key: cord-1045707-vzavgkgu
authors: Collins, Alexander B.; Zhao, Lei; Zhu, Ziwen; Givens, Nathan T.; Bai, Qian; Wakefield, Mark R.; Fang, Yujiang
title: Impact of COVID-19 on male fertility
date: 2022-01-08
journal: Urology
DOI: 10.1016/j.urology.2021.12.025
sha: 6c5d4a34fd420f946a5144daf14a5b9cb2c3cb03
doc_id: 1045707
cord_uid: vzavgkgu

COVID-19, the clinical condition caused by the SARS-CoV-2 virus, has been associated with massive cytokine storm and damage to multiple organ systems. Although evidence for the detection of SARS-CoV-2 virus in the testis remains scarce, testicular damage and dysregulation of gonadotropins associated with inflammation has been reported. Additionally, as a result of the rapidly evolving pandemic, frequently updated medical interventions and public policies leading to delays of care can play a role in fertility. This narrative review aims to summarize the current literature on how COVID-19 may influence male fertility.

Since December 2019, much of the world's news, economy, and focus has been on the [1, 2] . COVID-19 is now understood to be the clinical disease caused by SARS-CoV-2. The SARS-CoV-2 virus originated in Wuhan, China. Throughout history, multiple zoonotic coronavirus pathogens have emerged and coronaviruses have been shown to adapt to different animal hosts [3] . SARS-CoV-2 shares over 96% of its genome with the bat coronavirus BatCoV RaTg13, supporting the theory that SARS-CoV-2 evolved from a bat coronavirus with an unknown intermediate host [4] .

Clinically, COVID-19 presents with a persistent fever, cough, pneumonia, and loss of smell and taste. There has also been pathological evidence of massive intravascular micro-thrombotic phenomenon in multiple organs, including the lungs, heart, kidneys, brain, and testes. The interaction of the SARS-CoV-2 viral Spike protein and ACE2 on cells co-expressing ACE2 and the cellular transmembrane protease serine 2 (TMPRSS2) has been identified as the mechanism of cellular entry for the SARS-CoV-2 virus. Although not all tissues that express ACE2 are susceptible to SARS-CoV-2 infection, organ involvement has been found to be positively correlated with ACE2 expression [5] . Since the testes express ACE2 receptors, investigations into the possible influences of COVID-19 on male fertility are being actively explored [6] .

The hypothalamic-pituitary-gonadal axis (HPG) endocrinologically links the brain and testis. This link is achieved through the production of gonadotropins and testosterone and the HPG feedback loop. Precise regulation of this axis is required for optimal sex hormone production and fertility. COVID-19's effects on the hypothalamic-pituitary-gonadal axis require further evaluation, however, abnormal levels of gonadotropins have been identified in COVID-19 patients [7] .

The pandemic has dramatically impacted our way of life and our medical systems and remains an ongoing and evolving public health concern. Staying current with new literature is challenging due to the high volume of studies being published. This narrative review aims to summarize the current information available investigating the relationship of COVID-19 and male infertility. We explore this relationship as it relates to hormonal regulation and the hypothalamic pituitary axis (HPG), systemic inflammation, the potential of direct testicular infection, semen parameters, interactions of medical interventions for COVID-19, and access to urologic care during the pandemic.

An adequate hypothalamic-pituitary gonadal axis is crucial for maintaining normal testosterone production. Low testosterone secondary to hypergonadotropic hypogonadism, or primary hypogonadism, can be congenital as in Klinefelter Syndrome, or caused by environmental or biological disruptions to gonadal function. Low testosterone secondary to hypogonadotropic hypogonadism can lead to a secondary testicular failure. Causes for hypogonadotropic hypogonadism can be congenital, in cases such as Kallmann syndrome, or acquired secondarily from numerous causes including medication, pituitary lesions, infection, or inflammation [8] . Fertility issues associated with acquired hypogonadotropic hypogonadism can generally be corrected by fixing the underlying issue.

