Abstract
Background
Undernutrition can lead to impaired physical growth, restricted intellectual skills, low school performance, reduced working capacity, and rooted disability in adult life. Thus, this study was designed to assess the prevalence and associated factors of undernutrition among children aged 6 to 59 months.
Methods
A community-based cross-sectional study was conducted among 432 children aged 6 to 59 months in the Menz Gera Midir District. A multi-stage sampling technique was applied to recruit the study participants. Socio-demographic and socio-economic variables were collected by using structured questionnaires. Anthropometric measurements of the children were measured according to the World Health Organization’s recommendation. A data collection sheet was used to collect information on the types of foods and number of meals consumed by the child. A bivariable and multivariable logistic regression was performed to identify factors associated with undernutrition.
Result
In this study, about 11.3% (95% CI: 8.3–14.3%), 50.2% (95% CI: 45.5–55.0%), and 28% (95% CI: 23.8–32.3%) were wasted, stunted, and underweight, respectively. Children aged 12–23 months (AOR: 1.97; 95% CI: 1.01–3.87), 36–47 months (AOR: 2.05; 95% CI: 1.00–4.19), and being anemic (AOR: 2.92; 95% CI: 1.73–4.92) were found to be an independent predictor of stunting. Moreover, being anemic was found to be significantly associated with wasting (AOR: 6.84; 95% CI: 3.16–14.82).
Conclusion
According to the findings of this study, undernutrition was a serious public health issue among 6–59 month old children in the Menz Gera Midir District. Children’s age and anemia status were significantly associated with stunting and wasting. Therefore, community-based nutrition programs are vital to reduce childhood undernutrition
Background
Malnutrition is a global public health issue that affects every country [1]. It is caused by unbalanced diets that lack all the necessary nutrients (macronutrients and micronutrients), a condition called undernutrition. It is also caused by excessive consumption of nutrients, which is called "over nutrition" [2,3].
Undernutrition can be classified as stunting, wasting, and being underweight. Stunting is characterized by low height-for-age (HAZ) and is the result of long-term nutritional deficiency. Wasting is low weight-for-height (WHZ), which indicates short-term poor nutritional status. On the other hand, underweight is a low weight-for-age (WAZ) that shows reduced public situations in both the long and short term [4]. Undernutrition has both short-term and long-term consequences. Of these consequences, child undernutrition could cause decreased physical growth, restricted intellectual skills, low academic performance, reduced working ability at maturity, lead to chronic illness and disability in adult life, and affect national economic growth [5] Also, there is an increased risk of cardiovascular disease, diabetes mellitus, cancer, and mental health issues in adulthood [6].
Globally, about 8–11 million preschool children die each year, and more than 35% of these deaths are due to undernutrition [4]. According to the 2020 World Health Organization (WHO) report, about 149 million children under 5 were stunted, 45 million were wasted, and 38.9 million were overweight globally [7]. Undernutrition contributes to more than 50% of the child mortality rate in developing nations [5]. Furthermore, Asia and Africa were the most heavily impacted by wasting [8]. The levels of wasting and stunting in preschool children have become the highest problem in developing countries like Ethiopia [9]. Data from the Ethiopia demographic and health survey (EDHS) in 2019 showed that the prevalence of stunting, wasting, and underweight in preschool children was 38%, 10%, and 24%, respectively [10].
Studies on the associated factors of undernutrition showed that being male, parents with lower educational level, families with poor socioeconomic status, paternal occupation type, living in a large family size, having more than two offspring, children having non-breast milk feeding practice, children who had diarrhea, children whose mother had never visited an antenatal clinic, children who received butter as pre-lacteal feeding, the family did not follow family planning, and using an unprotected water source for drinking were some of the predictors of undernutrition [11–20].
Undernutrition is still a high-magnitude problem in developing countries. However, there is limited data regarding the nutritional status of preschool children in the Menz Gera Midir District. Therefore, this study was aimed at determining the prevalence and associated factors of undernutrition among preschool children in Menz Gera Midir District. As a result, researchers specializing in child health and nutrition, health policymakers, and other undernutrition experts will benefit from this study.
Materials and methods
Study setting, design and period
A community-based cross-sectional study was done in the Menz Gera Midir district from January to May 2017. The Menz Gera Midir district is located in the North Shewa zone of the Eastern Amhara Region of Ethiopia. The administrative center of the district is Mehal Meda town. The town has an elevation of 3037 meters above sea level with a latitude and longitude of 10018172 N/390 312. Based on the central statistics agency of Ethiopia, the district has a total population of 138,708 people, of whom 67,567 are men and 16,361 are urban inhabitants [21]. Approximately 46,235 households are found within the 28 smallest administrative units of the district. Of these, 5453 are urban households. In 2020, there were 13,422 children under the age of five [22].
Study population
All children aged 6–59 months residing in Menz Gera Midir District were taken as a source population, whereas children aged 6–59 months in Menz Gera Midir District who volunteered to participate during the study period were considered as a study population. Children aged 6–59 months residing in the selected smallest administration unit for at least 6 months and whose parents/guardians were willing to fully participate in the study were included in this study. On the other hand, children with mental illnesses and severely ill children who could not give a response were excluded from the study.
Study variables
In this study, wasting, stunting, and underweight were considered as dependent variables. While socio-demographic characteristics of preschool children (age group, sex) and respective parents/caregivers such as the mother’s sex, education, religion, marital status, occupation, family size, place of residence, socioeconomic status of the households, presence of anemia, intestinal infection, access to clean water, use of a toilet, vitamin A supplementation, vaccination status, and duration of breastfeeding practice of the mother were taken as independent variables.
Sample size determination and sampling technique
A single population proportion formula was used to decide the sample size, and the expected prevalence of undernutrition was set at 25%, taken from Menz Keya [23], and the marginal error (d) of 5% and a 95% confidence interval were used to calculate the sample size. Furthermore, considering the affordable resources for the investigations, a design effect of 1.5 was applied, and the final sample size became 432. A multi-stage sampling technique was used to assess the prevalence of undernutrition in children aged 6–59 months. First, from all the smallest administrative units, about 25% were selected, which is seven, and then, from seven, one from urban and six from rural areas were recruited by a simple random sampling technique. In the second stage, a proportional sample allocation was applied to seven of the smallest administrative units, and a systematic sampling technique was used to select the total study participants. During the systematic sampling technique, the first study participant was selected by the lottery method, and the next study participant was selected by using the Kth interval. If there were two or more eligible children in the household, we used only one child by using the lottery method. If the selected household is closed, we returned to the household for a second visit, and if it is closed again, we moved on to the next household.
Operational definitions
Anemia: When hemoglobin (Hgb) level is less than 11g/dl for both sex [24,25]
Mildly undernutrition: when weight for height/length is between -1SD and 1SD
Moderately undernutrition: weight for height/length is between -2SD and -3SD with no edema
Severely undernutrition: the presence of edema of both feet, or severe wasting or both (weight for height/length ≤ -3SD)
Anthropometric indices: these are calculated from anthropometric measurements of weight, height and age
Stunting: When young children have a low HAZ <-2SD
Underweight: When children are too light for their age (WAZ) <-2SD
Data collection procedures and laboratory methods
Household demographic and socio-economic data collection
The socio-demographic data of children (age, sex, residence, delivery status, birth order, and vaccination status) and socio-demographic and socio-economic data of the parents or caretakers of the child (age, sex, household wealth, occupation, religion, and marital status) were collected by a questionnaire which was prepared from the national survey and accordingly modified based on the reviewed literature [26]. In addition, food and nutritional technical assistance, the Helen Keller international food frequency questionnaire, and a 24-hour dietary recall questionnaire were used to assess household food security, food consumption pattern, and dietary diversity scores [27–29]. The questionnaire has five sections which contain socio-demographic, breastfeeding practices, household wealth index related questions, food and dietary frequency related questions, and questions on morbidity and vaccination data of the child. To complete this questionnaire, about 15 to 20 minutes are required.
