The impact of heavy metals exposure on male fertility: a scoping review of human studies
-
Carlo Giulioni
, Federico Falsetti
, Valentina Maurizi , Francesco Del Giudice , Felice Crocetto , Ciro Imbimbo and Angelo Cafarelli
Abstract
Introduction
Male infertility is a critical global health issue, with environmental and occupational exposure to heavy metals, such as lead (Pb), cadmium (Cd), mercury (Hg), and arsenic (As), impacting male reproductive health. This scoping review aims to evaluate the effects of heavy metal exposure on semen parameters.
Content
This study adhered to the 2020 PRISMA framework. A broad literature search was performed on January 2025, using Embase, PUBMED, and Scopus. A comprehensive literature search was performed using PubMed, Embase, and Scopus on January 12, 2025, using a combination of Medical Subject terms and keywords.
Summary
Of the 1,709 identified studies, 21 met the inclusion criteria and were analyzed. Findings indicate that lead exposure negatively impacts sperm concentration, motility, and morphology, primarily through oxidative stress and enzymatic inhibition. Cadmium disrupts the blood-testis barrier and acrosomal function, leading to sperm abnormalities. Arsenic exposure is linked to oxidative stress, apoptosis, and impaired sperm motility.
Outlook
The cumulative evidence supports a strong association between heavy metal exposure and male infertility. This review underscores the need for stricter occupational safety regulations and environmental policies to mitigate heavy metal exposure.
Acknowledgments
CG: project development, manuscript writing, and data collection, FF: project development. VM: Data collection and analysis. FDG: Data collection. FC: Manuscript editing. CI: Manuscript editing. AC: Project development and manuscript editing.
-
Research ethics: Not applicable.
-
Informed consent: Not applicable.
-
Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
-
Use of Large Language Models, AI and Machine Learning Tools: None declared.
-
Conflict of interest: Authors state no conflict of interest.
-
Research funding: Not applicable.
-
Data availability: Not applicable.
References
1. Agarwal, A, Farkouh, A, Saleh, R, Abdel-Meguid Hamoda, TA, Harraz, AM, Kavoussi, P, et al.. Controversy and consensus on indications for sperm DNA fragmentation testing in male infertility: a global survey, current guidelines, and expert recommendations. World J Mens Health 2023;41:575–602. https://doi.org/10.5534/wjmh.220282.Search in Google Scholar PubMed PubMed Central
2. Babakhanzadeh, E, Nazari, M, Ghasemifar, S, Khodadadian, A. Some of the factors involved in male infertility: a prospective review. Int J Gen Med 2020;13:29–41. https://doi.org/10.2147/IJGM.S241099.Search in Google Scholar PubMed PubMed Central
3. Shah, R, Rambhatla, A, Atmoko, W, Martinez, M, Ziouziou, I, Kothari, P, et al.. Global practice patterns in the evaluation of non-obstructive azoospermia: results of a world-wide survey and expert recommendations. World J Mens Health 2024;42:727–48. https://doi.org/10.5534/wjmh.230333.Search in Google Scholar PubMed PubMed Central
4. Rambhatla, A, Shah, R, Ziouziou, I, Kothari, P, Salvio, G, Gul, M, et al.. Global practice patterns and variations in the medical and surgical management of non-obstructive azoospermia: results of a world-wide survey, guidelines and expert recommendations. World J Mens Health 2025;43:92–122. https://doi.org/10.5534/wjmh.230339.Search in Google Scholar PubMed PubMed Central
5. Cannarella, R, Shah, R, Ko, E, Kavoussi, P, Rambhatla, A, Hamoda, TAA, et al.. Effects of varicocele repair on testicular endocrine function: a systematic review and meta-analysis. World J Mens Health 2024. https://doi.org/10.5534/wjmh.240109.Search in Google Scholar PubMed
