Skip to main content
PLOS One logoLink to PLOS One
. 2019 Jul 3;14(7):e0219170. doi: 10.1371/journal.pone.0219170

Association between malnutrition and anemia in under-five children and women of reproductive age: Evidence from Bangladesh Demographic and Health Survey 2011

M Shafiqur Rahman 1,*, Muntaha Mushfiquee 1, Mohammad Shahed Masud 1, Tamanna Howlader 1
Editor: Seth Adu-Afarwuah2
PMCID: PMC6609031  PMID: 31269082

Abstract

Background

Bangladesh is one of the most anemia prone countries in South Asia. Children of age under five years and women of reproductive age are particularly vulnerable in this region. Although several studies have investigated the risk factors of anemia, only few have explored its association with malnutrition, despite its high prevalence in the same group. The objective of this paper is to investigate the association of malnutrition with anemia by conducting separate analyses for under-five children and women of reproductive age using data from the nationally representative 2011 Bangladesh Demographic and Health Survey.

Methods

Two binary outcome variables are considered separately: presence of anemia in children under five years of age (Hb<11.0 g/dl) and presence of anemia in women of childbearing age (Hb<12.0 g/dl). The exposures of interest corresponding to these two outcomes are stunting (low height-for-age) and low BMI (<18.5 kg/m2), respectively. Preliminary analysis involves estimating the association between exposure and outcome while controlling for a single confounder by computing adjusted odds ratios (adjOR) using the Cochran-Mantel-Haenszel approach in stratified analysis. Later, associations between the exposures and outcomes are estimated separately for under-five children and women of reproductive age by fitting multivariable regression models that adjust simultaneously for several confounders.

Results

The prevalence of anemia is found to be higher among both the stunted children and women with low BMI compared to their healthy counterparts (Children: 56% vs 48%; women: 50% vs 43%). Furthermore, stunted children and women with low BMI have significantly increased odds of developing anemia, as reflected by the adjusted ORs of 1.76 (95% CI:1.10–2.83) and 1.81 (95% CI: 1.11–3.48), respectively. The association of stunting with anemia in children was modified by their age and socio-economic condition, where risk of being anemic decreases with increasing age but with a lower rate for stunted children from richest family. In addition, stunted children of anemic mothers are at greater risk of being anemic compared to non-stunted children of anemic or non-anemic mothers. Again the association between BMI and anemia in women is modified by the level of education, with risk of anemia being lowest among women with low BMI and higher education.

Conclusion

Evidence–based policies targeting the vulnerable groups are required to combat anemia and nutritional deficiencies simultaneously under the same program.

Introduction

Anemia, which is characterized by low level of hemoglobin in the blood, is one of the major public health hazards affecting people in both developed and developing countries [13]. Anemia may occur at all stages of life, however, young children and women in the childbearing age are the most vulnerable [4, 5]. When anemia occurs in children, it could affect their cognitive performance and physical growth [6]. In women, anemia could adversely affect their capacity to work and may lead to poor pregnancy outcomes [7]. According to the World Health Organization (WHO), globally about 38% of women of reproductive age and 43% of children under five years of age were affected by anemia in 2011 [2, 3]. Anemia is more prevalent in developing countries [4, 8] contributing to about one million deaths each year world-wide. Three-quarters of these deaths occur in Africa and South-East Asia [2, 3, 9, 10]. Bangladesh has been reported as one of the most anemia prone countries in South Asia [1113]. According to the National Nutrition Project (NNP), the prevalence of anemia among children of ages 6–59 months was estimated to be 47% in 2004 and 68% in 2013 [14, 15]. The National Micronutrient Survey 2011–12 estimated an anemia prevalence of 33% among the children of the age group 6–59 months and 26% among the non-pregnant and non-lactating women [14]. Another study reported that childhood anemia decreased with increasing age, with a prevalence of 64% among children of ages 6–23 months and 42% among children of ages 24–59 months [15, 16]. Such high prevalence reported by multiple studies indicates that anemia is a major public health threat in Bangladesh. Although Bangladesh has made remarkable progress in health and social development achieving most of the Millenium Development Goals (MDGs) in the last decade [17], it is still struggling to tackle the burden of some diseases including anemia.

Several studies [1, 1821] have been conducted to identify the factors associated with anemia among the vulnerable groups of the population. Most of these studies reported iron deficiency as the primary cause of anemia in developing countries along with other associated causes including malaria, parasitic infection, nutritional deficiencies, and haemoglobinpathies (a genetic condition). However, recent evidence suggests that iron deficiency may not be the primary cause of anemia in Bangladesh [22, 23]. The reason is that iron is abundant in groundwater and majority of the country’s population relies on groundwater for drinking purposes [24]. Thus consumption of iron occurs through consumption of groundwater. Furthermore, there are studies that have found a link between the amount of iron intake through groundwater and the level of iron in the body [23, 25]. Thus, iron deficiency does not appear to be the most important risk factor of anemia, which explains why most of the iron-supplementation intervention programmes are ineffective in reducing the burden of anemia in Bangladesh [26].