A selection of studies has produced data to support that COVID-19 can impact testicular hormone production. When reviewing these studies, it is important to recall that physiological stressors such as illness are associated with fluctuations in baseline hormone levels. A study by Ma et al. compared 119 reproductive aged males with SARS-CoV-2 to 273 age matched controls. They found high luteinizing hormone (LH) levels and lower testosterone to LH ratios in SARS-CoV-2 patients. The authors suggest these findings are associated with the systemic inflammation present in the evaluated patients. These abnormalities could indicate disruption in sex hormone secretion associated with COVID-19 disease [9] . Another study compared 89 COVID-19 patients to 30 patients suffering from other respiratory infections and 143 healthy controls. The COVID-19 patients were found to have significantly lower testosterone, higher LH and prolactin, and equivalent FSH when compared to both sets of controls [10] . Rastrelli et al. found that in a group of 31 patients, the 12.9% of patients who died or had severe COVID-19 exhibited lower total and free testosterone and elevated LH when compared to more moderate cases [11] .

Hypothalamic pathology associated with SARS-CoV-2 infection in the brain is still being studied. SARS-CoV-2 has been shown to cross the blood brain barrier [7] . Once past the barrier, it infects ACE2 expressing cells, leading to neuroinflammation. This inflammation can disrupt normal physiologic functions such as temperature regulation and hormone balance [12] [13] [14] .

Testicular pathology associated with hyperthermia has been established previously. Fevers are the body's response to systemic inflammation, and over 80% of COVID-19 patients are reported to develop a fever, which tends to be prolonged with an average duration of 10 days [15] . It has been reported that a fever of > 39C for over three days can lead to significant reduction in semen concentration and motility [16] . While interpreting these findings, it is worth noting that the standardized reported definitions of fever for COVID-19 patients has been poor [17] .1/7/2022 10:55:00 PM Few studies have attempted to link circulating gonadotropin levels to neuropathology in COVID -19 patients. Neuroimaging findings from a single patient study revealed a hyperintense signaling suggestive of hypothalamic lesions as well as an enlarged pituitary gland [13] . While far from conclusive, these findings suggest that hypothalamic involvement in COVID-19 patients could alter regulation of gonadotropin release leading to subsequent reduction in testosterone levels [7] .

Although unlikely to lead to permanent effects on fertility, the use of glucocorticoids for the management of COVID-19 can impact fertility. Dexamethasone is one of the only medications proven to reduce mortality in COVID-19 patients and is now routinely administered [18] . A precisely balanced concentration of glucocorticoids is required to maintain gonadal function. Exogenous glucocorticoid use can disrupt the hypothalamo-pituitary-gonadal axis, which is well known to lead to temporary effects on fertility [19] .

The blood testes barrier provides privileged immunity to the testicles. However, this barrier is imperfect. The presence of systemic and local inflammation can increase this permeability and allow invasion of immune cells. SARS-CoV-2 is a cytopathic virus that creates a proinflammatory state and can lead to cell pryoptosis. Pryoptosis is an inflammatory form of programmed cell death that leads to the release of potent pro-inflammatory cytokines.

Inflammatory cytokines lead to immune cell recruitment that can assist in disease clearance and further increase the production of inflammatory cytokines; in some cases, this can create a cytokine storm, leading to uncontrolled systemic inflammation that impacts multiple organ systems [20] .

Leukocytospermia often accompanies a systemic increase in IL-6, MCP-1, and TNF-α, and can be associated with systemic inflammation or viral and bacterial infections [7] . Several studies have reported an increase in inflammatory markers, including IL-6, IL-8 and TNF-α, have been identified in semen samples from patients recovering or suffering from COVID-19 compared to controls [21] [22] [23] . Additionally, CD3+, CD68+ and IgG have been identified in the seminiferous tubules of COVID-19 patients [22] . Inflammatory states, as well as states of low oxygen tension, are associated with oxidative stress and production of free radicals. Both inflammatory cytokines and oxidative stress have been found to damage cellular components of testes [24] . Oxidative stress leads to Leydig cell damage, thus disrupting capacity for testosterone production and germinal epithelial damage, which hinders spermatogenesis [25] [7] .

