Prevalence and Risk Factors of Schistosomiasis among School-Age Children and Adolescents in Zaria, Kaduna State, Nigeria
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335-345
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10.58578/ajmsphr.v3i3.11652
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Authors:Tanko A. Nanret1*, Suchi K. Nanret2, Orinya Alfred3, Ejembi Joan4, Olanrewaju Jimoh5, Dimowo C. Palangutde6, Ahmed S. Opaluwa7, Abdulaziz M. Mukhtar8, Medugu Nubua9
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Abstract
Nigeria bears the world’s highest burden of schistosomiasis, with school-aged children and adolescents experiencing particularly high prevalence and infection intensity. In Zaria metropolis, the abundance of water bodies and frequent water-contact activities, including irrigation farming and swimming, may increase the risk of transmission. This study aimed to determine the prevalence of schistosomiasis and identify its associated risk factors among school-aged children and adolescents in Zaria metropolis. A community-based cross-sectional study was conducted among individuals aged 6–19 years using a multistage sampling technique to select communities, clusters, and households. Stool and urine samples were collected from eligible participants and examined for ova of Schistosoma species using standard laboratory techniques. Demographic characteristics and potential risk factors were assessed using a structured questionnaire, and the data were analysed using SPSS version 26. A total of 423 participants were recruited from the Biye, Bomo, Wuchichiri, and Kufena communities. The overall prevalence of schistosomiasis was 10.6% (45/423), comprising 9.5% (40/423) urinary schistosomiasis caused by Schistosoma haematobium and 1.2% (5/423) intestinal schistosomiasis caused by Schistosoma mansoni. Frequent water contact through swimming and irrigation farming was significantly associated with increased odds of infection (adjusted odds ratio [AOR] = 2.688, 95% confidence interval [CI]: 1.341–5.386, p = .005), while geographical location was also independently associated with schistosomiasis (AOR = 0.275, 95% CI: 0.102–0.740, p = .011). These findings indicate a high prevalence of schistosomiasis among school-aged children and adolescents in Zaria metropolis and demonstrate the importance of water-contact behaviour and geographical context in sustaining transmission. The study provides epidemiological evidence to support geographically targeted interventions, health education, reduced exposure to infested water bodies, and strengthened schistosomiasis prevention and control programmes.
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References
Boutayeb, A. (2010). The impact of infectious diseases on the development of Africa. In V. R. Preedy & R. R. Watson (Eds.), Handbook of disease burdens and quality of life measures (pp. 1171–1188). Springer. https://doi.org/10.1007/978-0-387-78665-0_66
Aula, O. P., McManus, D. P., Jones, M. K., & Gordon, C. A. (2021). Schistosomiasis with a focus on Africa. Tropical Medicine and Infectious Disease, 6(3), 109. https://doi.org/10.3390/tropicalmed6030109
Colley, D. G., Bustinduy, A. L., Secor, W. E., & King, C. H. (2014). Human schistosomiasis. The Lancet, 383(9936), 2253–2264. https://doi.org/10.1016/S0140-6736(13)61949-2
Weerakoon, K. G., Gordon, C. A., Williams, G. M., Cai, P., Gobert, G. N., Olveda, R. M., Ross, A. G., Olveda, D. U., & McManus, D. P. (2018). Co-parasitism of intestinal protozoa and Schistosoma japonicum in a rural community in the Philippines. Infectious Diseases of Poverty, 7, Article 121. https://doi.org/10.1186/s40249-018-0504-6
GBD 2016 Disease and Injury Incidence and Prevalence Collaborators. (2017). Global, regional, and national incidence, prevalence, and years lived with disability for 328 diseases and injuries for 195 countries, 1990–2016: A systematic analysis for the Global Burden of Disease Study 2016. The Lancet, 390(10100), 1211–1259. https://doi.org/10.1016/S0140-6736(17)32154-2
Onyekwere, A. M., Rey, O., Nwanchor, M. C., Alo, M., Angora, E. K., Allienne, J. F., & Boissier, J. (2022). Prevalence and risk factors associated with urogenital schistosomiasis among primary school pupils in Nigeria. Parasite Epidemiology and Control, 18, e00255. https://doi.org/10.1016/j.parepi.2022.e00255
Uneke, C., Ugwuoke-Adibuah, S., Nwakpu, K., & Ngwu, B. (2009). An assessment of Schistosoma haematobium infection and urinary tract bacterial infection amongst school children in rural eastern Nigeria. The Internet Journal of Laboratory Medicine, 4(1), 1–6. https://ispub.com/IJLM/4/1/3651
Bishop, H. G., & Akoh, R. I. (2018). Risk factors, symptoms and effects of urinary schistosomiasis on anthropometric indices of school children in Zaria, Kaduna State, Nigeria. Open Access Journal of Science, 2(1), 61–65. https://doi.org/10.15406/oajs.2018.02.00045
Marege, A., Seid, M., Boke, B., Thomas, S., Arage, M., Mouze, N., Yohanes, T., Woldemariam, M., & Manilal, A. (2021). Prevalence of Schistosoma mansoni–Salmonella coinfection among patients in southern Ethiopia. New Microbes and New Infections, 40, 100842. https://doi.org/10.1016/j.nmni.2021.100842
Weerakoon, K. G., & McManus, D. P. (2016). Cell-free DNA as a diagnostic tool for human parasitic infections. Trends in Parasitology, 32(5), 378–391. https://doi.org/10.1016/j.pt.2016.01.006
Gray, D. J., Ross, A. G., Li, Y.-S., & McManus, D. P. (2011). Diagnosis and management of schistosomiasis. BMJ, 342, d2651. https://doi.org/10.1136/bmj.d2651
Cheesbrough, M. (2006). Microbiological tests. In M. Cheesbrough, District laboratory practice in tropical countries: Part 2 (2nd ed., pp. 1–266). Cambridge University Press. https://doi.org/10.1017/CBO9780511543470.002
Bishop, H. G., & Akoh, R. I. (2018). Risk factors, symptoms and effects of urinary schistosomiasis on anthropometric indices of school children in Zaria, Kaduna State, Nigeria. Open Access Journal of Science, 2(1), 61–65. https://doi.org/10.15406/oajs.2018.02.00045
Iyanam, R. (2017). Prevalence of schistosomiasis among primary school children in Dakace District, Zaria Local Government Area, Kaduna State, Nigeria [Master’s dissertation, Ahmadu Bello University]. https://kubanni.abu.edu.ng/items/9e057fd0-4d3e-439f-9bc0-1475254e10c2/full