期刊论文详细信息
Particle and Fibre Toxicology
Schistosoma mansoni among pre-school children in Musozi village, Ukerewe Island, North-Western-Tanzania: prevalence and associated risk factors
Gerald M. Mkoji2  Domenica Morona3  Rebecca Waihenya4  Humphrey D. Mazigo3  Deodatus M. Ruganuza1 
[1] Institute of Tropical Medicine and Infectious Diseases (ITROMID), Jomo Kenyatta University of Agriculture and Technology, Nairobi, Kenya;Centre for Biotechnology Research and Development, Kenya Medical Research Institute (KEMRI), Nairobi, Kenya;Department of Medical Parasitology and Entomology, School of Medicine, Catholic University of Health and Allied Sciences, Mwanza, Tanzania;Department of Zoology, Jomo Kenyatta University of Agriculture and Technology, Nairobi, Kenya
关键词: Tanzania;    Pre-school children;    Intensity of infection;    S. mansoni prevalence;   
Others  :  1222207
DOI  :  10.1186/s13071-015-0997-9
 received in 2015-07-01, accepted in 2015-07-09,  发布年份 2015
PDF
【 摘 要 】

Background

Recent evidence indicates that pre-school children (PSC) living in S. mansoni highly endemic areas are at similar risk of schistosomiasis infection and morbidity as their school aged siblings. Recognizing this fact, the World Health Organization (WHO) is considering including this age group in highly endemic areas in control programmes using mass drug administration (MDA). However, detailed epidemiological information on S. mansoni infection among PSC is lacking for many endemic areas, specifically in Tanzania. This study was conducted to determine the prevalence of S. mansoni infection and its associated risk factors among PSC in Ukerewe Island, North-Western Tanzania.

Methods

This was a cross-sectional study, which studied 400 PSC aged 1–6 years. The Kato-Katz (K-K) technique and the point of care circulating cathodic antigen (CCA) immunodiagnostic test were used to diagnose S. mansoni infection in stool and urine samples respectively. A pre-tested questionnaire was used to collect demographic data and water contact behaviour of the children from their parents/guardians.

Results

Based on the K-K technique, 44.4 % (95 % CI: 39.4–49.4) pre-school children were infected with S. mansoni and the overall geometric mean eggs per gram of faeces (GM-epg) was 110.6 epg with 38.2 and 14.7 % having moderate and heavy intensity infections respectively. Based on the CCA, 80.1 %, (95 % CI: 76.0–84.0) were infected if a trace was considered positive, and 45.9 %, (95 % CI: 40.9–50.9), were infected if a trace was considered negative. Reported history of lake visits (AOR = 2.31, 95 % CI: 1.06–5.01, P < 0.03) and the proximity to the lake shore (<500 m) (AOR = 2.09, 95 % CI: 1.05–4.14, P < 0.03) were significantly associated with S. mansoni infection. Reported lake visit frequency (4–7 days/week) was associated with heavy intensities of S. mansoni infection (P < 0.00).

Conclusion

The prevalence of S. mansoni infection in the study population using K-K and CCA-trace-negative was moderate. The frequency of lake visits and the proximity to the lake shore were associated with the infection of S. mansoni and its intensity. These findings call for the need to include the PSC in MDA programmes, public health education and provision of safe water for bathing.

【 授权许可】

   
2015 Ruganuza et al.

【 预 览 】
附件列表
Files Size Format View
20150805113206836.pdf 1039KB PDF download
Fig. 4. 18KB Image download
Fig. 3. 83KB Image download
Fig. 2. 36KB Image download
Fig. 1. 79KB Image download
【 图 表 】

Fig. 1.

Fig. 2.

Fig. 3.

Fig. 4.

