Next Article in Journal
Tuberculosis Diagnosis: Current, Ongoing, and Future Approaches
Previous Article in Journal
Survival Trends for Uterine Sarcomas from a Tertiary Center: The Oxford Experience
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Diseases
Volume 12
Issue 9
10.3390/diseases12090201
diseases-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Systematic Review

The Effect of COVID-19 and COVID-19 Vaccination on Assisted Human Reproduction Outcomes: A Systematic Review and Meta-Analysis

by
Andrea Milostić-Srb
1,†,
Nika Srb
1,†,
Jasminka Talapko
1,
Tomislav Meštrović
2,3,4,
Tihomil Žiger
1,
Stana Pačarić
1,5,
Rajko Fureš
1,6,
Vedrana Makarović
1,7,* and
Ivana Škrlec
1,*
1
Faculty of Dental Medicine and Health, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia
2
University Centre Varaždin, University North, 42000 Varaždin, Croatia
3
Institute for Health Metrics and Evaluation, University of Washington, Seattle, WA 98195, USA
4
Department for Health Metrics Sciences, School of Medicine, University of Washington, Seattle, WA 98195, USA
5
Department of Surgery, University Hospital Centre Osijek, 31000 Osijek, Croatia
6
Department of Gynecology and Obstetrics, Zabok General Hospital and Croatian Veterans Hospital, 49210 Zabok, Croatia
7
University Hospital Center Osijek, 31000 Osijek, Croatia
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Diseases 2024, 12(9), 201; https://doi.org/10.3390/diseases12090201
Submission received: 26 June 2024 / Revised: 24 August 2024 / Accepted: 25 August 2024 / Published: 3 September 2024
Browse Figures
Versions Notes

Abstract

:
The most discussed infectious disease is coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus. Many research endeavors have focused on the effects of the virus on reproductive organs, as these have also been shown to carry the receptors to which the virus attaches. The results of assisted reproductive technology (ART) have been significantly affected by the pandemic, with some in vitro fertilization (IVF) centers being closed due to the risk of further spread of the disease. According to World Health Organization statistics, 17.5% of adults worldwide suffered from fertility problems in 2023; in other words, one in six people in the world have reproductive health problems. As infertility is a growing problem in the modern world and new developments in assisted reproduction are always a topic of profound interest, it is important to understand the impact of SARS-CoV-2 on reproductive health. This systematic review aimed to examine studies describing patients undergoing ART procedures with a COVID-19-positive history and to shed light on the recent evidence on the safety of COVID-19 vaccination in the ART context. A meta-analysis was conducted to confirm the results of the systematic review. The results showed a significant difference in clinical pregnancy rates between the vaccinated and unvaccinated groups and an increased miscarriage rate in those with a COVID-19-positive history. However, no significant difference in clinical pregnancy and birth rates was found in participants with a previous COVID-19 infection. The results show that further studies and research are needed, even though the spread and impact of the virus have decreased. Evidence-based information for individuals and couples undergoing infertility treatment is vital to enable informed decision-making.

1. Introduction

Coronaviruses are highly contagious viruses that cause mild to severe respiratory infections [1]. The global pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was declared by the World Health Organization (WHO) on 11 March 2020 [2]. SARS-CoV-2 uses angiotensin-converting enzyme 2 (ACE2) as a cellular receptor for viral entry, as well as a cellular protease called transmembrane protease serine-2 (TMPRSS2) [2,3]. Replication of the virus takes place in the nasopharyngeal epithelium and spreads to the distal alveoli [2,4].
After the infection, the human body activates pattern recognition receptors (PRRs) that recognize foreign bodies called pathogen-associated molecular patterns (PAMPs) and danger-associated molecular patterns (DAMPs) [5]. The Toll-like receptor groups TLR3 and TLR7 recognize the virus and produce several type I interferons and proinflammatory cytokines [2,4]. The interferons bind to the surface receptors of the cell and initiate a signaling cascade via the JAK-STAT pathway, thereby activating transcriptional regulation of hundreds of interferon-regulated genes like oligoadenylate synthetase 1 (OAS1), OAS2, and OAS3 [6].
Extrapulmonary organs such as the heart, liver, kidney, colon, esophagus, brain, breasts, placenta, gallbladder, and testes have mRNA expressions of both ACE2 and TMPRSS2; this explains why SARS-CoV-2 may be able to affect these organs [7,8]. The virus induces the release of ACE2, causes cytokine storms, and leads to oxidative stress and increased body temperature. All this can become a severe threat to the reproductive health and fertility of the host [9]. Apart from the fertility aspect, it is important to know that respiratory viruses can lead to multiorgan failure through activation of the complement system and cytokine storms, dysregulation of the immune system response, and infiltration of the inflammatory cells [10].
The SARS-CoV-2 virus affects the reproductive organs via the ACE2 receptor. ACE2 is mainly found in men in spermatogonia, Sertoli, and Leydig cells [11,12]. In Leydig cells, the physiological function of ACE2 is to regulate testosterone production and modulate the conversion of angiotensin II to angiotensin I, thus balancing the interstitial fluid volume. During coronavirus disease 2019 (COVID-19), host ACE2 receptors are saturated by binding with the virus, which increases the availability of angiotensin II as it is not converted [13]. Infection can lead to inflammation, possibly affecting spermatogenesis and testosterone production. The high expression of ACE2 indicates that SARS-CoV-2 enters the testicular interstitium via the blood and causes hormonal dysregulation. In infected COVID-19 patients, serum luteinizing hormone (LH) was significantly elevated, and the ratio of testosterone to LH and the ratio of follicle-stimulating hormone (FSH) to LH were decreased considerably [14,15]. Apart from the effects on hormones, there may also be damage to the testicular tissue, causing orchitis or orchiepididymitis [11,16,17,18]. Autoimmune orchitis can result from a triggered immune response in the testes [19]. A study conducted on knockout mouse lines found that sperm have reduced sperm motility, resulting in a lower fertilization rate in vitro. Those data showed that TMPRSS12, which is predominantly expressed in the testis, impacts the regulation of sperm motility [20]. Recent studies have shown a difference between the sexes regarding contracting COVID-19 [21,22,23].
In women, ACE2 and TMPRSS2 are expressed together in the endometrium, ovarian cortex, and ovarian medulla, especially in oocytes of different stages, as well as in the membrane of the trophectoderm, in the hypoblast, in epiblast cells in blastocysts, and partially in granulosa cells [3,24,25]. The cellular ACE2 receptor and TMPRSS2 protease expression increased with oocyte maturation, but ACE2 was expressed at all stages of follicle maturation [12,26,27]. Thus, there is a link between infection and ovarian dysfunction [8]. Moreover, binding SARS-CoV-2 to the ACE2 receptor might affect ovulation, the menstrual cycle, and pregnancy. It appears that cytokine levels correlate with the severity of disease in pregnant women with the virus [28]. The virus disrupts the microenvironment of the follicle, potentially affecting reproductive outcomes and interfering with embryo implantation and pregnancy itself [8,12,29]. Studies also show that it is not only pregnancy but also birth outcome that is affected by the virus. For instance, the incidence of preterm births and cesarean deliveries were above the international averages [30,31]. Even older studies concluded that the SARS virus can cause higher rates of spontaneous miscarriages, premature births, and intrauterine growth disorders during pregnancy [32]. Side effects of the COVID-19 infection in infants include respiratory distress and fetal problems, low platelets with abnormal liver function, and, in some cases, even death [33,34]. However, most studies agree that males were more affected than females [35].
According to the WHO statistics, 17.5% of adults worldwide suffered from fertility problems in 2023 [36]. The present review summarizes the current impact of SARS-CoV-2 and COVID-19 on fertility and assisted human reproduction procedure outcomes. These include the clinical pregnancy rate, miscarriage rate, and birth rate. The basic genetic characteristics of COVID-19, its receptors, its impact on human fertility, and assisted reproduction since the pandemic’s beginning are discussed based on recently published evidence.

