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Article

Under-5 Malaria and Fever Morbidities as Correlates of Anaemia in Niger: A Heteroscedasticity-Consistent Ordered Probit Approach

by
Thonaeng Charity Molelekoa
* and
Abayomi Samuel Oyekale
Department of Agricultural Economics and Extension, North-West University Mafikeng Campus, Mmabatho 2735, South Africa
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2024, 21(12), 1687; https://doi.org/10.3390/ijerph21121687
Submission received: 11 September 2024 / Revised: 26 November 2024 / Accepted: 30 November 2024 / Published: 18 December 2024
(This article belongs to the Special Issue Socio-Economic Inequalities in Child Health)

Abstract

:
Background: The relationship between malaria/other febrile infections and anaemia among under-5 children is a subject of significant policy relevance among African health policy makers. The international significance of addressing anaemia is prominently underscored in the third Sustainable Development Goal (SDG). This paper therefore analysed the effect of malaria/other febrile infections and other maternal and child’s demographic variables on the prevalence of anaemia in Niger. Methods: We utilized the under-5 children’s module of the Malaria Indicator Survey (MIS) for 2021, which was collected from women of reproductive age (15–49) in selected households. The data were analysed with heteroscedasticity-consistent ordered probit regression model. Results: The results showed that 73.73% of the children was anaemic, while malaria and other febrile infections were present in 14.00% and 33.87%, respectively. Anaemia was highest in the Tillaberi and Dosso regions, where 84.12% and 79.12% of the children were anaemic. The ordered probit regression revealed that anaemia was promoted by malaria, other febrile infections, being a male child, second of multiple birth, and birth order, while wealth index, age, urban residence, and access to newspaper and television reduced it. Conclusions: Anaemia remains a major public health problem among under-5 children in Niger. A comprehensive healthcare intervention to address the problem should consider regional, sectoral, and gender differences in the incidences, with drastic efforts towards prevention of malaria and other fever-inducing illnesses. In addition, interventions to promote households’ economic status, reduce maternal fertility, and facilitate preventive practices through nutrition enhancement and health-related media programs hold some promise.

1. Introduction

Anaemia and fever are health problems of significant public health concern, particularly among under-5 children in developing countries [1]. Children under the age of five are said to be anaemic when they have a low concentration of blood haemoglobin below 11 g/dL [2,3]. Moreover, fever in children is diagnosed at the body temperature of 38.5 °C or more (101.3 °F) for children older than three months and 38.0 °C (100.4 °F) or more for those who are three months or less [4]. Some statistics have shown that around 43% of under-5 children are anaemic globally, while fever is the leading cause of hospital admissions among these children [5,6]. In sub-Saharan Africa (SSA), 28.5% of under-5 children are anaemic [7,8]. The adverse health consequences of anaemia in children include stunting, the impairment of cognitive development, immune system compromise, and a high risk of morbidity and mortality [9].
In Niger, different interrelated health issues such as infections and malaria manifest as severe fever that impact under-5 children [10,11,12,13]. Therefore, fever often indicates an underlying infection, although diagnosing the exact cause can be challenging, especially in developing countries where malaria is commonly presumed [14]. By age five, children in these countries experience around 40 fever episodes, often managed with antibiotics or antimalarial drugs [15]. Specifically, fever-related illnesses and anaemia are remarkably interlinked and contribute to high rates of severe morbidity and mortality among under-5 children [16]. This emphasizes the need for thorough research and targeted interventions to promote Nigerien children’s health, for the reduction of child mortality and promotion of cognitive and physical development [17].
Furthermore, anaemia results from insufficient red blood cells or haemoglobin levels, which are crucial for transporting oxygen within the body’s cells [18,19]. Anaemia promotes a reduction in oxygen delivery to the body’s cells, causing symptoms like fatigue and shortness of breath [17]. The causes of anaemia in under-5 children include poor diet, infections, inflammation, chronic diseases, and genetic disorders [20,21]. However, iron deficiency is a primary cause of anaemia, along with deficiencies in folate, vitamins B12, and Vitamin A [21]. Nigerien children face significant nutritional challenges due to growing poverty and inadequate access to nutritious food [22]. Moreover, 80% of the population living in rural areas has inadequate access to essential services like clean water, healthcare services, and education [22]. The cumulative impacts of these deprivations influence a child’s health with serious survival consequences.
Several studies have shown the socioeconomic factors influencing anaemia severity among under-5 children. Specifically, it had been noted that the effect of anaemia and other febrile infections can manifest with severe symptoms, including convulsions [8,23]. In some empirical analyses, fever morbidity was found to increase the probability of being anaemic [24]. Also, Elmardi et al. [25] found anaemia prevalence to be higher among children with malaria or a two-week history of fever. Some other authors with similar findings include White [26], Kweku et al. [27], and Stoltzfus et al. [28]. However, other factors such as twin birth [29,30,31], small size at birth, higher birth order, recent fever, and distance to healthcare are linked to higher anaemia levels [30] and altitude [32,33].
Understanding fever and anaemia’s relationship is crucial for achieving Sustainable Development Goal 3. Given the complex relationship between fever and anaemia in young children, it is essential to conduct thorough studies to inform evidence-based interventions and policies, particularly focusing on the socioeconomic factors that contribute to these health challenges in Niger [33]. This study therefore provides some valuable insights into the effect of malaria/other febrile infections and other maternal demographic variables on anaemia prevalence among under-5 children in Niger, utilizing data from the Demographic Health Survey (DHS). This study seeks to identify some key correlates of anaemia infection among under-5 children in Niger and propose some intervention strategies.

2. Materials and Methods

2.1. The Data

We used the Niger’s Malaria Indicator Survey (MIS) for 2021 in this study. The survey was conducted through the DHS programme by the l’Institut National de la Statistique (INS) from 12 August to 27 October 2021 through financial and technical assistance from by the United States Agency for International Development (USAID), the government of the Republic of Niger, the United States President’s Malaria Initiative (PMI), Catholic Relief Services (CRS), and the National Malaria Control Program.
The sampling targeted every eligible household in Niger, with adequate urban/rural and regional representativeness (see Figure 1 for the list of regions). Four survey instruments were used for data collection, which were household, women’s, biomarker, and field survey outcome questionnaires. This paper used the data collected with the women’s questionnaire, focusing on those who were 15–49 years of age and eligible children who were 6–59 months old. Mothers who consented to anaemia and malaria tests had their children’s blood collected for haemoglobin and rapid malaria tests, respectively. In addition, children’s temperatures were measured with thermometers.
The data collection protocols were pre-tested by 12 enumerators and 8 health officers who went through some collective and specialized trainings for two weeks. Between 12 July and 7 August 2021, the general enumerators, comprising 50 qualified persons (16 men and 34 women), were trained on the procedures and ethical requirements for the survey. The field surveys were conducted among 210 cluster samples. Due to insecurity, interviews were not conducted in two Tillabéri clusters and one cluster from Diffa. Therefore, the survey took place in a total of 207 clusters.
At the end of the survey, the number of selected households was 1272 and 3694 in urban and rural areas, respectively, while 1183 and 3546 were successfully interviewed. The number of eligible women (15–49 years of age) in the selected households was 1690 and 4263 in urban and rural areas, respectively, while those who granted their consent to participate and completed the surveys numbered 1619 and 4176 [34].

2.2. Limitations of the Study

One of the major limitations of this study is that not all the eligible women eventually participated. Although the response rate was quite high, the omission of some important groups could have biased our estimators. In addition, among the eligible children, many of them objected to taking their blood samples for the haemoglobin test and rapid malaria tests. However, since our sample for this study was primarily based on the state of anaemia, some level of bias could have been introduced by the non-participants.

2.3. Ethical Approval and Interview Consent

The protocols for conducting the survey as well as the tests for haemoglobin level and parasitaemia were reviewed and approved by the National Ethics Committee for Health Research (CNERS) of the Ministry of Public Health of Population and Social Affairs and the ICF Institutional Review Board. Also, the parents or caregivers of the children who participated in the biomarker testing were informed of the risks and benefits of participation to secure their final authorization. The results of the tests were communicated to the parents/caregivers, while some severe cases were referred to the nearest healthcare centres.

