1 Introduction

In 2021, the share of the global population who could not afford a healthy diet—that is energy sufficient, nutritionally adequate and sourced from diverse foods – was estimated at 42.2% (FAO et al., 2023). The corresponding share in low-income and lower-middle-income countries was estimated at 86.1% and 70.2%, respectively. In Ethiopia, the corresponding share was 83.8% (FAO et al., 2023). This has huge implications on undernutrition in the population in general and young children in particular. This is because undernutrition in early years is associated with shorter adult height, lower attained schooling, reduced economic productivity (Victoria et al., 2008), and can result in intergenerational transfer of poor birth outcomes in the next generation (Addo et al., 2015; Victoria et al., 2008). Child stunting (being short for their age) together with deficiencies of iodine and iron can contribute to children not reaching their developmental potential; and deficiencies of vitamin A and zinc can result in deaths (Black et al., 2013).

In Ethiopia, despite a reduction of stunting prevalence by about 14 percentage points between 2005 and 2019 among children under 5 years of age, child undernutrition remains high (EPHI & ICF, 2021). The same report indicates that, in 2019, the prevalence of stunting among children under two years of age ranged between 17 and 36%. Unless the current trend in the reduction of stunting in Ethiopia will be accelerated, the country will be offtrack to meeting one of the SDG targets and its ambitious plan to end stunting in children under two years of age by 2030, also called the Seqota Declaration (FDRE, 2016).

There is a vast literature on the determinants of child linear growth outcomes or stunting in Ethiopia. Based on a systematic literature review, Tasic et al. (2020) found that child characteristics such as age, sex, and the incidence of diarrhea; parental characteristics including maternal education and height; and household characteristics including wealth status, food security, access to improved water sources and sanitation facilities, are among major determinants of child stunting in Ethiopia. The aforementioned study further grouped stunting determinants in Ethiopia into immediate, underlying, and the enabling determinants, according to the conceptual framework on maternal and child nutrition (UNICEF, 2021) which also guides this study.

Chief among immediate causes of child stunting in Ethiopia includes inadequate dietary intakes of energy and different nutrients needed for child growth (e.g. Haile et al., 2016; Wirth et al., 2017). Various studies show that energy and nutrient intakes among young children in Ethiopia are far below the WHO recommendations (e.g. Haileselassie et al., 2022; Feyisa et al., 2020; Mengistu et al., 2017; EPHI, 2016, 2013; Baye et al., 2012). Yet, much of existing studies on the determinants of child stunting in Ethiopia examined the importance of diet quality and adequacy using proxy indicators such as dietary diversity score (e.g. Gebreayohanes & Dessie, 2022; Mohammed et al., 2019; Motbainor et al., 2015), notwithstanding the strong associations between dietary diversity and nutrient adequacy (e.g. Mekonnen et al., 2020; Arimond et al., 2010; Arimond & Ruel, 2004; Ruel, 2003). This study contributes to the literature by examining the quality of diets consumed in the household, taking into account the type of foods consumed and adequacy of nutrient intakes.

Studies elsewhere documented the importance of animal source foods (ASFs) for improving diet quality and children’s linear growth or stunting (e.g. Grillenberger et al., 2006; Headey et al., 2018; Iannotti et al., 2017, 2019; Murphy & Allen, 2003; Neumann et al., 2002; Parikh et al., 2021), and some studies also in Ethiopia (e.g. Hoddinott et al., 2015; Mekonnen et al., 2022; Omer et al., 2019, 2022). However, evidence on the longer-term effect of ASFs consumption on linear growth is inconclusive. For example, a randomized controlled trial involving egg intervention during early complementary feeding in Ecuador found improved linear growth and reduced stunting (Iannotti et al., 2017). A follow up study, however, did not find the effect of the intervention in linear growth after two years (Iannotti et al., 2019). Relatedly, using observational data from the Demographic and Health Surveys for several countries, a recent study identified the independent association of ASFs consumption and children’s linear growth or stunting (e.g. Headey et al., 2018). The aforementioned study, however, lacks information on whether sustained consumption of ASFs is associated with child linear growth. This study adds to the growing literature by considering sustained (past as well as current) consumption of ASFs.

