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Renal abnormalities and its associated factors among school-aged children living in Schistosoma mansoni endemic communities in Northwestern Tanzania

Tropical Medicine and Health volume 48, Article number: 55 (2020) Cite this article

Abstract

Background

In sub-Saharan Africa, renal abnormalities are a major public health concern, especially in children living in Schistosoma haematobium endemic areas. However, there is a dearth of data on renal abnormalities among children living in Schistosoma mansoni endemic areas. The objective of the study was to assess the prevalence of renal abnormalities among school children in a Schistosoma mansoni endemic community in Northwestern Tanzania.

Methods

A cross-sectional study was conducted between January and March 2017 among school children aged 6–13 years, attending three primary schools located along the shoreline of Lake Victoria. A single urine sample was collected from each child and screened for S. mansoni using circulating cathodic antigen and for S. haematobium eggs using a urine filtration technique. A urine dipstick was used to screen for urine protein levels, creatinine levels, microalbuminuria, and red blood cells. Venous blood was obtained for estimation of creatinine level and for malaria diagnosis. The primary outcomes were the prevalence of renal abnormalities, defined by the presence of low estimated glomerular filtration rate (eGFR), proteinuria or microalbuminuria, and hematuria in urine.

Results

Of 507 children included in the final analysis, 49.9% (253/507) were male with a mean age of 8.51 ± 1.3 years. Overall, 64.0% (326/507) of the children were infected with S. mansoni, and 1.6% (8/507) of the children were infected with S. haematobium. A total of 71 (14%) of the children had proteinuria, 37 (7.3%) had hematuria, and 8 (1.6%) had a low estimated glomerular filtration rate (eGFR). Overall prevalence of renal abnormalities was 22.9%. Renal abnormalities (proteinuria) were associated with S. mansoni infection (OR = 4.9, 95% CI 2.1–11.2, p < 0.001) and having red blood cells in urine (OR = 5.3, 95% CI 2.5–11.2, p < 0.001).

Conclusion

Twenty-two percent of school children who participated in this study had renal abnormalities associated with S. mansoni infection. Given the high prevalence of S. mansoni, longitudinal epidemiological surveillance is warranted to measure the burden of renal abnormalities and assess the impact of the praziquantel treatment on these abnormalities.

Background

Early detection and identification of renal diseases in children and adolescents is very important in the prevention of chronic renal diseases. Childhood renal diseases can lead to treatable disorders without long-term consequences and in other cases life-threatening conditions for children [1]. Proteinuria/microalbuminuria and hematuria are important early markers for progression to end-stage renal disease and cardiovascular diseases [2, 3].

In Africa, the causes of renal diseases in children are multifactorial [4]. These causes range from non-infectious diseases (intrauterine injury to the kidney, malnutrition, and sickle cell nephropathy) to infectious diseases (malaria, post-infection glomerulo-nephritis, and HIV nephropathy) [5, 6]. Studies from sub-Saharan Africa have reported the association of S. haematobium with renal abnormalities. The presence of hematuria has remained an important marker of renal disease associated with S. haematobium [7]. However, the association between S. mansoni and renal abnormalities is poorly understood. A few studies have reported the associations between both S. haematobium and S. Mansoni and markers of renal abnormalities such as hematuria and proteinuria [8, 9]. When diagnostic tests were repeated in the same location, years after treatment for S. haematobium, a lower prevalence of proteinuria and hematuria was consistently observed [10, 11]. Kayange et al. reported that S. mansoni was highly associated with proteinuria in a hospital-based study [12]. The mechanisms behind the association of S. mansoni and renal abnormalities can be explained by deposition of immune complex formed by Schistosoma antigen and IgG/IgM antibodies in the glomerular basement membrane [13, 14].

In the Mwanza region, previous studies have demonstrated that there is a high prevalence of schistosomiasis, which contributes to a high prevalence of persistence proteinuria and later to a chronic kidney disease [12]. Therefore, the objective of the study was to assess the prevalence of renal abnormalities based on creatinine, proteinuria, and hematuria levels in children living in an endemic S. mansoni community.