【 参考文献 】
  • [1]Hotez PJ, Kamath A. Neglected tropical diseases in sub-saharan Africa: review of their prevalence, distribution, and disease burden. PLoS Negl Trop Dis. 2009; 3(8):e412.
  • [2]van der Werf MJ, de Vlas SJ, Brooker S, Looman CW, Nagelkerke NJ, Habbema JD et al.. Quantification of clinical morbidity associated with schistosome infection in sub-Saharan Africa. Acta Trop. 2003; 86(2–3):125-39.
  • [3]King CH, Dickman K, Tisch DJ. Reassessment of the cost of chronic helmintic infection: a meta-analysis of disability-related outcomes in endemic schistosomiasis. Lancet. 2005; 365(9470):1561-9.
  • [4]King CH, Dangerfield-Cha M. The unacknowledged impact of chronic schistosomiasis. Chronic Illn. 2008; 4(1):65-79.
  • [5]Koukounari A, Fenwick A, Whawell S, Kabatereine NB, Kazibwe F, Tukahebwa EM et al.. Morbidity indicators of Schistosoma mansoni: relationship between infection and anemia in Ugandan schoolchildren before and after praziquantel and albendazole chemotherapy. Am J Trop Med Hyg. 2006; 75(2):278-86.
  • [6]Lwambo NJ, Siza JE, Brooker S, Bundy DA, Guyatt H. Patterns of concurrent hookworm infection and schistosomiasis in schoolchildren in Tanzania. Trans R Soc Trop Med Hyg. 1999; 93(5):497-502.
  • [7]Mazigo HD, Waihenya R, Lwambo NJ, Mnyone LL, Mahande AM, Seni J et al.. Co-infections with Plasmodium falciparum, Schistosoma mansoni and intestinal helminths among schoolchildren in endemic areas of northwestern Tanzania. Parasites Vectors. 2010; 3:44. BioMed Central Full Text
  • [8]Kinung’hi SM, Magnussen P, Kaatano GM, Kishamawe C, Vennervald BJ. Malaria and helminth co-infections in school and preschool children: a cross-sectional study in Magu district, north-western Tanzania. PLoS One. 2014; 9(1):e86510.
  • [9]Tanzania demographic and health survey 2010. National bureau of statistics (NBS) [Tanzania], ICF Macro, Dar es Salaam, Tanzania; 2011.
  • [10]Sousa-Figueiredo JC, Pleasant J, Day M, Betson M, Rollinson D, Montresor A et al.. Treatment of intestinal schistosomiasis in Ugandan preschool children: best diagnosis, treatment efficacy and side-effects, and an extended praziquantel dosing pole. Int Health. 2010; 2(2):103-13.
  • [11]Verani JR, Abudho B, Montgomery SP, Mwinzi PN, Shane HL, Butler SE et al.. Schistosomiasis among young children in Usoma, Kenya. Am J Trop Med Hyg. 2011; 84(5):787-91.
  • [12]Smith FM. Bilharziasis in the African infant and child in the Mtoko District, Southern Rhodesia. Cent Afr J Med. 1958; 4(7):287-8.
  • [13]Perel Y, Sellin B, Perel C, Arnold P, Mouchet F. Use of urine collectors for infants from 0 to 4 years of age in a mass survey of urinary schistosomiasis in Niger. Med Trop (Mars). 1985; 45(4):429-33.
  • [14]Kabatereine NB, Brooker S, Koukounari A, Kazibwe F, Tukahebwa EM, Fleming FM et al.. Impact of a national helminth control programme on infection and morbidity in Ugandan schoolchildren. Bull World Health Organ. 2007; 85(2):91-9.
  • [15]Bosompem KM, Bentum IA, Otchere J, Anyan WK, Brown CA, Osada Y et al.. Infant schistosomiasis in Ghana: a survey in an irrigation community. Trop Med Int Health. 2004; 9(8):917-22.
  • [16]Odogwu SE, Ramamurthy NK, Kabatereine NB, Kazibwe F, Tukahebwa E, Webster JP et al.. Schistosoma mansoni in infants (aged < 3 years) along the Ugandan shoreline of Lake Victoria. Ann Trop Med Parasitol. 2006; 100(4):315-26.
  • [17]Mafiana CF, Ekpo UF, Ojo DA. Urinary schistosomiasis in preschool children in settlements around Oyan Reservoir in Ogun State, Nigeria: implications for control. Trop Med Int Health. 2003; 8(1):78-82.
  • [18]Stothard JR, Gabrielli AF. Schistosomiasis in African infants and preschool children: to treat or not to treat? Trends Parasitol. 2007; 23(3):83-6.
