Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Unable to obtain approval
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Study rationale
Male infertility results from impaired sperm function, and account for half of all infertility. Fertility services have been reported to cost £325M annually in the UK(4) (REF). Testosterone deficiency is one of the most common hormonal problems affecting men, leading to osteoporosis, type 2 diabetes, obesity and depression(5).
Concerns have been raised about the potential effects of COVID-19 on male reproductive dysfunction (male infertility and testosterone deficiency). A recent study has suggested that COVID-19 may enter human cells by binding to receptors (special gates on cells that recognise a specific molecule) for angiotensin converting enzyme 2 (ACE2)(6) . ACE2 receptors are found at very high levels in the testes. Within the testes, ACE2 is found on developing sperm, the 'nurse cells' that help the sperm grow (Sertoli cells), and also on Leydig cells which are needed to make the male sex hormone testosterone. In summary, this evidence suggests that there is a plausible link why COVID-19 would cause male infertility and testosterone deficiency.
All fertility treatment in the UK is regulated by the Human Fertility and Embryology Authority (HFEA). The HFEA has prohibited on all non-cancer fertility treatment in the UK between April 15th and May 12th 2020 due to the COVID-19 epidemic. It is important to rapidly screen and report whether COVID-19 has any obvious effects in causing male infertility and testosterone deficiency. It must be noted that a recent study(1) reported that COVID-19 is not spread by human semen and therefore, semen processing should not risk staff to COVID-19 infection.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Case group |
|
| |
| Control Group |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Exposure: Covid-19 infection | Other | Previous history of COVID-19 infection. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Semen parameters | Sperm concentration (x10^6/ml) between case and control group. | 3 visits (up to 75 days apart) |
| Sperm Parameters | Sperm Motility (%) between case and control group. | 3 visits (up to 75 days apart) |
| Sperm Parameters | Sperm normal morphology (%) between case and control group. | 3 visits (up to 75 days apart) |
| Hormones measurement | Testosterone (nmol/L) between case and control group. | 3 visits (up to 75 days apart) |
| Hormones measurement | Follicle Stimulating Hormone(IU/L) between case and control group. | 3 visits (up to 75 days apart) |
| Hormones measurement | Luteinising hormone(IU/L) between case and control group. | 3 visits (up to 75 days apart) |
| Measure | Description | Time Frame |
|---|---|---|
| Seminal Reactive oxygen species | Compare seminal reactive oxidative species (RLU/second/10^6sperm) between case and control group. | 3 visits (up to 75 days apart) |
| Sperm DNA fragmentation rate |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Male
We will be recruiting participants by the following means:
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Channa Jayasena | London | Outside U.S./Canada | W12 0HS | United Kingdom |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 32283711 | Background | 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 Apr 9;9(4):920. doi: 10.3390/cells9040920. | |
| 32313110 | Background | Wang S, Zhou X, Zhang T, Wang Z. The need for urogenital tract monitoring in COVID-19. Nat Rev Urol. 2020 Jun;17(6):314-315. doi: 10.1038/s41585-020-0319-7. |
| Label | URL |
|---|---|
| The state of the fertility sector 2017-2018 | View source |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D007248 | Infertility, Male |
| D007246 | Infertility |
| D007006 | Hypogonadism |
| ID | Term |
|---|---|
| D005832 | Genital Diseases, Male |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |
Not provided
Not provided
Not provided
Not provided
Not provided
Sperm DNA fragmentation testing only. No sequencing of human genomic DNA will take place.
Compare Sperm DNA fragmentation rate (%) between case and control group.
| 3 visits (up to 75 days apart) |
| 28318076 | Background | Hackett G, Kirby M, Edwards D, Jones TH, Rees J, Muneer A. UK policy statements on testosterone deficiency. Int J Clin Pract. 2017 Mar;71(3-4):e12901. doi: 10.1111/ijcp.12901. Epub 2017 Mar 20. |
| 32007145 | Background | Lu R, Zhao X, Li J, Niu P, Yang B, Wu H, Wang W, Song H, Huang B, Zhu N, Bi Y, Ma X, Zhan F, Wang L, Hu T, Zhou H, Hu Z, Zhou W, Zhao L, Chen J, Meng Y, Wang J, Lin Y, Yuan J, Xie Z, Ma J, Liu WJ, Wang D, Xu W, Holmes EC, Gao GF, Wu G, Chen W, Shi W, Tan W. Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. Lancet. 2020 Feb 22;395(10224):565-574. doi: 10.1016/S0140-6736(20)30251-8. Epub 2020 Jan 30. |
| Reference 1 | View source |
| D006058 | Gonadal Disorders |
| D004700 | Endocrine System Diseases |