Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 24
Filter
1.
Infect Dis Poverty ; 11(1): 73, 2022 Jun 25.
Article in English | MEDLINE | ID: mdl-35752864

ABSTRACT

BACKGROUND: Schistosomiasis and soil-transmitted helminths (STHs) contribute high disease burdens amongst the neglected tropical diseases (NTDs) and are public health problems in Angola. This study reports the prevalence, intensity and risk factors for schistosomiasis and STH infection in Huambo, Uige and Zaire provinces, Angola, to inform a school-based preventive chemotherapy program. METHODS: A two-stage cluster design was used to select schools and schoolchildren to participate in parasitological and water, sanitation and hygiene (WASH) surveys across Huambo, Uige, and Zaire provinces. Point-of-care circulating cathodic antigen and urinalysis rapid diagnostic tests (RDTs) were used to determine the prevalence of Schistosoma mansoni and S. haematobium, respectively. Kato-Katz was used to identify and quantify STH species and quantify and compare with RDTs for S. mansoni. Urine filtration was used to quantify and compare with RDTs for S. haematobium. Descriptive statistics were used for prevalence and infection intensity of schistosomiasis and STH infection. Performance of RDTs was assessed through specificity and Cohen's Kappa agreement with microscopy. A multivariate regression analysis was used to determine demographic and WASH factors associated with schistosomiasis and STH infection. RESULTS: A total 575 schools and 17,093 schoolchildren participated in the schistosomiasis survey, of which 121 schools and 3649 schoolchildren participated in the STH survey. Overall prevalence of S. mansoni was 21.2% (municipality range 0.9-74.8%) and S. haematobium 13.6% (range 0-31.2%), with an overall prevalence of schistosomiasis of 31.4% (range 5.9-77.3%). Overall prevalence of Ascaris lumbricoides was 25.1% (range 0-89.7%), hookworm 5.2% (range 0-42.6%), and Trichuris trichiura 3.6% (range 0-24.2%), with an overall prevalence of STH infection of 29.5% (range 0.8-89.7%). Ecological zone and ethnicity were factors associated with schistosomiasis and STH infection, with older age and female sex additional risk factors for S. haematobium. CONCLUSIONS: Most municipalities met World Health Organization defined prevalence thresholds for a schistosomiasis preventive chemotherapy program. A STH preventive chemotherapy program is indicated for nearly all municipalities in Uige and select municipalities in Huambo and Zaire. The association between ecological zone and ethnicity with schistosomiasis and STH infection necessitates further evaluation of home and school environmental, sociodemographic and behavioural factors to inform targeted control strategies to complement preventive chemotherapy programs.


Subject(s)
Helminthiasis , Helminths , Schistosomiasis , Angola/epidemiology , Animals , Child , Democratic Republic of the Congo/epidemiology , Feces/parasitology , Female , Helminthiasis/parasitology , Humans , Neglected Diseases , Prevalence , Schistosomiasis/parasitology , Soil/parasitology
2.
mBio ; 7(4)2016 08 09.
Article in English | MEDLINE | ID: mdl-27507822

ABSTRACT

UNLABELLED: Each year, millions of African children receive praziquantel (PZQ) by mass drug administration (MDA) to treat schistosomiasis at a standard single dose of 40 mg/kg of body weight, a direct extrapolation from studies of adults. A higher dose of 60 mg/kg is also acceptable for refractory cases. We conducted the first PZQ pharmacokinetic (PK) and pharmacodynamic (PD) study in young children comparing dosing. Sixty Ugandan children aged 3 to 8 years old with egg patent Schistosoma mansoni received PZQ at either 40 mg/kg or 60 mg/kg. PK parameters of PZQ racemate and enantiomers (R and S) were quantified. PD outcomes were assessed by standard fecal egg counts and novel schistosome-specific serum (circulating anodic antigen [CAA]) and urine (circulating cathodic antigen [CCA]) antigen assays. Population PK and PD analyses were performed to estimate drug exposure in individual children, and the relationship between drug exposure and parasitological cure was estimated using logistic regression. Monte Carlo simulations were performed to identify better, future dosing regimens. There was marked PK variability between children, but the area under the concentration-time curve (AUC) of PZQ was strongly predictive of the parasitological cure rate (CR). Although no child achieved antigenic cure, which is suggestive of an important residual adult worm burden, higher AUC was associated with greater CAA antigenic decline at 24 days. To optimize the performance of PZQ, analysis of our simulations suggest that higher doses (>60 mg/kg) are needed, particularly in smaller children. IMPORTANCE: Schistosomiasis is a neglected tropical disease, typically associated with chronic morbidity, and its control is a global health priority. Praziquantel (PZQ) is the only available antiparasitic drug and is often given out, as a single oral dose (40 mg/kg), to school-aged children by mass drug administration (MDA) schemes operating within preventive chemotherapy campaigns as endorsed by the World Health Organization (WHO). This current strategy has several limitations. (i) It excludes preschool children who can be patently infected. (ii) It delivers PZQ at a dose directly extrapolated from adult pharmacological studies. To address these problems, we conducted the first pharmacokinetic and pharmacodynamic study of young children within an area of Uganda where Schistosoma mansoni is hyperendemic. Our results demonstrate that a higher dose (>60 mg/kg) is required, especially in smaller children, and draw attention to the need for further optimization of PZQ treatment based on schistosome antigenic assays, which are more sensitive to pharmacodynamic markers.