This study is embedded in two related strands of literature on child linear growth determinants. The first is on nutrient intakes which has been found strongly linked with child linear growth outcomes (e.g. Gibson et al., 2009; Grillenberger et al., 2006; Puentes et al., 2016), even though the role of micro-nutrients is considered rather supportive for optimal functioning of immune system and optimal growth outcomes (Ramakrishnan et al., 2009; Sanin et al., 2018). The second is on the importance of ASFs as described above. This study contributes to both strands of the literature because many of previous studies drew from cross-sectional or pooled panel observations even though the effect of dietary consumption on child growth would only be observed with time lag. Studies with repeated observations over a child’s consumption and linear growth are either scarce (Puentes et al., 2016; Zaharia et al., 2021), or those available are mainly from nonrepresentative sample with limited geographic coverage (e.g. Belayneh et al., 2021; Puentes et al., 2016). Further, the aforementioned longitudinal studies, with the exception of Puentes et al. (2016), relied on proxy indicators such as dietary diversity score or indicators of consumed food groups without measuring the quantity and adequacy of nutrient intakes, even though dietary diversity is strongly associated with nutrient adequacy as described above.

In sum, the main objective of this study is to examine the associations between household’s food and nutrient acquisition capacity and linear growth in children in rural and small towns in Ethiopia. Specifically, we examine whether household’s sustained intake of multiple nutrients (measured by the mean nutrient adequacy (MPA)) is linked with child’s linear growth. In addition, we examine whether household’s sustained acquisition of animal sourced foods (ASFs) is strongly linked with child’s linear growth. This study differs from previous research in Ethiopia in at least two ways: (1) it evaluates the actual quantities consumed and their adequacy (the MPA) instead of using other proxy indicators for nutrient consumption; and (2) compares the association of past (lagged) consumption of food (including ASFs) and nutrients against current (contemporaneous) consumption on child linear growth outcomes using nationally representative longitudinal data.

2 Material and methods

2.1 Data

We used all the three waves of the Ethiopia Socioeconomic Panel Survey (ESS) collected by the Ethiopia Central Statistics Agency in collaboration with the World Bank as part of the Living Standards Measurement Study–Integrated Surveys on Agriculture (LSMS-ISA) project. The ESS was implemented every two years: the households in the survey were visited in 2011/2012, re-visited in 2013/2014, and then re-visited again in 2015/2016. The first wave was a nationally representative survey of 3,969 households living in rural and small town areas. The subsequent waves added samples from large town areas, increasing the total sample to over 5000 households in waves 2 and 3 (CSA and World Bank 2020). For the purpose of establishing associations between child linear growth and past consumption patterns, we limited our analysis to the same set of households that were interviewed at the baseline (wave 1) and subsequent waves.

This study considered 1708 households with children aged less than 59 months at the baseline (i.e. wave 1) and had complete information on other household level indicators. Some of the households had multiple children under five years of age. In total 2386 children were considered in the study, including those younger than 6 months at the baseline. The panel survey therefore interviewed each study panel household up to three times. For children 6—59 months of age we calculated two indicators of child growth status using the 2006 World Health Organization (WHO) growth standards: the height for age z scores (HAZ) and a binary indicator for stunting based on whether the HAZ score was below two standard deviations from the WHO growth standards (WHO, 2006).Footnote 1 Children aged 6—59 months with height measurement outside of the normal growth standards (i.e. less than or above five standard deviations) according to the WHO growth reference were excluded from the baseline analysis but were kept in the sample. That is, some of these children were included back in the analysis of the subsequent survey waves because their height measurement in those surveys was within the normal growth standards described above. Similarly, children younger than six months at the baseline were excluded from the baseline analysis but were included in the analysis of the last two survey waves, yielding unbalanced panel. Hence, the total number of children with HAZ scores within the WHO growth standards at the baseline, the second- and third- survey waves was 1605, 2297 and 2376, respectively. Only 1022 children were observed in all three survey waves whereas the remaining children were observed only twice (i.e. either in waves 1 and 2, waves 2 and 3, or waves 1 and 3). Finally, the overall attrition rate was quite small since it was only ten children and nine households that completely dropped out from the analysis.

Besides height measurements for children under five years of age,Footnote 2 the ESS contains information on a wide range of household socioeconomic and demographic characteristics in each round of the survey including age and education status of each household member, and household level information such as access to water and sanitation, nonfood spending, food consumption and spending, among others. We calculated the nutrient content of foods consumed in the household using the Ethiopian food composition table (Ågren & Gibson, 1968), and other sources including the USDA (2016), Langenhoven et al. (1991), West et al. (1989), where nutrient information was missing. Waste and retention factors were applied to raw foods to account for nutrient losses during preparation (USDA, 2016). As this study is concerned mainly with household nutrient and dietary consumption and child linear growth, we checked whether the daily total food consumption per adult equivalent was feasible based on criteria from a human nutrition perspective; excluding households whose estimated energy consumption per adult female equivalent (AFE) was below 500 kilocalories per day and those above 5,000 kilocalories per day (Voortman et al., 2017). More detailed procedures followed including the use of AFE are described elsewhere (Mekonnen et al., 2020).