6. Barone, B, Finati, M, Cinelli, F, Fanelli, A, Del Giudice, F, De Berardinis, E, et al.. Bladder cancer and risk factors: data from a multi-institutional long-term analysis on cardiovascular disease and cancer incidence. J Pers Med 2023;13:512. https://doi.org/10.3390/jpm13030512.Search in Google Scholar PubMed PubMed Central
7. Giulioni, C, Phuoc, NHV, Cayan, S. Ex vivo microscopic testicular sperm extraction at the time of radical orchiectomy in men with nonobstructive azoospermia (NOA): a scoping review. Asian J Androl 2024. https://doi.org/10.4103/aja202387.Search in Google Scholar PubMed PubMed Central
8. Giulioni, C, Maurizi, V, Scarcella, S, Di Biase, M, Iacovelli, V, Galosi, AB, et al.. Do environmental and occupational exposure to pyrethroids and organophosphates affect human semen parameters? Results of a systematic review and meta-analysis. Andrologia 2021;53:e14215. https://doi.org/10.1111/and.14215.Search in Google Scholar PubMed
9. Giulioni, C, Maurizi, V, Castellani, D, Scarcella, S, Skrami, E, Balercia, G, et al.. The environmental and occupational influence of pesticides on male fertility: a systematic review of human studies. Andrology 2022;10:1250–71. https://doi.org/10.1111/andr.13228.Search in Google Scholar PubMed PubMed Central
10. Ma, Y, He, X, Qi, K, Wang, T, Qi, Y, Cui, L, et al.. Effects of environmental contaminants on fertility and reproductive health. J Environ Sci 2019;77:210–17. https://doi.org/10.1016/j.jes.2018.07.015.Search in Google Scholar PubMed
11. Crocetto, F, Risolo, R, Colapietro, R, Bellavita, R, Barone, B, Ballini, A, et al.. Heavy metal pollution and male fertility: an overview on adverse biological effects and socio-economic implications. Endocr Metab Immune Disord Drug Targets 2023;23:129–46. https://doi.org/10.2174/1871530322666220627141651.Search in Google Scholar PubMed
12. Giulioni, C, Maurizi, V, De Stefano, V, Polisini, G, Teoh, JY, Milanese, G, et al.. The influence of lead exposure on male semen parameters: a systematic review and meta-analysis. Reprod Toxicol 2023;118:108387. https://doi.org/10.1016/j.reprotox.2023.108387.Search in Google Scholar PubMed
13. Morán-Martínez, J, Carranza-Rosales, P, Morales-Vallarta, M, A Heredia-Rojas, J, Bassol-Mayagoitia, S, Denys Betancourt-Martínez, N, et al.. Chronic environmental exposure to lead affects semen quality in a Mexican men population. Iran J Reprod Med 2013;11:267–74.Search in Google Scholar
14. Xu, DX, Shen, HM, Zhu, QX, Chua, L, Wang, QN, Chia, SE, et al.. The associations among semen quality, oxidative DNA damage in human spermatozoa and concentrations of cadmium, lead and selenium in seminal plasma. Mutat Res 2003;534:155–63. https://doi.org/10.1016/s1383-5718(02)00274-7.Search in Google Scholar PubMed
15. Hernández-Ochoa, I, García-Vargas, G, López-Carrillo, L, Rubio-Andrade, M, Morán-Martínez, J, Cebrián, ME, et al.. Low lead environmental exposure alters semen quality and sperm chromatin condensation in northern Mexico. Reprod Toxicol 2005;20:221–8. https://doi.org/10.1016/j.reprotox.2005.01.007.Search in Google Scholar PubMed
16. Telisman, S, Colak, B, Pizent, A, Jurasović, J, Cvitković, P. Reproductive toxicity of low-level lead exposure in men. Environ Res 2007;105:256–66. https://doi.org/10.1016/j.envres.2007.05.011.Search in Google Scholar PubMed
17. Telisman, S, Cvitković, P, Jurasović, J, Pizent, A, Gavella, M, Rocić, B. Semen quality and reproductive endocrine function in relation to biomarkers of lead, cadmium, zinc, and copper in men. Environ Health Perspect 2000;108:45–53. https://doi.org/10.1289/ehp.0010845.Search in Google Scholar PubMed PubMed Central