Food consumption patterns
A qualitative household food security and dietary diversity score questionnaire was used to collect information on the types of foods and number of meals consumed by the index child over the past 24 hours. Probing questions were used to get information on the food types consumed, ingredients used to prepare meals, the type of snacks used, and the number of times the child ate the particular food within 24 hours of recall [30].
Anthropometric data for nutritional status
Anthropometric measurements such as children’s weight and height, as well as their mid-upper arm circumference (MUAC), were taken in accordance with a WHO recommendation from 2006 [31]. Children’s weight was measured through light-weight wear. The weight of children aged 24–59 months was measured to the nearest 0.1 kg by beam balance. For children aged less than 24 months, weight was measured to the nearest 0.1 kg using the Salter scale. A measuring board was used to measure the length and height; the height of children aged 6–23 months was measured in a recumbent position to the nearest 0.1 cm, while the height of children aged 24–59 months was measured to the nearest 0.1 cm while standing straight on a horizontal surface with their heels together and eyes straight forward. Anthropometric data from children was entered into the WHO Anthro software version 3.2.2.1. The WHO multi-center growth reference standards for the Z-scores of indices, such as WAZ, WHZ, and HAZ, were calculated. The children were classified as stunted, underweight, and wasted when their HAZ, WAZ, and WHZ scores were less than 2 SD from the median of the reference population, respectively [24].
Sample collection and laboratory investigation
Measurement of Hgb. Blood samples from capillary blood were sampled from all preschool children and the Hgb value was determined by a Hemocue analyzer (Hb 301+, Norway), which is recommended by WHO to measure population anemia prevalence [32]. The study area was located > 1000 m above sea level, and the results of Hgb were adjusted to its respective sea level (altitude) as recommended by WHO [25].
Stool examinations. Stool samples were collected from each study participant. Stool samples were labeled, clean, leak-proof containers. The wet mount was done with normal saline and direct microscopy was observed by using a light microscope. A formal ether concentration technique was performed for further parasitic detection.
Data management and quality control
The questionnaire, which was originally developed in English, was translated into the Amharic language and back-translated into English to ensure its consistency. Then the questioner was pretested by Dija’s smallest administration unit. Training was given for the data collectors on data recording, handling, and managing. The completeness and legibility of every questionnaire were checked daily by the principal investigator.
The weight measurement scales were adjusted daily (using standardized weighing grams) before use. All the measurements of weight and height were taken twice, and the average weight was taken. The cleanliness of microscope lenses (eyepiece and objective) was maintained by performing daily cleaning. Anthropometric measurements were taken twice, and the average of the two was taken.
Appropriate labeling, storage, packaging, and transportation methods and daily internal quality control with the known results that were available in the laboratory were implemented before use in and out of the laboratory. Recommended containers and collection procedures were employed. For delayed samples, an appropriate preservative (10% formalin for stool) was used for stability. A sample of inappropriate preservatives, transportation media, and temperature, and inadequate volume was rejected.
Data processing and analysis
Firstly, data was entered and stored using EPI-info version 7 and checked for consistency. The data was sorted and cleaned before being exported to the Statistical Package for Social Sciences (SPSS) version 25 for further analysis. Also, WHO Anthro software version 3.2.2.1 was used for anthropometric indices. Descriptive statistics such as frequencies, means, medians, and standard deviations were used to summarize the characteristics of the study participants. To identify factors associated with undernutrition a bivariable and multivariable logistic regression was performed. The bivariable logistic regression analyses were done to determine factors associated with wasting, stunting, and underweight. Predictor variables having a p-value less than or equal to 0.2 in the bivariable analysis were included in the multivariable analysis to control the confounders. A Hosmer-Lemeshow goodness-of-fit test was used to assess the model’s fitness. The crude odds ratio (COR) and adjusted odds ratio (AOR), along with the 95% confidence interval (CI), were used to determine the strength of association between the predictors and dependent variables. Variables with a p-value of less than 0.05 were considered statistically significant.
Ethical considerations
Ethical clearance and approval was granted by the University of Gondar, College of Medicine and Health Sciences, School of Biomedical and Laboratory Sciences Ethical Review Committee (Reference number SBMLS/625/09). A permission letter was also obtained from the district health office and each village administrative office. The purpose of the research was explained to the study subjects and written informed consent was obtained from the mother or guardian of the child, and then those who were willing to participate were included in the study. Participation was fully voluntarily and refusal at any time during data collection was permitted. Information obtained in any course of study was kept confidential. Confidentiality was maintained by numeric coding of questionnaires. Any abnormal findings were linked to the nearby health center. Additionally, when the hemoglobin level of the children was below 11 g/dL, their mothers/care givers were informed to take them to a health facility for follow-up care.
Results
Child socio-demographic and health related characteristics
In this study, a total of 432 households, 390 (90.3%) from rural areas and 42 (9.7%) from urban areas, were included. Of them, 227 (52.5%) and 27 (6.3%) were females from rural and urban residences, respectively. The median age of the children was 24, IQR (14–42) months, with a median of the birth interval from their preceding elders, IQR (14–42). Moreover, 41 (9.5%) and 210 (48.6%) of the children were positive and negative for parasite infection, respectively, whereas 181 (41.9%) of the children were not assessed for parasitic infection. Concerning the anemia status of the children, 123 (28.5%) of the children were anemic (Table 1).
Table 1. Socio-demographic and health related characteristics of children aged 6 to 59 months in the Menz Gera Midir district Northeast Ethiopia in 2021, (N = 432).
| Variables | Category | Frequency (n) | Percentage (%) |
|---|---|---|---|
| Sex | Male | 178 | 41.2 |
| Female | 254 | 58.8 | |
| Age (months) | 6–11 | 90 | 16.7 |
| 12–23 | 107 | 25.0 | |
| 24–35 | 70 | 17.1 | |
| 36–47 | 76 | 18.8 | |
| 48–59 | 89 | 22.5 | |
| Place of Child Birth | Health Facility | 297 | 68.8 |
| Home | 136 | 31.2 | |
| Delivery Status | Post term | 0 | 0 |
| Term | 425 | 98.4 | |
| Preterm | 7 | 1.6 | |
| Nutritional Status (MUAC) | ≥ 13.5cm | 167 | 38.7 |
| < 13.5cm | 265 | 61.3 | |
| Vaccination Status | Not vaccinated | 5 | 1.2 |
| Partially Vaccinated | 58 | 13.4 | |
| Fully Vaccinated | 369 | 85.4 | |
| History of illness in two weeks | Yes | 17 | 3.9 |
| No | 415 | 96.1 | |
| Intestinal parasites (n = 251) | Positive | 35 | 13.9 |
| Negative | 215 | 86.1 | |
| Anemia status of child | Anemic | 123 | 28.5 |
| Non-anemic | 309 | 71.5 |
Parental socio-demographic, health related and economic characteristics
Of the total respondents, almost all (98.8%) were Orthodox, whereas the remaining 0.9% and 0.3% were Protestant and Muslim religion followers, respectively. In addition, the majority (402, or 93%) of the mother respondents were married. Regarding paternal educational status, more than one-third (158; 36.6%) of the mothers cannot read and write. Moreover, 411 (95.2%) of them were housewives. Economically, nearly half of the households are classified in the lower socio-economic class. The median household size in rural and urban areas was 5, IQR (4–6) and 4, IQR (3–5) people per household, respectively. Of the total rural study participants, 134 (34.4%) did not have access to clean drinking water, but all urban respondents did. Concerning the defecation system, 376 (96.4%) of the rural and 42 (100%) of the urban respondents use traditional pit latrines and improved well-ventilated toilets, respectively. Around 72.9% of the total households suffered from household food insecurity, and almost half (49.5%) of them consumed 4–6 food groups per day (Table 2).