Having calculated the nutrient contents from foods consumed at home, we estimated the mean probability of nutrient adequacy (MPA) per AFE based on 11 nutrients including protein, iron, zinc, thiamin, riboflavin, niacin, vitamin B6, folate, vitamin B12, vitamin C, and vitamin A. The probability approach to calculating nutrient adequacy is considered robust to misspecification of variance so long as the distribution of requirements is symmetric (Wiesmann et al., 2009). The probability approach makes use of the estimated average requirements (EAR), which is the daily nutrient intake value estimated to meet the requirements of half of the healthy individuals in a given population (IOM, 2006). Assuming normal distribution of nutrient requirements of non-pregnant, non-lactating adult women, we calculated the probability of adequacy for each of the above nutrients (excluding iron) by solving for the standardized score (z-score):

$${{\text{z}}-{\text{score}}}_{i}=\frac{{usual\,intake}_{i}-{EAR}_{i}}{{SD}_{i}},$$
$$SD=CV \times EAR$$
(1)

where \(SD\) and \(CV\) respectively represent the standard deviation and coefficient of variation for nutrient \(i\). We replaced usual intake by observed daily nutrient consumption per AFE. Note that even though we used per AFE values to proxy for intra-household distribution of food (Coates et al., 2017; Sununtnasuk & Fiedler, 2017), actual food distribution may differ from that implied by the AFE scale, which is one of the limitations of this study. We used the EAR and CV values from WHO/FAO (2004) for an adult female (19–65 years) (see Supplementary Table A1). Using the standardized z-scores and the property of standard normal distribution, we computed the probability of adequacy for each nutrient. As the requirements for iron are known to be skewed for non-pregnant, non-lactating women (see IOM, 2006, 43–44), the probability of adequacy for iron was calculated using the probability of adequacy table (see Wiesmann et al., 2009, p 206, adapted from IOM, 2006) assuming a bioavailability of 5%. Last, we calculated the MPA by averaging the probability of adequacy of 11 nutrients described above.

Further, we examined which food groups were consumed in the household over the previous 7 days, based on information whether anyone in the household consumed any food during the recall period. Specifically, we considered 7 food groups which are important for child growth according to WHO guidance, including (1) cereals, roots and tubers; (2) legumes and nuts; (3) milk and its derivatives; (4) meat products (meat, poultry, offal, and fish); (5) eggs; (6) vitamin A-rich fruits and vegetables (leafy green vegetables, yellow fruits and vegetables); and (7) other fruits and vegetables (WHO, 2010). Even though the standard recall period for this type of research is twenty-four hours, our data is available for seven days. However, considering household consumption data over seven days period is likely to be closer to the household’s normal consumption pattern. In addition, the seven days reference may take into account religious restrictions among orthodox Christians in Ethiopia on the consumption of animal sourced foods on specific days in a week which otherwise a twenty-four hours recall may not capture (Haileselassie et al., 2022; Desalegn et al., 2019; Melesse & van den Berg, 2020).

3 Empirical strategy

As noted above, the effect of dietary consumption on child’s linear growth would be observed with time lag. Hence, to examine the relationship between current child outcomes and household’s dietary consumption in the previous period, we run panel regressions of the following form, following Zaharia et al. (2021) and informed by the concept of nutrition production function described in Behrman and Deolalikar (1988):

$${Child\,outcome}_{it}=\alpha {MPA}_{i,t-1} +{{\varvec{X}}}_{{\varvec{i}},{\varvec{t}}}\mathbf{^{\prime}}{\varvec{\upbeta}}+{\lambda \delta }_{j,t}+{e}_{i,t}$$
(2)

