Skip to main content
BMJ Open logoLink to BMJ Open
. 2022 Nov 10;12(11):e060692. doi: 10.1136/bmjopen-2021-060692

Seasonality and predictors of childhood stunting and wasting in drought-prone areas in Ethiopia: a cohort study

Bereket Yohannes Kabalo 1,2,, Bernt Lindtjørn 1,2
PMCID: PMC9660553  PMID: 36356996

Abstract

Background and objectives

Over centuries, Ethiopia has experienced severe famines and periods of serious drought, and malnutrition remains a major public health problem. The aims of this study were to estimate seasonal variations in child stunting and wasting, and identify factors associated with both forms of child malnutrition in drought-prone areas.

Methods

This cohort study was conducted among a random sample of 909 children in rural southern Ethiopia. The same children were followed for 1 year (2017–2018) with quarterly repeated measurements of their outcomes: height-for-age and weight-for-height indices (Z-scores). Linear regression models were used to analyse the association between both outcomes and baseline factors (eg, household participation in a social safety net programme and water access) and some time-varying factors (eg, household food insecurity).

Results

Child wasting rates varied with seasonal household food insecurity (ᵪ2trend = 15.9, p=0.001), but stunting rates did not. Household participation in a social safety net programme was associated with decreased stunting (p=0.001) and wasting (p=0.002). In addition to its association with decreased wasting (p=0.001), protected drinking water access enhanced the association between household participation in a social safety net programme and decreased stunting (p=0.009). Absence of a household latrine (p=0.011), lower maternal education level (p=0.001), larger family size (p=0.004) and lack of non-farming income (p=0.002) were associated with increased child stunting.

Conclusions

Seasonal household food insecurity was associated with child undernutrition in rural Ethiopia. Strengthening community-based food security programmes, such as the Ethiopian social safety net programme, could help to reduce child undernutrition in drought-prone areas. Improving clean water access and sanitation could also decrease child undernutrition.

Key terms: Z-scores; Social safety net program; Water access

Keywords: nutrition & dietetics, primary care, nutrition, epidemiology, public health


STRENGTHS AND LIMITATIONS OF THIS STUDY.

  • This study accounted for agroecological strata and random selection of households; however, we did not initially estimate separate samples for the different strata (eg, by household participation in social safety net programme).

  • Seasonality was accounted for in our repeated measurements using some time-varying exposure variables (eg, household food insecurity and child diarrhoeal illness); however, we did not assess other illnesses, such as malaria, measles and tuberculosis.

  • We did not initially estimate separate samples for our repeated measurements, but our analytical sample (ie, counts of observations compiled from the repeated measurements) showed adequate statistical power of estimation to meet the primary aims of the study.

  • This study analysed height-for-age Z-score and weight-for-height Z-score indices as continuous measures using linear regression models; our estimates were adjusted for the observed clustering effects at the primary sampling stage (at the kebele level) and time series effects of our repeated measurements.

  • As our data were analysed in a cohort design, a certain underestimated time element may exist in our repeated measurements beyond the scope of our time-varying exposures.

Introduction

Over the centuries, Ethiopia has experienced droughts and famine events, averaging once per decade.1 2 The Intergovernmental Panel on Climate Change (IPCC) also predicts that climate change will lead to more desertification and crop failures in vulnerable areas, such as Ethiopia3–5 where malnutrition remains one of the major public health problems.6–9

In communities that rely on subsistence agriculture, food insecurity often peaks seasonally in preharvest periods.10 11 Affected households adapt by reducing the frequency and size of daily meals; selling livestock or dairy products; borrowing food or money from merchants or local social networks; selling wood, charcoal or grass; engaging in paid labour and renting out farm land.12 However, such coping mechanisms are often insufficient, leading to a vicious cycle of poverty and food insecurity.

Following many years of food provision for famine-prone populations, the Ethiopian government launched the Productive Safety Net Programme (PSNP) in 2005.13 PSNP’s stated aims are to prevent household asset depletion and strengthen communities.13 This programme provides cash or food payments in exchange for labour to produce public works, local infrastructure and environmental projects, or direct payments for households that are unable to provide labour.14

Researchers use several methods to assess the impact of food scarcity on populations. One common outcome is the level of household food insecurity (HFI) and occurrence of malnutrition among vulnerable populations (eg, young children), and both these outcomes are subjected to the impacts of climate change.15 16 Recent literature has emphasised the importance of understanding seasonal variations in nutrition status among young children as an indicator of vulnerability to food insecurity.17 Population’s vulnerability in this context could be described as the level of susceptibility to food insecurity challenges due to lack of capacity to cope and adapt to those challenges.18

Since the 1970s, undernutrition has been classified in two major ways: wasting (ie, low weight-for-height or small mid-upper arm circumference) and stunting (ie, low height-for-age).19 However, this categorical classification neglects many children with borderline measurements who are undernourished.20 Height-for-age and weight-for-height indices (Z-scores) as continuous outcome measures could reflect shared factors and pathophysiological processes that should be viewed as composite measures of undernutrition.21

Wolaita, a densely populated area in southern Ethiopia, has experienced severe droughts and famines.2 10 As such, the population’s experiences and coping mechanisms related to severe food insecurity are relevant for other famine-prone areas in the country and across Africa. The aims of this study were to estimate seasonal variations in child stunting and wasting, and identify factors associated with both these forms of child malnutrition in drought-prone areas.

Methods

Study design and setting

We conducted a prospective cohort study using a random sample of 909 households in the rural Wolaita area in southern Ethiopia. We recruited one child per household at the start of the study (in June 2017), and followed the same children by measuring their outcomes, that is, height-for-age and weight-for-height indices, every 3 months for 1 year (June 2017 to June 2018). Our exposure variables included background factors (measured at baseline) and some time-varying factors (measured each season). Quarterly repeated measurements were performed in the first month of each season (ie, June, September, December and March).10

Wolaita is located between the Great Rift Valley and the Omo Valley in southern Ethiopia. Rural villages in this area mainly represent two agro-ecological areas: the hot and semi-dry ‘lowlands’ and the relatively cooler and subhumid ‘midlands’.3 22 Mean annual rainfall ranges from 800 mm in the lowlands to 1200 mm in the midlands, with a bimodal distribution.10 Farming of staple crops, such as maize, occurs during the Belg rains from approximately March to early May.10 23 Root crops, such as taro and sweet potato, are farmed in both seasons and help to bridge seasonal gaps in food security.3 10

Outcomes

The main outcome measures were height-for-age and weight-for-height indices (Z-scores), measured each season for 1 year and defined based on the WHO 2006 child growth standards.24 Stunting and wasting were defined as HAZ (height-for-age Z-scores) and WHZ (weight-for-height Z-scores) of −2 SD below the respective WHO standard median.

