Fertilizers and Human Health—A Systematic Review of the Epidemiological Evidence
Abstract
:1. Introduction
2. Materials and Methods
2.1. Search Strategy
2.2. Study Eligibility and Selection
2.3. Exposure and Outcome Definitions
2.4. Data Extraction
2.5. Quality of the Assessed Evidence
2.6. Evidence Synthesis
3. Results
3.1. Evidence Base Overview-Study Characteristics-Methodological Assessment
3.2. Health-Related Effects and Exposure to Inorganic Fertilizers
3.2.1. Neurological Outcomes
3.2.2. Other Non-Malignant Outcomes
3.2.3. Cancerous Outcomes
Solid Organ Tumors
Blood-Related Malignancies
3.3. Health-Related Effects and Exposure to Organic Fertilizers
3.3.1. Infectious-Related Outcomes
3.3.2. Allergies and Atopy
3.3.3. Other Non-Malignant Outcomes
3.3.4. Cancerous Outcomes
4. Discussion
Supplementary Materials
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
- European Commission. Fertilizers in the EU; European Commission: Brussels, Belgium, 2019; Volume 8, Available online: https://agriculture.ec.europa.eu/system/files/2019-07/market-brief-fertilisers_june2019_en_0.pdf (accessed on 4 May 2024).
- Mnif, W.; Hassine, A.I.H.; Bouaziz, A.; Bartegi, A.; Thomas, O.; Roig, B. Effect of endocrine disruptor pesticides: A review. Int. J. Environ. Res. Public Health 2011, 8, 2265–2303. [Google Scholar] [CrossRef] [PubMed]
- (UNEP) TUNEP. Fertilizers: Challenges and Solutions. Ecosystems and Biodiversity. 2020. Available online: https://www.unep.org/news-and-stories/story/fertilizers-challenges-and-solutions (accessed on 9 November 2020).
- International Fiscal Association. “Fertilizer Outlook 2020–2024” Market Intelligence and Agriculture Services; IFA: Berlin, Germany, 2020. [Google Scholar]
- UNEP. Synthesis Report on the Environmental and Health Impacts of Pesticides and Fertilizers and Ways to Minimize Them; UNEP: Geneva, Switzerland, 2022. [Google Scholar]
- Wallace, B.C.; Small, K.; Brodley, C.E.; Lau, J.; Trikalinos, T.A. Deploying an interactive machine learning system in an evidence-based practice center: Abstrackr. In Proceedings of the 2nd ACM SIGHIT International Health Informatics Symposium, Miami, FL, USA, 28–30 January 2012; pp. 819–824. [Google Scholar]
- Morgan, R.L.; Whaley, P.; Thayer, K.A.; Schünemann, H.J. Identifying the PECO: A framework for formulating good questions to explore the association of environmental and other exposures with health outcomes. Environ. Int. 2018, 121 Pt 1, 1027. [Google Scholar] [CrossRef] [PubMed]
- Viswanathan, M.; Berkman, N.D. Development of the RTI item bank on risk of bias and precision of observational studies. J. Clin. Epidemiol. 2012, 65, 163–178. [Google Scholar] [CrossRef]
- Ballal, S.G.; Ali, B.A.; Albar, A.A.; Ahmed, H.O.; al-Hasan, A.Y. Bronchial asthma in two chemical fertilizer producing factories in eastern Saudi Arabia. Int. J. Tuberc. Lung Dis. 1998, 2, 330–335. [Google Scholar]
- Behrens, T.; Lynge, E.; Cree, I.; Lutz, J.M.; Eriksson, M.; Guenel, P.; Merletti, F.; Morales-Suarez-Varela, M.; Afonso, N.; Stengrevics, A.; et al. Pesticide exposure in farming and forestry and the risk of uveal melanoma. Cancer Causes Control 2012, 23, 141–151. [Google Scholar] [CrossRef] [PubMed]
- Belongia, E.A.; Chyou, P.H.; Greenlee, R.T.; Perez-Perez, G.; Bibb, W.F.; DeVries, E.O. Diarrhea incidence and farm-related risk factors for Escherichia coli O157:H7 and Campylobacter jejuni antibodies among rural children. J. Infect. Dis. 2003, 187, 1460–1468. [Google Scholar] [CrossRef] [PubMed]
- Blair, A.; White, D.W. Death certificate study of leukemia among farmers from Wisconsin. J. Natl. Cancer Inst. 1981, 66, 1027–1030. [Google Scholar] [CrossRef]
- Bulbulyan, M.A.; Jourenkova, N.J.; Boffetta, P.; Astashevsky, S.V.; Mukeria, A.F.; Zaridze, D.G. Mortality in a cohort of Russian fertilizer workers. Scand. J. Work Environ. Health 1996, 22, 27–33. [Google Scholar] [CrossRef]
- Cantor, K.P.; Blair, A. Farming and mortality from multiple myeloma: A case-control study with the use of death certificates. J. Natl. Cancer Inst. 1984, 72, 251–255. [Google Scholar]
- Carlton, E.J.; Liu, Y.; Zhong, B.; Hubbard, A.; Spear, R.C. Associations between schistosomiasis and the use of human waste as an agricultural fertilizer in China. PLoS Negl. Trop. Dis. 2015, 9, e0003444. [Google Scholar] [CrossRef]
- Casey, J.A.; Curriero, F.C.; Cosgrove, S.E.; Nachman, K.E.; Schwartz, B.S. High-density livestock operations, crop field application of manure, and risk of community-associated methicillin-resistant Staphylococcus aureus infection in Pennsylvania. JAMA Intern. Med. 2013, 173, 1980–1990. [Google Scholar] [CrossRef] [PubMed]