Table 2. Socio- demographic, health related and economic, characteristics of care givers in the Menz Gera Midir district Northeast Ethiopia in 2021, (N = 432).
| Variable | Category | Frequency (n) | Percentage (%) |
|---|---|---|---|
| Sex of the child care giver | Female | 420 | 97.2 |
| Male | 12 | 2.8 | |
| Residence | Rural | 390 | 90.3 |
| Urban | 42 | 9.7 | |
| Religions | Orthodox | 427 | 98.8 |
| Others | 5 | 1.2 | |
| Relationship of the care giver to the child | Mother | 414 | 95.8 |
| Father | 12 | 2.8 | |
| Others | 6 | 1.4 | |
| Marital Status | Married | 402 | 93.0 |
| Divorced | 25 | 5.8 | |
| Single | 5 | 1.2 | |
| Sex of the head of the household | Male | 406 | 93.99 |
| Female | 26 | 6.01 | |
| Occupation of Mother | Housewife | 411 | 95.2 |
| Government employed | 14 | 3.2 | |
| Merchant | 7 | 1.6 | |
| Father’s Occupation | Farmer | 365 | 84.5 |
| Governmental Employee | 22 | 5.1 | |
| Labor | 19 | 4.4 | |
| Merchant | 26 | 6.0 | |
| Maternal Educational status | No Education | 158 | 36.6 |
| Primary School | 155 | 35.9 | |
| Secondary completed | 98 | 22.7 | |
| Higher Education Completed | 21 | 4.9 | |
| Father’s Educational status | No Education | 94 | 21.8 |
| Primary School | 191 | 44.2 | |
| Secondary completed | 125 | 28.9 | |
| Higher Education complete | 22 | 5.1 | |
| Wealth quintile | Higher | 64 | 14.8 |
| Medium | 164 | 38.0 | |
| Lower | 204 | 47.2 | |
| Family size in the household | < = 3 | 98 | 22.7 |
| 4–6 | 275 | 63.7 | |
| > = 7 | 59 | 13.6 | |
| Type of toilet used | Traditional Pit latrine | 376 | 87.0 |
| Ventilated improved latrine | 44 | 10.2 | |
| Others | 12 | 2.8 | |
| Access to clean drinking water | Yes | 298 | 69 |
| No | 134 | 31 | |
| Household Food Security (HHFS) | Food Secured | 117 | 27.1 |
| Food in secured | 315 | 72.9 | |
| Household Dietary Diversity Score | 0–3 food groups | 188 | 43.5 |
| 4–6 food groups | 214 | 49.5 | |
| 7–8 food groups | 30 | 6.9 | |
| > = 9 food groups | 0 | 0.0 |
Prevalence of undernutrition
From the total of 432 children, 11.3% (95% CI: 8.3–14.3%), 50.2% (95% CI: 45.5–55.0%), and 28% (95% CI: 23.8–32.3%) were wasted, stunted, and underweight, respectively (Fig 1).
Fig 1. Prevalence of under-nutrition among children aged 6 to 59 months in Menz Gera Midir District, Northeast Ethiopia, in 2021 (N = 432).
Factors associated with undernutrition
In bivariable logistic regression analysis, sex of the child, age of the child, anemia status of the child, the severity of food insecurity, and anemia status of the mother were significantly associated with stunting with a p-value of less than 0.2. Hence, these variables were fitted into a multivariable logistic regression model. However, only child age and child anemia remained significantly associated with stunting. The odds of stunting among children aged 12–23 and 36–47 months were 1.97 (95% CI: 1.01–3.87) and 2.05 (95% CI: 1.00–4.19) compared to children aged 6–11 months, respectively. Anemic children were 2.92 (95% CI: 1.73–4.92) times more likely to be stunted compared to non-anemic children (Table 3).
Table 3. Bivariable and multivariable logistic regression analysis of stunting among children aged 6 to 59 months in the Menz Gera Midir district Northeast Ethiopia in 2021, (N = 432).
| Variable | Category | Stunting n (%) | COR (95% CI) | AOR (95% CI) | P value |
|---|---|---|---|---|---|
| Sex | Female | 121 (47.6) | 1 | 1 | 0.112 |
| Male | 96 (53.9) | 1.28 (0.71–1.89) | 1.40 (0.92–2.13) | ||
| Age of the child | 6–11 | 33 (45.8) | 1 | 1 | |
| 12–23 | 43 (39.8) | 1.54 (0.84–2.86) | 1.97 (1.01–3.87) | 0.048 | |
| 24–35 | 41 (56.9) | 1.39 (0.74–2.63) | 1.68 (0.85–3.35) | 0.138 | |
| 36–47 | 45 (54.2) | 1.56 (0.81–3.03) | 2.05 (1.00–4.19) | 0.05 | |
| 48–59 | 55 (56.7) | 0.78 (0.43–1.43) | 0.82 (0.43–1.56) | 0.546 | |
| Residence | Rural | 199 (51.0) | 1.39 (0.73–2.64) | - | 0.314 |
| Urban | 18 (42.9) | 1 | - | ||
| Child anemia status | Anemic | 79 (64.2) | 2.23 (1.45–3.43) | 2.92 (1.73–4.92) | <0.001 |
| Non-anemic | 138 (44.7) | 1 | 1 | ||
| Family size | ≤3 | 48 (49.0) | 1 | - | |
| 4–6 | 141 (51.3) | 1.10 (0.69–1.74) | - | 0.697 | |
| ≥7 | 28 (47.5) | 0.94 (0.49–1.80) | - | 0.853 | |
| Care giver sex | Female | 211 (50.2) | 1 | - | 0.853 |
| Male | 6 (50.0) | 0.99 (0.31–3.12) | - | ||
| Age of the mother | ≤30 | 143 (48.3) | 1 | 0.239 | |
| >30 | 74 (54.4) | 1.23 (0.85–1.92) | |||
| Food security | Secured | 64 (54.7) | 1 | - | 0.258 |
| Insecure | 153 (48.6) | 0.78 (0.51–1.20) | - | ||
| Dietary diversity score | ≤3 | 96 (51.1) | 1 | - | |
| 4–6 | 108 (50.5) | 0.73 (0.34–1.59) | - | 0.433 | |
| ≥7 | 13 (43.3) | 0.98 (0.66–1.45) | - | 0.905 | |
| Anemia status of the mother | Anemic | 60 (60.6) | 1.67 (1.05–2.64) | 1.28 (0.76–2.13) | 0.353 |
| Non-anemic | 146 (48.0) | 1 | 1 | ||
| Wealth index | Low | 68 (47.2) | 1 | - | |
| Medium | 71 (49.3) | 1.32 (0.83–2.10) | - | 0.239 | |
| High | 78 (54.2) | 1.09 (0.69–1.73) | - | 0.724 | |
| Mother occupation | Housewife | 206 (50.1) | 1 | - | 0.840 |
| Others | 11 (52.4) | 1.10 (0.46–2.63) | - | ||
| Mother educational status | No formal education | 157 (50.2) | 1 | - | |
| Certificate/ diploma | 50 (51.0) | 1.04 (0.66–1.63) | - | 0.882 | |
| Degree and above | 10 (47.6) | 0.90 (0.37–2.19) | - | 0.822 | |
| Marital status | Married | 203 (50.5) | 1.17 (0.55–2.45) | - | 0.686 |
| Single/Divorce | 14 (46.7) | 1 | - | ||
| Parasite infection | Positive | 18 (43.9) | 1 | ||
| Negative | 109 (51.9) | 1.38 (0.70–2.71) | - | 0.350 | |
| Illness in the past 2 weeks | Yes | 9 (52.9) | 1.12 (0.41–2.96) | - | 0.820 |
| No | 208 (50.1) | 1 | - | ||
| Birth order | 1–2 | 120 (48.2) | 1 | - | 0.323 |
| ≥3 | 97 (53.0) | 1.21 (0.83–1.78) | - |
Note: AOR; Adjusted Odds Ratio, CI; Confidence Interval, COR; crude Odds Ratio.