Methods

Study area

The study was conducted at Ilemela district of Mwanza region in Northwestern Tanzania. The region has 139 primary schools which enroll over 95% of all school-aged children in the region [15]. Specifically, the study was conducted in Ilemela District at Kayenze, Kabangaja, and Sangabuye primary schools located in Kayenze, Sangabuye, and Bugongwa villages respectively. These schools were selected because they are located close to the shores of Lake Victoria where previous studies have reported a high prevalence of intestinal schistosomiasis [16]. Communities in this area are at an increased risk of schistosomiasis infection because of daily activities such as bathing/swimming, washing cloth, and fetching water for domestic use from the lake [17]. Primary school children in this area receive an annual mass drug administration of praziquantel to control schistosomiasis infection.

Study design, population, and inclusion and exclusion criteria

We conducted a cross-sectional study among school children between January and March 2017 at the three primary schools. Standard II class (second grade) pupils were enrolled in the study because for this class, no praziquantel had been administered in the previous year. We excluded children with fever since fever is known to cause proteinuria. We also excluded children with preexisting renal disease since it is difficult to determine acute kidney injury in a child with preexisting renal disease without serial creatinine measurement.

Sample size calculation

Our sample size was 507. We calculated the sample size using the Yamane Taro formula (1967) \( n=\frac{N}{1+N{e}^2} \), where n is the sample size, N is the population size of all standard II pupils in the district (94,000), and e is the level of precision at a 95% confidence level, and p = 0.05 is assumed for the equation [18].

Sampling technique

Three villages alongside Lake Victoria and their corresponding primary schools were selected based on convenience and feasibility. A systematic sampling method was used to select study participants, using the class register as a sampling frame. Attempt was made to sample an equal number of girls and boys by reviewing participant’s recruitment logs.

Data collection

A week before urine and blood sample collection, the study objectives were explained to the teachers and children. The children were then provided with informed consent forms to take home to their parents/guardians. They were instructed to tell their parents/guardians to read the informed consent forms and sign if they had understood and agreed to their child’s participation. The signed forms were then brought back to school, and the meeting was also held between the study team and the children and their parents/guardians to facilitate understanding of the objective of the study and associated risks and benefits of participation.

Physical examination of school children

A brief physical examination was done to check for facial or leg edema, temperature, weight (by digital weighing machine), and height. Blood pressure was measured in an enclosed room using a pediatric digital blood pressure monitor which was calibrated before each use. Hypertension was determined using the World Health Organization age-based blood pressure reference charts [19]. The nutritional status of each child was calculated using the WHO 2013 BMI percentile charts according to the child’s age and sex [20].

Laboratory procedures

Urine sampling

A single early morning urine sample was collected from each participating child. Urine albumin and creatinine concentrations were measured using a 25 Biosystems Clinical Chemistry Analyzer according to standard laboratory procedure at the National Institute for Medical Research laboratory, Mwanza, Tanzania. Urine albumin-creatinine ratio (ACR) was calculated and classified using the following categories [21]: normal ≤ 30 mg/g, moderately increased = 30–300 mg/g, and severely increased ≥ 300 mg/g.

Proteinuria measurement

Proteinuria was measured using urine dipsticks (Multistix™, Bayer, Germany), and proteinuria level was reported as negative, 1+ (30 mg/dL), 2+ (100 mg/dL), 3+ (300 mg/dL), or 4+ (1000 mg/dL) as per manufacturer instructions. Children were considered to have proteinuria if they scored 2+, 3+, or 4+. Other indicators recorded using a urine dipstick were leukocytes esterase, hematuria, nitrates, glucose, and ketones. The urinalysis was considered positive if any of these indicators were detected in urine samples. Positive nitrate and leukocyte esterase were considered an indicator for urinary tract infection [22].

Examination of creatinine level in serum

Serum creatinine level was measured using a Cobas 400 clinical chemistry machine (Roche, Germany), calibrated by the Creatinine Jaffe 2 method. Two milliliters of blood was poured into the test tube and then into the machine. An estimated glomerular filtration rate (eGFR) was calculated using modified Schwartz equation (taking into account estimation of GFR in children using serum creatinine and height) as recommended by the Kidney Disease Improving Global Outcomes (KDIGO) guidelines and validated in children with and without CKD [21, 23, 24].

