Risk Factors for Childhood Stunting in 137 Developing Countries: A Comparative Risk Assessment Analysis at Global, Regional, and Country Levels

Using risk factor and height data from population-based surveys, Goodarz Danaei estimate the greatest contributors to childhood stunting worldwide.

Published in the journal: . PLoS Med 13(11): e32767. doi:10.1371/journal.pmed.1002164
Category: Research Article
doi: 10.1371/journal.pmed.1002164


Using risk factor and height data from population-based surveys, Goodarz Danaei estimate the greatest contributors to childhood stunting worldwide.


Child survival has improved substantially over the past fifty years. The annual number of child deaths under age 5 y declined from 17.6 million in 1970 to 6.3 million in 2013, and under-five mortality declined from 143 per 1,000 live births to 44 during the same period [1]. Global progress in improving childhood growth has been less impressive [2]. While the prevalence of stunting (height-for-age z-score less than two standard deviations below the global median, as defined by the 2006 World Health Organization Child Growth Standards [3]) among children under 5 y declined from 47% in 1985 to 30% in 2011 globally, only minor improvements have been achieved in some of the poorest regions of the world, especially South Asia and sub-Saharan Africa [2]. In recognition of the large disparities across the globe in the areas of early life nutrition and development, the World Health Assembly set a target to reduce by 40% the number of stunted children worldwide by 2025 [4].

To reach this target, information on ways to alleviate stunting in each country is essential. Randomized trials and observational studies have identified a large number of risk factors for poor childhood growth [57]. However, the impact of these risk factors on stunting at the population level (globally, regionally, and at the country level) is not known.

To address this gap, we conducted a global comparative risk assessment analysis of stunting risk factors. We used country-level data on the prevalence of risk factors from global pooling projects of population health surveys, in combination with effect sizes for each risk factor on stunting from recent meta-analyses of epidemiological studies. This report focuses on 18 risk factors for stunting, while a forthcoming paper uses similar methodology to examine four psychosocial risk factors.


We estimated the burden of stunting among children 2 y (24–35 mo) of age (i.e., right at the end of the first 1,000 days of life) that is attributable to 18 risk factors in 137 developing countries. The selected countries included all countries designated as developing by the Global Burden of Disease Study [8], which closely correspond to the countries designated as developing by the United Nations for tracking progress towards the Millennium Development Goals [9]. These risk factors were selected from an extensive list of modifiable (i.e., behavioral or environmental; nongenetic) risk factors for stunting based on (i) the availability of high-quality exposure data (i.e., nationally representative data using standard measurements such as measured weight rather than self-report, and using appropriate statistical methods for pooling and imputing data [10]), (ii) strong evidence for an association with stunting, and (iii) the availability of evidence on the effect size on stunting from recent meta-analyses of epidemiological studies (criteria described in detail in S1 Text; see also [57] and S2 Table). Estimating the burden of stunting attributable to various risks does not in itself establish causality, but because we have included only risk factors for which there is convincing evidence of a causal relationship with stunting, the relationships examined here can be interpreted as our current best estimates of their causal effect. Stunting was defined as height-for-age z-score < −2 based on the World Health Organization Child Growth Standards [3]. We grouped risk factors into five clusters: maternal nutrition and infection, teenage motherhood and short birth intervals, fetal growth restriction (FGR) and preterm birth, child nutrition and infection, and environmental factors (i.e., unimproved water and sanitation and use of biomass fuels) (Table 1). These categories were based on the similarity of risk factors and of their corresponding interventions. We estimated the proportion of stunting that is attributable to each risk factor and cluster of risk factors in each country, as detailed below.

Tab. 1. Sources of data on the selected risk factors and their effect size for stunting.
Sources of data on the selected risk factors and their effect size for stunting.
aAll effect sizes are reported as ORs for stunting unless otherwise stated.

Data Sources

We derived the prevalence of exposure to each risk factor for the year 2010 (or as close to 2010 as possible) from published literature and from available surveys such as Demographic and Health Surveys (DHS) (Table 1). Estimates of stunting prevalence for children under 5 y for each country for the year 2011 were provided by the Nutrition Impact Model Study [2], which provides regional and global levels similar to those estimated by WHO [40]. We chose 2010 as the index year for risk factor exposure and 2011 as the index year for stunting exposure to allow a temporal sequence such that risk factors are measured or estimated before stunting. To estimate the prevalence of stunting and number of stunted children at age 2 y (i.e., 24 to 35 mo of age), we calculated the ratio of stunting prevalence among children age 2 y to that among children under 5 y in 104 surveys available from the WHO Global Database on Child Growth and Malnutrition (available from the Nutrition Landscape Information System) [38]. For 33 countries without surveys, we used population-weighted sub-regional averages to generate a correction factor (see S2 Text for more detail and S3 Table for the country-specific ratios). Data on cohort size (population of children at age 2 y) were provided by the United Nations Population Division World Population Prospects 2015 Revision [41]. Data on prevalence of teenage motherhood and short birth spacing were available for 64 countries with recent DHS surveys (73 countries did not have a recent DHS survey). For countries without DHS data, we used a sub-regional average if estimates from at least one country in the region were available (or a regional average when no data were available within the sub-region; see S3 Fig for sub-region and region classifications). The analysis of child HIV infection without highly active antiretroviral therapy (HAART) before 2 y of age (untreated HIV infection) was conducted only for 45 countries with available HIV prevalence data. To inform the effect size of each risk factor on stunting, we identified the most recent meta-analyses of epidemiological studies or conducted de novo systematic reviews (S1 Text; S2 Table).

