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. 2021 Mar 25;16(3):e0248637. doi: 10.1371/journal.pone.0248637

Pooled prevalence and associated factors of chronic undernutrition among under-five children in East Africa: A multilevel analysis

Getayeneh Antehunegn Tesema 1,*, Yigizie Yeshaw 1,2, Misganaw Gebrie Worku 3, Zemenu Tadesse Tessema 1, Achamyeleh Birhanu Teshale 1
Editor: Jane Anne Scott4
PMCID: PMC7993805  PMID: 33765094

Abstract

Background

Childhood undernutrition is the leading cause of under-five mortality and morbidity in the world particularly in East African countries. Although there are studies on child undernutrition in different East African countries, our search of the literature revealed that there is limited evidence of a pooled analysis of these studies. Therefore, this study aimed to investigate the pooled prevalence and associated factors of chronic undernutrition (i.e. stunting) among under-five children in East Africa.

Methods

A pooled analysis of the Demographic and Health Surveys (DHSs) in 12 East African countries was conducted. A total weighted sample of 79744 under-five children was included in the study. Mixed-effect logistic regression analysis was used to identify significant factors associated with chronic undernutrition since the DHS data has a hierarchical structure. The intra-class correlation coefficient (ICC), Median Odds Ratio (MOR), Likelihood Ratio (LR)-test, and deviance was used for model comparison. Variables with p-value <0.2 in the bivariable mixed-effect logistic regression analysis were considered for the multivariable analysis. In the multivariable multilevel analysis model, the Adjusted Odds Ratio (AOR) with the 95% Confidence Interval (CI) were reported for significant factors.

Results

The pooled prevalence of chronic undernutrition among underfive children in East Africa was 33.3% (95% CI: 32.9%, 35.6%) ranging from 21.9% in Kenya to 53% in Burundi. Children whose mothers lived in rural area (AOR = 1.11, 95% CI: 1.06, 1.16), born to mother who had no formal education (AOR = 1.42, 95% CI: 1.34, 1.50) and primary education (AOR = 1.37, 95% CI: 1.31, 1.44), being in poor household (AOR = 1.66, 95% CI: 1.58, 1.74), and middle household (AOR = 1.42, 95% CI: 1.35, 1.49), child aged 36–48 months (AOR = 1.09, 95% CI: 1.04, 1.14), being male (AOR = 1.19, 95% CI: 1.15, 1.23), 2nd - 4th birth order (AOR = 1.08, 95% CI: 1.03, 1.13), and above 4th 1.27 (AOR = 1.27, 95% CI: 1.19, 1.35), home delivery 1.09 (AOR = 1.09, 95% CI: 1.05, 1.13), small size at birth (AOR = 1.35, 95% CI: 1.29, 1.40) and being multiple births (AOR = 1.98, 95% CI: 1.81, 2.17) were associated with increased odds of stunting. While, antenatal care visit (AOR = 0.89, 95% CI: 0.86, 0.93), mothers aged 25–34 (AOR = 0.83, 95% CI: 0.79, 0.86) and ≥ 35 years (AOR = 0.76, 95% CI: 0.72, 0.81), large size at birth (AOR = 0.85, 95% CI: 0.81, 0.88), and family size >8 (AOR = 0.92, 95% CI: 0.87, 0.98) were associated with decreased odds of stunting.

Conclusion

The study revealed that stunting among under-five children remains a major public health problem in East Africa. Therefore, to improve child nutrition status the governmental and non-governmental organizations should design public health interventions targeting rural residents, and the poorest households. Furthermore, enhancing health facility delivery, ANC visit, and maternal health education is vital for reducing child chronic undernutrition.

Background

Adequate nutrition is vital for healthy growth, and neurological and cognitive development in early childhood [1, 2]. The first 1000 days after conception are the critical period for infant growth and development [3]. Stunting is a linear growth failure that causes both physical and cognitive delays in growth and development [4] and it is the best predictor of chronic child undernutrition and household well-being [5]. Stunting is defined as the inability to attain potential height for age and under-five children are particularly vulnerable to malnutrition [6]. A child is considered to be stunted when their height for age is minus two standard deviations below the median population [7].

Malnutrition is the leading cause of morbidity and mortality in under-five children [8]. Globally, an estimated 178 million under-five children are stunted, of whom more than 90% live in Africa and Asia [9]. It affects one-third of under-five children in low and middle-income countries [10]. The prevalence of stunting among under-5 children is highest in Africa (36%), of these the largest number of stunted children is found in East Africa [11]. More than half (54%) of under-five mortality each year is due to malnutrition and its related complication [12].

It is well known that childhood malnutrition has significant consequences on child growth and development [13, 14]. It has both short and long-term adverse effects [15]. The short term consequences are recurrent infections [16], increased diseases severity [17], and delayed recovery from the disease [18], delayed physical and mental development [19], whereas the long term consequences of stunting are poor academic performance [20], premature death [14] and increased the risk of chronic diseases such as Diabetic Mellitus (DM), Hypertension (HTN) and heart disease [21, 22]. In addition, malnutrition has a significant negative consequence on the future reproductive health of female children [23, 24].

Previous studies on stunting among under-five children revealed that the causes of stunting are multifactorial [2528]. Commonly reported predictors of stunting among under-five children include residence, duration of breastfeeding, wealth status, media exposure, maternal education, husband education, Antenatal Care (ANC) visit during pregnancy, Postnatal Care (PNC), place of delivery, health care access, women decision making autonomy, childhood illness, congenital diseases, maternal Body Mass Index (BMI), birth order and family size [2933].

According to UNICEF data, the global progress of stunting has declined from 255 million to 159 million from 1990 to 2014 [34]. Nevertheless, today, one in four under-five children in East African countries is stunted [35]. Despite the Sustainable Development Goal (SDG) ambitious target to reduce stunting among children by 40% by 2025 [36, 37], the prevalence in East Africa remains unacceptably high [38, 39].

Though there are studies conducted on stunting in East African countries [3032, 40, 41], these were mainly based on hospital records, and are unable to capture the pooled prevalence and associated factors of stunting among under-five children in East Africa. Therefore, this study aimed to investigate the pooled prevalence and associated factors of chronic undernutrition among under-five children in East Africa. The study findings could help to inform the design of evidence-based public health interventions for reducing childhood undernutrition, and subsequently reduce child mortality, in East Africa.