Exposures

Our exposure variables included background factors (baseline data) and some time-varying factors (measured each season). Baseline factors comprised the following: (1) child age and sex; (2) parent age and education; (3) household socioeconomic conditions, such as family size, source of income, wealth index and participation in the food security programme (PSNP); (4) household latrine ownership and (5) drinking water access. We considered HFI, dietary diversity and child diarrhoeal illness as time-varying exposures, for which we carried out repeated measurements.

Repeated measurements

Our repeated measurements were performed during the four seasons based on agricultural cycles: Kiremt is the sowing season in June, July and August; Belg is the main harvest season in September, October and November; Bega is the postharvest season in December, January and February and Tsedey is the dry preharvest season in March, April and May.10 These quarterly repeated measurements were carried out at the same time for outcomes and time-varying exposures.

Participants

A multistage random selection of households was conducted. First, we selected two rural districts, or Woredas, representing the two agroecological strata in Wolaita: the Humbo district in the lowlands and Soddo Zuria district in the midland area, with the assumption that HFI would be more prevalent in the lowland areas.25 26 Population density was higher in the midland villages than in the lowland villages in the study area. As such, we selected three kebeles (the smallest administrative unit) from the lowland district and two kebeles from the midland district using the complex samples selection feature in SPSS V.25.0 (IBM). Finally, we selected households with children under 5 years-old and enrolled one child aged 6–59 months per household.

To estimate the sample size, we followed an earlier cohort study assessing seasonal variations in wasting prevalence.27 The estimated sample size to estimate differences in prevalence rates of wasting 6.6% and 13%, with a 95% level of confidence and 80% power, was 820 children (OpenEpi software). Our study included 909 children.

Patient and public involvement

No subject involvement.

Outcome measurements

Height and weight measurements were performed each season. We trained four data collectors on standard techniques for height and weight measurements. After the training, we validated the consistency of their measurements by recruiting 10 children aged below 5 years from another rural village and having all four data collectors (observers) measure each child’s height twice. The overall measurements showed approximately 92% average internal consistency. These four observers recorded height and weight measurements for the actual study. Height (or recumbent length for children younger than 24 months) was measured to the nearest 0.1 cm using a local wooden length board. Weight was measured to the nearest 0.1 kg using a Seca weight scale (Seca GmbH & Co. Kg, Hamburg, Germany).

Exposure measurements

Time-invariant factors (baseline)

Children’s age in months, mothers’ age in years and highest grade of school completed by both parents were recorded. We also recorded family size (number of household members), source of income (exclusively farming vs generates other additional income), possession of common household assets and participation in the food security programme (data collectors observed PSNP beneficiary cards during household visits). In addition, we recorded household latrine ownership (yes vs no) and drinking water access (protected vs unprotected), and only water piped via public tap was as a protected source.28 We used principal component analysis to construct a wealth index based on common household assets: (1) housing material of the roof, interior ceilings, floors and walls; (2) number of livestock owned by the household; (3) land size in hectares and (4) possession of common assets, such as a radio, mobile telephone, bed and mattress, kerosene lamp, watch, electric or solar panels, chairs and tables, wooden boxes, and donkey carts.10 29

Time-varying factors (measured each season)

The time-varying variable, that is, HFI, was measured using nine questions in the Household Food Insecurity Access Scale, which has been validated in the study area.10 Household dietary diversity was scored using 24-hour recall measurements. Household members were asked about the 12 common food groups in Ethiopia: (1) cereals and breads; (2) potatoes and other roots or tubers; (3) vegetables; (4) fruits; (5) eggs; (6) dairy products; (7) pulses; (8) fish; (9) meat; (10) oil, fat or butter; (11) sugar or honey and (12) other foods or condiments (eg, coffee, tea, other spices, etc.). The responses for the 12 food-groups were used to generate a scale of food intake diversity, that is, the household dietary diversity score (HDDS).30 The occurrence of childhood diarrhoeal illness was also assessed, which was defined as the passage of three or more loose or watery stools in the preceding 24-hours,31 32 and was assessed during the 2 weeks prior to the survey dates.33

We generated two categorical variables from the actual HFI observations in our data set and the time series of our repeated measurements. Quantified as person-time observations, an ordinal HFI measure (ie, number of seasons with HFI) was generated as an exposure variable to explore dose–response relationships (eg, between child wasting and HFI). Quantified also as person-time observations, we generated a multinomial HFI measure summarising incidence rates of HFI by the four seasons (0=food-secure; 1=HFI in the sowing season; 2=HFI in the main harvest season; 3=HFI in the postharvest season and 4=HFI in the dry preharvest season) as an exposure variable in our main analysis (ie, multivariable models). As household food security and dietary diversity are highly correlated entities, we accounted for HDDS as the null category for HFI multinomial measure (ie, 0=food-secure) as an exposure variable in our main analysis. Moreover, child diarrhoeal illness was considered as a covariate for the effect of the other time-varying exposures (eg, seasonal HFI).

Conceptual framework

Based on a systematic review paper, Phalkey and colleagues suggested complex pathways from climate variability to undernutrition in subsistence communities.34 Our current work used their work, but we adapted it to the scope of our study, and we focused on human nutrition (figure 1).

Figure 1.

Figure 1

Conceptual framework for a possible chain of relationships between seasonal food insecurity and child undernutrition, Wolaita, rural Ethiopia, 2017–2018.

Data and measurements

Data entry and cleaning

Data were double-entered in EpiData software V.3.1 (EpiData Association 2000–2021, Aarhus, Denmark) and corrected for entry errors. First, we entered our baseline data by unique identification numbers for the subjects (ID). We then entered repeated measurements by the subject ID and recorded each round of measurement with different variable names for each variable. After cleaning our data in the short format (by ID), we reshaped the data set into long format for statistical analysis, with which a new variable (season) was generated to specify the discrete time series of our repeated measurements. We generated nutritional indices (HAZ and WHZ) from anthropometric data using ENA and WHO Anthro software 3.2.2 (WHO, Geneva, Switzerland).

Units of analysis

As we measured each child in each of the four seasons, we compiled counts of observations totalling 3636 HAZ and WHZ measurements at the end of the study period. However, we excluded 46 HAZ and 126 WHZ observations that had incomplete data or that were severe outliers.35 Accordingly, our units of analysis were counts of measurements totalling 3571 HAZ estimates and 3510 WHZ estimates (figure 2). We analysed complete WHZ data (n=3510) of 897 children and complete HAZ data (n=3571) of 907 children.

Figure 2.

Figure 2

Flow chart of child anthropometric measurements considered for this cohort study, Wolaita, rural Ethiopia, 2017–2018.