Given the low prevalence of iron deficiency but high prevalence of anemia among women and children in Bangladesh, some recent studies in similar [27, 28] or different socio-economic settings [2931] were conducted to examine whether socio-demographic factors are associated with anemia. Most of these studies identified household socioeconomic status, food insecurity, and geographical location as risk factors. Although some of these studies identified stunting and low body-mass-index (BMI) as one of the risk factors of anemia in under-five children and women of reproductive age, respectively, limited studies have explicitly explored the association of these malnutrition indicators with anemia, despite their high prevalence in both women and children. According to recent evidence from the national surveys and studies [32, 33], about 36% of under-five children are stunted (low height-for-age), 33% are underweight (low weight-for-age) and 14% are wasted (low weight- for-height). Similarly 19% of women of reproductive age are malnourished (low BMI against the standard level 18.5). Thus, women of reproductive age and under-five children in Bangladesh are also vulnerable to malnutrition [32, 34]. High prevalence of anemia and malnutrition in both populations hints at a possible link between these two conditions. Thus, an intensive investigation is required to determine how and to what extent the nutritional statuses of women and children are associated with their anemia levels and whether the association is modified by other risk factors. Although some studies have [35, 36] tried to identify common factors associated with anemia and growth (measured by stunting, underweight and wasting in children and low BMI in women) through separate analysis of anemia and growth data, such an analysis may not be useful in identifying whether there is any association between growth and anemia. Against this backdrop, the current paper examines the association between anemia and stunting in under-five children and the association between anemia and BMI in childbearing women using nationally representative data extracted from the Bangladesh Demographic and Health Survey 2011. Findings of the study will be useful in providing new insights that may help design effective policies for reducing the burden of anemia as well as malnutrion in both women and children.

Methods

Data

Data on anemia, stunting and BMI were extracted from the 2011 Bangladesh Demographic and Health Survey (BDHS) [37] conducted during November 2010- March 2011. BDHS is a nationally representative health survey conducted every three years since 1993 with collaborative efforts of the National Institute of Population Research and Training (NIPORT), ICF International (USA), and Mitra and Associates under the demographic and health survey (DHS) program based on developing countries across the world. It is a cross-sectional study based on a two-stage stratified cluster sampling design. The entire population was stratified into 14 strata based on 7 administrative divisions and urban-rural areas in each division. In the first stage, the primary sampling units (PSUs) consisting of ward in rural area or sub-ward in urban area were randomly selected from a list of PSUs in each stratum. An equal number of households were then randomly selected from each PSU in the second stage. The survey collected information on health, nutrition and demographic history for men, women and children. In particular, data on anemia were collected from women of reproductive age and children in the age group 6–59 months belonging to every third household in the selected sampled households by screening the hemoglobin(Hb) levels (g/dl) in their blood samples at the time of survey. The 2011 BDHS used HemoCue®Hb 201+ rapid testing methodology, which consists of a battery-operated photometer and a disposible microcuvatte to measure Hb levels in the blood sample (a drop of capillary blood taken from fingertip). The classification of women and children as anemic or non-anemic was performed after adjusting their Hb levels for altitude, and in the case of women, pregnancy status was also adjusted for using Centre for Disease Control (CDC) formula [38]. Information on stunting and BMI were also collected at the time of the survey by taking anthropometric measurments such as height, weight and age of the women and children. For more details on survey methodology and methods for measurement of anemia, see elsewhere [37].

Ethical considerations

The Ethics committee at NIPORT, Mitra and Associates, and ICF international approved a waiver from ethical approval for this retrospective study. As the de-identified data for this study came from the secondary sources, this study does not require eithical approval.

Variables

The present study considered two populations, i.e., under-five children (6–59 months) and women of reproductive age (15–49 years) and therefore separate outcome-exposure pairs for the two populations. The outcome variables were ‘maternal-anemia’ (yes, no) representing anemia status in women and ‘child-anemia’ (yes, no) representing anemia status in children. Children were classified as anemic if their adjusted hemoglobin levels (Hb) were less than the cuttoff of 11.0 g/dl, and women were classified as anemic if Hb<12.0g/dl. The exposure variables of interest were BMI in the case of women and stunting in the case of children. BMI is a quantitative variable that was calculated using height and weight measurements of women and is a commonly used nutritional status indicator. BMI was convereted to a binary exposure with categories low (BMI<18.5) and high (BMI ≥18.5). Thus, women were considered malnourished if their BMI was less than 18.5. Similarly stunting (low height for age), which is a good nutritional status indicator for children, was also converted to a binary exposure (stunted vs normal). Children having z-score for the height-for-age index less than two standard deviations from the median of WHO reference population [37] were considered as stunted.

In addition to the above exposures, a set of background factors were chosen based on previous literature to control for potential confounders of the association between the exposure and outcome [27, 39]. Tables 1 and 2 list the qualitative background risk factors and their corresponding levels/categories for the outcomes child anemia and maternal anemia, respectively. In Table 1, a child was considered to have access to food if he/she had three square meals per day regularly. Otherwise, the child had limited access. In Table 2, information on size at birth was collected retrospectively by asking mothers to recall whether the child’s size was ‘very small’, ‘smaller than average’, ‘average’, or ‘above average’ at birth. This information is commonly used as proxy for birth weight in many studies [40, 41] as majority of births in Bangladesh occur at home where there is usually no facility for taking the baby’s weight. The binary risk factor ‘size at birth’ was created by classifying a child as ‘small’ if the mother reported ‘very small’ or ‘smaller than average’. Otherwise, the child’s size was considered normal. The variable socio-economic status (SES) was determined from wealth index that was calculated by performing principal component analysis on the assests owned by the households. The first principal component, which explains maximum variability of the data, gives the wealth index. The wealth index was then used to categorize the individuals into five equal groups, where the first quintile refers to the poorest group and the fifth quintile refers to the richest group [37].

Table 1. Distribution of anemic children by their background characteristics.