Examination of Schistosoma mansoni and Schistosoma haematobium

To screen for S. mansoni infection, point-of-care circulating cathodic antigen tests (CCA) (rapid medical diagnostic batch number: 170331037) were used. The same urine samples obtained earlier were used for the CCA test [25, 26]. Results were recorded as per manufacturer instructions [26].

For screening of S. haematobium infection, a urine filtration technique was used in which the urine sample was filtered (pore aperture 20 μm; Sefar AG, Heiden, Switzerland) and the filter was then placed on a slide and examined under a microscope for presence of S. haematobium eggs [27].

Malaria diagnosis

Malaria diagnosis was determined using an mRDT (Malaria Antigen P.f/Pan 05FK60, Standard Diagnostics (SD) Bioline, India) and interpreted according to the manufacturer’s instructions.

Definition of renal abnormalities

In this study, renal abnormalities were operationally defined as eGFR < 60 ml/min/1.73 m2 or microalbuminuria (urine for ACR > 30 mg/g or proteinuria of ≥ 2+ or hematuria ≥ 2+).

Data analysis

Data were double entered into Microsoft Excel and analyzed using STATA version 15. Results were summarized using proportions (%) for categorical data and means (SD) or medians (IQR) for continuous variables. Categorical variables were compared using either Pearson’s chi-squared or Fisher’s exact test. Determination of predictors of proteinuria and microalbuminuria was done by univariate logistic regressions followed by multivariable logistic regression. Odds ratios (OR) with 95% confidence interval (CI) were reported.

Results

Characteristics of the study participants

A total of 554 school children from Kayenze, Kabangaja, and Sangabuye primary school were enrolled into the study (Fig. 1). We excluded 47 children because of the following reasons: 25 had features suggestive of UTI (proteinuria, nitrate, and leucocytes on urine dipstick), 10 failed to produce urine specimen, 9 with fever, and 3 children with preexisting renal disease. Five hundred and seven children were included in the final analysis. Of these children, 49.9% (253/507) were male with a mean age of 8.5 ± 1.3 years. The majority of children (84.2%) had been in contact with the lake within 1 week prior to the survey administration, and 60% used the lake as a source of water for bathing, cooking, washing, and drinking (Table 1).

Fig. 1
figure 1

Study enrollment overview

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Table 1 Characteristics of 507 primary school children
Full size table

Prevalence of schistosomiasis and malaria

The prevalence of S. mansoni and S. haematobium was 64.3% and 1.6% respectively. Prevalence of S. mansoni was higher in younger children 6 to 9 years compared to participants 10 to 13 years (76% vs. 23%, p = 0.062), but the prevalence did not differ by sex (50% vs. 49%, p = 0.538). The prevalence of asymptomatic malaria was 17.4% (88/507). Males were slightly more affected than females (56% and 43%). Younger children aged 6 to 9 years were also more affected by malaria than older children aged 10 to 13 years although this was not statistically significant (p = 0.153).

Renal abnormalities

Eight (1.6%) of the study participants had an eGFR less than 60, which meets the criteria for severe renal abnormalities. Twenty (3.9%) participants had an eGFR of < 90 ml/min/1.73 m3. Due to the small number of cases with eGFR < 60, this study could not conduct univariate and multivariate analysis. Overall, 33 (6.5%) participants had microalbuminuria in the nephrotic range with severely increased ACR (> 300gm/g), and 241 (47.5%) had moderately increased ACR range 30–300 mg/g. Seventy-one (71/507) (14.0%) participants had proteinuria of 2+ to 4+, and 37 (7.3%) had blood in their urine. Prevalence of renal abnormalities was 22.9% (Table 2).

Table 2 Laboratory renal abnormalities among 507 study participants
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Factors associated with proteinuria

All presenting demographic and clinical characteristics were evaluated as possible factors predictive of proteinuria. Significant predictors of proteinuria on multivariable analysis included schistosomiasis and blood in the urine. We observed that children infected with S. mansoni had 4 times higher odds of having proteinuria compared to those without S. mansoni (OR [95% CI] = 4.9 [2.1–11.2], p < 0.001). Also, children with blood in their urine had five times higher odds of having proteinuria compared with those without blood in their urine (OR [95% CI] = 5.3 [2.5–11.0], p < 0.001 (Table 3).