Time-varying data considerations

As we measured the same children in each season, age changes during the study period could lead to certain deviations in outcome estimates (ie, cohort effects). As such, we generated a separate variable (age in months divided by age in the logarithmic scale) to account for cohort effects. Time-varying effects could also be due to external factors (eg, seasonality). Accordingly, we considered HFI as a multinomial variable to estimate the seasonally variable effect of HFI on child undernutrition. Furthermore, we accounted for the time series of our repeated measurements using some dummy variables as measurement components of time-varying exposures.

Statistical methods

We used Stata V.15 (Stata Corp LLC, College Station, TX, USA) for our statistical works. To explore our data distributions (bivariate analysis), we used parametric tests, such as t-tests to compare two means, analysis of variance tests to compare more than two means, and correlation tests to assess the associations between two continuous variables. We analysed our normally distributed data for both outcomes with background factors (baseline data) and some time-varying factors (repeated measurements) using hierarchical linear regression models. Our data comprised two categories: (1) clustering effects at the primary sampling stage (at the kebele level) or (2) time-varying effects within our repeated measurements.

Multivariable analysis

We first estimated between-variations as main effects of baseline factors on our outcome measures, and then analysed within-variations as main effects to explore time-varying exposure effects on outcome estimates (additional details are provided under separate subheadings hereafter).

Between-variation models

HAZ data were analysed using a multivariable linear regression model with adjustment for the clustering effect of stunting at the primary sampling stage, but we ignored observed insignificant clustering when analysing the WHZ data.36 37 HAZ and WHZ estimates in the preceding season were considered to control for cohort effects when analysing baseline factors associated with stunting and wasting.

Within-variation models

At this stage, we aimed to estimate the time-varying exposure effects on outcome estimates, and further analysed the fit between-variation models to account for an exposure-season interaction effect (eg, HFI by the four seasons as a multinomial exposure variable) to estimate seasonally variable effects of relevant exposure variables on outcome estimates. Time-varying exposure effects were estimated as main effects with adjustment for other time-varying effects (ie, cohort and time series effects) and main effects of all baseline factors included in the fitted models for between-variations.

Further analysis

We further analysed the fitted models for both outcomes to explore interactions, for example, additive, or multiplicative effects (eg, PSNP participation and protected drinking water access on our outcome estimates) or effect modification (eg, variations in the effect of PSNP participation on child wasting across HFI levels).

Model reports and meanings

We reported main effects for between-variations and within-variations using standardised model coefficients (β) with 95% CIs. Decreased model coefficients refer to increased stunting (HAZ) and wasting (WHZ).

Results

Participants

Table 1 presents the baseline characteristics of the 907 study participants with complete HAZ data.

Table 1.

Baseline characteristics of the study participants in Wolaita, rural Ethiopia, 2017–2018 (n=907)

Variable # (%)*
Child’s sex
 Male 462 (50.9)
 Female 445 (49.1)
Child’s age in months, mean (SD) 33.4 (11.7)
Mother’s age in years, mean (SD) 29.3 (3.3)
Mother’s education (grade completed)
 0–4 325 (32.8)
 5–8 285 (31.4)
 9–12 or higher education 297 (32.7)
Father’s education (grade completed)
 0–4 452 (49.8)
 5–8 277 (30.5)
 9–12 or higher education 178 (19.6)
Household family size, median (IQR) 6 (4–7)
Household work, any non-farming income?
 Yes (additional income) 237 (26.1)
 No (exclusively farming) 670 (73.9)
Household owns a latrine
 Yes 784 (86.4)
 No 123 (13.6)
Household has protected drinking water access
 Yes 406 (44.8)
 No 501 (55.2)
Household PSNP participation
 Yes 434 (47.9)
 No 473 (52.1)
Household PSNP participation and protected drinking water access(cat)
 Neither PSNP participation nor protected water access 307 (33.9)
 PSNP participation (alone) 191 (21.1)
 Protected water access (alone) 165 (18.2)
 Both PSNP participation and protected water access 244 (26.9)

*Unless otherwise indicated. Participates in the Productive Safety Net Programme (PSNP). Household PSNP participation and protected drinking water access(cat) is a categorical variable generated from two dichotomous variables (PSNP participation and protected drinking water access): 1=households who neither had protected drinking water access nor participated in PSNP; 2=households who participated in PSNP, but did not have protected drinking water access; 3=households who had protected drinking water access, but did not participate in PSNP; 4=households who had protected drinking water access and also participated in PSNP.

Summary results from repeated measurements

Table 2 summarises prevalence rates of HFI, childhood diarrhoeal illness and stunting and wasting. The overall prevalence of child stunting was 32.1% (1145 of 3571 measurements) and that of wasting was 10.3% (360 of 3510 measurements). Child wasting rates varied across seasons (ᵪ2trend = 20.5, p=0.001), but stunting rates did not exhibit any seasonal variations.

Table 2.

Prevalence rates of household food insecurity, child diarrhoeal illness and undernutrition (stunting and wasting) rates (Wolaita, rural Ethiopia, 2017–2018)

Variable Season Prevalence
% 95% CI
Household food insecurity Sowing season (n=902) 77.2 71.6 83.2
Main harvest season (n=904) 60.2 55.3 65.5
Postharvest season (n=893) 76.0 70.5 82.0
Dry preharvest season (n=872) 84.0 78.1 90.4
Child diarrhoeal illness Sowing season (n=902) 30.9 27.4 34.7
Main harvest season (n=904) 26.5 23.3 30.1
Postharvest season (n=893) 22.6 19.6 26.0
Dry preharvest season (n=872) 24.0 21.0 27.6
Child stunting Sowing season (n=902) 32.2 28.7 36.2
Main harvest season (n=904) 32.2 28.7 36.2
Postharvest season (n=893) 31.1 27.6 35.0
Dry preharvest season (n=872) 33.6 29.9 37.7
Child wasting Sowing season (n=894) 9.4 7.6 11.6
Main harvest season (n=887) 8.9 7.1 11.1
Postharvest season (n=872) 10.0 8.1 12.3
Dry preharvest season (n=857) 12.8 10.6 15.5

Household food insecurity

The overall prevalence of HFI was 74.2% (95% CI 72.8 to 75.6) during the study period (2651 of 3571 measurements), and HFI varied across seasons (ᵪ2trend = 29.2, p=0.001). Quantified as person-time observations, the risk of experiencing HFI in just one season was 7.5%, compared with 17.0% in two seasons, 39.0% in three seasons and 34.8% throughout all four seasons. The median HDDS was 3 (out of the 12 food groups, IQR of 3–4), but the overall HDDS did not show seasonal variations. As shown in figure 3, dietary diversity decreased with increasing durations of HFI (Z=−7.3, p=0.001).

Figure 3.

