- Open Access
Malaria, anaemia and under-nutrition: three frequently co-existing conditions among preschool children in rural Rwanda
© Kateera et al. 2015
- Received: 22 April 2015
- Accepted: 28 October 2015
- Published: 5 November 2015
Malaria, anaemia and under-nutrition are three highly prevalent and frequently co-existing diseases that cause significant morbidity and mortality particularly among children aged less than 5 years. Currently, there is paucity of conclusive studies on the burden of and associations between malaria, anaemia and under-nutrition in Rwanda and comparable sub-Saharan and thus, this study measured the prevalence of malaria parasitaemia, anaemia and under-nutrition among preschool age children in a rural Rwandan setting and evaluated for interactions between and risk determinants for these three conditions.
A cross-sectional household (HH) survey involving children aged 6–59 months was conducted. Data on malaria parasitaemia, haemoglobin densities, anthropometry, demographics, socioeconomic status (SES) and malaria prevention knowledge and practices were collected.
The prevalences of malaria parasitaemia and anaemia were 5.9 and 7.0 %, respectively, whilst the prevalence of stunting was 41.3 %. Malaria parasitaemia risk differed by age groups with odds ratio (OR) = 2.53; P = 0.04 for age group 24–35 months, OR = 3.5; P = 0.037 for age group 36–47 months, and OR = 3.03; P = 0.014 for age group 48–60 months, whilst a reduced risk was found among children living in high SES HHs (OR = 0.37; P = 0.029). Risk of anaemia was high among children aged ≥12 months, those with malaria parasitaemia (OR = 3.86; P ≤ 0.0001) and children living in HHs of lower SES. Overall, under-nutrition was not associated with malaria parasitaemia. Underweight was higher among males (OR = 1.444; P = 0.019) and children with anaemia (OR = 1.98; P = 0.004).
In this study group, four in 10 and one in 10 children were found stunted and underweight, respectively, in an area of low malaria transmission. Under-nutrition was not associated with malaria risk. While the high prevalence of stunting requires urgent response, reductions in malaria parasitaemia and anaemia rates may require, in addition to scaled-up use of insecticide-treated bed nets and indoor residual insecticide spraying, improvements in HH SES and better housing to reduce risk of malaria.
Malaria, anaemia and under-nutrition are each associated with significant morbidity and mortality, particularly among children in sub-Saharan Africa [1–3]. Globally, malaria is responsible for over 450,000 deaths among children under 5 years ; anaemia is prevalent in 273 million (43 %) of children aged 6–59 months ; and severe under-nutrition affects about 20 million preschool-aged children living mostly in African and South-East Asia Regions . In the majority of the affected children, all three conditions frequently co-exist and have been associated with long-term complications, including deficits in physical and cognitive development and poor school performance [5–8].
Anaemia is characterized by a reduction in haemoglobin concentration causing impairment in meeting the oxygen demands of the body. Anaemia results broadly from either ineffective erythropoiesis or increased loss of erythrocytes or both. The main causes of anaemia include acute or chronic blood loss, nutritional deficiencies (including vitamins A, B12, C and folic acid and iron) , infectious diseases [10–12] and genetic disorders [13, 14].
Malaria causes a substantial proportion of anaemia observed in malaria endemic settings [15, 16]. However, how much of the anaemia burden is associated with malaria, relative to other causes, and across the different strata of malaria endemicities has not been studied.
Studies elucidating associations between malaria and under-nutrition yield conflicting results ; with some suggesting that under-nutrition is associated with higher malaria morbidity and all-cause mortality outcomes [17–19], while others show no effect of under-nutrition on malaria . Conversely, some studies have associated malaria with increased risk of under-nutrition  and Plasmodium falciparum infection has been associated with acute weight loss . Additionally, improvements in growth and other anthropometric indexes have been described in children protected from malaria, by using both malaria chemoprophylaxis  and long-lasting insecticide-treated bed nets (LLINs) .
Given the extensive temporal and spatial correlation between malaria, anaemia and under-nutrition, any interaction (causal or increasing the likelihood of poor health outcomes on either diseases) may lead to synergistic deleterious effects on child health and development. Studies on interactions between malaria, anaemia and under-nutrition particularly among community preschool-aged children are few and inconclusive . Most of these children carry these disease conditions in “hidden” pre-clinical stages and rarely present to medical personnel in the national health care system. This study measured the prevalence, investigated co-existence and assessed for risk determinants of malaria parasitaemia, anaemia and under-nutrition among preschool-going children in a rural Rwandan community.
Study design and selection of study participants
A larger descriptive cross-sectional survey involving all study area HHs was conducted to study social, economic, entomological and biomedical determinants of residual asymptomatic malaria burden and transmission intensity. In summary, the night prior to the survey, a village community health care worker identified HHs to be visited from an enumeration list and requested heads of households (HoH) and family members to stay in-house. Upon providing consent, the study team (consisting of an interviewer and a laboratory technician) visited the notified HH and administered an interviewer-guided questionnaire to HoHs. In HHs where no member or no HoH or spouse was found present, a return visit was scheduled and attempted within 7 days. All HHs where the study team failed to conduct a survey on the return visit were excluded. Study findings from this larger sector-wide HH survey conducted between June and November 2013 have since been published . For this sub-study, final data analysis was performed for only children aged 6–59 months who had complete laboratory and questionnaire data.