Statistical Analyses

We calculated the population attributable fraction (PAF) of stunting for each risk factor using methods that have been described elsewhere [42]. The estimated PAF for each risk factor quantifies the independent effect of that specific risk factor on stunting (holding all other risk factors constant); the PAF is estimated using the following relationship:

where RRi is the relative risk of stunting comparing category i with the reference (or optimal) category and Pi is the prevalence of exposure to the risk factor of interest.

For most risk factors, epidemiological studies have reported effect sizes on stunting. For maternal malaria, underweight, and anemia, as well as biomass fuel use, meta-analyses of effect sizes were available only on low birth weight (LBW), which is itself associated with stunting [20]. For these risk factors, we calculated the PAF of stunting by multiplying the proportion of LBW attributable to the risk factor (i.e., the PAF) by the proportion of stunting attributable to LBW in each country. For example, if in a particular country 20% of LBW is attributable to maternal underweight and 30% of stunting is attributable to LBW, then it can be easily inferred that 6% of stunting is attributable to maternal underweight. Similarly, the effects of nonexclusive and discontinued breastfeeding were reported only on diarrhea, which itself is associated with stunting [24]. We used these reported effect sizes to estimate the effect on stunting through diarrhea by multiplying the PAF of diarrhea attributable to these risk factors by the PAF of stunting attributable to diarrhea.

We further estimated the combined effect of several risk factors within each of the five clusters. The number of stunting cases attributable to multiple risk factors in one cluster is less than the sum of the number of stunting cases attributable to each risk factor because one case of stunting can be due to multiple risk factors (i.e., multicausality) and because one risk factor may affect stunting partly through another risk factor in the same cluster (i.e., mediation). To prevent “double counting” due to multicausality, we used a relationship to estimate the combined effects of multiple risk factors based on their individual PAFs [42]. The relationship is captured by the following formula, which assumes that there is no correlation and no effect modification for relative risks:

where PAFi is an individual PAF for a risk factor in cluster j, and all individual risk factors (from 1 to R) in cluster j are combined using the formula above to estimate PAFj, which is the fraction of stunting attributable to all the risk factors in cluster j.

To use this relationship in the child nutrition and infection cluster of risk factors, discontinued and nonexclusive breastfeeding were excluded because their effects on stunting are mediated through diarrhea, and we did not include childhood untreated HIV infection because data on this risk factor were not available for all countries. For this risk factor cluster, we had to make an additional modification because part of the effect of zinc deficiency on stunting is mediated by diarrhea. Therefore, using the above formula for this cluster would lead to overestimation if the effect of diarrhea and zinc deficiency were both included in the combined PAF (PAFj). To correct this, we replaced the overall effect of zinc on stunting with the part of the effect of zinc on stunting that is not mediated through diarrhea. We conducted a literature review but did not find any studies that quantified this relationship and therefore assumed that 50% of the excess relative risk of stunting due to zinc deficiency is mediated by diarrhea. For example, in Nigeria, the overall relative risk of zinc deficiency for stunting was estimated to be 1.04 (based on a 0.06 lower mean height-for-age z-score in zinc-deficient children; see notes below Table 1, and S3 Text, for more details), which corresponds to an excess relative risk of 0.04. Using the 50% proportion mentioned above, we calculated that the excess relative risk of zinc deficiency not mediated through diarrhea was 0.02, and that calculation in turn yields a “direct” relative risk of 1.02. This relative risk does not include the effect of zinc deficiency on diarrhea and can be combined with the effect of diarrhea on stunting to estimate the combined effect of both risk factors on stunting without creating a bias due to overestimation. We conducted a sensitivity analysis using 0% and 100% as the mediated proportion (S4 Table).

We calculated the attributable prevalence of stunting by multiplying the PAF by the prevalence of stunting in each country. We also calculated the attributable number of stunting cases in children aged 2 y by multiplying the PAF by the number of stunted children at age 2 y. To quantify uncertainty, we used the mean and standard error for each exposure prevalence and effect size, separately, to generate 1,000 simulations for the prevalence of the risk factor and its odds ratio for stunting, then calculated the PAF and attributable prevalence of stunting at age 2 y 1,000 times (once per simulation). The 95% confidence intervals of PAFs and numbers of attributable stunting cases were calculated by using the 2.5th and the 97.5th percentiles of draws. All analyses were conducted using STATA SE version 13.1. This study was conducted solely using secondary and existing datasets and therefore did not require institutional review board review.