Subject(s)
Anthelmintics/administration & dosage , Anthelmintics/pharmacokinetics , Praziquantel/administration & dosage , Praziquantel/pharmacokinetics , Schistosoma mansoni/drug effects , Schistosomiasis mansoni/drug therapy , Animals , Anthelmintics/pharmacology , Antigens, Helminth/blood , Antigens, Helminth/urine , Child , Child, Preschool , Feces/parasitology , Female , Humans , Male , Parasite Egg Count , Praziquantel/pharmacology , Schistosomiasis mansoni/parasitology , Uganda
3.
Biomed Res Int ; 2015: 717261, 2015.
Article in English | MEDLINE | ID: mdl-25705680

ABSTRACT

This study documented the population dynamics of Biomphalaria and associated natural infections with digenetic trematodes, along the shores of Lake Albert and Lake Victoria, recording local physicochemical factors. Over a two-and-a-half-year study period with monthly sampling, physicochemical factors were measured at 12 survey sites and all freshwater snails were collected. Retained Biomphalaria were subsequently monitored in laboratory aquaria for shedding trematode cercariae, which were classified as either human infective (Schistosoma mansoni) or nonhuman infective. The population dynamics of Biomphalaria differed by location and by lake and had positive relationship with pH (P < 0.001) in both lakes and negative relationship with conductivity (P = 0.04) in Lake Albert. Of the Biomphalaria collected in Lake Albert (N = 6,183), 8.9% were infected with digenetic trematodes of which 15.8% were shedding S. mansoni cercariae and 84.2% with nonhuman infective cercariae. In Lake Victoria, 2.1% of collected Biomphalaria (N = 13,172) were infected with digenetic trematodes with 13.9% shedding S. mansoni cercariae, 85.7% shedding nonhuman infective cercariae, and 0.4% of infected snails shedding both types of cercariae. Upon morphological identification, species of Biomphalaria infected included B. sudanica, B. pfeifferi, and B. stanleyi in Lake Albert and B. sudanica, B. pfeifferi, and B. choanomphala in Lake Victoria. The study found the physicochemical factors that influenced Biomphalaria population and infections. The number and extent of snails shedding S. mansoni cercariae illustrate the high risk of transmission within these lake settings. For better control of this disease, greater effort should be placed on reducing environmental contamination by improvement of local water sanitation and hygiene.


Subject(s)
Biomphalaria/genetics , Population Dynamics , Schistosoma mansoni/pathogenicity , Schistosomiasis mansoni/epidemiology , Animals , Biomphalaria/pathogenicity , Humans , Lakes/parasitology , Schistosoma mansoni/genetics , Schistosomiasis mansoni/genetics , Schistosomiasis mansoni/parasitology , Uganda/epidemiology
4.
Parasitology ; 141(14): 1947-61, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25158604

ABSTRACT

Within the World Health Organization 2012-2020 roadmap for control and elimination of schistosomiasis, the scale-up of mass drug administration with praziquantel is set to change the epidemiological landscape across Africa and Arabia. Central in measuring progress is renewed emphasis upon diagnostics which operate at individual, community and environmental levels by assessing reductions in disease, infections and parasite transmission. However, a fundamental tension is revealed between levels for present diagnostic tools, and methods applied in control settings are not necessarily adequate for application in elimination scenarios. Indeed navigating the transition from control to elimination needs careful consideration and planning. In the present context of control, we review current options for diagnosis of schistosomiasis at different levels, highlighting several strengths and weaknesses therein. Future challenges in elimination are raised and we propose that more cost-effective diagnostics and clinical staging algorithms are needed. Using the Kingdom of Saudi Arabia as a contemporary example, embedding new diagnostic methods within the primary care health system is discussed with reference to both urogenital and intestinal schistosomiasis.


Subject(s)
Anthelmintics/administration & dosage , Diagnostic Tests, Routine/methods , Praziquantel/administration & dosage , Schistosoma/isolation & purification , Schistosomiasis/diagnosis , Africa/epidemiology , Animals , Diagnostic Tests, Routine/economics , Disease Eradication/economics , Disease Eradication/methods , Female , Humans , Male , Saudi Arabia/epidemiology , Schistosoma/drug effects , Schistosomiasis/drug therapy , Schistosomiasis/epidemiology , Schistosomiasis/prevention & control , Time Factors
5.
Parasitology ; 141(14): 1819-25, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25088228