Variables Number at risk % of anemic children Variables2 Number at risk % of aanemic children
Stunting Maternal anemia status
Stunted 925 56.5 not anemic 1239 45
 Normal 1309 48.5 anemic 1000 61.3
Sex Size at birth
Male 1173 53.1 Normal 1883 52.3
Female 1110 51.1 Small 399 51.6
Age in months Birth order
24-Jun 780 71 First 791 52.2
25–48 1019 44.5 2–3 1020 51.5
48–59 484 38 4+ 472 53.6
Maternal Education Child had fever recently
No education 432 53.5 no 1366 49.6
Primary 744 54.6 Yes 917 56.1
Secondary 947 52.1 Child had diarrhea recently
Higher 160 38.1 no 2154 51.8
SES Yes 129 58.1
Poorest 521 59.5 Received Vitamin A supplement
Poorer 445 58 Yes 531 58
Middle 408 52.4 no 1740 50.3
Richer 431 45.7 Access to food
Richest 408 44 Yes 1830 51.3
Region Limited 453 55.6
Barisal 256 59.4 Area of residence
Chittagong 437 52.2 Urban 686 48.3
Dhaka 370 47.8 rural 1597 53.8
Khulna 254 54.3 Total 2271 52.1
Rajshahi 281 48.4
Rangpur 305 57.7
Sylhet 380 48.4

Table 2. Distribution of anemic women by their background characteristics.

Variables Number at risk % of anemic women
BMI
BMI<18.5 719 49.5
BMI> = 18.5 1739 43.2
Births in last five years
1 1713 42.6
2–4 754 50.5
Age in years
15–19 307 46.3
20–29 1530 43.5
30+ 628 48.3
Education
No education 486 51.6
Primary 798 47.2
Secondary 1010 41.4
Higher 173 38.2
SES
Poorest 562 51.6
Poorer 494 50.4
Middle 458 47.2
Richer 457 41.6
Richest 496 33.7
Region
Barisal 270 48.5
Chittagong 465 41.7
Dhaka 404 49.7
Khulna 274 35.8
Rajshahi 313 45.7
Rangpur 328 48.8
Sylhet 413 44.8
Area of residence
Urban 747 41.2
Rural 1720 46.7
Access to food
Yes 1977 43.5
Limited 490 51.2

Statistical analysis

First, univariate analysis was performed by calculating descriptive statistics that were used to summarize the data. Next, bivariate analysis was performed by calculating odds ratios from 2x2 contigency tables for the exposure and outcome variables. However, the true association between stunting and child-anemia or BMI and maternal-anemia may be confounded by other risk factors known as confounders that are associated with both the outcome and exposure of interest. To mitigate the effects of confounders, stratified analysis was performed by constructing 2x2 contigency tables for the exposure and outcome at each level of the confounder and computing the stratum specific odds ratios (OR). These odds ratios are then combined using Cochran-Mantel-Haenszel approach [42], which takes the weighted average of the strafum specific odds ratios to obtain the adjusted odds ratio (adjOR). The stratum specific analyses are also useful for identifying potential confounders and effect modifiers thereby providing insights for building a good multivariable regression model. Following stratified analysis, the net effects of malnutrition on child-anemia and maternal-anemia were assessed separately while controlling for the effects of all confounders simultaneously by fitting multivariable logistic models containing both main and interaction effects. Although several confounders were identified during the bivariate analysis, the final model contained the main and interaction effects of only a few confounders. The other confounders were excluded one by one based on the p-value (>0.10) of the likelihood ratio-test performed by adding the confounder to the model starting with stunting (for the model with child anemia) and BMI (for model with maternal anemia) in different combinations either as main effects and/or interaction effect. The non-linearity of the continuous covariate was assessed by introducing a quadratic term for the covariate and observing whether it is significant. If the quadratic term was significant, it was retained along with the linear term to capture the non—linear effect of the covariate on the outcome. Each estimate from the above analysis including the model fitting was obtained by employing sampling weight. All statistical analyses were performed using combination of Stata package ‘svy’, svyset, ‘epitab’, and ‘logit’ in Stata version 14.

Results

The analysis was based on a sample of 2283 children of ages between 6–59 months (male 41.4% and female 58.6%) and 2467 women of ages between 15–49 years. The average age of the children was 33.03 months with standard deviation (SD) of 15.86 months (results not shown). More than two-fifth of the children (41.4%) were stunted. Fifty one percent of children (n = 2234) with ages between 6 to 59 months were estimated to be anemic. The average age of the women in the sample was 25.91 years with SD of 5.97 years. The percentage of women of reproductive age having BMI<18.5 was 29.25%. Forty five percent of the women (n = 2467) were found to be affected by anemia. Table 1 presents the percentage of anemic children in the different categories of the background risk factors. Results indicate that the prevalence of anemia is higher among stunted children than among normal children (56.5% vs 48.5%). The prevalence of anemia is higher among women with low BMI (<18.5) than among women with normal BMI (>18.5) (49.5% vs 43.2%). Furthermore, prevalence of anemia is found to be higher among stunted children compared to non-stunted children and among women with low BMI compared to those with normal BMI at each level of the confounder in stratified analysis (Tables 3 and 4).

Table 3. Association between stunting and anemia in children of age 6–59 months.