In 2011, we estimated that 44.1 million children aged 2 y in the selected 137 developing countries were stunted, corresponding to 36% of the 2-y-old population. The most important individual risk factor for stunting was being term, small for gestational age (TSGA), with 10.8 million (95% CI 9.1 million–12.6 million) stunting cases attributable at age 2 y in 2011. Unimproved sanitation, with 7.2 million (95% CI 6.3 million–8.2 million) attributable cases of stunting, and diarrhea, with 5.8 million (95% CI 2.4 million–9.2 million) attributable cases, were the second and third most important risk factors for stunting worldwide, respectively (Fig 1). When clusters of risk factors were considered, FGR and preterm birth (preterm, small for gestational age; TSGA; preterm, appropriate for gestational age [PAGA]) were the leading risk factors for stunting prevalence, with 32.5% of stunting prevalence being attributed to these factors (14.4 million cases, 95% CI 12.6 million–16.2 million). This cluster of risk factors was followed by environmental factors (unimproved water, unimproved sanitation, and biomass fuel use), with 21.7% (9.6 million cases, 95% CI 8.4 million–10.8 million), maternal nutrition and infection risk factors, with 14.4% (6.4 million cases, 95% CI 5.3 million–7.5 million), and child nutrition and infection risk factors, with 13.5% (6.0 million cases, 95% CI 2.6 million–9.4 million) of attributable stunting cases. Teenage motherhood and short birth intervals had the fewest attributable stunting cases, with 1.9% (0.86 million cases, 95% CI 0.77 million–0.95 million) (Table 2; Fig 2).

Risk factors ranked within each cluster by number of attributable stunting cases in children aged 2 y in 137 developing countries in 2011.
Fig. 1. Risk factors ranked within each cluster by number of attributable stunting cases in children aged 2 y in 137 developing countries in 2011.
Whiskers indicate 95% confidence intervals. Effects are not additive because each case of stunting can be attributed to more than one risk factor. Untreated HIV infection is not included because exposure data for all countries were not available. PAGA, preterm, appropriate for gestational age; PSGA, preterm, small for gestational age; TSGA, term, small for gestational age.

Tab. 2. Population attributable fraction and number of stunting cases in children aged 2 y in 2011 attributable to risk factor clusters by region.
Population attributable fraction and number of stunting cases in children aged 2 y in 2011 attributable to risk factor clusters by region.
95% confidence intervals presented in parentheses.

Number of stunting cases in children aged 2 y in 2011 attributable to risk factor clusters, stratified by region.
Fig. 2. Number of stunting cases in children aged 2 y in 2011 attributable to risk factor clusters, stratified by region.
Effects are not additive because each case of stunting can be attributed to more than one risk factor. Untreated HIV infection is not included because exposure data for all countries were not available.

The risk factor cluster FGR and preterm birth was associated with the largest attributable burden of stunting in all regions. The cluster of environmental factors, most importantly unimproved sanitation, was the second leading cluster of risk factors in South Asia, sub-Saharan Africa, and East Asia and Pacific, whereas in Central Asia, Latin America and Caribbean, and North Africa and Middle East, the second leading cluster was child nutrition and infection (mostly childhood diarrhea). Central Asia had the highest proportion of stunting attributable to child nutrition and infection risk factors across all regions, at 18.9%, and sub-Saharan Africa had the largest proportion of stunting attributable to environmental risk factors across all regions, at 27.0%. Of all stunting cases attributable to each risk factor cluster, South Asia and sub-Saharan Africa had the largest shares across all regions (ranging from 34% to 50%, and 29% to 43%, respectively, across risk factor clusters) due to having both high exposures to the selected risk factors and large numbers of stunted children.

Within these larger regions, there were important differences across sub-regions in the burden of stunting attributable to risk factors and risk factor clusters. Within the sub-Saharan Africa region, the attributable prevalence of stunting associated with unimproved sanitation in southern Africa was less than half that of central, east, and west Africa. Similarly, diarrhea was associated with almost three times the burden of stunting in Andean and central Latin America as in tropical and southern Latin America. The burden of diarrhea also differed substantially within Asia, with much smaller attributable prevalence of stunting in the East Asia sub-region (1.9 percentage points) than in the Central Asia, South Asia, and Southeast Asia sub-regions (all greater than 3.5 percentage points).

At the country level, nations with high stunting prevalence such as Niger, Burundi, Yemen, Eritrea, Ethiopia, Afghanistan, Timor-Leste, and Zambia (all with prevalence greater than 50%) had, as expected, a large burden of stunting attributable to all risk factor clusters (Fig 3; S4 Fig displays the PAFs). However, several countries with a relatively lower prevalence of stunting also had a relatively large attributable burden due to high exposure to specific risk factors. For example, Somalia had the largest prevalence of stunting attributable to discontinued breastfeeding and the second largest prevalence attributable to nonexclusive breastfeeding (0.9 and 1.4 percentage points, respectively). Malawi had the top rank for PAGA, at 4.9 percentage points, and Bangladesh had the top rank for teenage motherhood, at 0.9 percentage points (country-level PAFs and numbers of attributable stunting cases are available in S5 Text and on the study website: http://www.healthychilddev.sph.harvard.edu/).