2.4. Estimated Econometric Model

We used heteroscedasticity-consistent ordered probit regression to analyse the data with the variance of error modelled by the households’ wealth index. The ordered probit model is appropriate when the dependent variable is more than two groups and they are ordinally coded. In the proposed model, there are four ordinal groups of anaemia, coded as 1 for severe, 2 for moderate, 3 for mild, and 4 for non-anaemic. It should be noted that the values of each group are irrelevant, only a particular order of arrangement should be followed. The model estimates a linear relationship of some independent variables and some unknown cutpoints. The estimated probability of observing an outcome y j = h , where h = 1 , 2 , 3 , 4 H is equivalent to the likelihood that the sum of the linear function and the error term is in the range of the cutpoints that are associated with the outcome.
Pr y j = h = P r ( k h < X j β + e j k h + 1 )
Pr y j = h = Φ k h + 1 X j β Φ k h X j β
y j refers to the outcome variables, X j are the explanatory variables which are malaria infection (yes = 1, 0 otherwise), other febrile infections (yes = 1, 0 otherwise), mother’s age (years), Diffa region (yes = 1, 0 otherwise), Dosso region (yes = 1, 0 otherwise), Maradi region (yes = 1, 0 otherwise), Tahoua region (yes = 1, 0 otherwise), Tillaberi region (yes = 1, 0 otherwise), Zinder region (yes = 1, 0 otherwise), Niamey (yes = 1, 0 otherwise), urban (yes = 1, 0 otherwise), altitude (meters), primary (yes = 1, 0 otherwise), secondary (yes = 1, 0 otherwise), tertiary (yes = 1, 0 otherwise), household size, male headship (yes = 1, 0 otherwise), head age (years), read newspaper (yes = 1, 0 otherwise), listen to radio (yes = 1, 0 otherwise), watch television (yes = 1, 0 otherwise), 2nd birth order (yes = 1, 0 otherwise), 3rd birth order (yes = 1, 0 otherwise), 4th birth order (yes = 1, 0 otherwise), 5th birth order (yes = 1, 0 otherwise), 1st of multiple (yes = 1, 0 otherwise), 2nd of multiple (yes = 1, 0 otherwise), gender (male = 1, 0 otherwise), and child age (months). k h is the cutpoints, and Φ . is the cumulative distribution function. The conventional ordinal probit assumes that the error is independently identically distributed (iid) normal with constant variance. When this assumption is violated, the estimated parameters are going to violate the BLUE (best linear unbiased estimator) assumptions. This will compel the estimation of a heteroscedasticity-consistent model where the variance of the error can be modelled as a multiplicative or additive function of selected independent variables [35]). In STATA 18, which was used for data analysis, the hetoprobit command estimated the log of standard deviation as a linear function of explanatory variables. In this study, the estimated model is presented as follows:
l n σ j = z j π
where z j is the household’s wealth index. When the error variance is different across different groups, Equation (2) becomes the following:
Pr y j = h = Φ k h + 1 X j β exp z j π Φ k h X j β exp z j π  
To ensure the identifiability of the estimated models, Equations (2) and (3) are without any constant term. The analysis was also implemented with due recognition of the likelihood of multicollinearity among the variables. Therefore, the variance inflation factor (VIF) was used to evaluate the presence of multicollinearity.

3. Results

3.1. Descriptive Statistics of Selected Mothers’ and Children’s Demographic Variables

Table 1 presents the descriptive statistics of selected demographic variables across mothers and children in Niger. The table shows that the number of observations is 4142. The results revealed that the average age of the mothers was 28.88 years. The Maradi region had the highest number of children with 25.46%. This was followed by the Zinder, Tahoua, and Tillaberi regions with 23.14%, 20.21%, and 13.42%, respectively. It was also revealed that 16.23% of the children resided in urban areas. The average altitude of the regions was 354.43 m. In terms of education level, 75.34% of the mothers had no form of formal education, while primary education was attained by 14.98%. The average household size was 8.46, and the average age of the household heads was 42.53 years. In terms of media/sources of information used by households, 25.69% were listening to radio, compared to 12.79% who were watching TV and 1.51% who were reading newspapers. Furthermore, 96.99% of the children were singletons. Based on the birth order, 59.28% were first-born and 35.37% were second-born. The results further revealed that 50.86% of the children were male and the average age was 31.36 months. The average wealth index was 2579.24.

3.2. Malaria and Fever Morbidity Among Under-5 Children

Table 2 shows the distribution of malaria and other febrile infections across the regions and economic sectors in Niger. It reveals that 14.00% and 33.87% of the children had malaria and other febrile infections, respectively. Among those with malaria, the majority were from the Zinder region (23.10%) and Dosso region (20.69%). Moreover, among those children with other febrile infections, the majority were from Zinder (20.67%) and Tillaberi (17.89%). Across the economic sectors, rural children accounted for 83.28% and 84.39% of those with malaria and other febrile infections, respectively.

3.3. Distribution of Anaemia Across Selected Demographic Variables

Figure 2 presents the distribution of children’s anaemia levels across the regions. The figure shows that 4.85% of the children from the Agadez region were severely anaemic. Other regions with relatively high severe anaemia were Dosso (4.81%), Maradi (4.58%), and Tillaberi (4.51%). The figure also shows that majority of children in Niger were moderately anaemic, with those from Tillaberi (51.26%), Zinder (50.29%), and Dosso (50.21%) being among the highest. Mild anaemia was highest in Diffa (31.26%), Niamey (29.29%), Tillaberi (28.34%), Tahoua (27.74%), and Maradi (24.31%). The results further show that Agadez had the highest (37.88%) number of children who were not diagnosed with anaemia. This was followed by the Niamey (36.98%), Maradi (30.33%), and Diffa (26.83%) regions.
Figure 3 shows the distribution of children’s anaemia levels regarding malaria and fever comorbidity in Niger. The results revealed that 6.55% of the children in Niger who were diagnosed with severe anaemia were infected with malaria, while 5.84% had other febrile infections. Among the children who had moderate anaemia, the majority (55.69%) were infected with malaria while 55.32% experienced fever episodes. Also, 41.69% of moderately anaemic children were not infected with malaria, and 39.21% did not report fever. Regarding children with mild anaemia, 27.09% had no fever and 26.70% had no malaria. It is also revealed that 30.49% of Nigerien children who were non-anaemic did not experience any fever episodes, while 27.91% were not infected with malaria. The figure also shows that non-anaemic children with other febrile and malaria infections were among the least, with 18.03% and 18.21%, respectively.
Figure 4 presents the distribution of children’s anaemia levels based on their birth orders and multiple birth in Niger. The figure shows that among children with severe anaemia, with regard to birth order, 11.11% were the fourth-born in the family, compared to 3.73% who were the first-born. The figure further shows that across those who were twins, severe anaemia was higher among second children with 10.77% compared to 8.77% for first children. In terms of children with moderate anaemia across birth orders, 66.67% were the fourth-born, compared to 31.34% who were the first-born. Moderate anaemia was higher among children who were the first child of twins (45.61%), compared to the second-born of twins (33.85%). Mild anaemia across birth orders was highest among the third-born (28.04%) compared to 26.01% for the first-born. Among twins, mild anaemia was higher among the second-born (26.15%) compared to the first-born (21.05%). Also, 30.92% of children who were first-born were not anaemic, compared to those who were fourth-born (11.11%). In addition, the absence of anaemia was higher among the second-born of twins (29.23%).