  • [19]Opara KN, Udoidung NI, Ukpong IG. Genitourinary schistosomiasis among pre-primary schoolchildren in a rural community within the Cross River Basin, Nigeria. J Helminthol. 2007; 81(4):393-7.
  • [20]Ekpo UF, Laja-Deile A, Oluwole AS, Sam-Wobo SO, Mafiana CF. Urinary schistosomiasis among preschool children in a rural community near Abeokuta, Nigeria. Parasites Vectors. 2010; 3:58. BioMed Central Full Text
  • [21]Jordan P, Webbe G. Human schistosomiasis. Human schistosomiasis. 1969.
  • [22]van Lieshout L, Polderman AM, Deelder AM. Immunodiagnosis of schistosomiasis by determination of the circulating antigens CAA and CCA, in particular in individuals with recent or light infections. Acta Trop. 2000; 77(1):69-80.
  • [23]Berhe N, Medhin G, Erko B, Smith T, Gedamu S, Bereded D et al.. Variations in helminth faecal egg counts in Kato-Katz thick smears and their implications in assessing infection status with Schistosoma mansoni. Acta Trop. 2004; 92(3):205-12.
  • [24]Bergquist R, Johansen MV, Utzinger J. Diagnostic dilemmas in helminthology: what tools to use and when? Trends Parasitol. 2009; 25(4):151-6.
  • [25]Johansen MV, Sithithaworn P, Bergquist R, Utzinger J. Towards improved diagnosis of zoonotic trematode infections in Southeast Asia. Adv Parasitol. 2010; 73:171-95.
  • [26]Utzinger J, Booth M, N’Goran EK, Muller I, Tanner M, Lengeler C. Relative contribution of day-to-day and intra-specimen variation in faecal egg counts of Schistosoma mansoni before and after treatment with praziquantel. Parasitology. 2001; 122(Pt 5):537-44.
  • [27]Booth M, Vounatsou P, N’Goran EK, Tanner M, Utzinger J. The influence of sampling effort and the performance of the Kato-Katz technique in diagnosing Schistosoma mansoni and hookworm co-infections in rural Cote d’Ivoire. Parasitology. 2003; 127(Pt 6):525-31.
  • [28]Yu JM, de Vlas SJ, Jiang QW, Gryseels B. Comparison of the Kato-Katz technique, hatching test and indirect hemagglutination assay (IHA) for the diagnosis of Schistosoma japonicum infection in China. Parasitol Int. 2007; 56(1):45-9.
  • [29]Lin DD, Liu JX, Liu YM, Hu F, Zhang YY, Xu JM et al.. Routine Kato-Katz technique underestimates the prevalence of Schistosoma japonicum: a case study in an endemic area of the People’s Republic of China. Parasitol Int. 2008; 57(3):281-6.
  • [30]Legesse M, Erko B. Field-based evaluation of a reagent strip test for diagnosis of Schistosoma mansoni by detecting circulating cathodic antigen in urine before and after chemotherapy. Trans R Soc Trop Med Hyg. 2007; 101(7):668-73.
  • [31]Ashton RA, Stewart BT, Petty N, Lado M, Finn T, Brooker S et al.. Accuracy of circulating cathodic antigen tests for rapid mapping of Schistosoma mansoni and S. haematobium infections in Southern Sudan. Trop Med Int Health. 2011; 16(9):1099-103.
  • [32]Coulibaly JT, N’Gbesso YK, N’Guessan NA, Winkler MS, Utzinger J, N’Goran EK. Epidemiology of schistosomiasis in two high-risk communities of south Cote d’Ivoire with particular emphasis on pre-school-aged children. Am J Trop Med Hyg. 2013; 89(1):32-41.
  • [33]Navaratnam AM, Mutumba-Nakalembe MJ, Stothard JR, Kabatereine NB, Fenwick A, Sousa-Figueiredo JC. Notes on the use of urine-CCA dipsticks for detection of intestinal schistosomiasis in preschool children. Trans R Soc Trop Med Hyg. 2012; 106(10):619-22.
  • [34]Standley CJ, Lwambo NJ, Lange CN, Kariuki HC, Adriko M, Stothard JR. Performance of circulating cathodic antigen (CCA) urine-dipsticks for rapid detection of intestinal schistosomiasis in schoolchildren from shoreline communities of Lake Victoria. Parasites Vectors. 2010; 3(1):7. BioMed Central Full Text
  • [35]Stothard JR, Kabatereine NB, Tukahebwa EM, Kazibwe F, Rollinson D, Mathieson W et al.. Use of circulating cathodic antigen (CCA) dipsticks for detection of intestinal and urinary schistosomiasis. Acta Trop. 2006; 97(2):219-28.