On the other hand, in the bivariable logistic regression model, child anemia, family size, severity of household food insecurity, and anemia status of the mother/caregiver were predictors of wasting with a p-value of less than 0.2. However, in the multivariable logistic regression model, only child anemia was found to be significantly associated with wasting. The odds of wasting were 6.84 (95% CI: 3.16–14.82) times more likely in anemic children compared to non-anemic children (Table 4).
Table 4. Bivariable and multivariable logistic regression analysis of wasting among children aged 6 to 59 months in the Menz GeraMidir district Northeast Ethiopia in 2021, (N = 432).
| Variable | Category | Wasting n (%) | COR (95% CI) | AOR (95% CI) | P value |
|---|---|---|---|---|---|
| Sex | Female | 26 (10.2) | 1 | 1 | 0.387 |
| Male | 23 (12.9) | 1.30 (0.72–2.36) | - | ||
| Age of the child | 6–11 | 8 (11.1) | 1 | - | |
| 12–23 | 16 (14.8) | 1.13 (0.44–2.93) | - | 0.802 | |
| 24–35 | 4 (5.6) | 0.97 (0.36–2.67) | - | 0.958 | |
| 36–47 | 9 (10.8) | 0.47 (0.14–1.64) | - | 0.236 | |
| 48–59 | 12 (12.4) | 1.39 (0.56–3.45) | - | 0.475 | |
| Residence | Rural | 45 (11.5) | - | Fisher exact | 1 |
| Urban | 4 (9.5) | - | - | ||
| Child anemia status | Anemic | 33 (26.8) | 6.72 (3.53–12.76) | 6.84 (3.16–14.82 | <0.001 |
| Non-anemic | 16 (5.2) | 1 | 1 | ||
| Family size | ≤3 | 15 (15.3) | 1 | 1 | 0.099 |
| 4–6 | 24 (8.7) | 0.53 (0.27–1.06) | 0.52 (0.24–1.13) | ||
| ≥7 | 10 (16.9) | 1.13 (0.47–2.71) | 1.60 (0.60–4.32) | 0.351 | |
| Care giver sex | Female | 48 (11.4) | - | Fisher exact | 1 |
| Male | 1 (8.3) | - | - | ||
| Age of the mother | ≤30 | 33 (11.1) | 1 | - | 0.851 |
| >30 | 16 (11.8) | 1.06 (0.56–2.01) | - | ||
| Food security | Secured | 11 (9.4) | 1 | - | 0.439 |
| Insecure | 38 (12.1) | 1.32 (0.65–2.68) | - | ||
| Dietary diversity score | ≤3 | 23 (12.2) | 1 | - | 0.901 |
| 4–6 | 23 (10.7) | 1.08 (0.31–3.86) | - | ||
| ≥7 | 3 (10.0) | 1.26 (0.35–4.47) | - | 0.726 | |
| Anemia status of the mother | Non-anemic | 24 (7.9) | 1 | 1 | 0.504 |
| Anemic | 19 (19.2) | 2.77 (1.45–5.31) | 1.30 (0.61–2.76) | ||
| Wealth index | Poor | 19 (13.2) | 1 | - | |
| Medium | 14 (9.4) | 0.82 (0.41–1.67) | - | 0.589 | |
| Rich | 16 (11.1) | 0.71 (0.34–1.47) | - | 0.357 | |
| Mother occupation | Housewife | 45 (10.9) | - | Fisher exact | 0.280 |
| Others | 4 (19.0) | - | - | ||
| Mother educational status | No formal education | 35 (11.2) | - | Fisher exact | 0.884 |
| Certificate/ diploma | 11 (11.2) | - | - | ||
| Degree and above | 3 (14.3) | - | - | ||
| Marital status | Married | 47 (11.7) | - | Fisher exact | 0.558 |
| Single/Divorce | 2 (6.7) | - | - | ||
| Parasite infection | Positive | 2 (4.9) | - | Fisher exact | 0.155 |
| Negative | 21 (10.0) | - | - | ||
| Illness in the past 2 weeks | Yes | 2 (11.8) | - | Fisher exact | 0.595 |
| No | 47 (11.3) | - | - | ||
| Birth order | 1–2 | 1 | - | 0.590 | |
| ≥3 | 0.85 (0.46–1.56) | - |
Note: AOR; Adjusted Odds Ratio, CI; Confidence Interval, COR; crude Odds Ratio.
In bivariable logistic regression analysis of factors associated with underweight, age of the child, residence, child anemia status, family size, and age of mother/caregiver, anemia status of the mother, wealth index, and parasite infection were predictors of underweight at p-value less than 0.2. However, in multivariable logistic regression, controlling for the cofounder, all of the predictors were not statistically associated with underweight (Table 5).
Table 5. Bi-variable and multi-variable logistic regression of underweight among children aged 6 to 59 months in the Menz Gera Midir district Northeast Ethiopia in 2021, (N = 432).
| Variable | Category | Underweight n (%) | COR (95% CI) | AOR (95% CI) | P value |
|---|---|---|---|---|---|
| Sex | Female | 74 (29.1) | 1 | - | 0.534 |
| Male | 47 (26.4) | 0.87 (0.57–1.34) | - | ||
| Age of the child | 6–11 | 24 (33.3) | 1 | 1 | |
| 12–23 | 31 (28.7) | 0.81 (0.42–1.53) | 0.77 (0.39–1.54) | 0.461 | |
| 24–35 | 19 (26.4) | 0.72 (0.35–1.47) | 0.87 (0.40–190) | 0.718 | |
| 36–47 | 26 (31.3) | 0.91 (0. 47–1.79) | 1.03 (0.49–2.16) | 0.0.939 | |
| 48–59 | 21 (21.6) | 0.55 (0.28–1.10) | 0.75 (0.35–1.58) | 0.455 | |
| Residence | Rural | 114 (29.2) | 1 | 1 | 0.245 |
| Urban | 7 (16.7) | 0.48 (0.21–1.12) | 0.59 (0.24–1.44) | ||
| Child anemia | Non-anemic | 72 (23.3) | 1 | 1 | 0.062 |
| Anemic | 49(39.8) | 2.18 (1.39–3.41) | 1.68 (0.98–2.88) | ||
| Family size | ≤3 | 32 (32.7) | 1 | 1 | 0.207 |
| 4–6 | 68 (24.7) | 0.88 (0.45–1.73) | 0.69 (0.39–1.23) | ||
| ≥7 | 21 (35.6) | 0.59 (0.33–1.08) | 1.50 (0.67–3.32) | 0.323 | |
| Care giver sex | Female | 119 (28.3) | - | Fisher exact | 0.523 |
| Male | 2 (16.7) | - | - | ||
| Age of the mother | ≤30 | 92 (31.1) | 1 | 1 | 0.099 |
| >30 | 29 (21.3) | 0.60 (0.37–0.97) | 0.62 (0.35–1.10) | ||
| Food security | Secured | 31 (26.5) | 1 | - | 0.669 |
| Insecure | 90 (28.6) | 1.11 (0.60–1.79) | - | ||
| Dietary diversity score | ≤3 | 51(27.1) | 1 | - | |
| 4–6 | 59 (27.6) | 0.66 (0.30–1.46) | - | 0.305 | |
| ≥7 | 11(36.7) | 0.64 (0.29–1.44) | - | 0.285 | |
| Anemia status of the mother | Anemic | 33 (33.3) | 1.45(0.88–2.37) | 1.20 (0.69–2.09) | 0.520 |
| Non-anemic | 78 (25.7) | 1 | 1 | ||
| Wealth index | Poor | 48 (33.3) | 1.50 (0.90–2.50) | 1.08 (0.58–2.03) | 0.808 |
| Medium | 37 (25.7) | 1.04 (0.61–1.76) | 0.90 (0.50–1.65) | 0.744 | |
| Rich | 36 (25.0) | 1 | 1 | ||
| Mother occupation | Housewife | 115 (28.0) | 1 | - | 0.953 |
| Others | 6 (28.6) | 1.03 (0.39–2.72) | - | ||
| Mother educational status | No formal education | 93 (29.7) | 1.06 (0.40–2.81) | - | 0.912 |
| Certificate/ diploma | 22 (22.4) | 0.72 (0.25–2.09) | - | 0.549 | |
| Degree/above | 6 (28.6) | 1 | - | ||
| Marital status | Married | 113 (28.1) | 1 | - | |
| Single/Divorce | 8 (26.7) | 1.08 (0.47–2.49) | - | 0.856 | |
| Parasite infection | Yes | 9 (22.0) | 1 | 1 | 0.903 |
| No | 52 (24.8) | 1.70 (0.52–2.61) | 1.06 (0.45–2.50) | ||
| Illness in the past 2 weeks | Yes | 2 (11.8) | Fisher exact | 0.101 | |
| No | 119 (28.7) | - | - | ||
| Birth order | 1–2 | 74 (29.7) | 1 | - | 0.356 |
| ≥3 | 47 (25.7) | 0.82 (0.53–1.26) | - |
Note: AOR; Adjusted Odds Ratio, CI; Confidence Interval, COR; crude Odds Ratio.