- Cocco, P.; Palli, D.; Buiatti, E.; Cipriani, F.; DeCarli, A.; Manca, P.; Ward, M.H.; Blot, W.J.; Fraumeni, J.F., Jr. Occupational exposures as risk factors for gastric cancer in Italy. Cancer Causes Control 1994, 5, 241–248. [Google Scholar] [CrossRef] [PubMed]
- Cocco, P.; Ward, M.H.; Dosemeci, M. Risk of stomach cancer associated with 12 workplace hazards: Analysis of death certificates from 24 states of the United States with the aid of job exposure matrices. Occup. Environ. Med. 1999, 56, 781–787. [Google Scholar] [CrossRef]
- Dal Pozzo, F.; Martinelle, L.; Leonard, P.; Renaville, B.; Renaville, R.; Thys, C.; Smeets, F.; Czaplicki, G.; Van Esbroeck, M.; Saegerman, C. Q Fever Serological Survey and Associated Risk Factors in Veterinarians, Southern Belgium, 2013. Transbound Emerg. Dis. 2017, 64, 959–966. [Google Scholar] [CrossRef]
- Dang-Xuan, S.; MacDonald, L.E.; Schurer, J.M.; Nguyen-Viet, H.; Pham-Duc, P. Household Exposure to Livestock and Health in the CHILILAB HDSS Cohort, Vietnam. Asia Pac. J. Public Health 2017, 29 (Suppl. S5), 72s–83s. [Google Scholar] [CrossRef]
- Dorn, C.R.; Reddy, C.S.; Lamphere, D.N.; Gaeuman, J.V.; Lanese, R. Municipal sewage sludge application on Ohio farms: Health effects. Environ. Res. 1985, 38, 332–359. [Google Scholar] [CrossRef]
- Efird, J.T.; Holly, E.A.; Preston-Martin, S.; Mueller, B.A.; Lubin, F.; Filippini, G.; Peris-Bonet, R.; McCredie, M.; Cordier, S.; Arslan, A.; et al. Farm-related exposures and childhood brain tumours in seven countries: Results from the SEARCH International Brain Tumour Study. Paediatr. Perinat. Epidemiol. 2003, 17, 201–211. [Google Scholar] [CrossRef]
- El-Tras, W.F.; Holt, H.R.; Tayel, A.A.; El-Kady, N.N. Campylobacter infections in children exposed to infected backyard poultry in Egypt. Epidemiol. Infect. 2015, 143, 308–315. [Google Scholar] [CrossRef] [PubMed]
- Fandrem, S.I.; Kjuus, H.; Andersen, A.; Amlie, E. Incidence of cancer among workers in a Norwegian nitrate fertiliser plant. Br. J. Ind. Med. 1993, 50, 647–652. [Google Scholar] [CrossRef]
- Fluegge, K. Exploring the potential confounder of nitrogen fertilizers in the relationship between pesticide exposures and risk of leukemia: A Poisson regression with two-way fixed-effects analysis. Chin. J. Cancer 2017, 36, 58. [Google Scholar] [CrossRef]
- Garcia-Perez, J.; Lope, V.; Lopez-Abente, G.; Gonzalez-Sanchez, M.; Fernandez-Navarro, P. Ovarian cancer mortality and industrial pollution. Environ. Pollut. 2015, 205, 103–110. [Google Scholar] [CrossRef]
- Garcia-Perez, J.; Morales-Piga, A.; Gomez, J.; Gomez-Barroso, D.; Tamayo-Uria, I.; Pardo Romaguera, E.; Fernandez-Navarro, P.; Lopez-Abente, G.; Ramis, R. Association between residential proximity to environmental pollution sources and childhood renal tumors. Environ. Res. 2016, 147, 405–414. [Google Scholar] [CrossRef] [PubMed]
- Getachew, M.; Tafess, K.; Zeynudin, A.; Yewhalaw, D. Prevalence soil transmitted helminthiasis and malaria co-infection among pregnant women and risk factors in Gilgel Gibe Dam area, southwest Ethiopia. BMC Res. Notes 2013, 6, 263. [Google Scholar] [CrossRef] [PubMed]
- Gijon-Robles, P.; Abattouy, N.; Merino-Espinosa, G.; El Khalfaoui, N.; Morillas-Marquez, F.; Corpas-Lopez, V.; Porcel-Rodriguez, L.; Jaaouani, N.; Diaz-Saez, V.; Riyad, M.; et al. Risk factors for the expansion of cutaneous leishmaniasis by Leishmania tropica: Possible implications for control programmes. Transbound. Emerg. Dis. 2018, 65, 1615–1626. [Google Scholar] [CrossRef] [PubMed]
- Gomzi, M. Respiratory health of children at schools near a fertilizer plant. Arh. Hig. Rada Toksikol. 1996, 47, 145–155. [Google Scholar]
- Gorman Ng, M.; Stjernberg, E.; Koehoorn, M.; Demers, P.A.; Winters, M.; Davies, H.W. Fertilizer use and self-reported respiratory and dermal symptoms among tree planters. J. Occup. Environ. Hyg. 2013, 10, 36–45. [Google Scholar] [CrossRef]
- Haughey, B.P.; Graham, S.; Brasure, J.; Zielezny, M.; Sufrin, G.; Burnett, W.S. The epidemiology of testicular cancer in upstate New York. Am. J. Epidemiol. 1989, 130, 25–36. [Google Scholar] [CrossRef]
- Hebert, R.; Lindsay, J.; Verreault, R.; Rockwood, K.; Hill, G.; Dubois, M.F. Vascular dementia: Incidence and risk factors in the Canadian study of health and aging. Stroke 2000, 31, 1487–1493. [Google Scholar] [CrossRef]