Figure 3

Dietary diversity score (HDDS) by duration of food insecurity for households who participated in the Productive Safety Net Programme (PSNP) and households that did not participate in the programme, Wolaita, rural Ethiopia, 2017–2018.

Child diarrhoeal illness

The overall prevalence of child diarrhoeal illness was 26% (95% CI 24.6 to 27.5; 930 of 3571 measurements), and the occurrence of child diarrhoeal illness varied across seasons (ᵪ2trend = 12.0, p=0.001), with a peak in the rainy (sowing) season.

Outcome data distributions

Table 3 shows HAZ and WHZ data distributions by background characteristics (baseline data).

Table 3.

Distributions of height-for-age Z-score (n=907 children) and weight-for-height Z-score (n=897 children) indices by baseline factors (rural Wolaita, Ethiopia, 2017–2018)

Variable Categories HAZ (n=3571) WHZ (n=3510)
Mean 95% CI Mean 95% CI
Child’s sex Female −1.057 −1.137 −0.976 −0.638 −0.690 −0.586
Male −1.308 −1.385 −1.230 −0.600 −0.654 −0.545
Mother’s age in years 15–24 −1.667 −1.761 −1.573 −0.434 −0.503 −0.364
25–34 −1.191 −1.285 −1.097 −0.529 −0.589 −0.469
>35 −0.688 −0.784 −0.593 −0.902 −0.964 −0.839
Mother’s education 0–4 −1.308 −1.443 −1.173 −0.599 −0.681 −0.516
5–8 −1.220 −1.319 −1.121 −0.669 −0.737 −0.601
9–12 or higher −1.161 −1.257 −1.065 −0.623 −0.690 −0.555
Father’s education 0–4 −1.308 −1.443 −1.173 −0.599 −0.681 −0.516
5–8 −1.144 −1.247 −1.042 −0.686 −0.753 −0.619
9–12 or higher −1.200 −1.298 −1.101 −0.592 −0.665 −0.519
Household has a latrine Yes −1.172 −1.232 −1.112 −0.620 −0.661 −0.579
No −1.269 −1.427 −1.111 −0.608 −0.702 −0.514
Non-farm-related work Yes −1.060 −1.171 −0.950 −0.680 −0.752 −0.608
No −1.228 −1.293 −1.164 −0.597 −0.641 −0.553
Household wealth status Poorest −1.203 −1.331 −1.074 −0.649 −0.726 −0.572
Poor −1.101 −1.223 −0.978 −0.774 −0.861 −0.686
Medium −1.308 −1.436 −1.181 −0.601 −0.690 −0.513
Rich −1.123 −1.248 −0.997 −0.501 −0.584 −0.418
Richest −1.190 −1.312 −1.068 −0.565 −0.647 −0.483
Household size <4 −1.064 −1.172 −0.956 −0.563 −0.633 −0.493
5–7 −1.238 −1.313 −1.163 −0.667 −0.720 −0.614
>8 −1.217 −1.349 −1.085 −0.571 −0.651 −0.490
Protected drinking water access Yes −1.204 −1.287 −1.121 −0.395 −0.449 −0.341
No −1.169 −1.245 −1.093 −0.803 −0.854 −0.752
PSNP participation Yes −1.051 −1.133 −0.969 −0.505 −0.560 −0.450
No −1.307 −1.383 −1.231 −0.723 −0.774 −0.671
PSNP participation and protected drinking water access* (cat) Neither† −1.369 −1.468 −1.270 −0.842 −0.907 −0.777
PSNP‡ −0.893 −1.016 −0.771 −0.717 −0.801 −0.634
Water§ −1.250 −1.371 −1.130 −0.486 −0.566 −0.405
Both¶ −1.218 −1.335 −1.102 −0.336 −0.408 −0.264

*PSNP participation and protected drinking water access (cat) is a categorical variable generated from two dichotomous variables (PSNP participation and protected drinking water access).

†Households who neither had protected drinking water access nor participated in PSNP.

‡Households who participated in PSNP, but did not have protected drinking water access.

§Households who had protected drinking water access, but did not participate in PSNP.

¶Households who had protected drinking water access and also participated in PSNP.

PSNP, Productive Safety Net Programme.

Boys had lower HAZ indices than girls (t=−4.2, p=0.001). HAZ indices increased (t=11.6, p=0.001), but WHZ decreased (t=−9.4, p=0.001), with increasing maternal age. Both HAZ and WHZ increased with increasing maternal education level: HAZ (t=3.8, p=0.001) and WHZ (t=2.0, p=0.039). Children who lived in exclusively farming households had lower HAZ indices than those who lived in households with additional income (t=−2.9, p=0.004), and WHZ decreased with decreasing household wealth (t=3.2, p=0.002).

HAZ and WHZ by PSNP and drinking water access

As shown in table 3, both HAZ and WHZ indices were higher among children whose households participated in PSNP than those whose households did not participate in PSNP: mean HAZ difference=0.251 (95% CI 0.136 to 0.365) and mean WHZ difference=0.216 (95% CI 0.141 to 0.291). Moreover, children whose households had protected drinking water access had higher WHZ indices than those whose households had no protected drinking water access: mean difference=0.399 (95% CI 0.324 to 0.474). HAZ did not vary by drinking water access.

Protected drinking water access had a confounding effect on the observed association between PSNP participation and increased WHZ: mean difference=0.136 (95% CI 0.060 to 0.212). Figure 4 shows WHZ data distributions by categories for a multinomial variable that disentangles PSNP participation and protected drinking water access.

Figure 4.

Figure 4

Mean weight-for-height Z-score indices of children aged 6–59 months by household participation in the Productive Safety Net Programme (PSNP) and protected drinking water access, Wolaita, rural Ethiopia, 2017–2018.

Baseline factors associated with child nutritional status

Table 4 presents results of multivariable regression models for factors independently associated with HAZ and WHZ. PSNP participation was found to be independently associated with increased HAZ and WHZ. In addition, protected drinking water access was associated with increased WHZ. Furthermore, protected water access enhanced the association between PSNP participation and increased HAZ. Being a boy, a lower level of maternal education, and a lack of a household latrine were associated with decreased HAZ.

Table 4.