ABSTRACT

Malaria microscopy in sub-Saharan Africa is often restricted by access to light microscopes. To address this gap, a novel portable inverted monocular microscope, the Newton Nm1, was designed and is now commercially available. Its diagnostic performance was assessed in a blinded-slide trial at ×1000 (oil) of Giemsa-stained thick blood films against a conventional microscope as undertaken by four Ugandan Ministry of Health technicians. With the Newton Nm1, diagnostic performance was: sensitivity 93.5% (95% confidence interval (CI) 78.6-99.2%), specificity 100.0% (95% CI 82.4-100.0%), positive predictive value 100.0% (95% CI 88.1-100.0%) and negative predictive value 90.5% (95% CI 69.6-98.8%). Discordance was due to a systematic error underestimating parasitaemia by ~45%; when counting Plasmodium parasites against 200 white blood cells, blood films with low parasitaemia (i.e. <100 µL(-1) of blood) could be overlooked and misclassified. By contrast, specificity was excellent with no false positives encountered. Whilst proven useful, especially in resource-poor environments, it is still unclear how we can ensure the uptake of the Newton Nm1 within sub-Saharan Africa.


Subject(s)
Malaria/diagnosis , Microscopy/instrumentation , Plasmodium/isolation & purification , Humans , Malaria/epidemiology , Observer Variation , Parasitemia , Predictive Value of Tests , Prevalence , Sensitivity and Specificity , Uganda/epidemiology
6.
Parasitology ; 141(14): 1880-90, 2014 Dec.
Article in English | MEDLINE | ID: mdl-24837880

ABSTRACT

During a longitudinal study investigating the dynamics of malaria in Ugandan lakeshore communities, a consistently high malaria prevalence was observed in young children despite regular treatment. To explore the short-term performance of artemether-lumefantrine (AL), a pilot investigation into parasite carriage after treatment(s) was conducted in Bukoba village. A total of 163 children (aged 2-7 years) with a positive blood film and rapid antigen test were treated with AL; only 8.7% of these had elevated axillary temperatures. On day 7 and then on day 17, 40 children (26.3%) and 33 (22.3%) were positive by microscopy, respectively. Real-time PCR analysis demonstrated that multi-species Plasmodium infections were common at baseline, with 41.1% of children positive for Plasmodium falciparum/Plasmodium malariae, 9.2% for P. falciparum/ Plasmodium ovale spp. and 8.0% for all three species. Moreover, on day 17, 39.9% of children infected with falciparum malaria at baseline were again positive for the same species, and 9.2% of those infected with P. malariae at baseline were positive for P. malariae. Here, chronic multi-species malaria infections persisted in children after AL treatment(s). Better point-of-care diagnostics for non-falciparum infections are needed, as well as further investigation of AL performance in asymptomatic individuals.


Subject(s)
Antimalarials/therapeutic use , Artemisinins/therapeutic use , Ethanolamines/therapeutic use , Fluorenes/therapeutic use , Malaria/diagnosis , Plasmodium/isolation & purification , Artemether , Child , Child, Preschool , Coinfection , Diagnostic Tests, Routine , Drug Therapy, Combination , Female , Follow-Up Studies , Humans , Longitudinal Studies , Lumefantrine , Malaria/drug therapy , Malaria/epidemiology , Malaria/parasitology , Male , Plasmodium/genetics , Plasmodium/immunology , Plasmodium falciparum/genetics , Plasmodium falciparum/immunology , Plasmodium falciparum/isolation & purification , Plasmodium ovale/genetics , Plasmodium ovale/immunology , Plasmodium ovale/isolation & purification , Point-of-Care Systems , Prevalence , Uganda/epidemiology
7.
PLoS Negl Trop Dis ; 7(12): e2561, 2013.
Article in English | MEDLINE | ID: mdl-24349589

ABSTRACT

Significant numbers of pre-school children are infected with Schistosoma mansoni in sub-Saharan Africa and are likely to play a role in parasite transmission. However, they are currently excluded from control programmes. Molecular phylogenetic studies have provided insights into the evolutionary origins and transmission dynamics of S. mansoni, but there has been no research into schistosome molecular epidemiology in pre-school children. Here, we investigated the genetic diversity and population structure of S. mansoni in pre-school children and mothers living in lakeshore communities in Uganda and monitored for changes over time after praziquantel treatment. Parasites were sampled from children (<6 years) and mothers enrolled in the longitudinal Schistosomiasis Mothers and Infants Study at baseline and at 6-, 12- and 18-month follow-up surveys. 1347 parasites from 35 mothers and 45 children were genotyped by direct sequencing of the cytochrome c oxidase (cox1) gene. The cox1 region was highly diverse with over 230 unique sequences identified. Parasite populations were genetically differentiated between lakes and non-synonymous mutations were more diverse at Lake Victoria than Lake Albert. Surprisingly, parasite populations sampled from children showed a similar genetic diversity to those sampled from mothers, pointing towards a non-linear relationship between duration of exposure and accumulation of parasite diversity. The genetic diversity six months after praziquantel treatment was similar to pre-treatment diversity. Our results confirm the substantial genetic diversity of S. mansoni in East Africa and provide significant insights into transmission dynamics within young children and mothers, important information for schistosomiasis control programmes.