- Holly, E.A.; Aston, D.A.; Ahn, D.K.; Kristiansen, J.J. Ewing’s bone sarcoma, paternal occupational exposure, and other factors. Am. J. Epidemiol. 1992, 135, 122–129. [Google Scholar] [CrossRef]
- Hovland, K.H.; Skogstad, M.; Bakke, B.; Skare, O.; Skyberg, K. Longitudinal lung function decline among workers in a nitrate fertilizer production plant. Int. J. Occup. Environ. Health 2013, 19, 119–126. [Google Scholar] [CrossRef]
- Hovland, K.H.; Skogstad, M.; Bakke, B.; Skare, O.; Skyberg, K. Longitudinal decline in pulmonary diffusing capacity among nitrate fertilizer workers. Occup. Med. 2014, 64, 181–187. [Google Scholar] [CrossRef] [PubMed]
- Illi, S.; Depner, M.; Genuneit, J.; Horak, E.; Loss, G.; Strunz-Lehner, C.; Buchele, G.; Boznanski, A.; Danielewicz, H.; Cullinan, P.; et al. Protection from childhood asthma and allergy in Alpine farm environments-the GABRIEL Advanced Studies. J. Allergy Clin. Immunol. 2012, 129, 1470–1477. [Google Scholar] [CrossRef]
- Issaragrisil, S.; Kaufman, D.W.; Anderson, T.; Chansung, K.; Leaverton, P.E.; Shapiro, S.; Young, N.S. The epidemiology of aplastic anemia in Thailand. Blood 2006, 107, 1299–1307. [Google Scholar] [CrossRef] [PubMed]
- Jayasumana, C.; Paranagama, P.; Agampodi, S.; Wijewardane, C.; Gunatilake, S.; Siribaddana, S. Drinking well water and occupational exposure to Herbicides is associated with chronic kidney disease, in Padavi-Sripura, Sri Lanka. Environ. Health 2015, 14, 6. [Google Scholar] [CrossRef]
- Karakosta, M.; Delicha, E.M.; Kouraklis, G.; Manola, K.N. Association of various risk factors with chronic lymphocytic leukemia and its cytogenetic characteristics. Arch. Environ. Occup. Health 2016, 71, 317–329. [Google Scholar] [CrossRef] [PubMed]
- Khuder, S.; Milz, S.A.; Bisesi, M.; Vincent, R.; McNulty, W.; Czajkowski, K. Health survey of residents living near farm fields permitted to receive biosolids. Arch. Environ. Occup. Health 2007, 62, 5–11. [Google Scholar] [CrossRef]
- Kobrossi, R.; Nuwayhid, I.; Sibai, A.M.; El-Fadel, M.; Khogali, M. Respiratory health effects of industrial air pollution on children in North Lebanon. Int. J. Environ. Health Res. 2002, 12, 205–220. [Google Scholar] [CrossRef]
- Kristensen, P.; Andersen, A.; Irgens, L.M.; Bye, A.S.; Vagstad, N. Testicular cancer and parental use of fertilizers in agriculture. Cancer Epidemiol. Biomark. Prev. 1996, 5, 3–9. [Google Scholar]
- Kristensen, P.; Irgens, L.M.; Andersen, A.; Bye, A.S.; Sundheim, L. Birth defects among offspring of Norwegian farmers, 1967–1991. Epidemiology 1997, 8, 537–544. [Google Scholar] [CrossRef]
- Lindsay, J.; Hebert, R.; Rockwood, K. The Canadian Study of Health and Aging: Risk factors for vascular dementia. Stroke 1997, 28, 526–530. [Google Scholar] [CrossRef]
- Lope, V.; Pollan, M.; Gustavsson, P.; Plato, N.; Perez-Gomez, B.; Aragones, N.; Suarez, B.; Carrasco, J.M.; Rodriguez, S.; Ramis, R.; et al. Occupation and thyroid cancer risk in Sweden. J. Occup. Environ. Med. 2005, 47, 948–957. [Google Scholar] [CrossRef] [PubMed]
- Melkonian, S.; Argos, M.; Pierce, B.L.; Chen, Y.; Islam, T.; Ahmed, A.; Syed, E.H.; Parvez, F.; Graziano, J.; Rathouz, P.J.; et al. A prospective study of the synergistic effects of arsenic exposure and smoking, sun exposure, fertilizer use, and pesticide use on risk of premalignant skin lesions in Bangladeshi men. Am. J. Epidemiol. 2011, 173, 183–191. [Google Scholar] [CrossRef] [PubMed]
- Menvielle, G.; Luce, D.; Fevotte, J.; Bugel, I.; Salomon, C.; Goldberg, P.; Billon-Galland, M.A.; Goldberg, M. Occupational exposures and lung cancer in New Caledonia. Occup. Environ. Med. 2003, 60, 584–589. [Google Scholar] [CrossRef] [PubMed]
- Morris, P.D.; Koepsell, T.D.; Daling, J.R.; Taylor, J.W.; Lyon, J.L.; Swanson, G.M.; Child, M.; Weiss, N.S. Toxic substance exposure and multiple myeloma: A case-control study. J. Natl. Cancer Inst. 1986, 76, 987–994. [Google Scholar]
- Musicco, M.; Filippini, G.; Bordo, B.M.; Melotto, A.; Morello, G.; Berrino, F. Gliomas and occupational exposure to carcinogens: Case-control study. Am. J. Epidemiol. 1982, 116, 782–790. [Google Scholar] [CrossRef]
- Musicco, M.; Sant, M.; Molinari, S.; Filippini, G.; Gatta, G.; Berrino, F. A case-control study of brain gliomas and occupational exposure to chemical carcinogens: The risk to farmers. Am. J. Epidemiol. 1988, 128, 778–785. [Google Scholar] [CrossRef]
- Nisse, C.; Haguenoer, J.M.; Grandbastien, B.; Preudhomme, C.; Fontaine, B.; Brillet, J.M.; Lejeune, R.; Fenaux, P. Occupational and environmental risk factors of the myelodysplastic syndromes in the North of France. Br. J. Haematol. 2001, 112, 927–935. [Google Scholar] [CrossRef]