where \({Child\,outcome}_{it}\) is either the HAZ score of child \(i\) in time \(t\), or a binary variable indicating whether or not the child is stunted at time\(t\). MPA is the key variable of interest and denotes the consumption of multiple nutrients (the mean probability of nutrient adequacy) by the \(i{\prime}th\) child in the household at time \(t-1\). \(X\) measured at time \(t\) denotes a vector of controls including the child’s age (including third-degree polynomial to capture the nonlinear relationship between child growth and dietary consumption (Alderman & Headey, 2018; Haile et al., 2016; Puentes et al., 2016), sex, and whether the child recently had diarrhea, maternal education, and whether the household had access to improved water sources and improved sanitation facilities. Controls were selected based on the concept of nutrition production function (Behrman & Deolalikar, 1988), the conceptual framework on maternal and child nutrition (UNICEF, 2021), and previous studies especially in Ethiopia (Tasic et al., 2020). Also in \(X\) is the number of days between height measurements for each child across successive survey waves. This is to account for linear growth differences among children due to differences in the dates of measurement since children experience high growth and growth spurts during the first two years (Puentes et al., 2016; Victoria et al., 2010). \({e}_{i,t}\) is a random error. Since there is potential for error \({e}_{i,t}\) variances to be correlated over time for a given child or over children within a given cluster, we cluster standard errors at enumeration area level (Abadie et al., 2017).

\({\delta }_{j,t}\) denotes location by survey wave fixed effects that control for unobserved temporal characteristics such as food prices, market availability, the health environment, etc. that affect children’s outcomes that are common to all children in a given location. In some specifications we use child fixed effects to control for unobserved child characteristics that do not change over time, such as maternal height, health and nutrition during pregnancy, birth outcome and exclusive breastfeeding before the age of 6 months, together with survey wave fixed effects to account for temporal shocks that affect all children in a survey.

Further, we examine the relationships between ASFs consumption and child growth outcomes by modifying Eq. 2, and replacing MPA by ASFs and other food groups measured at time t-1:

$${Child\,outcome}_{it}= {{\varvec{A}}{\varvec{S}}{\varvec{F}}}_{{\varvec{i}},{\varvec{t}}-1}\mathbf{^{\prime}}{\varvec{\upphi}}+{{\varvec{O}}}_{{\varvec{i}},{\varvec{t}}-1}\mathbf{^{\prime}}{\varvec{\uppsi}}+{{\varvec{X}}}_{{\varvec{i}},{\varvec{t}}}\mathbf{^{\prime}}{\varvec{\upbeta}}+{\lambda \delta }_{j,t}+{\mu }_{i,t}$$
(3)

where \({\varvec{O}}\) denotes a vector of food groups other than ASFs (including binary indicators for starchy staples, legumes, vegetables, and fruits), the controls \(X\) and \(\delta\) are the same as in Eq. 2 and \({\mu }_{i,t}\) is error terms of cluster and enumeration area fixed effects. Variants of this model consider two definitions of ASFs consumption: by type of individual ASF and the total number of ASFs consumed. The latter is considered because different ASFs contain different growth-stimulating nutrients and previous studies also found stronger associations between multiple ASFs consumption and child growth outcomes (Headey et al., 2018).

To check the robustness of results, we rerun the above models after including contemporaneous consumption in \(X\); based purely on contemporaneous consumption; by changing controls and fixed effects; and by running separate regressions for different age groups. The analysis of the longitudinal panel on contemporaneous consumption and child growth outcomes re-examines findings of previous cross-sectional and pooled panel studies that found strong links between child growth outcomes and contemporaneous consumption, since the effect of current consumption on child growth outcomes would be observed with time lag. We run regressions with user written Stata command, reghdfe, that efficiently absorbs multiple levels of fixed effects (Correia, 2014). The main advantage of this method is that it iteratively removes groups with only one observation which otherwise can overstate statistical significance and lead to incorrect inference (Correia, 2015).

Last, despite the use of lagged explanatory variables and fixed effects estimations, we interpret the results as associations rather than causal relations since lagging explanatory variables may not sufficiently address endogeneity concerns (Bellemare et al., 2017) i.e. factors that might determine the household’s food and nutrition acquisition capacity might still affect nutritional status through other channels.