2. Materials and Methods

2.1. Literature Search

The systematic review was conducted based on the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement, and the study protocol is registered in the PROSPERO database (CRD42024520979). The literature included English libraries such as PubMed, NIH, EMBASE, iCite COVID-19 portfolio, Cochrane Library, Google Scholar databases, and WHO and ESHRE statistics. Aside from this, the review was not limited to English and thoroughly examined literature available in other languages to gain insight into practices in central and south-eastern Europe. The search included articles from 1 January 2020 until 1 December 2023. The search keywords were: COVID-19; SARS-CoV-2; COVID-19 vaccine; IVF; ART; assisted reproduction; infertility; in vitro fertilization; intracytoplasmic sperm injection; ICSI; outcome; pregnancy; embryo; implantation; and birth; these were combined using Boolean operators AND, OR, and NOT.

2.2. Eligibility Criteria

The main focus of this review was on the outcomes of COVID-19 patients undergoing ART treatment. Therefore, the inclusion criteria for a study were the description of original data on COVID-19-positive or COVID-19 vaccinated patients and the impact on their fertility. The outcomes included miscarriages, clinical pregnancy, and birth. Clinical pregnancy data were defined as the presence of an intrauterine gestational sac detected by ultrasound examination and the detection of human chorionic gonadotropin in serum. The miscarriage rate was characterized as the proportion of pregnancies ending in miscarriage within the first three months expressed as a ratio to the number of clinical pregnancies. The birth rate was calculated as the number of births per clinical pregnancy. All articles that included cohort, case-control, and cross-sectional studies were included. Studies that did not provide original data on fertility and COVID-19 were excluded. If the article described the pregnancy outcomes of patients with a positive COVID-19 history but did not abstain from a type of assisted reproduction, these studies were not included. If a study described the effects of the pandemic on infertile couples and not the virus or the vaccine itself, it was also excluded.

2.3. Data Extraction

The articles, papers, and statistical data were independently assessed by the two authors (A.M.-S. and N.S.), and each study was included or excluded from the list according to the criteria for inclusion and exclusion. Complete access to all data was given to every author in this research. Discrepancies were resolved by discussion.

2.4. Study Quality

To assess the risk of bias, the quality of the included studies was rated using the Newcastle–Ottawa Scale (NOS) [37]. The scale is divided into three parts. The parts include the Selection, Comparability, and Exposure for case-control studies. In the categories of Selection and Exposure, the maximum is one star for each numbered item in a study. However, a maximum of two stars can be given in the category of Comparability. The total number of items is eight, and a maximum of nine stars can be awarded for a study. For cohort studies, the categories include the Selection, Comparability, and Outcome. The same star system is applied. Though there is no validated rating, most researchers agree that studies with 7–9 stars are considered high quality, and those rated with 0–4 are at a very high risk of bias. The studies included in this review are divided into two tables based on the study type. For the cohort-study group, the mean value of the studies was 7.27 since most of the studies had been awarded 7 or 8 stars (Supplement Table S1). In the case-control study table, the mean value of the quality was 7.5, with one study being awarded a maximum of 9 stars. In contrast, one study was given six stars, the lowest-rated included study (Supplement Table S2).

2.5. Statistical Analysis

Meta-analyses were performed using Jeffreys’s Amazing Statistics Program (JASP) software ver. 0.18.3.0 (by the University of Amsterdam). Due to insufficient data, many studies could not be included in the quantitative analysis. Thus, only eight studies were included on the history of the SARS-CoV-2 virus infection and seven studies on the administration of vaccines. The value of the I2 index and Q-test assessed statistical heterogeneity. I2 values > 75% and the p value < 0.001 were considered high heterogeneity; thus, random effects models were used. Potential publication bias was examined using the symmetry of the funnel plot and rank correlation test. A forest plot, with the principal outcome of the odds ratio (OR) and 95% confidence interval (95% CI), was used to display the results. p ≤ 0.05 was considered statistically significant. Only data about the clinical pregnancy rate were subjected to analysis.

3. Results

A total of 1069 articles were found in the databases. After removing duplicates and screening the titles and abstracts based on the eligibility criteria, our search identified 90 records. Articles describing the experience with ART treatments of COVID-19-positive patients but not providing data on treatment outcomes were also excluded. The relevant full-text articles were then reviewed and evaluated after the inclusion and exclusion criteria were applied, and 18 studies remained (Figure 1). Of these 18 studies, 11 described the effects of COVID-19 and 7 described the impact of the vaccine on ART outcomes of infertile couples. In addition, 15 studies were included in the quantitative analyses.

3.1. Characteristics of the Reviewed Studies

Although the total number of all participants cannot be added as some studies reported the number of ART treatment cycles instead of the number of participants, there were over 2096 participants with a positive history of COVID-19 or SARS-CoV-2 infection (Table 1). The exact number could not be calculated, as the study by Eckstein et al. [38] does not state the number of participants but rather the number of treatment cycles performed. The total number of vaccinated patients was 2362, with 4920 vaccinated couples (Table 2). The potential clinical outcomes of the treatments were miscarriage, clinical pregnancy, and birth. The included studies were published between early 2021 and October 2023. There were five observational, seven cohort, and six retrospective studies. Four were multicenter studies, and all reported at least one of the outcomes. Some even stated that specific data, such as birth rates, were unavailable during the study.
Approximately 562 pregnancies were recorded in the studies included in this review (Table 1). When calculating birth rates, the study by Banker et al. was not included because their data describe specific ART-like outcomes and not overall birth rates [48]. The same logic was applied when calculating the total birth rates in the studies. Thus, the number of live births is above 335. The same applies to the miscarriage rate, which is 188. In all studies, the participants were in their thirties according to their average age. This is consistent with other ART studies, which show that over 60% of ART patients are around 35 years old [49,50].
Table 2. Studies describing patients undergoing ART procedures vaccinated for COVID-19.
Table 2. Studies describing patients undergoing ART procedures vaccinated for COVID-19.
StudyStudy TypeCity, CountryPublication DateNo. COVID-19 Vaccinated ParticipantsMean Age ± SDPregnancyBirthMiscarriage
Huang et al. [51]retrospective cohort studyChina9 February 20226633.7 ± 5.639/66 (59.1)
Dong et al. [52]prospective cohort studyChina27 June 2022735 infertile couples33.15  ±  3.5570/132 (53.03)
Wang et al. [53]cohort studyChina16 December 20224185 couples31.49 (3.70)603 couples with clinical pregnancies
Chen et al. [54]retrospective studyChina11 January 2023268 women with inactivated or recombinant COVID-1933.32 ± 5.14 (inactivated)
33.00 ± 5.16 (recombinant)		(inactivated)
46/77 (57.94)
(recombinant)
11/15 (3.33)		No data yet(inactivated)
2/77 (2.60)
(recombinant)
2/15 (13.33)
Yang et al. [55]retrospective studyChina11 October 202389930.71  ±  3.84141
Chillon et al. [56]observational studyAustria, Germany17 March 20234535.53 (7.00%)1 (2.2%)6 (13%)
Zhang et al. [57]case-control studyChina8 August 2023108432.00 (30.00–35.00)248/1084 (22.88)180/1084
(16.61)		70/504
(13.89)
TOTAL 2362
4920 couples		 115918674
SD—standard deviation.
The number of vaccinated patients undergoing ART in the studies included was 2362, and 4920 couples had received the vaccination. The average age of the participants in the included studies was similar and in line with the previously mentioned facts about ART patients [49,50]. As the studies were conducted relatively recently, only 186 births were recorded, of which 180 belonged to one study. The total number of pregnancies in the studies was 1159, and the number of miscarriages was 74. It is interesting to note that six of the seven studies were conducted in China.