Methods

Data source

This study was based on the most recent Demographic and Health Surveys (DHS) conducted in the 12 East African countries (Burundi, Ethiopia, Comoros, Uganda, Rwanda, Tanzania, Mozambique, Madagascar, Zimbabwe, Kenya, Zambia, and Malawi). These datasets were merged to determine the pooled prevalence and associated factors of stunting among under-five children in East Africa. The DHS is a nationally representative survey that collects data on basic health indicators like mortality, morbidity, family planning service utilization, fertility, maternal and child health. The data were derived from the https://dhsprogram.com/data/available-datasets.cfm. The DHS has different datasets (men, women, children, birth, and household datasets). For this study, we used the child data set (KR file). In the KR file, all children who were born in the last five years preceding the survey in the selected enumeration area were included. The DHS used two stages of stratified sampling technique to select the study participants. We pooled the DHS surveys conducted in the 12 East African countries and a total weighted sample of 79744 under-five children was included in the study.

Variables of the study

The outcome variable was stunted (chronic undernutrition) or not stunted in children aged 6–59 months. In DHS to assess whether a child was stunted or not, the height for age measurement status was used. Children with a height for age measurement of < -2 standard deviation from the median of the reference population were considered to be short for their age (stunted), and children with a measurement of ≥ 2 standard deviation units were considered as not stunted. The response variable for the ith child is represented by a random variable Yi with two possible values coded as 1 and 0. So, the response variable of the ith child Yi was measured as a dichotomous variable with possible values Yi = 1, if the child was stunted and Yi = 0 if a child was not stunted.

The independent variables were classified into four themes as community-level, maternal, household, and child-related variables. Community-level factors included were the place of residence, country, and distance to the health facility. The maternal factors included were maternal age, maternal education, marital status, maternal Body Mass Index (BMI), woman’s health care decision making autonomy, maternal occupation, place of delivery, the mode of delivery, Antenatal Care (ANC) visit during pregnancy, Postnatal Care (PNC), media exposure, paternal education, and maternal height. Child-related variables included the sex of the child, age of the child, type of birth, birth order, child-size at birth, exclusive breastfeeding for six months, and nutritional status (wasting, and underweight). The household factors included covered by health insurance, type of toilet, source of fuel for cooking, wealth status, sex of household head, and family size.

Media exposure was calculated by aggregating three variables such as watching television, listening to the radio, and reading newspapers. Then categorised as having media exposure if a mother has been exposed to at least one of the three and not if she had no exposure to any of the media sources.

Data management and analysis

We pooled the DHS data from the 12 East African countries together after extracting the variables based on the literature. Before any statistical analysis, the data were weighted using sampling weight, primary sampling unit, and strata to restore the representativeness of the survey and to account for sampling design when calculating standard errors and reliable estimates. "Svy set" STATA command was used for analysis to take into account the complex survey design. Cross tabulations and summary statistics were done using STATA version 14 software. The pooled prevalence of stunting across countries was presented in a forest plot. The DHS data had a hierarchical nature, this could violate the independence of observations and equal variance assumption of the traditional logistic regression model. Hence, children are nested within a cluster and we expect that children within the same cluster are more likely to be related to each other than children in another cluster. This implies that there is a need to take into account the between cluster variability by using advanced models. Therefore, for the associated factors, we used the mixed-effect logistic regression analysis method. Model comparison and fitness were assessed based on the Intra-class Correlation Coefficient (ICC), Likelihood Ratio (LR) test, Median Odds Ratio (MOR), and deviance (-2LLR) values since the models were nested. Accordingly, a mixed effect logistic regression model (both fixed and random effect) was the best-fitted model since it had the lowest deviance value. Variables with a p-value <0.2 in the bi-variable analysis were considered in the multivariable mixed-effect logistic regression model. Adjusted Odds Ratios (AOR) with a 95% Confidence Interval (CI) and p-value ≤ 0.05 in the multivariable model were used to declare significant factors associated with stunting.

Ethics considerations

Ethical approval and participant consent were not necessary for this particular study since the study was a secondary data analysis based on the publically available DHS data. We requested the data from the MEASURE DHS Program and permission was granted to download and use the data for this study. There are no names of individuals or household addresses in the data files.

Results

Characteristics of the study population

A total of 79744 under-five children were included in the study, of these 40171 (50.4%) were males. The median (±IQR) age of children was 31 (±13.5) months. About 19.7% of the children were from Kenya and the majority (76.2%) of the children were living in rural areas. The majority of the mothers had attained a primary level of education and 49.4% were aged 25–34 years. The majority (68.6%) of children were delivered at a health facility (Table 1).

Table 1. Maternal, child, household and community level characteristics of the study population in East Africa (N = 79744).