Head of household interviews
A structured questionnaire was administered to the child’s primary caregiver to collect data on (1) demographics (sex, age, literacy, occupation, religion and marital status); (2) malaria prevention bed net (LLIN ownership, number and use) and indoor residual spraying (IRS) experience; (3) SES related variables (incomes, savings, land ownership, animals and sources of utilities like water, lighting and cooking) and HH structural features including type of outside wall, floor and roof materials); and (4) fever management practices. For each HH, location data was captured using a geographic positioning function based on the Samsung Galaxy 2 Android platforms (Samsung Electronics Co. Ltd, South Korea). The questionnaire used was written in English and was field-tested at three sites in order to minimize ambiguity, ensure consistency of comprehension of questions by both interviewers and respondents. Field workers were trained to administer the interviews in the local dialect (Kinyarwanda). Questionnaire data was collected using an electronic format developed using the open source Open Data Kit Collect setup on Android tablets .
Measures of under-nutrition indices (stunted, underweight, and wasted) were deduced from data on (1) age-in-months as reported by parents, (2) weight measured using UNICEF provided a digital Seca 874 weight scales (seca GmbH & Co. KG.) to the nearest 0.1 kg, and (3) height measured using a mobile measuring Seca 210 (seca GmbH & Co. KG.) mat for children 0 to 99 centimetres and a recumbent length board for children of height > 99 centimetres to the nearest centimetre, respectively.
From all HH members aged ≥6 months, finger-prick blood samples for malaria smear-based diagnosis and haemoglobin measurement were collected. Each smear was stained with 2 % Giemsa, processed and read independently by two study-trained microscopists at Ruhuha Health Centre laboratory. In case of a discrepancy, a tie-breaker third microscopist determined the final result. Expert microscopists at the National Reference Laboratory, Kigali, conducted quality control for all positive slides and a random sample of 5 % of all negative slides. Haemoglobin densities were measured on the spot in the field using a portable automated HemoCue® Hb 301 haemoglobinometer system (HemoCue AB, Angelholm, Sweden) according to the product instruction.
Outcome and predictor variables
A blood smear was considered negative when light microscopy examination of 100 high-power fields did not reveal any asexual parasites and considered positive if any asexual parasites were detected on thick blood microscopy. In this study, malaria diagnosis was assessed based on presence of malaria parasites in blood by microscopy only. Data on reported symptoms or clinical signs was not collected. Anaemia was defined as moderate-to-severe haemoglobin levels of <90 g/L as recommended for disease surveillance, especially in areas of high anaemia prevalence . Weight-for-height (wasting), height-for-age (stunting) and weight-for-age (underweight) z scores were calculated on the basis of the WHO Global Database on Child Growth and Malnutrition . Z scores of <−2 SD were considered indicative of wasting, stunting, and underweight, respectively, while corresponding Z scores of <−3 SD were considered indicative of severe under-nutrition.
Predictor variables included HoH demographics (including age, sex, religion, marital status), cell of residence), malaria prevention practices (including availability and use of LLINs, HH use of IRS, reported prior fever management experiences, HH structure materials including type of floor (soil/clay/dung vs. brick/cement), roof (iron sheets vs. grass/tents), and outside walls (cement/brick versus mud/wood wall). A HH level SES/wealth index (used to categorize each HH as low, middle and high SES category) was generated using 10 indicator variables using principal component analysis .
Study consent and ethical approval
Written informed consent to participate in the study as well to allow study findings to be published in a relevant scientific journal was obtained from the HoH on behalf of all household members including minors. The National Health Research Committee (NHRC) and the Rwanda National Ethics Committee, Kigali, Rwanda (No 384/RNEC/2012) granted ethical and scientific approval for the study protocol.
Data was collected using handheld android platforms on which open data kit software-hosted electronic questionnaire was loaded. These data was then relayed onto a server. Laboratory and anthropometric data was manually recorded in laboratory registers and later entered into Microsoft Access software. The two datasets were then merged and transferred into STATA 12.1 (STATA Corp., College Station, TX, USA) for analysis. Continuous variables were compared between groups (including stratification by age and sex) using Mann–Whitney U tests, and variable proportions were compared by Χ2 test. Associations between predictor variables and primary outcomes were statistically assessed for using both bivariate and multivariate logistic regression analysis. Odds ratios (ORs) and 95 % confidence intervals (CIs) were computed. Any covariate with a p value <0.15 in bivariate analysis were subsequently included in the final multivariable logistic model. Multi-collinearity tests were performed for all potentially correlated variables included in the final multivariate model for each of the five primary outcomes. Any risk estimate with a p-value <0.05 was considered statistically significant after adjustment for HH-level clustering and influence of other variables.
As reported in the earlier publication for the larger survey, a total of 4705 HHs were surveyed and of these, data from 12,965 (all-ages) individuals from 3968 (84.3 %) HHs that had complete laboratory and questionnaire data was aggregated in the primary database . From this primary database, data for 3182 children (aged 6–59 months) from 2228 HHs were extracted and analysed in this study. However for the final analysis, only 1882 (59.1 %) children with complete data on all primary outcome covariates (malaria slide positivity, haemoglobin densities and anthropometric data on age by months, height and weight) were considered.
