Hostname: page-component-586b7cd67f-gb8f7 Total loading time: 0 Render date: 2024-11-23T20:48:15.404Z Has data issue: false hasContentIssue false

Energy, protein and iron densities of dabi teff-field pea-based optimised novel complementary flour and its contribution to daily energy and nutrients demand by 6–23-month-old children

Published online by Cambridge University Press:  08 November 2023

Diriba Chewaka Tura*
Affiliation:
Department of Nutrition and Dietetics, Institute of Health, Jimma University, Jimma, Ethiopia Department of Human Nutrition, Wollega University, Nekemte, Ethiopia
Tefera Belachew
Affiliation:
Department of Nutrition and Dietetics, Institute of Health, Jimma University, Jimma, Ethiopia
Dessalegn Tamiru
Affiliation:
Department of Nutrition and Dietetics, Institute of Health, Jimma University, Jimma, Ethiopia
Kalkidan Hassen Abate
Affiliation:
Department of Nutrition and Dietetics, Institute of Health, Jimma University, Jimma, Ethiopia
*
*Corresponding author: Diriba Chewaka Tura, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Inadequate intake of age-specific energy and nutrients is among the prime immediate causes of child malnutrition. Thus, this study aimed to determine the energy, protein and Fe densities of pre-processed dabi teff-field pea-based optimised novel complementary flour and its contribution to daily energy and nutrients demand by 6–8, 9–11 and 12–23 month-old children. The optimal formula at overall optimisation was identified to be 34·66 % dabi teff, 25 % barley, 15 % oats, 15·34 % field pea, 5 % linseed and 5 % maize with response values of 15·74 % protein, 5·09 % fat, 2·26 % ash, 2·88 % fibre, 73·05 % carbohydrate, 1591·72 kJ/100 g (380·43 kcal/100 g) energy, 32·21 mg/100 g Fe, 77·51 mg/100 g Ca and 2·59 mg/100 g Zn. The energy density of the optimised novel complementary flour was 1·27 kcal/g which fulfilled the Pan American Health Organization/WHO recommendation (≥ 0·8 kcal/g), protein density was 4·14 g/100 kcal and the Fe density was 8·47 mg/100 kcal, which was 2·12 to 10·59 times higher than the recommended value where the optimal had demonstrated to contribute more than 100 % of the daily energy and protein demand and notably more than 200 % of daily Fe demand at moderate bioavailability (0·8–4 mg/100 kcal). These findings showed that the daily recommended dietary allowance for energy, protein and Fe could be attained by the developed dabi teff-field pea-based optimised novel complementary flour and its contribution to the children’s daily energy and nutrients demand met the standard, where the product can be used as food-based nutrition intervention to manage protein-energy malnutrition and Fe deficiency anemia in children sustainably.

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2023. Published by Cambridge University Press on behalf of The Nutrition Society

Adequate nutrition during childhood is a key factor to support the rapid rate of physical growth and mental development that occurs in the first 2 years of life(Reference Dewey and Adua Afarwuah1,Reference Vallinoto, Moreira and Maihara2) as well as for healthy life and future productivity of children(Reference Michaelsen and Greer3,Reference Skau, Bunthang and Chamnan4) . Stunting or declined linear growth of children usually occurs during the period of complementary feeding, particularly around the end of the second year of life, and ends irreversible(Reference Onyango, Borghi and de Onis5). Additionally, Fe deficiency anaemia is more prevalent in early childhood (between 6 and 24 months) than at any other time in the life cycle where the major causes are inadequate dietary intake of bioavailable Fe, malaria and parasitic infections(Reference Hallberg and Rossander6,Reference Ogbonnaya, Ketiku and Mojekwu7) . During this critical time, there is a high dietary requirement of Fe per body weight, where some health firms recommend that infants should be primarily introduced at first to Fe-rich complementary foods such as Fe-fortified or meat foods to meet their Fe requirements and alleviate long-life developmental impairments(8,Reference Qasem and Friel9) .

Infants and young children need adequate energy and a nutrient-dense diet both through exclusive breast-feeding followed by quality complementary feeding(Reference Dewey and Adua Afarwuah1,Reference Vallinoto, Moreira and Maihara2,Reference Arsenault and Brown10) . In the first 6 months after birth, breast milk is adequate for energy and nutrient requirements by infants(Reference Vallinoto, Moreira and Maihara2) after which the milk is no longer sufficient and children transfer from ideal and uncontaminated breast milk to poor-quality complementary foods (often regular family food) with the highest chance of vulnerability to malnutrition and infectious diseases(Reference Abebe, Stoecker and Hinds11,12) .

The energy density of a food refers to the amount of calories per unit weight of the food and is expressed as kcal/g, whereas nutrient density refers to the amount in grams of macro- and micronutrient nutrients in a food per 100 kcal(Reference Shiriki, Igyor and Gernah13,Reference van der Merwe, Kluyts and Bowley14) . The energy needs from complementary foods for infants with ‘average’ breast milk intake in developing countries are approximately 200 kcal per day at 6–8 months of age, 300 kcal per day at 9–11 months of age and 550 kcal per day at 12–23 months of age(Reference Dewey15,Reference Michaelsen16) . According to FAO/WHO(12) guidelines, the critical values of nutrient contents in formulated complementary food should be 400–425 kcal/100 g energy, ≥ 15 % protein, 10–25 % fat, 64 (sd 4) % carbohydrate, 16 mg/100 g Fe, 500 mg/100 g Ca and 3·2 mg/100 g Zn to be nutritional adequate(12).

Complementary foods need to be far more nutritious compared with family foods to fill the energy and nutrient gap. It should contain protein of high-biological value comprising the essential amino acids. Yet, the opposite is the case in low-income countries. Apart from a major source of essential amino acids, protein is a good energy source at times of energy deprivation(Reference Forsido, Kiyak and Belachew17,18) . Low energy intake accompanied by inadequate intake of protein leads to protein-energy malnutrition, the commonest lethal form of malnutrition revealed to us ‘the silent emergency of the world’(Reference Rolfes, Pinna and Whitney19). Thus, infants and young children need adequate protein where the recommended daily amount of protein in grams for a 6–8-month-old child is 9·1 g, for a 9–11-month-old child is 9·6 g and for a 12–23-month-old child is 10·9 g(Reference Dewey15). The ratio of energy from protein to the total energy content of a given food, which is referred to us the protein-energy ratio, is one of the indicators used to assess the adequacy and quality of protein in complementary foods. The Codex Alimentarius commission(12) specifies that the daily energy needs from protein (protein-calorie) should be between 6 and 15 % of the total daily energy requirements and typically should not exceed 15 %. This is because while protein is still crucially required for growth and development, a higher protein-calorie ratio beyond 15 % in complementary foods may increase the renal solute load (the non-metabolised nitrogenous end products) and interfere with appetite(20).

In addition to protein, infants and young children require an adequate amount of micronutrients such as Fe, Zn, Ca and vitamins to meet their physiological needs, particularly in the first 2 years of life and they are prone to micronutrient deficiencies and associated diseases(18,Reference Huffman and Schofield21) . Ahmed et al. (Reference Ahmed, Hossain and Sanin22) stated that globally, 7·3 % of the disease burden in children is accounted for by micronutrient deficiencies. The contribution of dietary minerals from breast milk declines with a child’s age and would be almost zero after 12 months, which makes these nutrients limiting nutrients(Reference Abeshu, Lelisa and Geleta23). The percentage of total daily micronutrient requirement from complementary foods may range from 30 to 100 %. For instance, for 9–11-month-old children, about 97 % of Fe, 86 % of Zn, 72 % of Ca, 76 % of Mg, 81 % of P and 73 % of Na requirements of children 6–24 months should come from complementary food, assuming average breast milk intake(Reference Dewey15,Reference Dewey and Brown24) .

Pan American Health Organization (PAHO) and WHO(Reference Dewey15) recommend Fe intake by children at 6–8, 9–11 and 12–23 months should be 11, 11 and 7 mg/d, respectively, where these figures are 4·1, 4·3 and 5·8 mg/d for Zn and 400, 400 and 500 mg/d for Ca for the respective age groups. Meeting such high demand is unlikely to be attained through a traditional complementary food, which calls for searching for other promising alternatives such as exploring locally available underutilised/forgotten nutritious cereals and legume crops and developing optimised complementary flour.

The theoretical gastric capacity of infants and young children is 30 g/kg body weight per meal, but their functional gastric capacity is much lower than this figure in usual settings. For instance, Abeshu et al. (Reference Abeshu, Adish and Haki25) have reported that the functional gastric capacity of 6–23-month-old children on average was around 20 g/kg body weight per meal for the study done at Wolayita Zone of Ethiopia, whereas Baye et al. (Reference Baye, Guyot and Icard-Verniere26) had reported a very low functional gastric capacity at 9 g/kg body weight per meal for 12–23-month-old children for the study done at North Wollo of Ethiopia. Because of this lower functional gastric capacity, children need to be fed energy and nutrient-dense food to satisfy their daily demands and served more frequently than adults WHO(20). PAHO/WHO(Reference Dewey15) recommends the required minimum energy density from processed cereal–legume-based complementary food should be 0·8 kcal/g, protein density should be up to 5·5 g/100 kcal and Fe density needs to be 0·8–4 mg/100 kcal where the required number of meals to be served to children per day was estimated to be 2–3 times for 6–8-month-old children and 3–4 times for 9–23-month-old children to provide adequate daily energy and nutrients requirements by children with additional one or two nutritional snacks based on the appetite of the child.