Variables Weighted frequency (%)
Community level variables
Country
Burundi 5580 (7.0)
Comoros 2221 (2.8)
Ethiopia 8455 (10.6)
Kenya 15705 (19.7)
Madagascar 4522 (5.7)
Malawi 4635 (5.8)
Mozambique 8818 (11.1)
Rwanda 3258 (4.1)
Tanzania 7782 (9.8)
Uganda 3881 (4.9)
Zambia 10259 (12.8)
Zimbabwe 4624 (5.8)
Residence
Rural 60751 (76.2)
Urban 18993 (23.8)
Distance to health facility
Not a big problem 47147 (59.1)
A big problem 32597 (40.9)
Maternal related characteristics
Mothers age
15–24 21556 (27.0)
25–34 39398 (49.4)
35–49 18790 (23.6)
Maternal education status
No 20178 (25.3)
Primary 41170 (51.6)
Secondary and higher 18396 (23.1)
Marital status
Never married 59331 (74.4)
Married/living together 11337 (14.2)
Divorced/widowed/separated 9076 (11.4)
Working status
No 27941 (35.0)
Yes 51803 (65.0)
Maternal BMI
Underweight 15834 (19.9)
Normal 49750 (62.4)
Overweight 14160 (17.7)
Women health care decision making autonomy
Respondent alone 14389 (18.0)
Jointly with husband/partner 31519 (39.5)
Husband/partner only 33836 (42.5)
Media exposure
No 26221 (32.9)
Yes 53523 (67.1)
Husband education status
No 14503 (18.2)
Primary 32181 (40.4)
Secondary and above 33060 (41.4)
Maternal height
Short 9371 (11.8)
Normal 70373 (88.2)
Place of delivery
Home 25055 (31.4)
Health facility 54689 (68.6)
Mode of delivery
Vaginal 75240 (94.3)
Caesarean 4504 (5.7)
ANC visit during pregnancy
No 28566 (35.8)
Yes 51177 (64.2)
PNC visit (n = 41430)
No 23295 (56.2)
Yes 18135 (43.8)
Household level characteristics
Type of toilet facility
Improved 29686 (37.2)
Not improved 50058 (62.8)
Source of fuel
Modern fuel 5137 (6.4)
Traditional fuel 74607 (93.6)
Covered by health insurance
No 63723 (79.9)
Yes 16021 (20.1)
Wealth status
Poor 36630 (45.9)
Middle 15670 (19.7)
Rich 27444 (34.4)
Sex of household head
Male 61510 (77.1)
Female 18234 (22.9)
Family size
1–4 23288 (29.2)
5–8 44878 (56.3)
≥ 9 11578 (14.5)
Child characteristics
Sex of child
Male 40171 (50.4)
Female 39573 (49.6)
Age of child (in months)
< 24 28195 (35.3)
24–35.9 17524 (22.0)
36–47.9 17295 (21.7)
48–60 16730 (21.0)
Type of birth
Single 77558 (97.3)
Twin 2186 (2.7)
Birth order
First 17399 (21.8)
2–4 38958 (48.9)
≥ 4 23387 (29.3)
Exclusively breast feed for 6 months
No 69273 (86.7)
Yes 10471 (13.2)
Child size at birth
Small 20114 (25.2)
Average 36513 (45.8)
Large 23117 (29.0)
Wasting status
Normal 76044 (95.4)
Wasted 3700 (4.6)
Underweight status
Normal 15767 (19.8)
Underweight 63977 (80.2)

Prevalence of stunting among under-five children in East Africa

The pooled prevalence of stunting among under-five children in East Africa was 33.3% (95% CI: 32.9, 35.6). The prevalence was varied across countries, it was highest in Burundi (53%) and lowest in Kenya (21.9%) (Fig 1).

Fig 1. The prevalence of stunting among under-five children in East African countries.

Fig 1

Associated factors of stunting among under-five children

The mixed-effect logistic regression model was the best-fitted model for the data because of the smallest value of deviance (Table 2). Furthermore, the ICC value in the null model was 18.9% [95% CI: 15.3%, 23.3%], it showed that about 18.9% of the total variability of stunting among under-five children was attributed to the between cluster variability whereas the remaining 81.1% of the total variability was explained by the between-individual variation. The MOR was 1.61 and showed that if we randomly select two children from two different clusters, a child from a cluster with a high risk of stunting was 1.61 times more likely to be stunted than a child from the cluster with a lower risk of stunting. Furthermore, the likelihood ratio test was (LR test vs. Logistic model: chibar2 (01) = 6623.18, Prob > = chiba2 = <0.001) significant which informed that the mixed-effect logistic regression model (GLMM) is the better model over the basic model (Table 2).

Table 2. Model comparison and model fitness.

Parameter Standard logistic regression model Null model Mixed-effect logistic regression model
LLR -47182.02 -47117.89
Deviance 94364.04 94235.6
ICC 18.9% (95% CI: 15.3%, 23.3%)
MOR 1.61 (1.57, 1.65)
LR-test LR test vs. logistic model: chibar2(01) = 245.15 Prob > = chibar2 = 0.001

ICC: Intra-class Correlation Coefficient, LLR: Log-likelihood Ratio, LR: Likelihood Ratio, MOR: Median Odds Ratio

In the multivariable mixed-effect logistic regression analysis; residence, country, maternal education, wealth status, child age, sex of the child, child-size at birth, type of birth, place of delivery, and birth order were significantly associated with increased odds of stunting among under-five children. Whereas, maternal age, ANC visit, and family size were significantly associated with decreased odds of stunting among under-five children. The odds of stunting among children living in the rural area were 1.11 (AOR = 1.11, 95% CI: 1.06, 1.16) times higher compared to those children in urban areas. Under-five children in Kenya had higher odds of stunting than children in other East African countrieso. Children born to mothers who had no formal education and primary education had 1.42 (AOR = 1.42, 95% CI: 1.34, 1.50) and 1.37 (AOR = 1.37, 95% CI: 1.31, 1.44) times higher likelihood to be stunted than children born to mothers who attained secondary education and above, respectively.

Children born to poor wealth households and middle wealth households had 1.66 (AOR = 1.66, 95% CI: 1.58, 1.74), and 1.42 (AOR = 1.42, 95% CI: 1.35, 1.49) times higher odds of stunting compared to children born to the rich wealth household, respectively. Children who were 2nd -4th born and above 4th born had 1.08 (AOR = 1.08, 95% CI: 1.03, 1.13), and 1.27 (AOR = 1.27, 95% CI: 1.19, 1.35) times more likely to be stunted as compared to the first birth. Children born at home were 1.09 (AOR = 1.09, 95% CI: 1.05, 1.13) times more likely to be stunted compared to children born at a health facility.

Children aged 36–47.9 months were 1.09 times (AOR = 1.09, 95% CI: 1.04, 1.14) higher odds of stunting compared to children aged < 24 months. Being male increased the odds of stunting by 19% (AOR = 1.19, 95% CI: 1.15, 1.23) compared to female children. The odds of stunting among multiple births were 1.98 times (AOR = 1.98, 95% CI: 1.81, 2.17) higher than singletons. Children who were small size at birth were 1.35 (AOR = 1.35, 95% CI: 1.29, 1.40) times more likely to be stunted compared to those children who were average size at birth whereas the odds of stunting among children who were large size at birth were decreased by 15% (AOR = 0.85, 95% CI: 0.81, 0.88) compared to average size children at birth. The odds of stunting for children born to mothers aged 25–34 and ≥ 35 years were decreased by 17% (AOR = 0.83, 95% CI: 0.79, 0.86) and 24% (AOR = 0.76, 95% CI: 0.72, 0.81) compared to children born to mothers aged 15–24 years, respectively. The odds of stunting among children belonging to households with eight and above family members were decreased by 8% (AOR = 0.92, 95% CI: 0.87, 0.98). The odds of stunting among children whose mothers had ANC visits during pregnancy were decreased by 11% (AOR = 0.89, 95% CI: 0.86, 0.93) than children whose mothers didn’t have ANC during pregnancy (Table 3).