Stunting prevalence attributable to the selected risk factor clusters by country.
Fig. 3. Stunting prevalence attributable to the selected risk factor clusters by country.
(A) Maternal nutrition and infection. (B) Teenage motherhood and short birth intervals. (C) Fetal growth restriction and preterm birth. (D) Child nutrition and infection. (E) Environmental factors.

The ranking of risk factors within each country was generally consistent with global and regional ranking of risk factors (S5 Table). Nevertheless, specific risk factors imposed a larger burden of stunting in particular countries irrespective of the burden of stunting in the country: unimproved sanitation surpassed TSGA as the leading risk factor in China and in many sub-Saharan African countries, and nonexclusive and discontinued breastfeeding had a substantially higher rank in middle-income countries (e.g., Mexico, South Africa, Iran, Turkey, and Argentina) than in low-income countries.


Our results suggest that a large proportion of childhood stunting in developing countries could be prevented if exposure to a few key risk factors could be eliminated. Globally, TSGA was associated with the largest stunting burden, followed by unimproved sanitation and childhood diarrhea. This pattern highlights the success of current clinical and public health interventions to prevent and manage childhood infections and improve childhood nutrition in many developing countries [43,44], but also calls for a new focus on interventions before and during pregnancy to address intergenerational effects of malnutrition among girls and women [45,46], as well as interventions to improve the environment in which mothers and families live, with specific attention to improving sanitation.

A previous analysis of FGR and preterm births in developing countries reported smaller fractions of stunting attributable to TSGA (e.g., a PAF of 16% for TSGA compared with 24% in our analysis) [20]. However, the value reported in this previous analysis may be an underestimation, as the regional and global effects were estimated using regional prevalence of stunting as opposed to estimating the attributable stunting in each country, as we did here.

The large burden of stunting attributable to FGR is perhaps unsurprising given that prenatal restricted growth is logically strongly related to postnatal restricted growth; nevertheless, our findings serve to further emphasize the importance of early intervention during pregnancy. Several recent reviews have identified maternal iron, balanced protein-energy, and multiple micronutrient supplementation as the most effective interventions to alleviate FGR [17,47]. However, providing these interventions before pregnancy or in its early months is logistically difficult because in many developing countries, the majority of pregnant women start attending antenatal clinics in their second or third trimester.

Environmental factors (i.e., unimproved water, unimproved sanitation, and biomass fuel use) had the second largest global attributable burden. Particularly, 7.2 million cases of stunting worldwide were attributable to unimproved sanitation. The attributable burden of unimproved sanitation for stunting was larger (though not significantly) than that of childhood diarrhea, as some of the effects of improved sanitation may be through prevention of other childhood infections and improvement of maternal health and nutrition in pregnancy [48,49]. This further underscores the importance of ongoing water, sanitation, and hygiene (WASH) programs [50] to increase access to, and use of, safe water and sanitation for children and families worldwide.

We found that one in seven cases of stunting was attributable to child nutrition and infection risk factors. Programs to promote adequate complementary feeding [51] and rotavirus and cholera vaccines [52] may reduce the attributable burden of this group of risks. Childhood HIV infection remains a significant contributor to child mortality [53] but was not a major risk for stunting at the population level. In Swaziland and Lesotho, the countries with the highest prevalence of this risk factor, the prevalence of stunting attributable to untreated HIV infection was estimated to be 0.7 and 0.8 percentage points, respectively. We may have slightly underestimated the fraction of stunting attributable to HIV as we were only able to estimate the effect of untreated child HIV infection, due to lack of data on the growth of HIV-infected children who receive HAART before 2 y of age compared with HIV-uninfected peers in developing countries (S2 Fig). Nevertheless, the contribution of HIV-infected children who receive HAART before 2 y to population-level stunting is likely small, given that young children initiating HAART exhibit rapid linear growth catch-up [54]. Teenage motherhood and short birth intervals had a fairly small effect on stunting at the population level due to both lower prevalence of exposure in many developing countries and smaller effect sizes for stunting compared with other risk factors.