18. Mahmoud, A, Kiss, P, Vanhoorne, M, De Bacquer, D, Comhaire, F. Is inhibin B involved in the toxic effect of lead on male reproduction? Int J Androl 2005;28:150–5. https://doi.org/10.1111/j.1365-2605.2005.00524.x.Search in Google Scholar PubMed
19. Bonde, JP, Joffe, M, Apostoli, P, Dale, A, Kiss, P, Spano, M, et al.. Sperm count and chromatin structure in men exposed to inorganic lead: lowest adverse effect levels. Occup Environ Med 2002;59:234–42. https://doi.org/10.1136/oem.59.4.234.Search in Google Scholar PubMed PubMed Central
20. Kasperczyk, A, Kasperczyk, S, Horak, S, Ostałowska, A, Grucka-Mamczar, E, Romuk, E, et al.. Assessment of semen function and lipid peroxidation among lead exposed men. Toxicol Appl Pharmacol 2008;228:378–84. https://doi.org/10.1016/j.taap.2007.12.024.Search in Google Scholar PubMed
21. Eibensteiner, L, Del Carpio Sanz, A, Frumkin, H, Gonzales, C, Gonzales, GF. Lead exposure and semen quality among traffic police in Arequipa, Peru. Int J Occup Environ Health 2005;11:161–6. https://doi.org/10.1179/oeh.2005.11.2.161.Search in Google Scholar PubMed
22. Jurasović, J, Cvitković, P, Pizent, A, Colak, B, Telisman, S. Semen quality and reproductive endocrine function with regard to blood cadmium in Croatian male subjects. Biometals 2004;17:735–43. https://doi.org/10.1007/s10534-004-1689-7.Search in Google Scholar PubMed
23. Wang, YX, Wang, P, Feng, W, Liu, C, Yang, P, Chen, YJ, et al.. Relationships between seminal plasma metals/metalloids and semen quality, sperm apoptosis and DNA integrity. Environ Pollut 2017;224:224–34. https://doi.org/10.1016/j.envpol.2017.01.083.Search in Google Scholar PubMed
24. Pant, N, Kumar, G, Upadhyay, AD, Patel, DK, Gupta, YK, Chaturvedi, PK. Reproductive toxicity of lead, cadmium, and phthalate exposure in men. Environ Sci Pollut Res Int 2014;21:11066–74. https://doi.org/10.1007/s11356-014-2986-5.Search in Google Scholar PubMed
25. Jeng, HA, Huang, YL, Pan, CH, Diawara, N. Role of low exposure to metals as male reproductive toxicants. Int J Environ Health Res 2015;25:405–17. https://doi.org/10.1080/09603123.2014.958137.Search in Google Scholar PubMed PubMed Central
26. Choy, CM, Yeung, QS, Briton-Jones, CM, Cheung, CK, Lam, CW, Haines, CJ. Relationship between semen parameters and mercury concentrations in blood and in seminal fluid from subfertile males in Hong Kong. Fertil Steril 2002;78:426–8. https://doi.org/10.1016/s0015-0282(02)03232-6.Search in Google Scholar PubMed
27. Leung, TY, Choy, CM, Yim, SF, Lam, CW, Haines, CJ. Whole blood mercury concentrations in sub-fertile men in Hong Kong. Aust N Z J Obstet Gynaecol 2001;41:75–7. https://doi.org/10.1111/j.1479-828x.2001.tb01298.x.Search in Google Scholar PubMed
28. Rignell-Hydbom, A, Axmon, A, Lundh, T, Jönsson, BA, Tiido, T, Spano, M. Dietary exposure to methyl mercury and PCB and the associations with semen parameters among Swedish fishermen. Environ Health 2007;6:14. https://doi.org/10.1186/1476-069X-6-14.Search in Google Scholar PubMed PubMed Central
29. Mocevic, E, Specht, IO, Marott, JL, Giwercman, A, Jönsson, BA, Toft, G, et al.. Environmental mercury exposure, semen quality and reproductive hormones in Greenlandic Inuit and European men: a cross-sectional study. Asian J Androl 2013;15:97–104. https://doi.org/10.1038/aja.2012.121.Search in Google Scholar PubMed PubMed Central
30. Zeng, Q, Feng, W, Zhou, B, Wang, YX, He, XS, Yang, P, et al.. Urinary metal concentrations in relation to semen quality: a cross-sectional study in China. Environ Sci Technol 2015;49:5052–9. https://doi.org/10.1021/es5053478.Search in Google Scholar PubMed