Oxidative stress has been proposed as a potential mechanism for the testicular damage found in COVID-19 patients. However, few studies have produced data to support this claim. Moghimi et al. evaluated the production of reactive oxygen species (ROS) and glutathione disulfide (GSH) concentration in an autopsy study of six COVID-19 patients vs. six controls. They revealed a statistically significant increase in ROS and decrease of GSH in COVID-19 patients when compared to controls. These findings indicate an increase in oxidative stress and a corresponding decrease in cellular defense to oxidative stress in patients suffering from COVID-19 [26] .

Several known single stranded RNA viruses, including other coronavirus variants like HIV, Mumps, and Zika, are known to cause orchitis and can be found in semen [27] . There is conflicting evidence regarding the ability of SARS-CoV-2 to directly infect the testis. The mechanism of proposed entry of SARS-CoV-2 is through the binding of the SARS-CoV-2 spike protein (S-protein) viral ligand and host ACE2 receptor. The S protein is then cleaved by a serine protease co-receptor TMPRSS2, leading to membrane fusion between the virus and cell [28] . The testes express a high level of ACE2 receptors on spermatogonia, seminiferous tubules, Sertoli and Leydig cells. The endogenous function of this receptor is not yet fully understood [5] .

ACE2 has a regulatory role in the male reproductive system, namely in the modulation of steroidogenesis. Additionally, ACE2 receptors are thought to play a role in fertility. This association is based on a study that observed lower levels of ACE2 in infertile men with severe spermatogenesis impairment when compared with fertile subjects [29] . Men have higher levels of TMPRSS2 expression than women. This is likely due to an androgen response element being a transcriptional promotor for TMPRSS2. It is thought that co-expression of ACE2 and TMPRSS2 are required for viral entry into cells [28] .

There is discrepancy regarding the levels of ACE2 and TMPRSS2 co-expression on individual cells. Stanley et al. found that levels of ACE2 and TMPRSS2 co-expression in testicular cells occurs less than 0.05% of the time [30] . These findings are supported by a study by Pan et al. showing minimal co-expression in individuals cells [31] . Lack of co-expression would indicate minimal risk of direct infection or an alternate mechanism of entry. Levels of ACE2 mRNA and TMPRSS2 in the testis have been also examined in an autopsy study. The study examining five COVID-19 patients found that all patients had elevated levels of ACE2 and TMPRSS2 expressed in seminiferous tubules compared to controls. Immunohistochemistry showed increased expression and RT-qPCR was notable for increased mRNA levels of ACE2 and TMPRSS2. Of note, this study did not attempt to prove co-expression of ACE2 and TMPRSS2 on an individual cell level [32] . Increased expression supports the likelihood of direct testicular invasion and damage by SARS-CoV-2. However, it remains unclear whether this increased expression of ACE2 and TMPRSS2 is actually co-expression. Additionally, increased expression of ACE2 could be secondary to underlying comorbidities such as hypertension, cancer, and smoking, rather than COVID-19 infection [33] .

Several autopsy studies have attempted to identify the presence of SARS-CoV-2 virus in the testis. Only a few of these studies have successfully reported the presence of SARS-CoV-2 viral particles in the testes. These studies have small sample sizes and reports of errors in tissue sampling. Errors in sampling, including the sampling of vascular structures, has drawn questions to the validity of viral particle identification in the testis. However, the majority of studies support an association between COVID-19 and a loss of testicular architecture via changes to seminiferous tubules, Leydig cells, and germ cells. Contrary to initial theories, the data from these studies suggest that COVID-19 indirectly, rather than directly, affects testicular function [34] .

Yang et al., studied the testes of 12 men who died from complications associated with COVID-19. RT-PCR identified SARS-CoV-2 RNA in one patient's testes, but electron microscopy did not confirm the presence of the SARS-CoV-2 virus in any of the 12 patients.

Later discussions have suggested that this sample was fibrovascular tissue and that the viral RNA was present in sampled blood opposed to testicular tissue [35] . All 12 patients possessed a lower number of Leydig cells when compared to controls. Additionally, all COVID-19 patients showed evidence of seminiferous tubule cellular injury and a diminished population with mild lymphocytic inflammation [36] . The authors postulated that damage to seminiferous tubules and Leydig cells may be secondary to viral membrane proteins such as the Spike protein.