Discussion
To prevent the health complications of under five children attributable to undernutrition, it is important to assess the prevalence of undernutrition and factors associated with its prevalence. Therefore, the main objective of this study was to determine the prevalence of undernutrition and assess associated factors among under-five children. The finding revealed that the prevalence of stunting, wasting, and underweight was 50.2% (95% CI: 45.5–55.0%), 11.3% (95% CI: 8.3–14.3%), and 28% (95% CI: 23.8–32.3%), respectively. The findings were high, which revealed that undernutrition is still a public health problem in Ethiopia, especially in the Amhara region. According to the 2016 EDHS report, undernutrition was a public health problem in the Amhara region [33].
The prevalence of stunting (50.2%) among children aged 6–59 months in this study was comparable with the results of other similar studies conducted in Hawassa, southern Ethiopia (53.1%) [34], Bule Hora district, South Ethiopia (47.6%) and Ilu Abba Bora Zone, Southwest Ethiopia (50.8%) [35]. It was also in line with the findings in India; Madhya Pradesh, Jabalpur (51.6%) [36] and Rajasthan, Jodhpur districts (53%) [37]. However, the finding was higher than other studies conducted in east Gojjam, northwest Ethiopia (44.7%) [38], slum areas of Gondar city, northwest Ethiopia (42.3%) [39], Somali region, eastern Ethiopia (27.4%) [40], Jimma, Southwest Ethiopia (21.8%), [2] orphanage centers, and Addis Ababa, Ethiopia (34.8%) [41]. Moreover, it was higher than other east African countries, including Tanzania; Kilosa District (41.0%) [42] and Rwanda; Ngoma District (33.7%) [43]. It was 6–13 times higher than the studies conducted in China [44–46]. It was also higher than the study conducted in central India (34.8%) [47] and the city of Maharashtra, India (40.5%) [48] and Roma, Italy (11.7%) [49]. On the other hand, the current finding was lower than studies done in Dabat District, northwest Ethiopia (64.5%) [50], and East Belesa District, northwest Ethiopia (57.7%) [51]. The possible reasons for this variation might be socio-demographic and socio-economic differences and the difference in geographic settings. Socio-demographic and socio-economic status have an effect on the nutritional status of children [47,48,52]. Geographic location also affects the cultivation of food crops, which in turn affects access and availability of food for household consumption. The impact of geographical location could be because of environmental variability in the occupation practiced, which could influence food security and consequently affect child nutrition, growth and development. Geographic locations are also favorable for climatic conditions, which affect food production [53].
Previous studies showed that the prevalence of stunting was significantly associated with family size, wealth index, child age, food security, source of drinking water, and dietary diversity [35,54–57]. However, in the current study, only child age and child anemia status were significantly associated with stunting. Children aged 12–23 and 36–47 months were about 2 times more likely to be stunted compared to children aged 6–11 months (AOR; 1.97 (95% CI: 1.01–3.87) and 2.05 (95% CI: 1.00–4.19, respectively). The finding was in line with a study done in southern Ethiopia [54]. East African Districts (Rwanda’s Gicumbi District, Uganda’s Kitgum District, and Tanzania’s Kilindi District) [53], India [48] and China [45]. This might be because of a high prevalence of childhood stunting, which reflects undernutrition, starts in the first years of life (6–24 months) [58] and becomes worse at different phases of growth and results in short adult stature [59]. The older children undergo rapid growth, which creates a high demand for energy and other nutrients. Moreover, for older children, the only source of nutrients was complimentary foods, while the younger children benefited from both breast milk and complimentary foods. These factors might compromise the child’s nutritional status at this age [42]. An increased interaction of the older child with its immediate environment might also be the other reason. Environmental interaction leads to an increased risk of infections and exposure to childhood diseases either through drinking of unimproved water sources, consumption of contaminated foods, poor hygiene, or poor environmental sanitation [60].
The odds of stunting among anemic children were 2.92 times more likely compared to their counterparts. This finding was consistent with studies conducted in Ethiopia [33,61]. Undernourished children are more likely to suffer from inadequate bioavailability of micronutrients such as iron, vitamin B12, and folate, which are important for the formation of blood cells. Undernourished children are unable to produce as many blood cells as needed, leading to the development of nutritional deficiency anemia, which is common, particularly in developing countries [62].
In the current study, the prevalence of wasting (11.3%) was similar to studies conducted in Damot Gale district, south Ethiopia (9%) [63], Bule Hora district, South Ethiopia (13.4%) [4], and the east Gojjam zone, Northwest Ethiopia (10–11.3%) [38]. However, it was lower than other studies conducted in the Somali region, Ethiopia (22.7%) [33], Hawassa, Southern Ethiopia (28.2%) [34], East Belesa District, Northwest Ethiopia (16%) [51], North Sudan (21%) [64], Australia (15%) [65] and Maharashtra, India (16%-17.1%) [48,66]. On the other hand, the current finding was higher than studies conducted in Gondar Town, Northwest Ethiopia (6.8%) [67], slum areas of Gondar City, Northwest Ethiopia (7.3%) [39], orphanage centers, Addis Ababa, Ethiopia (4.4%) [41], Ngoma District, Rwanda (3.6%) [68], South Sudan (2.3%) [69], Italy (2.9%) [49], and China (2–4%) [44–46]. This might be due to the difference in the sample size, study setting, socio-demographic characteristics, socio-economic status, geographic location, and study period.
