BMC Infectious Diseases | |
Micro-geographical variation in exposure to Schistosoma mansoni and malaria, and exacerbation of splenomegaly in Kenyan school-aged children | |
David W Dunne8  Eric Muchiri2  John H Ouma4  Amos Otedo6  Joseph K Mwatha6  Gachuhi Kimani6  Clifford Amaganga5  Edmund Ireri6  Hilda Kadzo1  Henry C Kariuki2  Anthony E Butterworth7  LeeCarol Kenty8  Birgitte J Vennervald3  Mark Booth8  | |
[1] Kenyatta National Hospital, Nairobi, Kenya;Division of Vector Borne Diseases, Ministry of Health, P.O Box 54840, Nairobi, Kenya;Danish Bilharziasis Laboratory, Jægersborg Alle 1D, 2920 Charlottenlund, Denmark;Maseno University, Maseno, Kenya;Kakamega Provincial Hospital, P.O. Box 560, Kakamega, Kenya;Kenya Medical Research Institute, Nairobi, Kenya;Biomedical Research and Training Institute, P.O. Box CY 1753, Causeway, Harare, Zimbabwe;Division of Microbiology and Parasitology, Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge, CB2 1QP, UK | |
关键词: GIS; children; Kenya; splenomegaly; malaria; S. mansoni; | |
Others : 1177095 DOI : 10.1186/1471-2334-4-13 |
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received in 2003-11-17, accepted in 2004-05-17, 发布年份 2004 | |
【 摘 要 】
Background
Schistosoma mansoni and Plasmodium falciparum are common infections of school aged children in Kenya. They both cause enlargement of the spleen, but their relative contribution to the condition of splenomegaly remains unknown in areas where both infections are endemic. Here, we have investigated whether relatively high exposure to both infections has a clinically measurable effect on this condition.
Methods
96 children aged 6–16 years living along a ten kilometre stretch and within 4 km south of a river that is a source of both S. mansoni and malaria infections were examined clinically for splenomegaly along the mid clavicular line (MCL) and mid axillary line (MAL). The survey was conducted outside the malaria transmission season. The consistency of the organ was recorded as soft, firm or hard. Mapping of the locations of houses and the course of the river was undertaken. Egg counts were mapped at the household level, as were IgG3 responses to Plasmodium falciparum schizont antigen (anti-Pfs IgG3), in order to identify areas with relatively high exposure to both infections, either infection or neither infection. ANOVA was used to test for differences in egg counts, IgG3 levels and the magnitude of spleen enlargement between these areas.
Results
4 contiguous sectors were identified, one where anti-Pfs IgG3 responses and S. mansoni egg counts were both high, one where only anti-Pfs IgG3 responses were high, one where only egg counts were high, and one where both anti-Pfs IgG3 responses and egg counts were low. Spleen MAL and MCL values were significantly higher amongst children from the sector with highest IgG3 levels and highest egg counts but similar amongst children from elsewhere. Both egg counts and anti-Pfs IgG3 responses were significantly higher in children with MAL values >=4 cm. Hardening of spleens was associated with proximity of domicile to the river.
Conclusions
Micro-geographical variation in exposure to S. mansoni and malaria infections can be exploited to investigate the chronic impact of these two infections. These results provide firm evidence that relatively high exposure to both infections exacerbates splenomegaly even outside the malaria transmission season. Major implications include assessing the burden of infection in school age-children.
【 授权许可】
2004 Booth et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
【 预 览 】
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【 参考文献 】
- [1]Buck AA, Anderson RI, MacRae AA: Epidemiology of poly-parasitism. I. Occurrence, frequency and distribution of multiple infections in rural communities in Chad, Peru, Afghanistan, and Zaire. Tropenmed Parasitol 1978, 29:61-70.
- [2]Booth M, Bundy DA: Estimating the number of multiple-species geohelminth infections in human communities. Parasitology 1995, 111 ( Pt 5):645-653.
- [3]Howard SC, Donnell CA, Chan MS: Methods for estimation of associations between multiple species parasite infections. Parasitology 2001, 122:233-251.