Table 3 Factors associated with proteinuria
Full size table

Factors associated with microalbuminuria

Presence of blood in urine was the only factor associated with microalbuminuria on multivariable analysis in this study. Children with blood in the urine had two times higher odds of having microalbuminuria compared to those without blood in their urine (OR [95% CI] 2.3 [1.1–4.9], p = 0.035 (Table 4).

Table 4 Factors associated with microalbuminuria
Full size table

Discussion

In this study, the overall prevalence of renal abnormalities was 22.9% and factors associated with proteinuria were S. mansoni infection and RBCs in urine.

Based on CCA, close to two thirds of the children participating in this study were infected with S. mansoni with a small percentage infected with S. haematobium. Similarly, a marginal proportion of children were diagnosed with proteinuria and hematuria, all of whom had low eGFR.

Based on eGFR, only a small percentage of the children included in the present study had renal abnormalities. The observed prevalence was lower than the 7.4% reported in another study done in Northwestern Tanzania and 4.6 reported in a systematic study done in Africa [12, 28]. This variation could be due to the different age group or type of exposure of participants in this study.

Although urogenital schistosomiasis is known to contribute to renal abnormalities, no association was observed between S. haematobium and low eGFR in this study. This can partly be explained by the low prevalence of S. haematobium found, as studies in areas with a higher prevalence of S. haematobium have reported an association between low eGFR and S. haematobium [7].

On the other hand, the prevalence of proteinuria observed in the present study was lower than what was observed in previous studies which range from 32 to 44% in the same region [7, 29]. This may be due to the fact that previous studies involved children with sickle cell anemia and HIV infection and our study was done in the general population of children in primary schools.

Microalbuminuria is known to be an early predictive factor for renal and cardiovascular diseases, not only for patients with diabetes mellitus, hypertension, or sickle cell anemia, but also in the general population [30]. In this study, almost half of the participants had moderately increased ACR and 6.5% had severely increased ACR. This was much higher than the levels that were found among Korean children aged 5–14 years [31]. It is unclear why there is such difference, and future research should investigate reasons for disparity.

Hematuria found in 37 participants may have originated from the glomerular, renal tubules and interstitial space, or urinary tract. In children with S. haematobium, the deposition of eggs in the bladder and ureter and subsequent granulomatous inflammation cause hematuria [32, 33]. Studies in Africa have reported rates of hematuria ranging from 0.6 to 67%, though most of the studies were done more than 20 years ago in areas with high prevalence of S. haematobium [7].

Our study showed an alarmingly high S. mansoni prevalence of 64% among primary school children living along the shores of Lake Victoria. We used a more sensitive test point-of-care CCA test, which is reported to be more sensitive than Kato Katz slides (86% sensitive versus 62%) [25]. Similar prevalence of 62% and 64% was observed in Sengerema and Ukerewe, two nearby communities, using a mixed method of POC-CCA and Kato Katz slides [34]. The high prevalence of schistosomiasis found here can be explained by an inadequate clean water supply, poor sanitation, domestic activities such as farming and fishing, recreational swimming, and also a high density of intermediate hosts along Lake Victoria [17].

In the present study, the prevalence of S. haematobium by single filtration test was low. This prevalence is slightly lower compared to what was reported in Zanzibar (Unguja and Pemba), in which the prevalence of 2.7% and 7% in primary school children was found [35]. The low prevalence may be because the location of communities in our study was along the lakeshores, which are less affected by S. haematobium [17]. The different species of snail hosts that transmit Schistosoma species have different preferences for location, with those transmitting S. mansoni preferring larger bodies and those transmitted S. haematobium preferring small water bodies away from the lakeshore line [17].

S. mansoni infection was strongly associated with proteinuria. Participants with proteinuria had four times higher odds of having proteinuria compared to those with no infection. Glomerular lesion associated with S. mansoni results from circulating antigen of Schistosoma eggs. The immune complex when deposited in the glomerulus results in injury and a cascade of immunological reaction. Previous studies in sub-Saharan Africa have reported similar findings [7].

Our studies had several limitations. First, renal ultrasound could have been helpful in identifying morphological changes consistent with schistosomiasis but was not done in this study. Second, this was a cross-sectional study with no control group; therefore, causality in the relationship between kidney injury and schistosomiasis infection could not be examined. Third, children with fever and preexisting renal disease were excluded; this may limit the generalization of our results. Also, identification of schistosomiasis using a gold standard test (stool microscopy) was not done in this study. Despite these limitations, this study contributed to the few studies that have evaluated the relationship between schistosomiasis and renal abnormalities.

