. 1
Flowchart of the systematic review. * Consider, if feasible to do so, reporting the number of records identified from each database or register searched (rather than the total number across all databases/ registers). ** If automation tools were used, indicate how many records were excluded by a human and how many were excluded by automation tools. From: Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 2021;372:n71. doi:10.1136/bmj.n71. For more information, visit: http://www.prisma-statement.org/.

Drawing on Page et al., 2020,1717 Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 2021;372:n71. the P (Population) in the P.I.C.O. of this systematic review is patients, i.e., the female research participants who were selected to take exogenous melatonin and who had or had not ovarian hyperstimulation syndrome, depending on the article; the I (Intervention) is the administration of exogenous melatonin; the C (Comparison) is the comparison of the control group and the experimental group (exposed to melatonin); the O (Outcomes) is the outcomes as described in Table 1.

Table 1
Exogenous melatonin in previous clinical studies.

This review was conducted following the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analysis) recommendations.1515 Berstock JR, Whitehouse MR. How to prepare and manage a systematic review and meta-analysis of clinical studies Vol. 4 EFORT Open Reviews 2019;4(5):213–20.

Inclusion and exclusion criteria

The exclusion criteria covered animal studies (n = 74), articles whose titles or abstracts did not fall within the scope of the present study (n = 11), and review articles (n = 8). An additional 16 articles were excluded for lack of access to the full text because they were not freely accessible. The remaining 24 articles were fully read. By applying a second round of exclusion criteria, 7 more studies were screened out. The 17 articles that remained met the inclusion criteria of this study (see Table 1 for details) and were thus included in the study (Fig. 1). The inclusion and exclusion criteria were based on Page et al., 2020.1717 Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 2021;372:n71.

Statistical analysis

For descriptive analysis, calculations were made for means, standard deviations, mean differences, and odd ratios with a 95 % Confidence Interval. Meta-analysis was carried out with the Review Manager 5.4.1 software program (Cochrane Collaboration, Oxford, UK). For the 95 % CI and the overall effect size, values of p ≤ 0.05 were assumed for significant differences.

Results

Melatonin is involved in a number of the body’s physiological processes, one of which is regulating fertility. The articles included in this study are detailed in Table 1, which also includes information about the authors, publication year, methods, melatonin treatment, rationale for article inclusion, and key results or outcomes. A significant finding of this systematic review was that melatonin plays a role in the improvement of oocyte and embryo quality.1919 Jing T, Shile S, Sun Y, Li H, Li WP, Cong Z, et al. Melatonin levels in follicular fluid as markers for IVF outcomes and predicting ovarian reserve. Reproduction 2017;153 (4):443–51.,2020 Fernando S, Osianlis T, Vollenhoven B, Wallace E, Rombauts L. A pilot double-blind randomised placebo-controlled dose-response trial assessing the effects of melatonin on infertility treatment (MIART): study protocol. BMJ Open 2014;4(8):e005986.,2121 Batiioǧlu AS, Şahin U, Grlek B, Öztrk N, Ünsal E. The efficacy of melatonin administration on oocyte quality. Gynecol Endocrinol 2012;28(2):91–3.,2222 Espino J, Macedo M, Lozano G, Ortiz Á, Rodríguez C, Rodríguez AB, et al. Impact of melatonin supplementation in women with unexplained infertility undergoing fertility treatment. Antioxidants 2019;8(9):338.,2323 Tong J, Sheng S, Sun Y, Li H, Li WP, Zhang C, et al. Melatonin levels in follicular fluid as markers for IVF outcomes and predicting ovarian reserve. Reproduction 2017;153 (4):443–51.,2424 Zheng M, Tong J, Li WP, Chen ZJ, Zhang C. Melatonin concentration in follicular fluid is correlated with antral follicle count (AFC) and in vitro fertilization (IVF) outcomes in women undergoing assisted reproductive technology (ART) procedures. Gynecol Endocrinol 2018;34(5):446–50.,2525 Jahromi BN, Sadeghi S, Alipour S, Mohammad, Parsanezhad E, Alamdarloo SM. Effect of melatonin on the outcome of assisted reproductive technique cycles in women with diminished ovarian reserve: a double-blinded randomized clinical trial. Irian J Med Sci 2017;42(1):73–8.,2626 Unfer V, Raffone E, Rizzo P, Buffo S. Effect of a supplementation with myo-inositol plus melatonin on oocyte quality in women who failed to conceive in previous in vitro fertilization cycles for poor oocyte quality: a prospective, longitudinal, cohort study. Gynecol Endocrinol 2011;27(11):857–61.,2727 Ma T, Niu Y, Wei B, Xu L, Zou L, Che X, et al. Moderate-to-severe ovarian hyperstimulation syndrome: a retrospective multivariate logistic regression analysis in Chinese patients. Adv Clin Exp Med 2020;29(1):85–90.,2828 Fernando S, Wallace EM, Rombauts L, White N, Hong J, Vollenhoven B, et al. The effect of melatonin on ultrasound markers of follicular development: a double-blind placebo-controlled randomised trial. Aust N Z J Obstet Gynaecol 2020;60(1):141–8.,3232 Li X, Mu Y, Elshewy N, Ding D, Zou H, Chen B, et al. Comparison of IVF and IVM outcomes in the same patient treated with a modified IVM protocol along with an oocytes-maturing system containing melatonin: a pilot study. Life Sci 2021;264:118706.,3333 Nishihara T, Hashimoto S, Ito K, Nakaoka Y, Matsumoto K, Hosoi Y, et al. Oral melatonin supplementation improves oocyte and embryo quality in women undergoing in vitro fertilization-embryo transfer. Gynecol Endocrinol 2014;30(5):359–62.,3434 Zheng M, Liu M, Zhang C. Melatonin ameliorates ovarian hyperstimulation syndrome (OHSS) through SESN2 regulated antiapoptosis. Obstet Gynecol Int 2023; 2023:1121227.