4 Results

4.1 Descriptive statistics

Characteristics of the sample and variables used in this study are described in Table 1 and Figs. 1, 2 and 3. The average height-for-age z-score (HAZ) of children was -1.41, and the prevalence of stunting in children was 38%. The household’s mean nutrient adequacy (MPA) was 0.41. Figures 1 and 2 show the distribution of both the HAZ score and the MPA by survey wavesFootnote 3. The share of households who consumed only one type of animal sourced food (ASF), and two or more types of ASFs was 31% and 13%, respectively (Fig. 3). When individual food groups were evaluated, the share of households consuming starchy staples was above 60%, and those consuming legumes and vegetables was between 30%-36%. Whereas the share of households consuming eggs, dairy, and meat was between 13%—24% (Fig. 3). The average age of children was 33 months. Nearly half of the children were girls, and only about 8% of the children had experienced diarrhea in the one month preceding the survey. Only 4% of mother’s had above 8 years of education. The share of households who had access to improved water source and improved latrines were 60% and 19%, respectively. A little over 90% of households reported that all household members eat the same diet during the study period. Descriptive statistics of key variables for the sub-sample corresponding to children age 6–59 month are presented as Annex Table 9.

Table 1 Descriptive statistics of key variables
Fig. 1
figure 1

Distribution of the Height for age z score (HAZ) across survey waves

Fig. 2
figure 2

Distribution of the mean nutrient adequacy (MPA) across survey waves

Fig. 3
figure 3

The average share of households who consumed food group

4.2 Econometric results

4.2.1 The average nutrient adequacy (MPA) and child linear growth outcomes

Table 2 summarizes the results of fixed effects (FE) panel estimations of variants of Eq. 2.Footnote 4 The Column headers in Table 2 indicate the dependent variables including the HAZ score (Columns 1, 2, 5, & 6) and stunting (Columns 3, 4, 7 & 8). For the binary outcome stunting, fixed effects estimations imply linear probability models. Besides the list of controls reported in the result Tables, Columns 1—4 and Columns 5—8 control for the enumeration area by survey fixed effects and child and survey fixed effects, respectively. Additional control in all specifications include the number of days between successive height measurements for each child as described in Table 1.

Table 2 Links between child outcomes and lagged and contemporaneous consumption of the mean nutrient adequacy (MPA) for children 6–114 months

The results presented in columns 1–8 (with the exception of column 6) show that lagged MPA, but not contemporaneous MPA, was significantly associated with child linear growth outcomes, regardless of whether child linear growth was measured in terms of the HAZ score or stunting. The magnitude of the coefficient estimates to lagged MPA implies that, on average, a standard deviation increase in lagged consumption of an MPA was associated with a 0.14 unit increase in the HAZ score (Columns 1&2). This is roughly a 10 percent increase over the mean HAZ score. Correspondingly, results suggest that a 10% increase in lagged MPA was associated with a 1.4 percentage points reduction in the likelihood of being stunted (Columns 3&4). Since the overall stunting rate in the sample is 38 percent, these percentage points translate into a 3.7 percent reduction in stunting rate. The reduction in the stunting rate associated with a 10% increase in lagged MPA increased to 4.2–5.2 percent when child and survey fixed effects were used instead of enumeration area by survey fixed effects (Columns 7 and 8). These are all important findings as coefficient estimates remained statistically significant even after controlling for child specific unobserved heterogeneities beside other controls. Further, the null hypotheses for joint tests for equality of the estimated coefficients across specifications were rejected, suggesting that the results were not spurious significant correlations. Footnote 5 Among controls, the incidence of diarrhea and child’s age (including its polynomial roots capturing the non-linear relationships between child growth and age) were significantly associated with the HAZ score with the expected signs (see Columns 1–4). We re-run Columns 1- 8 after replacing the household’s access to improved water sources and improved sanitation facilities by the household’s socioeconomic status score. Corresponding results presented in the Annex Table 10 show that the results are robust to specification changes.

We further checked the robustness of the results by limiting our analysis to children only aged 6–59 months. Even though the number of observations reduced by over one-third, results suggest that past consumption of an MPA, but not contemporaneous MPA, was indeed significantly associated with child linear growth outcomes (Table 3). Considering the mean HAZ score of -1.47 for this age group (see Annex Table 9), Columns 1 and 2 suggest that a standard deviation increase in lagged, but not contemporaneous, MPA was associated with a 10–11 percent increase over the mean HAZ score.Footnote 6 These estimates are roughly the same as those reported above for the full sample. Similarly, Columns 3 and 4 and Columns 7 and 8 of Table 3, suggest that a 10% increase in lagged MPA was associated with a 1.3—2.3 percentage point reduction in the likelihood of being stunted. Considering the overall stunting rate of 41 percent for this age group, this translates roughly into a range of 3.2 – 5.6 percent reduction in stunting rate. This range is slightly wider than the 3.7 – 5.2 percent reduction in the stunting rate that we found for the full sample (Table 2). Overall these estimates for lagged MPA on both the HAZ score and stunting show the robustness of the results. Also, the joint hypotheses tests for the equality of the estimated coefficients across specifications were rejected, suggesting that the results were not spurious significant correlations.Footnote 7