Conclusion

Our study findings show that 1 out 5 of primary school children have renal abnormalities. The study also identified a very high prevalence of S. mansoni and low prevalence of S. haematobium. Children with schistosomiasis had higher odds of having proteinuria. Screening and mass treatment of schistosomiasis should be a priority in this community in order to prevent long-term effect of renal injury. We also recommend longitudinal studies to identify causal relationship between S. mansoni and renal abnormalities.

Availability of data and materials

The datasets collected and/or analyzed during the current study are available from the corresponding author upon request.

Abbreviations

ACR:

Urine for albumin creatinine ration

mRDT:

Malaria rapid diagnostic test

eGFR:

Glomerular filtration rate

CI:

Confidence interval

IQR:

Interquartile range

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Acknowledgements

The authors wish to thank MEPIJF Tanzania for financial support. We appreciate the support provided by the Mwanza region commissioner, Ilemela District Medical and Education Officers. We would like also to thank the teachers, parents, and children from all three primary schools for their participation in the study. We are grateful for the research team, Mr. Honest Nagai, Dr. Christopher Kasanda, Mr. Julius Mungai, and Mr. Peter Nandi. Special thanks to Prof. Daniel Fitzgerald and Prof. Robert Peck for their comments on the earlier version of the manuscript.

Funding

Research reported in this publication was supported by the Fogarty International Center (and list ALL co-funding partners) of the National Institutes of Health under Award Number D43 TW010138. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

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Authors and Affiliations

  1. Department of Pediatrics, Weill Bugando School of Medicine, Catholic University of Health and Allied Sciences, Mwanza, United Republic of Tanzania

    Neema M. Kayange & Adolfine Hokororo

  2. Kilimanjaro Fertility Institute (KFi), Kilimanjaro, Tanzania

    Nicholaus Mazuguni

  3. Department of Biochemistry and Molecular Biology, Weill Bugando School of Medicine, Catholic University of Health and Allied Sciences, Mwanza, United Republic of Tanzania

    Benson R. Kidenya

  4. Department of Medical Parasitology and Entomology, Weill Bugando School of Medicine, Catholic University of Health and Allied Sciences, Mwanza, United Republic of Tanzania

    Humphrey D. Mazigo

  5. Department of Population Health Sciences, Duke University, Durham, NC, USA

    Charles Muiruri

  6. Centre for Global Health at Weill Cornell, New York, USA

    Karl Reis

  7. Department of Epidemiology and Biostatistics, Kilimanjaro Christian Medical University College, Moshi, Tanzania

    Charles Muiruri

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  1. Neema M. Kayange
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Contributions

NMK is the principal investigator and contributed to the study design, data collection, analysis, and manuscript preparation. NM and AH contributed to the study design and manuscript preparation. CM, BRK, HDM, and KR contributed to data analysis and interpretation. All authors contributed to the study design, interpretation, and drafting of the article. All authors read and approve the final version of the paper.

Corresponding author

Correspondence to Neema M. Kayange.

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The authors declare that they have no competing interests.

Ethics approval and consent to participate

Ethical approval was obtained from the Joint Catholic University of Health and Allied Sciences/Bugando Medical Centre (CUHAS, Research Clearance Certificate No: (CREC/121/2016) of Tanzania. Permission also was obtained from Ilemela District commissions and the headmasters of Kayange, Sangabuye, and Kabangaja schools. All parents/guardians of the participants were informed in Kiswahili about the study. Written informed consent and assent were obtained. All participants found to have S. mansoni infection, malaria, and/or UTI were treated according to the National guideline [40].

Consent for publication

Permission to publish was obtained from ethical clearance committee, Catholic University of Health and Allied Sciences, certificate number CREC/121/2016.

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Kayange, N.M., Mazuguni, N., Hokororo, A. et al. Renal abnormalities and its associated factors among school-aged children living in Schistosoma mansoni endemic communities in Northwestern Tanzania. Trop Med Health 48, 55 (2020). https://doi.org/10.1186/s41182-020-00243-6

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Keywords

Tropical Medicine and Health

ISSN: 1349-4147

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