Results of multivariable linear regression models for factors associated with child stunting and wasting (Wolaita, rural Ethiopia, 2017–2018)

Variables HAZ (n=3571) WHZ (n=3510)
β 95% CI β 95% CI
Child’s age in months (ln) −2.022*** −3.093 −0.951 −0.196** −0.309 −0.083
Child’s sex (ref=female) −0.327*** −0.441 −0.213 −0.034 −0.110 0.043
Mother’s age in years, continuous −0.039 −0.079 0.002 −0.005 −0.032 0.022
Mother’s education level, continuous 0.121*** 0.074 0.169 0.023 −0.009 0.054
Father’s education level, continuous −0.032 −0.084 0.019 −0.027 −0.062 0.008
Household latrine (ref=yes) −0.175* −0.343 −0.007 0.024 −0.088 0.137
Family size, continuous −0.123 −0.209 −0.037 −0.019 −0.077 0.038
Wealth index, continuous −0.075 −0.179 0.029 0.024 −0.045 0.094
Work, non-farming income (ref=yes) −0.182*** −0.316 −0.047 −0.043 −0.133 0.047
Drinking water access(W) 0.234 0.066 0.403 −0.363 −0.476 −0.250
PSNP participation(P) −0.092 −0.265 0.081 −0.172 −0.288 −0.056
Interaction term(W×P) −0.367*** −0.600 −0.133 0.005 −0.152 0.162
Child diarrhoeal illness −0.038 −0.166 0.090 0.017 −0.069 0.103
Household food insecurity 0.063 −0.066 0.192 0.020 −0.067 0.106

Our units of analysis here are HAZ (height-for-age Z-scores) measurements on 902 children and WHZ (weight-for-height Z-scores) measurements on 897 children in the preceding season. Drinking water access (0=protected vs 1=unprotected); PSNP=Productive Safety Net Programme (0=PSNP participant or beneficiary vs PSNP non-participant or non-beneficiary); interaction term: included households who neither had protected drinking water access nor PSNP participation. Child age and cohort-effect: we considered the child’s age in months in the logarithmic scale (ln) to account for the observed inconsistencies in child age data distributions. All model coefficients here are adjusted for the effect of child age changes during the study period (cohort-effect).

*P<0.05; **p<0.01; ***p<0.001.

Seasonality

As shown in figure 5, child wasting rates varied with seasonal HFI, and child wasting rates increased with increasing duration of HFI (ᵪ2trend = 5.9, p=0.015). Moreover, table 5 presents the association between seasonal HFI and child WHZ indices adjusted for baseline factors, child age changes during the study period and time series of our repeated measurements. It was found that seasonal HFI was independently associated with decreased WHZ.

Figure 5.

Figure 5

Seasonal variations in child wasting rates among overall measurements and measurements within food-insecure households, Wolaita, rural Ethiopia, 2017–2018.

Table 5.

Results of multivariable linear regression models for seasonality of child wasting, Wolaita, rural Ethiopia, 2017–2018 (n=3510)

Variables β 95% CI
Child’s age in months −0.150** −0.263 −0.036
Child’s sex (ref=female) −0.009 −0.083 0.065
Mother’s age, continuous 0.013 −0.019 0.045
Mother’s education, continuous 0.021 −0.010 0.052
Father’s education, continuous −0.021 −0.054 0.013
Household latrine (ref=yes) 0.050 −0.059 0.159
Family size, continuous −0.026 −0.082 0.030
Wealth index, continuous 0.020 −0.048 0.087
Work, non-farming income (ref=yes) −0.033 −0.120 0.055
PSNP participation −0.122** −0.199 −0.044
Drinking water access −0.349 *** −0.431 −0.267
Child diarrhoeal illness (ref=yes) 0.006 −0.081 0.093
Household food insecurity (ref=yes) 0.077 −0.058 0.211
Seasonal household food insecurity (ref=main harvest season)
Sowing season 0.003 −0.131 0.137
Postharvest season −0.170* −0.302 −0.037
Dry preharvest season −0.345*** −0.481 −0.209
Child age changes during the study period (cohort) 0.638* 0.066 1.211
Child diarrhoeal illness (time series)
At first season −0.020 −0.133 0.092
At second season 0.004 −0.104 0.112
At third season −0.157 −0.279 −0.034
At fourth season 0.054 −0.053 0.161
Household food insecurity (time series)
At first season 0.167 0.071 0.263
At second season −0.143 −0.225 −0.061
At third season 0.192 0.052 0.333
At fourth season −0.083 −0.246 0.079

**P<0.05; **p<0.01; ***p<0.001.

PSNP, Productive Safety Net Programme.

Effect modification

Table 6 presents the results of further analysis of the fitted WHZ model by duration of HFI. The results showed that seasonal HFI modified the effect of PSNP participation and protected drinking water access on increased WHZ estimates.

Table 6.

Variations in the effects of household PSNP participation and protected drinking water access on weight-for-height Z-scores of children aged 6–59 months by durations of household food insecurity, Wolaita, rural Ethiopia, 2017–2018

Duration of household food insecurity
1or 2 seasons 3 or 4 seasons
β 95% CI β 95% CI
Child age (lnmonths), continuous 1.279 −0.039 2.598 1.417 0.596 2.238
Child age changes (cmonths), continuous −0.266 −0.461 −0.070 −0.242 −0.361 −0.124
Child sex (ref=female) −0.141 −0.277 −0.004 0.031 −0.056 0.119
Mother’s age, continuous −0.046 −0.097 0.005 −0.034 −0.065 −0.004
Mother’s education, continuous −0.141 −0.198 −0.083 0.068 0.032 0.105
Father’s education, continuous 0.156 0.092 0.220 −0.080 −0.120 −0.041
Household latrine (ref=yes) −0.382 −0.592 −0.171 0.178 0.049 0.307
Family size, continuous −0.004 −0.112 0.105 0.004 −0.062 0.070
Wealth index, continuous −0.099 −0.227 0.030 0.061 −0.018 0.141
Work, non-farming income −0.273 −0.438 −0.108 0.038 −0.065 0.142
PSNP participation and protected drinking water access(cat) (ref=both)*
Neither† −0.679 −0.867 −0.491 −0.395 −0.518 −0.273
PSNP‡ −0.350 −0.556 −0.143 −0.296 −0.430 −0.162
Water§ −0.421 −0.616 −0.225 −0.058 −0.194 0.079
Both¶
Child diarrhoeal illness (ref=no) 0.015 −0.144 0.173 0.008 −0.094 0.110
Child diarrhoeal illness (first season) −0.066 −0.275 0.142 0.088 −0.046 0.222
Child diarrhoeal illness (second season) 0.077 −0.126 0.280 0.000 −0.127 0.127
Child diarrhoeal illness (third season) −0.010 −0.232 0.211 −0.150 −0.296 −0.003
Child diarrhoeal illness (fourth season) −0.088 −0.286 0.110 0.143 0.016 0.270

Decreased (β) coefficients refer to increased child wasting and vice-versa. Child age changes (cmonths)=child age in months divided by child age in the logarithmic scale; cmonths was used to account and adjust for child age changes during the study period.

*PSNP participation and protected drinking water access (cat) is a categorical variable generated from two dichotomous variables (PSNP participation and protected drinking water access).