Subject(s)
Genetic Variation , Schistosoma mansoni/classification , Schistosoma mansoni/genetics , Schistosomiasis mansoni/epidemiology , Schistosomiasis mansoni/parasitology , Africa , Animals , Anthelmintics/therapeutic use , Child, Preschool , Electron Transport Complex IV/genetics , Family Health , Female , Genetics, Population , Genotype , Humans , Infant , Longitudinal Studies , Male , Molecular Epidemiology , Molecular Sequence Data , Mothers , Praziquantel/therapeutic use , Schistosoma mansoni/isolation & purification , Schistosomiasis mansoni/drug therapy , Sequence Analysis, DNA , Uganda/epidemiology
8.
PLoS Negl Trop Dis ; 7(11): e2542, 2013 Nov.
Article in English | MEDLINE | ID: mdl-24244777

ABSTRACT

BACKGROUND: Calprotectin is a calcium-binding cytoplasmic protein found in neutrophils and increasingly used as a marker of bowel inflammation. Fecal occult blood (FOB) is also a dependable indicator of bowel morbidity. The objective of our study was to determine the applicability of these tests as surrogate markers of Schistosoma mansoni intestinal morbidity before and after treatment with praziquantel (PZQ). METHODS: 216 children (ages 3-9 years old) from Buliisa District in Lake Albert, Uganda were examined and treated with PZQ at baseline in October 2012 with 211 of them re-examined 24 days later for S. mansoni and other soil transmitted helminths (STH). POC calprotectin and FOB assays were performed at both time points on a subset of children. Associations between the test results and infection were analysed by logistic regression. RESULTS: Fecal calprotectin concentrations of 150-300 µg/g were associated with S. mansoni egg patent infection both at baseline and follow up (OR: 12.5 P = 0.05; OR: 6.8 P = 0.02). FOB had a very strong association with baseline anemia (OR: 9.2 P = 0.03) and medium and high egg intensity schistosomiasis at follow up (OR: 6.6 P = 0.03; OR: 51.3 P = 0.003). Both tests were strongly associated with heavy intensity S. mansoni infections. There was a significant decrease in FOB and calprotectin test positivity after PZQ treatment in those children who had egg patent schistosomiasis at baseline. CONCLUSIONS: Both FOB and calprotectin rapid assays were found to correlate positively and strongly with egg patent S. mansoni infection with a positive ameloriation response after PZQ treatment indicative of short term reversion of morbidity. Both tests were appropriate for use in the field with excellent operational performance and reliability. Due to its lower-cost which makes its scale-up of use affordable, FOB could be immediately adopted as a monitoring tool for PC campaigns for efficacy evaluation before and after treatment.


Subject(s)
Feces/parasitology , Leukocyte L1 Antigen Complex/blood , Occult Blood , Schistosoma mansoni/pathogenicity , Schistosomiasis mansoni/blood , Animals , Child , Child, Preschool , Female , Humans , Intestines/parasitology , Male , Schistosomiasis mansoni/parasitology
9.
Trans R Soc Trop Med Hyg ; 107(10): 639-47, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23976783

ABSTRACT

BACKGROUND: A sensitive and reliable rapid diagnostic test (RDT) which should have comparable diagnostic performance against reference host serological methods is urgently needed for use in point-of-care (POC) diagnosis of intestinal schistosomiasis in pre school-aged children. METHODS: The diagnostic accuracy of a RDT incorporating Schistosoma mansoni cercarial transformation fluid (SmCTF) for anti-schistosome antibody detection was evaluated with serum samples from a cohort of children from Uganda: 42 children aged under the age of 3 years and 40 children aged between 3 and 5 years. The infection status of these children had been previously determined by inspection of quadruplicate Kato-Katz faecal smears, a single urine circulating cathodic antigen (CCA) dipstick and antibody titres to S. mansoni soluble egg antigen (SmSEA) with a commercially available ELISA. RESULTS: Upon comparison with quadruplicate Kato-Katz the sensitivity and specificity of the RDT were 75.7% and 31.1%, respectively. When using the SmSEA-ELISA as an alternate reference test, the RDT achieved 81.3% sensitivity and 61.1% specificity. Sensitivity and specificity compared to the urine-CCA test was 74.5% and 32.3% respectively. Sensitivity differed significantly according to age group. CONCLUSIONS: The performance of the RDT within this study appeared favourable when compared with the currently-available SmSEA-ELISA. Looking to the future a serological POC test would be particularly promising for use in disease mapping in younger children especially in guiding administration of praziquantel treatment in selective treatment settings.