Study population baseline and demographic characteristics
N = 1882
Study group median age
31.1 (IQR: 18.4–45.70)
Study group mean weight in Kilograms
Study group mean height in meters
Study group mean haemoglobin density in g/dl
Number of children per cell
Number of children with malaria parasite carriage (Yes)
110/1876 (5.9 %)
Number of children with moderate-severe anaemia (<90 g/l)
132/1876 (7.0 %)
Number of children with under weight (Z score of <−2 SD of mean)
297/1882 (15.8 %)
Number of children with stunting (Z score of <−2 SD of mean)
777/1882 (41.3 %)
Number of children with wasting (Z score of <−2 SD of mean)
166/1876 (8.8 %)
Number of children reported ownership of ≥1 Bednet in HH (Yes)
1799/1882 (95.6 %)
Number of HHs with reported IRS done in last 12 months (Yes)
1805/1882 (95.9 %)
Number of children with reported fever in last 6 months (Yes)
1293/1882 (68.7 %)
Number of HoH per education level None
620 (33 %)
1259 (67 %)
Number of HH occupants
298 (15.83 %)
1373 (72.95 %)
211 (11.22 %)
Number of children per age group (in months)
225 (11.96 %)
435 (23.11 %)
434 (23.06 %)
372 (19.77 %)
416 (22.10 %)
Frequency of malaria, anaemia and under-nutrition co-morbidities
Malaria, n (%)
Anaemia, n (%)
Under-nutrition, n (%)
Factors associated with malaria
Malaria parasitaemia and anaemia distributions and bivariate analysis stratified by sex, residence and age group
OR (95 % CI), P-value
OR (95 % CI), P-value
0.796 (0.540–1.173), 0.248
1.139 (0.799–1.624), 0.470
1.659 (0.653–4.216), 0.287
0.555 (0.327–0.940), 0.029
2.531 (1.032–6.206), 0.042
0.502 (0.293–0.860), 0.012
2.625 (1.059–6.502), 0.037
0.404 (0.225–0.728), 0.003
3.028 (1.246–7.356), 0.014
0.323 (0.177–0.591), <0.0001
0.743 (0.398–1.390), 0.353
1.156 (0.638–2.092), 0.633
1.674 (0.943–2.969), 0.078
1.503 (0.829–2.728), 0.180
0.843 (0.450–1.577), 0.592
1.011 (0.544–1.881), 0.971
0.330 (0.137–0.798), 0.014
1.152 (0.605–2.193), 0.667
Multivariate risk factors analysis for anaemia, under-nutrition parameters and malaria parasitaemia
Anaemia OR (95 % CI), P-value
Stunting OR (95 % CI), P-value
Wasting OR (95 % CI), P-value
Underweight OR (95 % CI), P-value
Malaria OR (95 % CI), P-value
Malaria parasitaemia (Positive)
3.857 (2.208–6.740), <0.0001
Presence of anaemia (yes)
1.857 (1.093–3.155), 0.022
3.898 (2.297–6.615), <0.0001
Presence of stunting (yes)
1.428 (0.960–2.126), 0.079
0.046 (0.024–0.088), <0.0001
20.412 (12.304–33.862), <0.0001
Presence of wasting (yes)
0.055 (0.030–0.098), <0.0001
59.139 (32.506–107.594), <0.0001
Presence of under weight (yes)
1.979 (1.240–3.158), 0.004
20.256 (12.464–32.921), <0.0001
60.71 (31.994–115.197), <0.0001
1.444 (1.061–1.966), 0.019
1.331 (1.070–1.656), 0.010
Is HH in an economic group? (Yes)
0.758 (0.618–0.931), 0.008
Was IRS done in HH (Yes)
0.589 (0.397–0.873), 0.008
Does the HH owns ≥1 bednet (Yes)
0.551 (0.338–0.899), 0.017
Study participant age group
0.522 (0.297–0.916), 0.023
1.262 (0.697–2.283), 0.443
1.989 (0.766–5.169), 0.158
0.405 (0.227–0.721), 0.002
1.849 (1.031–3.316), 0.039
3.157 (1.259–7.920), 0.014
0.340 (0.181–0.639), 0.001
2.124 (1.159–3.894), 0.015
3.528 (3.1384–8.992), 0.008
0.257 (0.135–0.490), <0.0001
2.123 (1.169–3.855), 0.013
3.699 (1.479–9.251), 0.005
HH SES level
0.588 (0.373–0.928), 0.022
0.793 (0.415–1.516), 0.483
0.568 (0.352–0.916), 0.020
0.372 (0.152–0.906), 0.029
Does HH have a closed water source (Yes)
1.465 (0.969–2.214), 0.070
0.620 (0.377–1.018), 0.059
House wall material (Bricks and stones vs. wood/mud/tent)
0.615 (0.370–1.024), 0.061
House floor material (cement/concrete vs. mud/earth/dung)
0.447 (0.276–0.723), 0.001
Highest HoH education level (None vs. any)
0.633 (0.404–0.990), 0.045
Factors associated with anaemia
Anaemia distribution was similar across both sexes but decreased with increasing age and, similar to malaria parasitaemia, showed a higher proportion among children in Gikundamvura cell (10.2 %) vs. children in the other four cells with proportions ranging from 5.4 to 6.3 % (Table 3). By bivariate analysis, living in Gikundamvura was associated with a 1.9-fold (P = 0.008) higher odds of having anaemia compared to living in Biharwe cell while the risk of anaemia decreased with increasing age group (Table 3). In the final multivariate model, anaemia risk was high among children with malaria infection (OR = 3.86) and underweight (OR = 1.98) and decreased with increasing age, and among children living in wealthier HHs of middle and high SES (OR = 0.59; P = 0.022 and OR = 0.57; P = 0.020, respectively) (Table 4).