According to the previous studies, a number of determinants of wasting were identified. These include exclusive breast feeding, acute diarrhea [66], family size [46] presence of a fever in the previous 2 weeks [39] and illness in the last two weeks [41]. In the current study, only child anemia was found to be significantly associated with wasting. The odds of wasting were 6.84 times more likely in anemic children compared to their counterparts. The finding was in agreement with studies done in Menz Gera Midir district, Eastern Amhara, Ethiopia [70], and rural areas of Shaanxi, northwestern China [71]. Anemia and undernutrition often have common causes. Undernutrition and anemia have an interplaying association. Childhood anemia might occur as a result of a macro-nutrient deficiency or it precipitates the occurrence of under-nutrition owing to the poor synthesis of macronutrients. In other words, undernourished children more often suffer from inadequate availability of micronutrients such as iron, B12, and folate, which are important for erythropoiesis. Therefore, those children who are undernourished will have impaired production of adequate red blood cells as much as required. Consequently, this leads to the development of nutritional deficiency anemia [62,70,72].
This study also showed that the prevalence of underweight was 28%. This finding was consistent with other findings reported in the Damot-Galle district, south Ethiopia (27.6%) [63], Hawassa, Southern Ethiopia (28.2%) [34], Bule Hora district, South Ethiopia (29.2%) [4], and Kerala, India (28.3%) [73]. However, it was higher than the studies conducted in East Gojjam zone, Northwest Ethiopia (15.3%) [38], East Belesa District, northwest Ethiopia (16%) [51], Takusa district, Northwest Ethiopia (19.5%) [74], Jimma town, southwest Ethiopia (15.2%) [2], orphanage centers, Addis Ababa, Ethiopia (12.3%) [41], South Sudan (4.8%) [75], Ngoma District, Rwanda (6.6%) [68] and Kilosa District, Tanzania (11.5%) [42]. In contradiction, the result was lower than the studies conducted in urban slums and rural areas of Maharashtra, India (35.4%) and the urban slums of Pune (34.3%) [76]. Differences in socioeconomic, cultural, and child feeding patterns, seasonal variance in study time, and age group of the study population, study setting, and genetic factors could all contribute to the disparity.
According to this study, undernutrition is a community health problem in the Menz-Gera Midir district. Therefore, policies which are currently applied in the study area should be considered that children’s, specifically those who are aged 6 to 59 months, are highly affected by undernutrition, and they also need an advanced policy to eliminate undernutrition in the study area.
This study has its strength, which uses a concentration technique that helps to identify lower parasitic load. However, the major limitation of this study is that the micronutrient status of children was not measured (except anemia) and its real association with undernutrition was not known. Moreover, subclinical infections other than intestinal parasites were not assessed, which could limit the generalizability of the findings. Besides, as the study is cross-sectional, no causal link can be inferred.
Conclusion
In this study, undernutrition was a highly prevalent health problem among 6–59 month old children in the Menz Gera Midir District. This shows that early intervention, including community-based nutrition education programs and health programs, is vital to reduce childhood stunting, wasting, and being underweight, especially in the first 2 years of life. Childhood anemia and child age were linked to stunting. On the other hand, only anemia was a risk factor for wasting. As a result, community-based intervention and implementation should be strengthened in order to reduce the effect of anemia and the high burden of undernutrition among children under the age of five.
Acknowledgments
The authors would like to acknowledge Mehal Meda Hospital, the state of Amhara Health Bureau, and all the study participants.
Abbreviations
- AOR
Adjusted Odds Ratio
- COR
crude odds ratio
- EDHS
Ethiopian demographic health survey
- HAZ
Height for age
- Hgb
Hemoglobin
- MUAC
Mid-upper Arm Circumferences
- WAZ
weight-for-age
- WHZ
Weight for height
- WHO
World Health Organization
Data Availability
All data generated and/or analyzed in this study are available within the paper.
Funding Statement
The author(s) received no specific funding for this work.
References
- 1.Unicef. Improving child nutrition: the achievable imperative for global progress. New York: UNICEF. 2013:1–14. [Google Scholar]
- 2.Melese ST, Bedatu G, Kalkidan H. Prevalence of undernutrition and associated factors among preschool children in Jimma town, South West Ethiopia. African Journal of Food, Agriculture, Nutrition and Development. 2020;20(3):15954–77. [Google Scholar]
- 3.Haddad L, Achadi E, Bendech MA, Ahuja A, Bhatia K, Bhutta Z, et al. The Global Nutrition Report 2014: actions and accountability to accelerate the world’s progress on nutrition. The Journal of nutrition. 2015;145(4):663–71. doi: 10.3945/jn.114.206078 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Asfaw M, Wondaferash M, Taha M, Dube L. Prevalence of undernutrition and associated factors among children aged between six to fifty nine months in Bule Hora district, South Ethiopia. BMC Public health. 2015;15(1):1–9. doi: 10.1186/s12889-015-1370-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.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 nutrition. 2018;4(1):1–15. doi: 10.1186/s40795-018-0236-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Gamecha R, Demissie T, Admasie A. The Magnitude of Nutritional Underweight and Associated Factors Among Children Aged 6–59 Months in Wonsho Woreda, Sidama Zone Southern Ethiopia. The Open Public Health Journal. 2017;10:7–16. [Google Scholar]
- 7.World Health Organization (2021). Malnutrition. [online] Who.int. Available at: https://www.who.int/news-room/fact-sheets/detail/malnutrition [Accessed 05 Nov 2022]. [Google Scholar]
- 8.UNICEF DATA. (2018). 2018 Joint Child Malnutrition Estimates (JME). [online] Available at: https://data.unicef.org/resources/levels-and-trends-in-child-malnutrition-2018 [Accessed 25 May 2022]. [Google Scholar]
- 9.Alemu M, Nicola J, Bekele T. Tackling child malnutrition in Ethiopia: Do the sustainable development poverty reduction program’s underlying policy assumptions reflect local realities? Young Lives, An International Study of Childhood Poverty. An International Study of Childhood. 2005. [Google Scholar]
- 10.Ababa A, Calverton E. Central statistical agency (Ethiopia) and ICF international. Ethiopia and Calverton: Ethiopia Demographic and Health Survey. 2011;14. [Google Scholar]
- 11.Tamiru MW, Tolessa BE, Abera SF. Under nutrition and associated factors among under-five age Children of Kunama ethnic groups in Tahtay Adiyabo Woreda, tigray regional state, Ethiopia. Community Based Study Sciences 2015;4(2):277–88. [Google Scholar]
- 12.Asfaw M, Wondaferash M, Taha M, Dube L. Prevalence of undernutrition and associated factors among children aged between six to fifty nine months in Bule Hora district, South Ethiopia. BMC Public Health. 2015;15(1):41. doi: 10.1186/s12889-015-1370-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Eticha K, Shiferaw S, Tesfaye F. Prevalence and determinants of child malnutrition in Gimbi district, Oromia region, Ethiopia. Thesis In press. 2007. [Google Scholar]
- 14.Sapkota VP, Gurung CK. Prevalence and predictors of underweight, stunting and wasting in under-five children. Health Res Counc 2009;7(15):120–6. [Google Scholar]
- 15.Basit A, Nair S, Chakraborthy KB, Darshan B, Kamath A. Risk factors for under-nutrition among children aged one to five years in Udupi talukof Karnataka, India: A case control study. Australas Med J. 2012;5(3):163–7. doi: 10.4066/AMJ.20121022 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Brhane G, Regassa N. Nutritional status of children under five years of age in Shire Indaselassie, North Ethiopia: Examining the prevalence and risk factors. Kontakt. 2014;16(3):161–70. [Google Scholar]