3.4. Determinants of Anaemia Among Under-5 Children

Table 3 presents the results of the ordered probit regression. The included variables were examined for multicollinearity using the variance inflation factor (VIF). The computed value of 2.39 shows that multicollinearity was not a serious problem [36]. Also, the model was examined for heteroscedasticity with the variance of error being modelled by the wealth index. The results showed that the lnsigma parameter that was generated with the wealth index showed statistical significance (p < 0.05). Therefore, heteroscedasticity was a problem, and modelling the variance of error by the wealth index was appropriate. The model was run with the inclusion of the setting of the survey’s sampling design. Therefore, the survey setting menu of STATA 17 software was used for data analysis. The results revealed that the model produced a good fit to the data, with computed F-statistics being statistically significant (p < 0.01).
The ordered probit regression results in Table 3 show that malaria infection significantly reduced the probability of being non-anaemic (p < 0.05). The marginal parameters revealed that infection with malaria increased the probability of severe and moderate anaemia by 1.10% and 4.36%, respectively, while it reduced the probability of mild anaemia by 1.34% and non-anaemia by 4.11%. Similarly, the parameter of other febrile infections is with a negative sign and statistically significant (p < 0.01). This implies that other febrile infections reduced the probability of being non-anaemic. Marginally, infection with other febrile infections significantly increased (p < 0.01) the probability of being severely and moderately anaemic by 1.88% and 7.67%, respectively, while it reduced the probability of mild anaemia by 2.26% and being non-anaemic by 7.29%.
Although none of the regional parameters showed statistical significance (p > 0.10), the sectoral parameter of the ordered probit (urban residence) is statistically significant (p < 0.01) with a positive sign. This implies that urban children had a higher probability of being non-anaemic. The marginal parameters showed that urban residence reduced the probability of being severely anaemic and moderately anaemic by 2.04 and 11.30%, respectively. However, residence in urban areas increased the probability of being mild anaemic and non-anaemic by 2.00% and 11.34%, respectively.
Among the variables that captured access to media, the parameters of reading newspapers and watching television showed statistical significance (p < 0.05). These results indicate that children whose mothers read newspapers had a higher probability of being non-anaemic. Based on the marginal parameters, reading newspapers by under-5 children’s mothers reduced the probability of being severely and moderately anaemic by 1.93% and 12.11%, respectively, while it increased the probability of mild anaemia by 1.56% and non-anaemia by 12.48%. Furthermore, children whose mothers watched television had a significantly higher (p < 0.05) probability of being non-anaemic. The marginal parameters further revealed that access to television by the mothers of under-5 children reduced the probability of being severely and moderately anaemic by 0.98% and 4.87%, respectively, while it increased the probability of mild anaemia by 1.10% and not being anaemic by 4.76%.
Among the variables that were included to capture birth order, the parameters of second birth order and fifth birth order showed statistical significance (p < 0.05). These results revealed that being second-born reduced the probability of being non-anaemic. Furthermore, being second-born increased the probability of severe and moderate anaemia by 0.91% and 3.84%, respectively, while it reduced the probability of mild anaemia by 1.09% and being non-anaemic by 3.66%. Moreover, being fifth-born increased the probability of being non-anaemic, while it decreased the probability of severe, moderate, and mild anaemia by 3.32%, 4.55%, and 27.24%, respectively. In addition, being fifth-born increased the probability of being non-anaemic by 76.06%.
Among the variables that captured multiple birth, the parameter of being the second-born of a multiple birth showed statistical significance (p < 0.05) in the general ordered probit regression, as well as marginal parameters for moderate anaemia and non-anaemia. The results revealed that being the second-born of a multiple birth reduced the probability of being non-anaemic. Also, being the second-born in a multiple birth increased the probability of moderate anaemia by 13.04%, while it reduced the probability of non-anaemia by 12.12%.
The parameter of the gender of the child is statistically significant (p < 0.05) in the ordered probit model, as well as marginal parameters of moderate anaemia and non-anaemia. The results indicate that male children had a lower probability of being non-anaemic. Also, male children had their probability of being moderately anaemic increased by 3.02%, while their probability of being non-anaemic decreased by 2.89%. The parameter of children’s age is statistically significant (p < 0.01) across all the results. These showed that a unit increase in a child’s age increased the probability of being non-anaemic. The marginal parameters revealed that a unit increase in a child’s age reduced the probability of severe and moderate anaemia by 0.09% and 0.40%, respectively, while it increased the probability of mild anaemia and non-anaemia by 0.11% and 0.38%, respectively. Finally, the parameter of the household’s wealth index showed statistical significance (p < 0.05). The results showed that if the wealth index increases by a unit, the probability of being non-anaemic reduces. Specifically, among the estimated marginal parameters, the wealth index increased the probability of moderate and mild anaemia, while it reduced the probability of severe anaemia and being non-anaemic.

4. Discussion

Malaria infection is one of the major determinants of under-5 anaemia. More importantly, Africa remains the hotspot of malaria. Some statistics have shown that in 2022, 95% of the 236 million global malaria cases was in Africa, where most of the recorded deaths also occurred [37]. Similarly, SSA accounts for about 88.00% of global malaria mortalities [38], while under-5 children account for 80% of malaria mortality in Africa [39]. Our findings have shown that malaria incidence among the selected under-5 children was 14.00%. The implication is that Niger’s under-5 children have a relatively high burden of malaria, and existing interventions to address malaria like the use of insecticide-treated nets are either being jettisoned or ineffective. The fundamental problems with malaria eradication in Niger can be viewed considering households’ poverty, the poor coverage of healthcare facilities, the development of resistance to medication by malaria pathogens, and a low level of education [40,41,42].
It should be noted that emphasizing malaria prevention among under-5 children is of significance in addressing child mortality. In some previous studies, the prevalence of malaria among under-5 children varied between 0.7% [43] and 80.3% [44]. Although some studies reported less than 10% positive malaria cases [45,46,47,48,49], Ilol et al. [44] and Tusting et al. [50] reported 79.8% and 80.3%, respectively.
The results also showed that the incidence of other febrile infections was 33.87% among the selected under-5 children. Fever is one of the most common symptoms of major illnesses among under-5 children, including measles, malaria, diarrhoea, and other bacterial and viral infections [51,52]. In some previous studies, incidences of fever were 29.60% in Zambia [53] and 33.10% in Bangladesh [54]. A study by Crump et al. [55] reported that although 60.7% of under-5 children in Tanzania had malaria, it was only in 1.6% that malaria had caused fever. In another study, D’acremont et al. [14] found that among children with fever, viral infections were diagnosed in 70.5%, bacterial infections in 22.0%, and parasitic infections in 10.9%.
The findings also revealed a high incidence of anaemia among Nigerien under-5 children. With only 26.27% of the children being non-anaemic and 4.10% severe cases detected, anaemia among under-5 Nigerien children is a problem of serious public health concern. It should be noted that global under-5 anaemia prevalence has been estimated at 16.42% [56], while that for SSA is 59.9% [32]. Seifu and Tesema [30] also estimated that 76.60% of 6–23-month-old children in SSA were anaemic. In some nationally representative studies, anaemia prevalence rates were 49.40% in Sudan [25], 61.30% in South Africa [57], 47.5% in Sudan [58], 65.9% in Ghana [59], 51.8% in 6–36-month-old Swaziland children [60], 71.93% in 6–23-month-old Ethiopian children [61], 70.9% in Togo [62], 53.22% in Uganda [63], and 58.6% in Tanzania [64]. Other studies that were not nationally representative found under-5 anaemia prevalence rates at 11.10% in Nigeria [65], 3.9% in the United States of America [66], and 51.3% in rural central and western China [67].
Our findings showed that malaria and other febrile infections promoted under-5 anaemia. Malaria and anaemia are interlinked because at the initial stage when malaria parasites infect the blood, there is massive internalization and degrading of haemoglobin from the red blood cell [68]. The finding in this study is in line with some previous studies that reported a positive association between malaria and anaemia among under-5 children [69,70,71]. Our finding is, however, contrary to those of Elmardi et al. [25] among children under 24 months in Sudan. Other febrile infections also promoted anaemia among under-5 children. The channels through which fever influenced anaemia can be viewed from the fact that it is one of the major symptoms of malaria, and febrile infection promotes the destruction of red blood cells. In addition, some illnesses with fever symptoms are closely linked to infections and inflammation that decrease red blood cell production [72]. This finding is in line with the findings of Ewusie et al. [73], Semba et al. [24], Zhao et al. [74], and Gebrehaweria and Lemma [75]. However, the finding is contrary to that of Elmardi et al. [25].
Contrary to the findings of Gebrehaweria and Lemma [75], regional variables did not significantly influence anaemia among under-5 children. Although the parameters of the regional variables are statistically insignificant, some differences were obtained in the levels of anaemia across the regions. Specifically, in comparison to other regions, the anaemia incidence among children was lowest in the Agadez and Niamey regions. It should be noted that Niamey is the capital of Niger, with the highest population density, while Agadez has the lowest population density. In terms of anaemia among women of reproductive age, UNICEF [22] noted that anaemia was highest in the southwestern part of Niger, where inadequate access to clean drinking water was also predominant.
The sector of residence was found to significantly influence anaemia among under-5 children. Specifically, urban children had a lower probability of being anaemic. This is expected because of prevailing social services, such as healthcare facilities in urban centres, and the likelihood of lower income and multidimensional poverty in urban households. It should also be noted that the lower prevalence of anaemia in urban areas can be due to the expected higher literacy of urban mothers [76]. Our finding is in line with those of Khan et al. [77] and Dey et al. [76].
The wealth index was found to promote the non-anaemia condition among under-5 children. The level of wealth of under-5 children’s parents will influence the standard of living through materials for housing, asset acquisition, and the affordability of nutritious food. Our finding is in line with the findings of Dey et al. [76], who found a higher likelihood of anaemia among children from low and medium living standard. The finding also corroborates those of Assunção et al. [78] in Brazil and Mamiro et al. [79] in Tanzania. Gebrehaweria and Lemma [75] also found that community poverty promoted anaemia among under-5 children in Ethiopia, while Zhao et al. [74] and Xin et al. [80] found a higher prevalence of anaemia among children from low-income households. Relatedly, access to newspaper and television reduced the likelihood of anaemia among under-5 children. Specifically, newspapers and televisions are sources of vital information on child-related issues that can promote adequate nutrition and health. This result is in accordance with the findings of Gebrehaweria and Lemma [75] and Baranwal et al. [81].
The gender of the children showed that male children had a higher likelihood of being anaemic. This is in line with the findings of Assunção et al. [78] but contrary to those of Ewusie et al. [73]. The age of the children was positively associated with being non-anaemic. This is expected due to the higher prevalence of anaemia among infants. Therefore, our findings can be supported by the findings of Assunção et al. [78], Ewusie et al. [73] and Zhao et al. [74] but are contrary to the findings of Gebrehaweria and Lemma [75]. The child’s birth order was found to influence anaemia. Specifically, children who were the fifth-born had a higher probability of being non-anaemic, while second-born children had higher anaemic probability. Our findings are in accordance with those of Moschovis et al. [32] but contrary to those of Yadav et al. [82]. We also found that being the second of multiple births increased the probability of being anaemic. Our finding can be explained from the fact that in some in some instances, the second-born twin may be underweight, thereby promoting growth retardation, stunting, and anaemia [30]. Our finding is in line with those of Asmare and Agmas [83], as well as Seifu and Tesema [30].
We also found that although access to radio did not have a significant effect on prevalence of anaemia, access to newspapers and television had significant influences. This may have reflected the role of media programmes in facilitating awareness and prevention of anaemia among under-5 children. The results are in alignment with those of Baranwal et al. [81] and Anteneh and Van Geertruyden [84], who reported a decrease in the odds of being anaemic with access to media programmes through newspapers, television, and radio.