- Parks, C.G.; Hoppin, J.A.; De Roos, A.J.; Costenbader, K.H.; Alavanja, M.C.; Sandler, D.P. Rheumatoid Arthritis in Agricultural Health Study Spouses: Associations with Pesticides and Other Farm Exposures. Environ. Health Perspect. 2016, 124, 1728–1734. [Google Scholar] [CrossRef]
- Pasqualetti, P.; Casale, R.; Colantonio, D.; Collacciani, A. Occupational risk for hematological malignancies. Am. J. Hematol. 1991, 38, 147–149. [Google Scholar] [CrossRef]
- Pasqualetti, P.; Collacciani, A.; Casale, R. Risk of monoclonal gammopathy of undetermined significance: A case-referent study. Am. J. Hematol. 1996, 52, 217–220. [Google Scholar] [CrossRef]
- Pham-Duc, P.; Nguyen-Viet, H.; Hattendorf, J.; Cam, P.D.; Zurbrugg, C.; Zinsstag, J.; Odermatt, P. Diarrhoeal diseases among adult population in an agricultural community Hanam province, Vietnam, with high wastewater and excreta re-use. BMC Public Health 2014, 14, 978. [Google Scholar] [CrossRef]
- Pham-Duc, P.; Nguyen-Viet, H.; Hattendorf, J.; Zinsstag, J.; Phung-Dac, C.; Zurbrugg, C.; Odermatt, P. Ascaris lumbricoides and Trichuris trichiura infections associated with wastewater and human excreta use in agriculture in Vietnam. Parasitol. Int. 2013, 62, 172–180. [Google Scholar] [CrossRef] [PubMed]
- Rahman, M.H.; Bratveit, M.; Moen, B.E. Exposure to ammonia and acute respiratory effects in a urea fertilizer factory. Int. J. Occup. Environ. Health 2007, 13, 153–159. [Google Scholar] [CrossRef] [PubMed]
- Schmeisser, N.; Behrens, T.; Mester, B.; Gottlieb, A.; Langner, I.; Ahrens, W. Local cluster of germ cell cancer in a cohort of male automotive workers in Germany not explained by previous or concurrent activities and exposures in farming and forestry. Cancer Epidemiol. 2011, 35, 73–77. [Google Scholar] [CrossRef]
- Schwartzbaum, J.A.; George, S.L.; Pratt, C.B.; Davis, B. An exploratory study of environmental and medical factors potentially related to childhood cancer. Med. Pediatr. Oncol. 1991, 19, 115–121. [Google Scholar] [CrossRef]
- Shi, R.; Gao, Y.; Zhang, Y.; Gao, Y.J.; Zhu, S.; Wang, X.J.; Jin, P.; Tian, Y. Relationship between parental exposure to chemicals and risk of childhood acute leukemia. Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi 2013, 31, 413–417. [Google Scholar] [PubMed]
- Tangkanakul, W.; Tharmaphornpil, P.; Plikaytis, B.D.; Bragg, S.; Poonsuksombat, D.; Choomkasien, P.; Kingnate, D.; Ashford, D.A. Risk factors associated with leptospirosis in northeastern Thailand, 1998. Am. J. Trop. Med. Hyg. 2000, 63, 204–208. [Google Scholar] [CrossRef]
- Ton, T.G.; Longstreth, W.T., Jr.; Koepsell, T.D. Environmental toxins and risk of narcolepsy among people with HLA DQB1*0602. Environ. Res. 2010, 110, 565–570. [Google Scholar] [CrossRef]
- Valcin, M.; Henneberger, P.K.; Kullman, G.J.; Umbach, D.M.; London, S.J.; Alavanja, M.C.; Sandler, D.P.; Hoppin, J.A. Chronic bronchitis among nonsmoking farm women in the agricultural health study. J. Occup. Environ. Med. 2007, 49, 574–583. [Google Scholar] [CrossRef]
- van Duijn, C.M.; Delasnerie-Laupretre, N.; Masullo, C.; Zerr, I.; de Silva, R.; Wientjens, D.P.; Brandel, J.P.; Weber, T.; Bonavita, V.; Zeidler, M.; et al. Case-control study of risk factors of Creutzfeldt-Jakob disease in Europe during 1993-95. European Union (EU) Collaborative Study Group of Creutzfeldt-Jakob disease (CJD). Lancet 1998, 351, 1081–1085. [Google Scholar] [CrossRef]
- Wang, J.; Xia, K.; Waigi, M.G.; Gao, Y.; Odinga, E.S.; Ling, W.; Liu, J. Application of biochar to soils may result in plant contamination and human cancer risk due to exposure of polycyclic aromatic hydrocarbons. Environ. Int. 2018, 121, 169–177. [Google Scholar] [CrossRef] [PubMed]
- Welton, M.; Robb, S.W.; Shen, Y.; Guillebeau, P.; Vena, J. Prostate cancer incidence and agriculture practices in Georgia, 2000–2010. Int. J. Occup. Environ. Health 2015, 21, 251–257. [Google Scholar] [CrossRef] [PubMed]
- Wong, O.; Harris, F.; Yiying, W.; Hua, F. A hospital-based case-control study of acute myeloid leukemia in Shanghai: Analysis of personal characteristics, lifestyle and environmental risk factors by subtypes of the WHO classification. Regul. Toxicol. Pharmacol. 2009, 55, 340–352. [Google Scholar] [CrossRef] [PubMed]
- Wong, O.; Harris, F.; Armstrong, T.W.; Hua, F. A hospital-based case-control study of acute myeloid leukemia in Shanghai: Analysis of environmental and occupational risk factors by subtypes of the WHO classification. Chem. Biol. Interact. 2010, 184, 112–128. [Google Scholar] [CrossRef] [PubMed]