Confounder Categories Nutritional Status Number at risk % anemic child OR (95%CI) adj OR (95% CI)
Sex of child
Male stunted 465 58.5 1.47(1.16–1.87) 1.39(1.18–1.66)
normal 679 48.9
Female stunted 465 54.8 1.32(1.04–1.68)
normal 625 47.8
Age of a child
6 to 24 stunted 294 75.2 1.42(1.02–1.97) 1.50(1.26–1.79)
normal 467 68.1
25 to 48 stunted 447 49.2 1.46(1.13–1.87)
normal 553 39.9
48 to 59 stunted 189 45.5 1.74(1.19–2.54)
Size of a child
Normal size stunted 732 56.0 1.32(1.09–1.59)
normal 1115 49.2
Below average stunted 198 59.1 1.87(1.25–2.79)
Birth order
First stunted 308 56.5 1.35(1.01–1.80) 1.39(1.17–1.65)
normal 463 49.0
2 to 3 stunted 383 54.3 1.24(.96–1.60)
normal 619 48.9
4+ stunted 239 60.7 1.85(1.28–1.67)
normal 222 45.5
Child recently had diarrhea
No stunted 873 56.6 1.42(1.19–1.69) 1.39(1.18–1.65)
normal 1234 47.9
Yes stunted 57 57.9 1.03(.51–2.08)
normal 70 57.1
Child had fever recently
No stunted 544 54.6 1.44(1.16–1.79) 1.33(1.17–1.64)
normal 795 45.5
Yes stunted 386 59.6 1.32(1.00–1.72)
normal 509 52.6
Currently breast feeding
No stunted 306 47.1 1.61(1.20–2.16) 1.37(1.15–1.62)
normal 481 35.6
Yes stunted 624 61.4 1.25(1.01–1.55)
Normal 823 55.9
Mother’s education
No education stunted 232 56.5 1.34(.91–1.97) 1.34(1.13–1.59)
normal 189 49.2
Primary stunted 363 55.1 1.07(.79–1.43)
normal 365 53.4
Secondary stunted 304 59.9 1.63(1.23–2.15)
normal 623 47.8
Higher stunted 31 45.2 1.50(.69–3.29)
normal 127 35.4
SES
Poorest stunted 295 58.3 .91(.63–1.29) 1.26(1.06–1.50)
normal 216 60.7
Poorer stunted 210 60.0 1.22(.84–1.78)
normal 234 55.1
Middle stunted 161 52.8 1.06(.71–1.59)
normal 238 51.3
Richer stunted 149 53.7 1.66(1.11–2.48)
normal 272 41.2
Richest stunted 115 55.7 1.89(1.24–2.90)
normal 344 39.8
Region
Barisal stunted 112 62.5 1.34(.80–2.22) 1.40(1.18–1.67)
normal 137 55.5
Chittagong stunted 185 58.4 1.60(1.09–2.36)
normal 238 46.6
Dhaka stunted 158 47.5 1.00(.66–1.52)
normal 205 47.3
Khulna stunted 86 63.9 1.75(1.02–2.99)
normal 165 50.3
Rajshahi stunted 99 55.6 1.60(.98–2.62)
normal 178 43.8
Rangpur stunted 122 63.1 1.48(.92–2.36)
normal 177 53.4
Sylhet stunted 168 51.8 1.33(.89–2.00)
normal 204 44.6
Type of place of residence
Urban stunted 247 59.5 2.09(1.52–2.87) 1.38(1.16–1.63)
normal 426 41.3
Rural stunted 683 55.6 1.17(.95–1.43)
normal 878 51.8
Overall stunted 925 56.5 1.38(1.17, 1.63)
normal 1309 48.5

Table 4. Association between BMI and anemia in women of age 15–49 years.

Confounder categories BMI Numbers’ at risk % of anemic women OR (95%CI) adjOR (95%CI)
Mother’s age
15 to 19 BMI<18.5 153 51.6 1.36(.89–2.07) 1.29(1.08–1.53)
BMI> = 18.5 214 43.9
20 to 29 BMI<18.5 428 48.1 1.25(1.00–1.56)
BMI> = 18.5 1187 42.6
30 to 39 BMI<18.5 144 55.6 1.35(.93–1.98)
BMI> = 18.5 425 48
40 to 49 BMI<18.5 24 50.0 1.19(.45–3.16)
BMI> = 18.5 46 45.7
Food
Access to food BMI<18.5 549 47.2 1.17(.96–1.42) 1.25(1.05–1.48)
BMI> = 18.5 1565 43.3
Limited access to food BMI<18.5 200 59 1.55(1.08–2.21)
BMI> = 18.5 307 48.2
Birth in last 5 year
1 BMI<18.5 472 46.0 1.17(.95–1.44) 1.25(1.06–1.49)
BMI> = 18.5 1339 42.1
2–4 BMI<18.5 277 57.8 1.43(1.06–1.91)
BMI> = 18.5 533 48.9
SES
Poorest BMI<18.5 242 55.4 1.12(.81–1.56) 1.13(.95–1.35)
BMI> = 18.5 343 52.5
Poorer BMI<18.5 183 56.3 1.48(1.03–2.13)
BMI> = 18.5 329 47.1
Middle BMI<18.5 144 48.6 1.09(.75–1.62)
BMI> = 18.5 350 46.3
Richer BMI<18.5 119 45.4 1.20(.79–1.81)
BMI> = 18.5 376 40.9
Richest BMI<18.5 61 24.6 .56(.31–1.03)
BMI> = 18.5 474 36.7
Region
Barisal BMI<18.5 79 50.6 1.06(.63–1.78) 1.26(1.06–1.49)
BMI> = 18.5 193 49.2
Chittagong BMI<18.5 123 48.0 1.38(.92–2.08)
BMI> = 18.5 390 40.0
Dhaka BMI<18.5 125 58.4 1.60(1.05–2.43)
BMI> = 18.5 295 46.9
Khulna BMI<18.5 66 40.9 1.23(.71–2.15)
BMI> = 18.5 228 36.0
Rajshahi BMI<18.5 84 45.2 .98(.60–1.61)
BMI> = 18.5 243 45.7
Rangpur BMI<18.5 113 52.2 1.06(.68–1.65)
BMI> = 18.5 281 42.7
Type of place of residence
Urban BMI<18.5 160 46.8 1.32(.94–1.88) 1.25(1.05–1.48)
BMI> = 18.5 641 39.9
Rural BMI<18.5 589 51.3 1.22(1.00–1.49)
BMI> = 18.5 1231 46.2
Mother’s education
No education BMI<18.5 172 60.5 1.66(1.15–2.42) 1.22(1.03–1.45)
BMI> = 18.5 330 47.9
Primary BMI<18.5 282 52.5 1.24(.93–1.66)
BMI> = 18.5 527 42.1
Secondary BMI<18.5 279 42.7 1.04(.79–1.36)
BMI> = 18.5 842 41.8
Higher BMI<18.5 16 37.5 .95(.34–2.64)
BMI> = 18.5 173 38.7
Overall BMI<18.5 719 49.5 1.29 (1.08, 1.53)
BMI> = 18.5 1739 43.2