†Households who neither had protected drinking water access nor participated in PSNP.

‡Households who participated in PSNP, but did not have protected drinking water access.

§Households who had protected drinking water access, but did not participate in PSNP.

¶Households who had protected drinking water access and also participated in PSNP.

PSNP, Productive Safety Net Programme.

Discussion

Key results

Our cohort study suggested seasonal variations in WHZ indices among children aged 6–59 months in rural southern Ethiopia, with dose–response relationships. Household participation in the Ethiopian government’s social safety net (PSNP) and having protected drinking water access were main factors associated with increased HAZ or WHZ. Lower level of maternal education, lack of non-farming household income and absence of a household latrine were associated with decreased HAZ indices.

Limitations and strengths

This study was based on a random sample of households, and our units of analysis were counts of total observations compiled from four repeated measurements undertaken for 1 year. However, our one sample estimation could constitute a limitation of this study, especially as certain background factors (eg, household wealth, PSNP participation and drinking water access) clustered in the lowland areas. Subjectivity bias could also exist in our food insecurity measurements, especially as this study was conducted in a chronically food-insecure setting.38 39 We used the Household Food Insecurity Access Scale questionnaire, which had been validated in the study area.10 To ensure accuracy of the current study data, measurements were repeated and, although we used the same data collectors for the repeated data rounds, it was sometimes not possible to maintain the same data collectors. We did not initially estimate separate samples for our repeated measurements, but our analytical sample (ie, counts of observations compiled from the repeated measurements) showed adequate statistical power. We analysed HAZ and WHZ indices as composite measures of child nutritional status as continuous variables using linear regression models which enhanced the accuracy of our estimates.21 Moreover, we accounted and adjusted our estimates for the observed clustering effects at the primary sampling stage (at the kebele level). We accounted for seasonality through some time-varying exposures (HFI and child diarrhoeal illness), but we did not assess other illnesses, such as malaria, measles and tuberculosis.40–43 We considered some dummy variables to account for the time series random effects beyond the scope of our time-varying exposures.

Comparative discussions

Our prevalence estimates for stunting and wasting rates are consistent with recent estimates from Ethiopian demographic and health surveys.44 Our study indicated that household socioeconomic conditions, such as low level of maternal education, lack of non-farming income and absence of PSNP participation were associated with HAZ or WHZ indices (table 4), which complements previous reports.32 45–47 The country’s persistently low socioeconomic status is often described as a main cause for child undernutrition in Ethiopia.32 45–47

Our study suggested that household PSNP participation could improve HAZ and WHZ (table 4), which complements some extant literature,48 49 but contradictory reports also exist.50–52 These inconsistencies could be due to variations in the study designs, participants and data approaches. Nonetheless, a growing body of literature indicates that PSNP improves household food security and consumption.

Our study points to the lack of clean water access and a household latrine as independent predictors for child undernutrition (table 4), which aligns with previous reports.6 53 The lack of clean water access and sanitation could predispose populations to recurrent infections, such as diarrhoea and intestinal parasites.54 55 Indeed, improving clean water, sanitation and hygiene are frequently identified as priority interventions to reduce child undernutrition.56

Our study suggested seasonal HFI as an independent predictor of decreased WHZ (table 5), which is in accordance with previous investigations.57 58 This could be attributable to seasonal fluctuations in household food consumption patterns,11 59 and some scholars describe seasonality as a grossly neglected dimension of poverty.11 17 60

Meanings and possible explanations

Seasonal HFI could contribute to decreased WHZ indices in rural Ethiopia, suggesting that this population is vulnerable to food insecurity.17 Strengthening the PSNP intervention through effective targeting of the neediest households might further enhance its impacts on child undernutrition. Yet, the criteria for household PSNP eligibility remain controversial;61 for example, if geographic criteria prioritise the lowland areas,13 then poorer households in the midland villages (as in our study setting) could be neglected. Improving clean water access and sanitation have widely been described as nutrition-sensitive interventions.62 63 In our study area context, expanding the coverage of protected drinking water access in the midland villages might contribute to reducing child undernutrition. Moreover, addressing seasonal variations in HFI could help decrease child undernutrition.17

Supplementary Material

Reviewer comments
Author's manuscript

Acknowledgments

The authors express gratitude to the Centre for International Health at the University of Bergen in Norway and Hawassa University in Ethiopia for providing facilities to conduct this study. Dr Eskindir Loha is sincerely acknowledged for his important contribution in carrying out this study. Our field supervisors and enumerators are deeply thanked for their invaluable commitment. The authors gratefully acknowledge the study respondents for their cooperation in repeated rounds of interviews.

Footnotes

Contributors: Bereket conceived the research idea, designed the study protocol, implemented the study, made major statistical analyses and wrote the draft and final versions of the scientific report. Bernt conceived the research idea, made substantial contributions to the design, field methods, major statistical analyses and writing. Both authors read and approved this manuscript for submission. Both authors accept full responsibility for the work and/or the conduct of the study.

Funding: This study was funded by the South Ethiopia Network of Universities in Public Health project, under the Norwegian Program for Capacity Development in Higher Education and Research for Development (Grant Number: ETH-13/0025 'SENUPH'). The funder had no role in associated conduct, writing or decisions to publish this manuscript.

Competing interests: None declared.

Patient and public involvement: Patients and/or the public were not involved in the design, or conduct, or reporting or dissemination plans of this research.

Provenance and peer review: Not commissioned; externally peer reviewed.

Data availability statement

All data relevant to the study are included in the article or uploaded as supplementary information.

Ethics statements

Patient consent for publication

Consent obtained from parent(s)/guardian(s).

Ethics approval

This study involves human participants. The institutional review committee at Hawassa University in Ethiopia (IRB/002/09) and the Regional Committee for Medical and Research Ethics in Western Norway (2016/482/REK vest) approved the study protocol. Participants gave informed consent to participate in the study before taking part.