Table 3 Links between child outcomes and lagged and contemporaneous consumption of the mean nutrient adequacy (MPA) for children 6–59 months

4.2.2 Animal sourced foods consumption and child linear growth outcomes

In this section, we explore the relationships between lagged consumption of animal sourced foods to current linear growth outcomes while controlling for other food groups consumption and relevant covariates. Previous studies found that consumption of animal sourced foods is strongly associated with child’s linear growth outcomes. As noted above, however, previous studies, with a few exceptions, relied on cross-sectional or pooled panel observations that do not allow establishing associations between past consumption history to child’s current linear growth outcomes. This section attempts to add some evidence to the literature using longitudinal data. Table 4 reports the results of estimating various versions of Eq. 3, using the full sample. As in Sect. 4.1., the dependent variable takes two forms: Columns 1, 2, 5, and 6 consider the HAZ score, and Columns 3,4,7, and 8 employ a dummy variable if the child was stunted. Columns 1—4 and Columns 5—8 control for the enumeration area by survey fixed effects, and child and survey fixed effects, respectively.

Table 4 Links between child outcomes and the number of ASF consumed for children 6–114 months

The results presented in Table 4 appear to show a lack of strong relationships between the number of ASFs consumed in the past and child’s current linear growth outcomes in any of the specifications. In contrast, there appears to be some negative association between the likelihood of the child being stunted and contemporaneous consumption of one type of ASF (Columns 4),Footnote 8 and with two or more types of ASFs, even though the association was only significant at p < 0.10 (Columns 4 and 8). Since accessibility of each ASF may not be similar and aggregation may hide some of the variations among ASF types in the data, we re-run Columns 1- 8 after replacing the number of ASFs consumed by types of ASFs (Table 5).

Table 5 Links between child outcomes and lagged and contemporaneous consumption of ASF for children 6–114 months

Results presented in Table 5 suggest that there was a strong negative relationship between lagged eggs consumption and the likelihood of being stunted (Columns 3 and 4). The results suggest that sustained consumption of eggs in the past was associated with a 7–8 percentage point reduction in the likelihood of being stunted. On average, this translates into a 18–21 percent reduction in the likelihood being stunted, since the overall stunting rate in the sample is 38 percent. In addition, contemporaneous consumption of meat and fish was strongly associated with increased HAZ score (Column 6) and with a reduced likelihood of being stunted (Column 8). Similarly, results suggest that contemporaneous consumption of dairy was associated with increased HAZ score (Column 2), and with a reduced likelihood of being stunted (Column 4). The joint hypotheses tests for the equality of the estimated coefficients across specifications (including for eggs, dairy, and meat) were rejected, suggesting that the results were not spurious significant correlations.Footnote 9

As in the preceding section, we conducted additional analysis by limiting the sample to children only aged 6–59 months. Tables 6 and 7 present the results with similar specifications corresponding to Table 4 and 5, respectively. According to Table 6, consumption of two or more ASFs in the past, but not current consumption, was strongly associated with the likelihood of being stunted (Columns 3 and 4). Considering the average stunting rate of 41 percent for this age group, the results suggest that sustained consumption of two or more types of ASFs in the past was associated with a 24–27 percent reduction in the likelihood being stunted, on average.Footnote 10

Table 6 Links between child outcomes and the number of ASF consumed for children 6–59 months
Table 7 Links between child outcomes and lagged and contemporaneous consumption of ASF for children 6–59 months

Among ASF types, lagged consumption of dairy appear to be strongly associated with the HAZ score (Table 7, Columns 1 and 2). Results suggest that sustained dairy consumption in the past was associated with about 34 percentage point increase in the HAZ score. This, on average, translates into about 23 percent increase in the HAZ score since the mean HAZ score for this age group was -1.47. Columns 3 and 4 also show negative associations between meats consumption in the past and the likelihood of being stunted, even though it was significant only at 10% level (Columns 3 and 4). The null hypotheses for joint tests for equality of the estimated coefficients across specifications for past consumption of dairy were rejected, suggesting that the results were not spurious significant correlations.Footnote 11

4.2.3 Contemporaneous consumption and child linear growth outcomes

As noted above, much of previous studies reported evidence of strong associations between child linear growth outcomes and contemporaneous consumption mainly using one-time observations. However, as shown in Sects. 4.1 and 4.2 above, such association disappears (in the case of MPA) or becomes less strong (in the case of ASFs) when past consumption status is taken into account. This section re-examines such association using longitudinal data.