31. Shen, H, Xu, W, Zhang, J, Chen, M, Martin, FL, Xia, Y, et al.. Urinary metabolic biomarkers link oxidative stress indicators associated with general arsenic exposure to male infertility in a han Chinese population. Environ Sci Technol 2013;47:8843–51. https://doi.org/10.1021/es402025n.Search in Google Scholar PubMed
32. Ghaffari, MA, Motlagh, B. In vitro effect of lead, silver, tin, mercury, indium and bismuth on human sperm creatine kinase activity: a presumable mechanism for men infertility. Iran Biomed J 2011;15:38–43.Search in Google Scholar
33. Hsu, PC, Guo, YL. Antioxidant nutrients and lead toxicity. Toxicology 2002;180:33–44. https://doi.org/10.1016/s0300-483x(02)00380-3.Search in Google Scholar PubMed
34. Pant, N, Banerjee, AK, Pandey, S, Mathur, N, Saxena, DK, Srivastava, SP. Correlation of lead and cadmium in human seminal plasma with seminal vesicle and prostatic markers. Hum Exp Toxicol 2003;22:125–8. https://doi.org/10.1191/0960327103ht336oa.Search in Google Scholar PubMed
35. Kiziler, AR, Aydemir, B, Onaran, I, Alici, B, Ozkara, H, Gulyasar, T, et al.. High levels of cadmium and lead in seminal fluid and blood of smoking men are associated with high oxidative stress and damage in infertile subjects. Biol Trace Elem Res 2007;120:82–91. https://doi.org/10.1007/s12011-007-8020-8.Search in Google Scholar PubMed
36. Apostoli, P, Porru, S, Bisanti, L. Critical aspects of male fertility in the assessment of exposure to lead. Scand J Work Environ Health 1999;25:40–3.Search in Google Scholar
37. Figà-Talamanca, I, Traina, ME, Urbani, E. Occupational exposures to metals, solvents and pesticides: recent evidence on male reproductive effects and biological markers. Occup Med 2001;51:174–88. https://doi.org/10.1093/occmed/51.3.174.Search in Google Scholar PubMed
38. Batra, N, Nehru, B, Bansal, MP. Influence of lead and zinc on rat male reproduction at ’biochemical and histopathological levels. J Appl Toxicol 2001;21:507–12. https://doi.org/10.1002/jat.796.Search in Google Scholar PubMed
39. Centers for Disease Control and Prevention (CDC). Third national report on human exposure to environmental chemicals NCEH Publication No. 05-0570; 2005. Available from: https://stacks.cdc.gov/view/cdc/21809.Search in Google Scholar
40. Chung, NP, Cheng, CY. Is cadmium chloride-induced inter-sertoli tight junction permeability barrier disruption a suitable in vitro model to study the events of junction disassembly during spermatogenesis in the rat testis? Endocrinology 2001;142:1878–88. https://doi.org/10.1210/endo.142.5.8145.Search in Google Scholar PubMed
41. ATSDR. Agency for toxic substances and disease registry. Atlanta, GA: U.S. Department of Health and Human Services; 2007. The 2007 CERCLA priority list of hazardous substances.Search in Google Scholar
42. Siu, MK, Mruk, DD, Lee, WM, Cheng, CY. Adhering junction dynamics in the testis are regulated by an interplay of beta 1-integrin and focal adhesion complex-associated proteins. Endocrinology 2003;144:2141–63. https://doi.org/10.1210/en.2002-221035.Search in Google Scholar PubMed
43. Beardsley, A, Robertson, DM, O’Donnell, L. A complex containing alpha6beta1-integrin and phosphorylated focal adhesion kinase between Sertoli cells and elongated spermatids during spermatid release from the seminiferous epithelium. J Endocrinol 2006;190:759–70. https://doi.org/10.1677/joe.1.06867.Search in Google Scholar PubMed
44. Ranganathan, P, Rao, KA, Sudan, JJ, Balasundaram, S. Cadmium effects on sperm morphology and semenogelin with relates to increased ROS in infertile smokers: an in vitro and in silico approach. Reprod Biol 2018;18:189–97. https://doi.org/10.1016/j.repbio.2018.04.003.Search in Google Scholar PubMed