- Yiin, J.H.; Daniels, R.D.; Kubale, T.L.; Dunn, K.L.; Stayner, L.T. A study update of mortality in workers at a phosphate fertilizer production facility. Am. J. Ind. Med. 2016, 59, 12–22. [Google Scholar] [CrossRef] [PubMed]
- Yu, Y.; Su, F.C.; Callaghan, B.C.; Goutman, S.A.; Batterman, S.A.; Feldman, E.L. Environmental risk factors and amyotrophic lateral sclerosis (ALS): A case-control study of ALS in Michigan. PLoS ONE 2014, 9, e101186. [Google Scholar] [CrossRef]
- Zhang, N.; Yu, C.; Wen, D.; Chen, J.; Ling, Y.; Terajima, K.; Akazawa, K.; Shan, B.; Wang, S. Association of nitrogen compounds in drinking water with incidence of esophageal squamous cell carcinoma in Shexian, China. Tohoku J. Exp. Med. 2012, 226, 11–17. [Google Scholar] [CrossRef]
- Contreras, J.D.; Trangucci, R.; Felix-Arellano, E.E.; Rodríguez-Dozal, S.; Siebe, C.; Riojas-Rodríguez, H.; Meza, R.; Zelner, J.; Eisenberg, J.N.S. Modeling Spatial Risk of Diarrheal Disease Associated with Household Proximity to Untreated Wastewater Used for Irrigation in the Mezquital Valley, Mexico. Environ. Health Perspect. 2020, 128, 77002. [Google Scholar] [CrossRef]
- Essien, E.E.; Said Abasse, K.; Côté, A.; Mohamed, K.S.; Baig, M.; Habib, M.; Naveed, M.; Yu, X.; Xie, W.; Jinfang, S.; et al. Drinking-water nitrate and cancer risk: A systematic review and meta-analysis. Arch. Environ. Occup. Health 2022, 77, 51–67. [Google Scholar] [CrossRef]
- Fraser, P.; Chilvers, C. Health aspects of nitrate in drinking water. Sci. Total Environ. 1981, 18, 103–116. [Google Scholar] [CrossRef]
- Grosse, Y.; Baan, R.; Straif, K.; Secretan, B.; El Ghissassi, F.; Cogliano, V. Carcinogenicity of nitrate, nitrite, and cyanobacterial peptide toxins. Lancet Oncol. 2006, 7, 628–629. [Google Scholar] [CrossRef] [PubMed]
- Ward, M.H.; Jones, R.R.; Brender, J.D.; De Kok, T.M.; Weyer, P.J.; Nolan, B.T.; Villanueva, C.M.; Van Breda, S.G. Drinking Water Nitrate and Human Health: An Updated Review. Int. J. Environ. Res. Public Health 2018, 15, 1557. [Google Scholar] [CrossRef] [PubMed]
- Correa, P. A human model of gastric carcinogenesis. Cancer Res. 1988, 48, 3554–3560. [Google Scholar]
- Mirvish, S.S. Role of N-nitroso compounds (NOC) and N-nitrosation in etiology of gastric, esophageal, nasopharyngeal and bladder cancer and contribution to cancer of known exposures to NOC. Cancer Lett. 1995, 93, 17–48. [Google Scholar] [CrossRef]
- Keszei, A.P.; Goldbohm, R.A.; Schouten, L.J.; Jakszyn, P.; Van Den Brandt, P.A. Dietary N-nitroso compounds, endogenous nitrosation, and the risk of esophageal and gastric cancer subtypes in the Netherlands Cohort Study. Am. J. Clin. Nutr. 2013, 97, 135–146. [Google Scholar] [CrossRef] [PubMed]
- Morales-Suárez-Varela, M.; Llopis-Gonzalez, A.; Tejerizo-Perez, M. Impact of nitrates in drinking water on cancer mortality in Valencia, Spain. Eur. J. Epidemiol. 1995, 11, 15–21. [Google Scholar] [CrossRef]
- Ward, M.H.; Rusiecki, J.A.; Lynch, C.F.; Cantor, K.P. Nitrate in public water supplies and the risk of renal cell carcinoma. Cancer Causes Control 2007, 18, 1141–1151. [Google Scholar] [CrossRef]
- Anthony, A.A.; Oluyemi, O.A.; Thor, A.S. Organic Fertilizers: Public Health Intricacies. In Organic Fertilizers; Marcelo, L.L., Sonia, S., Eds.; IntechOpen: Rijeka, Croatia, 2016; p. Ch. 16. [Google Scholar]
- Steelman, V.M. Creutzfeld-Jakob disease: Recommendations for infection control. Am. J. Infect. Control 1994, 22, 312–318. [Google Scholar] [CrossRef]
- Brandel, J.P.; Vlaicu, M.B.; Culeux, A.; Belondrade, M.; Bougard, D.; Grznarova, K.; Denouel, A.; Plu, I.; Bouaziz-Amar, E.; Seilhean, D.; et al. Variant Creutzfeldt-Jakob Disease Diagnosed 7.5 Years after Occupational Exposure. N. Engl. J. Med. 2020, 383, 83–85. [Google Scholar] [CrossRef] [PubMed]
- Cocco, P.L.; Caperna, A.; Vinci, F. Occupational risk factors for the sporadic form of Creutzfeldt-Jakob disease. Med. Lavoro 2003, 94, 353–363. [Google Scholar]
- Safar, J.G.; Lessard, P.; Tamgüney, G.; Freyman, Y.; Deering, C.; Letessier, F.; DeArmond, S.J.; Prusiner, S.B. Transmission and Detection of Prions in Feces. J. Infect. Dis. 2008, 198, 81–89. [Google Scholar] [CrossRef] [PubMed]
- United Nations; United Nations Environment Programme. Environmental Dimensions of Antimicrobial Resistance: Summary for Policymakers; United Nations: New York, NY, USA, 2022. [Google Scholar]
- Levy, S.B.; Marshall, B. Antibacterial resistance worldwide: Causes, challenges and responses. Nat. Med. 2004, 10, S122–S129. [Google Scholar] [CrossRef] [PubMed]