Factors associated with under-nutrition
Stunting, under-weight and wasting distributions and bivariate analysis stratified by sex, residence and age group
OR (95 % CI), P-value
OR (95 % CI), P-value
OR (95 % CI), P-value
1.146 (0.953–1.377), 0.147
1.346 (1.049–1.727), 0.020
0.897 (0.652–1.235), 0.506
1.314 (0.945–1.827), 0.105
1.255 (0.763–2.066), 0.371
0.963 (0.558–1.660), 0.891
1.344 (0.967–1.869), 0.079
1.753 (1.082–2.840), 0.023
0.894 (0.515–1.553), 0.692
1.084 (0.771–1.525), 0.641
1.694 (1.033–2.777), 0.037
0.871 (0.493–1.540), 0.635
1.081 (0.774–1.511), 0.646
1.618 (0.993–2.639), 0.053
0.795 (0.451–1.399), 0.427
1.348 (1.003–1.812), 0.048
0.996 (0.680–1.459), 0.984
0.870 (0.519–1.458), 0.598
1.055 (0.771–1.442), 0.738
0.975 (0.652–1.458), 0.902
1.041 (0.614–1.763), 0.881
0.971 (0.715–1.318), 0.852
0.746 (0.496–1.121), 0.158
0.986 (0.588–1.654), 0.957
1.231 (0.891–1.699), 0.207
0.678 (0.433–1.059), 0.088
0.972 (0.558–1.692), 0.920
Collinearity analysis between all variables included in each of final multivariate model for the five primary outcomes showed mean variance inflation factor (VIF) values ranging from 2.17 to 7.23. For each of the five-outcome models, no variable showed a VIF >10: This is the cutoff marker of multicolinearity.
At least 4/10 and 1/10 preschool-age children in this rural setting were found stunted and underweight, respectively. Observed malaria parasite rates of <10 % suggest that this area is hypo-endemic for malaria. In this study, the proportion of children aged under 5 years with malaria (6.5 %) was almost two-fold higher than the 3.4 % reported in the same province in 2010 . These differences in proportions infected with malaria may be partially explained by malaria-associated temporal patterns, seasonality and/or differences in sampling technique used in the two surveys. However, the parasite rates observed in this study are comparable to the <10 % malaria infection rates reported among community members previously [25, 26, 31] suggesting that this area is of hypo-endemic transmission intensity .
In this study, risk of malaria increased with increasing age. Findings in this study are consistent with an increasingly observed trend of higher malaria risk among older age groups, as reported previously elsewhere and in this area, following the scale-up of control interventions [25, 26, 32, 33]. A reduction in malaria transmission and hence a lower frequency of exposure to malaria parasite inoculation and the associated infections impedes and, plausibly, delays development of a malaria protective immunity leading to an increased risk of malaria in older age groups. However, two reasons may account for the higher risk in older children observed in this study: (1) younger children are more likely to sleep under ITNs and hence be more protected, and (2) in contrast, older children are likely to tolerate malaria parasites without developing a fever and hence have an increased prevalence of asymptomatic malaria parasitaemia.
In this study, a protective malaria risk was associated with living in a high SES HHs. However, studies on associations between malaria and SES have hitherto yielded conflicting results, with some indicating no associated effect [34, 35] while others have shown that higher SES induces a protective effect [36–40]. It is plausible that a protective effect may exist where improved house structural features lead to a reduction in indoor malaria transmission by restricting mosquito entry . Individuals living in houses whose wall structure were made of wood/mud (vs cement/bricks) showed a significantly higher risk of malaria in this study. Houses whose walls are made of mud have been associated with having more eaves (that support mosquito entry), higher risk of indoor mosquito bites and, by creating cooler and darker conditions in comparison to brick/cement houses, creating a favourable indoor resting environment for mosquitoes [41–43].