When the strength of the association between anemia and stunting in children, or anemia and BMI in women was quantified by calculating the stratum-specific odds ratio at each level of the confounder, strong and significant associations were observed in each stratum. Tables 3 and 4 also show the adjOR, which measures the association between anemia and the exposure variable (stunting or BMI) after adjusting for the confounder and are calculated using the Cochran-Mantel-Haenszel approach. One observes that the associations remain significant even after adjusting for the effect of the confounder. For example, after controlling for the effect of sex, stunted children had 39% greater odds of developing anemia than normal children with estimated adjOR of 1.39 (95% CI: 1.18–1.66) (Table 3). Higher odds of being anemic among stunted children compared to non-stunted children were also observed after controlling for each of the other confounders, such as, age, SES etc, separately. Again, women with low BMI (BMI<18.5) had 29% greater odds of having anemia than women with normal BMI [adjOR = 1.29 (95% CI: 1.08–1.53)], after controlling for the effect of age (Table 4). Similar findings were observed when controlling for the other confounders such as age, education, and SES etc, separately.

Further, the associations between stunting and anemia in children and low BMI and anemia in women were assessed by controlling for several confounders simultaneously in a multivariable binary logistic model, where confounders were selected based on p-value (<0.10) of the likelihood ratio test. In the final model for child anemia, the exposure stunting along with the covariate child’s age and its quadratic form, and the confounders maternal anemia and SES, and three—way interaction between stunting, SES and age were found to be significant (Table 5). The results suggest that stunted children are more likely to develop anemia compared to normal children with the estimated adjOR being 1.76 (95% CI: 1.10–2.83). The significant interaction effect of stunting with SES and age suggests that the effect of stunting could be modified by SES and age of the child. Fig 1 describes how stunting interacts with age and SES. It suggests that the likelihood of developing anemia decreases with increasing age and the rate of decrease is comparatively high till the age of 36 months. In addition, the risk of developing anemia decreases with the improvement of household economic condition, especially in the case of normal children. For stunted children, the decline is less. The differences in risk between stunted children and normal children at various ages are largest in the richest category, while the curves for the risk cross in the poorest category. SES is a strong modifier of the effect of stunting on anemia. Improvement in SES results in rapid decline in the risk of developing anemia among normal children but not in stunted children. (Fig 2: left). The effect of stunting also varies across the levels of maternal anemia and SES (Fig 2: right). The stunted children of anemic mothers are at greatest risk of developing anemia whereas the normal children of non-anemic mothers are at the lowest risk of developing anemia. The difference in risk between these groups increases slightly with increasing SES. Interestingly, non-stunted children of anemic mothers have elevated risk of developing anemia compared to non-stunted children of anemic mothers across all SES. Improvement in SES results in rapid decline in risk among normal children but not as much among stunted children. Thus, both maternal anemia and SES are strong effect modifiers of stunting.

Table 5. Results from multivariable logistic regression analysis of child anemia data.

Variables OR P-value 95% CI
Stunting
normal RC
stunted 1.763 <0.01 1.099 2.829
Child age 0.929 <0.001 0.902 0.956
Child age^2 1.003 <0.01 1.001 1.004
maternal anemia 1.801 <0.001 1.501 2.160
Stunting*SES*child age
normal*poorest RC
normal*poorer 0.995 0.320 0.984 1.005
normal*middle 0.992 0.145 0.982 1.003
normal*richer 0.984 <0.01 0.974 0.994
normal*richest 0.976 <0.001 0.966 0.986
stunted*poorest 0.987 0.085 0.972 1.002
stunted*poorer 0.988 0.129 0.972 1.004
stunted*middle 0.982 <0.05 0.967 0.998
stunted*richer 0.981 <0.05 0.965 0.997
stunted*richest 0.987 0.150 0.970 1.005
Constant 4.347 <0.001 2.824 6.692

Fig 1. Interaction plot describing the effect of interaction between stunting, SES and age on the risk of child anemia.

Fig 1

Fig 2. Interaction plots describing the association of stunting interact with SES, and maternal anemia, anemia separately on the risk of child anemia.

Fig 2

Similarly, in the final multivariable model for women anemia, BMI is found to be significantly associated with anemia status, with the estimated adjOR of 1.80 (95% CI: 1.10–3.48) (Table 6). The interaction plot for BMI, age and education suggests that the risk of maternal anemia increases with increasing age for women with no education or primary education and decreases with age for women with secondary and higher education (Fig 3). In addition, the differences in risk at various ages between women with low BMI and women with normal BMI are significantly greater for uneducated women and diminish with increasing levels of education. Interestingly, for women with higher education, the risk of developing anemia is less in women with low BMI and the risk decreases with age. Fig 4 shows how SES and education modify the effect of BMI in women. The risk of being anemic decreases with increasing SES and the differences in risk between the two groups (low BMI and normal BMI) remain almost the same across all SES levels (Fig 4: left). Increasing education leads to significant drop in the risk of developing anemia among women with low BMI. In contrast, education does not appear to have any significant effect among women with normal BMI levels (Fig 4: right).

Table 6. Results from multivariable logistic regression analysis of maternal anemia data.