In another autopsy study by Ma et al., testicles from five COVID-19 patients were studied compared to controls. All five patients were found to have degenerated germ cells sloughed off into the seminiferous tubules. In four out of five patients, almost all the germ cells lining the seminiferous tubules were lost. There was also a corresponding loss of cells expressing the germ cell marker DDX4. These findings were in direct contrast to three controls studied. The number of Sertoli cells appear consistent between control and COVID-19 patients studied [37] . There have been few reports of testicular pain associated with COVID-19. One study looked at 34 men with mild to moderate COVID-19. Six men in the study complained of scrotal discomfort and tenderness. No further exam or testing such as ultrasound was completed to confirm or rule out orchitis [31] . Another study from Jordan followed 253 male patients with COVID-19 through their hospital stay and 21-day recovery period to observe for signs and symptoms of orchitis. Each patient was evaluated every two days by a urologist, but none of the patients were found to have signs or symptoms of orchitis. It was noted that most of the patients were asymptomatic or had mild-to-moderate symptoms. It remains unclear if orchitis would develop with higher viral loads, or at a later course in time [39] . In a retrospective cohort study by Liao et al., 142 patients who tested positive for COVID-19 underwent scrotal ultrasound at time of diagnosis. 22.5% of these patients were found to have increased tunica thickness and increased vascular flow consistent with orchitis, epididymitis, or epididymo-orchitis [40] .

Nearly 30 viruses have been identified in human semen [41] . Of these, the most notable are Most semen studies have involved recovering patients and have found that after one month, recovering patients did not have detectable levels of SARS-CoV-2 in their semen [31] was retested and found to be negative [21] . In studies showing viral RNA in semen, the results may be explained by sampling error or urinary or accessory sex organ involvement instead of direct testicular involvement. It is also important to recognize that even if COVID-19 is transmissible through semen, it is unlikely to provide a significant source of infection in comparison to respiratory droplets. However, consideration should be made for those attempting to become pregnant or those donating or preserving sperm [51] .

Delayed treatment across multiple pathologies has been seen during the time of the pandemic, with people expressing fear of hospitals and avoiding medical care even in emergencies. An estimated 40.9% of surveyed US adults reported avoiding medical care, with 12% avoiding urgent or emergency care, and 31.5% avoiding routine care [52] . The delayed treatment of testicular pathology, in cases of testicular cancer or sexually transmitted infections, may impact male fertility. The concept of delayed treatment during the era of COVID-19 can be expanded to include fertility treatments.

In March of 2020 the American Society for Reproductive Medicine (ASRM) recommended the suspension of non-urgent gamete cryopreservation, new fertility treatment, and elective non urgent diagnostic procedures. Sperm banking was deemed a low priority except for patients undergoing oncological treatment [51] . At that time, concerns were raised for those suffering from non-oncological conditions that could benefit from elective fertility treatment or gamete cryopreservation. Conditions discussed included patients with hypogonadotropic hypogonadism requiring long term treatment, those with infertility thought to be associated with varicocele, and patients suffering from systemic inflammatory or autoimmune disease requiring treatments that maybe gonadotoxic [53] . At the time of authorship, restrictions for fertility services have been lifted. It is unclear what effect, if any, these temporary restrictions had on male fertility. However, being aware of previous delays in treatment may aid providers in assessing fertility concerns.

Remdesivir is currently the only drug that is officially FDA approved for the treatment of COVID-19. There are seven drugs approved by the FDA under emergency use authorizations (EUA). These medications include Tocilizumab, Sotrovimab, Bamlanivimab and Etesevimab, Regen-COV (Casirivimab and Imdevimab), Baricitinib (Olumiant) and Propofol-Lipuro 1%. To our knowledge, there have been no conclusive studies to suggest that these drugs affect male fertility [54, 55] .