3.2. Meta-Analysis

A meta-analysis was conducted on eight studies of the COVID-19 history group, all of which had clearly described and presented their data. In the vaccine administration group, seven studies were included and quantitatively analyzed. The excluded studies did not provide information on the total number of pregnancies or birth rates, so the information was unavailable for our research. The data of 10,389 participants from the COVID-19 positive group and the 254,816 participants from the control group (the COVID-19 negative group) were pooled (Supplement Table S3). The Q-test and I2 index showed high heterogeneity in clinical pregnancy outcomes (p < 0.001, Q = 0.143; and τ2 = 0.043, I2 = 90.32). The high heterogeneity of the results becomes apparent in the forest plot (Figure 2). The random effects method was used as only a few studies were included. Thus, the differences in clinical pregnancy rates were compared for the COVID-19 positive and COVID-19 negative groups, and there were no differences (OR = −0.03; 95% CI: −0.18–0.12; p = 0.705; Figure 2). In Figure 2, study Banker et al. a) represents the fresh ET group and study Banker et al. b) represents the frozen ET group.
The data from the vaccinated and unvaccinated groups were analyzed and the random effects method was used to test whether the COVID-19 vaccines affected clinical pregnancy outcomes (Supplement Table S4). The Q-test and I2 index showed substantial heterogeneity (p < 0.001; τ2 = 0.025, I2 = 74.04). This is visible in the graphical representation of the forest plot (Figure 3). Clinical pregnancy rates were compared between vaccinated and unvaccinated participants undergoing IVF. Statistically significant differences were found (OR = −0.17; 95% CI: −0.32–(−0.01); p = 0.029; Figure 3).
Subsequently, the data of 10,096 participants were pooled for the birth rates of the COVID-19 positive group and 254,478 participants in the control groups (the COVID-19 negative group) (Supplement Table S3). As with pregnancy rates, the Q-test and I2 index showed high heterogeneity in birth outcomes (p < 0.001, Q = 0.809; and τ2 = 0.328, I2 = 98.69). The high heterogeneity of the results is displayed in the forest plot (Figure 4), and thus the random effects method was used. The differences in the birth rates were compared for the COVID-19 positive and COVID-19 negative groups and there were no differences (OR = −0.21; 95% CI: −0.68–0.25; p = 0.719; Figure 4).
The overall number of birth rate participants was 1292 in the vaccinated group and 1440 in the unvaccinated group. The data from the vaccinated and unvaccinated groups were analyzed using the random effects method to investigate whether COVID-19 vaccines affected birth outcomes (Supplement Table S4). The Q-test and I2 index showed considerable heterogeneity in birth rates (p = 0.002; τ2 = 0.097, I2 = 79.70). This is visible in the graphical representation of the forest plot (Figure 5). The birth rates of the vaccinated and unvaccinated participants were then compared. There were no statistically significant differences between vaccinated and unvaccinated participants (OR = −0.18; 95% CI: −0.59–0.23); p = 0.399; Figure 5).
The number of participants in the miscarriage rates for the COVID-19 positive group was 4692 and 5754 for the COVID-19 negative group (Supplement Table S3). The Q-test and I2 index showed substantial heterogeneity in miscarriage outcomes (p < 0.001, Q = 4.514; and τ2 = 0.034, I2 = 77.49), which is displayed in the forest plot (Figure 6). The differences in the miscarriage rates were compared for the COVID-19 positive and COVID-19 negative groups, and there were significant differences (OR = 0.21; 95% CI: 0.02–0.40; p = 0.034; Figure 6).
The total number of participants in the miscarriage rates for the vaccinated group was 581 and was 748 in the control group (the unvaccinated group) (Supplement Table S4). The Q-test and I2 index showed no heterogeneity in miscarriage rates (p = 0.520; τ2 = 0.00, I2 = 0.00). The birth rates of vaccinated and unvaccinated participants were compared. There were no statistically significant differences in birth rates between vaccinated and unvaccinated participants (OR = −0.05; 95% CI: −0.24–0.13); p = 0.561; Figure 7).

3.3. Publication Bias

In addition, the potential publication bias was estimated for all included studies. The funnel plot of the studies included in the clinical pregnancy rate was approximately symmetrical in both analyses, COVID-19 positive vs. negative and vaccinated vs. unvaccinated, with Kendall’s τ values of −0.111 and −0.429 (p = 0.761 and p = 0.293), respectively (Figure 8A,B). Almost all studies are at the top in the vaccinated vs. unvaccinated groups, showing that these are studies with high strength.
The funnel plot for the positive vs. negative birth rates of the COVID-19 groups is shown in Figure 9A and is mostly symmetrical with Kendall’s τ values of −0.200 (p = 0.719). Figure 9B shows the funnel plot for the vaccinated vs. unvaccinated birth rates, where Kendall’s τ values are 0.333 (p = 1.00), indicating no publication bias.
The funnel plot for the miscarriage rates of COVID-19 positive vs. negative groups is shown in supplementary Figure S1A. It is symmetrical with Kendall’s τ values 0.200 (p = 0.719). In supplementary Figure S1, the funnel plot for the miscarriage rates of vaccinated vs. unvaccinated groups is also displayed, with Kendall’s τ values of −1.00 (p = 1.00), indicating no publication bias.

4. Discussion

4.1. Clinical Pregnancy Rate of COVID-19 Patients

The studies examined over 500 pregnant women with a positive COVID-19 history (Table 1). The results of the meta-analysis showed no statistically significant difference in clinical pregnancy rates between the COVID-19 positive and COVID-19 negative groups (Figure 2). In 2018, the European Society of Human Reproduction and Embryology (ESHRE) announced that their results for that year showed a continued increase in the reported number of ART treatment cycles and children born in Europe [58]. In 2019, the year the pandemic began, ESHRE also reported an increase in ART treatment cycles and birth rates, with an increase in abandonment rates for fresh IVF or intracytoplasmic sperm injection (ICSI) cycles [59]. Frozen embryo transfers (FET) showed higher pregnancy rates (PRs), intrauterine insemination (IUI) cycles decreased with no change in outcomes, and there was a decrease in multiple embryo transfers [59]. In 2020, preliminary results were published, including 1157 IVF clinics in different countries and 1176 IUI units. These 35 countries reported that their clinical pregnancy rates (PR) per aspiration and transfer were similar to 2019 [60]. Data from the pandemic years have yet to be published. In China, where the pandemic began, 63.6% of ART treatment providers and 95.5% of sperm banks ceased operations due to the pandemic [61]. Wei et al. described data on clinical pregnancy and delivery rates, which showed a steady upward trend in the post-pandemic period [62].

4.2. Birth Rates of COVID-19 Patients

Over 300 births were described in the studies examined (Table 1). As previously mentioned, birth rates after ART procedures increased in the years before the pandemic [37,38,39,40]. In their systemic review and meta-analysis, Allotey et al. reported that COVID-19-infected pregnant women are more likely to experience preterm birth, have an increased risk of maternal death, and that babies are more likely to be admitted to the neonatal intensive care unit compared to women without a history of infection [63]. In 2018, it was reported that around 1.5 million IVF cycles are performed worldwide each year, resulting in around 400,000 live births, and that the overall rate of live births after ART is 0.3% [64]. A Canadian study found that the risk of COVID-19 for women of childbearing age appears to be low and that there is evidence of low risk for pregnant patients and their fetuses. In addition, the study suggested that ART procedures and fertility treatments should not have been postponed due to the pandemic [49]. Furthermore, our meta-analysis revealed no statistically significant differences in the birth rates of the two groups, namely those who tested positive for COVID-19 and those who tested negative (Figure 4).

4.3. Miscarriage Rates of COVID-19 Patients

Table 1 describes a total of 188 miscarriages in the considered studies. The results of the meta-analysis suggest that individuals infected with the SARS-CoV-2 virus may have an increased risk of early miscarriage during ART treatment (p = 0.034, Figure 6). These findings are consistent with those of a large cohort study from the UK, which showed that COVID-19 infection is associated with an increased incidence of first-trimester abortion and that pregnant women infected with the SARS-CoV-2 virus are at a higher risk of miscarriage [65]. An increased miscarriage rate in the ART procedure was observed in couples with a previous COVID-19 infection. Considering the high contagiousness of SARS-CoV-2, many questions have arisen regarding the risk of transmission to and between human embryos, gametes, and reproductive tissues during cryostorage in ART laboratories [49]. Opinions on the effects of COVID-19 on the embryo and fetus remain divided. Kotlyar et al. state in their study that vertical transmission of SARS-CoV-2 is possible and occurs in a few cases of maternal SARS-CoV-2 infection in the third trimester. The infection rates are similar to other pathogens that cause congenital infections [66]. On the other hand, Setti et al. reported that their data set showed no increased risk of miscarriage in the first trimester of ART pregnancies achieved during the onset of COVID-19 [67]. A Canadian review summarized the knowledge on the impact of SARS-CoV-2 infection on reproductive health [49]. No transmission cases during ART treatments, such as cryopreservation, embryo culture, or storage, were recorded, so authors have concluded that the likelihood of COVID-19 affecting embryos or their recipients is low [49].