Application of some simple processing techniques like fermentation, germination, soaking, roasting and dehulling can improve the nutrient densities and absorption of nutrients from cereal–legume foods as well as boost organoleptic qualities(12). Dietary factors such as meat, poultry, fish and citrus fruits are also good sources and important enhancers of non-haem Fe and Zn absorption from plant foods(Reference Etcheverry, Hawthorne and Liang27,Reference Hallberg and Hulthan28) . But in many developing countries, these products are too expensive and consumed on special occasions only, if not at all, where it is even unthinkable to purchase meat by people with poor socio-economic classes. Currently, the development of energy and nutrient-dense complementary foods from local and readily available nutrient-rich cereals and legumes combinations has received a lot of attention in many developing countries since it is cost-effective, sustainable and can be adapted to different cultural and dietary traditions and locally feasible strategies(Reference Ruel and Levin29,Reference Usha, Lakshmi and Ranjani30) . The food-based dietary guidelines by the International Life Science Institute(Reference Harris31) focus on the combination of foods that can meet nutrient requirements rather than on how each specific nutrient is provided in adequate amounts. This guideline was based on the fact that people eat foods, not nutrients or food tablets(Reference Thompson and Amoroso32). Recently, nutrition has got an increasing attention with stronger political involvement at both the national and international levels. For instance, the Ethiopian food and nutrition policy and strategy which was recently formulated supports the development and promotion of local production of complementary foods meeting acceptable standards as on one of its operationalising the strategy(33).

Generally, inadequate intake (both in quantity and quality) of age-specific essential nutrients together with infectious diseases is the prime immediate causes of child malnutrition leading to anthropometric deficits (stunting, wasting, underweight), anaemia, impaired cognitive development and finally increased morbidity and mortality. According to the Ethiopian Public Health Institute survey(34), 37 % of children under 5 years old were stunted, 21 % were underweight, 7 % were wasted, 2·9 % were overweight and 57 % anaemic. Thus, it was hypothesised that the development of energy, protein and Fe-dense complementary foods from locally available food crops including the underutilised/forgotten crops that could meet acceptable standards for energy and nutrient requirements by children and its promotion could be used to sustainably manage child malnutrition and its aligned consequences.

The sub-Saharan African region including Ethiopia is endowed with a rich diversity of ‘orphan crops’ having improved nutritional and medicinal values as well as sources of income generation(Reference Tura, Belachew and Tamiru35). Little or no attention was given to such crops in terms of research and development and policy framework that could promote their extensive agricultural production, industrial utilisation and home consumption. In Ethiopia, the food culture of teff grains, ‘a widely utilised orphan crop’, is both historical, an integral part of the country’s antiquity, and mostly traded domestically where more than 70 % of the Ethiopian population use teff grains as a traditional staple meal.

Dabi teff (Eragrostis tef), a farmer variety teff grain, is one of the underutilised/marginalised or forgotten food crops grown in Ethiopia (Oromia region) that could be utilised to combat macro- and micronutrient malnutrition. Dabi teff is the ‘afaan oromoo language’ name for an early maturing variety of dark red teff grain. The early maturing property of the grain makes the crop to be harvested twice within one rainy season (at early rainfall called ‘daabi gannoo’ and late rainfall called ‘daabi birraa’). Farmers in Wollega and Illuababor zones, Western Ethiopia, cultivate dabi teff either for its grain seeds or its straw. The contribution of the grains to household food and nutrition security is considerable when viewed through a food security lens while the straw is composed of fine stems used for plastering (finishing) mud hut walls during house construction and rated higher among others for animal fodder especially oxen feeding(Reference Tura, Belachew and Tamiru35). There are many social beliefs regarding the nutritional and health benefits of dabi teff among rural elderly people in particular and consumers in general (Personal communication). Price-wise, the red teff varieties grown in Ethiopia including dabi teff are the cheapest. For example, Rashid and Negasa(Reference Rashid and Negassa36) reported that the market price of mixed teff and red teff was 24 and 55 % less than the white teff. In addition to lower prices, red teff varieties have been implicated in the low incidence of anaemia in Ethiopia, which is presumed to be due to the grain’s high Fe content(Reference Gebremariam, Zarnkow and Becker37). The other cereals and legume components included in our current formulation for optimisation were thoughtfully selected to develop a wholesome and nutritionally complete novel complementary product. For example, the legumes/pulses field pea and linseed were selected because of their naturally containing high amounts of protein and to complement the lysine-limited cereals. Additionally, linseed is a popularly cultivated oil crop by the community in the sample collection area and its oil is among the leading sources of α-linolenic acid and n-3 PUFA from plant foods(Reference Lee, Kim and Kim38), which is crucially important for brain neural and cognitive development in utero and early childhood(Reference Campoy, Escolano-Margarit and Anjos39).

On the other hand, the cereals maize, barley and oats were selected because of their high carbohydrate contents and also for complementing the cysteine, methionine and tryptophan-limited legumes. All these nutritional qualities of the components would make the complementary product developed novel and superior quality. Hence in this study, the energy, protein and Fe densities of dabi teff-field pea-based optimised novel complementary flour and its contribution to daily energy and nutrient demand by 6–23-month-old children were investigated in comparison with FAO/WHO(12) recommended nutrient contents of complementary foods and PAHO/WHO(Reference Dewey15) recommended daily energy and nutrients requirements for 6–23-month-old children to ensure adequate energy and nutrients daily intake from the optimised complementary flour for children’s optimal growth and development.

Materials and methods

Food crops sample collection

Eight mothers who were judged to have good knowledge of complementary foods assisted by health extension workers in the village were asked about the types and affordability of common complementary crops used for feeding infants and young children in Nedjo area, west Wollega, Ethiopia and its presence in the market was inspected. Six food samples including dabi teff (Eragrostis tef (Zucc.) farmer variety), maize (Zea mays L.), barley (Hordeum vulgare), white field pea (Pisum sativum), oats (Avena sativa) and linseed (Linum usitatissimum) (Fig. 1) were purchased from an open market of Nedjo town, which is located at 575 km away to the west of Addis Ababa where Nedjo district is a potential dabi teff growers. The nutrient contents of these crops were initially literature searched, later verified through laboratory experimentation (nutrient analysis of each crop) (Table 1) and were carefully selected to add one or more nutrients to their mixture to be nutritionally complemented. Three kilograms of each apparently healthy sample was purchased from the centre and corners of the market on two different market days to assure representativeness, packed separately in polyethylene bags and transported to the Food Science and Nutrition Laboratory of Ethiopian Institute of Agricultural Research for analysis. All laboratory analysis of the nutritional composition of each crop sample and the formulated complementary food was conducted in the stated laboratory, which was certified by the International Organization for Standardization (ISO-17025:2017) by International Laboratory Accreditation Cooperation.

Fig. 1. Collected complementary food crops (photo by the researcher).

Table 1. Major macro- and mineral compositions of each crop sample collected

Values are means of the triplicate determinations. Values in the same column followed by different superscripts are significantly different at P < 0·05.

Sample processing

The collected crop samples underwent various controlled processing techniques (Fig. 2). In brief, dabi teff was manually cleaned by winnowing to remove chaff, straw, dust and other extraneous and washed with tap water and sundried for 2 d at an average temperature of 27°C while the other cereals (maize, barley and oats) and the legumes (field pea and linseed) were sorted out from sands, sticks, stones and defective seeds, later washed and sundried for 2 d at an average temperature of 27°C and were ready for further individual processing. Due to the small size of dabi teff seeds, it was made into whole-seed milled flour, which could be the reason for the higher nutrient contents of the crop. Barley and oats samples were soaked in clean tap water for 2 h. The water used for soaking was drained off and the crops were immediately decorticated (while the seeds were still wet) using a wooden decorticator and the hulls were removed by winnowing.

Fig. 2. Process flow chart diagram of the crop samples and formulations.

Germination of maize seeds was adopted from the method previously described by Rasane et al. (Reference Rasane, Jha and Kumar40) with little modification. Briefly, the maize grains were soaked in water (1:3 w/v) for 3 h to achieve hydration, drained, spread on a clean jute sack placed on a wooden platform and covered with another jute sack for germination at room temperature (25 (sd 2)°C) for 72 h and water was sprayed every 12 h to stay humid (60 % relative humidity). This 72 h was used because Rasane et al. (Reference Rasane, Jha and Kumar40) reported that the maximum amylase activity was obtained at 72 h of germination time. After 72 h, the germinated seeds were rinsed, drained for 10 min, transferred to aluminium trays and dried in an air oven at 40°C for 5 h to terminate the germination process. The dried germinated sample was further roasted at 120 (sd 5)°C for 10 min and allowed to cool.