The global scope of this analysis and the large number of risk factors included result in several limitations. Although we included only risk factors with strong evidence of an association with stunting, causality can never be guaranteed by observational studies (which were the sources of nearly all effect sizes available for the risk factors analyzed here). Although the list of risk factors is extensive, we had to exclude several risk factors because country-level data on exposure or effect size on stunting were not available. Examples are maternal smoking, prenatal alcohol use, and illicit drug use. Similarly, global data on environmental pollutant exposures in childhood, such as lead and arsenic exposure, were not available. In addition, we had to use approximate estimates for prevalence of use of biomass fuels, maternal malaria, maternal short stature, and maternal underweight. We used the prevalence of relying mainly on biomass fuels for cooking as a proxy for all exposure to biomass fuels, underweight among women of reproductive age as a proxy for maternal underweight, height among women aged 18 to 49 y as a proxy for maternal height, and prevalence of P. falciparum infection among children aged 2 to 10 y as a proxy for maternal malaria prevalence. Estimates of uncertainty in the exposures to maternal malaria, maternal short stature, childhood zinc deficiency, untreated HIV infection, LBW, and PAGA were unavailable, so uncertainty in the estimates of the effect of these risk factors is underestimated. Relatedly, we did not incorporate the uncertainty from converting the prevalence of stunting among children under 5 y to the prevalence of stunting among children age 2 y. Another limitation is that we estimated the effect of six risk factors through either LBW (maternal anemia, malaria, and underweight and biomass fuel use) or diarrhea (nonexclusive and discontinued breastfeeding), which may have led to underestimation of the effect of the maternal and childhood nutrition and infection risk factor clusters. As is standard in global risk factor analyses [42], we assumed that proportional effects are fairly similar across countries. Evidence from analyses of FGR and preterm birth supports this assumption as the odds ratios for stunting across different regions were fairly similar [20]. Multi-country studies are required to evaluate variation of effect sizes for other risk factors, but such studies are currently not available. Finally, the effect sizes for most risk factors were reported as odds ratios, which overestimate the relative risk when exposure is not rare and could lead to overestimating the effect of these risk factors on stunting. Correcting this bias requires information on the incidence of stunting among unexposed children for each risk factor and in each country [55], and these data are currently not available.

Our analysis also had several major strengths. We included all major risk factors for stunting after considering an extensive set and limiting our analysis to those with convincing evidence on their effect on stunting and high-quality data on country-level exposure. We reviewed and did not include risk factors with insufficient evidence on their effect on stunting, including child HIV infection with HAART [56], maternal and childhood iodine deficiency [57], child hookworm infection [58], acute lower respiratory infection [59], and childhood malaria [60]. We also excluded risk factors for which meta-analyses of observational studies and/or randomized trials identified no significant effect on childhood stunting. These were childhood anemia [61], maternal hookworm infection [62], and vitamin A deficiency [63]. For the included risk factors, we used the most recent and reliable meta-analyses of effect sizes on stunting. We quantified uncertainty at each step of estimation and reported overall uncertainty in the final results.

Our results represent a consistent and comparable set of global estimates of the impact of 18 risk factors on stunting. FGR, unimproved sanitation, and diarrhea are the leading risk factors for stunting globally, with larger estimated impacts on stunting in sub-Saharan Africa and South Asia compared with other regions. According to our findings, reducing the burden of stunting requires continuing the current efforts to diagnose and treat maternal and child infections, especially diarrhea, along with a new focus on clinical and public health interventions that focus on improving nutrition and sanitation among mothers and families.

Supporting Information

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1. Wang H, Liddell CA, Coates MM, Mooney MD, Levitz CE, Schumacher AE, et al. Global, regional, and national levels of neonatal, infant, and under-5 mortality during 1990–2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet. 2014;384:957–79. doi: 10.1016/S0140-6736(14)60497-9 24797572

2. Stevens GA, Finucane MM, Paciorek CJ, Flaxman SR, White RA, Donner AJ, et al. Trends in mild, moderate, and severe stunting and underweight, and progress towards MDG 1 in 141 developing countries: a systematic analysis of population representative data. Lancet. 2012;380:824–34. doi: 10.1016/S0140-6736(12)60647-3 22770478

3. World Health Organization. Child growth standards: length/height-for-age. Geneva: World Health Organization; 2015 [cited 2015 Apr 8]. Available from: http://www.who.int/childgrowth/standards/height_for_age/en/.

4. World Health Organization. WHA global nutrition targets 2025: stunting policy brief. Geneva: World Health Organization; 2014 [cited 2015 Jul 31]. Available from: http://www.who.int/nutrition/topics/globaltargets_stunting_policybrief.pdf.

5. Black RE, Allen LH, Bhutta ZA, Caulfield LE, de Onis M, Ezzati M, et al. Maternal and child undernutrition: global and regional exposures and health consequences. Lancet. 2008;371:243–60. doi: 10.1016/S0140-6736(07)61690-0 18207566

6. Black RE, Victora CG, Walker SP, Bhutta ZA, Christian P, de Onis M, et al. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet. 2013;382:427–51. doi: 10.1016/S0140-6736(13)60937-X 23746772

7. Bhutta ZA, Das JK, Rizvi A, Gaffey MF, Walker N, Horton S, et al. Evidence-based interventions for improvement of maternal and child nutrition: what can be done and at what cost? Lancet. 2013;382:452–77. doi: 10.1016/S0140-6736(13)60996-4 23746776

8. Global Burden of Disease Cancer Collaboration, Fitzmaurice C, Dicker D, Pain A, Hamavid H, Moradi-Lakeh M, et al. The global burden of cancer 2013. JAMA Oncol. 2015;1:505–27. doi: 10.1001/jamaoncol.2015.0735 26181261

9. United Nations. Millennium Development indicators: world and regional groupings. 2014 [cited 2016 Apr 24]. Available from: http://mdgs.un.org/unsd/mdg/Host.aspx?Content=Data/RegionalGroupings.