4.4. Clinical Pregnancy Rate of COVID-19 Vaccinated Patients

The second table describes the vaccinated patients and their ART results. Approximately 1159 pregnancies were recorded in the studies examined. Opinions also differ on the safety of vaccines in terms of fertility. A study published in 2023 reported that pregnancy outcomes were not affected by taking the inactivated vaccine before frozen embryo transfer [57]. It also states that the number of vaccine doses and the interval between them had no effect, thus providing evidence for the safety of administering the vaccine during pregnancy in patients undergoing ART [57]. However, another reasonably recent study concluded that while the vaccine did not affect egg quality and embryo transfer, the impact on reproductive outcomes and health remains uncertain [68]. Nevertheless, Shi et al. have shown that vaccination before the IVF procedure is associated with a lower pregnancy rate [69]. Regardless of these results, the data from this meta-analysis showed a statistically significant difference between the vaccinated and unvaccinated groups (p = 0.029, Figure 3). It can, therefore, be postulated that the administration of the SARS-CoV-2 vaccine may have an impact on the frequency of pregnancies in individuals undergoing ART, with a significantly higher prevalence observed in those who had not received the vaccine.

4.5. Birth Rates of COVID-19 Vaccinated Patients

The total number of births in all included studies was 186. As divergent viewpoints exist regarding the vaccine’s effects on pregnancy, similar divisions emerge concerning its influence on overall birth rates among healthy individuals. When comparing the birth rates of vaccinated and unvaccinated participants undergoing IVF, no statistically significant differences were found in the present meta-analysis (Figure 5). According to Zhang et al., the vaccine protects the mother and child, reducing the likelihood of fetal infection after birth [57]. Another study comparing unvaccinated and vaccinated women undergoing frozen embryo transfer found that live birth rates did not differ between the two groups [70]. The study also showed that the length and weight of the newborns did not change after vaccination [70]. Another Chinese study, in which the subjects were divided into four groups according to the vaccination status of both partners, provided evidence that the vaccination had no negative impact on the live birth rate [15].

4.6. Miscarriage Rates of COVID-19 Vaccinated Patients

The overall rate of miscarriage in the studies was 74. A meta-analysis showed that the COVID-19 vaccine did not impact the risk of miscarriage, although the analysis was based on only two studies (Figure 7). Zauche et al. compared the natural miscarriage rate in the first six weeks of pregnancy and found that vaccination before or during pregnancy did not increase the miscarriage rate [71]. A 2022 study compared the pregnancy outcomes of unvaccinated and vaccinated patients undergoing ART and found no statistically significant difference in miscarriage rates between the groups [72]. As early as 2021, researchers showed that data from clinical trials indicate that the vaccination does not harm reproductive health or increase the number of miscarriages [73].

4.7. Study Limitations

The strict inclusion and exclusion criteria demonstrate the study’s validity, proven by the non-significant difference between the groups regarding the baseline characteristics. The main limitation of this study is the relatively small number of studies found, as the inclusion criteria were quite strict, and artificial human reproduction is still a newer branch of medicine that needs more research. Due to the strict inclusion criteria, there is a potential selection bias in the included studies. Additionally, the study’s timeframe is constrained by the relatively short duration of the pandemic. Likewise, the critical studies are limited, although the systematic review included a moderate number of participants. The variability in methodologies and definitions across the included studies may have also introduced heterogeneity, reflected in the synthesis of findings. The studies’ heterogeneity should be considered a limitation of the research. Furthermore, we only included clinical pregnancy rate data in the meta-analysis. Most included studies were conducted in Europe, but most studies investigating the effects of the COVID-19 vaccine on ART were conducted in China. Also, the number of couples undergoing ART in each study varied considerably, from 4000 to as few as 6, which can significantly affect the results of individual studies. In addition, many of the included studies did not consider potential confounding factors such as the presence of various comorbidities (diabetes, hypertension) and sleep disorders in couples undergoing ART. The included studies did not specify which type of SARS-CoV-2 virus was affecting their patients (e.g., Delta and Omicron), and so we cannot determine whether all viruses have the same impact on ART methods and what impact each form of the virus has on IVF outcomes. Another issue is that not all studies mentioned which vaccine type was administrated. Furthermore, some of the included studies did not provide data on the children’s births, as they were either published before birth or did not have these data. Therefore, an accurate assessment of the impact of COVID-19 and the vaccine in such studies is highly subjective. It is also worth noting that publication bias could have influenced the findings when studies assessing ART procedures in COVID-19 vaccinated patients are concerned; however, it was insignificant.

5. Conclusions

Overall, there is still much to discover about the effects of SARS-CoV-2 infection on reproductive organs. It is important to prioritize the health and safety of people with infertility issues. When examining those currently undergoing ART treatment, the infection and the vaccine are compelling topics that need to be explored. Further research is needed to investigate the link between infertility and COVID-19 thoroughly. The safety and potential effects of the vaccine are also not yet fully known, as the long-term consequences for reproductive health are not yet known. The couples and individuals in the studies analyzed were not initially affected by their coronavirus infection. Nevertheless, the results of this meta-analysis suggest that SARS-CoV-2 infection was associated with an increased miscarriage rate. At the same time, vaccine administration was associated with decreased clinical pregnancy rates. However, the limited number of studies included in the meta-analysis should be considered when interpreting the results. Providing accurate information to individuals and couples undergoing infertility treatment can help allay concerns and enable informed decision-making. Finally, fostering an ongoing dialog between healthcare providers, researchers, and patients can contribute to a better understanding of the evolving landscape of COVID-19 and its impact on reproductive health.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/diseases12090201/s1, PRISMA 2020 Checklist [74]; Table S1: Newcastle-Ottawa Scale (NOS)—for cohort study; Table S2: Newcastle-Ottawa Scale (NOS)—for case-control study; Table S3: Quantitative data based on the history of the SARS-CoV-2 virus infection of studies included in the meta-analysis; Table S4: Quantitative data based on the vaccine administration of studies included in the meta-analysis; Figure S1: Funnel plots of miscarriage rate. (A) COVID-19 positive vs. negative participants, (B) vaccinated vs. unvaccinated participants.

Author Contributions

Conceptualization, A.M.-S. and N.S.; literature search, A.M.-S. and N.S.; writing—original draft preparation, A.M.-S., N.S., J.T., T.M., T.Ž., S.P., R.F., V.M. and I.Š.; writing—proofreading, review and editing, A.M.-S., V.M., N.S., T.M. and I.Š., supervision, N.S. and I.Š. A.M.-S. and N.S. contributed equally to this work. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by a grant from the Croatian Ministry of Science and Education and dedicated to multi-year institutional financing of scientific activity at the Josip Juraj Strossmayer University of Osijek, Faculty of Dental Medicine and Health, Osijek, Croatia, grant number IP8-FDMZ-2023 (to J.T.).

Conflicts of Interest

The authors declare no conflicts of interest. The funders had no role in the study’s design, in the collection, analyses, or interpretation of data, in the writing of the manuscript, or in the decision to publish the results.