The crop samples viz., barley, oats, field pea and germinated maize were minimally roasted in an oven at 120°C for 20 min until light brown coloured and then cooled to room temperature (25 (sd 2)°C) as described by Rasane et al. (Reference Rasane, Jha and Kumar40). The roasting process was carefully controlled to prevent over-roasting and the formation of a Maillard reaction that may lead to protein quality damage. The linseed sample was minimally cooked for 5 min at 90°C(Reference Castro-Alba, Lazarte and Bergenståhl41) with a small amount of water to condition the seeds to release oil from the oil cells and later sundried without draining the water used for cooking.

Flour preparation and handling

All the six processed samples were milled into flours using a standard miller (Cyclotec 1093 sample mill, Foss Analytical) to obtain smooth and consistent particle sizes and sieved through a 0·5 mm mesh sieve size. The flours were then packed in air-tight high-density polyethylene bags as described by the American Association of Cereal Chemists(42), separately coded and stored safely at room temperature till formulation.

Experimental design

Flour formulation

A mixture of cereals, legumes, pulse and/or oilseed flours constitutes an appropriate source of nutrients and energy density, essential fatty acids and limiting amino acids and ends up with many functional and health benefits as well as improved organoleptic characteristics(12). In the current study, Stat-Ease Design-Expert® software 11 (Randomized Mixture Design, D-optimal, Minneapolis, USA, 2018) was used to generate the formulation design matrix.

Macro-compositions analysis

In this study, Associations of Official Analytical Chemists (AOAC)(43) modified methods were used to determine the macro-composition of each crop sample and the formulated complementary flours. The moisture content was determined by air convection drying oven (Model No. DHG-9121A) using the method described by 925.10, AOAC(43) for 1 h at 130 (sd 3)°C. Crude protein content was determined by Kjeldahl (Kjeltec 8400, Auto Sample Systems, Foss Analytical) using a nitrogen conversion factor of 6·25 following the official method 954.10, AOAC(43). Soxhlet method (Soxtec 8000, Tecator Line, Foss Analytical) was used to determine the crude fat content by N-Hexane extract according to the method number 2003.06, AOAC(43). Ash content was determined using the combustion method by box type muffle furnace (Model No.SX2-4-10GJ, China) at 550°C for 4 h following method 923.03, AOAC(43). Crude fibre content was determined by Fibertec 8000, Foss analytical, following official method 978.10, AOAC(43). Utilisable carbohydrate was estimated by difference: 100 - (% Moisture + % Crude protein + % Crude fat + % Crude fibre + % Ash)(Reference Ayele, Teferra and Frank44). The gross energy (kcal/100 g) of each crop sample and the formulated flours were computed based on FAO/WHO(45) recently amended in the 2021 codex guideline by multiplying the values obtained for crude protein, crude fat and utilisable carbohydrate (the energy-yielding macronutrients) with Atwater conversion factors where E (kcal/100 g) = ((% crude fat × 9) + (% crude proteins × 4) + (% utilisable carbohydrates × 4)].

Dietary mineral analysis

Analysis of aqueous solutions by inductively coupled plasma-optical emission spectrometry with radial plasma observation method was used to determine the dietary mineral contents (Fe, Zn, Ca, Mg, K, P, Na) of each crop sample and the formulated complementary flours with radial plasma observation method(Reference de Souza, Leocádio and da Silveira46). All the measurements were performed using a sector ARCOS optical emission spectrometer optimised with small volume and thirty-two linear charge-coupled devices detectors in the wave length range between 130 and 770 nm and simultaneously analysed. A nebuliser was used to introduce sample solution into the argon gas field plasma and the energy excitement was proceeded in the single spectra and the energy was expressed in intensity, which is directly proportion to concentration, the concentration was calculated on the linear graph of the standard concentration and the corresponding intensities. All the measuring conditions, like plasma power, gas flows, torch positions and measuring time, are configured. It was a concentration measurement. According to the standard, the calibration and standardisation of the spectra method were performed and standardisation was done daily and it is a quick procedure for correcting measuring intensities so that the correct concentration is obtained using the original calibration curve.

Variables optimisation and validation

Numerical and graphical optimisation techniques were employed to identify the optimum formula (sweet spot) using the Deign-Expert (D-optimal mixture design). Simultaneous numerical values of independent variables and multi-responses optimisation were performed by setting the desired goals for each independent and dependent (response) variable. In brief, the major components used; dabi teff, field pea and germinated maize flours were set in range and the responses were set to maximise energy, protein, ash, fat, carbohydrate, Fe, Ca and Zn; whereas to minimise the moisture and crude fibre (Table 2). In addition to goal setting, the relative importance of each dependent variable in the overall optimisation solution was set to be ‘++++’ for protein and carbohydrate while it was set as ‘+++++’ for Fe, Ca and Zn.

Table 2. Goals set, the relative importance of each variable and the optimal values at optimal conditions

The graphical optimisation was carried out by superimposition of contour plots for all the responses with respect to component ratios. To confirm the validity of the optimisation, a laboratory experiment was conducted on the component ratios identified at the optimal formula and the obtained results were then compared with predicted values of the responses at optimal conditions and with values of the control flour and finally reported as the formula with optimal nutritional (macro-and micronutrients) profile of all the possible combinations or solutions.

Determination of energy and nutrient Densities of the optimised formula

The energy density of complementary foods, expressed as kcal/g, can be calculated by dividing the total energy from complementary foods by the amount in g of complementary foods served to the children per day, taking into account the theoretical gastric capacity of infants and young children to be 30 g/kg body weight per meal and the required number of meals to be served to the children per day for the respective age group. However, this theoretical gastric capacity may not usually be functional due to a lack of responsive feeding, inappropriate consistency of the foods or underlying health conditions where the children take less(Reference Dewey and Brown24).

The nutrient densities of the optimised flour were computed by dividing the respective nutrient contents obtained at optimal condition by energy value at optimal and given as g/100 kcal for macro and mg/100 kcal for micronutrients. To make it brief, the protein density or protein-energy ratio was calculated by dividing the crude protein content of the optimised flour by its corresponding energy value expressed as g/100 kcal. Similarly, the Fe density or Fe energy ratio was calculated by dividing the Fe content of the optimised flour by its corresponding energy value expressed as mg/100 kcal.

The amount of food needed per day by children in their respective age groups to satisfy their energy and nutrient intake demand is a function of the amount of energy and nutrient densities that can be provided by the complementary foods(Reference van der Merwe, Kluyts and Bowley14). Abeshu et al. (Reference Abeshu, Lelisa and Geleta23) estimated that for complementary food having energy density range of 0·6–1·0 kcal/g, the amount of food served to provide the daily energy requirement is 263·3 g for 6–8-month-old children, 317·09 g for 9–11-month-old children and 334·92 g for 12–23-month-old children for the study done at Wolayita Zone of Ethiopia and the children could consume an average amount of 212·82 g of the complementary food per day due to their low functional gastric capacity. Another report by Wasswa et al. (Reference Wasswa, Fungo and Kaaya47) stated that the amount of porridge eaten by children in rural settings of Uganda was estimated at around 200 g per day for children aged 6–12 months.

Consequently, based on these two reports and the Ethiopian complementary feeding guidelines(48), we have estimated the daily amounts of our optimised complementary food to be served to an age group of 6–8, 9–11 and 12–23-month-old children to meet their daily requirements to be 225, 300 and 450 g, respectively (i.e. 75, 100 and 150 g per meal for the respective age group) and 3 meals/d. The lower the energy density of a complementary diet, the greater the quantity of the diet required to meet the energy and nutrient demands by infants and young children(Reference van der Merwe, Kluyts and Bowley14). PAHO/WHO(Reference Dewey15) and WHO(20) complementary feeding guideline recommends that 5 meals/d are needed for a lower energy density of 0·6 kcal/g, 4 meals/d for 0·8 kcal/g and 3 meals/d when the energy density is at least 1·0 kcal/g. The standard also specifies that meal frequency that is greater than necessary may lead to excessive displacement of breast milk and preparing and feeding five meals per day requires a considerable amount of time and effort by caregivers. This may prompt them to hold prepared food over from one meal to the next, thereby potentially increasing the risk of microbial contamination which needs to be considered when developing messages regarding meal frequency due to which 1–2 nutritious snacks per day, such as a piece of fruit or a piece of bread would be recommended that takes less time for preparation and may also be less likely to displace breast milk(Reference Dewey15).

Contribution of the optimised complementary flour to the daily recommended energy and nutrient intake demand by infants and young children

Considering the estimated daily amount of complementary food to be served to the children and the amount of daily energy and nutrient demand by the respective age group as described in the introduction section above, the likely contribution (percentage) of the optimised complementary flour to the recommended daily requirement specified by PAHO/WHO(Reference Dewey15) was computed. Further, the energy and nutrient content of the optimised flour was compared with the recommended value specified by FAO/WHO(12) standards, which were also described in the introduction section earlier.

Statistical analysis

Numerical multi-response optimisation was performed using the Design-Expert®, D-optimal version 11 to identify the optimal condition while one-way ANOVA of SPSS version 24 was employed to test whether there is a significant difference between the nutrient contents of the optimised, the Cerifam® faffa (the popular commercial complementary flour in Ethiopia) and the control flours and significant differences were declared at P < 0·05. The mean nutrient contents were checked against the critical limits set by FAO/WHO(12). The energy density (kcal/g), protein, carbohydrate and fat densities (g/100 kcal), and Fe, Ca and Zn densities (mg/100 kcal) of the optimised flour were compared with PAHO/WHO(Reference Dewey15) recommendations and finally, the likely daily energy and nutrients contribution by the optimised complementary flour, the Cerifam® faffa and the control flour were computed for 6–8, 9–11 and 12–23-month-old children after adjusting for an estimated daily amount to be served to the children and compared with the RDA as per the PAHO/WHO(Reference Dewey15).

Results

Macro- and mineral compositions of each crop and the formulated complementary flours

The mean macro-compositions of each crop samples collected are presented in Table 1 where field pea and linseed flours were determined to contain a significantly higher (P < 0·05) protein content at 20·95 and 20·57 %, respectively, while barley, oats, maize and linseed were determined to contain a significantly higher (P < 0·095) energy value at 380·22, 381·01, 376·77 and 519·96 kcal/100 g, respectively, which were the bases to develop protein and energy-dense complementary flour. On the other hand, dabi teff has shown to contain significantly higher (P < 0·05) Fe and Ca content at 86·50 and 123·59 mg/100 g, respectively, which was the bases to develop Fe-dense novel complementary flour. The mean macro-compositions of the formulated complementary flours that were subjected to the optimisation process were 4·89%, 15·49, 4·91, 2·23, 3·48, 68·99 % and 382·14 kcal/100 g for moisture contents, protein, fat, ash, fibre, carbohydrate and energy contents, respectively, whereas the mean dietary mineral contents of the formulated complementary flours that were subjected to the optimisation process were 28·12, 76·25, 2·47, 120·57, 287·99 and 439·33 mg/100 g for Fe, Ca, Zn, Mg, P and K, respectively (Table 3).

Table 3. Macro- and mineral composition of the formulated mean, the optimised, the control and FAO/WHO specifications

Values are means of the triplicate determinations. Values in the same column followed by different superscripts are significantly different at P < 0·05.

Macro- and mineral compositions of the optimised complementary flours

The macro- and mineral compositions of the optimised novel complementary flour, the formulated mean, the control and the FAO/WHO(12) critical limits are presented in Table 3 where the overall optimised formula was identified to be 34·66 % dabi teff, 25 % barley, 15 % oats, 15·34 % field pea, 5 % linseed and 5 % germinated maize flours with response values of 15·74 % protein, 73·05 % carbohydrate, 5·09 % fat and 380·43 kcal/100 g energy, 32·21 mg/100 g Fe, 77·52 mg/100 g Ca and 2·59 mg/100 g Zn, 118·64 mg/100 g Mg, 287·99 P and 439·33 mg/100 g K at the optimal point with the overall desirability function of 0·651 (Fig. 3). The control flour contained 10·77 %, 74·41 %, 3·78 % and 374·74 kcal/100 g for protein, carbohydrate, fat and energy contents, respectively, whereas it had 7·25 mg/100 g Fe, 49·45 mg/100 g Ca, 2·64 mg/100 g Zn, 96·45 mg/100 g Mg, 282·65 mg/100 g P and 398·67 mg/100 g K, respectively. Cerifam® faffa flour contains 14 % protein, 76 % carbohydrate, 4 % fat and 396 kcal/100 g, and it contains 6 mg/100 g Fe, 5 mg/100 g Zn and 100 mg/100 g Ca, respectively (Table 3). Both the formulated mean and the optimised value fulfilled the FAO/WHO(12) critical standard limit. The energy, protein and Fe contents of the optimised and the formulated mean were significantly higher (P < 0·05) than the values for the control and the Cerifam® faffa flours, while there was no significant difference (P > 0·05) between the ash and Zn contents of the optimised, the formulated mean, the control and the Cerifam® faffa flours.

Fig. 3. 3D surface graph of desirability function at the overall optimisation.

The validation analysis result was 5·34 %, 15·86 %, 5·12 % 2·21 %, 2·85 %, 68·82 %, 384·80 kcal/100 g, 31·76 mg/100 g, 76·88 mg/100 g and 2·53 mg/100 g for moisture, protein, fat, ash, fibre, energy, Fe, Ca and Zn contents, respectively (Table 4). This showed that there was a good agreement between the predicted response values at optimal conditions and the validation laboratory values. The optimisation process was verified using the graphical optimisation technique (Fig. 4) where the overlay counter plot was generated for the most important variables to identify the optimum regions. Any design points that fall within the yellow region (with the very conservative silver-grey region) in the overlay plot represent an optimal combination of dabi teff flour, field pea and germinated maize flours in combination with the other constant components that can bear optimal macro- and micronutrient contents within 95 % CI.

Table 4. Experimental validation of optimal condition and comparison with the control flour

Values are means of the triplicate determinations. Values in the same column followed by different superscripts are significantly different at P < 0·05.

Fig. 4. Graphical overlay contour plot for the overall graphical optimisation.

Energy and macro-nutrient densities of the optimised, the control flours and PAHO/WHO recommendation

The energy and macro-nutrient densities of the formulated mean, the optimised, the control flours and the PAHO/WHO(Reference Dewey15) recommendations for complementary food for average breastfed children are presented in Table 5. After adjusting for the amount of food to be served to the children, the energy density of our current optimised complementary flour for all the age groups (6–8, 9–11 and 12–23-month-old children) was computed to be 1·27 kcal/g. The protein density of our optimised complementary flour was computed to be 4·14 g/100 kcal and which was 1·44 times higher than the protein density of the control (traditional) flour while the fat density was computed to be 1·34 g/100 kcal and the carbohydrate density of the optimised flour was computed to be 19·20 g/100 kcal.

Table 5. Energy and nutrient densities of the formulated mean, the optimal and the control flours and PAHO/WHO standards

Source of PAHO/WHO: Codex Stan 074–1981, Rev. 1–2006; PHO/WHO, 2001.

Minerals densities of the optimised, the control flours and PAHO/WHO recommendation

The dietary minerals densities of the formulated mean, the optimised and the control flours and the PAHO/WHO(Reference Dewey15) recommendations for complementary food for average breastfed children are presented in Table 5. The Fe density of our optimised complementary flour was computed to be 8·47 mg/100 kcal, and it was 4·39 times higher than the control which could be accredited to the higher Fe content of dabi teff flour at 86·50 mg/100 g (Table 1) which was one of the major ingredients in our formulations. The Zn density of our optimised flour was determined to be 0·68 mg/100 kcal and the Ca density was determined to be 20·37 mg/100 kcal.

Contribution of the optimised complementary flour

Contribution of the optimised complementary flour to daily energy and protein demand by 6–23-month- old children

Table 6 shows the required daily meal frequency and the estimated amount of solid portions of complementary food per meal for age groups of 6–8, 9–11 and 12–23-month-old children and the recommended daily requirements of energy and protein from a complementary food based on PAHO/WHO Guiding Principles for Complementary Feeding of the Breastfed Child. After adjusting for the amount of complementary food a child in its respective age group needs to be served, the likely daily contribution (in percentage) of the currently developed optimal complementary food to the recommendation and the daily requirements was computed for energy and protein. It was further compared with the relative contribution of the control and Cerifam® faff flour (the popular commercial complementary flour in Ethiopia). In the above section, it was estimated that the daily amounts of complementary foods to be served to an age group of 6–8, 9–11 and 12–23-month-old children to be 225, 300 and 450 g, respectively. Based on adjusting for this estimated daily serving amount and the daily requirements of the nutrients, the currently developed optimised complementary product could likely contribute up to 143, 127 and 104 % of daily energy requirements for the age group of 6–8, 9–11 and 12–23-month-old child, respectively (Table 6). Similarly, after adjusting, the optimised complementary flour could be able to contribute up to 130, 164 and 217 % of the daily protein requirements for the respective age groups. This contribution of the optimised complementary flour to the PHO/WHO recommended requirements (demand) was significant (more than 100 %) and the product can considerably fulfil the energy and protein demand by the children under each respective age group, which showed the protein-energy deficit would be less likely to occur if the children would be fed the estimated serving amount properly.

Table 6. Contribution of the optimised flour to the daily energy and protein demands by 6–23-month-old children from complementary flour as recommended by PAHO/WHO (2001)

PAHO/WHO, 2001; CF, complementary food; %CTB, percentage contribution.

The relative contributions of the optimal, the control and the Cerifam® faffa flour to the daily energy and protein demand by the children are presented in Table 6, which was calculated to be 143, 141 and 149 % by the optimal, the control and Cerifam® faffa flours for the 6–8-month-old children, 127, 125 and 132 % for the 9–11-month-old children and 104, 102 and 108 % for the age group of 12–23-month-old children, respectively. When compared with the control and the Cerifam® faffa flour, the contribution of energy by the optimised complementary flour was slightly higher than that of the control flour and slightly lower than that of the Cerifam® faffa flour for the entire age category. This relatively comparable energy content of the control and Cerifam® faffa flour to the optimal flour could be attributed to the cereals, barley and wheat flours in their formulation, which are claimed as higher energy-containing cereals. The relative contribution of the optimal complementary flour to the daily protein demand was calculated to be higher than both the control and Cerifam® faffa flour and was determined to be 130, 89 and 115 % by the optimal, control and Cerifam® faffa flours for the 6–8-month-old- children, 164, 146 and 112 % for the 9–11-month-old children and 217, 148 and 193 % for the age group of 12–23-month-old children, respectively (Table 6).

Contribution of the optimised complementary flour to daily Fe, Ca and Zn demand by 6–23-month-old children

Table 7 shows the required daily meal frequency and the estimated amount of solid portions of a complementary food per meal for age groups of 6–8, 9–11 and 12–23-month-old children and the recommended daily requirements (RDA) of Fe, Ca and Zn from a complementary food based on PAHO/WHO Guiding Principles for Complementary Feeding of the Breastfed Child. After adjusting for the estimated daily serving amount and the daily requirements of the minerals as well as based on the assumption of moderate bioavailability, the currently optimised complementary flour was computed to contribute up to 220, 293 and 690 % of the daily Fe requirement for 6–8, 9–11 and 12–23-month-old children, respectively, with daily Fe demand of 11, 11 and 7 mg by 6–8, 9–11 and 12–23-month-old children, respectively (Table 7). This contribution of the optimised complementary flour to the PHO/WHO recommended requirements (demand) for Fe was significant (more than 200 %) and the product can considerably fulfil the Fe demand by the children under each respective age group, which showed the Fe deficiency anaemia would be less likely to occur if the children would be fed the estimated serving amount properly.

Table 7. Contribution of the optimised flour to the daily Fe, Ca and Zn demands by 6–23-month-old children from complementary flour as recommended by PAHO/WHO (2001)

PAHO/WHO, 2001; CF, complementary food; %CTB, percentage contribution. All the calculations were based on the moderate bioavailability of the minerals.

Regarding Zn, the optimised flour was demonstrated to contribute up to 47·32, 60·23and 67·07 % of daily Zn demand of 4·1, 4·3 and 5·8 mg by the respective age groups. On the other hand, the new optimised dabi teff-field-based complementary flour could only contribute up to 14·53, 19·37 and 23·3 % of daily Ca requirement (demand) of 400, 400 and 500 mg by the respective age group (Table 7).

Regarding the relative Fe contribution by the optimised complementary flour to the daily Fe demand by the children, the optimal flour had a significantly higher (non-comparably higher) percentage contribution than both the control and Cerifam® faffa flour where it was calculated to be 220, 50 and 41 % by the optimal, the control and the Cerifam® faffa flours for the 6–8-month-old children, 293, 66 and 55 % for the 9–11-month-old children and 690, 155 and 129 % for the age group of 12–23-month-old children, respectively (Table 7). This higher Fe contribution by the optimised complementary flour was ascribed to the higher Fe content of dabi teff flour at 86·5 mg/100 g (Table 1).

On the other hand, the relative contribution by the optimised complementary flour to daily Zn demand was comparable with that of the control flour, while it was lower than that of the Cerifam® faffa flour for all the age groups where it was calculated to be 47, 48 and 91 % by the optimal, the control and the Cerifam® faffa flours for the 6–8-month-old children, 60, 61 and 166 % for the 9–11-month-old children and 67, 68 and 129 % for the age group of 12–23-month-old children, respectively (Table 7) and this higher Zn content of the Cerifam® faffa flour could be attributed to the ingredients used during its formulation. Regarding the relative contribution of the three flours to daily Ca demand, the optimised, the control and the Cerifam® faffa flour were found to be very low for all the age groups ranging from 9 % to 30 % (Table 7) with relatively higher contribution by Cerifam® faffa flour, which could account for the milk powder in its formulation.

Discussion

The complementary crop samples collected have shown to contain varied and higher energy and nutrient contents, and each of the crop samples was designed to add one or more nutrients to their mixture, which were used to develop nutritionally complemented optimised novel complementary flour.

When compared with the FAO/WHO(12) recommended guideline for nutrient content requirements of formulated complementary foods, the mean macronutrients values of the formulations and the response values at the optimal condition of the currently developed complementary flour were adequately met the recommended critical limits for all the macro-compositions except for fat content at ≤ 5, ≥ 15, 10–25, ≤ 3, ≤ 5, 64 (sd 4) % and 400–425 kcal/100 g for moisture, protein, fat, ash, fibre, carbohydrate and energy contents, respectively (Table 3). Similarly, the mineral contents adequately met the recommended critical limits for Fe at 16 mg/100 gm for both the formulated mean and the optimised complementary flours (Table 3) where the mean formulation was 1·76 times higher and the optimal value was 2·01 times higher than the recommendation for Fe content. The Ca and Zn contents, however, did not meet the recommendation at 500 and 3·2 mg/100 g, respectively, though Zn could meet up to 77·19 % of the required value, which was marginal.

According to PAHO/WHO(Reference Dewey15) complementary feeding guidelines, the energy density of cereal-based complementary foods for infants and young children should be ≥ 0·8 kcal/g. Hence, our optimised complementary flour had demonstrated to meet beyond the minimum energy density requirements from complementary foods at 1·27 kcal/g for infants and young children aged 6–23 months old and the children can meet their daily energy demand if served the estimated amounts for the respective age group described in the above section and if fed three times per day as the guideline specifies that 3 meals/d would satisfy the energy demand of the children if the complementary food contains an energy density of at least 1 kcal/g.

It was unable to compare the energy density of our current optimised product with some past reports because of the wrong energy density calculation which said, ‘Simply dividing the energy contents of the complementary foods by 100’. For example, Tenagashaw et al. (Reference Tenagashaw, Kinyuru and Kenji49) reported energy density of complementary food formulated from blends of teff, soyabean and orange-fleshed sweet potato ranged from 3·70 to 3·76 kcal/g, and Ayele et al. (Reference Ayele, Teferra and Frank44) reported the energy density of complementary foods from kocho, pumpkin fruit, red kidney bean and maize at 3·3 kcal/g following the same calculation, which was overexaggerated. Even higher energy-dense foods have energy density of 1·07–1·46 kcal/g where in this case, the approximate quantity of complementary food that would meet the energy needs of the children is 137–187 g/d at 6–8 months, 206–281 g/d at 9–11 months and 378–515 g/d at 12–23 months old as specified by PAHO/WHO(Reference Dewey15,Reference Abeshu, Lelisa and Geleta23) recommendation. However, the current energy density determined was higher than the energy density reported by Abebe et al. (Reference Abebe, Stoecker and Hinds11) where the traditional corn-based porridge consumed as complementary foods in rural villages of Sidama zone of Southern Ethiopia contained an energy density of 0·53 kcal/g, while kocho-based contained 0·49 kcal/g, both of which were very low energy density levels.

The FAO/WHO Codex Alimentarius committee recommends the protein density of cereal-based formulated complementary foods for infants and young children should not exceed 5·5 g/100 kcal (upper threshold) where the determined protein density of our optimised complementary flour at 4·14 g/100 kcal was near to the upper threshold. This showed that our optimised complementary food is super and can meet the recommended standard and could provide the daily protein demand by 6–23-month-old children if served the estimated amount in the above section for the respective age group and fed three times per day. This finding was in agreement with the report by Tenagashaw et al. (Reference Tenagashaw, Kinyuru and Kenji49) where the protein density of complementary foods from blends of teff, soyabean and orange-fleshed sweet potato was in the range of 3·50–4·79 g/100 kcal. It also agreed with the report by Ayele et al. (Reference Ayele, Teferra and Frank44) where the protein density of an optimised formula from kocho, pumpkin fruit, red kidney bean and maize was 3·0 g/100 kcal. Alternatively, the protein density of homemade complementary foods in Wolayita zone of Ethiopia contained lower protein density ranging from 2·13 to 2·48 g/100 kcal as reported by Abeshu et al. (Reference Abebe, Stoecker and Hinds11).

Fat is among the major factors determining the energy density of foods; it provides essential fatty acids needed for the effective absorption of fat-soluble vitamins, and it boosts the sensory qualities of processed foods, PAHO/WHO(Reference Dewey15). The fat density determined at 1·34 g/100 kcal in our optimised flour was below the recommended standard set by codex (2·5–4·5 g/100 kcal) for cereal-based complementary foods for infants and young children, FAO/WHO(12). This finding was in agreement with the report by Tenagashaw et al. (Reference Tenagashaw, Kinyuru and Kenji49) that the fat density of complementary foods from blends of teff, soyabean and orange-fleshed sweet potato was in the range of 1·26–1·66 g/100 kcal where it did not even meet the minimum standard value that calls for additional fat-energy source. The current carbohydrate density of the optimised flour determined at 19·20 g/100 kcal agreed with the report by Tenagashaw et al. (Reference Tenagashaw, Kinyuru and Kenji49) that the carbohydrate density ranged from 18·22 to 20·05 g/100 kcal and this higher carbohydrate density could be attributed to the cereal–legume blends used to optimise the complementary flour, which were claimed to contain higher carbohydrate contents and maybe also due to the pre-processing techniques applied.

Dietary minerals such as Fe, Ca and Zn are the limiting nutrients in the diets of infants and young children(Reference Dewey and Brown24). The Fe density of our optimised flour as compared with the recommendation by PAHO/WHO(Reference Dewey15) complementary feeding guideline of cereal–legume-based complementary foods for infants and young children (6–24 months) accounted for high, moderate and low bioavailability of Fe where the recommended value is 2·5, 1·5 and 0·5 mg/100 kcal for 6–8, 9–11 and 12–23-month-old children when accounted for high bioavailability, while it is 4·0, 2·4 and 0·8 mg/100 kcal when accounted for moderate bioavailability and 7·7, 4·6 and 1·6 mg/100 kcal when accounted for low bioavailability for 6–8, 9–11, and 12–23-month-old children, respectively(Reference Ogbonnaya, Ketiku and Mojekwu7,Reference Dewey15,Reference Michaelsen16) .

The Fe density of our current optimised complementary flour that was computed to be 8·47 mg/100 kcal was 2·12–10·59 times higher than the recommended value when accounted for moderate bioavailability. This finding showed that the optimised complementary flour could even meet the recommendation when accounted for the low bioavailability of Fe density at 7·7 mg/100 kcal. Hence, it had demonstrated to meet the Fe density requirements from the complementary foods for infants and young children aged 6–23 months and the children can meet their daily Fe demand if properly fed. Such products with higher Fe content can be considered as meat substitutes given the Fe bioavailability would be comparable with that of red meat and the ‘novelty’ of this study would be accredited to the incorporation of dabi teff flour into the formulations containing high Fe at 86·50 mg/100 g (Table 1) and the presence of linseed which is a leading source of α-linolenic acid and n-3 PUFA that would make the formulated and optimised product super.

The present finding was higher than the Fe density of complementary blends of teff, soyabean and orange-fleshed sweet potato that range from 2·42 to 5·19 mg/100 kcal as reported by Tenagashaw et al. (Reference Tenagashaw, Kinyuru and Kenji49). Fe in plant foods exists in non-hem form, and it may also bind with anti-nutrients found in cereal–legume foods where its absorption can be impaired(Reference Hurrell and Egli50); but in our case, the pre-processing technique applied could reduce the effect of the anti-nutrients in inhibiting absorption.

Zn is an important mineral used for the management of diseases such as diarrhoea, pneumonia and sometimes malaria in children. It is also used for tissue growth and maintenance and wound healing where its deficiency leads to stunted growth though its effect is less recognised and referred to us the ‘hidden hunger’(Reference van der Merwe, Kluyts and Bowley14). PAHO/WHO(Reference Dewey15) recommends Zn density at 1·6, 1·1 and 0·6 mg/100 g for 6–8, 9–11 and 12–23 months of age children from complementary food when accounted for lower bioavailability(Reference Ogbonnaya, Ketiku and Mojekwu7). In the present study, the determined Zn density at 0·68 mg/100 kcal has shown fulfilment for 12–23-month-old children while at a marginal level (61·82 %) when accounted for the requirements for 9–11-month-old children and below the recommended for 6–8-month-old children. The present finding was higher than the Zn density of complementary food at 0·4 mg/100 kcal as reported by Ayele et al. (Reference Ayele, Teferra and Frank44) while it was lower than the report by Tenagashaw et al. (Reference Tenagashaw, Kinyuru and Kenji49) with a Zn density range of 1·41–1·49 mg/100 kcal.

The Ca density of our optimised flour determined at 20·37 mg/100 kcal could only meet 25·46 % of the required Ca density in formulated complementary food for infant and young children as set by codex standard (> 80 mg/100 kcal) FAO/WHO(12). The present finding was slightly lower than the report by Ayele et al. (Reference Ayele, Teferra and Frank44) which was 24·1 mg/100 kcal but by far lower than the report by Tenagashaw et al. (Reference Tenagashaw, Kinyuru and Kenji49) with a Ca density range of 60·68–67·84 mg/100 kcal from complementary blends of teff, soyabean and orange-fleshed sweet potato, which could be attributed to the variety of soyabean and the orange-fleshed sweet potato used.

Collectively speaking, our optimised complementary food was super Fe, protein and energy sources meeting the FAO/WHO(12) and PAH/WHO(Reference Dewey15) recommended standard and could provide the daily energy, protein, carbohydrate, Fe and Zn (to a considerable extent) demands by 6–23-month-old children if served 225 g of the optimised complementary food for 6–8 month-old children, 300 g for 9–11-month-old children and 450 g for 12–23-month-old children and feed three times per day accompanied by additional nutritional snacks during any signs of hunger and satiety and average breast-feeding.

Of the examined nutrients, the determined fat density at 1·34 g/100 kcal and Ca density at 20·37 mg/100 kcal (Table 5) were found to be unfavourably lower than the required standard at 2·5–4·5 g/100 kcal of fat density and at > 80 mg/100 kcal of Ca density where these two nutrients were frequently reported to be lower in cereal-based complementary foods(Reference Baye, Guyot and Icard-Verniere26,Reference Tenagashaw, Kinyuru and Kenji49,Reference Walle and Moges51) . The lower fat and Ca densities might be matched by advising mothers/caretakers to add Ca and vitamin-rich foods such as eggs, dried meat powder (quanta powder), refined butter and vegetable oil (the usual practice), mashed vegetables and replacing water with milk as well as adding mashed vegetables during porridge preparation for infants and young children which might aid to enhance energy density and to meet the recommendations. The energy density of a meal can be increased from 0·6 kcal/g to 1·0 kcal/g by adding one teaspoon of oil/butter or one piled teaspoon of mashed avocado or some amount of meat to 100 g of porridge(Reference Wolmarans, Kunneke and Laubscher52).

PAHO/WHO(Reference Dewey15,Reference Dewey and Brown24) recommends that the energy needs from complementary foods for infants and young children with average breast milk intake in developing countries are approximately 200, 300 and 550 kcal per day for 6–8 months, 9–11 months and, at 12–23 months of age children, respectively. Complementary foods are expected to be energy-dense and fill these deficits of daily energy and nutrient demand by the children apart from the amount obtained from breast-feeding(Reference Abeshu, Adish and Haki25). Among the energy-yielding macronutrients, protein should provide 6–15 % of total daily energy requirements, which corresponds to 9·1, 9·6 and 10·9 g of protein per day for 6–8, 9–11 and 12–23-month-old children, respectively, PAHO/WHO(Reference Dewey15).

From the other energy-yielding macronutrients, the standard states 55–65 % of total daily energy requirements should come from carbohydrate and the suggested amount ranging from 30 to 45 % need to come from fat energy(Reference Dewey and Brown24). From the optimal points of the optimised complementary flour, the contribution of energy from protein and carbohydrate to the total energy of the complementary flour was 16·55 and 76·81 %, respectively, which was adequately considerable and agreed with the recommended values, whereas the energy from fat was determined to be 12·04 %, which was below the desired range.

From these findings, it could be deduced that the contribution of Fe that can be obtained from the optimised dabi teff-field pea-based complementary flour to the daily Fe demand by the children was extraordinarily high that it could even meet the daily requirement under low bioavailability. Thus, the product could demonstrate to fill the huge gap of Fe demand by children that should come from complementary food (97 %) and can serve as a sustainable food-based nutrition intervention against Fe deficiency anaemia.

It might not be surprising that the optimised complementary flour could demonstrate to contribute a higher amount of Fe because dabi teff flour had Fe content at 86·5 mg/100 g, which was one of the major ingredients in our formulations. It is unlikely that the high levels of Fe in the optimal complementary flour can cause any danger to infants and young children since Fe overload in body fluid is mostly hereditary where the intestine continues to absorb Fe at a high rate despite the excess Fe builds up in the body tissue. Fe deficiency is the most common problem rather than its toxicity and some adverse health effects of Fe overload like fatigue, mental depression, abnormal heartbeat, intestinal side effects and diabetes are severe with alcohol abusers because alcohol damages the intestine and impairs its defense against absorbing too much Fe(Reference Diress and Endalifer53). However, the use of such high Fe-containing food in malaria-endemic areas needs to be stressed to avoid complications and may require following the WHO/UNICEF recommendation(Reference Zlotkin, Newton and Aimone54).