- Martínez, J.L.; Coque, T.M.; Baquero, F. What is a resistance gene? Ranking risk in resistomes. Nat. Rev. Microbiol. 2015, 13, 116–123. [Google Scholar] [CrossRef] [PubMed]
- Bengtsson-Palme, J.; Kristiansson, E.; Larsson, D.G.J. Environmental factors influencing the development and spread of antibiotic resistance. FEMS Microbiol. Rev. 2017, 42, fux053. [Google Scholar] [CrossRef]
- Bürgmann, H.; Frigon, D.; H Gaze, W.; M Manaia, C.; Pruden, A.; Singer, A.C.; F Smets, B.; Zhang, T. Water and sanitation: An essential battlefront in the war on antimicrobial resistance. FEMS Microbiol. Ecol. 2018, 94, fiy101. [Google Scholar] [CrossRef] [PubMed]
- Vikesland, P.; Garner, E.; Gupta, S.; Kang, S.; Maile-Moskowitz, A.; Zhu, N. Differential Drivers of Antimicrobial Resistance across the World. Acc. Chem. Res. 2019, 52, 916–924. [Google Scholar] [CrossRef]
- Zhu, B.; Chen, Q.; Chen, S.; Zhu, Y.G. Does organically produced lettuce harbor higher abundance of antibiotic resistance genes than conventionally produced? Environ. Int. 2017, 98, 152–159. [Google Scholar] [CrossRef]
- Hubballi, M.; Johnson, I.; Anjali, V.A.; Archana, T.S.; Nakkeeran, S. Detection and Identification of Soil-Borne Pathogens: Classical to Recent Updates. In Rhizosphere Microbes: Biotic Stress Management; Singh, U.B., Sahu, P.K., Singh, H.V., Sharma, P.K., Sharma, S.K., Eds.; Springer: Singapore, 2022; pp. 1–45. [Google Scholar]
- Hu, J.; Wu, F.; Wu, S.; Sun, X.; Lin, X.; Wong, M.H. Phytoavailability and phytovariety codetermine the bioaccumulation risk of heavy metal from soils, focusing on Cd-contaminated vegetable farms around the Pearl River Delta, China. Ecotoxicol. Environ. Saf. 2013, 91, 18–24. [Google Scholar] [CrossRef]
- Khan, A.; Khan, S.; Khan, M.A.; Qamar, Z.; Waqas, M. The uptake and bioaccumulation of heavy metals by food plants, their effects on plants nutrients, and associated health risk: A review. Environ. Sci. Pollut. Res. Int. 2015, 22, 13772–13799. [Google Scholar] [CrossRef]
- Bandara, J.M.; Wijewardena, H.V.; Liyanege, J.; Upul, M.A.; Bandara, J.M. Chronic renal failure in Sri Lanka caused by elevated dietary cadmium: Trojan horse of the green revolution. Toxicol. Lett. 2010, 198, 33–39. [Google Scholar] [CrossRef]
- Reuss, J.; OReuss, J.O.; Dooley, H.L.; Griffis, W.; Corvallis Environmental Research Laboratory. Plant Uptake of Cadmium from Phosphate Fertilizer; US Environment Protection Agency: Portland, OR, USA, 1976. [Google Scholar]
- Jayasumana, C.; Orantes, C.; Herrera, R.; Almaguer, M.; Lopez, L.; Silva, L.C.; Ordunez, P.; Siribaddana, S.; Gunatilake, S.; De Broe, M.E. Chronic interstitial nephritis in agricultural communities: A worldwide epidemic with social, occupational and environmental determinants. Nephrol. Dialysis Transplant. Off. Public. Eur Dialysis Transpl. Assoc. Eur. Renal Assoc. 2017, 32, 234–241. [Google Scholar] [CrossRef] [PubMed]
- Chandrajith, R.; Seneviratna, S.; Wickramaarachchi, K.; Attanayake, T.; Aturaliya, T.N.C.; Dissanayake, C.B. Natural radionuclides and trace elements in rice field soils in relation to fertilizer application: Study of a chronic kidney disease area in Sri Lanka. Environ. Earth Sci. 2010, 60, 193–201. [Google Scholar] [CrossRef]
- Tóth, G.; Hermann, T.; Da Silva, M.R.; Montanarella, L. Heavy metals in agricultural soils of the European Union with implications for food safety. Environ. Int. 2016, 88, 299–309. [Google Scholar] [CrossRef] [PubMed]
- Loganathan, P.; Hedley, M.J.; Grace, N.D. Pasture soils contaminated with fertilizer-derived cadmium and fluorine: Livestock effects. Rev. Environ. Contamin. Toxicol. 2008, 192, 29–66. [Google Scholar] [CrossRef]
- Barančíková, G.; Madams, M.; Rybàr, O. Crop contamination by selected trace elements. J. Soils Sediments 2004, 4, 37–42. [Google Scholar] [CrossRef]
- Dharma-wardana, M.W.C. Chronic kidney disease of unknown etiology and the effect of multiple-ion interactions. Environ. Geochem. Health 2018, 40, 705–719. [Google Scholar] [CrossRef]
- Ndambi, O.A.; Pelster, D.E.; Owino, J.O.; de Buisonjé, F.; Vellinga, T. Manure Management Practices and Policies in Sub-Saharan Africa: Implications on Manure Quality as a Fertilizer. Front. Sustain. Food Syst. 2019, 3, 29. [Google Scholar] [CrossRef]
- United States Department for Agriculture (USDA) Economic Research Service. International Agricultural Productivity. 2023. Available online: https://www.ers.usda.gov/data-products/international-agricultural-productivity (accessed on 1 September 2024).