References

  1. Hu, B.; Guo, H.; Zhou, P.; Shi, Z.-L. Characteristics of SARS-CoV-2 and COVID-19. Nat. Rev. Microbiol. 2021, 19, 141–154. [Google Scholar] [CrossRef] [PubMed]
  2. Niemi, M.E.K.; Daly, M.J.; Ganna, A. The Human Genetic Epidemiology of COVID-19. Nat. Rev. Genet. 2022, 23, 533–546. [Google Scholar] [CrossRef]
  3. Xue, Y.; Xiong, Y.; Cheng, X.; Li, K. Impact of SARS-CoV-2 Infection on Clinical Outcomes of in Vitro Fertilization Treatments: A Systematic Review and Meta-Analysis. Front. Endocrinol. 2023, 14, 1233986. [Google Scholar] [CrossRef] [PubMed]
  4. Zou, X.; Chen, K.; Zou, J.; Han, P.; Hao, J.; Han, Z. Single-Cell RNA-Seq Data Analysis on the Receptor ACE2 Expression Reveals the Potential Risk of Different Human Organs Vulnerable to 2019-nCoV Infection. Front. Med. 2020, 14, 185–192. [Google Scholar] [CrossRef]
  5. Kasuga, Y.; Zhu, B.; Jang, K.-J.; Yoo, J.-S. Innate Immune Sensing of Coronavirus and Viral Evasion Strategies. Exp. Mol. Med. 2021, 53, 723–736. [Google Scholar] [CrossRef] [PubMed]
  6. Schneider, W.M.; Chevillotte, M.D.; Rice, C.M. Interferon-Stimulated Genes: A Complex Web of Host Defenses. Annu. Rev. Immunol. 2014, 32, 513–545. [Google Scholar] [CrossRef]
  7. Dong, M.; Zhang, J.; Ma, X.; Tan, J.; Chen, L.; Liu, S.; Xin, Y.; Zhuang, L. ACE2, TMPRSS2 Distribution and Extrapulmonary Organ Injury in Patients with COVID-19. Biomed. Pharmacother. 2020, 131, 110678. [Google Scholar] [CrossRef]
  8. Herrero, Y.; Pascuali, N.; Velázquez, C.; Oubiña, G.; Hauk, V.; de Zúñiga, I.; Peña, M.G.; Martínez, G.; Lavolpe, M.; Veiga, F.; et al. SARS-CoV-2 Infection Negatively Affects Ovarian Function in ART Patients. Biochim. Biophys. Acta Mol. Basis Dis. 2022, 1868, 166295. [Google Scholar] [CrossRef]
  9. Rajak, P.; Roy, S.; Dutta, M.; Podder, S.; Sarkar, S.; Ganguly, A.; Mandi, M.; Khatun, S. Understanding the Cross-Talk between Mediators of Infertility and COVID-19. Reprod. Biol. 2021, 21, 100559. [Google Scholar] [CrossRef]
  10. Mokhtari, T.; Hassani, F.; Ghaffari, N.; Ebrahimi, B.; Yarahmadi, A.; Hassanzadeh, G. COVID-19 and Multiorgan Failure: A Narrative Review on Potential Mechanisms. J. Mol. Histol. 2020, 51, 613–628. [Google Scholar] [CrossRef]
  11. Wang, Z.; Xu, X. scRNA-Seq Profiling of Human Testes Reveals the Presence of the ACE2 Receptor, A Target for SARS-CoV-2 Infection in Spermatogonia, Leydig and Sertoli Cells. Cells 2020, 9, 920. [Google Scholar] [CrossRef] [PubMed]
  12. Zhang, Y.; Geng, X.; Tan, Y.; Li, Q.; Xu, C.; Xu, J.; Hao, L.; Zeng, Z.; Luo, X.; Liu, F.; et al. New Understanding of the Damage of SARS-CoV-2 Infection Outside the Respiratory System. Biomed. Pharmacother. 2020, 127, 110195. [Google Scholar] [CrossRef]
  13. Verrienti, P.; Cito, G.; Di Maida, F.; Tellini, R.; Cocci, A.; Minervini, A.; Natali, A. The Impact of COVID-19 on the Male Genital Tract: A Qualitative Literature Review of Sexual Transmission and Fertility Implications. Clin. Exp. Reprod. Med. 2022, 49, 9–15. [Google Scholar] [CrossRef] [PubMed]
  14. Verma, S.; Saksena, S.; Sadri-Ardekani, H. ACE2 Receptor Expression in Testes: Implications in Coronavirus Disease 2019 Pathogenesis†. Biol. Reprod. 2020, 103, 449–451. [Google Scholar] [CrossRef] [PubMed]
  15. Ma, L.; Xie, W.; Li, D.; Shi, L.; Mao, Y.; Xiong, Y.; Zhang, Y.; Zhang, M. Effect of SARS-CoV-2 Infection upon Male Gonadal Function: A Single Center-Based Study. MedRxiv 2020, 2020-03. [Google Scholar] [CrossRef]
  16. Bridwell, R.E.; Merrill, D.R.; Griffith, S.A.; Wray, J.; Oliver, J.J. A Coronavirus Disease 2019 (COVID-19) Patient with Bilateral Orchitis. Am. J. Emerg. Med. 2021, 42, 260.e3–260.e5. [Google Scholar] [CrossRef]
  17. Xu, J.; Qi, L.; Chi, X.; Yang, J.; Wei, X.; Gong, E.; Peh, S.; Gu, J. Orchitis: A Complication of Severe Acute Respiratory Syndrome (SARS)1. Biol. Reprod. 2006, 74, 410–416. [Google Scholar] [CrossRef]
  18. Gagliardi, L.; Bertacca, C.; Centenari, C.; Merusi, I.; Parolo, E.; Ragazzo, V.; Tarabella, V. Orchiepididymitis in a Boy with COVID-19. Pediatr. Infect. Dis. J. 2020, 39, e200. [Google Scholar] [CrossRef]
  19. Li, H.; Xiao, X.; Zhang, J.; Zafar, M.I.; Wu, C.; Long, Y.; Lu, W.; Pan, F.; Meng, T.; Zhao, K.; et al. Impaired Spermatogenesis in COVID-19 Patients. EClinicalMedicine 2020, 28, 100604. [Google Scholar] [CrossRef]
  20. Larasati, T.; Noda, T.; Fujihara, Y.; Shimada, K.; Tobita, T.; Yu, Z.; Matzuk, M.M.; Ikawa, M. Tmprss12 Is Required for Sperm Motility and Uterotubal Junction Migration in Mice†. Biol. Reprod. 2020, 103, 254–263. [Google Scholar] [CrossRef]
  21. Batiha, O.; Al-Deeb, T.; Al-zoubi, E.; Alsharu, E. Impact of COVID-19 and Other Viruses on Reproductive Health. Andrologia 2020, 52, e13791. [Google Scholar] [CrossRef]
  22. Wang, Q.; Zhang, Y.; Wu, L.; Niu, S.; Song, C.; Zhang, Z.; Lu, G.; Qiao, C.; Hu, Y.; Yuen, K.-Y.; et al. Structural and Functional Basis of SARS-CoV-2 Entry by Using Human ACE2. Cell 2020, 181, 894–904.e9. [Google Scholar] [CrossRef]
  23. Scopus Preview—Scopus—Document Details—Single-Cell Transcriptome Analysis of the Novel Coronavirus (SARS-CoV-2) Associated Gene ACE2 Expression in Normal and Non-Obstructive Azoospermia (NOA) Human Male Testes. Available online: https://www.scopus.com/record/display.uri?eid=2-s2.0-85085124021&origin=inward&txGid=c40616db96674ffe52e0079abee92424 (accessed on 4 March 2024).
  24. Rajput, S.K.; Logsdon, D.M.; Kile, B.; Engelhorn, H.J.; Goheen, B.; Khan, S.; Swain, J.; McCormick, S.; Schoolcraft, W.B.; Yuan, Y.; et al. Human Eggs, Zygotes, and Embryos Express the Receptor Angiotensin 1-Converting Enzyme 2 and Transmembrane Serine Protease 2 Protein Necessary for Severe Acute Respiratory Syndrome Coronavirus 2 Infection. F&S Sci. 2021, 2, 33–42. [Google Scholar] [CrossRef]
  25. Wu, M.; Ma, L.; Xue, L.; Zhu, Q.; Zhou, S.; Dai, J.; Yan, W.; Zhang, J.; Wang, S. Co-Expression of the SARS-CoV-2 Entry Molecules ACE2 and TMPRSS2 in Human Ovaries: Identification of Cell Types and Trends with Age. Genomics 2021, 113, 3449–3460. [Google Scholar] [CrossRef] [PubMed]
  26. Stanley, K.E.; Thomas, E.; Leaver, M.; Wells, D. Coronavirus Disease-19 and Fertility: Viral Host Entry Protein Expression in Male and Female Reproductive Tissues. Fertil. Steril. 2020, 114, 33–43. [Google Scholar] [CrossRef] [PubMed]