  • [36]Shane HL, Verani JR, Abudho B, Montgomery SP, Blackstock AJ, Mwinzi PN et al.. Evaluation of urine CCA assays for detection of Schistosoma mansoni infection in Western Kenya. PLoS Negl Trop Dis. 2011; 5(1):e951.
  • [37]Garba A, Barkire N, Djibo A, Lamine MS, Sofo B, Gouvras AN et al.. Schistosomiasis in infants and preschool-aged children: Infection in a single Schistosoma haematobium and a mixed S. haematobium-S. mansoni foci of Niger. Acta Trop. 2010; 115(3):212-9.
  • [38]Rollinson D, Knopp S, Levitz S, Stothard JR, Tchuem Tchuente LA, Garba A et al.. Time to set the agenda for schistosomiasis elimination. Acta Trop. 2013; 128(2):423-40.
  • [39]2012 census database. 4th ed. National bureau of statistics, Tanzania; 2012.
  • [40]Katz N, Chaves A, Pellegrino J. A simple device for quantitative stool thick-smear technique in Schistosomiasis mansoni. Revista Instituto de Medicine Tropica Sao Paulo. 1972; 14(6):397-400.
  • [41]Barreto ML, Smith D, Sleigh AC. Implications of feacal egg count variation when using the Kato Katz method to assess S. mansoni infections. Trans R Soc Trop Med Hyg. 1990; 84:554-5.
  • [42]Van Dam G, Wichers J, Ferreira TF, Ghati D, Van Amerongen A, Deelder A. Diagnosis of schistosomiasis by reagent strip test for detection of circulating cathodic antigen. J Clin Microbiol. 2004; 42(12):5458-61.
  • [43]Basic laboratory methods in medical parasitology. 1991.
  • [44]Prevention and control of schistosomiasis and soil-transmitted helminthiasis. World Health Organ Tech Rep Ser. 2002; 912:i.
  • [45]Sousa-Figueiredo JC, Betson M, Kabatereine NB, Stothard JR. The urine circulating cathodic antigen (CCA) dipstick: a valid substitute for microscopy for mapping and point-of-care diagnosis of intestinal schistosomiasis. PLoS Negl Trop Dis. 2013; 7(1):e2008.
  • [46]Malenganisho WL, Magnussen P, Friis H, Siza J, Kaatano G, Temu M et al.. Schistosoma mansoni morbidity among adults in two villages along Lake Victoria shores in Mwanza District, Tanzania. Trans R Soc Trop Med Hyg. 2008; 102(6):532-41.
  • [47]Kardorff R, Gabone RM, Mugashe C, Obiga D, Ramarokoto CE, Mahlert C et al.. Schistosoma mansoni-related morbidity on Ukerewe Island, Tanzania: clinical, ultrasonographical and biochemical parameters. Trop Med Int Health. 1997; 2(3):230-9.
  • [48]Kloos H, Gazzinelli A, Van Zuyle P. Microgeographical patterns of schistosomiasis and water contact behavior; examples from Africa and Brazil. Mem Inst Oswaldo Cruz. 1998; 93 Suppl 1:37-50.
  • [49]Boisier P, Ramarokoto CE, Ravoniarimbinina P, Rabarijaona L, Ravaoalimalala VE. Geographic differences in hepatosplenic complications of schistosomiasis mansoni and explanatory factors of morbidity. Trop Med Int Health. 2001; 6(9):699-706.
  • [50]Berhe N, Myrvang B, Gundersen SG. Intensity of Schistosoma mansoni, hepatitis B, age, and sex predict levels of hepatic periportal thickening/fibrosis (PPT/F): a large-scale community-based study in Ethiopia. Am J Trop Med Hyg. 2007; 77(6):1079-86.
  • [51]Gurarie D, Wang X, Bustinduy AL, King CH. Modeling the effect of chronic schistosomiasis on childhood development and the potential for catch-up growth with different drug treatment strategies promoted for control of endemic schistosomiasis. Am J Trop Med Hyg. 2011; 84(5):773-81.
  • [52]Terer CC, Bustinduy AL, Magtanong RV, Muhoho N, Mungai PL, Muchiri EM et al.. Evaluation of the health-related quality of life of children in Schistosoma haematobium-endemic communities in Kenya: a cross-sectional study. PLoS Negl Trop Dis. 2013; 7(3):e2106.
  • [53]Handzel T, Karanja DM, Addiss DG, Hightower AW, Rosen DH, Colley DG et al.. Geographic distribution of schistosomiasis and soil-transmitted helminths in Western Kenya: implications for anthelminthic mass treatment. Am J Trop Med Hyg. 2003; 69(3):318-23.
  文献评价指标  
  下载次数:7次 浏览次数:3次