References

  • 1.Kloos H, Lindtjorn B. Malnutrition and mortality during recent famines in Ethiopia: implications for food aid and rehabilitation. Disasters 1994;18:130–9. 10.1111/j.1467-7717.1994.tb00294.x [DOI] [PubMed] [Google Scholar]
  • 2.Cochrane L. Strengthening food security in rural Ethiopia [PhD] University of British Columbia; 2017. [Google Scholar]
  • 3.Cochrane L, Bekele YW. Average crop yield (2001-2017) in Ethiopia: trends at national, regional and zonal levels. Data Brief 2018;16:1025–33. 10.1016/j.dib.2017.12.039 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Shukla P, Skea J, Calvo Buendia E. IPCC, 2019: Climate Change and Land: an IPCC special report on climate change, desertification, land degradation, sustainable land management, food security, and greenhouse gas fluxes in terrestrial ecosystems 2019.
  • 5.Mohammed Y, Yimam A. Analysis of meteorological droughts in the Lake’s Region of Ethiopian Rift Valley using reconnaissance drought index (RDI). Geoenvironmental Disasters 2021;8:13. 10.1186/s40677-021-00183-1 [DOI] [Google Scholar]
  • 6.Abate KH, Belachew T. Chronic malnutrition among under five children of Ethiopia may not be economic. A systematic review and meta-analysis. Ethiop J Health Sci 2019;29:265–77. 10.4314/ejhs.v29i2.14 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Yazew KG, Kassahun CW, Ewnetie AW, et al. Recovery rate and determinants of severe acute malnutrition children treatment in Ethiopia: a systematic review and meta-analysis. Syst Rev 2019;8:323. 10.1186/s13643-019-1249-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Bitew ZW, Alemu A, Worku T. Treatment outcomes of severe acute malnutrition and predictors of recovery in under-five children treated within outpatient therapeutic programs in Ethiopia: a systematic review and meta-analysis. BMC Pediatr 2020;20:335. 10.1186/s12887-020-02188-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Zerga AA, Tadesse SE, Ayele FY, et al. Impact of malnutrition on the academic performance of school children in Ethiopia: a systematic review and meta-analysis. SAGE Open Med 2022;10:20503121221122398. 10.1177/20503121221122398 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Kabalo BY, Gebreyesus SH, Loha E, et al. Performance of an adapted household food insecurity access scale in measuring seasonality in household food insecurity in rural Ethiopia: a cohort analysis. BMC Nutr 2019;5:54. 10.1186/s40795-019-0323-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Hirvonen K, Taffesse AS, Worku Hassen I. Seasonality and household diets in Ethiopia. Public Health Nutr 2016;19:1723–30. 10.1017/S1368980015003237 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Jufare AT. Livelihood adaptation, risks and vulnerability in rural Wolaita, Ethiopia [PhD] Norwegian University of Life Sciences; 2008. [Google Scholar]
  • 13.Ministry of Agriculture . Productive safety net programme phase IV programme implementation manual. Addis Ababa, Ethiopia; 2014: 179. [Google Scholar]
  • 14.Doocy S, Teferra S, Norell D, et al. Credit program outcomes: coping capacity and nutritional status in the food insecure context of Ethiopia. Soc Sci Med 2005;60:2371–82. 10.1016/j.socscimed.2004.10.025 [DOI] [PubMed] [Google Scholar]
  • 15.MacVicar S, Berrang-Ford L, Harper S, et al. How seasonality and weather affect perinatal health: comparing the experiences of Indigenous and non-Indigenous mothers in Kanungu district, Uganda. Soc Sci Med 2017;187:39–48. 10.1016/j.socscimed.2017.06.021 [DOI] [PubMed] [Google Scholar]
  • 16.Dodd W, Gómez Cerna M, Orellana P, et al. Factors associated with seasonal food insecurity among small-scale Subsistence farming households in rural Honduras. Int J Environ Res Public Health 2020;17. 10.3390/ijerph17030706. [Epub ahead of print: 22 01 2020]. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Baye K, Hirvonen K. Seasonality: a missing link in preventing undernutrition. Lancet Child Adolesc Health 2020;4:e3. 10.1016/S2352-4642(19)30343-8 [DOI] [PubMed] [Google Scholar]
  • 18.Mumby PJ, Chollett I, Bozec Y-M, et al. Ecological resilience, robustness and vulnerability: how do these concepts benefit ecosystem management? Curr Opin Environ Sustain 2014;7:22–7. 10.1016/j.cosust.2013.11.021 [DOI] [Google Scholar]
  • 19.Waterlow JC. Note on the assessment and classification of protein-energy malnutrition in children. Lancet 1973;2:ii:87–9. 10.1016/s0140-6736(73)93276-5 [DOI] [PubMed] [Google Scholar]
  • 20.Bille JC, Assefa E, Corra M. Ecology and ecosystems of the Borana deep wells area. Addis Ababa: ILCA, 1983. [Google Scholar]
  • 21.Wells JCK, Briend A, Boyd EM, et al. Beyond wasted and stunted-a major shift to fight child undernutrition. Lancet Child Adolesc Health 2019;3:831–4. 10.1016/S2352-4642(19)30244-5 [DOI] [PubMed] [Google Scholar]
  • 22.Esayas B, Simane B, Teferi E, et al. Trends in extreme climate events over three Agroecological zones of southern Ethiopia. Advances in Meteorology 2018;2018:1–17. 10.1155/2018/7354157 [DOI] [Google Scholar]
  • 23.Korecha D, Sorteberg A. Validation of operational seasonal rainfall forecast in Ethiopia. Water Resour Res 2013;49:7681–97. 10.1002/2013WR013760 [DOI] [Google Scholar]
  • 24.Bloem M. The 2006 WHO child growth standards. BMJ 2007;334:705–6. 10.1136/bmj.39155.658843.BE [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Webb P. Coping with drought and food insecurity in Ethiopia. Disasters 1993;17:33–47. 10.1111/j.1467-7717.1993.tb00486.x [DOI] [PubMed] [Google Scholar]
  • 26.Eze E, Girma A, Zenebe A, et al. Predictors of drought-induced crop yield/losses in two agroecologies of southern Tigray, Northern Ethiopia. Sci Rep 2022;12:6284. 10.1038/s41598-022-09862-x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Roba KT, O'Connor TP, Belachew T, et al. Variations between post- and pre-harvest seasons in stunting, wasting, and Infant and Young Child Feeding (IYCF) practices among children 6-23 months of age in lowland and midland agro-ecological zones of rural Ethiopia. Pan Afr Med J 2016;24:163. 10.11604/pamj.2016.24.163.9387 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.van Cooten MH, Bilal SM, Gebremedhin S, et al. The association between acute malnutrition and water, sanitation, and hygiene among children aged 6-59 months in rural Ethiopia. Matern Child Nutr 2019;15:e12631. 10.1111/mcn.12631 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Naik GR. Advances in principal component analysis: research and development; 2018.
  • 30.Swindale A, Bilinsky P. Household dietary diversity score (HDDS) for measurement of household food access: indicator guide; 2006.
  • 31.Alemayehu B, Ayele BT, Melak F, et al. Exploring the association between childhood diarrhea and meteorological factors in southwestern Ethiopia. Sci Total Environ 2020;741:140189. 10.1016/j.scitotenv.2020.140189 [DOI] [PubMed] [Google Scholar]