45. Seong, JB, Bae, YC, Lee, HS, Huh, JW, Lee, SR, Lee, HJ, et al.. Increasing ERK phosphorylation by inhibition of p38 activity protects against cadmium-induced apoptotic cell death through ERK/Drp1/p38 signaling axis in spermatocyte-derived GC-2spd cells. Toxicol Appl Pharmacol 2019;384:114797. https://doi.org/10.1016/j.taap.2019.114797.Search in Google Scholar PubMed
46. Ali, A, Derar, DR, Abdel-Elmoniem, EM, Almundarij, TI. Cadmium in seminal plasma of fertile and infertile male dromedary camels. Biol Trace Elem Res 2020;193:162–5. https://doi.org/10.1007/s12011-019-01688-5.Search in Google Scholar PubMed
47. Fang, Y, Xiang, Y, Lu, X, Dong, X, Zhang, J, Zhong, S. Epigenetic dysregulation of Mdr1b in the blood-testis barrier contributes to dyszoospermia in mice exposed to cadmium. Ecotoxicol Environ Saf 2020;190:110142. https://doi.org/10.1016/j.ecoenv.2019.110142.Search in Google Scholar PubMed
48. ATSDR. Toxicological profile for cadmium (draft for public comment). Atlanta, GA, USA: U.S. Department of Health and Human Services. Public Health Service; 2008a.Search in Google Scholar
49. Rao, MV, Sharma, PS. Protective effect of vitamin E against mercuric chloride reproductive toxicity in male mice. Reprod Toxicol 2001;15:705–12. https://doi.org/10.1016/s0890-6238(01)00183-6.Search in Google Scholar PubMed
50. El-Desoky, GE, Bashandy, SA, Alhazza, IM, Al-Othman, ZA, Aboul-Soud, MA, Yusuf, K. Improvement of mercuric chloride-induced testis injuries and sperm quality deteriorations by Spirulina platensis in rats. PLoS One 2013;8:e59177. https://doi.org/10.1371/journal.pone.0059177.Search in Google Scholar PubMed PubMed Central
51. Grotto, D, Barcelos, GR, Valentini, J, Antunes, LM, Angeli, JP, Garcia, SC, et al.. Low levels of methylmercury induce DNA damage in rats: protective effects of selenium. Arch Toxicol 2009;83:249–54. https://doi.org/10.1007/s00204-008-0353-3.Search in Google Scholar PubMed
52. Boujbiha, MA, Hamden, K, Guermazi, F, Bouslama, A, Omezzine, A, Kammoun, A, et al.. Testicular toxicity in mercuric chloride treated rats: association with oxidative stress. Reprod Toxicol 2009;28:81–9. https://doi.org/10.1016/j.reprotox.2009.03.011.Search in Google Scholar PubMed
53. Al Hashimi, M, Pinggera, GM, Mostafa, T, Rambhatla, A, Hamoda, T, Shah, R, et al.. Regenerative therapy in erectile dysfunction: a survey on current global practice trends and GAF expert recommendations. World J Mens Health 2024. https://doi.org/10.5534/wjmh.240086.Search in Google Scholar PubMed PubMed Central
54. Pi, J, Yamauchi, H, Kumagai, Y, Sun, G, Yoshida, T, Aikawa, H, et al.. Evidence for induction of oxidative stress caused by chronic exposure of Chinese residents to arsenic contained in drinking water. Environ Health Perspect 2002;110:331–6. https://doi.org/10.1289/ehp.02110331.Search in Google Scholar PubMed PubMed Central
55. Uckun, FM, Liu, XP, D’Cruz, OJ. Human sperm immobilizing activity of aminophenyl arsenic acid and its N-substituted quinazoline, pyrimidine, and purine derivatives: protective effect of glutathione. Reprod Toxicol 2002;16:57–64. https://doi.org/10.1016/s0890-6238(01)00195-2.Search in Google Scholar PubMed
56. Kim, YJ, Chung, JY, Lee, SG, Kim, JY, Park, JE, Kim, WR, et al.. Arsenic trioxide-induced apoptosis in TM4 Sertoli cells: the potential involvement of p21 expression and p53 phosphorylation. Toxicology 2011;285:142–51. https://doi.org/10.1016/j.tox.2011.04.013.Search in Google Scholar PubMed
57. Polimanti, R, Piacentini, S, De Angelis, F, De Stefano, GF, Fuciarelli, M. Human GST loci as markers of evolutionary forces: GSTO1*E155del and GSTO1*E208K polymorphisms may be under natural selection induced by environmental arsenic. Dis Markers 2011;31:231–9. https://doi.org/10.3233/DMA-2011-0821.Search in Google Scholar PubMed PubMed Central