The proportion of children under 5 years found with anaemia in this study (6.8 %) was three-fold higher than the 2.0 % reported for the same province in 2010 . After adjusting for all predictors, anaemia risk was associated with malaria parasitaemia, age group, HH SES and underweight, with a borderline significant outcome noted among children with stunting and those coming from HHs where IRS was applied. Individuals found with moderate-to-severe anaemia had an almost four-fold increased risk of being malaria-infected. In malaria-endemic settings, malaria is the most common cause of anaemia  and among parasitaemic patients in comparable settings, a similarly increased risk of anaemia has been previously demonstrated [35, 44, 45]. In one study among preschool-going children in Uganda, malaria was found to be the only risk determinant for anaemia . Additionally, effective malaria control programmes have been shown to significantly reduce anaemia burden, with anaemia now considered a surrogate indicator of impact of malaria control programmes [46, 47]. Interestingly in this study, the risk of anaemia decreased with increasing age groups in contrast to the observed increasing risk of malaria across the same age groups in our study and some studies other malaria-endemic settings [15, 35, 48]. However, in all the other settings, the reported malaria parasite carriage rates were significantly higher than the 6.8 % reported in this study. In study areas of lower parasitaemia carriage, and especially following reduction in malaria burden, malaria may make a less significant attributable contribution to anaemia relative to other risk factors .
Anaemia, but not malaria, was significantly associated with underweight in this study. Evidence for the impact of under-nutrition on development of anaemia in young children living in malaria-endemic areas had been reported previously . Previous studies on malaria and under-nutrition associations have shown contrasting results. In Ghana and in The Gambia, under-nutrition was associated with increased risks of malaria-associated mortality and the risk of having multiple malaria episodes, respectively [17, 18]. In contrast, in Burkina Faso and Uganda, no association between under-nutrition and malaria morbidity was demonstrated [35, 49]. Although this study did not assess for other causal factors associated with anaemia, it is plausible that children who are malnourished are more likely to also have had micronutrient deficiencies that may have partly contributed to the burden of anaemia observed.
Children from middle and high SES HHs were found to have a significantly reduced risk of having anaemia than children from low SES HHs. Two plausible reasons for this are the differential nutritional intakes and house structural features that determine risk of indoor malaria transmission between the two SES levels. Presumably, children from low SES HHs are likely to have poorer nutritional intake and also live in houses whose structure are more conducive for indoor malaria transmission, with the increased risk of malaria causing a concurrent deleterious effect on anaemia risk.
Among preschool-aged children in the same province in 2010, stunting, wasting and underweight proportions in comparison to findings in this study were 43.9 %, 3.2 % and 11.5 % vs. 41.6 %, 8.8 % and 15.8 %, respectively . Both surveys point to very high prevalence of stunting in this age group in this area. In our study, male sex was associated with a 1.44-fold increase in risk of underweight. Sex differences in risk of under-nutrition have been shown elsewhere [50, 51], but studies elucidating the observed sex-dependent risk of under-nutrition are lacking. As reported previously, the risk of being underweight significantly increased with increasing age in this study [52, 53]. Possible reasons for increased risk of underweight with increasing age could include but are not limited to (1) short birth intervals with mothers not having adequate gestational weight gains and hence having smaller than expected babies at birth; (2) reduced breast feeding periods; (3) poor weaning diets and; (4) reduced care given to older children following successive births .
Other risk determinants for malaria, anaemia and under-nutrition metrics were also identified. Living in houses where the HoH was not educated and in houses where domestic water was sourced from an open source compared to HHs where domestic water was drawn a closed source were associated with a high risk of malaria infection. Lack of education may likely be associated with low SES status and limited malaria control-associated knowledge and practice factors, which may be related to lower availability and use of malaria control measures like LLINs. Regarding the domestic water sources, open water sources may also serve as potential mosquito breeding sites and hence pose an increased risk. Anaemia risk was interestingly found to be lower by almost 50 % among individuals living in HHs where IRS was carried out. It is plausible that the IRS effect on lower anaemia risk was mediated primariry through reducing malaria risk. However, other unmeasured risk determinants may have contributed to the high risk among individuals from HHs where no IRS was applied of anaemia. Other identified risk determinants for under-nutrition included SES indicator variables (HoH belonging to an economic group and type of material house floor is made of) and prior fever experience and malaria control measures (LLIN availability and IRS experience). Given that the study area is predominantly agricultural, HHs where the HoHs reported being a member of an economic group are more likely to have better food security and hence a lower risk of under-nutrition. Individuals who reported having had a fever during the past 6 months are likely to have had malaria: A risk determinant of stunting . The use of malaria control measures (LLIN and IRS) could have reduced the risk of malaria and limited long-term development of under-nutrition.
This study had several limitations. Being a cross-sectional study design, associations observed may have been confounded by unmeasured factors. Also, causal inferences cannot be drawn from study findings due to the study design employed. The lack of additional haematological assessments including mean cell volume, micronutrients and haemolysis parameters limited the characterization of anaemia types. With regard to under-nutrition, only weight and height measurements were collected. The lack of other under-nutrition related data including skin fold thickness, oedema and body mass index did not allow for a more robust nutritional assessment. In this survey, statistical adjustments for correlation with and between HH members were conducted to ensure study finding were robust. However, given the multi-factorial causal factors associated with anaemia and under-nutrition, data on important covariates including but not limited to helminthic infection, micronutrient levels, co-infections like HIV, genetic haemoglobin disorders and breast feeding need to be collected in future studies to be able to perform a more robust analysis.