Subject(s)
Antibodies, Helminth/blood , Parasitology/methods , Schistosoma mansoni/immunology , Schistosomiasis mansoni/diagnosis , Animals , Child, Preschool , Diagnostic Tests, Routine/methods , Female , Humans , Immunoassay/methods , Infant , Infant, Newborn , Male , Schistosomiasis mansoni/immunology , Schistosomiasis mansoni/urine , Sensitivity and Specificity , Uganda/epidemiology , Urine/parasitology
10.
Expert Rev Anti Infect Ther ; 11(7): 733-52, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23879611

ABSTRACT

Preventive chemotherapy campaigns against schistosomiasis have progressively scaled-up during the last decade, administering single standard dose praziquantel (40 mg/kg) treatments to millions of African children. Steps taken in securing international advocacy and national level implementation are traced to highlight an international treatment platform set for further expansion, including surveillance of schistosomiasis, school-level targeting with better on-site drug administration and annual reporting of programmatic indicators (i.e., treatment coverage), potentially in real-time. Several shortcomings in need of resolution are identified and efficacy of praziquantel is assessed by a systematic review. If WHO predictions in reduction of schistosomiasis are to be realized, careful international harmonization and tailoring of national resources are required. Maintaining an effective drug distribution system and regularly checking drug efficacy are paramount.


Subject(s)
Anthelmintics/therapeutic use , Disease Eradication , Praziquantel/therapeutic use , Schistosomiasis/prevention & control , Africa/epidemiology , Anthelmintics/administration & dosage , Child , Epidemiological Monitoring , Humans , Praziquantel/administration & dosage , Schistosomiasis/drug therapy , Schistosomiasis/epidemiology , Treatment Outcome
11.
Trends Parasitol ; 29(4): 197-205, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23465781

ABSTRACT

The occurrence of schistosomiasis within African infants and preschool children has been much better documented in recent years, revealing an important burden of disease previously overlooked. Despite mounting evidence showing that treatment with praziquantel is safe, beneficial, and could be delivered within ongoing public health interventions, young children still do not have satisfactory access to this drug, and a significant treatment gap exists. Progress towards resolution of this unfortunate health inequity is highlighted, including the development of an appropriate paediatric praziquantel formulation, and present blocks are identified on securing this issue within the international health agenda.


Subject(s)
Anthelmintics/therapeutic use , Praziquantel/therapeutic use , Schistosomiasis/drug therapy , Africa/epidemiology , Animals , Anthelmintics/administration & dosage , Anthelmintics/pharmacokinetics , Child, Preschool , Humans , Infant , Praziquantel/administration & dosage , Praziquantel/pharmacokinetics , Prevalence , Public Health , Schistosomiasis/epidemiology
12.
Acta Trop ; 128(2): 292-302, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23022016

ABSTRACT

Following major water development schemes in the 1980s, schistosomiasis has become a serious parasitic disease of children living in the Senegal River Basin. Both urogenital (Schistosoma haematobium) and intestinal (Schistosoma mansoni) schistosomiasis can be highly prevalent in school-aged children, with many individuals infected with both parasites. In order to investigate the transmission and re-infection dynamics of both parasite species, single and mixed infection foci at three villages (Nder and Temeye; S. mansoni and S. haematobium foci and Guia; S. haematobium focus) were studied. In each focus infected children were identified and selected for a 12-month study involving two treatments with praziquantel (40mg/kg) three weeks apart at the beginning of the study and again 6 months into the study. Urine and stool samples were examined for schistosome eggs before and at 6 weeks and 6 months after chemotherapy. Prevalence and intensity of infection were recorded for each child at each time point. Before treatment, in all three villages, the prevalence and intensity of infection was extremely high for both S. mansoni (79-100%) and S. haematobium (81-97%). With the first round of chemotherapy sufficient cure rates (CRs) of both species were achieved in all villages (38-96%) with high egg reduction rates (ERRs) (97-99%). The data show that high and rapid re-infection rates occur, especially for S. mansoni, within a six-month period following treatment. Re-infection must be highly linked to ecological and seasonal factors. The persistence of S. mansoni in Nder could raise concern as levels of infection intensity remain high (geometric mean intensity at baseline 653epg changed to 705epg at 12 months) after four rounds of chemotherapy. This phenomenon could be explained by extremely rapid re-infection dynamics or a sub-optimal efficacy of praziquantel against S. mansoni in this village. High intensities in mixed infections may influence disease epidemiology and control warranting further studies. The disease situation in the SRB must be monitored closely and new treatment regimes should be designed and implemented to control schistosomiasis in the school-age population.


Subject(s)
Anthelmintics/therapeutic use , Praziquantel/therapeutic use , Schistosoma haematobium/isolation & purification , Schistosoma mansoni/isolation & purification , Schistosomiasis haematobia/drug therapy , Schistosomiasis mansoni/drug therapy , Adolescent , Animals , Child , Child, Preschool , Coinfection/drug therapy , Feces/parasitology , Female , Humans , Male , Recurrence , Rural Population , Senegal , Treatment Outcome , Urine/parasitology
13.
J Infect Dis ; 207(2): 362-6, 2013 Jan 15.
Article in English | MEDLINE | ID: mdl-23125445

ABSTRACT

Specific immunoglobulin E (IgE) responses are upregulated during chronic schistosome infection and during allergy. These responses are tightly regulated during schistosomiasis. We have previously shown that IgE regulation depends on the extent and length of exposure to individual parasite allergen-like proteins. Here we compare the development of IgE and immunoglobulin G4 (IgG(4)) responses to the differentially expressed allergen-like proteins SmTAL1 and SmTAL2 among preschool-aged children from 2 villages with different levels of Schistosoma mansoni transmission. We found a lack of SmTAL1 responsiveness among all children, but evidence for IgG(4)-dependent IgE-SmTAL2 desensitization in both villages, occurring earlier among children from the village where the level of transmission was greater. Findings provide insights into the development and regulation of allergic-type immune responses.