Table 8 presents a summary of results from fixed effects estimations of the HAZ score and stunting for children aged 6–113 months, and 6–59 months only. Results in each panel and column in Table 8 come from separate regressions. From Panel a, there was only one out of 8 specifications that show a weakly significant association between contemporaneous MPA and child linear growth outcome (Column 2). From Panel b, there was a strong association between contemporaneous consumption of 1 ASF and child stunting (Column 2). Columns 2 and 8 also showed some weak association (that is significant only at p < 0.10) between contemporaneous consumption of two or more ASFs and linear child growth outcomes. From Panel c, consumption of meat and fish (Column 3 and 4) and consumption of dairy (Columns 2 and 7) appear to be associated with child linear growth outcomes, even though two of these four coefficients were significant only at p < 0.10. Regression results that take into account location and time fixed effects appear to show some associations between contemporaneous consumption of ASFs and child linear growth outcomes, especially when older children were included in the analysis. Nonetheless, results were not as strong as those reported in previous studies with cross-sectional data.

Table 8 Contemporaneous consumption and child linear growth outcomes

5 Discussion and conclusions

5.1 Discussion

Less than seven years remain till the globally agreed date to end all forms of malnutrition, including stunting in children under 5 years of age, one of the targets of the Sustainable Development Goals (SDG 2 zero hunger). However, the prevalence of child stunting in Ethiopia is still high and the progress to date in the reduction of stunting appears to be slow according to survey data used in this study and a more recent survey by MOH (MOH, 2023). Identifying optimal conditions to end hunger and improve diets within the limits of planetary boundaries is one of the evidence-based priorities that the Scientific Group to the United Nations Food Systems Summit suggested (von Braun et al., 2021). This study examined whether household’s average nutrient acquisition capacity (measured as MPA) predicts linear growth in children, and whether household’s sustained acquisition of animal sourced foods is associated with child linear growth in rural and small towns in Ethiopia. Much of previous studies on child linear growth determinants used proxy indicators such as dietary diversity scores or simple indicators of consumed food groups without measuring the quantity and adequacy of nutrient intakes, and relied mostly on cross-sectional observations even though the effect of dietary consumption on child linear growth would be observed with time lag. This study contributes to filling the gap in the literature using longitudinal data.

Results suggest that household’s lagged MPA, but not contemporaneous MPA, was strongly associated with current child growth outcomes, regardless of whether child growth was measured in terms of the HAZ score or stunting. For example, for children 6–59 months of age, a standard deviation increase in lagged MPA was associated with a 10–11 percent increase over the mean HAZ score. Similarly, a 10% increase in lagged MPA was associated with a 3.2 – 5.6 percent reduction in stunting rate. When older children (aged up to 114 months) were included in the analysis, the corresponding increase in the average HAZ score was 10 percent and the reduction in stunting rate was 4.2–5.2 percent, respectively. The results were robust to specifications even after controlling for child specific unobserved heterogeneities and survey fixed effects beside other controls. Since the MPA comprises both macro- and micronutrients, results suggest that both types of nutrients were important predictors of child growth. However, the specific contribution of micronutrients in linear growth outcomes could either be small (Ramakrishnan et al., 2009; Sanin et al., 2018), or that their role is rather indirect—via supporting the optimal functioning of immune system and development potential (Black et al., 2013). Identifying the independent roles of macro- and micronutrients for linear growth outcomes is beyond the scope of this study.

Animal source foods are known to be rich in high quality protein and other growth-stimulating nutrients (Dror & Allen, 2011). Recent observational studies such as Headey et al. (2018) found strong associations between contemporaneous ASFs consumption and child linear growth or stunting. Nonetheless, findings of some randomized control trials in low-income countries suggest that the longer-term effect of ASFs consumption on linear growth is inconclusive (Allen & Dror, 2011; Iannotti et al., 2019). In this context, this study sheds some light using longitudinal data from rural and small towns in Ethiopia. For children 6–59 months of age, results suggest that lagged (sustained) consumption of two or more ASFs was associated with an average of 24–27 percent reduction in the likelihood of being stunted. Among ASF types, lagged consumption of meats was associated with stunting reduction, and lagged consumption of dairy was associated with improvement in the HAZ score. When older children (aged up to 114 months) were included in the analysis, results did not show strong relationships between the number of ASFs consumed in the past and the child’s current linear growth outcomes. However, among ASFs results suggest that sustained consumption of eggs was associated with a 18–21 percent reduction in the likelihood of being stunted. Further, there appears to be some association between child linear growth outcomes and contemporaneous ASFs consumption.