10. Finucane MM, Paciorek CJ, Danaei G, Ezzati M. Bayesian estimation of population-level trends in measures of health status. Stat Sci. 2014;29:18–25.

11. Özaltin E, Hill K, Subramanian SV. Association of maternal stature with offspring mortality, underweight, and stunting in low- to middle-income countries. JAMA. 2010;303:1507–16. doi: 10.1001/jama.2010.450 20407060

12. NCD Risk Factor Collaboration. A century of trends in adult human height. Elife. 2016;5:e13410. doi: 10.7554/eLife.13410 27458798

13. Han Z, Mulla S, Beyene J, Liao G, McDonald SD, Knowledge Synthesis Group. Maternal underweight and the risk of preterm birth and low birth weight: a systematic review and meta-analyses. Int J Epidemiol. 2011;40:65–101. doi: 10.1093/ije/dyq195 21097954

14. NCD Risk Factor Collaboration. Trends in adult body-mass index in 200 countries from 1975 to 2014: a pooled analysis of 1698 population-based measurement studies with 19·2 million participants. Lancet. 2016;387:1377–96. doi: 10.1016/S0140-6736(16)30054-X 27115820

15. Radeva-Petrova D, Kayentao K, ter Kuile FO, Sinclair D, Garner P. Drugs for preventing malaria in pregnant women in endemic areas: any drug regimen versus placebo or no treatment. Cochrane Database Syst Rev. 2014;(10):CD000169. doi: 10.1002/14651858.CD000169.pub3 25300703

16. Gething PW, Patil AP, Smith DL, Guerra CA, Elyazar IR, Johnston GL, et al. A new world malaria map: Plasmodium falciparum endemicity in 2010. Malar J. 2011;10:378. doi: 10.1186/1475-2875-10-378 22185615

17. Haider BA, Olofin I, Wang M, Spiegelman D, Ezzati M, Fawzi WW. Anaemia, prenatal iron use, and risk of adverse pregnancy outcomes: systematic review and meta-analysis. BMJ. 2013;346:f3443. doi: 10.1136/bmj.f3443 23794316

18. Stevens GA, Finucane MM, De-Regil LM, Paciorek CJ, Flaxman SR, Branca F, et al. 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:e16–25. doi: 10.1016/S2214-109X(13)70001-9 25103581

19. Fink G, Sudfeld CR, Danaei G, Ezzati M, Fawzi WW. Scaling-up access to family planning may improve linear growth and child development in low and middle income countries. PLoS ONE. 2014;9:e102391. doi: 10.1371/journal.pone.0102391 25020132

20. Christian P, Lee SE, Donahue Angel M, Adair LS, Arifeen SE, Ashorn P, et al. Risk of childhood undernutrition related to small-for-gestational age and preterm birth in low- and middle-income countries. Int J Epidemiol. 2013;42:1340–55. doi: 10.1093/ije/dyt109 23920141

21. Lee AC, Katz J, Blencowe H, Cousens S, Kozuki N, Vogel JP, et al. National and regional estimates of term and preterm babies born small for gestational age in 138 low-income and middle-income countries in 2010. Lancet Glob Health. 2013;1:e26–36. doi: 10.1016/S2214-109X(13)70006-8 25103583

22. Imdad A, Bhutta ZA. Effect of preventive zinc supplementation on linear growth in children under 5 years of age in developing countries: a meta-analysis of studies for input to the lives saved tool. BMC Public Health. 2011;11:S22. doi: 10.1186/1471-2458-11-S3-S22 21501440

23. Wessells KR, Brown KH. Estimating the global prevalence of zinc deficiency: results based on zinc availability in national food supplies and the prevalence of stunting. PLoS ONE. 2012;7:e50568. doi: 10.1371/journal.pone.0050568 23209782

24. Checkley W, Buckley G, Gilman RH, Assis AM, Guerrant RL, Morris SS, et al. Multi-country analysis of the effects of diarrhoea on childhood stunting. Int J Epidemiol. 2008;37:816–30. doi: 10.1093/ije/dyn099 18567626

25. Walker CLF, Rudan I, Liu L, Nair H, Theodoratou E, Bhutta ZA, et al. Global burden of childhood pneumonia and diarrhoea. Lancet. 2013;381:1405–16. doi: 10.1016/S0140-6736(13)60222-6 23582727

26. Lamberti LM, Walker CLF, Noiman A, Victora C, Black RE. Breastfeeding and the risk for diarrhea morbidity and mortality. BMC Public Health. 2011;11:S15.