Study findings pointed to high rates of under-nutrition and anaemia but not malaria parasitaemia in preschool-going children. A strong association between malaria and anaemia but not between malaria and under-nutrition was observed. Although the study design limits the interpretation of cause and effect between these three disease determinants, control of malaria may have a substantial indirect reduction on anaemia burden among preschool-going children in this area. Integrated rather than vertical programmes covering nutritional rehabilitation, malaria control including the scaled up LLIN and IRS coverage, improvements in HH SES and better housing that limits mosquito entry are need to realize optimal child health outputs.
FK conceived the study, participated in study design, coordinated study implementation, performed statistical analysis and drafted the manuscript. CMI participated in study design and implementation. EH participated in design of study questionnaire and study implementation. PK was involved in study implementation and coordinated data management. PFM reviewed statistical analysis processes and critically reviewed the manuscript. MPG provided guidance on the data analysis process and critically reviewed the manuscript. LM participated in study implementation. MV participated in study conception, participated in its implementation and helped in draft and reviewing the manuscript. All authors read and approved the final manuscript.
We thank the Ruhuha community members, Ruhuha Health Centre leadership and the sector leadership for their support and study participation.
The Netherlands Organization for Tropical Scientific Research (NWO–WOTRO (AMC Project Number SA358001) funded the study.
The authors have declared that they have no competing interests.
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- WHO: World Malaria Report 2013. Geneva: World Health Organization. 2013. http://www.who.int/iris/…/9789241564694_eng.pdf. Accessed 24 Sept 2014.
- Stevens GA, Finucane MM, De-Regil LM, Paciorek CJ, Flaxman SR, Branca F, et al. Global regional, and national trends in hemoglobin concentration and prevalence of total and severe anemia in children and pregnant and non-pregnant women for 1995–2011: a systematic analysis of population representative data. Lancet Global Health. 2013;1:16–25.View ArticleGoogle Scholar
- UNICEF: United Nations Interagency Group for Child Mortality Estimation. Levels and trends in child mortality. 2014, New York: United Nations Children’s Fund. http://www.childmortality.org/files_v17/download/UNICEF%202014%20IGME%20child%20mortality%20Report_Final.pdf. Accessed 12 Oct 2014.
- WHO. Guideline: Updates on the management of severe acute malnutrition in infants and children 2012, Geneva: World Health Organization. http://apps.who.int/iris/bitstream/10665/95584/1/9789241506328_eng.pdf. Accessed 13 Mar 2014.
- Hall A, Khanh LN, Son TH, Dung NQ, Lansdown RG, Dar DT, et al. An association between chronic undernutrition and educational test scores in Vietnamese children. Eur J Clin Nutr. 2001;55:801–4.View ArticlePubMedGoogle Scholar
- Grantham-McGregor S, Ani C. A review of studies on the effect of iron deficiency on cognitive development in children. J Nutr. 2001;131:649S–66S.PubMedGoogle Scholar
- Agarwal DK, Upadhyay SK, Agarwal KN. Influence of malnutrition on cognitive development assessed by Piagetian tasks. Acta Paediatr Scand. 1989;78:115–22.View ArticlePubMedGoogle Scholar
- Hutchinson SE, Powell CA, Chang SPW, Grantham-Mc SM, Gregor SM. Nutrition, anaemia, geohelminth infection and school achievement in rural Jamaican primary school children. Eur J Clin Nutr. 1997;51:729–35.View ArticlePubMedGoogle Scholar
- Müller O, Traore C, Jahn A, Becher H. Severe anaemia in west African children: malaria or malnutrition? Lancet. 2003;361:86–7.View ArticlePubMedGoogle Scholar
- Best C, Neufingerl N, van Geel L, van den Briel T, Osendarp S. The nutritional status of school-aged children: why should we care? Food Nutr Bull. 2010;31:400–17.PubMedGoogle Scholar
- Menendez C, Fleming AF, Alonso PL. Malaria-related anaemia. Parasitol Today. 2000;16:469–76.View ArticlePubMedGoogle Scholar
- 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;85:91–9.PubMed CentralView ArticlePubMedGoogle Scholar
- Morris CR, Singer ST, Walters MC. Clinical hemoglobinopathies: iron, lungs and new blood. Curr Opin Hematol. 2006;13:407–18.PubMedGoogle Scholar
- Wambua S, Mwangi TW, Kortok M, Uyoga SM, Macharia AW, Mwacharo JK, et al. The effect of thalassaemia on the incidence of malaria and other diseases in children living on the coast of Kenya. PLoS Med. 2006;3:e158.PubMed CentralView ArticlePubMedGoogle Scholar
- Ehrhardt S, Burchard GD, Mantel C, Cramer JP, Kaiser S, Kubo M, et al. Malaria, anemia, and malnutrition in children—defining intervention priorities. J Infect Dis. 2006;194:108–14.View ArticlePubMedGoogle Scholar
- Green H, Sousa-Figueiredo J, Basáñez M, Betson M, Kabatereine NB, Fenwick A, et al. Anaemia in Ugandan preschool-aged children: the relative contribution of intestinal parasites and malaria. Parasitology. 2011;138:1534–45.View ArticlePubMedGoogle Scholar
- Mockenhaupt FP, Ehrhardt S, Burkhardt J, Bosomtwe SY, Laryea S, Anemana SD, et al. Manifestation and outcome of severe malaria in children in northern Ghana. Am J Trop Med Hyg. 2004;71:167–72.PubMedGoogle Scholar
- Deen JL, Walraven GE, von Seidlein L. Increased risk for malaria in chronically malnourished children under 5 years of age in rural Gambia. J Trop Pediatr. 2002;48:78.View ArticlePubMedGoogle Scholar
- Friedman JF, Kwena AM, Mirel LB, Kariuki SK, Terlouw DJ, Phillips-Howard PA, et al. Malaria and nutritional status among pre-school children: results from cross-sectional surveys in western Kenya. Am J Trop Med Hyg. 2005;73:698–704.PubMedGoogle Scholar
- Snow RW, Byass P, Shenton FC. The relationship between anthropometric measurements and measurements of iron status and susceptibility to malaria in Gambian children. Trans R Soc Trop Med Hyg. 1991;85:584–9.View ArticlePubMedGoogle Scholar
- Nyakeriga AM, Troye-Blomberg M, Chemtai AK, Marsh K, Williams TN. Malaria and nutritional status in children living on the coast of Kenya. Am J Clin Nutr. 2004;80:1604–10.PubMedGoogle Scholar
- Bayley NB. Scales of Infant Development. 2nd ed. San Antonio: PsychCorp Harcourt Assessment, Inc.; 1993.Google Scholar
- Bradley-Moore AM, Greenwood BM, Bradley AK, Kirkwood BR, Gilles HM. Malaria chemoprophylaxis with chloroquine in young Nigerian children. III. Its effect on nutrition. Ann Trop Med Parasitol. 1985;79:575–84.PubMedGoogle Scholar
- Ter Kuile FO, Terlouw DJ, Kariuki SK, Phillips-Howard PA, Mirel LB, Hawley WA, et al. Impact of permethrin-treated bed nets on malaria, anemia, and growth in infants in an area of intense perennial malaria transmission in western Kenya. Am J Trop Med Hyg. 2003;68:68–77.PubMedGoogle Scholar
- Rulisa S, Kateera F, Bizimana JP, Agaba S, Dukuzumuremyi J, Baas L, et al. Malaria prevalence, spatial clustering and risk factors in a low endemic area of eastern Rwanda: a cross sectional study. PLoS One. 2013;8:e69443.PubMed CentralView ArticlePubMedGoogle Scholar
- Kateera F, Mens PF, Hakizimana E, Ingabire CM, Muragijemariya L, Karinda P, et al. Malaria parasite carriage and risk determinants in a rural population: a malariometric survey in Rwanda. Malar J. 2015;14:16.PubMed CentralView ArticlePubMedGoogle Scholar
- Hartung C, Anokwa Y, Brunette W, Lerel A, Tseng C, Boriello G. Open Data Kit: tools to build information services for developing regions. Information and Communication Technologies and Development (ICTD). 2010. London, UK. http://opendatakit.org/wp-content/uploads/2010/10/ODK-Paper-ICTD-2010.pdf. Accessed 12 Aug 2014.
- Stoltzfus RJ. Rethinking anaemia surveillance. Lancet. 1997;349:1764–6.View ArticlePubMedGoogle Scholar
- WHO. Global Database on Child Growth and Malnutrition. 2006. Geneva: World Health Organization. http://www.who.int/nutgrowthdb/en/. Accessed 13 Nov 2014.
- Yvas S, Kumaranayake L. Constructing socio-economic status indices: how to use principal components analysis. Health Policy Plan. 2006;21:459–68.View ArticleGoogle Scholar
- National Institute of Statistics of Rwanda: Rwanda Demographic Health Survey. 2010. http://dhsprogram.com/pubs/pdf/FR259/FR259.pdf. Accessed 11 Nov 2014.
- Winskill P, Rowland M, Mtove G, Malima RC, Kirby MJ. Malaria risk factors in north-east Tanzania. Malar J. 2011;10:98.PubMed CentralView ArticlePubMedGoogle Scholar
- Smith T, Hii JL, Genton B, Müller I, Booth M, Gibson N, et al. Associations of peak shifts in age-prevalence for human malarias with bednet coverage. Trans R Soc Trop Med Hyg. 2001;95:1–6.View ArticlePubMedGoogle Scholar
- Luckner D, Lell B, Greve B, Lehman LG, Schmidt-Ott RJ, Matousek P, et al. No influence of socioeconomic factors on severe malarial anaemia, hyperparasitaemia or reinfection. Trans R Soc Trop Med Hyg. 1998;92:478–81.View ArticlePubMedGoogle Scholar
- Osterbauer B, Kapisi J, Bigira V, Mwangwa F, Kinara S, Kamya MR, et al. Factors associated with malaria parasitaemia, malnutrition, and anaemia among HIV-exposed and unexposed Ugandan infants: a cross-sectional survey. Malar J. 2012;11:432.PubMed CentralView ArticlePubMedGoogle Scholar
- Yé Y, Hoshen M, Louis V, Séraphin S, Traoré I, Sauerborn R. Housing conditions and Plasmodium falciparum infection: protective effect of iron-sheet roofed houses. Malar J. 2006;5:8.PubMed CentralView ArticlePubMedGoogle Scholar
- Koram KA, Bennett S, Adiamah JH, Greenwood BM. Socio-economic risk factors for malaria in a peri-urban area of The Gambia. Trans R Soc Trop Med Hyg. 1995;89:146–50.View ArticlePubMedGoogle Scholar
- Tshikuka JG, Scott ME, Gray-Donald K, Kalumba ON. Multiple infection with Plasmodium and helminths in communities of low and relatively high socio-economic status. Ann Trop Med Parasitol. 1996;90:277–93.PubMedGoogle Scholar
- Messina JP, Taylor SM, Meshnick SR, Linke AM, Tshefu AK, Atua B, et al. Population, behavioural and environmental drivers of malaria prevalence in the Democratic Republic of Congo. Malar J. 2011;10:161.PubMed CentralView ArticlePubMedGoogle Scholar
- Atieli H, Menya D, Githeko A, Scott T. House design modifications reduce indoor resting malaria vector densities in rice irrigation scheme area in western Kenya. Malar J. 2009;8:108.PubMed CentralView ArticlePubMedGoogle Scholar
- Kirby MJ, Green C, Milligan PM, Sismanidis C, Jasseh M, Conway DJ, et al. Risk factors for house-entry by malaria vectors in a rural town and satellite villages in The Gambia. Malar J. 2008;7:2.PubMed CentralView ArticlePubMedGoogle Scholar
- Harbison JE, Mathenge EM, Misiani GO, Mukabana WR, Day JF. A simple method for sampling indoor-resting malaria mosquitoes Anopheles gambiae and Anopheles funestus (Diptera: Culicidae) in Africa. J Med Entomol. 2006;43:473–9.View ArticlePubMedGoogle Scholar
- Lwetoijera DW, Kiware SS, Mageni ZD, Dongus S, Harris C, Devine GJ, et al. A need for better housing to further reduce indoor malaria transmission in areas with high bed net coverage. Parasit Vectors. 2013;6:57.PubMed CentralView ArticlePubMedGoogle Scholar
- McElroy PD, ter Kuile FO, Lal AA, Bloland PB, Hawley WA, Oloo AJ, et al. Effect of Plasmodium falciparum parasitemia density on hemoglobin concentrations among full-term, normal birth weight children in western Kenya, IV. The Asembo Bay Cohort Project. Am J Trop Med Hyg. 2000;62:504–12.PubMedGoogle Scholar
- Bloland PB, Boriga DA, Ruebush TK, McCormick JB, Roberts JM, Oloo AJ, et al. Longitudinal cohort study of the epidemiology of malaria infections in an area of intense malaria transmission II. Descriptive epidemiology of malaria infection and disease among children. Am J Trop Med Hyg. 1999;60:641–8.PubMedGoogle Scholar
- Korenromp EL, Armstrong-Schellenberg JR, Williams BG, Nahlen BL, Snow RW. Impact of malaria control on childhood anaemia in Africa—a quantitative review. Trop Med Int Health. 2004;9:1050–65.View ArticlePubMedGoogle Scholar
- Mathanga DP, Campbell CH, Vanden J, Wolkon EA, Bronzan RN, Malenga GJ, et al. Comparison of anaemia and parasitaemia as indicators of malaria control in household and EPI-health facility surveys in Malawi. Malar J. 2010;9:107.PubMed CentralView ArticlePubMedGoogle Scholar
- Knoblauch AM, Winkler MS, Archer C, Divall MJ, Owuor M, Yapo RM, et al. The epidemiology of malaria and anaemia in the Bonikro mining area, central Côte d’Ivoire. Malar J. 2014;13:194.PubMed CentralView ArticlePubMedGoogle Scholar
- Müller O, Garenne M, Kouyate B, Becher H. The association between protein-energy malnutrition, malaria morbidity and all-cause mortality in West African children. Trop Med Int Health. 2003;8:507–11.View ArticlePubMedGoogle Scholar
- Medhin G, Hanlon C, Dewey M, Alem A, Tesfaye F, Worku B, et al. Prevalence and predictors of undernutrition among infants aged six and twelve months in Butajira, Ethiopia: the P-MaMiE birth cohort. BMC Public Health. 2010;10:27.PubMed CentralView ArticlePubMedGoogle Scholar
- Wamani H, Astrom AN, Peterson S, Tumwine JK, Tylleskär T. Boys are more stunted than girls in sub-Saharan Africa: a meta-analysis of 16 demographic and health surveys. BMC Pediatr. 2007;7:17.PubMed CentralView ArticlePubMedGoogle Scholar
- Deribew A, Alemseged F, Tessema F, Sena L, Birhanu Z, Zeynudin A, et al. Malaria and under-nutrition: a community based study among under-five children at risk of malaria, south-west Ethiopia. PLoS One. 2010;5:e10775.PubMed CentralView ArticlePubMedGoogle Scholar
- Ethiopia Demographic and Health Survey: 2005. Addis Ababa, Ethiopia and Calverton, Maryland, USA: Central Statistical Agency and ORC. http://dhsprogram.com/pubs/pdf/FR179/FR179[23June2011].pdf. Accessed 13 Jul 2014.