58. Ramos-Treviño, J, Bassol-Mayagoitia, S, Hernández-Ibarra, JA, Ruiz-Flores, P, Nava-Hernández, MP. Toxic effect of cadmium, lead, and arsenic on the sertoli cell: mechanisms of damage involved. DNA Cell Biol 2018;37:600–8. https://doi.org/10.1089/dna.2017.4081.Search in Google Scholar PubMed
59. Rosenblatt, AE, Burnstein, KL. Inhibition of androgen receptor transcriptional activity as a novel mechanism of action of arsenic. Mol Endocrinol 2009;23:412–21. https://doi.org/10.1210/me.2008-0235.Search in Google Scholar PubMed PubMed Central
60. Shao, Y, Zhao, H, Wang, Y, Liu, J, Li, J, Chai, H, et al.. Arsenic and/or copper caused inflammatory response via activation of inducible nitric oxide synthase pathway and triggered heat shock protein responses in testis tissues of chicken. Environ Sci Pollut Res Int 2018;25:7719–29. https://doi.org/10.1007/s11356-017-1042-7.Search in Google Scholar PubMed
61. Ince, S, Avdatek, F, Demirel, HH, Arslan-Acaroz, D, Goksel, E, Kucukkurt, I. Ameliorative effect of polydatin on oxidative stress-mediated testicular damage by chronic arsenic exposure in rats. Andrologia 2016;48:518–24. https://doi.org/10.1111/and.12472.Search in Google Scholar PubMed
62. Wang, X, Zhang, J, Xu, W, Huang, Q, Liu, L, Tian, M, et al.. Low-level environmental arsenic exposure correlates with unexplained male infertility risk. Sci Total Environ 2016;571:307–13. https://doi.org/10.1016/j.scitotenv.2016.07.169.Search in Google Scholar PubMed
63. Benoff, S, Jacob, A, Hurley, IR. Male infertility and environmental exposure to lead and cadmium. Hum Reprod Update 2000;6:107–21. https://doi.org/10.1093/humupd/6.2.107.Search in Google Scholar PubMed
64. Agarwal, A, Farkouh, A, Saleh, R, Hamoda, TAA, Salvio, G, Boitrelle, F, et al.. Technical aspects and clinical limitations of sperm DNA fragmentation testing in male infertility: a global survey, current guidelines, and expert recommendations. World J Mens Health 2024;42:202–15. https://doi.org/10.5534/wjmh.230076.Search in Google Scholar PubMed PubMed Central
65. Farkouh, A, Agarwal, A, Hamoda, TAA, Kavoussi, P, Saleh, R, Zini, A, et al.. Controversy and consensus on the management of elevated sperm DNA fragmentation in male infertility: a global survey, current guidelines, and expert recommendations. World J Mens Health 2023;41:809–47. https://doi.org/10.5534/wjmh.230008.Search in Google Scholar PubMed PubMed Central
66. Wang, X, Tian, J. Health risks related to residential exposure to cadmium in Zhenhe County, China. Arch Environ Health 2004;59:324–30. https://doi.org/10.3200/AEOH.59.6.324-330.Search in Google Scholar PubMed
67. Joffe, M, Bisanti, L, Apostoli, P, Kiss, P, Dale, A, Roeleveld, N, et al.. Asclepios. Time to Pregnancy and occupational lead exposure. Occup Environ Med 2003;60:752–8. https://doi.org/10.1136/oem.60.10.752.Search in Google Scholar PubMed PubMed Central
68. Giulioni, C, Maurizi, V, Galosi, AB. The role of physical agents’ exposure in male infertility: a critical review. Arch Ital Urol Androl 2023;95:10890. https://doi.org/10.4081/aiua.2023.10890.Search in Google Scholar PubMed
69. Shah, R, Agarwal, A, Kavoussi, P, Rambhatla, A, Saleh, R, Cannarella, R, et al.. Consensus and diversity in the management of varicocele for male infertility: results of a global practice survey and Comparison with guidelines and recommendations. World J Mens Health 2023;41:164–97. https://doi.org/10.5534/wjmh.220048.Search in Google Scholar PubMed PubMed Central