- 17.Kavosi E, Hassanzadeh Rostami Z, Kavosi Z, Nasihatkon A, Moghadami M, Heidari M. Prevalence and determinants of under-nutrition among children under six: a cross-sectional survey in Fars province, Iran. Int J Health Policy Manag. 2014;3(2):71–6. doi: 10.15171/ijhpm.2014.63 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Stalin P, Bazroy J, Dimri D, Singh Z, Senthilvel V, Sathyanarayanan S. Prevalence of underweight and its risk factors among under five children in a rural area of Kancheepuram District in Tamil Nadu, India. IOSR-J Dental and Med Sci. 2013;3(6):71–4. [Google Scholar]
- 19.Hasnain SF, Hashmi SK. Consanguinity among the risk factors for underweight in children under five: a study from rural Sindh. J Ayub Med Coll Abbottabad. 2009;21(3):111–6. [PubMed] [Google Scholar]
- 20.Mengistu K, Alemu K, Destaw B. Prevalence of malnutrition and associated factors among children aged 6–59 months at Hidabu Abote District, North Shewa, Oromia Regional State. J Nutr Disord Ther. 2013;1(001):1–15. [Google Scholar]
- 21.Ababa A, Population Census Commission. The 2007 population and housing census of Ethiopia. 2007. [Google Scholar]
- 22.Mernie G, Kloos H, Adane M. Prevalence of and factors associated with acute diarrhea among children under five in rural areas in Ethiopia with and without implementation of community-led total sanitation and hygiene. BMC pediatrics. 2022;22(1):1–16. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Aweke K, Habtamu F, Akalu G. Nutritional status of children in food insecure households in two districts of North Showa Zone, Ethiopia. African Journal of Food, Agriculture, Nutrition and Development. 2012;12(2):5915–27. [Google Scholar]
- 24.World Health Organization, Unicef. WHO child growth standards and the identification of severe acute malnutrition in infants and children, A Joint Statement by the World Health Organization and the United Nations Children’s Fund. Geneva: World Health Organization. 2009. [PubMed] [Google Scholar]
- 25.WHO. Haemoglobin concentrations for the diagnosis of anaemia and assessment of severity. World Health Organization. 2011;11(1). [Google Scholar]
- 26.Hall A, Kassa T, Demissie T, Degefie T, Lee S. National survey of the health and nutrition of schoolchildren in Ethiopia. Tropical Medicine & International Health. 2008;13(12):1518–26. doi: 10.1111/j.1365-3156.2008.02168.x [DOI] [PubMed] [Google Scholar]
- 27.Coates J, Swindale A, Bilinsky P. Household Food Insecurity Access Scale (HFIAS) for measurement of food access: indicator guide: version 3. 2007. [Google Scholar]
- 28.Amare B, Moges B, Moges F, Fantahun B, Admassu M, Mulu A, et al. Nutritional status and dietary intake of urban residents in Gondar, Northwest Ethiopia. BMC public health. 2012;12(1):1–10. doi: 10.1186/1471-2458-12-752 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Belachew T, Lindstrom D, Gebremariam A, Hogan D, Lachat C, Huybregts L, et al. Food insecurity, food based coping strategies and suboptimal dietary practices of adolescents in Jimma zone Southwest Ethiopia. PloS one. 2013;8(3):e57643. doi: 10.1371/journal.pone.0057643 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Hoddinott John, Yohannes Y. Dietary Diversity as a Household Food Security Indicator. Food and Nutrition Technical Assistance Project. Academy for Educational Development. 2002. [Google Scholar]
- 31.World Health Organization, Unicef. WHO child growth standards and the identification of severe acute malnutrition in infants and children: a Joint Statement by the World Health Organization and the United Nations Children’s Fund. Geneva: World Health Organization. 2008. [PubMed] [Google Scholar]
- 32.Patel AJ, Wesley R, Leitman SF, BJ B. Capillary versus venous haemoglobin determination in the assessment of healthy blood donors. Vox sanguinis. 2013;104(4) 317–23. doi: 10.1111/vox.12006 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Kebede D, Merkeb Y, Worku E, Aragaw H. Prevalence of undernutrition and potential risk factors among children under 5 years of age in Amhara Region, Ethiopia: evidence from 2016 Ethiopian Demographic and Health Survey. Journal of Nutritional Science. 2021;10. doi: 10.1017/jns.2021.17 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Wolde T, Belachew T, Birhanu T. Prevalence of undernutrition and determinant factors among preschool children in Hawassa, Southern Ethiopia. Prevalence. 2014;29:16–24. [Google Scholar]
- 35.Bidira K, Tamiru D, Belachew T. Anthropometric failures and its associated factors among preschool-aged children in a rural community in southwest Ethiopia. Plos one. 2021;16(11):e0260368. doi: 10.1371/journal.pone.0260368 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Rao VG, Yadav R, Dolla CK, Kumar S, Bhondeley MK, Ukey M. Undernutrition & childhood morbidities among tribal preschool children. Indian J Med Res 2005;122:43–7. [PubMed] [Google Scholar]
- 37.Singh MB, Fotedar R, Lakshminarayana J, Anand PK. Studies on the nutritional status of children aged 0–5 years in a drought affected desert area of western Rajasthan, India. Public Health Nutr. 2006;9:961–7. doi: 10.1017/s1368980006009931 [DOI] [PubMed] [Google Scholar]
- 38.Zeray A, Kibret GD, Leshargie CT. Prevalence and associated factors of undernutrition among under-five children from model and non-model households in east Gojjam zone, Northwest Ethiopia: a comparative cross-sectional study. BMC nutrition. 2019;5(1):1–10. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Gelu A, Edris M, Derso T, Abebe Z. Undernutrition and associated factors among children aged 6–59 months living in slum areas of Gondar city, northwest Ethiopia: a cross-sectional study. Pediatric health, medicine and therapeutics. 2018;9:81. doi: 10.2147/PHMT.S172317 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Kebede D, Aynalem A. Prevalence of undernutrition and potential risk factors among children below five years of age in Somali region, Ethiopia: evidence from 2016 Ethiopian demographic and health survey. BMC nutrition. 2021;7(1):1–10. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Teferi H, Teshome T. Magnitude and Associated Factors of Undernutrition Among Children Aged 6–59 Months in Ethiopian Orphanage Centres. Pediatric Health, Medicine and Therapeutics. 2021;12:141. doi: 10.2147/PHMT.S289809 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Mrema JD, Elisaria E, Mwanri AW, Nyaruhucha CM. Prevalence and Determinants of Undernutrition among 6-to 59-Months-Old Children in Lowland and Highland Areas in Kilosa District, Tanzania: A Cross-Sectional Study. Journal of Nutrition and Metabolism. 2021 Apr 11;2021. doi: 10.1155/2021/6627557 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Alelign T, Degarege A, Erko B. Prevalence and factors associated with undernutrition and anaemia among school children in Durbete Town, northwest Ethiopia. Archives of Public Health. 2015;73(1):1–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Liu J, Sun J, Huang J, Huo J. Prevalence of Malnutrition and Associated Factors of Stunting among 6–23-Month-Old Infants in Central Rural China in 2019. International Journal of Environmental Research and Public Health. 2021;18(15):8165. doi: 10.3390/ijerph18158165 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Zhang Y, Huang X, Yang Y, Liu X, Yang C, Wang A, et al. Double burden of malnutrition among children under 5 in poor areas of China. PLoS One. 2018;13(9):e0204142. doi: 10.1371/journal.pone.0204142 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Li H, Yuan S, Fang H, Huang G, Huang Q, Wang H, et al. Prevalence and associated factors for stunting, underweight and wasting among children under 6 years of age in rural Hunan Province, China: a community-based cross-sectional study. BMC Public Health. 2022;22(1):1–12. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Dhok RS, Thakre SB. Chronic undernutrition amongst under-five in an urban slum of Central India. Int J Commun Med Public Health. 2016;3(3):700–4. [Google Scholar]
- 48.Purohit L, Sahu P, Godale LB. Nutritional status of under-five children in a city of Maharashtra: a community based study. Int J Community Med Public Health. 2017;4(4):1171–8. [Google Scholar]