Subject(s)
Allergens/immunology , Helminth Proteins/immunology , Immunoglobulin E/blood , Immunoglobulin G/blood , Schistosoma mansoni/immunology , Schistosomiasis mansoni/immunology , Adult , Animals , Child, Preschool , Female , Humans , Infant , Schistosomiasis mansoni/parasitology , Schistosomiasis mansoni/transmission , Uganda
14.
Geospat Health ; 7(1): 1-13, 2012 Nov.
Article in English | MEDLINE | ID: mdl-23242675

ABSTRACT

The establishment of a national control programme (NCP) in Uganda has led to routine treatment of intestinal schistosomiasis with praziquantel in the communities along Lake Albert. However, because regular water contact remains a way of life for these populations, re-infection continues to mitigate the sustainability of the chemotherapy-based programme. A six-month longitudinal study was conducted in one Lake Albert community with the aim of characterizing water contact exposure and infection among mothers and their young preschool-aged children as the latter are not yet formally included within the NCP. At baseline the cohort of 37 mothers, 36 preschool-aged children had infection prevalences of 62% and 67%, respectively, which diminished to 20% and 29%, respectively, at the 6-month post-treatment follow-up. The subjects wore global positioning system (GPS) datalogging devices over a 3-day period shortly after baseline, allowing for the estimation of time spent at the lakeshore as an exposure metric, which was found to be associated with prevalence at follow-up (OR = 2.1, P = 0.01 for both mothers and young children and odds ratio (OR) = 4.4, P = 0.01 for young children alone). A social network of interpersonal interactions was also derived from the GPS data, and the exposures were positively associated both with the number and duration of peer interaction, suggesting the importance of socio-cultural factors associated with water contact behaviour. The findings illustrate reduction in both prevalence and intensity of infection in this community after treatment as well as remarkably high rates of water contact exposure and re-infection, particularly among younger children. We believe that this should now be formally considered within NCP, which may benefit from more in-depth ethnographic exploration of factors related to water contact as this should provide new opportunities for sustaining control.


Subject(s)
Environmental Exposure/statistics & numerical data , Praziquantel/therapeutic use , Schistosomiasis mansoni/epidemiology , Water Microbiology , Albendazole/therapeutic use , Animals , Anthelmintics/therapeutic use , Cercaria/parasitology , Child , Child, Preschool , Environmental Exposure/adverse effects , Female , Geographic Information Systems , Humans , Longitudinal Studies , Male , Mothers/statistics & numerical data , Pilot Projects , Prevalence , Schistosoma mansoni/isolation & purification , Schistosoma mansoni/pathogenicity , Schistosomiasis mansoni/drug therapy , Schistosomiasis mansoni/prevention & control , Secondary Prevention , Social Behavior , Uganda/epidemiology
15.
PLoS Negl Trop Dis ; 6(10): e1864, 2012.
Article in English | MEDLINE | ID: mdl-23094120

ABSTRACT

BACKGROUND: In 2012 the WHO formally recognised that infants and preschool children are at significant risk of schistosomiasis and qualify for treatment with praziquantel (PZQ). Targeted surveys determining both the performance and safety of this drug are now needed in endemic areas. We have formally assessed parasitological cure and putative side-effects in a prospective cohort of Schistosoma mansoni-infected children (aged 5 months-7 years old) in lakeshore settings of Uganda. METHODOLOGY/PRINCIPAL FINDINGS: From a total of 369 children found to be egg-patent for intestinal schistosomiasis, 305 were followed-up three to four weeks after PZQ treatment and infection status re-assessed. Separately, a previously tested side-effect questionnaire was employed before and 24 hours after PZQ treatment to assess incidence and amelioration of symptoms in young children and their mothers. While the overall observed parasitological cure was 56.4%, a significant difference was found between a sub-set of children who had a history of multiple PZQ treatments (between one and four in an 18 month period), where cure rate was 41.7%, and those who had never received treatment (cure rate was 77·6%). PZQ proved to be safe, with only mild reported side effects which cleared within a month after treatment. Prevalence of reported symptoms was significantly lower in children than in mothers, and fewer side-effects were reported upon subsequent rounds of PZQ treatment. CONCLUSION/SIGNIFICANCE: Our findings show that PZQ treatment of young children resulted in satisfactory cure rates, and marked reduction in egg-output, with only mild and transient reported side-effects. However, the cure rate is clearly lower in younger children and those with history of previous treatment. Cure rate, but not egg reduction rate, was also lower in children with heavier pre-intervention infection intensity. With chemotherapy now recommended as a long-term strategy for disease control in young children, research into optimising the periodicity of targeted treatment strategies is now crucial.