  • 32.Abdulahi A, Shab-Bidar S, Rezaei S, et al. Nutritional status of under five children in Ethiopia: a systematic review and meta-analysis. Ethiop J Health Sci 2017;27:175–88. 10.4314/ejhs.v27i2.10 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Bogale GG, Gelaye KA, Degefie DT, et al. Spatial patterns of childhood diarrhea in Ethiopia: data from Ethiopian demographic and health surveys (2000, 2005, and 2011). BMC Infect Dis 2017;17:426. 10.1186/s12879-017-2504-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Phalkey RK, Aranda-Jan C, Marx S, et al. Systematic review of current efforts to quantify the impacts of climate change on undernutrition. Proc Natl Acad Sci U S A 2015;112:E4522–9. 10.1073/pnas.1409769112 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.WHO . Anthropometric indices and exclusion flags; 2006.
  • 36.Coelho C, Arnold B. Finite form representations for Meijer G and Fox H functions applied to multivariate likelihood ratio tests, 2019. [Google Scholar]
  • 37.Rabe-Hesketh S, Skrondal A. Multilevel and longitudinal modeling using Stata. Fourth ed, 2021. [Google Scholar]
  • 38.Headey, D D E, et al. Improving the measurement of food security 2012.
  • 39.Gebreyesus SH, Lunde T, Mariam DH. Is the adapted household food insecurity access scale (HFIAS) developed internationally to measure food insecurity valid in urban and rural households of Ethiopia? BMC Nutrition 2015;1. [Google Scholar]
  • 40.Doherty T, Rohde S, Besada D, et al. Reduction in child mortality in Ethiopia: analysis of data from demographic and health surveys. J Glob Health 2016;6:020401. 10.7189/jogh.06.020401 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Ambel AA, Andrews C, Bakilana AM, et al. Examining changes in maternal and child health inequalities in Ethiopia. Int J Equity Health 2017;16:152. 10.1186/s12939-017-0648-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Legesse D, Haji Y, Abreha S. Trend analysis of malaria occurrence in Wolaita zone, southern Ethiopia: retrospective cross-sectional study. Malar Res Treat 2015;2015:123682. 10.1155/2015/123682 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Gari T, Loha E, Deressa W, et al. Malaria increased the risk of stunting and wasting among young children in Ethiopia: results of a cohort study. PLoS One 2018;13:e0190983. 10.1371/journal.pone.0190983 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.CSA . Ethiopian demographic and health survey 2016; 2017.
  • 45.Golan J, Heacdey D, Hirvonen K. The Oxford Handbook of Ethiopian economy. in changes in child undernutriton in Ethiopia, 2000–2016. New York: Oxford University Press, 2019. [Google Scholar]
  • 46.UNDP . Human development report; 2019.
  • 47.UNDP . Human development report 2020; 2020.
  • 48.Astatkie A. Dynamics of stunting from childhood to youthhood in Ethiopia: evidence from the young lives panel data. PLoS One 2020;15:e0229011. 10.1371/journal.pone.0229011 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Bahru BA, Bosch C, Birner R, et al. Drought and child undernutrition in Ethiopia: a longitudinal path analysis. PLoS One 2019;14:e0217821. 10.1371/journal.pone.0217821 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Berhanu G, Mekonnen S, Sisay M. Prevalence of stunting and associated factors among preschool children: a community based comparative cross sectional study in Ethiopia. BMC Nutr 2018;4:28. 10.1186/s40795-018-0236-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Tesfaye A, Egata G. Stunting and associated factors among children aged 6-59 months from productive safety net program beneficiary and non-beneficiary households in Meta District, East Hararghe zone, Eastern Ethiopia: a comparative cross-sectional study. J Health Popul Nutr 2022;41:13. 10.1186/s41043-022-00291-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Bahru BA, Jebena MG, Birner R, et al. Impact of Ethiopia's productive safety net program on household food security and child nutrition: a marginal structural modeling approach. SSM Popul Health 2020;12:100660. 10.1016/j.ssmph.2020.100660 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Takele K, Zewotir T, Ndanguza D. Understanding correlates of child stunting in Ethiopia using generalized linear mixed models. BMC Public Health 2019;19:626. 10.1186/s12889-019-6984-x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Dake SK, Solomon FB, Bobe TM, et al. Predictors of stunting among children 6-59 months of age in Sodo Zuria District, South Ethiopia: a community based cross-sectional study. BMC Nutr 2019;5:23. 10.1186/s40795-019-0287-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Batiro B, Demissie T, Halala Y, et al. Determinants of stunting among children aged 6-59 months at Kindo Didaye woreda, Wolaita zone, southern Ethiopia: unmatched case control study. PLoS One 2017;12:e0189106. 10.1371/journal.pone.0189106 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.UNICEF . UNICEF conceptual framework on maternal and child nutrition; 2020.
  • 57.Belayneh M, Loha E, Lindtjørn B. Seasonal variation of household food insecurity and household dietary diversity on wasting and stunting among young children in a drought prone area in South Ethiopia: a cohort study. Ecol Food Nutr 2021;60:44–69. 10.1080/03670244.2020.1789865 [DOI] [PubMed] [Google Scholar]
  • 58.Mohsena M, Hossain M, Chakraborty B, et al. Fragile environment, seasonality and maternal and childhood undernutrition in Bangladesh. J Biosoc Sci 2018;50:579–603. 10.1017/S002193201700044X [DOI] [PubMed] [Google Scholar]
  • 59.Lindtjørn B, Alemu T, Bjorvatn B. Dietary pattern and state of nutrition among children in drought-prone areas of southern Ethiopia. Ann Trop Paediatr 1993;13:21–32. 10.1080/02724936.1993.11747621 [DOI] [PubMed] [Google Scholar]
  • 60.Steinbrink M, Niedenführ H. Africa on the move: migration, Translocal Livelihoods and rural development in sub-Saharan Africa. Springer International Publishing, 2020. [Google Scholar]
  • 61.Irenso AA, Atomsa GE. Implications of Ethiopian productive safety net programme on household dietary diversity and women's body mass index: a cross-sectional study. Food Nutr Res 2018;62. 10.29219/fnr.v62.1574. [Epub ahead of print: 01 11 2018]. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Tusa BS, Weldesenbet AB, Kebede SA. Spatial distribution and associated factors of underweight in Ethiopia: an analysis of Ethiopian demographic and health survey, 2016. PLoS One 2020;15:e0242744. 10.1371/journal.pone.0242744 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Anyanwu O, Ghosh S, Kershaw M, et al. Dietary outcomes, nutritional status, and household water, sanitation, and hygiene (WASH) practices. Curr Dev Nutr 2022;6:nzac020. 10.1093/cdn/nzac020 [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

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

Supplementary Materials

Reviewer comments
Author's manuscript

Data Availability Statement

All data relevant to the study are included in the article or uploaded as supplementary information.


Articles from BMJ Open are provided here courtesy of BMJ Publishing Group

RESOURCES