70. Romano, L, Pellegrino, R, Sciorio, C, Barone, B, Gravina, AG, Santonastaso, A, et al.. Erectile and sexual dysfunction in male and female patients with celiac disease: a cross-sectional observational study. Andrology 2022;10:910–18. https://doi.org/10.1111/andr.13186.Search in Google Scholar PubMed PubMed Central
© 2025 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Reviews
- Navigating nephropathy and nephrotoxicity: understanding pathophysiology unveiling clinical manifestations, and exploring treatment approaches
- Incretin-based therapies: advancements, challenges, and future directions in type 2 diabetes management
- Point-of-care testing: revolutionizing clinical biochemistry using decentralized diagnostics
- The impact of heavy metals exposure on male fertility: a scoping review of human studies
- Glucagon in glucose homeostasis and metabolic disease: from physiology to therapeutics
- The efficacy of dietary supplements on health status and performance of football players: a systematic review
- Original Articles
- Factors affecting self-care in heart failure patients: a cross-sectional study
- Physiological regulation of moderate-intensity exercise in improving the biomarkers visfatin and myonectin as a modulator of increasing metabolic performance in obese
- A comparative study of heart rate variability (HRV) among adult hypertensive and normotensive subjects in the supine position
- Elevated seminal plasma leptin may correlate with varicocele presence and BMI
- Clinical significance of detectable blood lead and cadmium in the Sarno river basin population: results from the PREVES-STOP study
- Outcomes of systemic thrombolysis with reteplase in high-risk acute pulmonary embolism
- The pharmacokinetics and comparative bioavailabilty of oral and subcutaneous semaglutide in healthy volunteers
- Short Communications
- Approaching a phenomenal contradiction in acid–base physiology
- Current trends and innovations in oral and maxillofacial surgery
- Letter to the Editor
- The need for quality certification for urological apps
Articles in the same Issue
- Frontmatter
- Reviews
- Navigating nephropathy and nephrotoxicity: understanding pathophysiology unveiling clinical manifestations, and exploring treatment approaches
- Incretin-based therapies: advancements, challenges, and future directions in type 2 diabetes management
- Point-of-care testing: revolutionizing clinical biochemistry using decentralized diagnostics
- The impact of heavy metals exposure on male fertility: a scoping review of human studies
- Glucagon in glucose homeostasis and metabolic disease: from physiology to therapeutics
- The efficacy of dietary supplements on health status and performance of football players: a systematic review
- Original Articles
- Factors affecting self-care in heart failure patients: a cross-sectional study
- Physiological regulation of moderate-intensity exercise in improving the biomarkers visfatin and myonectin as a modulator of increasing metabolic performance in obese
- A comparative study of heart rate variability (HRV) among adult hypertensive and normotensive subjects in the supine position
- Elevated seminal plasma leptin may correlate with varicocele presence and BMI
- Clinical significance of detectable blood lead and cadmium in the Sarno river basin population: results from the PREVES-STOP study
- Outcomes of systemic thrombolysis with reteplase in high-risk acute pulmonary embolism
- The pharmacokinetics and comparative bioavailabilty of oral and subcutaneous semaglutide in healthy volunteers
- Short Communications
- Approaching a phenomenal contradiction in acid–base physiology
- Current trends and innovations in oral and maxillofacial surgery
- Letter to the Editor
- The need for quality certification for urological apps