  27. Reis, F.M.; Bouissou, D.R.; Pereira, V.M.; Camargos, A.F.; dos Reis, A.M.; Santos, R.A. Angiotensin-(1-7), Its Receptor Mas, and the Angiotensin-Converting Enzyme Type 2 Are Expressed in the Human Ovary. Fertil. Steril. 2011, 95, 176–181. [Google Scholar] [CrossRef] [PubMed]
  28. Tanacan, A.; Yazihan, N.; Erol, S.A.; Anuk, A.T.; Yucel Yetiskin, F.D.; Biriken, D.; Ozgu-Erdinc, A.S.; Keskin, H.L.; Moraloglu Tekin, O.; Sahin, D. The Impact of COVID-19 Infection on the Cytokine Profile of Pregnant Women: A Prospective Case-Control Study. Cytokine 2021, 140, 155431. [Google Scholar] [CrossRef]
  29. Yu, N.; Li, W.; Kang, Q.; Xiong, Z.; Wang, S.; Lin, X.; Liu, Y.; Xiao, J.; Liu, H.; Deng, D.; et al. Clinical Features and Obstetric and Neonatal Outcomes of Pregnant Patients with COVID-19 in Wuhan, China: A Retrospective, Single-Centre, Descriptive Study. Lancet Infect. Dis. 2020, 20, 559–564. [Google Scholar] [CrossRef]
  30. Zeng, L.; Xia, S.; Yuan, W.; Yan, K.; Xiao, F.; Shao, J.; Zhou, W. Neonatal Early-Onset Infection With SARS-CoV-2 in 33 Neonates Born to Mothers with COVID-19 in Wuhan, China. JAMA Pediatr. 2020, 174, 722–725. [Google Scholar] [CrossRef]
  31. Matar, R.; Alrahmani, L.; Monzer, N.; Debiane, L.G.; Berbari, E.; Fares, J.; Fitzpatrick, F.; Murad, M.H. Clinical Presentation and Outcomes of Pregnant Women with Coronavirus Disease 2019: A Systematic Review and Meta-Analysis. Clin. Infect. Dis. 2021, 72, 521–533. [Google Scholar] [CrossRef]
  32. Wong, S.F.; Chow, K.M.; Leung, T.N.; Ng, W.F.; Ng, T.K.; Shek, C.C.; Ng, P.C.; Lam, P.W.Y.; Ho, L.C.; To, W.W.K.; et al. Pregnancy and Perinatal Outcomes of Women with Severe Acute Respiratory Syndrome. Am. J. Obstet. Gynecol. 2004, 191, 292–297. [Google Scholar] [CrossRef] [PubMed]
  33. Zhu, H.; Wang, L.; Fang, C.; Peng, S.; Zhang, L.; Chang, G.; Xia, S.; Zhou, W. Clinical Analysis of 10 Neonates Born to Mothers with 2019-nCoV Pneumonia. Transl. Pediatr. 2020, 9, 510–560. [Google Scholar] [CrossRef]
  34. Wei, M.; Yuan, J.; Liu, Y.; Fu, T.; Yu, X.; Zhang, Z.-J. Novel Coronavirus Infection in Hospitalized Infants Under 1 Year of Age in China. JAMA 2020, 323, 1313–1314. [Google Scholar] [CrossRef] [PubMed]
  35. Li, K.; Chen, G.; Hou, H.; Liao, Q.; Chen, J.; Bai, H.; Lee, S.; Wang, C.; Li, H.; Cheng, L.; et al. Analysis of Sex Hormones and Menstruation in COVID-19 Women of Childbearing Age. Reprod. Biomed. Online 2021, 42, 260–267. [Google Scholar] [CrossRef] [PubMed]
  36. 1 in 6 People Globally Affected by Infertility: WHO. Available online: https://www.who.int/news/item/04-04-2023-1-in-6-people-globally-affected-by-infertility (accessed on 23 November 2023).
  37. Lo, C.K.-L.; Mertz, D.; Loeb, M. Newcastle-Ottawa Scale: Comparing ‘Reviewers’ to ‘Authors’ Assessments. BMC Med. Res. Methodol. 2014, 14, 45. [Google Scholar] [CrossRef] [PubMed]
  38. Eckstein, V.; Glaß, K.; Leßmann, M.-E.; Schaar, J.; Klimova, A.; Wimberger, P.; Goeckenjan, M. Assisted Reproduction after SARS-CoV-2-Infection: Results of a Single-Center Cohort-Study. Arch. Gynecol. Obstet. 2023, 309, 305–313. [Google Scholar] [CrossRef]
  39. Huri, M.; Noferi, V.; Renda, I.; Piazzini, F.; Benemei, S.; Coccia, M.E. The COVID-19 Pandemic Impact on the Outcome of Medically Assisted Reproduction Pregnancies. Front. Reprod. Health 2022, 4, 860425. [Google Scholar] [CrossRef]
  40. Rageh, K.E.A.; Farag, E.A.; Behery, M.A.; Badreldin, M.A.; Ali, E.A. The Impact of Previous Exposure to COVID-19 on the Outcome of ICSI Cycles. JBRA Assist. Reprod. 2023, 27, 367–372. [Google Scholar] [CrossRef]
  41. Engels Calvo, V.; Cruz Melguizo, S.; Abascal-Saiz, A.; Forcén Acebal, L.; Sánchez-Migallón, A.; Pintado Recarte, P.; Cuenca Marín, C.; Marcos Puig, B.; Del Barrio Fernández, P.G.; Nieto Velasco, O.; et al. Perinatal Outcomes of Pregnancies Resulting from Assisted Reproduction Technology in SARS-CoV-2-Infected Women: A Prospective Observational Study. Fertil. Steril. 2021, 116, 731–740. [Google Scholar] [CrossRef]
  42. Rodríguez-Varela, C.; Mariani, G.; Dolz, P.; García-Velasco, J.A.; Serra, V.; Pellicer, A.; Labarta, E. Impact of COVID-19 on Infertility Treatments: Not Even a Global Pandemic Was Strong Enough to Hamper Successful Pregnancies. Life 2021, 12, 6. [Google Scholar] [CrossRef]
  43. Ata, B.; Gianaroli, L.; Lundin, K.; Mcheik, S.; Mocanu, E.; Rautakallio-Hokkanen, S.; Tapanainen, J.S.; Vermeulen, N.; Veiga, A. Outcomes of SARS-CoV-2 Infected Pregnancies after Medically Assisted Reproduction. Hum. Reprod. 2021, 36, 2883–2890. [Google Scholar] [CrossRef] [PubMed]
  44. Huang, J.; Liu, Y.; Xia, L.; Zhao, Y.; Tian, L.; Xu, D.; Su, Q.; Hu, Y.; Xie, Q.; Chen, J.; et al. Effect of Prior Female SARS-CoV-2 Infection on IVF Outcomes: A Prospective Cohort Study. Front. Endocrinol. 2023, 14, 1239903. [Google Scholar] [CrossRef]
  45. Epelboin, S.; Labrosse, J.; De Mouzon, J.; Fauque, P.; Gervoise-Boyer, M.-J.; Levy, R.; Sermondade, N.; Hesters, L.; Bergère, M.; Devienne, C.; et al. Obstetrical Outcomes and Maternal Morbidities Associated with COVID-19 in Pregnant Women in France: A National Retrospective Cohort Study. PLoS Med. 2021, 18, e1003857. [Google Scholar] [CrossRef] [PubMed]
  46. Ziert, Y.; Abou-Dakn, M.; Backes, C.; Banz-Jansen, C.; Bock, N.; Bohlmann, M.; Engelbrecht, C.; Gruber, T.M.; Iannaccone, A.; Jegen, M.; et al. Maternal and Neonatal Outcomes of Pregnancies with COVID-19 after Medically Assisted Reproduction: Results from the Prospective COVID-19-Related Obstetrical and Neonatal Outcome Study. Am. J. Obstet. Gynecol. 2022, 227, e1–e495. [Google Scholar] [CrossRef]
  47. Dolgushina, N.V.; Menzhinskaya, I.V.; Ermakova, D.M.; Frankevich, N.A.; Vtorushina, V.V.; Sukhikh, G.T. The Effect of COVID-19 Severity, Associated Serum Autoantibodies and Time Interval after the Disease on the Outcomes of Fresh Oocyte ART Cycles in Non-Vaccinated Patients. J. Clin. Med. 2023, 12, 4370. [Google Scholar] [CrossRef] [PubMed]
  48. Banker, M.; Arora, P.; Banker, J.; Shah, A.; Gupta, R.; Shah, S. Impact of COVID-19 Pandemic on Clinical and Embryological Outcomes of Assisted Reproductive Techniques. J. Hum. Reprod. Sci. 2022, 15, 150–156. [Google Scholar] [CrossRef]
  49. Madjunkov, M.; Dviri, M.; Librach, C. A Comprehensive Review of the Impact of COVID-19 on Human Reproductive Biology, Assisted Reproduction Care and Pregnancy: A Canadian Perspective. J. Ovarian Res. 2020, 13, 140. [Google Scholar] [CrossRef]