5. Conclusions

The interplay of malaria and other febrile infections in the promotion of anaemia is a subject of significant policy relevance in Africa. In addition, a clear understanding of essential correlates of anaemia is fundamental towards achievement of SDGs, especially the ones that are related to health. This study contributes to the existing body of knowledge on child anaemia and its relationships to malaria infection, fever, and other important correlates in Niger. Our adopted econometric model facilitates the robustness of the estimated parameters through an essential correction of heteroscedasticity. The results have shown a very high incidence of anaemia among under-5 children in Niger, which raises serious questions regarding the efficacy of some on-going programmes for promoting children’s health outcomes by addressing undernutrition and malaria prevalence. The high incidence of malaria necessitates some critical interventions for protecting Nigerien children from mosquito bites and the facilitation of effective healthcare treatment mechanisms for infected children. Of significant note is the fact that other febrile infections which were prevalent among under-5 children had significant impacts on child’s anaemia. Therefore, the existence of a sustainable framework for reducing illnesses among under-5 children will go a long way in addressing anaemia among under-5 children, more so that urban children were better off in all the studied health indicators.
Furthermore, there were some regional differences in anaemia, fever, and malaria prevalence in Niger. This calls for interventions that critically evaluate the vulnerability of each region for some direct marginal reforms. Specifically, children from Tillaberi and Dosso exhibited the highest vulnerability to anaemia. Our results have highlighted the role of information sources in addressing anaemia, with mothers’ access to newspaper and television showing some anaemia prevalence-reducing promise. Therefore, the integration of some essential child and health promoting information focusing on prevention of anaemia in Nigerien newspapers and television hold significant prospects in reducing the current high prevalence of anaemia. Another important finding is the role of maternal fertility, which was captured by children’s birth order, in promoting anaemia. Conventionally, high maternal fertility induces poverty, which will also breed diseases and anaemia among children. Interventions to educate women of reproductive age on the need for family planning may go a very long way in addressing anaemia in Niger. This can be further buttressed by the fact that households’ wealth was an important factor in reducing anaemia among under-5 children. Finally, our results emphasize the role of children’s age and gender in explaining anaemia. This reaffirms the need for an adequate consideration of gender and age in addressing child’s anaemia in Niger with a focus on males and infants.

Author Contributions

Methodology, T.C.M. and A.S.O.; Software, A.S.O.; Formal analysis, A.S.O.; Investigation, T.C.M. and A.S.O.; Writing—original draft, T.C.M.; Writing—review & editing, A.S.O. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki, and approved by the Institutional Review Board (or Ethics Committee) of the Ministry of Health, Niger and Demographic and Health Survey (DHS).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Restrictions apply to the availability of these data. Data were obtained from [DHS] and are available [www.dhs.com] with the permission of [DHS].