Many non-FDA approved treatments such as ribavirin, ivermectin, chloroquine and a myriad of antivirals have been used in COVID-19 patients. In rat studies, ribavirin was found to be gonadotoxic at all doses administered for a period of 105 days [56] . Some studies have suggested that prolonged use of chloroquine may impair sperm quality [57] . In general, effects of antiviral medications on male fertility require further studies [58] . Throughout 2021, ivermectin, an antiparasitic medication, gained traction across social media platforms as a potential treatment and prophylaxis for COVID-19. Claims of associations between ivermectin and male infertility also spread through social media [59] . These claims stemmed from the misinterpretation of a 2011 paper by Indonoji et. al studying sperm parameters in 37 patients with onchocerciasis treated with ivermectin [60] . Although the study identified a decrease in sperm parameters including sperm motility and count, it possessed serious limitations, including a lack of control group. Some other studies have shown ivermectin to be gonadotoxic in animal models [61] , but there have been no definitive findings to suggest that ivermectin is associated with male infertility in humans. Attention should be brought to the consequences that future medications used for COVID-19 treatment may have on fertility.

COVID-19 is responsible for mobilizing a collaborative effort to create a novel vaccine in record time. Prior to the COVID-19 vaccine, the fastest vaccine approved was the vaccine for the mumps virus in the 1960s, which took four years to develop. The COVID-19 vaccine was conceived, created, and approved for emergency use by the FDA in under one year. In August 2021, the Pfizer vaccine received full approval by the FDA.

Despite the pandemic ravaging the world, there is still vaccine hesitancy. Potential fertility implications after receiving a COVID-19 vaccine are a source of anxiety for many patients, as reproductive toxicity was not evaluated in clinical trials [62] . A vaccine that uses the actual virus could theoretically also directly affect the testes. However, the Pfizer and Moderna vaccines are only mRNA vaccines, which stimulate the recipient's immune system to produce the SARS-CoV-2 spike protein, and thus does not bind to receptors via the same mechanism that SARS-COV-2 virus does [63] . The Johnson & Johnson vaccine utilizes viral vector technology, combining SARS-CoV-2 spike gene with a weakened adenovirus. This leads to expression of the spike protein on cellular surfaces for immune cell interaction [64] . Although unlikely, there is a theoretical risk for expressed spike protein interaction in the testis.

A single centered prospective study out of the University of Miami investigated the effects of COVID-19 vaccination on semen parameters. A sample of 45 healthy male volunteers provided semen samples before the first vaccination dose and again, 70 days after the second dose administration. Semen samples were analyzed for the following parameters: semen volume, sperm concentration, sperm motility and total motile sperm count. No significant decreases in any of the above parameters were found [65] . There is a potential for a temporary decrease in sperm production post-vaccine, related to vaccine induced fevering. A fever can temporarily impact sperm count, and in the Pfizer vaccine clinical trials about 16% of men experienced a fever after the second vaccine dose. However, this brief impact on sperm after vaccination is likely of much less magnitude than any potential effects of having the full clinical syndrome of COVID-19 [63] .

Although there is limited data on the impact of the COVID-19 vaccines on male fertility, the Society for Male Reproduction and Urology (SMRU) and the Society for the Study of Male Reproduction (SSMR) have made two recommendations regarding vaccinations. Firstly, the COVID-19 vaccine should not be withheld from men desiring fertility who meet criteria for vaccination. Secondly, the COVID-19 vaccines should be offered to all men desiring fertility and all men not desiring fertility when they meet criteria for vaccination.

It is important to note that the data that has been presented on COVID-19 and infertility has surfaced within the short time frame since the virus was recognized in 2019. Sample sizes are generally small and many clinical studies are performed at single sites, making it unwise to draw definitive conclusions from their findings. This is an evolving virus and will continue to require dynamic research to truly understand it's lasting impacts on the male reproductive tract and fertility.

While much is left to be studied, COVID-19 does appear to impact male fertility, at least temporarily. From review of the current literature, it has become evident that COVID-19 can lead to a reduction in testosterone production and a state of temporary hypogonadism. It was originally hypothesized that since the testes are prone to direct infection by the SARS-CoV-2 virus due to their ACE2 expression, male fertility is adversely affected. Although controversy remains, the data supports that a reduction in testosterone production is more likely associated with indirect testicular damage due to systemic or local inflammation. Additionally, with the rapidly evolving pandemic, it is important to maintain vigilance for potential interventions and delays of care that can lead to lasting effects on fertility. Moving forward, further studies are required to investigate the potential long term fertility effects of the COVID-19 disease, treatments, and vaccines.

The authors declare no conflicts of interest.

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