- 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]
Element | Description |
---|---|
Population | Humans of all age groups without language or geographical limitations |
Exposure | Exposure to fertilizers (inorganic and organic) through occupational or residential exposure |
Comparator | Non-exposed individuals or those with lower levels of exposure |
Outcome | Health-related outcomes including cancer, multiple myeloma, infections, diarrhea, amyotrophic lateral sclerosis, rheumatoid arthritis, narcolepsy, polydactyly, aplastic anemia, and Creutzfeldt–Jakob disease |
Health Outcome | Type of Exposure | Study Type | Results | Quality Assessment |
---|---|---|---|---|
Non-Malignant Outcomes | ||||
(a) Infectious Diseases | ||||
Analytical Studies | ||||
Creutzfeldt–Jakob disease (CJD) | Both | Case-control | Inverse association, NS | Good |
Tuberculosis | Occupational | Exposure Cohort | Inverse association, NS | Poor |
(b) Allergies and Atopy | ||||
Descriptive Studies | ||||
Asthma | Both | Cross-sectional | Adverse association, NS | Moderate |
Asthma | Occupational | Cross-sectional | Adverse association, NS | Moderate |
(c) Neurological Outcomes | ||||
Analytical Studies | ||||
Amyotrophic Lateral Sclerosis (ALS) | Both | Case-control | Adverse association, NS | Moderate |
Narcolepsy | Occupational | Case-control | Adverse association, NS | Moderate |
Vascular Dementia | Occupational | Case-control | Adverse association * | Moderate |
(d) Other Outcomes | ||||
Analytical Studies | ||||
Alcoholism | Occupational | Cohort | Inverse association, NS | Poor |
All-cause mortality | Occupational | Cohort | Adverse association * | Poor |
Aplastic Anemia | Both | Case-control | Adverse association, SNR | Moderate |
Esophageal atresia | Occupational | Cohort | Adverse association, NS | Moderate |
Polydactyly | Occupational | Cohort | Adverse association, NS | Moderate |
Rheumatoid Arthritis | Occupational | Cohort | Adverse association * | Moderate |
Skin conditions (rash/lesions/ulcer) | Occupational | Case-control | Adverse association, NS | Moderate |
Skin conditions (rash/lesions/ulcer) | Occupational | Cohort | Adverse association ** | Poor |
Syndactyly | Occupational | Cohort | Adverse association * | Moderate |
Descriptive Studies | ||||
Bronchitis (acute and chronic) | Environmental | Cross-sectional | Inverse association, NS | Moderate |
Bronchitis (acute and chronic) | Environmental | Cross-sectional | Adverse association, NS | Moderate |
Bronchitis (acute and chronic) | Environmental | Cross-sectional | Adverse association * | Poor |
Bronchitis (acute and chronic) | Occupational | Cross-sectional | Adverse association * | Moderate |
Emphysema | Environmental | Cross-sectional | Adverse association * | Poor |
Skin conditions (rash/lesions/ulcer) | Environmental | Cross-sectional | Adverse association * | Poor |
Malignant Outcomes | ||||
Analytical Studies | ||||
Acute Leukemia (AML, ALL, ANLL) | Occupational | Case-control | Adverse association * | Moderate |
Acute Leukemia (AML, ALL, ANLL) | Occupational | Case-control | Adverse association * | Poor |
Acute Leukemia (AML, ALL, ANLL) | Occupational | Case-control | Adverse association * | Moderate |
All Cancer Mortality | Occupational | Exposure Cohort | Adverse association, NS | Poor |
All Cancer Mortality | Occupational | Exposure Cohort | Adverse association * | Poor |
All Cancer Mortality | Occupational | Exposure Cohort | Inverse association, NS | Poor |
B-cell neoplasms | Occupational | Case-control | Adverse association * | Moderate |
Brain tumors (glioma, meningioma, neuroblastoma) | Occupational | Case-control | Adverse association, NS | Moderate |
Brain tumors (glioma, meningioma, neuroblastoma) | Occupational | Case-control | Adverse association * | Moderate |
Brain tumors (glioma, meningioma, neuroblastoma) | Occupational | Case-control | Adverse association * | Poor |
Breast cancer | Occupational | Exposure Cohort | Inverse association, NS | Poor |
Buccal cavity and pharynx Cancer | Occupational | Exposure Cohort | Inverse association, NS | Poor |
Cancer of male genital organs | Occupational | Case-control | Adverse association * | Moderate |
Cancer of male genital organs | Occupational | Exposure Cohort | Adverse association * | Moderate |
Cancer of male genital organs | Occupational | Exposure Cohort | Adverse association, NS | Poor |
Cancer of other male genital organs | Occupational | Exposure Cohort | Adverse association * | Poor |
Cancer of other and unspecified organs | Occupational | Exposure Cohort | Adverse association, NS | Poor |
Cancer of trachea, bronchus, and lung | Occupational | Exposure Cohort | Adverse association * | Poor |
Chronic Leukemia (CLL, CML, SLL) | Both | Case-control | Adverse association * | Moderate |
Chronic Leukemia (CLL, CML, SLL) | Occupational | Case-control | Adverse association, NS | Moderate |
Colon cancer | Occupational | Exposure Cohort | Inverse association, NS | Poor |
Connective tissue cancer | Occupational | Exposure Cohort | Inverse association, NS | Poor |
Digestive system and peritoneum cancer | Occupational | Exposure Cohort | Inverse association, NS | Poor |
Gastric cancer | Occupational | Case-control | Adverse association, NS | Moderate |
Gastric cancer | Occupational | Case-control | Adverse Association, NS | Moderate |
Gastric cancer | Occupational | Exposure Cohort | Inverse association, NS | Poor |
Gastric cancer | Occupational | Exposure Cohort | Inverse association, NS | Poor |
Gastric cancer | Occupational | Exposure Cohort | Adverse Association, NS | Poor |
Germ cell cancer | Occupational | Case-control | Adverse Association, NS | Moderate |
Hematological Malignancies | Occupational | Case-control | Adverse association * | Poor |
Leukemia | Occupational | Exposure Cohort | Adverse association * | Poor |
Lung cancer | Occupational | Case-control | Adverse association, NS | Moderate |
Lung cancer | Occupational | Exposure Cohort | Adverse Association, NS | Poor |
Lung cancer | Occupational | Exposure Cohort | Adverse association, NS | Poor |
Monoclonal gammopathy of undetermined significance (MGUS) | Occupational | Case-control | Adverse association * | Poor |