  50. Age and Infertility: The Biological Clock: Fact or Fiction? Available online: https://fertilitycenterlv.com/blog/your-biological-clock-fact-or-fiction-the-effects-of-age-on-female-fertility/ (accessed on 22 November 2023).
  51. Huang, J.; Xia, L.; Lin, J.; Liu, B.; Zhao, Y.; Xin, C.; Ai, X.; Cao, W.; Zhang, X.; Tian, L.; et al. No Effect of Inactivated SARS-CoV-2 Vaccination on in Vitro Fertilization Outcomes: A Propensity Score-Matched Study. J. Inflamm. Res. 2022, 15, 839–849. [Google Scholar] [CrossRef]
  52. Dong, M.; Wu, S.; Zhang, X.; Zhao, N.; Qi, J.; Zhao, D.; Sang, Y.; Tan, J. Effects of COVID-19 Vaccination Status, Vaccine Type, and Vaccination Interval on IVF Pregnancy Outcomes in Infertile Couples. J. Assist. Reprod. Genet. 2022, 39, 1849–1859. [Google Scholar] [CrossRef]
  53. Wang, C.; Tang, D.; Liu, J.; Zhang, S.; Xu, Y.; Qiao, J.; Cao, Y. Association Between COVID-19 Vaccination and Artificial Insemination Outcomes for Couples Experiencing Infertility. JAMA Netw. Open 2022, 5, e2247216. [Google Scholar] [CrossRef]
  54. Chen, H.; Zhang, X.; Lin, G.; Gong, F.; Hocher, B. Safety of COVID-19 Vaccination in Women Undergoing IVF/ICSI Treatment—Clinical Study and Systematic Review. Front. Immunol. 2023, 13, 1054273. [Google Scholar] [CrossRef] [PubMed]
  55. Yang, Y.; Dong, Y.; Li, G.; Yin, B.; Tang, X.; Jia, L.; Zhang, X.; Yang, W.; Wang, C.; Peng, X.; et al. Pregnancy Outcomes Following Natural Conception and Assisted Reproduction Treatment in Women Who Received COVID-19 Vaccination Prior to Conception: A Population-Based Cohort Study in China. Front. Med. 2023, 10, 1250165. [Google Scholar] [CrossRef] [PubMed]
  56. Chillon, T.S.; Weiss, G.; Demircan, K.; Minich, W.B.; Schenk, M.; Schomburg, L. Antibodies to SARS-CoV-2 in Follicular Fluids and Their Association with Assisted Reproduction. Front. Immunol. 2023, 14, 1120328. [Google Scholar] [CrossRef] [PubMed]
  57. Zhang, X.-L.; Chen, Y.-H.; Zhang, S.-P.; Wu, X.-Q.; Wang, X.-P. Effects of the Severe Acute Respiratory Syndrome Coronavirus 2 Inactivated Vaccine on the Outcome of Frozen Embryo Transfers: A Large Scale Clinical Study. Int. J. Womens Health 2023, 15, 1305–1316. [Google Scholar] [CrossRef]
  58. European IVF Monitoring Consortium (EIM), for the European Society of Human Reproduction and Embryology (ESHRE); Wyns, C.; Geyter, C.D.; Calhaz-Jorge, C.; Kupka, M.S.; Motrenko, T.; Smeenk, J.; Bergh, C.; Tandler-Schneider, A.; Rugescu, I.A.; et al. ART in Europe, 2018: Results Generated from European Registries by ESHRE. Hum. Reprod. Open 2022, 2022, hoac022. [Google Scholar] [CrossRef]
  59. European IVF Monitoring Consortium (EIM) for the European Society of Human Reproduction and Embryology (ESHRE); Smeenk, J.; Wyns, C.; De Geyter, C.; Kupka, M.; Bergh, C.; Cuevas Saiz, I.; De Neubourg, D.; Rezabek, K.; Tandler-Schneider, A.; et al. ART in Europe, 2019: Results Generated from European Registries by ESHRE. Hum. Reprod. 2023, 38, dead197. [Google Scholar] [CrossRef]
  60. Smeenk, J.; Wyns, C.; De Geyter, C.; Bergh, C.; Cuevas, I.; de Neubourg, D.; Kupka, M.S.; Rezabek, K.; Rugescu, I.; Tandler-Schneider, A.; et al. O-153 Assisted Reproductive Technology (ART) in Europe 2020 and Development of a Strategy of Vigilance: Preliminary Results Generated from European Registers by the ESHRE EIM Consortium. Hum. Reprod. 2023, 38, dead093.014. [Google Scholar] [CrossRef]
  61. Qiao, J.; National Expert Group for Quality Management on Assisted Reproductive Technology. Impacts of COVID-19 pandemics on the services of assisted reproductive technology in Chinese mainland: A national cross-sectional survey. Chin. J. Reprod. Contracept. 2021, 41, 7–11. [Google Scholar]
  62. Wei, L.; Zhang, J.; Deng, X.; Luo, C.; Bo, L.; Gao, S.; Qian, F.; Lu, S.; Mao, C. Impacts of the COVID-19 Pandemic on Chinese Assisted Reproductive Technology Institutions and Human Sperm Banks: Reflections in the Post-Pandemic Era. J. Health Popul. Nutr. 2023, 42, 82. [Google Scholar] [CrossRef]
  63. Allotey, J.; Fernandez, S.; Bonet, M.; Stallings, E.; Yap, M.; Kew, T.; Zhou, D.; Coomar, D.; Sheikh, J.; Lawson, H.; et al. Clinical Manifestations, Risk Factors, and Maternal and Perinatal Outcomes of Coronavirus Disease 2019 in Pregnancy: Living Systematic Review and Meta-Analysis. BMJ 2020, 370, m3320. [Google Scholar] [CrossRef]
  64. Adamson, G.D.; de Mouzon, J.; Chambers, G.M.; Zegers-Hochschild, F.; Mansour, R.; Ishihara, O.; Banker, M.; Dyer, S. International Committee for Monitoring Assisted Reproductive Technology: World Report on Assisted Reproductive Technology, 2011. Fertil. Steril. 2018, 110, 1067–1080. [Google Scholar] [CrossRef] [PubMed]
  65. Balachandren, N.; Davies, M.C.; Hall, J.A.; Stephenson, J.M.; David, A.L.; Barrett, G.; O’Neill, H.C.; Ploubidis, G.B.; Yasmin, E.; Mavrelos, D. SARS-CoV-2 Infection in the First Trimester and the Risk of Early Miscarriage: A UK Population-Based Prospective Cohort Study of 3041 Pregnancies Conceived during the Pandemic. Hum. Reprod. 2022, 37, 1126–1133. [Google Scholar] [CrossRef]
  66. Kotlyar, A.M.; Grechukhina, O.; Chen, A.; Popkhadze, S.; Grimshaw, A.; Tal, O.; Taylor, H.S.; Tal, R. Vertical Transmission of Coronavirus Disease 2019: A Systematic Review and Meta-Analysis. Am. J. Obstet. Gynecol. 2021, 224, 35–53.e3. [Google Scholar] [CrossRef] [PubMed]
  67. Setti, P.E.L.-; Cirillo, F.; Immediata, V.; Morenghi, E.; Canevisio, V.; Ronchetti, C.; Baggiani, A.; Albani, E.; Patrizio, P. First Trimester Pregnancy Outcomes in a Large IVF Center from the Lombardy County (Italy) during the Peak COVID-19 Pandemic. Sci. Rep. 2021, 11, 16529. [Google Scholar] [CrossRef] [PubMed]
  68. Zhou, H.; Zou, Y.; Guo, Y.; Lv, X.; Chen, J.; Guo, X.; Liu, Q. Effect of COVID-19 Inactivated Vaccine on Peripheral Blood Anti-Β2-GPI Antibody and Outcomes in Vitro Fertilization-Embryo Transplantation. Int. Immunopharmacol. 2023, 122, 110596. [Google Scholar] [CrossRef] [PubMed]
  69. Shi, W.; Wang, M.; Xue, X.; Li, N.; Chen, L.; Shi, J. Association between Time Interval from COVID-19 Vaccination to In Vitro Fertilization and Pregnancy Rate after Fresh Embryo Transfer. JAMA Netw. Open 2022, 5, e2236609. [Google Scholar] [CrossRef]
  70. Cao, M.; Wu, Y.; Lin, Y.; Xu, Z.; Liang, Z.; Huang, Q.; Li, S.; Liu, H.; An, C.; Luo, Y.; et al. Inactivated Covid-19 Vaccine Did Not Undermine Live Birth and Neonatal Outcomes of Women with Frozen-Thawed Embryo Transfer. Hum. Reprod. 2022, 37, 2942–2951. [Google Scholar] [CrossRef]