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Kebede, D.; Getaneh, F.; Endalamaw, K.; Belay, T.; Fenta, A. Prevalence of anemia and its associated factors among under-five age children in Shanan gibe hospital, Southwest Ethiopia. BMC Pediatr. 2021, 21, 542. [Google Scholar] [CrossRef] [PubMed]
  2. WHO. Haemoglobin Concentrations for the Diagnosis of Anaemia and Assessment of Severity; World Health Organization: Geneva, Switzerland, 2011. [Google Scholar]
  3. Ministry of Health, Community Development, Gender, Elderly and Children (MoHCDGEC), [Tanzania Mainland, Ministry of Health (MoH) [Zanzibar], National Bureau of Statistics (NBS), Office of the Chief Government Statistician (OCGS) and ICF. 2015-16 Tanzania Demographic and Health Survey and Malaria Indicator Survey Key Findings; MoHCDGEC, MoH, NBS, OCGS, and ICF: Rockville, MD, USA, 2016. [Google Scholar]
  4. National Centre for Biotechnology Information. Overview: Fever in Children. 2022. Available online: https://www.ncbi.nlm.nih.gov/books/NBK279455/ (accessed on 28 June 2024).
  5. Mboya, I.B.; Mamseri, R.; Leyaro, B.J.; George, J.; Msuya, S.E.; Mgongo, M. Prevalnce and factors associated with anemia among children under five years of age in Rombo district, Kilimanjaro region, Northern Tanzania. F1000Research 2023, 9, 1102. [Google Scholar] [CrossRef]
  6. Andrews, J.R.; Vaidya, K.; Saha, S.; Yousafzai, M.T.; Hemlock, C.; Longley, A.; Aiemjoy, K.; Yu, A.T.; Bogoch, I.I.; Tamrakar, D. Healthcare utilization patterns for acute febrile illness in Bangladesh, Nepal, and Pakistan: Results from the Surveillance for Enteric Fever in Asia Project. Clin. Infect. Dis. 2020, 71 (Supp. 3), S248–S256. [Google Scholar] [CrossRef]
  7. MacLean, B.; Sholzberg, M.; Weyand, A.C.; Lim, J.; Tang, G.; Richards, T. Identification of women and girls with iron deficiency in the reproductive years. Int. J. Gynecol. Obstet. 2023, 162, 58–67. [Google Scholar] [CrossRef] [PubMed]
  8. Aliyo, A.; Jibril, A. Assessment of anemia and associated risk factors among children under-five years old in the West Guji Zone, southern Ethiopia: Hospital-based cross-sectional study. PLoS ONE 2022, 17, e0270853. [Google Scholar] [CrossRef] [PubMed]
  9. Takele, K.; Zewotir, T.; Ndanguza, D. Risk factors of morbidity among children under age five in Ethiopia. BMC Public Health 2019, 19, 942. [Google Scholar] [CrossRef]
  10. Ogobara Dougnon, A.; Charle-Cuéllar, P.; Toure, F.; Aziz Gado, A.; Sanoussi, A.; Lazoumar, R.H.; Alain Tchamba, G.; Vargas, A.; Lopez-Ejeda, N. Impact of integration of severe acute malnutrition treatment in primary health care provided by community health workers in rural Niger. Nutrients 2021, 13, 4067. [Google Scholar] [CrossRef]
  11. Aboagye, R.G.; Kugbey, N.; Ahinkorah, B.O.; Seidu, A.-A.; Cadri, A.; Bosoka, S.A.; Akonor, P.Y.; Takase, M. Nutritional status of school children in the South Tongu District, Ghana. PLoS ONE 2022, 17, e0269718. [Google Scholar] [CrossRef]
  12. Wessells, K.R.; Ouédraogo, C.T.; Young, R.R.; Faye, M.T.; Brito, A.; Hess, S.Y. Micronutrient status among pregnant women in Zinder, Niger and risk factors associated with deficiency. Nutrients 2017, 9, 430. [Google Scholar] [CrossRef]
  13. Kodish, S.R.; Matean, M.; Grey, K.; Palaniappan, U.; Northrup-Lyons, M.; Yalvigi, A.; Gwavuya, S.; Mclean, J.; Erasmus, W. Conceptualizing multi-level determinants of infant and young child nutrition in the Republic of Marshall Islands–a socio-ecological perspective. PLOS Global Public Health 2023, 2, e0001343. [Google Scholar] [CrossRef]
  14. D’Acremont, V.; Lengeler, C.; Genton, B. Reduction in the proportion of fevers associated with Plasmodium falciparum parasitaemia in Africa: A systematic review. Malar. J. 2010, 9, 240. [Google Scholar] [CrossRef] [PubMed]
  15. World Health Organization. Malaria. Available online: https://www.who.int/news-room/fact-sheets/detail/malaria (accessed on 27 October 2019).
  16. Wirth, J.P.; A Woodruff, B.; Engle-Stone, R.; Namaste, S.M.; Temple, V.J.; Petry, N.; Macdonald, B.; Suchdev, P.S.; Rohner, F.; Aaron, G.J. Predictors of anemia in women of reproductive age: Biomarkers Reflecting Inflammation and Nutritional Determinants of Anemia (BRINDA) project. Am. J. Clin. Nutr. 2017, 106, 416S–427S. [Google Scholar] [CrossRef] [PubMed]
  17. Obeagu, E.I.; Nimo, O.M.; Bunu, U.O.; Ugwu, O.P.; Alum, E.U. Anaemia in children under five years: African perspectives. Int. J. Curr. Res. Biol. Med. 2023, 1, 1–7. [Google Scholar]
  18. Brittenham, G.M.; Moir-Meyer, G.; Abuga, K.M.; Datta-Mitra, A.; Cerami, C.; Green, R.; Pasricha, S.-R.; Atkinson, S.H. Biology of anemia: A public health perspective. J. Nutr. 2023, 153, S7–S28. [Google Scholar] [CrossRef]
  19. Garcia-Casal, M.N.; Dary, O.; Jefferds, M.E.; Pasricha, S.R. Diagnosing anemia: Challenges selecting methods, addressing underlying causes, and implementing actions at the public health level. Ann. N. Y. Acad. Sci. 2023, 1524, 37–50. [Google Scholar] [CrossRef]
  20. Hess, S.Y.; Owais, A.; Jefferds, M.E.D.; Young, M.F.; Cahill, A.; Rogers, L.M. Accelerating action to reduce anemia: Review of causes and risk factors and related data needs. Ann. N. Y. Acad. Sci. 2023, 1523, 11–23. [Google Scholar] [CrossRef]
  21. World Health Organization. Countries and Territories Certified Malaria-Free by WHO, World Health Organization. Available online: https://www.who.int/teams/global-malaria-programme/elimination/countries-and-territories-certified-malaria-free-by-who (accessed on 11 December 2023).
  22. UNICEF. Regional Operational Guide on Maternal Anemia Leveraging the Systems Approach to Protect Women from Anemia in West and Central Africa. Available online: https://www.unicef.org/wca/media/10121/file/UNICEF_Regional_Operational_Guide_on_Maternal_Anemia.pdf.pdf (accessed on 6 August 2024).
  23. Sharif, M.R.; Kheirkhah, D.; Madani, M.; Kashani, H.H. The relationship between iron deficiency and febrile convulsion: A case-control study. Glob. J. Health Sci. 2015, 8, 185. [Google Scholar] [CrossRef]
  24. Semba, R.D.; de Pee, S.; Ricks, M.O.; Sari, M.; Bloem, M.W. Diarrhea and fever as risk factors for anemia among children under age five living in urban slum areas of Indonesia. Int. J. Infect. Dis. 2007, 12, 62–70. [Google Scholar] [CrossRef]
  25. Elmardi, K.A.; Adam, I.; Malik, E.M.; Ibrahim, A.A.; Elhassan, A.H.; Kafy, H.T.; Nawai, L.M.; Abdin, M.S.; Kremers, S. Anaemia prevalence and determinants in under 5 years children: Findings of a cross-sectional population-based study in Sudan. BMC Pediatr. 2020, 20, 1–14. [Google Scholar] [CrossRef]
  26. White, N.J. Anaemia and malaria. Malar. J. 2018, 17, 371. [Google Scholar] [CrossRef]
  27. Kweku, M.; Ofori, M.; Appiah, E.K.; Dinko, B.; Takramah, W.; Agboli, E.; Takase, M.; Doe, F.; Tarkang, E. Seasonal prevalence of malaria, fever, anaemia and factors associated with malaria prevalence among children less than five in an area with prolonged malaria transmission in Ghana. Int. J. Trop. Dis. Health 2017, 22, 1–11. [Google Scholar] [CrossRef] [PubMed]