Monoclonal gammopathy of undetermined significance (MGUS) | Occupational | Case-control | Adverse association * | Moderate |
Multiple myeloma | Both | Case-control | Adverse association, NS | Moderate |
Myelodysplastic syndrome | Occupational | Case-control | Adverse association * | Good |
Mesothelioma | Occupational | Exposure Cohort | Adverse Association, NS | Poor |
Mesothelioma | Occupational | Exposure Cohort | Adverse Association, SNR | Poor |
Pancreatic cancer | Occupational | Exposure Cohort | Adverse Association, NS | Poor |
Pancreatic cancer | Occupational | Exposure Cohort | Adverse association, NS | Poor |
Pharynx cancer | Occupational | Exposure Cohort | Inverse association, NS | Poor |
Rectum cancer | Occupational | Exposure Cohort | Inverse association, NS | Poor |
Rectum cancer | Occupational | Exposure Cohort | Inverse association, NS | Poor |
Respiratory system cancer | Occupational | Exposure Cohort | Adverse association * | Poor |
Skin cancer | Occupational | Exposure Cohort | Inverse association, NS | Poor |
Skin cancer | Occupational | Exposure Cohort | Adverse association, NS | Poor |
T/NK-cell neoplasms | Occupational | Case-control | Inverse association, NS | Moderate |
Tongue cancer | Occupational | Exposure Cohort | Inverse association, NS | Poor |
Uveal Melanoma | Occupational | Case-control | Adverse association * | Poor |
Urinary tract cancer (Renal and bladder) | Environmental | Case-control | Adverse association, NS | Poor |
Urinary tract cancer (Renal and bladder) | Occupational | Exposure Cohort | Adverse association, NS | Poor |
Urinary tract cancer (Renal and bladder) | Occupational | Exposure Cohort | Adverse association, NS | Poor |
Descriptive Studies | ||||
Acute Leukemia (AML, ALL, ANLL) | Environmental | Cross-sectional | Adverse association, SNR | Moderate |
Brain tumors (glioma, meningioma, neuroblastoma) | Environmental | Cross-sectional | Adverse association, SNR | Moderate |
Ewing’s sarcoma | Environmental | Cross-sectional | Adverse association, SNR | Moderate |
Leukemia | NR | Ecological study | Inverse association * | Poor |
Leukemia | Occupational | Ecological study | Adverse association * | Moderate |
Lymphoma (Hodgkin and Non-Hodgkin) | Environmental | Cross-sectional | Adverse association, SNR | Moderate |
Multiple myeloma | NR | Ecological study | Adverse Association, NS | Poor |
Multiple myeloma | Occupational | Ecological study | Adverse association * | Moderate |
Non-Hodgkin Lymphoma | NR | Ecological study | Adverse Association, NS | Poor |
Osteosarcoma | Environmental | Cross-sectional | Adverse association, SNR | Moderate |
Ovarian cancer mortality | NR | Ecological study | Adverse association * | Poor |
Wilm’s Tumor | Environmental | Cross-sectional | Inverse association, SNR | Moderate |
Health Outcome | Type of Exposure | Study Type | Results | Quality Assessment |
---|---|---|---|---|
Non-Malignant Outcomes | ||||
(a) Infectious Diseases | ||||
Analytical Studies | ||||
Community-acquired MRSA | Both | Nested case-control | Adverse association ** | Moderate |
Creutzfeldt–Jakob disease (CJD) | Both | Case-control | Adverse association ** | Good |
Cutaneous leishmaniasis | Environmental | Case-control | Adverse association (NS) | Poor |
Hospital-acquired MRSA | Both | Nested case-control | Inverse association * | Moderate |
Skin/soft tissue infection | Both | Nested case-control | Adverse association ** | Moderate |
Descriptive Studies | ||||
Acute Bronchitis | Environmental | Cross-sectional | Inverse association ** | Poor |
Escherichia coli O157 antibodies | Environmental | Cross-sectional | Adverse association ** | Good |
Helminth Infection | Environmental | Cross-sectional | Adverse association (NS) | Poor |
Household poultry positive for C. jejuni | Occupational | Cross-sectional | Adverse association ** | Good |
Malaria and Soil-Transmitted Helminthiasis | Environmental | Cross-sectional | Adverse association ** | Moderate |
Q fever seroprevalence against C. burnetii | NR | Cross-sectional | Adverse association ** | Poor |
Schistosomiasis | Environmental | Cross-sectional | Inverse association (NS) | Poor |
(b) Allergies and Atopy | ||||
Analytical Studies | ||||
Asthma | Environmental | Cohort | Inverse association ** | Good |
Atopic dermatitis | Environmental | Cohort | Inverse association ** | Good |
Hay Fever | Environmental | Cohort | Inverse association ** | Good |
(c) Other Outcomes, including symptoms | ||||
Analytical Studies | ||||
Aplastic anemia | Occupational | Case-control | Adverse association ** | Moderate |
Rheumatoid Arthritis | Occupational | Cohort | Inverse association (NS) | Moderate |
Descriptive Studies | ||||
Chronic Bronchitis | Occupational | Cross-sectional | Adverse association ** | Moderate |
Emphysema | Environmental | Cross-sectional | Adverse association * | Poor |
Skin ulcer | Environmental | Cross-sectional | Adverse association * | Poor |
Malignant Outcomes | ||||
Analytical Studies | ||||
Lung cancer | Occupational | Case-control | Adverse association (NS) | Moderate |
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. |
© 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Tagkas, C.F.; Rizos, E.C.; Markozannes, G.; Karalexi, M.A.; Wairegi, L.; Ntzani, E.E. Fertilizers and Human Health—A Systematic Review of the Epidemiological Evidence. Toxics 2024, 12, 694. https://doi.org/10.3390/toxics12100694
Tagkas CF, Rizos EC, Markozannes G, Karalexi MA, Wairegi L, Ntzani EE. Fertilizers and Human Health—A Systematic Review of the Epidemiological Evidence. Toxics. 2024; 12(10):694. https://doi.org/10.3390/toxics12100694
Chicago/Turabian StyleTagkas, Christos F., Evangelos C. Rizos, Georgios Markozannes, Maria A. Karalexi, Lydia Wairegi, and Evangelia E. Ntzani. 2024. "Fertilizers and Human Health—A Systematic Review of the Epidemiological Evidence" Toxics 12, no. 10: 694. https://doi.org/10.3390/toxics12100694
APA StyleTagkas, C. F., Rizos, E. C., Markozannes, G., Karalexi, M. A., Wairegi, L., & Ntzani, E. E. (2024). Fertilizers and Human Health—A Systematic Review of the Epidemiological Evidence. Toxics, 12(10), 694. https://doi.org/10.3390/toxics12100694