Subject(s)
Anthelmintics/administration & dosage , Anthelmintics/adverse effects , Praziquantel/administration & dosage , Praziquantel/adverse effects , Schistosomiasis mansoni/drug therapy , Animals , Child , Child, Preschool , Drug-Related Side Effects and Adverse Reactions/epidemiology , Feces/parasitology , Female , Humans , Incidence , Infant , Male , Parasite Egg Count , Schistosoma mansoni/drug effects , Schistosoma mansoni/isolation & purification , Surveys and Questionnaires , Treatment Outcome , Uganda
16.
Int Health ; 4(2): 95-102, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22876272

ABSTRACT

To facilitate administration of praziquantel (PZQ) to African infants and preschool-aged children using a dose pole, the performance of two downwardly extended versions (the first created in 2010 using biometric data from Uganda alone and the second version created here using data from 36 countries) was assessed against height/weight data from a total of 166 210 preschool-aged children (≤6 year olds) from 36 African countries. New and optimized thresholds for PZQ tablet administration at one tablet (600 mg), ¾ and ½ tablet divisions are suggested here. Both dose poles investigated estimated an acceptable PZQ dosage (30-60 mg/Kg) for more than 95% of children. Extension and optimization of the current PZQ dose pole, followed by theoretical validation using biometric data from preschool-aged children (0-6 years of age, 60-110 cm in height) from 36 African countries will help future mass drug administration campaigns incorporate younger children. This newly optimized dose pole with single 600 mg (height: 99-110 cm), ¾ (height: 83-99 cm) and ½ (height: 66-83 cm) tablet divisions, also reduces drug waste and facilitates inclusion of preschool-aged children. Our findings also have bearings on the use of other dose poles for treatment of young children.

17.
Parasit Vectors ; 4: 232, 2011 Dec 13.
Article in English | MEDLINE | ID: mdl-22166365

ABSTRACT

BACKGROUND: It is widely advocated that integrated strategies for the control of neglected tropical diseases (NTDs) are cost-effective in comparison to vertical disease-specific programmes. A prerequisite for implementation of control interventions is the availability of baseline data of prevalence, including the population at risk and disease overlap. Despite extensive literature on the distribution of schistosomiasis on the mainland in Uganda, there has been a knowledge gap for the prevalence of co-infections with malaria, particularly for island communities in Lake Victoria. In this study, nine lakeshore and island districts were surveyed for the prevalence of NTDs and malaria, as well as educational and health infrastructure. RESULTS: A total of 203 communities were surveyed, including over 5000 school-age children. Varying levels of existing health infrastructure were observed between districts, with only Jinja District regularly treating people for NTDs. Community medicine distributors (CMD) were identified and trained in drug delivery to strengthen capacity. Prevalence levels of intestinal schistosomiasis and soil-transmitted helminthiasis were assessed via Kato-Katz thick smears of stool and malaria prevalence determined by microscopy of fingerprick blood samples. Prevalence levels were 40.8%, 26.04% and 46.4%, respectively, while the prevalence of co-infection by Schistosoma mansoni and Plasmodium spp. was 23.5%. Socio-economic status was strongly associated as a risk factor for positive infection status with one or more of these diseases. CONCLUSIONS: These results emphasise the challenges of providing wide-scale coverage of health infrastructure and drug distribution in remote lakeshore communities. The data further indicate that co-infections with malaria and NTDs are common, implying that integrated interventions for NTDs and malaria are likely to maximize cost-effectiveness and sustainability of disease control efforts.


Subject(s)
Helminthiasis/epidemiology , Malaria/epidemiology , Schistosomiasis/epidemiology , Soil/parasitology , Adolescent , Child , Feces/parasitology , Female , Geography , Helminthiasis/transmission , Humans , Malaria/transmission , Male , Neglected Diseases/epidemiology , Prevalence , Rural Health , Schistosomiasis/transmission , Uganda/epidemiology
18.
Parasitology ; 138(12): 1534-45, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21819635

ABSTRACT

Anaemia is a severe public health issue among African preschool-aged children, yet little effective progress has been made towards its amelioration, in part due to difficulties in unravelling its complex, multifactorial aetiology. To determine the current anaemia situation and assess the relative contribution of malaria, intestinal schistosomiasis and infection with soil-transmitted helminths, two separate cross-sectional epidemiological surveys were carried out in Uganda including 573 and 455 preschool-aged children (≤6 years) living along the shores of Lake Albert and on the islands in Lake Victoria, respectively. Anaemia was found to be a severe public health problem in Lake Albert, affecting 68·9% of children (ninety-five percent confidence intervals (95% CI) 64·9-72·7%), a statistically significant higher prevalence relative to the 27·3% detected in Lake Victoria (95% CI: 23·3-31·7%). After multivariate analysis (controlling for sex and age of the child), the only factor found to be significantly associated with increased odds of anaemia in both lake systems was malaria (Lake Albert, odds ratio (OR)=2·1, 95% CI: 1·4-3·2; Lake Victoria, OR=1·9, 95% CI: 1·2-2·9). Thus intervention strategies primarily focusing on very young children and combating malaria appear to represent the most appropriate use of human and financial resources for the prevention of anaemia in this age group and area. Looking to the future, these activities could be further emphasised within the National Child Health Days(PLUS) agenda.