While findings of this study provide some support to the importance of ASFs to child’s linear growth in small towns and rural Ethiopia, results were not as strong as those reported in previous studies such as Headey et al. (2018) that used cross-sectional or pooled panel observations from several countries. However, to put our results in context, first, the surveys used this study were not designed primarily for nutrition research and the consumption data was for the household. Hence, our analysis may not have fully captured intrahousehold food allocations, specifically children’s access to ASFs and the adequacy of quantity consumed. This is because previous studies suggest that intra-household food allocation is determined by relative differences in household members’ income, bargaining power, food behaviors, social status, tastes and preferences, and interpersonal relationships (Harris-Fry et al., 2017), among others. Second, our reference period of consumption was seven days unlike the twenty-four hours reference used in Headey et al., (2018). This may have minimized potential variations in the consumption data that is needed for identification. Third, due to data limitation (the fact that the surveys used in this study were conducted in about two-year intervals), we were unable to conduct separate panel data estimations for children aged 6–23 months (age category that children experience higher growth faltering (Victoria et al., 2010)) and those older than 23 months. Fourth, due to attrition and missing observations, the sample used for analysis was unbalanced panel; hence, results may suffer from the corresponding bias. However, overall results did not show major differences (at least qualitatively) across specifications and when data were disaggregated across age groups, possibly suggesting that sample attrition may not have been systematic.

The first reason, however, may not carry too much weight in explaining the less strong associations between ASFs consumption and child linear growth outcomes observed in this study. This is because, over 90% households in this study reported that all household members eat roughly the same diet regardless of age, a pattern that has changed very little between 2011/12 and 2015/16 as described above. In fact, a study in rural Ethiopia found that children are favored in intrahousehold food allocations (Coates et al., 2018). Relatedly, based on the 2015/16 survey wave used in this study, Mekonnen et al. (2020) found estimates of household nutrient adequacy which were reasonably comparable to that of EPHI (2013)—a national food consumption survey that measured individual level consumption. Nonetheless, to better understand the contribution of ASFs to child’s linear growth would require better data—designed for nutrition research—with repeated measurements of length/height across age groups and the quantities consumed (including that of other food groups) over time, besides other socioeconomic determinants which are important especially for nutrition outcomes of older children (Alderman & Headey, 2018).

On the one hand, results of this study concerning the association of MPA and ASFs with child linear growth outcomes appear to suggest that the full diet perspective needs greater attention to improve linear growth outcomes of children in small towns and rural Ethiopia. On the other hand, the mean probability of nutrient adequacy (MPA) among study households was 41% or less, indicating the burden of multiple nutrient deficiencies. Since household diets in Ethiopia are monotonous whereby grains/starchy staples constitute a major part of children’s, women’s and men’s diet (EPHI, 2013), the enormity of the gap in the household MPA indicates the need for nutrient-dense foods especially that of ASFs in the household diets. Addressing nutrient gaps using ASFs may involve tradeoffs with sustainability, since ASFs have higher environmental impacts (e.g. Willet et al., 2019). Potential solutions may include stimulating farm-livestock systems that is sustainable, e.g. circular systems where there is no food-feed competition, that avoid losses, that recycle waste and use animals to unlock biomass that humans cannot eat (Oosting et al., 2022). Note however that due to the low level of ASFs consumption in Ethiopia, sustainability issues around ASFs may not be the prime concern as much as that of high-income countries where plant-based alternatives are more available or affordable year-round (Parlasca & Qaim, 2022). Further, despite the low level of ASFs consumption in Ethiopia, recent studies show that ASFs and other nutrient-rich foods in the country have become increasingly unaffordable especially to lower-income households (Bachewe et al., 2017; Daba et al., 2021; Haileselassie et al., 2020).

5.2 Conclusions

Given the study limitations described above, findings of this study provide suggestive evidence that policies and interventions aimed at improving linear growth outcomes of children in rural and small towns in Ethiopia should improve household’s access to ASFs and nutrient acquisition capacity. Since the association of ASFs consumption and child linear growth outcomes appears to be heterogenous across age groups, targeting households with younger children may be more beneficial.