Variables OR P-value 95% CI
BMI
BMI>18.5
BMI< = 18.5 1.807 <0.05 1.100 3.485
SES
poorest RC
poorer 1.022 0.866 0.798 1.308
middle 0.894 0.395 0.690 1.157
richer 0.731 <0.05 0.560 0.953
richest 0.519 0.000 0.388 0.694
Education*BMI*age
no educ*BMI> = 18.5 1.012 0.162 0.995 1.029
no educ*BMI<18.5 1.009 0.470 0.985 1.033
primary*BMI> = 18.5 1.015 0.111 0.997 1.034
primary*BMI<18.5 0.996 0.784 0.969 1.024
secondary*BMI> = 18.5 1.013 <0.05 1.011 1.034
secondary*BMI<18.5 0.987 0.411 0.958 1.018
higher*BMI> = 18.5 1.018 <0.05 1.012 1.040
higher*BMI<18.5 0.978 0.330 0.935 1.023
Constant 0.670 0.112 0.409 1.098

Fig 3. Interaction plot describing the association of BMI interact with education and age on the risk of maternal anemia.

Fig 3

Fig 4. Interaction plot describing the association of BMI interact with SES and education, separately on the risk of maternal anemia.

Fig 4

Discussion

This paper has investigated the association between anemia and stunting among children in age group 6–59 months as well as the association between anemia and BMI among women of reproductive. In general, the prevalence of anemia was markedly high both among stunted children and women of low BMI compared to their normal counterparts. However, the higher prevalence among children suggests that they are more vulnerable to anemia than women. In both cases, there was a positive association between nutritional deficiency (reflected by stunting or low BMI) and anemia that was statistically significant even after controlling for the effects of possible confounders. This study identified important interactions that have interesting interpretations. There was significant interaction between stunting, child’s age and household socio-economic condition (SES). The risk of child anemia decreased with increasing age, however, the rate of decline was lower for stunted children. The implication of this finding is that there is a greater prevalence of anemia among stunted children compared to non-stunted children. In general, improvements in socio-economic status decreased the risk of being anemic in both groups. Thus, very young children belonging to poor households and experiencing stunting form a high risk group and should be the focus of interventions. Again, the presence of maternal anemia significantly increased the risk of child anemia even when there was improvement in socio-economic condition. The interaction effect of stunting and maternal anemia status suggests that stunted children of anemic mothers are at greater risk of being anemic. The strong association observed between maternal anemia and child anemia may be explained by the fact that there are certain factors influencing anemia that are common to both [43]. For example, both the mother and child could have a common dietary pattern and access to the same source of iron-rich micronutrient food. In addition, they share the same environment, have access to the same health facilities and are likely to have similar genetic traits. On the other hand BMI, which reflects nutritional deficiency among the women of reproductive age, is found to be significantly associated with maternal anemia. Although the risk of being anemic decreases with improvements in household economic condition, the difference in risk between women with low BMI and those with normal BMI remained almost the same. On the other hand, education strongly modifies the effect of BMI and has a profound effect on women with low BMI. Higher education lowers the risk of being anemic even if the BMI is low. These findings are similar to those found in other studies conducted for relevant population with similar [27, 28, 44] or different settings [29, 31, 43].

The results obtained in the study have some important implications. The strong associations between stunting and anemia in children, and low BMI and anemia in women, could be due to several factors. Nutritional deficiency may not be directly associated with anemia, however, it leads to certain changes in the body that make it susceptible to health hazards that may cause anemia. One hypothesis is that children and women suffering from nutritional deficiency are more likely to have weaker immune systems which make them vulnerable to various illnesses and health hazards such as parasitic infections or chronic inflammation [4546]. Many of these conditions reduce the hemoglobin level in blood leading to increased anemia prevalence. The statement is supported by the evidence given in other studies [47] that nutritional deficiency causes several health hazards.

Strong associations between stunting and anemia in children as well as BMI and anemia in women indicate that it is necessary to tackle both nutritional deficiency and anemia simultaneously under the same program targeting both mother and children. Improving women’s education and empowerment might be one way to curb high anemia and malnutrition prevalence rates. Another possible tool to tackle anemia and malnutrition is mass-and-social-media campaign which works by increasing awareness and knowledge about these conditions and methods of prevention.

Strengths and limitations of the study

This study is based on data from a nationally representative survey, which is regularly conducted by an international expert group, and hence the quality of data is high. In addition, findings from nationally representative data are more helpful for policy makers to design appropriate interventions. Furthermore, based on data conditions, sophisticated epidemiological and statistical analyses have been performed to meet the main objective of the study.

However, this study has some limitations. These include i) unavailability of data on intake of iron rich food for all subjects [37], ii) data may suffer from re-call bias of information on SES, size of the child at birth and evidence of fever or diarrhea in last fifteen days of the survey, and iii) measurement errors in data on anemia (Hb level).

Acknowledgments

The authors acknowledge NIPORT, Mitra and Associates, and ICF international for providing the data used in this study.

Data Availability

All data are freely available upon request from the DHS website http://dhsprogram.com/data/.

Funding Statement

The author(s) received no specific funding for this work.