  71. Zauche, L.H.; Wallace, B.; Smoots, A.N.; Olson, C.K.; Oduyebo, T.; Kim, S.Y.; Petersen, E.E.; Ju, J.; Beauregard, J.; Wilcox, A.J.; et al. Receipt of mRNA Covid-19 Vaccines and Risk of Spontaneous Abortion. N. Engl. J. Med. 2021, 385, 1533–1535. [Google Scholar] [CrossRef]
  72. Wu, Y.; Cao, M.; Lin, Y.; Xu, Z.; Liang, Z.; Huang, Q.; Li, S.; Li, L.; Meng, Y.; An, C.; et al. Inactivated COVID-19 Vaccination Does Not Affect In Vitro Fertilization Outcomes in Women. Hum. Reprod. 2022, 37, 2054–2062. [Google Scholar] [CrossRef]
  73. Allahbadia, G. Will Procreation Ever Be The Same After COVID-19? J. Obstet. Gynaecol. India 2021, 71, 1–6. [Google Scholar] [CrossRef]
  74. Page, M.J.; McKenzie, J.E.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Shamseer, L.; Tetzlaff, J.M.; Akl, E.A.; Brennan, S.E.; et al. The PRISMA 2020 statement: An updated guideline for reporting systematic reviews. BMJ 2021, 372, n71. [Google Scholar] [CrossRef] [PubMed]
Diseases 12 00201 g001
Figure 1. PRISMA flow diagram.
Figure 1. PRISMA flow diagram.
Diseases 12 00201 g001
Diseases 12 00201 g002
Figure 2. Forest plot of studies of COVID-19 positive vs. COVID-19 negative for clinical pregnancy [38,39,40,42,44,45,47,48].
Figure 2. Forest plot of studies of COVID-19 positive vs. COVID-19 negative for clinical pregnancy [38,39,40,42,44,45,47,48].
Diseases 12 00201 g002
Diseases 12 00201 g003
Figure 3. Forest plot of included studies on clinical pregnancy rate for vaccinated vs. not vaccinated participants [51,52,53,54,55,56,57].
Figure 3. Forest plot of included studies on clinical pregnancy rate for vaccinated vs. not vaccinated participants [51,52,53,54,55,56,57].
Diseases 12 00201 g003
Diseases 12 00201 g004
Figure 4. Forest plot of studies of COVID-19 positive vs. COVID-19 negative for birth rates [39,42,45,47,48].
Figure 4. Forest plot of studies of COVID-19 positive vs. COVID-19 negative for birth rates [39,42,45,47,48].
Diseases 12 00201 g004
Diseases 12 00201 g005
Figure 5. Forest plot of included studies on birth rate for vaccinated vs. not vaccinated participants [55,56,57].
Figure 5. Forest plot of included studies on birth rate for vaccinated vs. not vaccinated participants [55,56,57].
Diseases 12 00201 g005
Diseases 12 00201 g006
Figure 6. Forest plot of studies of COVID-19 positive vs. COVID-19 negative for miscarriage rates [38,39,42,47,48].
Figure 6. Forest plot of studies of COVID-19 positive vs. COVID-19 negative for miscarriage rates [38,39,42,47,48].
Diseases 12 00201 g006
Diseases 12 00201 g007
Figure 7. Forest plot of included studies on miscarriage rate for vaccinated vs. not vaccinated participants [54,57].
Figure 7. Forest plot of included studies on miscarriage rate for vaccinated vs. not vaccinated participants [54,57].
Diseases 12 00201 g007
Diseases 12 00201 g008
Figure 8. Funnel plots of clinical pregnancy rate. (A) COVID-19 positive vs. negative participants, (B) vaccinated vs. unvaccinated participants.
Figure 8. Funnel plots of clinical pregnancy rate. (A) COVID-19 positive vs. negative participants, (B) vaccinated vs. unvaccinated participants.
Diseases 12 00201 g008
Diseases 12 00201 g009
Figure 9. Funnel plots of birth rate. (A) COVID-19 positive vs. negative participants, (B) vaccinated vs. unvaccinated participants.
Figure 9. Funnel plots of birth rate. (A) COVID-19 positive vs. negative participants, (B) vaccinated vs. unvaccinated participants.
Diseases 12 00201 g009
Table 1. Studies describing patients undergoing ART procedures with a COVID-19-positive history.
Table 1. Studies describing patients undergoing ART procedures with a COVID-19-positive history.
StudyStudy TypeCity, CountryPublication DateNo. COVID-19 Positive ParticipantsMean Age ± SDPregnancyBirthMiscarriage
Eckstein V et al. [38]cohort-studyGermany10 October 20231581 treatment cycles35.8  ±  4.1 (23.1–49.5)19/87 (21.84%)not published yet10/19 (52.63%)
Huri et al. [39]retro-prospective cohort studyFlorence, Italy25 April 2022749 219 (100%)165 (22.02%)98
Rageh et al. [40]observational studyManama, Bahrain; Kingdom of Saudi Arabia12 September 20238832.14 ± (4.773)32 (36.4%)
Engels Calvo et al.
[41]		multicenter, prospective, observational study78 Spanish centers12 April 20217439.674 (5.5%)
Rodríguez-Varela et al. [42]retrospective, multicentric, and double-arm studySpain, Lisbon and Rome21 December 2021638.66 39 (4.5%)-overall miscarriage rate
ESHRE COVID-19 Working Group et al. [43]retrospective, multicentric studies32 countries worldwide13 September 202110533.7 ± 6.1256710 (12.5%)
Huang J et al. [44]prospective cohort studyChina4 October 202325232.3 ± 5.083 (70.3%)
Epelboin et al. [45]prospective clinical studyFrance30 November 2021.1631.1 (±5.9) 16 (1.8%)No data
Ziert et al. [46]multicentric, prospective, observational studyGermany, Austria19 April 20226534.09 ± 5.126557/65 (87,69%)0/57 (0.0)
Dolgushina et al. [47]observational prospective studyRussia29 June 202313534 (31–37)39 (28.9%)30 (22.2%)31 (23.1%)
Banker et al. [48]retrospective cohort studyAhmedabad, India30 June 202260630.747.6% Fresh ET
68.7% Frozen ET		32.4% Fresh ET
46.3% Frozen ET		10% Fresh ET
6.73% Frozen ET
TOTAL 2096 562335188
SD—standard deviation; ET—embryo transfer.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Milostić-Srb, A.; Srb, N.; Talapko, J.; Meštrović, T.; Žiger, T.; Pačarić, S.; Fureš, R.; Makarović, V.; Škrlec, I. The Effect of COVID-19 and COVID-19 Vaccination on Assisted Human Reproduction Outcomes: A Systematic Review and Meta-Analysis. Diseases 2024, 12, 201. https://doi.org/10.3390/diseases12090201

AMA Style

Milostić-Srb A, Srb N, Talapko J, Meštrović T, Žiger T, Pačarić S, Fureš R, Makarović V, Škrlec I. The Effect of COVID-19 and COVID-19 Vaccination on Assisted Human Reproduction Outcomes: A Systematic Review and Meta-Analysis. Diseases. 2024; 12(9):201. https://doi.org/10.3390/diseases12090201

Chicago/Turabian Style

Milostić-Srb, Andrea, Nika Srb, Jasminka Talapko, Tomislav Meštrović, Tihomil Žiger, Stana Pačarić, Rajko Fureš, Vedrana Makarović, and Ivana Škrlec. 2024. "The Effect of COVID-19 and COVID-19 Vaccination on Assisted Human Reproduction Outcomes: A Systematic Review and Meta-Analysis" Diseases 12, no. 9: 201. https://doi.org/10.3390/diseases12090201

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop