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. 2018 May 23;14(4):e12620. doi: 10.1111/mcn.12620

Understanding the geographical burden of stunting in India: A regression‐decomposition analysis of district‐level data from 2015–16

Purnima Menon 1,, Derek Headey 1, Rasmi Avula 1, Phuong Hong Nguyen 1,
PMCID: PMC6175441  PMID: 29797455

Abstract

India accounts for approximately one third of the world's total population of stunted preschoolers. Addressing global undernutrition, therefore, requires an understanding of the determinants of stunting across India's diverse states and districts. We created a district‐level aggregate data set from the recently released 2015–2016 National and Family Health Survey, which covered 601,509 households in 640 districts. We used mapping and descriptive analyses to understand spatial differences in distribution of stunting. We then used population‐weighted regressions to identify stunting determinants and regression‐based decompositions to explain differences between high‐ and low‐stunting districts across India. Stunting prevalence is high (38.4%) and varies considerably across districts (range: 12.4% to 65.1%), with 239 of the 640 districts have stunting levels above 40% and 202 have prevalence of 30–40%. High‐stunting districts are heavily clustered in the north and centre of the country. Differences in stunting prevalence between low and high burden districts were explained by differences in women's low body mass index (19% of the difference), education (12%), children's adequate diet (9%), assets (7%), open defecation (7%), age at marriage (7%), antenatal care (6%), and household size (5%). The decomposition models explained 71% of the observed difference in stunting prevalence. Our findings emphasize the variability in stunting across India, reinforce the multifactorial determinants of stunting, and highlight that interdistrict differences in stunting are strongly explained by a multitude of economic, health, hygiene, and demographic factors. A nationwide focus for stunting prevention is required, while addressing critical determinants district‐by‐district to reduce inequalities and prevalence of childhood stunting.

Keywords: child undernutrition, decomposition analysis, determinants, India, spatial analysis, stunting


Key messages.

  • India carries a high burden of child stunting, but lack of disaggregated stunting data at the district level has been a challenge for policy and program strategies in a decentralized governance system.

  • This is the first study to use district‐level data from a recently released national survey to highlight spatial differences in stunting across 640 districts in India.

  • Our findings highlight the range of factors that explain differences between high and lower stunting burden districts.

  • These results emphasize the importance of focused strategic planning and action to address multiple, and different, district‐specific determinants of stunting across India.

1. INTRODUCTION

As a marker of poor nutrition, stunting in early childhood is strongly associated with numerous short‐term and long‐term consequences, including increased childhood morbidity and mortality (Black et al., 2013), delayed growth and motor development (Grantham‐McGregor et al., 2007), and long‐term educational and economic consequences (Dewey & Begum, 2011). In recognition of the high social and economic costs of stunting, the Sustainable Development Goals explicitly include reductions in global stunting, and many countries have adopted the World Health Assembly target of achieving a 40% reduction in stunting by 2025.

Achieving this reduction on a global scale, however, requires rapid progress against stunting in India, which accounts for approximately one third of the world's total population of stunted preschoolers (De Onis, Blössner, & Borghi, 2011). Understanding the underlying determinants of stunting in India—which has long been characterized as having unusually high stunting rates relative to its economic development (Ramalingaswami, Jonson, & Rohde, 1997)—has therefore been the subject of considerable investigation. An array of studies from many disciplines has drawn attention to the multifactorial nature of the problem of stunting in India. Explanations have addressed issues such as economic growth and agricultural production (Fenske, Burns, Hothorn, & Rehfuess, 2013; Headey, Chiu, & Kadiyala, 2012; Subramanyam, Kawachi, Berkman, & Subramanian, 2011), poor sanitation and open defecation (Fenske et al., 2013; Spears, Ghosh, & Cumming, 2013), discrimination against women and girls (Jayachandran & Pande, 2015), poor maternal undernutrition before and during pregnancy (Coffey, 2015), exceptionally poor infant and young child feeding practices (Menon, Bamezai, Subandoro, Ayoya, & Aguayo, 2015), and broader dietary deficiencies (Deaton & Dreze, 2008).

Some previous studies have shown that child undernutrition clusters in specific regions in developing countries (Fenn, Morris, & Frost, 2004; Gebreyesus, Mariam, Woldehanna, & Lindtjorn, 2016) and different types of spatial analysis studies have been conducted to identify geographical inequalities in child stunting (Fenn et al., 2004, Gebreyesus et al., 2016, Adekanmbi, Uthman, & Mudasiru, 2013, Alemu, Ahmed, Yalew, & Birhanu, 2016). However, much less has been done on explaining the factors that contribute to spatial variability in stunting (Di Cesare et al., 2015; Haile, Azage, Mola, & Rainey, 2016; Sharaf & Rashad, 2016; Srinivasan, Zanello, & Shankar, 2013), particularly in India. Although India is a highly populated country with a high burden of stunting, limited evidence exists on spatial analysis to examine the patterns of stunting across the country. To our knowledge, two previous assessments have been done; one at the state level (Cavatorta, Shankar, & Flores‐Martinez, 2015) and another that utilized data from a subset of Indian districts (112 of 640) from a privately conducted survey to examine the role of sanitation (Spears et al., 2013). The paucity of analysis on the geography of stunting in India is problematic for two reasons. First, there are significant economic, social, and cultural differences both across and within states that might well explain the stark geographical disparities in nutrition previously observed in India (Cavatorta et al., 2015). Second, although Indian governance has traditionally been dominated by federal and state governments, the past 20 years has seen a major push to decentralize decision making to the district and subdistrict levels. Hence, a more granular assessment of the differences in stunting across India's 640 districts is essential for targeting and planning purposes.

In this study, we address this knowledge gap with an analysis of a new district‐level data set created to address three research questions: (a) How do stunting prevalence and absolute numbers of stunted children vary across Indian states and districts? (b) Which determinants of stunting are associated with district stunting prevalence? and (c) Which determinants account for the variation in stunting observed across high‐ and low‐stunting districts?

2. METHODS

2.1. Data

This paper utilizes a district‐level data set generated from National Family Health Survey (NFHS)‐4 Fact Sheets (International Institute for Population Sciences, 2017) and the 2011 Census of India (Ministry of Home Affairs, 2012). The NFHS‐4 survey is unique in being the first national survey to provide data on stunting that is representative at the district level for all 640 districts spread across 36 states. NFHS‐4 was conducted from January 20, 2015 to December 4, 2016, gathering data from 601,509 households. The survey covered topics such as child anthropometrics, parental education levels, household demographics, and access to health and sanitation services. The fact sheets from all 640 districts were released on April 2017, but unit level data have not been released (as of November 2017). These district fact sheets provide summary data on 114 indicators including stunting and its key determinants. We supplemented these indicators with data from the Census of India (Ministry of Home Affairs, 2012), including estimates of the population aged 0–5 years, open defecation density, ownership of household durables, and housing characteristics.

2.2. Measures

Our outcome indicator of interest is the district level stunting prevalence, which is the proportion of children 0–59 months of age who have their height‐for‐age two standard deviations below the World Health Organization (WHO, 2006) growth reference (HAZ < −2). The key determinants of stunting in India were selected based on conceptual frameworks from the previous literature, particularly UNICEF (1990) and the Lancet Nutrition Series (Bhutta et al., 2013). The UNICEF framework distinguishes between immediate determinants (diets and disease burdens) and underlying determinants. The Lancet framework links these determinants to interventions, noting that nutrition‐specific interventions address immediate determinants, whereas interventions and policies in nutrition‐sensitive sectors address underlying determinants. In this paper, we distinguish between immediate determinants, nutrition‐specific interventions, and underlying determinants.

The immediate determinants included indicators related to maternal undernutrition and child feeding practices. We used women's low body mass index (BMI < 18.5 kg/m2) as a proxy for maternal undernutrition. Indicators for infant and young child feeding included early initiation of breastfeeding (proportion of infants 0–23 months who were breastfed within 1 hr of birth), exclusive breastfeeding (the proportion of infants 0–5.9 months of age who fed only breast milk), timely introduction of complementary foods (proportion of children 6–8.9 months of age who were introduced solid and semi‐solid foods), and adequate diet (proportion of children 6–23 months old who received four or more food groups and a minimum meal frequency). Some of these variables are only available for subsets of districts.

The nutrition‐specific interventions included antenatal care (ANC) during the first trimester, adequate ANC (at least four ANC visits), and iron and folic acid (IFA) consumption (at least 100 IFA during the last pregnancy). Indicators related to infant's postnatal care included full immunization, vitamin A supplementation, and oral rehydration solution during diarrhoea. Although some of these are health care interventions, they are considered nutrition‐specific interventions because they act as important platforms for delivery of nutrition‐specific interventions such as micronutrient supplements and nutrition counselling and reach households in the first 1,000 days of life.

The underlying determinants examined included mother's education (≥10 years of schooling), age at marriage (at 18 years or older), sanitation, an asset index, and household size. For sanitation, we used water within premises (with the assumption that more access to water may facilitate more hygienic practices) and open defecation density (the number of people estimated to engage in open defecation per square kilometre). An asset index was constructed from district‐level data, using the first principal component extracted from 19 different variables, including housing structure, house ownership, presence of a kitchen, access to electricity, clean cooking fuel, assets, and access to a bank account. We also included the proportion of scheduled caste/tribes (designated groups of historically disadvantaged people in India) in the district because it is an important dimension of inequality in India.

2.3. Statistical analyses

Several complementary methods of analysis were applied to these data. We first estimate the absolute numbers of stunted children by multiplying the stunting prevalence with the estimated number of children 0–5 years of age from the Census of India. We mapped stunting prevalence by district to graphically analyse patterns of stunting across India. We tabulated stunting prevalence and absolute numbers of stunted children by states and by three major state groupings (northern states, southern states, and north‐eastern and island states). District stunting prevalence was then categorized into four bins based on current WHO cut‐off values for public health significance (WHO, 2010): low prevalence (<20%), moderate prevalence (20–29.9%), high prevalence (30–39.9%), and very high prevalence (≥40%). The differences in determinants were tested for statistical significance across these different stunting burden categories, using analysis of variance and Bonferroni post hoc comparisons.

Second, to identify the determinants of stunting prevalence at the district level, we examined the bivariate associations between stunting and various determinants using scatter plots and tested for normality of the distributions using the Kolmogorow–Smirnov test. Three variables (4+ antenatal visits, open defecation density, and asset scores) were not normally distributed and showed non‐linear bivariate relationships with stunting; hence, they were log‐transformed. Multivariate linear regression was then used to examine the different factors associated with stunting. For this regression analysis, we dropped a few variables that were either highly correlated with another variable (e.g., ANC in the first trimester was highly correlated with 4+ ANC visits) or were only available for a subset of the districts (exclusive breastfeeding, timely introduction of foods, and oral rehydration solution during diarrhoea were only available for 425, 186, and 328 districts, respectively). Because we are primarily interested in explaining differences across districts rather than differences across states, all models included state‐fixed effects, meaning that we are analysing within‐state variation in stunting prevalence. We therefore report both total R 2, but also the within‐ and between‐state coefficients of determination. All regression models were weighted by the population of children under 5 years because the district population sizes vary substantially. In terms of specifications, we first estimated bivariate models for each variable. We then estimated a multivariable model including only immediate determinants and nutrition‐specific interventions and then estimated a full multivariable model that included underlying determinants. In addition to gauging whether the coefficients on immediate determinants are robust to potential confounding factors, this approach allows us to investigate potential causal pathways by examining how coefficients on immediate determinants change as underlying determinants are added to the model (MacKinnon, Krull, & Lockwood, 2000).

In the last step of our analysis, we applied a regression‐decomposition to assess the ability of the various determinants described above to predict spatial patterns in stunting and differences between very high‐burden and low‐burden districts. This approach has been used widely in literature to study mean outcome differences between groups (Jann, 2008), including differences in child malnutrition between geographical areas (Sharaf & Rashad, 2016; Spears et al., 2013; Srinivasan et al., 2013) and between populations measured at different points of time (Headey, Hoddinott, Ali, Tesfaye, & Dereje, 2015). This analysis effectively combines the analysis of differences in means of the explanatory variables (X) and regression estimates of the coefficients associated with these variables (βX). Specifically, the “explained” difference between one spatial unit (District A) and another unit (District B) is the product of the difference in the mean of X across the two samples (X A − X B) and the coefficient of X from a pooled regression model (βX). Intuitively, if a particular X variable has a large regression coefficient (“marginal effect”) and a large difference in means over two districts, then this variable will play a large role in explaining the interdistrict difference in stunting. An attractive feature of the decomposition approach is that it gauges the ability of all the variables in the model to predict interdistrict differences, as well as the ability of the model as a whole to account for these differences. In this analysis, we implemented a decomposition at means of the stunting differences between very high‐burden (stunting > 40%) and low‐burden districts (stunting < 20%) with the objective of understanding how high‐burden districts can move towards much lower rates of stunting. We report the share of actual stunting accounted for by this decomposition, as well as the share unexplained by the model as a whole.

3. RESULTS

India achieved a sizeable improvement in stunting between 2006 and 2016, with a decline from 48.0% to 38.4% among children below 5 years (International Institute for Population Sciences, 2017). Despite this, stunting in India remains high and variable across districts, ranging between 12.4% and 65.1% (Figure 1). In total, there are more than 63 million children stunted in the country, which is more than one third of the global estimate for 2013 (De Onis & Branca, 2016). Stunting varies substantially across major regions and states, both in terms of prevalence and absolute numbers of stunted children (Table 1). The populous northern states of India contain approximately 52.6 million stunted children, accounting for more than 80% of stunted children in the country. Average district stunting prevalence for these states varies from 25.2% in Himachal Pradesh to 48.2% in Bihar and 46.3% in Uttar Pradesh. These latter two states are very large, containing 9.2 million and 14.3 million stunted children, respectively. In comparison, all of the Southern states collectively contain 8.1 million stunted children and the north‐eastern and island states some 2.4 million. Even so, stunting prevalence in these other regions is relatively high in many instances, with one third of children in Andhra Pradesh and Karnataka estimated to be stunted, for example. Among reasonably populous states, only Kerala had an average district stunting prevalence below the 20% threshold.

Figure 1.

Figure 1

Maps of stunting prevalence in Indian districts, 2015–2016

Table 1.

Stunting prevalence and population stunted, by major regions and states of India

# districts District stunting prevalence (%) Population stunted
Mean Range (min, max)
Northern states 442 35.5 52,623,659
Bihar 38 48.2 35.6 57.3 9,208,676
Chandigarh 1 28.7 28.7 28.7 34,278
Chhattisgarh 18 38.9 30.6 49.0 1,368,203
Gujarat 26 39.4 22.6 50.6 2,991,236
Haryana 21 32.4 19.8 52.3 1,141,734
Himachal Pradesh 12 25.2 18.4 30.3 203,373
Jammu & Kashmir 22 27.4 18.2 43.1 541,625
Jharkhand 24 45.0 38.5 59.4 2,434,078
Madhya Pradesh 50 42.0 32.1 52.1 4,549,506
Maharashtra 35 35.2 21.3 47.6 4,561,180
NCT of Delhi 9 31.6 22.5 38.6 656,792
Odisha 30 34.8 15.3 47.5 1,811,802
Punjab 20 25.3 17.6 34.8 786,316
Rajasthan 33 39.1 28.4 54.3 4,146,682
Uttar Pradesh 71 46.3 32.2 65.1 14,300,000
Uttarakhand 13 31.4 22.9 39.1 449,780
West Bengal 19 32.7 23.3 45.5 3,438,399
Southern states 105 26.9 8,128,073
Andhra Pradesh 13 31.2 22.1 44.1 1,624,603
Goa 2 19.9 18.3 21.4 28,873
Karnataka 30 35.3 18.6 55.8 2,596,295
Kerala 14 19.2 12.4 27.7 689,068
Puducherry 4 26.6 19.0 32.0 31,701
Tamil Nadu 32 27.0 17.2 37.0 2,022,964
Telangana 10 29.4 15.7 38.3 1,134,569
North‐east and islands 93 31.0 2,404,214
Andaman & Nicobar 3 24.3 20.1 32.5 9,692
Arunachal Pradesh 16 29.4 20.5 42.0 63,165
Assam 27 35.3 24.6 47.4 1,686,136
Dadra and Nagar 1 41.7 41.7 41.7 21,223
Daman and Diu 2 28.1 18.9 37.3 6,282
Lakshadweep 1 27.0 27.0 27.0 1,959
Manipur 9 31.0 21.0 37.1 111,542
Meghalaya 7 40.1 16.8 51.6 242,762
Mizoram 8 29.6 23.7 36.9 47,720
Nagaland 11 28.4 18.7 41.8 81,906
Sikkim 4 30.8 24.0 42.3 19,651
Tripura 4 26.5 19.5 32.5 112,176
Total 640 36.0 63,155,946

Note. NCT = National Capital Territory.

The bold font means the overall number for the regions (eg. Northern States, Southern States, ect).

Across all 640 districts in India, 239 districts have stunting prevalence in excess of 40% (very high), and 441 districts have stunting prevalence between 30% and 40% (high; Table 2). Only 29 districts have stunting levels between 10% and 20%, and most of these are in South India. Although there is considerable clustering of stunting within states, intrastate variance in district stunting prevalence is still reasonably high. Specifically, inter‐state variation explains 56% of the variation in district stunting prevalence (see Table 4 below); hence, 44% of variation in interdistrict stunting prevalence is accounted for by intrastate variation.

Table 2.

Stunting prevalence and absolute numbers of stunted children, by stunting burden categories

No. districts Share of districts (%) Stunting rate (%) Stunted children Share of stunted children (%)
Stunting burden categories
Low prevalence (<20%) 29 4.5 16.9 723,651 1.1
Medium prevalence (20–29.9%) 170 25.6 25.9 8,872,991 14.1
High prevalence (30–39.9%) 202 31.6 35.2 16,363,830 25.9
Very high prevalence (≥ 40%) 239 37.3 46.9 37,179,537 58.9
Total 640 100.0 38.8 63,140,011 100.0

Table 4.

Multivariate linear regression models of stunting among children 0–5 years of age against its underlying determinants, with state‐fixed effects

Bivariate model Partial modela Full modelb

Coefficient

[95% CI]

Coefficient

[95% CI]

Coefficient

[95% CI]
Women with BMI <18.5 0.86**** [0.79, 0.94] 0.54**** [0.46, 0.62] 0.30**** [0.21, 0.40]
Initiated breastfeeding early −0.24**** [−0.29, −0.20] 0.05 [−0.00, 0.10] 0.02 [−0.03, 0.07]
Adequate diet −0.55**** [−0.64, −0.46] −0.21**** [−0.31, −0.11] −0.22**** [−0.32, −0.13]
4* ANC visits, log −1.30**** [−1.41, −1.20] −0.36**** [−0.53, −0.18] −0.17* [−0.36, 0.02]
IFA during pregnancy −0.35**** [−0.38, −0.32] −0.06** [−0.11, −0.00] 0.02 [−0.03, 0.08]
Full immunization −0.26**** [−0.30, −0.22] −0.05** [−0.09, −0.00] −0.00 [−0.04, 0.04]
Received vitamin A in last 6 months −0.24**** [−0.28, −0.19] −0.02 [−0.07, 0.02] −0.03 [−0.07, 0.01]
Women with ≥10 years school −0.44**** [−0.49, −0.40] −0.14**** [−0.22, −0.07]
Married after age of 18 −0.33**** [−0.38, −0.28] −0.09*** [−0.14, −0.04]
Water within premises −0.11**** [−0.14, −0.07] −0.02 [−0.05, 0.02]
Asset score, Quintile 1 0.00 [0.00, 0.00] 0.00 [0.00, 0.00]
Asset score, Quintile 2 −2.32** [−4.27, −0.37] −1.91** [−3.45, −0.37]
Asset score, Quintile 3 −5.17**** [−7.05, −3.29] −2.92*** [−4.84, −1.00]
Asset score, Quintile 4 −10.57**** [−12.56, −8.59] −2.99** [−5.44, −0.54]
Asset score, Quintile 5 −16.58**** [−18.54, −14.61] −3.43** [−6.47, −0.39]
Log open defecation density 0.52**** [0.45, 0.58] 0.11*** [0.03, 0.18]
Scheduled caste population 0.05 [−0.05, 0.15] −0.04 [−0.12, 0.03]
Household size 7.01**** [6.18, 7.84] 1.90**** [0.88, 2.92]
R 2, total .70 .74
R 2, between‐state .56 .56
R 2, within‐state .32 .41
N 635c 635

Note. All models included state‐fixed effects and are weighted by the number of children 0–5 years in each district. ANC = antenatal care; BMI = body mass index; IFA = iron and folic acid.

a

Partial model included immediate and nutrition‐specific interventions.

b

Full model included all factors such as immediate and underlying determinants as well as nutrition‐specific interventions.

c

Data for final model were available for 635 districts; 5 districts were excluded due to lack of data on full immunization.

*

p < .10.

**

p < .05.

***

p < .01.

****

p < .001.

National averages and district variability for various determinants across stunting burden categories of stunting are presented in Table 3. On average, nearly a quarter of women have low BMI. More than 40% of children were breastfed within an hour of birth, and only 55% were exclusively breastfed. Moreover, complementary feeding is of great concern with less than 10% of children receiving an adequately diverse diet. In case of underlying determinants, more than a third of women had at least 10 years of education, and two thirds of girls married after the age of 18. Open defecation is still prevalent in more than half of the population. Coverage is above 50% for several nutrition‐specific interventions. More than half of the women received ANC in the first trimester or had at least four ANC visits, but only 30% of the women consumed at least 100 IFA during pregnancy. Coverage of full immunization and vitamin A supplementation was nearly 60%. There was high interdistrict variability for most determinants across stunting burden category districts (Table 3). The most inequity among districts is observed for women's low BMI, women's education (≥10 years), asset score, ANC, and IFA consumption where the high‐burden stunting districts have levels that are 2–3 times lower than the low‐burden districts, and gaps range from 16% to 40%.

Table 3.

Differences in stunting prevalence and its determinants across stunting burden categories

Overall prevalence Low prevalence (<20%) Medium prevalence (20–<30%) High prevalence (30–<40%) Very high prevalence (≥40%)
Stunting 16.9 25.9 35.3 46.9
Immediate determinants
Women with BMI <18.5 22.9 12.5a 15.3a 21.9b 28.6c
Initiated breastfeeding early 41.6 52.5a 49.7a 47.1a 39.3b
Exclusive breastfeedinga 54.9 48.7a 59.0a 59.7a , b 53.3a , c
Timely introduction of foodsb 42.7 29.5a 63.2b 46.9c 34.2a
Adequate diet 9.6 17.3a 15.2a 9.8b 6.9c
Nutrition‐specific interventions
ANC first trimester 58.6 77.2a 67.9b 62.3c 50.7d
4+ ANC visits 51.2 74.4a 67.5a 54.5b 35.9c
Taken IFA during pregnancy 30.3 46.8a 42.4a 33.1b 20.2c
Full immunization 62.0 75.7a 67.7a 62.6b 56.7c
Received vitamin A in last 6 months 60.2 72.4a 66.0a 58.7b 55.5b
ORS during diarrhoeac 50.6 91.4a 65.7a 57.0b 48.5c
Underlying determinants
Women with ≥10 years school 35.7 56.1a 44.0b 33.9c 25.7d
Married after age of 18 73.2 90.3a 83.0b 76.5c 68.5d
Asset score (scale 0–100) 36.0 57.0a 55.4a 50.9b 46.9c
Water within premises 42.3 60.7a 50.4a 40.1a , b 36.3a , b
Open defecation density (km2) 252.8 130.4a 142.7a 187.7a 400.9b
Scheduled caste population 14.9 13.4 14.7 14.4 15.5
Household size 5.0 4.5a 4.6a 4.9a , b 5.4b

Note. Significant differences (p < .05) between groups are denoted by different subscript letters. ANC = antenatal care; BMI = body mass index; IFA = iron and folic acid; ORS = oral rehydration solution.

a

Data for exclusive breastfeeding are available for 425 districts only.

b

Data for timely introduction of foods are available for 186 districts only.

c

Data for ORS during diarrhoea are available for 328 districts only.

Bivariate analysis indicates that stunting is associated with a wide range of immediate and underlying determinants (Table 4). The strongest associations were observed for asset scores (β = −10.6 and −16.6 for Quintile 4 and 5, respectively) and low BMI in women (β = −0.73, 95% CI [0.66, 0.79]). The districts with higher coverage of nutrition specific‐interventions had lower prevalence of stunting (β ranged from −0.27 to −0.17).

In the partial multivariable regression analyses (Table 4), which only includes immediate determinants and nutrition‐specific interventions, we found significant relationships between women's BMI and adequate diet among children with stunting. For every 1‐percentage point increase in women with low BMI, there is an associated 0.54 percentage point increase in stunting. Districts with higher proportion of children with adequate diet had lower stunting prevalence (β = −0.21, 95% CI [−0.31, −0.11]). In terms of nutrition‐specific interventions, higher coverage of ANC (4 + ANC visits) had a large and statistically significant negative association with stunting (β = −0.36, 95% CI [−0.53, −0.18]), and IFA consumption had a much smaller association (β = −0.06, 95% CI [−0.11, −0.01]).

In the full model, where all the determinants were included together, all of the above associations (except for IFA consumption) remained significant; however, the magnitude of the coefficients decreased, suggesting that various underlying determinants explain variation in factors such as ANC and maternal BMI. For example, the coefficient on maternal BMI declines from 0.53 in the partial model to 0.30 in the full model, and the coefficient on ANC declines from −0.36 to −0.22. Interestingly, the coefficient on adequate diet is essentially unchanged. For both models, the total R 2 coefficients are high (0.70 and 0.74), although this is partly because state‐fixed effects explain 56% of the national variation in district stunting prevalence. In terms of the explanatory power of the various determinants, the more relevant statistic is the within‐state R 2 which shows that the explanatory variables in the partial and full models explain 31% and 42%, respectively, of the within‐state variation in district stunting prevalence.

The variables selected in the full regression model were used in the decomposition analysis to estimate the extent to which differences in these factors explained differences in stunting prevalence across very high‐ and low‐burden districts. Overall, the decomposition models performed well, explaining 71% of the observed differences in stunting prevalence between high‐ and low‐burden districts (Figure 2). This explained share is accounted for by the differences in women's low BMI (19%), women's education (12%), adequate diet among children (9%), asset scores (7%), open defecation (7%), age at marriage (7%), ANC (6%), and household size (5%). Decomposition analyses comparing low‐ and medium‐burden districts found similar results (results not shown).

Figure 2.

Figure 2

Factors contributing to the difference in stunting prevalence between very high‐burden (stunting > 40%) and low‐burden districts (stunting < 20%). ANC = antenatal care; BMI = body mass index; HH = household

4. DISCUSSION

In parallel with global attention and political commitment to reducing undernutrition, India has made considerable progress in reducing child malnutrition in the last decade. However, stunting prevalence remains high and extremely variable across districts and particularly high in populous northern states. High‐stunting districts are characterized by lower levels of immediate and underlying determinants and low levels of nutrition‐specific intervention coverage. The key factors associated with stunting were women's BMI, women's education, women's age at marriage, coverage of ANC, adequacy of child diets, household assets, and open defecation. These results suggest that if very high‐stunting districts could catalyse improvements in these social, economic, and dietary factors, they would eliminate 71% of the gap with low stunting districts.

Our analysis has several unique strengths. Previous studies have applied decomposition techniques to understand stunting differences between poor‐performing states and a single high‐performing state (Tamil Nadu) using child level data from NHFS‐III (Cavatorta et al., 2015) and to understand changes in India's national stunting prevalence between NHFS‐I (1992/1993) and NHFS‐III (2005–2006; Headey, Hoddinott, & Park, 2016). Our study uses the most recent data, is comprehensive in examining spatial variation across the entire country, and geographically granular in that it focuses on interdistrict variation in stunting in a country with tremendous spatial variation in nutrition and its proximate and underlying determinants. Geographical clustering of stunting in India is pronounced, as is the clustering of various immediate and underlying determinants and intervention coverage. These determinants account for around three quarters of the differences in stunting prevalence between the very high and low prevalence districts. A geographical lens, therefore, highlights spatial dimensions of undernutrition that might be overlooked in child‐level analyses. These findings also offer insights on the kinds of gaps that must be closed with equity‐enhancing, geographically targeted policy instruments and high‐quality implementation of these instruments. Our analysis, therefore, provides timely evidence for policymakers to tackle stunting in India, in a context of India's commitments to the global nutrition targets and the Sustainable Development Goals.

We acknowledge some of the limitations of this analysis. The cross‐sectional and geographically aggregated nature of our data means that our analysis is ecological in nature and could still be hampered by confounding factors. The richer unit level data from the NHFS‐4, which at the time of writing had still not been released, will permit a more extensive analysis. We were unable to examine changes in linear growth outcomes by different age categories, which can provide important clues about the aetiology of stunting. From a policy perspective, however, there is significant merit in understanding district‐level variation, because the district is an increasingly important unit in India's ongoing decentralization process and a district‐level focus is central to India's newly launched National Nutrition Strategy (NITI Aayog, 2017). Moreover, despite the more ecological nature of our analysis, our findings are well‐aligned with those from many other studies that have examined the determinants of stunting in India, using both unit‐level and district‐level data sets. For instance, almost all previous analyses of stunting determinants find strong associations with mother's education (Alderman & Headey, 2016). Several studies also link stunting in India to monotonous diets (Menon et al., 2015) and poor sanitation (Spears et al., 2013), even after controlling for wealth and parental education. Other studies have also found ANC visits in their last birth to be strongly associated with stunting in South Asia (Headey et al., 2016). A final limitation of note is that we were not able to examine relationships between all aspects of infant and young child feeding practices and child stunting because they are age‐specific indicators (exclusive breastfeeding (EBF) for children 0–5 months and timely introduction of foods for children 6–8 months), and data were only available for a subset districts.

A focus on addressing women's nutrition emerges as a key priority area in our analyses, similar to other studies of malnutrition in South Asia (Coffey, 2015). We find, for instance, that low women's BMI explained almost a fifth of the difference between high‐ and low‐burden stunting districts, corroborating results from previous studies that maternal undernutrition before and during pregnancy is a major determinant of poor fetal growth and child stunting (Black et al., 2013). Accounting for one fifth of the global population with 42% of low BMI prepregnant women (Coffey, 2015), India faces a critical challenge because preconception undernutrition among women can influence birth outcomes and child growth through influencing early placental and embryonic development, epigenetic effects, and competition for nutrients between mother and baby (King, 2016).

Including maternal BMI, variables reflecting women's well‐being—BMI, education, early marriage, and access to ANC—explain close to half the difference between high and low stunting districts. Discrimination against women is a widely suspected cause of India's unusually high rate of stunting, including small size at birth and low birth weight (Coffey, 2015). Although the variables in our analysis do not capture gender discrimination in terms of man–woman or boy–girl differences, the indicators used reflect several investments in girls and women—education levels, age at marriage, maternal nutrition, and use/access to ANC services. These indicators of investments in girls and women are likely to have both biological and social pathways to better nutrition for children. For example, early marriage, and consequently early child bearing, is more likely to lead to preterm births or small for gestational age births and perhaps also higher fertility prevalence over the life course (Branca, Piwoz, Schultink, & Sullivan, 2015; Temmerman, Khosla, Bhutta, & Bustreo, 2015).

Our study has significant policy implications. The high burden of stunting across most districts in India implies that strategies to address stunting must be rolled out across most of India, and a narrow spatial targeting is unlikely to deliver radical reductions in stunting. Moreover, the fact that 44% of interdistrict variation in stunting prevalence is explained by intrastate variation suggests that decentralization of the district level is critical. In addition to the intrastate variation, inter‐state differences were also prominent (56% of the variation in district stunting was explained by state‐fixed effects). This is likely due to vast differences across states in administrative and governance approaches, implementation capabilities, and economic and sociocultural differences.

The regression model used in this study has significant predictive power, suggesting that the variables used in this analysis could be used for monitoring multisectoral initiatives to reduce stunting. These initiatives should prioritize improving the socioeconomic, nutritional, and health status of girls and women—their nutrition, education, early marriage, and access to care during and after pregnancy—and improvements in sanitation and overall socioeconomic status of the household. We note, however, that many of these factors are rooted in social and cultural contexts that will require more holistic societal changes than policy instruments alone can deliver.

In conclusion, our findings reiterate the complex and multifaceted nature of the burden of stunting in India. The granular district‐focused analysis in this study, a first for India, highlights the concentration of this burden in the northern and eastern regions and the close associations between stunting and a wide range of nutrition‐specific and nutrition‐sensitive factors. The most important policy implications of our analysis are the need for a stunting prevention focus that is nationwide but focused on addressing critical determinants district‐by‐district to reduce inequalities and the prevalence of childhood stunting.

CONFLICTS OF INTEREST

The authors declare that they have no conflicts of interest.

CONTRIBUTIONS

PM conceived the manuscript, reviewed the analyses, and wrote significant sections of the manuscript. DH conducted the statistical analysis and wrote major sections of the manuscript. RA conducted the literature review, reviewed, and revised the manuscript. PHN conducted the statistical analysis and wrote significant sections of the manuscript. All authors read and approved the final submitted manuscript.

ACKNOWLEDGMENTS

We thank Lan Mai Tran for data preparation, analytic support, and preparation of figures and tables. We thank Sneha Mani for preparation of maps.

Menon P, Headey D, Avula R, Nguyen PH. Understanding the geographical burden of stunting in India: A regression‐decomposition analysis of district‐level data from 2015–16. Matern Child Nutr. 2018;14:e12620 10.1111/mcn.12620

Contributor Information

Purnima Menon, Email: p.menon@cgiar.org.

Phuong Hong Nguyen, Email: p.h.nguyen@cgiar.org.

REFERENCES

  1. Adekanmbi, V. T. , Uthman, O. A. , & Mudasiru, O. M. (2013). Exploring variations in childhood stunting in Nigeria using league table, control chart and spatial analysis. BMC Public Health, 13, 361. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Alderman, H. , & Headey, D. D. (2016). How important is parental education for child nutrition? World Development. Early online version [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Alemu, Z. A. , Ahmed, A. A. , Yalew, A. W. , & Birhanu, B. S. (2016). Non random distribution of child undernutrition in Ethiopia: spatial analysis from the 2011 Ethiopia demographic and health survey. International Journal for Equity in Health, 15, 198. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bhutta, Z. A. , Das, J. K. , Rizvi, A. , Gaffey, M. F. , Walker, N. , Horton, S. , … Maternal & Child Nutrition Study, G (2013). Evidence‐based interventions for improvement of maternal and child nutrition: What can be done and at what cost? Lancet, 382, 452–477. [DOI] [PubMed] [Google Scholar]
  5. Black, R. E. , Victora, C. G. , Walker, S. P. , Bhutta, Z. A. , Christian, P. , De Onis, M. , … Maternal & Child Nutrition Study, G (2013). Maternal and child undernutrition and overweight in low‐income and middle‐income countries. Lancet, 382, 427–451. [DOI] [PubMed] [Google Scholar]
  6. Branca, F. , Piwoz, E. , Schultink, W. , & Sullivan, L. M. (2015). Nutrition and health in women, children, and adolescent girls. BMJ, 351, h4173. [DOI] [PubMed] [Google Scholar]
  7. Cavatorta, E. , Shankar, B. , & Flores‐Martinez, A. (2015). Explaining cross‐state disparities in child nutrition in rural India. World Development, 76, 216–237. [Google Scholar]
  8. Coffey, D. (2015). Prepregnancy body mass and weight gain during pregnancy in India and sub‐Saharan Africa. Proceedings of the National Academy of Sciences of the United States of America, 112, 3302–3307. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. De Onis, M. , Blössner, M. , & Borghi, E. (2011). Prevalence and trends of stunting among pre‐school children, 1990–2020. Public Health Nutrition, 15, 142–148. [DOI] [PubMed] [Google Scholar]
  10. De Onis, M. , & Branca, F. (2016). Childhood stunting: A global perspective. Maternal & Child Nutrition, 12, 12–26. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Deaton, A. , & Dreze, J. (2008). Food and nutrition in India: Facts and interpretations. ( pp. 42–65). XLIV: Economic and Political Weekly. [PMC free article] [PubMed] [Google Scholar]
  12. Dewey, K. G. , & Begum, K. (2011). Long‐term consequences of stunting in early life. Maternal & Child Nutrition, 7(Suppl 3), 5–18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Di Cesare, M. , Bhatti, Z. , Soofi, S. B. , Fortunato, L. , Ezzati, M. , & Bhutta, Z. A. (2015). Geographical and socioeconomic inequalities in women and children's nutritional status in Pakistan in 2011: An analysis of data from a nationally representative survey. The Lancet Global Health, 3, e229–e239. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Fenn, B. , Morris, S. S. , & Frost, C. (2004). Do childhood growth indicators in developing countries cluster? Implications for intervention strategies. Public Health Nutrition, 7, 829–834. [DOI] [PubMed] [Google Scholar]
  15. Fenske, N. , Burns, J. , Hothorn, T. , & Rehfuess, E. A. (2013). Understanding child stunting in India: A comprehensive analysis of socio‐economic, nutritional and environmental determinants using additive quantile regression. PLoS One, 8, e78692. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Gebreyesus, S. H. , Mariam, D. H. , Woldehanna, T. , & Lindtjorn, B. (2016). Local spatial clustering of stunting and wasting among children under the age of 5 years: Implications for intervention strategies. Public Health Nutrition, 19, 1417–1427. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Grantham‐Mcgregor, S. , Cheung, Y. B. , Cueto, S. , Glewwe, P. , Richter, L. , Strupp, B. , & International Child Development Steering, G (2007). Developmental potential in the first 5 years for children in developing countries. Lancet, 369, 60–70. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Haile, D. , Azage, M. , Mola, T. , & Rainey, R. (2016). Exploring spatial variations and factors associated with childhood stunting in Ethiopia: Spatial and multilevel analysis. BMC Pediatrics, 16, 49. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Headey, D. , Chiu, A. , & Kadiyala, S. (2012). Agriculture's role in the Indian enigma: Help or hindrance to the malnutrition crisis? Food Security, 4, 87–102. [Google Scholar]
  20. Headey, D. , Hoddinott, J. , Ali, D. , Tesfaye, R. , & Dereje, M. (2015). The Other Asian Enigma: Explaining the Rapid Reduction of Undernutrition in Bangladesh. World Development, 66, 749–761. [Google Scholar]
  21. Headey, D. , Hoddinott, J. , & Park, S. (2016). Drivers of nutritional change in four South Asian countries: A dynamic observational analysis. Maternal & Child Nutrition, 12(Suppl 1), 210–218. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. International Institute for Population Sciences (2017). India Fact Sheet. NFHS‐4 (National Family Health Survey‐4), International Institute for Population Studies. Accessed April 2017. http://rchiips.org/NFHS/pdf/NFHS4/India.pdf.
  23. Jann, B. (2008). The Blinder–Oaxaca decomposition for linear regression models. The Stata Journal, 8, 453–479. [Google Scholar]
  24. Jayachandran, S. & Pande, R. (2015). Why are Indian children shorter than African children? In: Research NBoE, editor. NBER Working Paper 21036. Cambridge MA.
  25. King, J. C. (2016). A summary of pathways or mechanisms linking preconception maternal nutrition with birth outcomes. The Journal of Nutrition, 146, 1437S–1444S. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Mackinnon, D. P. , Krull, J. L. , & Lockwood, C. M. (2000). Equivalence of the mediation, confounding and suppression effect. Prevention science : the official journal of the Society for Prevention Research, 1, 173–181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Menon, P. , Bamezai, A. , Subandoro, A. , Ayoya, M. A. , & Aguayo, V. (2015). Age‐appropriate infant and young child feeding practices are associated with child nutrition in India: Insights from nationally representative data. Maternal & Child Nutrition, 11, 73–87. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Ministry of Home Affairs (2012). Census of India. New Delhi: Ministry of Home Affairs (MoHA), Government of India (GOI). [Google Scholar]
  29. National Institution for Transforming India Aayog 2017. NITI Aayog (National Institution for Transforming India), Government of India. Nourishing India‐National Nutrition Strategy.
  30. Ramalingaswami, V. , Jonson, U. , & Rohde, J. (1997). The Asian enigma In The progress of nations. New York: UNICEF. [Google Scholar]
  31. Sharaf, M. F. , & Rashad, A. S. (2016). Regional inequalities in child malnutrition in Egypt, Jordan, and Yemen: A Blinder‐Oaxaca decomposition analysis. Health Econ Rev, 6, 23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Spears, D. , Ghosh, A. , & Cumming, O. (2013). Open defecation and childhood stunting in India: an ecological analysis of new data from 112 districts. PLoS One, 8, e73784. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Srinivasan, C. S. , Zanello, G. , & Shankar, B. (2013). Rural‐urban disparities in child nutrition in Bangladesh and Nepal. BMC Public Health, 13, 581. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Subramanyam, M. A. , Kawachi, I. , Berkman, L. F. , & Subramanian, S. V. (2011). Is economic growth associated with reduction in child undernutrition in India? PLoS Medicine, 8, 424–437. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Temmerman, M. , Khosla, R. , Bhutta, Z. A. , & Bustreo, F. (2015). Towards a new global strategy for women's, children's and adolescents' health. BMJ, 351, h4414. [DOI] [PubMed] [Google Scholar]
  36. UNICEF (1990). Strategy for improved nutrition of children and women in developing countries. UNICEF Policy Review 1990‐1 (E/ICEF/1990/L.6). New York: UNICEF.
  37. World Health Organization (2006). WHO child growth standards based on length/height, weight and age. Acta Paediatrica Supplement, 450, 76–85. [DOI] [PubMed] [Google Scholar]
  38. World Health Organization (2010). Nutrition Landscape Information System (NLIS). COUNTRY PROFILE INDICATORS. Interpretation Guide. Geneva, Switzerland World Health Organization.

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