  28. Stoltzfus, R.J.; Tielsch, J.M.; Chwaya, H.M.; Montresor, A.; Albonico, M.; Savioli, L. Malaria, hookworms and recent fever are related to anemia and iron status indicators in 0-to 5-y old Zanzibari children and these relationships change with age. J. Nutr. 2000, 130, 1724–1733. [Google Scholar] [CrossRef] [PubMed]
  29. Sinha, N.; Deshmukh, P.; Garg, B. Epidemiological correlates of nutritional anemia among children (6–35 months) in rural Wardha, Central India. Indian J. Med. Sci. 2008, 62, 45–54. [Google Scholar] [PubMed]
  30. Seifu, B.L.; Tesema, G.A. Individual-and community-level factors associated with anemia among children aged 6–23 months in sub-Saharan Africa: Evidence from 32 sub-Saharan African countries. Arch. Public Health 2022, 80, 183. [Google Scholar] [CrossRef]
  31. Obasohan, P.E.; Walters, S.J.; Jacques, R.; Khatab, K. A scoping review of the risk factors associated with anaemia among children under five years in sub-Saharan African countries. Int. J. Environ. Res. Public Health 2020, 17, 8829. [Google Scholar] [CrossRef]
  32. Moschovis, P.P.; Banajeh, S.; MacLeod, W.B.; Saha, S.; Hayden, D.; Christiani, D.C.; Mino, G.; Santosham, M.; Thea, D.M.; Qazi, S.; et al. Childhood anemia at high altitude: Risk factors for poor outcomes in severe pneumonia. Pediatrics 2013, 132, e1156–e1162. [Google Scholar] [CrossRef]
  33. Ssentongo, P.; Ba, D.M.; Ssentongo, A.E.; Fronterre, C.; Whalen, A.; Yang, Y.; Ericson, J.E.; Chinchilli, V.M. Association of vitamin A deficiency with early childhood stunting in Uganda: A population-based cross-sectional study. PLoS ONE 2020, 15, e0233615. [Google Scholar] [CrossRef]
  34. Institut National de la Statistique (INS) et ICF. Enquête sur les Indicateurs du Paludisme au Niger 2021: Rapport Final; INS; ICF: Rockville, MD, USA, 2023; Available online: https://dhsprogram.com/pubs/pdf/MIS39/MIS39.pdf (accessed on 3 August 2024).
  35. Harvey, A.C. Estimating regression models with multiplicative heteroscedasticity. Econometrica 1976, 44, 461. [Google Scholar] [CrossRef]
  36. Shrestha, N. Detecting multicollinearity in regression analysis. Am. J. Appl. Math. Stat. 2020, 8, 39–42. [Google Scholar] [CrossRef]
  37. African Leaders Malaria Alliance. Malaria Progress & Challenges. Available online: https://alma2030.org/heads-of-state-and-government/african-union-malaria-progress-reports/2023-africa-malaria-progress-report/#:~:text=According%20to%20the%20WHO%2C%20there,African%20Member%20States%20in%202022 (accessed on 7 August 2024).
  38. World Health Organization. World Malaria Report 2023. WHO. 2023. Available online: https://www.who.int/teams/global-malaria-programme/reports/world-malaria-report-2023 (accessed on 15 June 2024).
  39. WHO. World Malaria Report 2022. 2022. Available online: https://www.who.int/teams/global-malaria-programme/reports/world-malaria-report-2022 (accessed on 18 July 2024).
  40. Tchole, A.I.M.; Ye, R.-Z.; Xu, Q.; Li, Z.-W.; Liu, J.-Y.; Wang, S.-S.; Wang, X.-Y.; Bachir, A.M.; Zhao, L.; Cao, W.-C. Epidemiological behaviour and interventions of malaria in Niger, 2010–2019: A time-series analysis of national surveillance data. Malar. J. 2024, 23, 30. [Google Scholar] [CrossRef]
  41. The Demographic and Health Surveys Program. [Niger DHS, 2012—Final Report]. 2012. Available online: https://dhsprogram.com/publications/publication-FR277-DHS-Final-Reports.cfm (accessed on 10 December 2023). (In French).
  42. President’s Malaria Initiative. Niger Malaria Profile. 2022. Available online: https://d1u4sg1s9ptc4z.cloudfront.net/uploads/2023/01/Niger-Malaria-Profile-1.pdf (accessed on 10 December 2023).
  43. Chanda, P.; Hamainza, B.; Mulenga, S.; Chalwe, V.; Msiska, C.; Chizema-Kawesha, E. Early results of integrated malaria control and implications for the management of fever in under-five children at a peripheral health facility: A case study of Chongwe rural health centre in Zambia. Malar. J. 2009, 8, 49. [Google Scholar] [CrossRef] [PubMed]
  44. Iloh, G.U.P.; Nnorom, O.U.; Amadi, A.N. Malaria morbidity among under-five Nigerian children: A study of its prevalence and health practices of primary care givers (mothers) in a resource-poor setting of a rural hospital in Eastern Nigeria. Eur. J. Prev. Med. 2013, 1, 50–57. [Google Scholar]
  45. West, P.A.; Protopopoff, N.; Rowland, M.; Cumming, E.; Rand, A.; Drakeley, C.; Wright, A.; Kivaju, Z.; Kirby, M.J.; Mosha, F.W.; et al. Malaria risk factors in North West Tanzania: The effect of spraying, nets and wealth. PLoS ONE 2013, 8, e65787. [Google Scholar] [CrossRef] [PubMed]
  46. Kateera, F.; Ingabire, C.M.; Hakizimana, E.; Kalinda, P.; Mens, P.F.; Grobusch, M.P.; Mutesa, L.; van Vugt, M. Malaria, anaemia and under-nutrition: Three frequently co-existing conditions among preschool children in rural Rwanda. Malar. J. 2015, 14, 440. [Google Scholar] [CrossRef] [PubMed]
  47. Escamilla, V.; Alker, A.; Dandalo, L.; Juliano, J.J.; Miller, W.C.; Kamthuza, P.; Tembo, T.; Tegha, G.; Martinson, F.; Emch, M.; et al. Effects of community-level bed net coverage on malaria morbidity in Lilongwe, Malawi. Malar. J. 2017, 16, 142. [Google Scholar] [CrossRef]
  48. Ambe, J.P.; Balogun, S.T.; Waziri, M.B.; Nglass, I.N.; Saddiq, A. Impacts of seasonal malaria chemoprevention on malaria burden among under five-year-old children in Borno State, Nigeria. J. Trop. Med. 2020, 2020, 9372457. [Google Scholar] [CrossRef]
  49. Tsegaye Negash, B.; Ayalew, M. Trend and factors associated with anemia among women reproductive age in Ethiopia: A multivariate decomposition analysis of Ethiopian Demographic and Health Survey. PLoS ONE 2023, 18, e0280679. [Google Scholar] [CrossRef]
  50. Tusting, L.S.; Bottomley, C.; Gibson, H.; Kleinschmidt, I.; Tatem, A.J.; Lindsay, S.W.; Gething, P.W. Housing improvements and malaria risk in sub-Saharan Africa: A multi-country analysis of survey data. PLoS Med. 2017, 14, e1002234. [Google Scholar] [CrossRef]
  51. Nnedu, O.N.; Rimel, B.; Terry, C.; Jalloh-Vos, H.; Baryon, B.; Bausch, D.G. Syndromic diagnosis of malaria in rural Sierra Leone and proposed additions to the national integrated management of childhood illness guidelines for fever. Am. J. Trop. Med. Hyg. 2010, 82, 525–528. [Google Scholar] [CrossRef]
  52. Novignon, J.; Nonvignon, J. Socioeconomic status and the prevalence of fever in children under age five: Evidence from four sub-Saharan African countries. BMC Res. Notes 2012, 5, 380. [Google Scholar] [CrossRef]
  53. Hamooya, B.M.; Chongwe, G.; Sitali, L.; Halwindi, H. Reported incidence of fever for under-5 children in Zambia: A longitudinal study. Arch. Public Health 2015, 73, 46. [Google Scholar] [CrossRef] [PubMed]
  54. Rahman, A.; Hossain, M.M. Prevalence and determinants of fever, ARI and diarrhea among children aged 6–59 months in Bangladesh. BMC Pediatr. 2022, 22, 117. [Google Scholar] [CrossRef]
  55. Crump, J.A.; Morrissey, A.B.; Nicholson, W.L.; Massung, R.F.; Stoddard, R.A.; Galloway, R.L.; Ooi, E.E.; Maro, V.P.; Saganda, W.; Kinabo, G.D.; et al. Etiology of Severe Non-malaria Febrile Illness in Northern Tanzania: A Prospective Cohort Study. PLoS Neglected Trop. Dis. 2013, 7, e2324. [Google Scholar] [CrossRef]
  56. Gedfie, S.; Getawa, S.; Melku, M. Prevalence and associated factors of iron deficiency and iron deficiency anemia among under-5 children: A systematic review and meta-analysis. Glob. Pediatr. Health 2022, 9, 2333794X221110860. [Google Scholar] [CrossRef] [PubMed]
  57. National Department of Health (NDoH); Statistics South Africa (Stats SA); South African Medical Research Council (SAMRC); ICF. South Africa Demographic and Health Survey 2016; NDOH: Pretoria, South Africa; Rockville, MD, USA, 2019. [Google Scholar]
  58. Hershey, C.L.; Florey, L.S.; Ali, D.; Bennett, A.; Luhanga, M.; Mathanga, D.P.; Salgado, S.R.; Nielsen, C.F.; Troell, P.; Jenda, G.; et al. Malaria Control Interventions Contributed to Declines in Malaria Parasitemia, Severe Anemia, and All-Cause Mortality in Children Less Than 5 Years of Age in Malawi, 2000–2010. Am. J. Trop. Med. Hyg. 2017, 97, 76–88. [Google Scholar] [CrossRef] [PubMed]
  59. Jones, A.D.; Colecraft, E.K.; Awuah, R.B.; Boatemaa, S.; Lambrecht, N.J.; Adjorlolo, L.K.; Wilson, M.L. Livestock ownership is associated with higher odds of anaemia among preschool-aged children, but not women of reproductive age in Ghana. Matern. Child Nutr. 2018, 14, e12604. [Google Scholar] [CrossRef] [PubMed]
  60. Machisa, M.; Wichmann, J.; Nyasulu, P.S. Biomass fuel use for household cooking in Swaziland: Is there an association with anaemia and stunting in children aged 6–36 months? Trans. R. Soc. Trop. Med. Hyg. 2013, 107, 535–544. [Google Scholar] [CrossRef]
  61. Mohammed, S.H.; Habtewold, T.D.; Esmaillzadeh, A. Household, maternal, and child related determinants of hemoglobin levels of Ethiopian children: Hierarchical regression analysis. BMC Pediatr. 2019, 19, 113. [Google Scholar] [CrossRef]
  62. Nambiema, A.; Robert, A.; Yaya, I. Prevalence and risk factors of anemia in children aged from 6 to 59 months in Togo: AnalysisfromTogodemographicandhealthsurveydata, 2013–2014. BMC Public Health 2019, 19, 215. [Google Scholar] [CrossRef]
  63. Ntenda, P.A.; Chirambo, A.C.; Nkoka, O.; El-Meidany, W.M.; Goupeyou-Youmsi, J. Implication of asymptomatic and clinical Plasmodium falciparum infections on biomarkers of iron status among school-aged children in Malawi. Malar. J. 2022, 21, 278. [Google Scholar] [CrossRef]
  64. Ojoniyi, O.O.; Odimegwu, C.O.; Olamijuwon, E.O.; Akinyemi, J.O. Does education o set the e ect of maternal disadvantage on childhood anaemia in Tanzania? Evidence from a nationally representative cross-sectional study. BMC Pediatr. 2019, 19, 89. [Google Scholar] [CrossRef] [PubMed]
  65. Akodu, O.S.; Disu, E.A.; Njokanma, O.F.; Kehinde, O.A. Iron deficiency anaemia among apparently healthy pre-school children in Lagos, Nigeria. Afr. Health Sci. 2016, 16, 61–68. [Google Scholar] [CrossRef] [PubMed]
  66. Gupta, P.M.; Perrine, C.G.; Mei, Z.; Scanlon, K.S. Iron, anemia, and iron deficiency anemia among young children in the United States. Nutrients 2016, 8, 330. [Google Scholar] [CrossRef] [PubMed]
  67. Hipgrave, D.B.; Fu, X.; Zhou, H.; Jin, Y.; Wang, X.; Chang, S.; Scherpbier, R.W.; Wang, Y.; Guo, S. Poor complementary feeding practices and high anaemia prevalence among infants and young children in rural central and western China. Eur. J. Clin. Nutr. 2014, 68, 916–924. [Google Scholar] [CrossRef]
  68. Elliott, D.A.; McIntosh, M.T.; Hosgood, I.I.I.H.D.; Chen, S.; Zhang, G.; Baevova, P.; Joiner, K.A. Four distinct pathways of hemoglobin uptake in the malaria parasite Plasmodium falciparum. Proc. Natl. Acad. Sci. USA 2008, 105, 2463–2468. [Google Scholar]
  69. Menon, M.P.; Yoon, S.S. Prevalence and factors associated with anemia among children under 5 years of age—Uganda, 2009. Am. J. Trop. Med. Hyg. 2015, 93, 521–526. [Google Scholar] [CrossRef]
  70. Sumbele, I.U.N.; Sama, S.O.; Kimbi, H.K.; Taiwe, G.S. Malaria, moderate to severe Anaemia, and malarial Anaemia in children at presentation to Hospital in the Mount Cameroon Area: A cross-sectional study. Anemia 2016, 2016, 5725634. [Google Scholar] [CrossRef]
  71. Ngesa, O.; Mwambi, H. Prevalence and risk factors of Anaemia among children aged between 6 months and 14 years in Kenya. PLoS ONE 2014, 9, e113756. [Google Scholar] [CrossRef]
  72. Quintero, J.P.; Siqueira, A.M.; Tobón, A.; Blair, S.; Moreno, A.; Arévalo-Herrera, M.; Lacerda, M.V.G.; Valencia, S.H. Malaria-related anaemia: A Latin American perspective. Mem. Inst. Oswaldo Cruz 2011, 106, 91–104. [Google Scholar] [CrossRef]
  73. Ewusie, J.E.; Ahiadeke, C.; Beyene, J.; Hamid, J.S. Prevalence of anemia among under-5 children in the Ghanaian population: Estimates from the Ghana demographic and health survey. BMC Public Health 2014, 14, 626. [Google Scholar] [CrossRef]
  74. Zhao, A.; Zhang, Y.; Peng, Y.; Li, J.; Yang, T.; Liu, Z.; Lv, Y.; Wang, P. Prevalence of anemia and its risk factors among children 6–36 months old in Burma. Am. J. Trop. Med. Hyg. 2012, 87, 306–311. [Google Scholar] [CrossRef] [PubMed]
  75. Gebrehaweria Gebremeskel, M.; Lemma Tirore, L. Factors associated with anemia among children 6–23 months of age in Ethiopia: A multilevel analysis of data from the 2016 Ethiopia demographic and health survey. Pediatr. Health Med. Ther. 2020, 11, 347–357. [Google Scholar] [CrossRef] [PubMed]
  76. Dey, S.; Goswami, S.; Dey, T. Identifying predictors of childhood anaemia in North-East India. J. Health Popul. Nutr. 2013, 31, 462–470. [Google Scholar] [CrossRef]
  77. Khan, J.R.; Awan, N.; Misu, F. Determinants of anemia among 6–59 months aged children in Bangladesh: Evidence from nationally representative data. BMC Pediatr. 2016, 16, 3. [Google Scholar] [CrossRef]
  78. Assunção, M.C.F.; da Silva dos Santos, I.; de Barros, A.J.D.; Gigante, D.P.; Victora, C.G. Anaemia in children under six: Population-based study in Pelotas, Southern Brazil. Rev. Saude Publ. 2007, 41, 328–335. [Google Scholar] [CrossRef]
  79. Mamiro, P.; Kolsteren, P.; Roberfroid, D.; Tatala, S.; Opsomer, A.; Van Camp, J. Feeding practices and factors contributing to wasting, stunting, and iron-deficiency anaemia among 3–23-month old children in Kilosa district, rural Tanzania. J. Health Popul. Nutr. 2005, 23, 222–230. [Google Scholar]
  80. Xin, Q.-Q.; Chen, B.-W.; Yin, D.-L.; Xiao, F.; Li, R.-L.; Yin, T.; Yang, H.-M.; Zheng, X.-G.; Wang, L.-H. Prevalence of anemia and its risk factors among children under 36 months old in China. J. Trop. Pediatr. 2017, 63, 36–42. [Google Scholar] [CrossRef]
  81. Baranwal, A.; Roy, N. Association of household environment and prevalence of anemia among children under-5 in India. Front. Public Health 2014, 2, 196. [Google Scholar] [CrossRef]
  82. Yadav, J.; Nilima, N. Geographic variation and factors associated with anemia among under-fives in India: A multilevel approach. Clin. Epidemiol. Glob. Health 2021, 9, 261–268. [Google Scholar] [CrossRef]
  83. Asmare, A.A.; Agmas, Y.A. Determinants of coexistence of undernutrition and anemia among under-five children in Rwanda; evidence from 2019/20 demographic health survey: Application of bivariate binary logistic regression model. PLoS ONE 2024, 19, e0290111. [Google Scholar] [CrossRef]