Meta-analysis of assisted reproduction outcome variables

The comparison between melatonin intake and the clinical pregnancy rate of assisted reproduction yielded no statistical difference. Only 6 studies included this variable and with the following results: p = 0.64, I2 = 37 % (Fig. 2); risk ratio of 1.22 (0.71‒2.09). Caution is needed in interpreting this outcome, for there are numerous other variables involved in a healthy pregnancy resulting from assisted reproduction techniques, including the physiological conditions necessary for achieving pregnancy.

Fig. 2
Meta-analysis of clinical pregnancy rate in patients receiving and not receiving melatonin.

The meta-analysis of the fertilization rate outcome in percentage (%) showed a positive effect of the melatonin treatment, as the difference between the melatonin treatment groups and the control groups was statistically significant (p ≤ 0.00001, I2 = 88 %, Fig. 3; risk ratio = 0.84 [0.79, 0.90]). The fertilization rate is an important indicator of reproductive outcomes, and the group of women who took melatonin had improved results compared to the group of women who did not take it (Fig. 3).

Fig. 3
Meta-analysis of fertilization rate in patients receiving and not receiving melatonin.

In the only four studies addressing follicle count, melatonin had positive effects on the growth of follicles as shown by p ≤ 0.00001, I2 = 85 % (Fig S2 Supplementary materials Supplementary material associated with this article can be found, in the online version, at http://doi:10.1016/j.clinsp.2024.100397. ), which points to statistical significance.

Five studies measured the Mature oocyte (MII). Statistically significant values were found, and they are p = 0.001, I2 = 87 % (Fig. S1 Supplementary materials Supplementary material associated with this article can be found, in the online version, at http://doi:10.1016/j.clinsp.2024.100397. ). The MII oocyte is the female germ cell in an ideal state of maturation for fertilization.

A meta-analysis of maternal age in years was performed in 11 studies, and no statistically significant difference was found (p = 0.64 and I2 = 64 %). Body mass index (kg/m2) was a sociodemographic variable analyzed in 8 studies, with no significant differences in outcome (p = 0.59, I2 = 77 %). A third sociodemographic variable was women’s infertility time, and it approached the significance level at best (p = 0.06, I2 = 0 %).