- [4]Booth M: The application of attributable risk analysis in helminth epidemiology. Parasitology Today 1998, 14:497 -4500.
- [5]Nelson GS: Schistosoma mansoni infection in the West Nile District of Uganda part III. the spleen and S. mansoni infection. East African Medical Journal 1957, 35:543 -5547.
- [6]Ongom VL, Bradley DJ: The epidemiology and consequences of Schistosoma mansoni infection in West Nile, Uganda. I. Field studies of a community at Panyagoro. Trans R Soc Trop Med Hyg 1972, 66:835-851.
- [7]Buck AA, Anderson RI, MacRae AA: Epidemiology of poly-parasitism. IV. Combined effects on the state of health. Tropenmed Parasitol 1978, 29:253-268.
- [8]Whittle H, Gelfand M, Sampson E, Purvis A, Weber M: Enlarged livers and spleens in an area endemic for malaria and schistosomiasis. Trans R Soc Trop Med Hyg 1969, 63:353-361.
- [9]Fulford AJ, Mbugua GG, Ouma JH, Kariuki HC, Sturrock RF, Butterworth AE: Differences in the rate of hepatosplenomegaly due to Schistosoma mansoni infection between two areas in Machakos District, Kenya. Trans R Soc Trop Med Hyg 1991, 85:481-488.
- [10]Mwatha JK, Jones FM, Mohamed G, Naus CW, Riley EM, Butterworth AE, Kimani G, Kariuki CH, Ouma JH, Koech D, Dunne DW: Associations between anti-Schistosoma mansoni and anti-Plasmodium falciparum antibody responses and hepatosplenomegaly, in Kenyan schoolchildren. J Infect Dis 2003, 187:1337-1341.
- [11]Clarke SE, Bogh C, Brown RC, Walraven GE, Thomas CJ, Lindsay SW: Risk of malaria attacks in Gambian children is greater away from malaria vector breeding sites. Trans R Soc Trop Med Hyg 2002, 96:499-506.
- [12]Vennervald BJ, Kenty LC, Butterworth AE, Kariuki CH, Kadzo H, Ireri E, Amaganga C, Gachuhi K, Mwatha JK, Otedo A, Booth M, Ouma JH, Dunne DW: Detailed clinical and ultrasound examination of children and adolescents in a Schistosoma mansoni endemic area in Kenya: hepatosplenic disease in the absence of portal fibrosis. Tropical Medicine and International Health 2004, 9:461 -4470.
- [13]Katz N, Chaves A, Pellegrino J: A simple device for quantitative stool thick-smear technique in schistosomiasis mansoni. Revista do Instituto de Medicina Tropical de Sao Paulo 1972, 14:397-400.
- [14]Naus CW, Jones FM, Satti MZ, Joseph S, Riley EM, Kimani G, Mwatha JK, Kariuki CH, Ouma JH, Kabatereine NB, Vennervald BJ, Dunne DW: Serological responses among individuals in areas where both schistosomiasis and malaria are endemic: cross-reactivity between Schistosoma mansoni and Plasmodium falciparum. J Infect Dis 2003, 187:1272-1282.
- [15]Greenwood BM: The microepidemiology of malaria and its importance to malaria control. Trans R Soc Trop Med Hyg 1989, 83 Suppl:25-29.
- [16]Smith T, Charlwood JD, Takken W, Tanner M, Spiegelhalter DJ: Mapping the densities of malaria vectors within a single village. Acta Trop 1995, 59:1-18.
- [17]Smith T, Charlwood JD, Kitua AY, Masanja H, Mwankusye S, Alonso PL, Tanner M: Relationships of malaria morbidity with exposure to Plasmodium falciparum in young children in a highly endemic area. Am J Trop Med Hyg 1998, 59:252-257.
- [18]Thomas CJ, Lindsay SW: Local-scale variation in malaria infection amongst rural Gambian children estimated by satellite remote sensing. Trans R Soc Trop Med Hyg 2000, 94:159-163.