  84. Anteneh, Z.A.; Van Geertruyden, J.P. Spatial variations and determinants of anemia among under-five children in Ethiopia, EDHS 2005–2016. PLoS ONE 2021, 16, e0249412. [Google Scholar] [CrossRef]
Figure 1. Map of Niger showing the different regions. Source: https://en.wikipedia.org/wiki/Regions_of_Niger (accessed on 20 October 2024).
Figure 1. Map of Niger showing the different regions. Source: https://en.wikipedia.org/wiki/Regions_of_Niger (accessed on 20 October 2024).
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Figure 2. Distribution of children’s anaemia levels across regions in Niger.
Figure 2. Distribution of children’s anaemia levels across regions in Niger.
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Figure 3. Distribution of children’s anaemia levels across malaria infection and other febrile infections in Niger.
Figure 3. Distribution of children’s anaemia levels across malaria infection and other febrile infections in Niger.
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Figure 4. Distribution of children’s anaemia levels across birth order and twins in Niger.
Figure 4. Distribution of children’s anaemia levels across birth order and twins in Niger.
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Table 1. Descriptive statistics of selected mothers and children’s variables (n = 4142).
Table 1. Descriptive statistics of selected mothers and children’s variables (n = 4142).
VariablesMeanStd. Err.[95% Confidence Interval]
Mother’s age28.87520.179128.521929.2285
Agadez0.02830.00360.02120.0355
Diffa0.02280.00200.01890.0268
Dosso0.07980.00590.06810.0914
Maradi0.25460.01860.21800.2913
Tahoua0.20210.01440.17370.2304
Tillaberi0.13420.01630.10210.1664
Zinder0.23140.01440.20290.2599
Niamey0.04680.00460.03770.0559
Urban0.16230.01530.13220.1925
Altitude354.43234.3246345.9018362.9628
Primary 0.14980.00920.13160.1679
Secondary0.09040.00730.07600.1049
Tertiary0.00640.00130.00380.0091
Household size8.46480.16608.13728.7923
Male headship1.06810.00821.05201.0842
Head age42.53060.356241.827943.2333
Newspaper0.01510.00260.01000.0203
Radio0.25690.01610.22520.2885
TV0.12790.01220.10380.1520
1st birth order0.59280.00820.57660.6090
2nd birth order0.35370.00690.34010.3674
3rd birth order0.05100.00410.04290.0591
4th birth order0.00210.00080.00050.0037
5th birth order0.00030.0003−0.00030.0010
Not twins0.96990.00440.96120.9787
1st of multiple0.01380.00210.00970.0179
2nd of multiple0.01630.00260.01120.0214
Gender of child0.50860.00930.49020.5269
Child age31.36240.260630.848331.8765
Wealth index2579.24405380.3780−8033.070313,192.1900
Table 2. Distribution of malaria and fever incidences across regions and sectors in Niger (n = 4142).
Table 2. Distribution of malaria and fever incidences across regions and sectors in Niger (n = 4142).
VariablesFreq.PercentFreq.Percent
RegionMalariaFever
Agadez122.07382.71
Diffa223.79976.91
Dosso12020.6924217.25
Maradi10618.2821315.18
Tahoua8013.7918713.33
Tillaberi7012.0725117.89
Zinder13423.1029020.67
Niamey366.21856.06
Urban/Rural
Rural48383.28118484.39
Urban9716.7221915.61
Total (% all children)58014.00140333.87
Table 3. Results of the heteroscedasticity-consistent ordered probit and their marginal values.
Table 3. Results of the heteroscedasticity-consistent ordered probit and their marginal values.
VariablesAllSevere AnaemiaModerate AnaemiaMild AnaemiaNon-Anaemic
Ordered ProbitMarginal CoeffMarginal CoeffMarginal CoeffMarginal Coeff
Coeffit-statCoeffit-statCoeffit-statCoeffit-statCoeffit-stat
Malaria−0.1367−1.990.01101.820.04362.04−0.0134−1.8−0.0411−2.06
Fever−0.2396−4.450.01883.790.07674.58−0.0226−3.92−0.0729−4.60
Mother’s age0.00491.47−0.0004−1.47−0.0016−1.470.00041.460.00151.48
Diffa0.13440.80−0.0088−0.89−0.0446−0.790.00971.010.04370.77
Dosso−0.0024−0.010.00020.010.00080.01−0.0002−0.01−0.0008−0.01
Maradi0.11900.90−0.0083−0.94−0.0391−0.890.00960.980.03780.88
Tahoua0.08720.62−0.0061−0.65−0.0286−0.620.00710.670.02760.61
Tillaberi−0.0433−0.210.00330.210.01400.22−0.0040−0.21−0.0133−0.22
Zinder−0.0405−0.330.00300.320.01310.33−0.0037−0.32−0.0125−0.33
Niamey0.07380.36−0.0051−0.38−0.0243−0.350.00590.40.02350.35
Urban0.33915.44−0.0204−5.27−0.1130−5.480.02006.580.11345.18
Altitude0.00050.970.0000−0.96−0.0002−0.980.00000.960.00010.98
Primary0.07501.09−0.0053−1.13−0.0246−1.090.00611.170.02381.08
Secondary−0.0222−0.260.00170.250.00720.26−0.0020−0.25−0.0069−0.26
Tertiary−0.0137−0.060.00100.060.00440.06−0.0012−0.06−0.0042−0.06
Household size0.00280.45−0.0002−0.45−0.0009−0.450.00020.450.00090.45
Male headship−0.0580−0.550.00430.550.01890.55−0.0051−0.55−0.0181−0.55
Head age−0.0011−0.480.00010.480.00040.48−0.0001−0.48−0.0003−0.48
Newspaper0.36112.50−0.0193−3.43−0.1211−2.510.01566.620.12482.30
Radio0.03840.73−0.0028−0.73−0.0125−0.730.00330.750.01200.73
TV0.14722.03−0.0098−2.24−0.0487−2.000.01102.490.04761.96
2nd Birth order−0.1189−2.260.00912.140.03842.27−0.0109−2.16−0.0366−2.28
3rd Birth order0.05890.69−0.0041−0.73−0.0194−0.690.00480.750.01870.68
4th Birth order−0.3899−0.580.04070.430.11200.71−0.0490−0.47−0.1038−0.70
5th Birth order8.534846.15−0.0332−9.16−0.4550−46.31−0.2724−28.370.760689.91
1st of Multiple−0.1279−0.800.00840.90.04240.79−0.0094−1.02−0.0415−0.77
2nd of Multiple−0.4698−2.290.05211.630.13043.02−0.0613−1.86−0.1212−2.89
Gender of child−0.0926−2.180.00682.210.03022.16−0.0081−2.17−0.0289−2.17
Child age0.01226.91−0.0009−6.87−0.0040−6.580.00116.440.00386.78
Wealth index −6.2 × 10−8−2.535.6 × 10−82.51.1 × 10−72.52−9.99 × 10−8−2.58
lnsigma
v191awealth−4.6 × 10−7−2.54
/cut1−1.4143
/cut20.3900
/cut31.1268
Number of strata16
Number of PSUs206
Number of obs4142
Population size4,213,981,348
Design df190
F (29,162)227.57 ***
Mean VIF2.39
***—statistically significant at 1% level.
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Molelekoa, T.C.; Oyekale, A.S. Under-5 Malaria and Fever Morbidities as Correlates of Anaemia in Niger: A Heteroscedasticity-Consistent Ordered Probit Approach. Int. J. Environ. Res. Public Health 2024, 21, 1687. https://doi.org/10.3390/ijerph21121687

AMA Style

Molelekoa TC, Oyekale AS. Under-5 Malaria and Fever Morbidities as Correlates of Anaemia in Niger: A Heteroscedasticity-Consistent Ordered Probit Approach. International Journal of Environmental Research and Public Health. 2024; 21(12):1687. https://doi.org/10.3390/ijerph21121687

Chicago/Turabian Style

Molelekoa, Thonaeng Charity, and Abayomi Samuel Oyekale. 2024. "Under-5 Malaria and Fever Morbidities as Correlates of Anaemia in Niger: A Heteroscedasticity-Consistent Ordered Probit Approach" International Journal of Environmental Research and Public Health 21, no. 12: 1687. https://doi.org/10.3390/ijerph21121687

APA Style

Molelekoa, T. C., & Oyekale, A. S. (2024). Under-5 Malaria and Fever Morbidities as Correlates of Anaemia in Niger: A Heteroscedasticity-Consistent Ordered Probit Approach. International Journal of Environmental Research and Public Health, 21(12), 1687. https://doi.org/10.3390/ijerph21121687

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