27. Roberts TJ, Carnahan E, Gakidou E. Can breastfeeding promote child health equity? A comprehensive analysis of breastfeeding patterns across the developing world and what we can learn from them. BMC Med. 2013;11:254. doi: 10.1186/1741-7015-11-254 24305597

28. Bailey RC, Kamenga MC, Nsuami MJ, Nieburg P, St Louis ME. Growth of children according to maternal and child HIV, immunological and disease characteristics: a prospective cohort study in Kinshasa, Democratic Republic of Congo. Int J Epidemiol. 1999;28:532–40. 10405861

29. McDonald CM, Manji KP, Kupka R, Bellinger DC, Spiegelman D, Kisenge R, et al. Stunting and wasting are associated with poorer psychomotor and mental development in HIV-exposed Tanzanian infants. J Nutr. 2013;143:204–14. doi: 10.3945/jn.112.168682 23256148

30. Taha T, Nour S, Li Q, Kumwenda N, Kafulafula G, Nkhoma C, et al. The effect of human immunodeficiency virus and breastfeeding on the nutritional status of African children. Pediatr Infect Dis J. 2010;29:514–8. doi: 10.1097/INF.0b013e3181cda531 20054287

31. Webb AL, Manji K, Fawzi WW, Villamor E. Time-independent maternal and infant factors and time-dependent infant morbidities including HIV infection, contribute to infant growth faltering during the first 2 years of life. J Trop Pediatr. 2009;55:83–90. doi: 10.1093/tropej/fmn068 18723575

32. Joint United Nations Programme on HIV/AIDS. Global report: UNAIDS report on the global AIDS epidemic 2013. 2013 Nov [cited 2016 Sep 29]. Available from: http://www.unaids.org/sites/default/files/media_asset/UNAIDS_Global_Report_2013_en_1.pdf.

33. Fink G, Günther I, Hill K. The effect of water and sanitation on child health: evidence from the demographic and health surveys 1986–2007. Int J Epidemiol. 2011;40:1196–204. doi: 10.1093/ije/dyr102 21724576

34. Wolf J, Bonjour S, Prüss-Ustün A. An exploration of multilevel modeling for estimating access to drinking-water and sanitation. J Water Health. 2013;11:64–77. doi: 10.2166/wh.2012.107 23428550

35. Bruce NG, Dherani MK, Das JK, Balakrishnan K, Adair-Rohani H, Bhutta ZA, et al. Control of household air pollution for child survival: estimates for intervention impacts. BMC Public Health. 2013;13:S8.

36. Bonjour S, Adair-Rohani H, Wolf J, Bruce NG, Mehta S, Prüss-Ustün A, et al. Solid fuel use for household cooking: country and regional estimates for 1980–2010. Environ. Health Perspect. 2013;121:784–90. doi: 10.1289/ehp.1205987 23674502

37. NCD Risk Factor Collaboration. Height: evolution of adult height over time. 2016 [cited 2016 Jul 29]. Available from: http://www.ncdrisc.org/d-height.html.

38. World Health Organization. Nutrition Landscape Information System (NLiS). 2016 [cited 2016 Apr 17]. Available from: http://apps.who.int/nutrition/landscape/search.aspx.

39. WHO/UNICEF Joint Monitoring Programme (JMP) for Water Supply and Sanitation. Improved and unimproved water and sanitation facilities. 2014 [cited 2014 Dec 19]. Available from: http://www.wssinfo.org/definitions-methods/watsan-categories/.

40. de Onis M, Blössner M, Borghi E. Prevalence and trends of stunting among pre-school children, 1990–2020. Public Health Nutr. 2012;15:142–8. doi: 10.1017/S1368980011001315 21752311

41. United Nations Population Division. World population prospects: 2015 revision. 2015 [cited 2016 Apr 17]. Available from: http://www.un.org/en/development/desa/population/events/other/10/index.shtml.

42. Ezzati M, Lopez AD, Rodgers A, Vander Hoorn S, Murray CJL, Comparative Risk Assessment Collaborating Group. Selected major risk factors and global and regional burden of disease. Lancet. 2002;360:1347–60.

43. Gordon JE, Béhar M, Scrimshaw NS. Acute diarrhoeal disease in less developed countries. Bull World Health Organ. 1964;31:1–7. 14230890

44. Arifeen SE, Hoque DME, Akter T, Rahman M, Hoque ME, Begum K, et al. Effect of the Integrated Management of Childhood Illness strategy on childhood mortality and nutrition in a rural area in Bangladesh: a cluster randomised trial. Lancet. 2009;374:393–403. doi: 10.1016/S0140-6736(09)60828-X 19647607

45. Stein AD, Barnhart HX, Wang M, Hoshen MB, Ologoudou K, Ramakrishnan U, et al. Comparison of linear growth patterns in the first three years of life across two generations in Guatemala. Pediatrics. 2004;113:e270–5. 14993588