- [19]Kloos H, Fulford AJ, Butterworth AE, Sturrock RF, Ouma JH, Kariuki HC, Thiongo FW, Dalton PR, Klumpp RK: Spatial patterns of human water contact and Schistosoma mansoni transmission and infection in four rural areas in Machakos District, Kenya. Soc Sci Med 1997, 44:949-968.
- [20]Klumpp RK, Webbe G: Focal, seasonal and behavioural patterns of infection and transmission of Schistosoma haematobium in a farming village at the Volta Lake, Ghana. J Trop Med Hyg 1987, 90:265-281.
- [21]Sturrock RF, Klumpp RK, Ouma JH, Butterworth AE, Fulford AJ, Kariuki HC, Thiongo FW, Koech D: Observations on the effects of different chemotherapy strategies on the transmission of Schistosoma mansoni in Machakos District, Kenya, measured by long-term snail sampling and cercariometry. Parasitology 1994, 109 ( Pt 4):443-453.
- [22]Boutlis CS, Fagan PK, Gowda DC, Lagog M, Mgone CS, Bockarie MJ, Anstey NM: Immunoglobulin G (IgG) responses to Plasmodium falciparum glycosylphosphatidylinositols are short-lived and predominantly of the IgG3 subclass. J Infect Dis 2003, 187:862-865.
- [23]John CC, Zickafoose JS, Sumba PO, King CL, Kazura JW: Antibodies to the Plasmodium falciparum antigens circumsporozoite protein, thrombospondin-related adhesive protein, and liver-stage antigen 1 vary by ages of subjects and by season in a highland area of Kenya. Infect Immun 2003, 71:4320-4325.
- [24]Ferrante A, Rzepczyk CM: Atypical IgG subclass antibody responses to Plasmodium falciparum asexual stage antigens. Parasitology Today 1997, 13:145 -1148.
- [25]Kariuki SK, ter Kuile FO, Wannemuehler K, Terlouw DJ, Kolczak MS, Hawley WA, Phillips-Howard PA, Orago AS, Nahlen BL, Lal AA, Shi YP: Effects of permethrin-treated bed nets on immunity to malaria in western Kenya I. Antibody responses in pregnant women and cord blood in an area of intense malaria transmission. Am J Trop Med Hyg 2003, 68:61-67.
- [26]Trape JF, Lefebvre-Zante E, Legros F, Ndiaye G, Bouganali H, Druilhe P, Salem G: Vector density gradients and the epidemiology of urban malaria in Dakar, Senegal. Am J Trop Med Hyg 1992, 47:181-189.
- [27]Vennervald B, Booth M, Butterworth AE, Kariuki CH, Kadzo H, Ireri E, Amaganga C, Gachuhi K, Kenty LC, Mwatha JK, Ouma JH, Dunne DW: Regression of hepatosplenomegaly in Kenyan school-aged children after praziquantel treatment and in the absence of re-infection by Schistosoma mansoni. Transactions of the Royal Society of Tropical Medicine and Hygiene, in press.
- [28]Tebo AE, Kremsner PG, Piper KP, Luty AJ: Low antibody responses to variant surface antigens of Plasmodium falciparum are associated with severe malaria and increased susceptibility to malaria attacks in Gabonese children. Am J Trop Med Hyg 2002, 67:597-603.
- [29]Stirnadel HA, Beck HP, Alpers MP, Smith TA: Genetic analysis of IgG subclass responses against RESA and MSP2 of Plasmodium falciparum in adults in Papua New Guinea. Epidemiol Infect 2000, 124:153-162.
- [30]Aucan C, Traore Y, Fumoux F, Rihet P: Familial correlation of immunoglobulin G subclass responses to Plasmodium falciparum antigens in Burkina Faso. Infect Immun 2001, 69:996-1001.
- [31]Brooker S, Guyatt H, Omumbo J, Shretta R, Drake L, Ouma J: Situation analysis of malaria in school-aged children in Kenya - what can be done? Parasitol Today 2000, 16:183-186.