Subject(s)
Anemia/epidemiology , Anemia/etiology , Malaria/complications , Schistosomiasis mansoni/complications , Animals , Child , Child Welfare , Child, Preschool , Cross-Sectional Studies , Female , Humans , Infant , Infant, Newborn , Lakes/parasitology , Longitudinal Studies , Malaria/epidemiology , Male , Malnutrition/complications , Maternal Welfare , Pregnancy , Prevalence , Schistosomiasis mansoni/epidemiology , Soil/parasitology , Surveys and Questionnaires , Uganda/epidemiology
19.
Parasitology ; 138(12): 1593-606, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21861945

ABSTRACT

Where very young children come into contact with water containing schistosome cercariae, infections occur and schistosomiasis can be found. In high transmission environments, where mothers daily bathe their children with environmentally drawn water, many infants and preschool-aged children have schistosomiasis. This 'new' burden, inclusive of co-infections with Schistosoma haematobium and Schistosoma mansoni, is being formally explored as infected children are not presently targeted to receive praziquantel (PZQ) within current preventive chemotherapy campaigns. Thus an important PZQ treatment gap exists whereby infected children might wait up to 4-5 years before receiving first treatment in school. International treatment guidelines, set within national treatment platforms, are presently being modified to provide earlier access to medication(s). Although detailed pharmacokinetic studies are needed, to facilitate pragmatic dosing in the field, an extended 'dose pole' has been devised and epidemiological monitoring has shown that administration of PZQ (40 mg/kg), in either crushed tablet or liquid suspension, is both safe and effective in this younger age-class; drug efficacy, however, against S. mansoni appears to diminish after repeated rounds of treatment. Thus use of PZQ should be combined with appropriate health education/water hygiene improvements for both child and mother to bring forth a more enduring solution.


Subject(s)
Anthelmintics/administration & dosage , Praziquantel/administration & dosage , Schistosomiasis haematobia/drug therapy , Schistosomiasis mansoni/drug therapy , Africa/epidemiology , Age Factors , Anemia/epidemiology , Animals , Anthelmintics/therapeutic use , Child, Preschool , Coinfection , Feces/parasitology , Female , Hepatomegaly , Humans , Infant , Praziquantel/therapeutic use , Prevalence , Schistosomiasis haematobia/epidemiology , Schistosomiasis haematobia/prevention & control , Schistosomiasis mansoni/epidemiology , Schistosomiasis mansoni/prevention & control , Splenomegaly , Water/parasitology , Water/standards
20.
Trans R Soc Trop Med Hyg ; 105(9): 500-6, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21714979

ABSTRACT

Point-prevalence recording of the distribution of tropical parasitic diseases at village level is usually sufficient for general monitoring and surveillance. Whilst within-village spatial patterning of diseases exists, and can be important, mapping infected cases in a household-by-household setting is arduous and time consuming. With the development of low-cost GPS-data loggers (< £40) and available GoogleEarth(TM) satellite imagery, we present a field-applicable method based on crowdsourcing for rapid identification of infected cases (intestinal schistosomiasis, malaria and hookworm) by household. A total of 126 mothers with their 247 preschool children from Bukoba village (Mayuge District, Uganda) were examined with half of these mothers given a GPS-data logger to walk home with, returning the unit the same day for data off-loading, after which, households were assigned GPS coordinates. A satellite image of Bukoba was annotated with households denoting the infection status of each mother and child. General prevalence of intestinal schistosomiasis, malaria and hookworm in mothers and children was: 27.2 vs 7.7%, 28.6 vs 87.0% and 60.0 vs 22.3%, respectively. Different spatial patterns of disease could be identified likely representing the intrinsic differences in parasite biology and interplay with human behaviour(s) across this local landscape providing a better insight into reasons for disease micro-patterning.


Subject(s)
Data Collection , Family Characteristics , Hookworm Infections/epidemiology , Malaria/epidemiology , Population Surveillance , Schistosomiasis mansoni/epidemiology , Adolescent , Adult , Animals , Child, Preschool , Data Collection/economics , Female , Hookworm Infections/transmission , Humans , Malaria/transmission , Male , Middle Aged , Mothers , Prevalence , Schistosomiasis mansoni/transmission , Uganda/epidemiology , Water Supply
SELECTION OF CITATIONS
SEARCH DETAIL
...