The contribution of Zn by the currently optimised complementary flour was lower as compared with the report by(Reference Desalegn, Abegaz and Kinfe55) for the formulation of complementary food from chickpea (kabuli variety), red teff (DZ-0199 variety) and quality protein maize (BHQPY-545 variety and Ipomoea batatas, Tulla variety) that the Zn content fulfilled 81–88·34 % of the RDA, which could be attributed to variety and component variation. In agreement with the present findings, Adetola et al. (Reference Adetola, Onabanjo and Stark56) reported that composite flour from orange-fleshed sweet potato, soyabean and carrot met 22–23 % of the daily recommended allowance for Ca for the 1–3 years age group.

The practical applications of the current study to the reality of shifting the optimised product into children’s diet are that dabi teff-field pea-based energy, protein and Fe-dense homemade complementary foods targeting infants and young children and school-going children can be prepared at home and can also be scaled up at industrial baby food production. The higher Fe density and the notably higher contribution of the product to the daily Fe requirements could make the product have paramount implications in sports nutrition. For example, recent studies have shown that athletic runners require 30–70 % more Fe due to losses from foot strike haemolysis and gastrointestinal blood loss(57) where the consumption of our new product could increase the Hb level of the blood helping more oxygen to be transmitted, which might aid in the higher resistance and increase endurance during athletics performance. It is also suggested that this study needs to be substantiated by conducting randomised controlled feeding trials combined with nutrition education through behavioural change communication to mothers/caretakers to adopt, practise and maintain our new food formula preparation in the rural community and determine the efficacy of the newly developed dabi teff-field pea-based energy, protein and Fe-dense optimised novel complementary flour in improving the nutritional and Fe status of infants and young children.

Conclusion

Nutritional well-being in early childhood is a major driver for optimal growth and development, healthy life, improved school performance as well as improved future productivity and earning potential of children. Children should be nourished with age-specific daily adequate energy and nutrient demands. In the present study, the optimised dabi teff-field pea-based novel complementary flour was demonstrated to provide adequate energy, protein and Fe densities meeting the standard and show the likely contribution of more than 100 % of daily demands for energy and protein, and notably more than 200 % of daily Fe demand by all the age groups (6–8, 9–11 and 12–23-month-old children) as per the by PAHO/WHO recommendation at moderate bioavailability where it even met at lower Fe bioavailability. Thus, children aged 6–23 months can meet their daily energy and nutrient demand if served the estimated amount of the novel complementary food and fed there times a day. The density and daily contribution of Zn from the developed product were marginal, whereas the fat and Ca densities and their daily contribution by the product were inadequate, which might require matching. This study gives the basis for the optimisation of cereal–legume blends from locally available, affordable and underutilised food crops that can serve as sustainable food-based nutrition intervention strategies to fight against protein-energy malnutrition and Fe deficiency anaemia in children.

Acknowledgements

The authors are thankful to the Ethiopian Institute of Agricultural Research (Food Science and Nutrition Laboratory), Addis Ababa; Awash Melkasa Research Center and Horticoop Laboratory International, Debre Zeit for allowing us to use their laboratory facilities for the analysis of the nutrient composition parameters. We thank Dr. Diriba Gelati, Dr. Kasayye Tolassa, Mr. Dinka Mulugeta, Mr. Hailu Reta, Mr. Girmay Tsegay, Mr. Dessalegn Dereje, Mrs. Zufan G/kidan and Mr. Demerew Abera for showing us their bright face and assisting in laboratory data generating activities.

No funding source is available.

D. C. T.: lead in conceptualisation and designing; formal analysis and interpretations; methodology; experimentation; software; writing original draft; writing – review and editing and approved the final version. K. H. A., T. B. and D. T.: conceptualisation and designing; methodology; analysis and interpretations; critical revision of the manuscript; writing – review and editing and approved the final version.

The authors declare that there is no conflict of interests.

References

Dewey, KG & Adua Afarwuah, S (2008) Systematic review of the efficacy and effectiveness of complementary feeding interventions in developing countries. Matern Child Nutr 4, 2485.CrossRefGoogle ScholarPubMed
Vallinoto, P, Moreira, EG & Maihara, VA (2022) Estimation of daily dietary intake of essential minerals and trace elements in commercial complementary foods marketed in Brazil. Food Chem Adv 1, 100039.CrossRefGoogle Scholar
Michaelsen, KF & Greer, FR (2014) Protein needs early in life and long-term health. Am J Clin Nutr 99, 718S722S.CrossRefGoogle ScholarPubMed
Skau, JK, Bunthang, T, Chamnan, C, et al. (2014) The use of linear programming to determine whether a formulated complementary food product can ensure adequate nutrients for 6- to 11-month-old Cambodian infants. Am J Clin Nutr 99, 130138.CrossRefGoogle ScholarPubMed
Onyango, AW, Borghi, E, de Onis, M, et al. (2014) Complementary feeding and attained linear growth among 6–23-month-old children. Public Health Nutr 17, 19751983.CrossRefGoogle Scholar
Hallberg, L & Rossander, L (1984) Improvement of iron nutrition in developing countries: comparison of adding meat, soy protein, ascorbic acid, citric acid, and ferrous sulphate on iron absorption from a simple Latin American-type of meal. Am J Clin Nutr 39, 577583.CrossRefGoogle ScholarPubMed
Ogbonnaya, JA, Ketiku, AO, Mojekwu, CN, et al. (2012) Energy, iron and zinc densities of commonly consumed traditional complementary foods in Nigeria. Br J Appl Sci Technol 2, 4857.CrossRefGoogle Scholar
Health-Canada (2012) Nutrition for healthy term infants: recommendations from birth to six months. Can J Diet Pract Res 73, 204.CrossRefGoogle Scholar
Qasem, W & Friel, J (2015) The recommended first complementary foods: a review of the literature. J Pediatr Neonatal Care 2, 00069.CrossRefGoogle Scholar
Arsenault, JE & Brown, KH (2003) Zinc intake of US preschool children exceeds new dietary reference intakes. Am J Clin Nutr 78, 10111017.CrossRefGoogle ScholarPubMed
Abebe, Y, Stoecker, BJ, Hinds, MJ, et al. (2006) Nutritive value and sensory acceptability of corn-and kocho-based foods supplemented with legumes for infant feeding in Southern Ethiopia. Afr J Food Agric Nutr Dev 6, 119.Google Scholar
FAO/WHO (1991) Guidelines on formulated complementary foods for older infants and young children, CAC/GL 8–1991, REV 2013. http://files.foodmate.com (accessed May 2022).Google Scholar
Shiriki, D, Igyor, MA & Gernah, DI (2015) Nutritional evaluation of complementary food formulations from maize, soybean and peanut fortified with Moringa oleifera leaf powder. Food Nutr Sci 6, 494.Google Scholar
van der Merwe, J, Kluyts, M, Bowley, N, et al. (2007) Optimizing the introduction of complementary foods in the infant’s diet: a unique challenge in developing countries. Matern Child Nutr 3, 259270.CrossRefGoogle Scholar
Dewey, K (2001) PAHO/WHO: Guiding Principles for Complementary Feeding of the Breastfed Child. Division of Health Promotion and Protection. Food and Nutrition Program. https://iris.paho.org/handle/10665.2/752 (accessed May 2022).Google Scholar
Michaelsen, KF (2000) Complementary Feeding of Young Children in Developing Countries: A Review of Current Scientific Knowledge: edited by Kenneth Brown, Kathryn Dewey, and Lindsay Allen, 1998, 178 pages, Softcover. Oxford: Oxford University Press.Google Scholar
Forsido, SF, Kiyak, N, Belachew, T, et al. (2019) Complementary feeding practices, dietary diversity, and nutrient composition of complementary foods of children 6–24 months old in Jimma Zone, Southwest Ethiopia. J Health Popul Nutr 38, 0190172.CrossRefGoogle ScholarPubMed
WHO, Geneva (2003) Global Strategy for Infant and Young Child Feeding. Geneva: WHO.Google Scholar
Rolfes, SR, Pinna, K & Whitney, E (2008) Understanding Normal and Clinical Nutrition. Canada by Nelson Education, Ltd.: Cengage learning.Google Scholar
WHO (2009) Proceedings of the WHO UNICEF WFP UNHCR informal consultation on the management of moderate malnutrition in under-5 children. Geneva, Oct. 2008. Food Nutr Bull 30, S464S474.Google Scholar
Huffman, SL & Schofield, D (2011) Consequences of malnutrition in early life and strategies to improve maternal and child diets through targeted fortified products. Matern Child Nutr 3, 14.CrossRefGoogle Scholar
Ahmed, T, Hossain, M & Sanin, KI (2013) Global burden of maternal and child undernutrition and micronutrient deficiencies. Ann Nutr Metab 61, 817.CrossRefGoogle Scholar
Abeshu, MA, Lelisa, A & Geleta, B (2016) Complementary feeding: review of recommendations, feeding practices, and adequacy of homemade complementary food preparations in developing countries - lessons from Ethiopia. Front Nutr 3, 19.CrossRefGoogle ScholarPubMed
Dewey, KG & Brown, KH (2003) Update on technical issues concerning complementary feeding of young children in developing countries and implications for intervention programs. Food Nutr Bull 24, 528.CrossRefGoogle ScholarPubMed
Abeshu, MA, Adish, A, Haki, GD, et al. (2016) Assessment of caregiver’s knowledge, complementary feeding practices, and adequacy of nutrient intake from homemade foods for children of 6–23 months in food insecure Woredas of Wolayita Zone, Ethiopia. Front Nutr 3, 2016.CrossRefGoogle ScholarPubMed
Baye, K, Guyot, JP, Icard-Verniere, C, et al. (2012) Nutrient intakes from complementary foods consumed by young children (aged 12–23 months) from North Wollo, northern Ethiopia: the need for agro-ecologically adapted interventions. Public Health Nutr 16, 17411750.CrossRefGoogle ScholarPubMed
Etcheverry, P, Hawthorne, KM, Liang, LK, et al. (2006) Effect of beef and soy proteins on the absorption of non-heme iron and inorganic zinc in children. J Am Coll Nutr 25, 3440.CrossRefGoogle ScholarPubMed
Hallberg, L & Hulthan, L (2000) Prediction of dietary iron absorption: an algorithm for calculating absorption and bioavailability of dietary iron. Am J Clin Nutr 71, 11471160.CrossRefGoogle ScholarPubMed
Ruel, MT & Levin, CE (2000) Assessing the potential for food-based strategies to reduce vitamin A and iron deficiencies. FCND briefs 92, 162.Google Scholar
Usha, R, Lakshmi, M & Ranjani, M (2010) Nutritional, sensory and physical analysis of pumpkin flour incorporated into weaning mix. Malays J Nutr 16, 379387.Google ScholarPubMed
Harris, SS (1997) Preventing Micronutrient Malnutrition: A Guide to Food-based Approaches: Why Policy Makers Should Give Priority to Food-based. Strategies. Rome, Italy: ILSI Press.Google Scholar
Thompson, B & Amoroso, L (2011) Combating Micronutrient Deficiencies: Food-Based Approaches. Rome, Italy: CAB International and FAO.CrossRefGoogle Scholar
FNPS (2021) Federal Democratic Republic of Ethiopia National Food and Nutrition Strategy. Addis Ababa: Ethiopia.Google Scholar
EPHI & ICF (2019) Ethiopia Mini Demographic and Health Survey 2019: Key Indictors. Rockville, MD: EPHI and ICF.Google Scholar
Tura, DC, Belachew, T, Tamiru, D, et al. (2023) Optimization of dabi teff-field pea based energy and protein dense novel complementary food with improved sensory acceptability using D–optimal mixture design. Heliyon 9, e19029.CrossRefGoogle ScholarPubMed
Rashid, S & Negassa, A (2011) Policies and Performance of Ethiopian Cereal Markets. Ethiopia Strategy Support Program, Addis Ababa, Ethiopia. ESSP II Working Paper No. 21, pp. 2.Google Scholar
Gebremariam, MM, Zarnkow, M & Becker, T (2014) Teff (Eragrostis tef) as a raw material for malting, brewing and manufacturing of gluten-free foods and beverages: a review. J Food Sci Technol 51, 28812895.CrossRefGoogle ScholarPubMed
Lee, SH, Kim, YB, Kim, DH, et al. (2021) Dietary soluble flaxseed oils as a source of n-3 polyunsaturated fatty acids for laying hens. Poultr Sci 100, 101276.CrossRefGoogle Scholar
Campoy, C, Escolano-Margarit, MV, Anjos, T, et al. (2012) n-3 fatty acids on child growth, visual acuity and neurodevelopment. Br J Nutr 107, S85S106.CrossRefGoogle ScholarPubMed
Rasane, P, Jha, A, Kumar, A, et al. (2015) Reduction in phytic acid content and enhancement of antioxidant properties of nutricereals by processing for developing a fermented baby food. J Food Sci Technol 52, 32193234.Google ScholarPubMed
Castro-Alba, V, Lazarte, CE, Bergenståhl, B, et al. (2019) Phytate, iron, zinc, and calcium content of common Bolivian foods and their estimated mineral bioavailability. Food Sci Nutr 7, 28542865.CrossRefGoogle ScholarPubMed
AACC (American Association of Cereal Chemists) (2000) Cereals and Grains Associations Technical Communities, 11th ed. Washington, DC: AACC.Google Scholar
AOAC (2016) Official Methods of Analysis of the Association of Official Analytical Chemists, 20th ed. Washington, DC: AOAC International.Google Scholar
Ayele, DA, Teferra, TF, Frank, J, et al. (2021) Optimization of nutritional and functional qualities of local complementary foods of southern Ethiopia using a customized mixture design. Food Sci Nutr 10, 239252.CrossRefGoogle ScholarPubMed
de Souza, RM, Leocádio, LG & da Silveira, CL (2008) ICP OES simultaneous determination of Ca, Cu, Fe, Mg, Mn, Na, and P in biodiesel by axial and radial inductively coupled plasma-optical emission spectrometry. Anal Lett 41, 16151622.CrossRefGoogle Scholar
Wasswa, M, Fungo, R & Kaaya, A (2021) Proximate composition and sensory characteristics of refractance window dried cowpea composite porridges. Afr J Food Agric Nutr Dev 21, 1896518979.Google Scholar
Federal Democratic Republic of Ethiopia & M.o.H (2012) Complementary Feeding of Children 6 up to 24 Months Old for IYCF Trainers and Promoters. Addis Ababa, Ethiopia: Federal Democratic Republic of Ethiopia.Google Scholar
Tenagashaw, MW, Kinyuru, JN, Kenji, GM, et al. (2017) Nutrient density of complementary foods formulated from a blend of teff, soybean and orange-fleshed sweet potato. Int J Food Sci Nutr Eng 7, 6169.Google Scholar
Hurrell, R & Egli, I (2010) Iron bioavailability and dietary reference values. Am J Clin Nutr 91, 1461S1467S.CrossRefGoogle ScholarPubMed
Walle, H & Moges, D (2017) Optimization of cereal-legume blend ratio to enhance the nutritional quality and functional property of complementary food. Ethiopian J Sci Technol 10, 109122.CrossRefGoogle Scholar
Wolmarans, P, Kunneke, E & Laubscher, R (2009) Use of the South African Food Composition Database System (SAFOODS) and its products in assessing dietary intake data: part II: invited review. S Afr J Clin Nutr 22, 5967.Google Scholar
Diress, G & Endalifer, ML (2022) Effect of alcohol consumption on haemoglobin level among non-pregnant reproductive age women in Ethiopia: a cross-sectional secondary data analysis of the 2016 Ethiopian Demographic Health Survey. BMJ Open 12, e046458.CrossRefGoogle Scholar
Zlotkin, S, Newton, S, Aimone, AM, et al. (2013) Effect of iron fortification on malaria incidence in infants and young children in Ghana: a randomized trial. JAMA 310, 938947.CrossRefGoogle ScholarPubMed
Desalegn, BB, Abegaz, K & Kinfe, E (2015) Effect of blending ratio and processing technique on physicochemical composition, functional properties and sensory acceptability of quality protein maize (QPM) based complementary food. Int J Food Sci Nutr Eng 5, 121129.Google Scholar
Adetola, OY, Onabanjo, OO & Stark, AH (2020) The search for sustainable solutions: producing a sweet potato based complementary food rich in vitamin A, zinc and iron for infants in developing countries. Sci Afr 8, e00363.Google Scholar
Micronutrients and Nutrition Board (2002) Dietary Reference Intakes for Vitamin A, Vitamin K, Arsenic, Boron, Chromium, Copper, Iodine, Iron, Manganese, Molybdenum, Nickel, Silicon, Vanadium, and Zinc. Dietary Reference Intakes. https://pubmed.ncbi.nlm.nih.gov/25057538/ (accessed May 2022).Google Scholar
Figure 0

Fig. 1. Collected complementary food crops (photo by the researcher).

Figure 1

Table 1. Major macro- and mineral compositions of each crop sample collected

Figure 2

Fig. 2. Process flow chart diagram of the crop samples and formulations.

Figure 3

Table 2. Goals set, the relative importance of each variable and the optimal values at optimal conditions

Figure 4

Table 3. Macro- and mineral composition of the formulated mean, the optimised, the control and FAO/WHO specifications

Figure 5

Fig. 3. 3D surface graph of desirability function at the overall optimisation.

Figure 6

Table 4. Experimental validation of optimal condition and comparison with the control flour

Figure 7

Fig. 4. Graphical overlay contour plot for the overall graphical optimisation.

Figure 8

Table 5. Energy and nutrient densities of the formulated mean, the optimal and the control flours and PAHO/WHO standards

Figure 9

Table 6. Contribution of the optimised flour to the daily energy and protein demands by 6–23-month-old children from complementary flour as recommended by PAHO/WHO (2001)

Figure 10

Table 7. Contribution of the optimised flour to the daily Fe, Ca and Zn demands by 6–23-month-old children from complementary flour as recommended by PAHO/WHO (2001)