46. Prentice AM, Ward KA, Goldberg GR, Jarjou LM, Moore SE, Fulford AJ, et al. Critical windows for nutritional interventions against stunting. Am J Clin Nutr. 2013;97:911–8. doi: 10.3945/ajcn.112.052332 23553163

47. Morris RK, Oliver EA, Malin G, Khan KS, Meads C. Effectiveness of interventions for the prevention of small-for-gestational age fetuses and perinatal mortality: a review of systematic reviews. Acta Obstet Gynecol Scand. 2013;92:143–51. doi: 10.1111/aogs.12029 23066728

48. Strunz EC, Addiss DG, Stocks ME, Ogden S, Utzinger J, Freeman MC. Water, sanitation, hygiene, and soil-transmitted helminth infection: a systematic review and meta-analysis. PLoS Med. 2014;11:e1001620. doi: 10.1371/journal.pmed.1001620 24667810

49. Dangour AD, Watson L, Cumming O, Boisson S, Che Y, Velleman Y, et al. Interventions to improve water quality and supply, sanitation and hygiene practices, and their effects on the nutritional status of children. Cochrane Database Syst Rev. 2013;(8):CD009382. doi: 10.1002/14651858.CD009382.pub2 23904195

50. UNICEF. Water, sanitation and hygiene: UNICEF in action. New York: UNICEF; 2014 Jan 10 [cited 2016 Mar 25]. Available from: http://www.unicef.org/wash/index_action.html.

51. Lassi ZS, Das JK, Zahid G, Imdad A, Bhutta ZA. Impact of education and provision of complementary feeding on growth and morbidity in children less than 2 y of age in developing countries: a systematic review. BMC Public Health. 2013;13:S13. doi: 10.1186/1471-2458-13-S3-S13 24564534

52. Das JK, Tripathi A, Ali A, Hassan A, Dojosoeandy C, Bhutta ZA. Vaccines for the prevention of diarrhea due to cholera, shigella, ETEC and rotavirus. BMC Public Health. 2013;13(Suppl 3):S11.

53. Liu L, Oza S, Hogan D, Perin J, Rudan I, Lawn JE, et al. Global, regional, and national causes of child mortality in 2000–13, with projections to inform post-2015 priorities: an updated systematic analysis. Lancet. 2015;385:430–40. doi: 10.1016/S0140-6736(14)61698-6 25280870

54. Shiau S, Arpadi S, Strehlau R, Martens L, Patel F, Coovadia A, et al. Initiation of antiretroviral therapy before 6 months of age is associated with faster growth recovery in South African children perinatally infected with human immunodeficiency virus. J Pediatr. 2013;162:1138–45. doi: 10.1016/j.jpeds.2012.11.025 23312691

55. Zhang J, Yu KF. What’s the relative risk?: a method of correcting the odds ratio in cohort studies of common outcomes. JAMA. 1998;280:1690–1. 9832001

56. Isanaka S, Duggan C, Fawzi WW. Patterns of postnatal growth in HIV-infected and HIV-exposed children. Nutr Rev. 2009;67:343–59. doi: 10.1111/j.1753-4887.2009.00207.x 19519675

57. Zimmermann MB. The role of iodine in human growth and development. Semin Cell Dev Biol. 2011;22:645–52. doi: 10.1016/j.semcdb.2011.07.009 21802524

58. Taylor-Robinson DC, Maayan N, Soares-Weiser K, Donegan S, Garner P. Deworming drugs for soil-transmitted intestinal worms in children: effects on nutritional indicators, haemoglobin and school performance. Cochrane Database Syst Rev. 2012;(7):CD000371. doi: 10.1002/14651858.CD000371.pub4 22786473

59. Victora CG, Barros FC, Kirkwood BR, Vaughan JP. Pneumonia, diarrhea, and growth in the first 4 y of life: a longitudinal study of 5914 urban Brazilian children. Am J Clin Nutr. 1990;52:391–6. 2375306

60. Dicko A, Barry A, Dicko M, Diallo AI, Tembine I, Dicko Y, et al. Malaria morbidity in children in the year after they had received intermittent preventive treatment of malaria in Mali: a randomized control trial. PLoS ONE. 2011;6:e23390. doi: 10.1371/journal.pone.0023390 21858096

61. Pasricha S-R, Hayes E, Kalumba K, Biggs B-A. Effect of daily iron supplementation on health in children aged 4–23 months: a systematic review and meta-analysis of randomised controlled trials. Lancet Glob Health. 2013;1:e77–86. doi: 10.1016/S2214-109X(13)70046-9 25104162

62. Imhoff-Kunsch B, Briggs V. Antihelminthics in pregnancy and maternal, newborn and child health. Paediatr Perinat Epidemiol. 2012;26(Suppl 1):223–38. doi: 10.1111/j.1365-3016.2012.01280.x 22742613

63. Ramakrishnan U, Aburto N, McCabe G, Martorell R. Multimicronutrient interventions but not vitamin A or iron interventions alone improve child growth: results of 3 meta-analyses. J Nutr. 2004;134:2592–602. 15465753

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