- 49.Giampaolo R, Marotta R, Biagiarelli FS, Zampa A, Moramarco S, Buonomo E. The exacerbated prevalence of acute malnutrition and growth retardation in Roma children living in camps. Italian Journal of Pediatrics. 2021;47(1):1–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Tariku A, Biks GA, Derso T, Wassie MM, Abebe SM. Stunting and its determinant factors among children aged 6–59 months in Ethiopia. Italian journal of pediatrics. 2017;43(1):1–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Fentahun W, Wubshet M, Tariku A. Undernutrition and associated factors among children aged 6–59 months in East Belesa District, northwest Ethiopia: a community based cross-sectional study. BMC public health. 2016;16(1):1–10. doi: 10.1186/s12889-016-3180-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Akombi BJ, Agho KE, Hall JJ, Merom D, Astell-Burt T, Renzaho AM. Stunting and severe stunting among children under-5 years in Nigeria: A multilevel analysis. BMC pediatrics. 2017;17(1):1–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Agho KE, Akombi BJ, Ferdous AJ, Mbugua I, Kamara JK. Childhood undernutrition in three disadvantaged East African Districts: a multinomial analysis. BMC pediatrics. 2019;19(1):1–11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Mengesha A, Hailu S, Birhane M, Belay MM. The Prevalence of Stunting and Associated Factors among Children Under Five years of age in Southern Ethiopia: Community Based Cross-Sectional Study. Annals of Global Health. 2021;87(1). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Mdimu EL, Massaga JJ, Sembuche SL, Abade AM, Leyna GH. Risk factors associated with under nutrition among children aged 6–59 months in Ngorongoro, Arusha region, Tanzania: a case-control study, 2017. The Pan African Medical Journal. 2020;37. doi: 10.11604/pamj.2020.37.315.21726 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.Wali N, Agho KE, Renzaho AM. Factors associated with stunting among children under 5 years in five South Asian countries (2014–2018): Analysis of demographic health surveys. Nutrients. 2020;12(12):3875. doi: 10.3390/nu12123875 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.Hall J, Walton M, Van Ogtrop F, Guest D, Black K, Beardsley J. Factors influencing undernutrition among children under 5 years from cocoa-growing communities in Bougainville. BMJ global health. 2020;5(8):e002478. doi: 10.1136/bmjgh-2020-002478 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Müller O, Krawinkel M. Malnutrition and health in developing countries. Cmaj. 2005;173(3):279–86. doi: 10.1503/cmaj.050342 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59.Luo ZC, Karlberg J. Critical growth phases for adult shortness. American journal of epidemiology. 2000;152(2):125–31. doi: 10.1093/aje/152.2.125 [DOI] [PubMed] [Google Scholar]
- 60.Akombi BJ, Agho KE, Hall JJ, Wali N, Renzaho AMN, Merom D. Stunting, wasting and underweight in sub-Saharan Africa: a systematic review. Int J Environ Res Public Health. 2017;14(8):863. doi: 10.3390/ijerph14080863 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Tekile AK, Woya AA, Basha GW. Prevalence of malnutrition and associated factors among under-five children in Ethiopia: evidence from the 2016 Ethiopia Demographic and Health Survey. BMC research notes. 2019;12(1):1–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.De Benoist B, Cogswell M, Egli I, McLean E. Worldwide prevalence of anaemia 1993–2005; WHO global database of anaemia. 2008. [DOI] [PubMed] [Google Scholar]
- 63.Abera L, Dejene T, Laelago T. Prevalence of malnutrition and associated factors in children aged 6–59 months among rural dwellers of damot gale district, south Ethiopia: community based cross sectional study. International journal for equity in health. 2017;16(1):1–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Sulaiman AA, Bushara SO, Elmadhoun WM, Noor SK, Abdelkarim M, Aldeen IN, et al. Prevalence and determinants of undernutrition among children under 5-year-old in rural areas: A cross-sectional survey in North Sudan. Journal of family medicine and primary care. 2018;7(1):104. doi: 10.4103/jfmpc.jfmpc_73_17 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.White M, Dennis N, Ramsey R, Barwick K, Graham C, Kane S, et al. Prevalence of malnutrition, obesity and nutritional risk of Australian paediatric inpatients: a national one-day snapshot. Journal of paediatrics and child health. 2015;51(3):314–20. doi: 10.1111/jpc.12709 [DOI] [PubMed] [Google Scholar]
- 66.Murarkar S, Gothankar J, Doke P, Pore P, Lalwani S, Dhumale G, et al. Prevalence and determinants of undernutrition among under-five children residing in urban slums and rural area, Maharashtra, India: a community-based cross-sectional study. BMC Public Health. 2020;20(1):1–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 67.Abebe Z, Zelalem Anlay D, Biadgo B, Kebede A, Melku T, Enawgaw B, et al. High prevalence of undernutrition among children in Gondar town, Northwest Ethiopia: a community-based cross-sectional study. International journal of pediatrics. 2017;2017. doi: 10.1155/2017/5367070 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 68.Dukuzimana MA, Bizimana EG, Michael H, Habineza A, Rutayisire E. Prevalence and Factors Associated with Under Nutrition among Children Aged 6 to 59 Months in Ngoma District, Rwanda. Journal of Public Health International. 2021;4(1):10–20. [Google Scholar]
- 69.Kiarie J, Karanja S, Busiri J, Mukami D, Kiilu C. The prevalence and associated factors of undernutrition among under-five children in South Sudan using the standardized monitoring and assessment of relief and transitions (SMART) methodology. BMC nutrition. 2021;7(1):1–11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 70.Engidaye G, Melku M, Yalew A, Getaneh Z, Asrie F, Enawgaw B. Under nutrition, maternal anemia and household food insecurity are risk factors of anemia among preschool aged children in Menz Gera Midir district, Eastern Amhara, Ethiopia: a community based cross-sectional study. BMC Public Health. 2019;19(1):968. doi: 10.1186/s12889-019-7293-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 71.Yang W, Li X, Li Y, Zhang S, Liu L, Wang X, et al. Anemia, malnutrition and their correlations with socio-demographic characteristics and feeding practices among infants aged 0–18 months in rural areas of Shaanxi province in northwestern China: a cross-sectional study. BMC Public Health. 2012;12(1):1127. doi: 10.1186/1471-2458-12-1127 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 72.Takele WW, Baraki AG, Wolde HF, Desyibelew HD, Derseh BT, Dadi AF, et al. Anemia and Contributing Factors in Severely Malnourished Infants and Children Aged between 0 and 59 Months Admitted to the Treatment Centers of the Amhara Region, Ethiopia: A Multicenter Chart Review Study. Anemia. 2021;2021:6636043. doi: 10.1155/2021/6636043 [DOI] [PMC free article] [PubMed] [Google Scholar] [Retracted]
- 73.Priyanka R, Vincent V, Jini M, Saju C. An assessment of the nutritional status of underfive children in a rural area of Thrissur district, Kerala, India. Int J Community Med Public Health. 2016;3(12):3479–86. [Google Scholar]
- 74.Nigatu G, Woreta SA, Akalu TY, Yenit MK. Prevalence and associated factors of underweight among children 6–59 months of age in Takusa district, Northwest Ethiopia. International journal for equity in health. 2018;17(1):1–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 75.Kiarie J, Karanja S, Busiri J, Mukami D, Kiilu C. The prevalence and associated factors of undernutrition among under-five children in South Sudan using the standardized monitoring and assessment of relief and transitions (SMART) methodology. BMC Nutrition. 2021;7(1):25. doi: 10.1186/s40795-021-00425-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 76.Mamulwar MS, Rathod HK, Jethani S, Dhone A, Bakshi T, Lanjewar B, et al. Nutritional status of under-five children in urban slums of Pune. International Journal of Medicine and Public Health. 2014;4(3). [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
All data generated and/or analyzed in this study are available within the paper.