In short, melatonin had beneficial effects as shown by the increased fertilization rate and other outcomes of the reproductive process. The clinical pregnancy rates, however, were not significantly different in the group comparison.

Discussion

The main findings were that women who took melatonin had an improved fertilization rate and reaped other benefits from assisted reproductive technologies. However, melatonin intake did not result in a higher clinical pregnancy rate.

Of the 17 studies selected for this systematic review, only two articles, those by Li et al., 20193535 Maganhin CC, Baracat MCP, Carvalho KC, Seganfredo IB, Luquetti CM, Dos Santos Simões R, et al. Evidence that melatonin increases inhibin beta-a and follistatin gene expression in ovaries of pinealectomized rats. Reprod Sci 2020;27(7):1455–64. and Zhang et al., 2023,3434 Zheng M, Liu M, Zhang C. Melatonin ameliorates ovarian hyperstimulation syndrome (OHSS) through SESN2 regulated antiapoptosis. Obstet Gynecol Int 2023; 2023:1121227. deal directly with the subject of ovarian hyperstimulation and the way in which melatonin can be a hormone that aids reproductive results. Li et al., 2019, concluded that melatonin produced by the follicular follicle helps predict OHSS, while Zhang et al., 2020, took a deeper approach. They demonstrated how melatonin, in addition to having anti-apoptotic properties, can improve oxidative stress in OHSS and concluded that it can indeed prevent OHSS. In a recent study by Hu et al., 2020,3636 Hu KL, Ye X, Wang S, Zhang D. Melatonin application in assisted reproductive technology: a systematic review and meta-analysis of randomized trials. Front Endocrinol (Lausanne) 2020;11:160.. Erratum in: Front Endocrinol (Lausanne). 2020;11:333. promising results were obtained, but they differ from those of this meta-analysis, in which the clinical pregnancy rate improved with the administration of melatonin to patients with an OR of 1.43. However, their study comprised only articles with an RTC design, an advantage offset mainly by the low-quality bias and the heterogeneity of the articles. In a recent meta-analysis by Mejihede et al. 20213535 Maganhin CC, Baracat MCP, Carvalho KC, Seganfredo IB, Luquetti CM, Dos Santos Simões R, et al. Evidence that melatonin increases inhibin beta-a and follistatin gene expression in ovaries of pinealectomized rats. Reprod Sci 2020;27(7):1455–64. with 7 articles from randomized controlled trials, oral melatonin supplementation resulted in an increase in the number of mature oocytes, and a trend for increasing CPR, albeit not significant.3232 Li X, Mu Y, Elshewy N, Ding D, Zou H, Chen B, et al. Comparison of IVF and IVM outcomes in the same patient treated with a modified IVM protocol along with an oocytes-maturing system containing melatonin: a pilot study. Life Sci 2021;264:118706. A recent study also verified the relationship between melatonin and the increase in gene expression in rats of follistatin and of Inhibin Beta-A, substances necessary for good hormonal regulation of the ovary and oocyte maturation.3535 Maganhin CC, Baracat MCP, Carvalho KC, Seganfredo IB, Luquetti CM, Dos Santos Simões R, et al. Evidence that melatonin increases inhibin beta-a and follistatin gene expression in ovaries of pinealectomized rats. Reprod Sci 2020;27(7):1455–64. One of the mechanisms may be through the melatonin receptor in ovarian follicles, but there are also other mechanisms that do not depend on the receptor and are related to antioxidant substances.3232 Li X, Mu Y, Elshewy N, Ding D, Zou H, Chen B, et al. Comparison of IVF and IVM outcomes in the same patient treated with a modified IVM protocol along with an oocytes-maturing system containing melatonin: a pilot study. Life Sci 2021;264:118706.,3434 Zheng M, Liu M, Zhang C. Melatonin ameliorates ovarian hyperstimulation syndrome (OHSS) through SESN2 regulated antiapoptosis. Obstet Gynecol Int 2023; 2023:1121227.,3535 Maganhin CC, Baracat MCP, Carvalho KC, Seganfredo IB, Luquetti CM, Dos Santos Simões R, et al. Evidence that melatonin increases inhibin beta-a and follistatin gene expression in ovaries of pinealectomized rats. Reprod Sci 2020;27(7):1455–64.,3737 Mejlhede MAB, Jepsen JB, Knudsen UB. Oral melatonin supplementation during in vitro fertilization treatment: a systematic PRISMA review and meta-analysis of randomized controlled trials. Gynecol Endocrinol 2021;37(12):1079–85.