Table 3. The bi-variable and multivariable mixed-effect logistic regression analysis of stunting among under 5 children in East Africa.

Variable Stunted Not stunted COR with 95% CI AOR with 95% CI
Residence
Urban 14535 4458 1 1
Rural 38691 22060 1.79 (1.72, 1.86) 1.11 (1.06, 1.16)*
Country
Kenya 12262 3443 1 1
Comoros 1597 3076 1.15 (1.03, 1.27) 1.36 (1.22, 1.52)*
Ethiopia 5379 3076 1.78 (1.68, 1.89) 1.88 (1.75, 2.20)*
Burundi 2620 2960 3.60 (3.37, 3.85) 4.76 (4.40, 5.14)*
Madagascar 2302 2220 2.95 (2.74, 3.17) 3.44 (3.18, 3.72)*
Malawi 3175 1460 1.48 (1.37, 1.59) 1.89 (1.74, 2.05)*
Mozambique 5361 3457 1.88 (1.77, 2.00) 2.51 (2.34, 2.70)*
Rwanda 2113 1145 1.77 (1.63, 1.93) 2.41 (2.20, 2.64)*
Tanzania 5410 2372 1.42 (1.33, 1.51) 1.78 (1.66, 1.91)*
Uganda 2943 939 1.09 (1.01, 1.19) 1.30 (1.19, 1.42)*
Zambia 6475 3784 1.93 (1.82, 2.04) 2.43 (2.28, 2.59)*
Zimbabwe 3588 1036 0.89 (0.82, 0.97) 1.45 (1.32, 1.59)*
Maternal age
15–24 14032 7523 1 1
25–34 26785 12613 0.91 (0.88, 0.95) 0.83 (0.79, 0.86)*
≥ 35 12409 6381 0.98 (0.94, 1.02) 0.76 (0.72, 0.81)*
Maternal education
No 11791 8387 2.40 (2.29, 2.51) 1.42 (1.34, 1.50)**
Primary 27003 14167 1.90 (1.83, 1.98) 1.37 (1.31, 1.44)*
Secondary and above 14431 3964 1 1
Wealth status
Poor 22149 14481 2.04 (1.97, 2.11) 1.66 (1.58, 1.74)**
Middle 10256 5413 1.67 (1.60, 1.75) 1.42 (1.35, 1.49)*
Rich 20820 6624 1 1
Media exposure
Yes 37494 16028 1 1
No 17732 10489 1.52 (1.47, 1.56) 1.04 (0.99, 1.08)
Women health care decision making autonomy
Respondent alone 9640 4749 1 1
Jointly with husband/ partner 20759 10760 1.06 (1.02, 1.11) 0.99 (0.94, 1.03)
Husband/partner only 22823 11008 1.03 (0.99, 1.08) 1.04 (0.99, 1.09)
Distance to health facility
Not a big problem 32729 14417 1 1
A big problem 20496 12101 1.33 (1.29, 1.37) 1.02 (0.98, 1.06)
Childs age in months
<24 19061 9134 1 1
24–35.9 11810 5714 1.03 (0.99, 1.08) 1.01 (0.97, 1.06)
36–47.9 11284 6011 1.12 (1.07, 1.16) 1.09 (1.04, 1.14)*
48–60 11070 5660 1.08 (1.03, 1.12) 1.02 (0.97, 1.07)
Sex of child
Male 26127 14043 1.15 (1.12, 1.19) 1.19 (1.15, 1.23)*
Female 27098 12475 1 1
Type of birth
Single 52082 25475 1 1
Multiple 1143 1044 2.04 (1.87, 2.22) 1.98 (1.81, 2.17)**
Place of delivery
Health facility 37519 17168 1 1
Home 15707 9348 1.29 (1.25, 1.34) 1.09 (1.05, 1.13)*
ANC visit during pregnancy
No 17874 10692 1 1
Yes 35352 15826 0.75 (0.73, 0.78) 0.89 (0.86, 0.93)*
Exclusively breast feed for 6 months
No 6941 3530 1 1
Yes 46285 22988 0.92 (0.88, 0.96) 0.95 (0.89, 1.01)
Child size at birth
Average 24347 12166 1 1
Small 13104 7010 1.12 (1.08, 1.16) 1.35 (1.29, 1.40)**
Large 15775 7342 0.89 (0.86, 0.92) 0.85 (0.81, 0.88)**
Birth order
First 11987 5412 1 1
2–4 26557 12401 1.06 (1.02, 1.10) 1.08 (1.03, 1.13)**
≥ 5 14682 8706 1.33 (1.28, 1.39) 1.27 (1.19, 1.35)*
Family size
1–4 15871 7416 1 1
5–8 29520 15358 1.15 (1.11, 1.19) 1.03 (0.99, 1.07)
>8 7835 3744 1.05 (1.01, 1.10) 0.92 (0.87, 0.98)*

* p-value<0.05,

** p-value<0.01, CI: Confidence interval, COR: Crude Odds Ratio, AOR: Adjusted Odds Ratio

This table includes only those variables for which the bi-variable analysis had a p <0.20

Discussion

This study provides evidence that stunting among under-five children continues to be a major public health problem in East African countries. Our study investigated the pooled prevalence and associated factors of stunting among under-five children in East African countries to understand the overall prevalence and associated factors of stunting in East Africa as well as the inter-country distribution of stunting among under-five children across the East African countries.

In this study, 33.3% of under-five children in East African countries were stunted. This is lower than the study reported in Sub-Saharan Africa [39] but higher than a study finding in Iran [42]. This could be due to East African countries being more vulnerable to food shortages because they rely on agriculture which is highly sensitive to weather and climate conditions such as temperature, precipitation, and light and extreme events, and low capacity for adaptation [43, 44]. Furthermore, stunting among under-five children is strongly associated with poverty [45, 46]. Iran is relatively wealthier and has good access to basic maternal and child health care services compared to East African countries, hence this could be the possible explanation for the decreased prevalence of stunting in Iran.

In the multivariable mixed-effect logistic regression; residence, country, maternal age, maternal education, wealth status, child age, sex of the child, type of birth, place of delivery, ANC visit, child-size at birth, birth order, and family size were significantly associated with stunting. In this study, under-five children in a rural area had higher odds of stunting than urban children. It was consistent with study findings [47, 48], this could be due to the reason that urban residents have good access to education, improved access to water and sanitation facilities that contributed to having good child nutrition. Besides, in urban areas maternal health care services such as ANC, health facility delivery, and PNC visit are available, that could raise community awareness to provide quality complementary feeding and uses child immunization services, this could contribute to the lower risk of child stunting in urban areas [49].

Children born to mothers with a lower level of education were more likely to be stunted compared to children born to mothers who attained a secondary and higher level of education. It is consistent with the study findings in Nairobi [50] and Bolivia [51]. It could be because educated mothers have good knowledge about child health and basic health care services, and an enhanced capacity to recognize childhood illness and seek treatment for their children [52]. Besides, educated women are more likely to exclusively breastfeed for 6 months and provide recommended complementary feeding compared to uneducated mothers [53].

In our study wealth status is one of the most important predictors of stunting. Children in the poor and middle household’s wealth were more likely to be stunted than children in the richest household wealth. This was consistent with studies in Indonesia [54], Bangladesh [55], and Angola [56], and stunting is considered to be an indicator of food insecurity and poverty [57]. Children who live in poor households typically have poor access to adequate food, safe water, and sanitation [58]. Consequently, they are at higher risk of childhood infectious diseases such as acute respiratory diseases, diarrheal diseases, and intestinal parasites, all of which contribute to chronic undernutrition [59].

Children in the age group of 36–48 months were more likely to be stunted compared to children aged less than 24 months. It is consistent with a study reported in Nigeria [60], this could be due to the reason that as children ages increase they had environmental exposure that could increase their risk of infections like tonsillopharyngitis, diarrheal diseases, pneumonia, and CROUP [61, 62]. The risk of malnutrition is highest mainly after the initiation of complementary feeding that has been directly linked with poor complementary feeding and breastfeeding weaning practices of mothers, together with high rates of infectious diseases could be the possible reason for the increased risk of stunting in older children [63, 64].

Males were more likely to be stunted than females. This is supported by previous study findings reported in sub-Saharan Africa [65], Pakistan [66], and Brazil [67]. This could be due to the slower lung maturation among males compared to females that predispose male children to repeated respiratory infections such as pneumonia, bronchiolitis, otitis media, and hyperactive airway disease which could contribute to the increased risk of stunting among males [68]. Children born with multiple births are at higher risk of being stunted compared to singletons. It is consistent with studies reported in India [69] and Nigeria [40] and the increased risk of stunting is likely explained by the fact that multiple births are more likely to be born prematurely with low birth weight, and experience increased competition for nutrition [70].

In our study, birth order and, family size were significant predictors of stunting among under-five children. Children of two and above birth order were more likely to be stunted than children of first birth order, it was in line with previous study findings [71, 72]. This might be due to the reason that the family unable to satisfy child dietary and other healthcare-related services because of more children as well as due to maternal nutrition depletion [73].

Children who were small size at birth were more likely to be stunted whereas large-sized babies at birth had lower odds of being stunted as compared to children who were average size at birth. It was consistent with studies [74, 75], this could be due to increased vulnerability of children with small size babies to infections mainly diarrheal and lower respiratory infections such as pneumonia, and otitis media, and increased risk of complications including sleep apnea, anemia, chronic lung disorders, fatigue and loss of appetite compared to children with normal birth weights [76, 77].

The odds of stunting for children born to mothers aged 25–34 and ≥ 35 years were lower than children born to mothers aged 15–24 years. It was in line with the study reported in Nigeria [60]. The possible explanation could be due to the reason that teenagers who gave birth are less likely to use health services like vaccination services, and have poor health-seeking behavior relative to mature mothers.

In our study, health facility delivery and ANC visit were protective of child chronic undernutrition. This finding is supported by studies reported in Indonesia [78] and Nepal [79], this could be due to the reason that ANC visit is an entry point for the other maternal health services, and births from mother who had ANC visit and health facility delivery are aware of danger signs of childhood illness, using childhood immunization services and appropriate childhood feeding practice [80].

The strength of this study was that it was based on a weighted large, nationally representative data set and could have adequate statistical power to detect the true association of factors with stunting among under-five children. Besides, the study is done using an advanced model to take into account the clustering effect (mixed-effect logistic regression) to get reliable standard error and estimate. However, the study finding is interpreted in light of limitations. First, as with other cross-sectional studies, the temporal relationship can’t be established. Second, the DHS didn’t incorporate information about health care availability and accessibility like distance to the health facility, medical-related factors, and the quality of maternal health services provided which might influence child nutrition status. Also, since data was collected from self-report from respondents there may be a possibility of social desirability and recall bias.

Conclusion

The pooled prevalence of stunting among under-five children in East Africa was 33.3% ranging from 21.9% in Kenya to 53% in Burundi. Chronic child undernutrition continues to be a major public health problem in East Africa. In this study; residence, country, maternal age, maternal education, wealth status, child age, sex of the child, type of birth, place of delivery, ANC visit, child-size at birth, birth order, and family size were significantly associated with stunting among under 5 children. Therefore, to improve child nutrition status the governmental and non-governmental organizations should design public health interventions targeting rural residents, and the poorest households. Furthermore, enhancing health facility delivery, ANC visit, and maternal health education is vital for reducing child chronic undernutrition.

Acknowledgments

We greatly acknowledge MEASURE DHS for granting access to the East African DHS data sets.

Abbreviations

ANC

Antenatal Care

AOR

Adjusted Odds Ratio

CI

Confidence Interval

DHS

Demographic Health Survey

GLMM

Generalized Linear Mixed Models

ICC

Intra-class Correlation Coefficient

LLR

log-likelihood Ratio

LR

Likelihood Ratio

MOR

Median Odds Ratio

SSA

Sub-Saharan Africa

WHO

World Health Organization

Data Availability

The data used in this study are from the Measure DHS program (www.dhsprogram.com) and can be accessed following the protocol outlined in the Methods section.

Funding Statement

The authors received no specific funding for this work.

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Pooled prevalence and associated  factors of chronic undernutrition among under-five children in East Africa: A multilevel analysis

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https://link.springer.com/article/10.1007/s10668-010-9278-0?code=17828610-9ce7-412d-b01f-238f1863e02f&error=cookies_not_supported

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In your revision ensure you cite all your sources (including your own works), and quote or rephrase any duplicated text outside the methods section. Further consideration is dependent on these concerns being addressed.

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Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

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The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

**********

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Reviewer #1: Yes

Reviewer #2: Yes

**********

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Reviewer #1: Yes

Reviewer #2: No

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The study is relevant and timeous considering that stunting remains persistent in most African countries. The authors determined the pooled prevalence of chronic undernutrition and associated factors. Data from 12 East African DHS was used (i.e. secondary analysis). The overall pooled prevalence for stunting and by country are reported. Regression analysis was used to study the associated factors, and the manuscript report several factors similar to other studies, such as residence, maternal age, maternal education, wealth status, birth size, sex of the child, ANC visit, place of delivery, family size, type of birth, birth order, country, and child age. The strength and the limitations of the study are well discussed and the conclusion summarizes the findings and the recommendation.

The manuscript has adhered to the standard format.

Abstract

Under the results; the third sentence should read "Children whose mothers" not mother.

Key words

The authors can consider to add stunting, pooled prevalence, associated factors, under-five children, East-Africa, DHS . Remove "mixed effect analysis".

Background

first paragraph sentence 7 - A child is considered stunted... The authors should remove "as"

second paragraph this sentence is missing something and should be rephrased "Malnutrition is the leading cause of under-five morbidity and mortality". Is it under-five 'children'?

Results

This sentence "The median age of children was 31 (IQR±13.5) months" should either report median (IQR) or mean±SD. It cant be IQR and SD.

Reviewer #2: In general, this is a well conducted study although the writing is awkward in places with some grammatical errors. A lack of line numbering made it difficult to highlight these issues so I have edited the paper and I attach a copy of this paper with changes marked. Further suggestions for improvements are listed below.

Abstract

1. The results section of the abstract contains a single, very long sentence which contains all of the factors significantly associated with undernutrition. I suggest breaking this into two sentences which first identifies those factors associated with an increased risk of stunting and then a second sentence which identifies those factors which were associated with a decreased risk of stunting.

Background

2. Is the statistic of 1 in 4 infants in East African countries being stunted actually for infants (i.e. children under 12 months of age) or for children under-five years, which is the target group for this study?

Methods

3. The explanatory variable ‘exclusive breastfeeding’ needs to be more clearly defined. Is this a continuous variable which indicates the duration of EBF or is it a binary variable which indicates whether a child was EBF to 6 months of age? The results in table 4 suggest it is the latter.

Results

4. Under the data management section you say that the pooled prevalence of stunting with the 95% Confidence Interval (CI) was reported using a forest plot. However, while you report the pooled prevalence in the results section you have not included the forest plot.

5. When reporting the findings from the multivariable mixed-effect logistic regression analysis you describe each variable individually and you move between variables that are associated with an increased risk of stunting and those with a decreased risk of stunting. I think it would be clearer if you were to first present those variables associated with a higher risk of stunting and then in a new paragraph identify those that are associated with a lower risk of stunting.

6. The sentence that compares the odds of stunting for each country compared to Kenya is very long and repeats results that are easily discernible from the table. I suggest simplifying this finding and only provide the results for the countries with the lowest and highest odds ratios e.g. “Compared with Kenya which had the lowest prevalence of stunting, all of the other countries had a significantly higher odds of stunting ranging from an odds of 1.30 (1.19, 1.42) for Uganda to 4.76 (4.40, 5.14) for Burundi.”

7. PNC is described in the methods section as an explanatory variable. While it is reported in table 1 there is no further reference to PNC. This variable isn’t included in Table 3 or reported in the results or discussion in terms of its association with stunting. You should either remove all reference to PNC or redo the analysis with this variable in the model. Or does table 3 only contain those variables which had a p-value above 0.2 in the bivariable analysis? This is not clear if this is the case.

Discussion

8. For clarity, I suggest discussing all of the factors associated with an increased risk of stunting and THEN discussing those factors associated with a decreased risk. You move between factors associated with increased and decreased risk and then back to increased risk.

References

9. A number of the references are very dated e.g. 1, 11, 16, 32, 41, 52, 57, 61, 65. Are they seminal papers or can they be replaced with more recent references?

10. Reference 7 The last ‘author’ appears to be a group/organisation but it is unclear which group. When entering the details of a group put a comma after the last word of the name to denote that this is a group. E.g.

WHO Child Health Epidemiology Reference Group,

Otherwise ENDNOTE treats the last word as the family name and initialises all of the other words e.g. Group,WCHERG

11. Reference 33 Some details appear to be missing. Is this a book or a chapter of a book?

12. Reference 35 Please do not abbreviate the institution which has published the report. Where was this report published?

13. Reference 59 Reference details are incomplete.

**********

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Reviewer #1: No

Reviewer #2: Yes: Jane A Scott

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Attachment

Submitted filename: PONE-D-20-18977_reviewer.docx

PLoS One. 2021 Mar 25;16(3):e0248637. doi: 10.1371/journal.pone.0248637.r002

Author response to Decision Letter 0


10 Feb 2021

PLOS ONE

Point by point response for editors/reviewers comments

Manuscript title: Pooled prevalence and associated factors of chronic undernutrition among under-five children in East Africa: A multilevel analysis

Manuscript ID: PONE-D-20-18977

Dear editor/reviewer.

Dear all,

We would like to thank you for these constructive, building, and improvable comments on this manuscript that would improve the substance and content of the manuscript. We considered each comment and reviewers on the manuscript thoroughly. Our point-by-point responses for each comment and question are described in detail on the following pages.

Response to reviewers comments

Reviewer#1

1. Abstract

Under the results; the third sentence should read "Children whose mothers" not mother.

Authors’ response: Thank you for the comments. We accept and modified it. (See Abstract section, line 41, page 2)

2. Key words

The authors can consider to add stunting, pooled prevalence, associated factors, under-five children, East-Africa, DHS . Remove "mixed effect analysis".

Authors’ response: Thank you for the concerns. We removed it in the revised manuscript. (See Abstract section, line 57, line 3)

3. Background

first paragraph sentence 7 - A child is considered stunted... The authors should remove "as"

second paragraph this sentence is missing something and should be rephrased "Malnutrition is the leading cause of under-five morbidity and mortality". Is it under-five 'children'?

Authors’ response: Thank you for the comments. We accepted and modified it. (See Background section, page 4)

4. Results

This sentence "The median age of children was 31 (IQR±13.5) months" should either report median (IQR) or mean±SD. It cant be IQR and SD.

Authors’ response: Thank you for the comments. We reported the median as a measure of central tendency and Inter-quartile Rage (IQR) as a measure of dispersion since the variable was not normally distributed (skewed) with Shapiro Wilks test p-value<0.05.

Reviewer #2

1. In general, this is a well conducted study although the writing is awkward in places with some grammatical errors. A lack of line numbering made it difficult to highlight these issues so I have edited the paper and I attach a copy of this paper with changes marked. Further suggestions for improvements are listed below.

Authors’ response: Thank you reviewer for the detailed comments and changes you made for the betterment of the paper. Sorry for the missing line number, and now, we insert the line number and address the comments you raised. (See the revised manuscript)

2. Abstract

The results section of the abstract contains a single, very long sentence which contains all of the factors significantly associated with undernutrition. I suggest breaking this into two sentences which first identifies those factors associated with an increased risk of stunting and then a second sentence which identifies those factors which were associated with a decreased risk of stunting.

Authors’ response: Thank you for the comments. We accept the comments and write accordingly. (See Abstract section, line 39 -52, page 2-3)

3. Background

Is the statistic of 1 in 4 infants in East African countries being stunted actually for infants (i.e. children under 12 months of age) or for children under-five years, which is the target group for this study?

Authors’ response: Thank you for the comments. We rewrote it as our target population is under-five children. (See the revised manuscript)

4. Methods

The explanatory variable ‘exclusive breastfeeding’ needs to be more clearly defined. Is this a continuous variable which indicates the duration of EBF or is it a binary variable which indicates whether a child was EBF to 6 months of age? The results in table 4 suggest it is the latter.

Authors’ response: Thank you for the comments. We consider the duration of EBF as a binary outcome by categorizing those children who breastfeed for a minimum of 6 months exclusively as yes and for those children who feed less than months as no. (See the revised manuscript)

5. Results

5. Under the data management section you say that the pooled prevalence of stunting with the 95% Confidence Interval (CI) was reported using a forest plot. However, while you report the pooled prevalence in the results section you have not included the forest plot.

Authors’ response: Thank you for the comments. We planned to present using a forest plot but we prefer to present it in a bar graph as this study was not a metanalysis. As you know while we have done, in the forest plot several columns were presented like weight but this may not be important to present it. So, we presented the pooled prevalence in the bar graph. (See Figure 1)

6. When reporting the findings from the multivariable mixed-effect logistic regression analysis you describe each variable individually and you move between variables that are associated with an increased risk of stunting and those with a decreased risk of stunting. I think it would be clearer if you were to first present those variables associated with a higher risk of stunting and then in a new paragraph identify those that are associated with a lower risk of stunting

Authors’ response: Thank you for the comments. We accept the comments and report the findings from factors that increase the odds of stunting to factors that decrease the odds of stunting. (See the Result section, line 195 – 228, page 9-11)

7. The sentence that compares the odds of stunting for each country compared to Kenya is very long and repeats results that are easily discernible from the table. I suggest simplifying this finding and only provide the results for the countries with the lowest and highest odds ratios e.g. “Compared with Kenya which had the lowest prevalence of stunting, all of the other countries had a significantly higher odds of stunting ranging from an odds of 1.30 (1.19, 1.42) for Uganda to 4.76 (4.40, 5.14) for Burundi.”

Authors’ response: Thank you for the comments. We revised it. (See Result section, line 202-203, page 10)

8. PNC is described in the methods section as an explanatory variable. While it is reported in table 1 there is no further reference to PNC. This variable isn’t included in Table 3 or reported in the results or discussion in terms of its association with stunting. You should either remove all reference to PNC or redo the analysis with this variable in the model. Or does table 3 only contain those variables which had a p-value above 0.2 in the bivariable analysis? This is not clear if this is the case.

Authors’ response: Thank you for the concern. We consider PNC in the method and result section. But, in the multivariable multilevel analysis, we did not use PNC as it has a p-value>0.2 in the bivariable analysis. As we stated in the method section we consider variables with a p-value in the bivariable multilevel analysis were included in the multivariable multilevel analysis, that is why we did not include PNC in the final model.

9. Discussion

For clarity, I suggest discussing all of the factors associated with an increased risk of stunting and THEN discussing those factors associated with a decreased risk. You move between factors associated with increased and decreased risk and then back to increased risk.

Authors’ response: Thank you for the suggestions. We accept it and rewrote it. (See discussion section)

10. References

A number of the references are very dated e.g. 1, 11, 16, 32, 41, 52, 57, 61, 65. Are they seminal papers or can they be replaced with more recent references?

Reference 7 The last ‘author’ appears to be a group/organisation but it is unclear which group. When entering the details of a group put a comma after the last word of the name to denote that this is a group. E.g.

WHO Child Health Epidemiology Reference Group,

Otherwise ENDNOTE treats the last word as the family name and initialises all of the other words e.g. Group,WCHERG

Reference 33 Some details appear to be missing. Is this a book or a chapter of a book?

Reference 35 Please do not abbreviate the institution which has published the report. Where was this report published?

Reference 59 Reference details are incomplete.

Authors’ response: Thank you for the comments. We modified all the suggested references. (See the revised manuscript)

Attachment

Submitted filename: Point by point response.docx

Decision Letter 1

Jane Anne Scott

23 Feb 2021

PONE-D-20-18977R1

Pooled prevalence and associated  factors of chronic undernutrition among under-five children in East Africa: A multilevel analysis

PLOS ONE

Dear Dr. Tesema,

Thank you for resubmitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but still does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the minor issues that I have identified at the end of this letter.

Please also note that your image file "Figure 1.tif" could not be opened and processed. It appears that the image file is corrupt or invalid. Please check and make sure that this problem is corrected when you resubmit your final version of the paper. 

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If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols

We look forward to receiving your revised manuscript.

Kind regards,

Jane Anne Scott, PhD, MPH Grad Dip Dietetics, BSc

Academic Editor

PLOS ONE

Journal Requirements:

Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

Additional Editor Comments (if provided):

Minor issues to be addressed

1. Line 49 Being small size at birth should be included with the factors that were associated with increased odds of stunting, not those associated with a decreased odds as the AOR is greater than 1 (AOR=1.35, 95% CI: 1.29, 1.40).

2. Line 55 How are ‘multiple births’ a modifiable factor unless a woman is having fertility treatment? The conclusions in your abstract should be consistent with the conclusions in your main paper on page 15.

3. Line 60 you have misquoted reference 3. It is the first 1000 days ‘post conception’ NOT ‘after birth’.

4. Line 304-305 The way in which you have worded this sentence makes it sound as though ‘health facility delivery and ANC visit’ are associated with an increased risk of chronic malnutrition and NOT that they are protective of chronic malnutrition. I suggest rewording this sentence

‘In our study, health facility delivery and ANC visit were protective of child chronic malnutrition.’

5. Table 3 please include a footnote explaining the meaning of the asterisks. Also I recommend that you included a footnote to explain that the table includes only those variables for which the bi-variable analysis had a p <0.20, otherwise readers may wonder why some of the variables listed in Table 1 are not included in Table 2, (as I was).

Minor grammatical errors

6. line 34 should read ‘Variables’ (plural)

7. line 37 should read ‘were reported for significant factors’

8. Line 45 2nd -4th birth order

9. line 72 the word half is a collective noun and is treated as a singular. Therefore this should read ‘More than half …… is due ….’

10. line 84 the word ‘to’ is not needed, should read ‘… children include residence…..’

11. Line 89 should read ‘ has declined from..’

12. Line 139 I suggest replacing the word ‘divided’ with ‘categorised’.

13. Line 149 should read ‘presented in a bar graph’.

14. Line 195 Given that the next paragraph describes the multivariable mixed-effect logistic regression analysis, shouldn’t this subheading read ‘The mixed effect results’?

15. Lines 260 to 262 should read ‘Besides, educated women are more likely to exclusively breastfeed for….”

16. Line 266 suggest rewording this sentence ‘Children who live in poor households typically have poor access to adequate food, safe water, and sanitation.’

[Note: HTML markup is below. Please do not edit.]

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2021 Mar 25;16(3):e0248637. doi: 10.1371/journal.pone.0248637.r004

Author response to Decision Letter 1


26 Feb 2021

Point by point response for editors/reviewers comments

PLOS ONE Journal

Manuscript title: Pooled prevalence and associated factors of chronic undernutrition among under-five children in East Africa: A multilevel analysis

Manuscript ID: PONE-D-20-18977R1

Dear editor/reviewer.

Dear all,

We would like to thank you for these constructive, building, and improvable comments on this manuscript that would improve the substance and content of the manuscript. We considered each comment and clarification questions of editors and reviewers on the manuscript thoroughly. Our point-by-point responses for each comment and question are described in detail on the following pages.

Response to Editors

1. Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

Authors’ response: Thank you for the comments. We have checked the references and it is correctly presented.

Response to reviewers

Minor issues to be addressed

1. Line 49 Being small size at birth should be included with the factors that were associated with increased odds of stunting, not those associated with a decreased odd as the AOR is greater than 1 (AOR=1.35, 95% CI: 1.29, 1.40).

Authors’ response: Thank you for the comments. We included with the factors that were associated with increased odds of stunting. (See Abstract section line 48, page 2)

2. 2. Line 55 How are ‘multiple births’ a modifiable factor unless a woman is having fertility treatment? The conclusions in your abstract should be consistent with the conclusions in your main paper on page 15

Authors’ response: Thank you for the comments. We rewrote it. (See Abstract section, line 53-57, page 3)

3. Line 60 you have misquoted reference 3. It is the first 1000 days ‘post conception’ NOT ‘after birth’

Authors’ response: Thank you for the comments. We rewrote it. (see Background section, line 61, page 4)

4. Line 304-305 The way in which you have worded this sentence makes it sound as though ‘health facility delivery and ANC visit’ are associated with an increased risk of chronic malnutrition and NOT that they are protective of chronic malnutrition. I suggest rewording this sentence

‘In our study, health facility delivery and ANC visit were protective of child chronic malnutrition.’

Authors’ response: Thank you for the suggestions. We accept it and revised the sentence. (See Discussion section, line 302-303, page 14)

5. Table 3 please include a footnote explaining the meaning of the asterisks. Also I recommend that you included a footnote to explain that the table includes only those variables for which the bi-variable analysis had a p <0.20, otherwise readers may wonder why some of the variables listed in Table 1 are not included in Table 2, (as I was).

Authors’ response: Thank you for the comments. We included the points you raised. (See Table 3)

Grammatical errors

6. line 34 should read ‘Variables’ (plural)

7. line 37 should read ‘were reported for significant factors’

8. Line 45 2nd -4th birth order

9. line 72 the word half is a collective noun and is treated as a singular. Therefore this should read ‘More than half …… is due ….’

10. line 84 the word ‘to’ is not needed, should read ‘… children include residence…..’

11. Line 89 should read ‘ has declined from..’

12. Line 139 I suggest replacing the word ‘divided’ with ‘categorised’.

13. Line 149 should read ‘presented in a bar graph’.

14. Line 195 Given that the next paragraph describes the multivariable mixed-effect logistic regression analysis, shouldn’t this subheading read ‘The mixed effect results’?

15. Lines 260 to 262 should read ‘Besides, educated women are more likely to exclusively breastfeed for….”

16. Line 266 suggest rewording this sentence ‘Children who live in poor households typically have poor access to adequate food, safe water, and sanitation.’

Authors’ response: We thank you a lot for your extensive effort to improve our work. We accept all the abovementioned comments and revised the manuscript. (See the revised manuscript)

Attachment

Submitted filename: Point by point response.docx

Decision Letter 2

Jane Anne Scott

3 Mar 2021

Pooled prevalence and associated  factors of chronic undernutrition among under-five children in East Africa: A multilevel analysis

PONE-D-20-18977R2

Dear Dr. Tesema,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

Kind regards,

Jane Anne Scott, PhD, MPH Grad Dip Dietetics, BSc

Academic Editor

PLOS ONE

Acceptance letter

Jane Anne Scott

17 Mar 2021

PONE-D-20-18977R2

Pooled prevalence and associated  factors of chronic undernutrition among under-five children in East Africa: A multilevel analysis

Dear Dr. Tesema:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Jane Anne Scott

Academic Editor

PLOS ONE

Associated Data

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

    Supplementary Materials

    Attachment

    Submitted filename: PONE-D-20-18977_reviewer.docx

    Attachment

    Submitted filename: Point by point response.docx

    Attachment

    Submitted filename: Point by point response.docx

    Data Availability Statement

    The data used in this study are from the Measure DHS program (www.dhsprogram.com) and can be accessed following the protocol outlined in the Methods section.


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