References

  • 1.K4Health. Anemia Prevalence, Causes, and Consequences. K4Health Toolkits, 2006.
  • 2.Benoist BD, McLean E, Egli I, Cogswell M. Worldwide prevalence of anemia 1993–2005: WHO Global Database on Anemia. Geneva, Switzerland: World Health Organization; 2008. [Google Scholar]
  • 3.World Health Organization. The Global Prevalence of Anaemia in 2011. Geneva, Switzerland: World Health Organization, 2015. [Google Scholar]
  • 4.Stevens GA, Finucane MM, De-Regil LM, Paciorek CJ, Flaxman SR, Branca F. Global, regional, and national trends in haemoglobin concentration and prevalence of total and severe anaemia in children and pregnant and non-pregnant women for 1995–2011: a systematic analysis of population-representative data. Lancet Glob Health. 2013;1(1):16–25. 10.1016/s2214-109x(13)70001-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Smagulova IE, Sharmanov TS, Balgimekov SA. The prevalence of anemia among children and women of reproductive age in Kazakhstan and basis of its prevention. Vopr Pitan. 2013;82(5):58–63. [PubMed] [Google Scholar]
  • 6.AT S V DS, S. K. Anemia and growth. Indian J Endocrinol Metab 2014;18(1):S1–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Scholl TO, Hediger ML, Fischer RL, Shearer JW. Anemia vs iron deficiency: increased risk of preterm delivery in a prospective study. Am J Clin Nutr. 1992;55. [DOI] [PubMed] [Google Scholar]
  • 8.Balarajan Y, Ramakrishnan U, Ozaltin E, Shankar AH, SV S. Anaemia in low-income and middle-income countries. Lancet. 2011;378(9809):2123–35. 10.1016/S0140-6736(10)62304-5 [DOI] [PubMed] [Google Scholar]
  • 9.Chaparro C, Oot L, Sethuraman K. Overview of the Nutrition Situation in Four Countries in South and Central Asia. Washington, DC: FHI 360/FANTA; 2014. [Google Scholar]
  • 10.Ayoya MA, Bendech MA, Zagré NM, Tchibindat F. Maternal anaemia in West and Central Africa: time for urgent action. Public Health Nutr. 2012;15 10.1017/s1368980011002424 [DOI] [PubMed] [Google Scholar]
  • 11.Helen Keller International. The Burden of Anemia in Rural Bangladesh: The Need for Urgent Action. Nutrition Surveillance Project Bulletin. 2006;16. [Google Scholar]
  • 12.Zhang Q, Ananth CV, Li Z, Smulian JC. Maternal anaemia and preterm birth: a prospective cohort study. Int J Epidemiol. 2009;38(5):1380–9. 10.1093/ije/dyp243 [DOI] [PubMed] [Google Scholar]
  • 13.Ahmed F. Anaemia in Bangladesh: a review of prevalence and aetiology. Public Health Nutr 2000;3(4):385–93. [DOI] [PubMed] [Google Scholar]
  • 14.Bangladesh Bureau of Statistics. Anemia prevalence survey of Urban Bangladesh and Rural Chittagong Hill Tracts 2003. Dhaka, Bangladesh: Bangladesh Bureau of Statistics, Statistics Division, Ministry of Planning, Government of the Peoples Republic of Bangladesh UNICEF; 2004.
  • 15.International Centre for Diarrheal Disease Research Bangladesh (icddr,b), United Nations Children’s Fund (UNICEF), Global Alliance for Improved Nutrition (GAIN), and Institute of Public Nutrition. National Micronutrients Status Survey 2011–12: Final Report. Dhaka, Bangladesh: Centre for Nutrition and Food Security, icddr,b; 2013.
  • 16.Rashid M, Flora MS, Moni MA, Akhter A, Mahmud Z. Reviewing Anemia and iron folic acid supplementation program in Bangladesh- a special article. Bangladesh Med J. 2010; 39(3). [Google Scholar]
  • 17.General Economics Division (GED). Millennium Development Goals: Bangladesh Progress Report 2015. Planning Commission, Government of the People’s Republic of Bangladesh, 2015.
  • 18.Arnold DL, Williams MA, Miller RS, Qiu C, Sorensen TK. Iron deficiency anemia, cigarette smoking and risk of abruptio placentae. J Obstet Gynaecol Res. 2009;35(3):446–52. 10.1111/j.1447-0756.2008.00980.x [DOI] [PubMed] [Google Scholar]
  • 19.Ndyomugyenyi R, Kabatereine N, Olsen A, Magnussen P. Malaria and hookworm infections in relation to hemoglobin and serum ferritin levels in pregnancy in Masindi district, western Uganda. Trans R Soc Trop Med Hyg. 2008;102 10.1016/j.trstmh.2007.09.015 [DOI] [PubMed] [Google Scholar]
  • 20.Rakic L, Djokic D, Drakulovic M, Pejic A, Radojicic Z, Marinkovic M. Risk factors associated with anemia among Serbian non-pregnant women 20 to 49 years old. A cross-sectional study. Hippokratia. 2013;17. [PMC free article] [PubMed] [Google Scholar]
  • 21.Rawat R, Saha KK, Kennedy A, Rohner F, Ruel M, Menon P. Anaemia in infancy in rural Bangladesh: contribution of iron deficiency, infections and poor feeding practices. Br J Nutr. 2014;111 10.1017/s0007114513001852 [DOI] [PubMed] [Google Scholar]
  • 22.Akash G.M.B. No iron deficiency in Bangladesh, but anaemia persists. SciDevNet. 2015. [Google Scholar]
  • 23.Rahman S, Ahmed T, Rahman AS, Alam N, Ahmed AS, Ireen S, et al. Determinants of iron status and Hb in the Bangladesh population: the role of groundwater iron. Public Health Nutr. 2016;19(10):1862–74. 10.1017/S1368980015003651 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Merrill R, Shamim AA, Ali H, West KP Jr.. Groundwater Iron Assessment and Consumption by Women in Rural Northwestern Bangladesh. International Journal for Vitamin and Nutrition Research 2012;82(1):5–14. 10.1024/0300-9831/a000089 [DOI] [PubMed] [Google Scholar]
  • 25.Merrill RD, Shamim AA, Ali H, Jahan N, Labrique AB, Schulze K, et al. Iron status of women is associated with the iron concentration of potable groundwater in rural Bangladesh. Journal of Nutrition. 2011;141(5):944–9. 10.3945/jn.111.138628 [DOI] [PubMed] [Google Scholar]
  • 26.Sanghvi TG, Harvey PW, Wainwright E. Maternal iron-folic acid supplementation programs: evidence of impact and implementation. Food Nutr Bull 2010;31(2):S100–7. [DOI] [PubMed] [Google Scholar]
  • 27.Khan JR, Awan N, Misu F. Determinants of anemia among 6–59 months aged children in Bangladesh: evidence from nationally representative data. BMC Pediatrics. 2016;16(1):1–12. 10.1186/s12887-015-0536-z [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Ghose B, Tang S, Yaya S, Feng Z. Association between food insecurity and anemia among women of reproductive age. PeerJ. 2016;5(4):e1945. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Legason ID, Atiku A, Ssenyonga R, Olupot-Olupot P, Barugahare JB. Prevalence of Anaemia and Associated Risk Factors among Children in North-western Uganda: A Cross Sectional Study. BMC Hematology. 2017;17(1):10 10.1186/s12878-017-0081-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Muchie KF. Determinants of severity levels of anemia among children aged 6–59 months in Ethiopia: further analysis of the 2011 Ethiopian demographic and health survey. BMC Nutrition. 2016;2(1):51 10.1186/s40795-016-0093-3 [DOI] [Google Scholar]
  • 31.Kuziga F, Adoke Y, Wanyenze RK. Prevalence and factors associated with anaemia among children aged 6 to 59 months in Namutumba district, Uganda: a cross- sectional study. BMC Pediatrics. 2017;17(1):25 10.1186/s12887-017-0782-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Save the Children. Malnutrition in Bangladesh: Harnessing social protection for the most vulnerable London, UK: Save the Children, 2015. [Google Scholar]
  • 33.Rahman MS, Howlader T, Masud MS, R ML. Association of Low-Birth Weight with Malnutrition in Children under Five Years in Bangladesh: Do Mother’s Education, Socio-Economic Status, and Birth Interval Matter?. PLoS ONE. 2016; 2016;11(6):e0157814 10.1371/journal.pone.0157814 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Ahmed T, Mahfuz M, Ireen S. Nutrition of Children and Women in Bangladesh: Trends and Directions for the Future. Journal of Health, Population, and Nutrition 2012;30(1):1–11. 10.3329/jhpn.v30i1.11268 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Gosdin L, Martorell R, Bartolini RM, Mehta R, Srikantiah S, MF Y. The co‐occurrence of anaemia and stunting in young children. Maternal & Child Nutrition. 2018;14(3):e12597. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Woodruff BA, Wirth JP, Ngnie-Teta I, Beaulière JM, Mamady D, Ayoya MA, et al. Determinants of Stunting, Wasting, and Anemia in Guinean Preschool-Age Children: An Analysis of DHS Data From 1999, 2005, and 2012. Food Nutr Bull. 2018. 39(1):39–53. 10.1177/0379572117743004 [DOI] [PubMed] [Google Scholar]
  • 37.NIPORT, Mitra and Associates, ICF International. Bangladesh Demographic and Health Survey, 2011. NIPORT, Mitra & Associates and ICF International, Dhaka, Bangladesh and Calverton, MD, USA2013.
  • 38.Centers for Disease Control and Prevention. Recommendations to prevent and control iron deficiency in the United States. GA, CDC: 1998. [Google Scholar]
  • 39.Kamruzzaman M, Rabbani MG, Saw A, Sayem MA, Hossain MG. Differentials in the prevalence of anemia among non-pregnant, ever-married women in Bangladesh: multilevel logistic regression analysis of data from the 2011 Bangladesh Demographic and Health Survey. BMC Women’s Health. 2015;15(1):1–8. 10.1186/s12905-015-0211-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Haque SMR, Tisha S, Huq N. Poor Birth Size a Badge of Low Birth Weight Accompanying Less Antenatal Care in Bangladesh with Substantial Divisional Variation: Evidence from BDHS—2011. Public Health Research 2015;5(6):184–91. [Google Scholar]
  • 41.Dhar B, Mowlah G, Nahar S, Islam N. Birth weight status of newborns and its relationship with other anthropometric parameters in a public maternity hospital in Dhaka, Bangladesh. J Health Popul Nutr. 2002;20:36–41. [PubMed] [Google Scholar]
  • 42.Agresti A. Categorical Data Analysis: Hooken, New Jersey: John Wiley & Sons; 2002. [Google Scholar]
  • 43.Mohammed SH, Larijani B, Esmaillzadeh A. Concurrent anemia and stunting in young children: prevalence, dietary and non-dietary associated factors. Nutr J. 2019. February 21;18(1):10 10.1186/s12937-019-0436-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Pala K, Dundar N. Prevalence & risk factors of anaemia among women of reproductive age in Bursa, Turkey. Indian J Med Res. 2008;128. [PubMed] [Google Scholar]
  • 45.Grantham-McGregor S (1995) A review of studies of the effect of severe malnutrition on mental development. Journal of Nutrition 125: 2233–2238. [DOI] [PubMed] [Google Scholar]
  • 46.Khanam R, Nghiem HS, Rahman MM (2011) The impact of childhood malnutrition on schooling: evidence from Bangladesh. Journal of Biosocial Science 43: 437–451. 10.1017/S0021932011000149 [DOI] [PubMed] [Google Scholar]
  • 47.Pelletier DL, Frongillo EA, Schroeder DG, Habichit JP. The effects of malnutrition on child mortality in developing countries. Bulletin of the World Health Organization. 1995;73(4):443–8. [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

All data are freely available upon request from the DHS website http://dhsprogram.com/data/.


Articles from PLoS ONE are provided here courtesy of PLOS

RESOURCES