Some recent studies demonstrate that melatonin either from follicular fluid, granulosa cells, or exogenous sources has important roles concerning the quality of oocytes. It can delay the aging of the ovaries and their functions and improve the antioxidant properties of the oocytes, leading to improved reproductive outcomes such as an improved fertilization rate.55 Tamura H, Jozaki M, Tanabe M, Shirafuta Y, Mihara Y, Shinagawa M, et al. Importance of melatonin in assisted reproductive technology and ovarian aging. Vol. 21, Int J Mol Sci. 2020;21(3):1135.,2828 Fernando S, Wallace EM, Rombauts L, White N, Hong J, Vollenhoven B, et al. The effect of melatonin on ultrasound markers of follicular development: a double-blind placebo-controlled randomised trial. Aust N Z J Obstet Gynaecol 2020;60(1):141–8.,3232 Li X, Mu Y, Elshewy N, Ding D, Zou H, Chen B, et al. Comparison of IVF and IVM outcomes in the same patient treated with a modified IVM protocol along with an oocytes-maturing system containing melatonin: a pilot study. Life Sci 2021;264:118706.,3434 Zheng M, Liu M, Zhang C. Melatonin ameliorates ovarian hyperstimulation syndrome (OHSS) through SESN2 regulated antiapoptosis. Obstet Gynecol Int 2023; 2023:1121227.,3535 Maganhin CC, Baracat MCP, Carvalho KC, Seganfredo IB, Luquetti CM, Dos Santos Simões R, et al. Evidence that melatonin increases inhibin beta-a and follistatin gene expression in ovaries of pinealectomized rats. Reprod Sci 2020;27(7):1455–64.

The strength of the present work lies in demonstrating through metaanalysis that variables analyzed at the onset of assisted reproduction techniques improved to benefit the women who used exogenous melatonin. On the other hand, in the author’s judgment, an important limitation is that in nearly half of the studies, the risk of bias was unclear or was not mentioned, impairing the quality of the studies. Another limitation, and the most important one, is that there was no difference in the clinical pregnancy rate between the groups. Further, there were not enough studies among the selected articles to analyze the main variable of assisted reproduction, namely the rate of live births.

Limitations of the study

This study has two main limitations. First, it is a systematic review and as such there is no data collection. Also, the results are those of previously published articles. Second, with respect to the meta-analysis of the clinical rate of pregnancy variable, there is no statistical difference between the use and the nonuse of melatonin, despite its beneficial molecular and cellular effects as judged by the values presented in the articles.

Conclusion and future perspectives

Melatonin is not a substance that has been used frequently in assisted reproduction. However, it has the following advantages for use in clinical practice: it is low cost; it is commercially available; it is a hormone produced by our own body and thus has no side effects; it has, as one of its main physiological actions, the capacity to reduce the oxidative stress of oocytes, but due to the few existing studies, this feature is still being overshadowed by the main results of human reproduction, such as clinical pregnancy rate and live birth rate. Therefore, the authors suggest that this line of research into melatonin use in assisted reproductive technologies be expanded with double-blind randomized multicenter studies. Melatonin had beneficial effects such as the improvement in the fertilization rate, although the authors did not obtain significance in the clinical pregnancy rate.

Additional studies, such as double-blind randomized clinical trials with many participants, are needed, particularly as regards melatonin action on ovarian hyperstimulation syndrome.

Supplementary materials

Supplementary material associated with this article can be found, in the online version, at http://doi:10.1016/j.clinsp.2024.100397.

  • Funding
    No funding.

References

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Publication Dates

  • Publication in this collection
    16 Aug 2024
  • Date of issue
    2024

History

  • Received
    23 Jan 2024
  • Reviewed
    01 Apr 2024
  • Accepted
    13 May 2024
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