Hostname: page-component-cd9895bd7-lnqnp Total loading time: 0 Render date: 2024-12-27T11:47:09.700Z Has data issue: false hasContentIssue false

Energy and nutrient intake by 11–13-year-old young adolescents attending private schools in Delhi, India

Published online by Cambridge University Press:  03 June 2024

Anupama Ivaturi*
Affiliation:
Adelaide Dental School, The University of Adelaide, Adelaide, SA, Australia
Lynne Giles
Affiliation:
School of Public Health, The University of Adelaide, Adelaide, SA, Australia
Loc G. Do
Affiliation:
School of Dentistry, University of Queensland, Herston, QLD, Australia
Tina Rawal
Affiliation:
Public Health Foundation of India, Gurgaon, Haryana, India
Monika Arora
Affiliation:
Public Health Foundation of India, Gurgaon, Haryana, India
Paula Moynihan
Affiliation:
Adelaide Dental School, The University of Adelaide, Adelaide, SA, Australia
*
*Corresponding author: Dr A. Ivaturi, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

There are no high-quality data on dietary behaviour of adolescents in India. This study aimed to assess the intake of energy (E), macronutrients and selected micronutrients in a sample of 11–13-year-old schoolchildren in Delhi, India. Participants from private schools (n=10) recorded dietary intake using a 3-d food diary. Information was entered into the dietary assessment tool, Intake24, to ascertain portion size and convert data into nutrient intake through integrated food tables. Of the 514 consenting participants, 393 (76·4 %) (169 girls, 224 boys) aged 11·4 (±1·8) years completed the study. The median (interquartile range (IQR) daily E intake was 2580 (2139·3–2989·8) kcal (10·8 (9·0 − 12·5) MJ) for girls and 2941·5 (2466·7–3599·3) kcal (12·3 (10·3–15·2) MJ) for boys. The median (IQR) daily nutrient intakes for girls and boys respectively were protein 64·6 (54·8–79·3) g, 74·4 (61·4; 89·4) g; carbohydrate 336·5 (285·3–393·6) g, 379·6 (317·8–461·8) g; and saturated fat 45·6 (34·8–58·3) g, 54·6 (41·9–69·5) g. There were no significant between-gender differences in percentage E from protein (10·2 (9·2–11·4)), or carbohydrate (52·4 (48·7–56·7)). Girls obtained less percentage E from saturated fat (16·1 (11·0–18·2) compared with boys 16·3 (14·2–19·1) (P < 0·05). E from saturated fat was above FAO recommendations in >74 % of participants. The estimated average requirement for iron was achieved by < 40 % of girls. In conclusion, strategies to optimise the dietary intake of adolescents in India should focus on preventing excess intakes of E and saturated fat and improving iron intake in girls.

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), 2024. Published by Cambridge University Press on behalf of The Nutrition Society

India has the largest adolescent population (>253 million) in the world(1). Early adolescence is a period of rapid development and growth(Reference Kupka, Siekmans and Beal2). Requirements of energy (E) peak as does the requirements for micronutrients, and therefore, adolescence is a period during which there is an increased risk of deficiency(Reference Sullivan, Childs and O’Connell3). The results of the Comprehensive National Nutrition Survey (2016–18)(4) show that a ‘triple burden’ of undernutrition, micronutrient deficiency(Reference Pandurangi, Mummadi and Challa5,Reference Meenakshi6) and overnutrition exists in the young Indian population(Reference Meenakshi6Reference Verma, Aditi and Kapoor8). Dietary preferences and habits that form in adolescence may last lifelong, and therefore, it is an appropriate time to encourage and build healthy eating habits(Reference Hollis, Collins and DeClerck9).

The transition of the traditional Indian diet towards a more ‘westernised’ diet that includes prepackaged and processed food has been reported previously(Reference Shetty10,Reference Popkin11) . Existing food environments in lower-middle-income countries (LMIC) like India negatively impact dietary intake(Reference Sawyer, van Lenthe and Kamphuis12). Children from the lower socio-economic status groups typically attend Government schools, and those from middle- and higher-income families attend private schools. Despite school feeding programmes actively operating in Government and Government-aided schools, children from lower income groups are disproportionately impacted by the unhealthy city food environments near schools with the offer and sale of processed food. On the other hand, children from middle- and high-income groups attending private schools have access to disposable income and are exposed to processed high-fat, sugar and salt foods within schools through cafeterias and through the location of outlets of multinational fast-food chains in the environment around school with no access to an organised school lunch programme(Reference Bassi, Bahl and Arora13). Therefore, all the children and adolescents attending schools in Delhi, irrespective of the socio-economic status, are at risk of exposure to unhealthy processed foods, with the young adolescents attending private educational institutions facing a significant impact of consistent exposure within and outside schools. This is concerning as it contributes to a high risk of noncommunicable diseases(Reference Bassi, Bahl and Arora13)

The most recent available evidence shows that there is an increasing trend of the combined prevalence of childhood obesity and overweight in India with the highest reported combined prevalence from New Delhi(4,Reference Ranjani, Mehreen and Pradeepa14) . This trend sustained in the latest (2019–21) report of the National Family Health Survey, which showed an increase in prevalence of overweight and obesity for men, women and children under 5 years compared with the previous survey year (2016). However, the prevalence data for obesity and overweight for the 11–14 years age group are not available in National Family Health Survey. The Comprehensive National Nutrition Survey data (2016–18) are the only available resource on prevalence of overweight (12·3 %) and obesity (3·6 %) for this age group(4). Despite these concerning figures, there are no data on the individual dietary behaviour of this population.

Addressing undernutrition and ensuring food security remains the priority of the Government of India(Reference Sankar and van den Briel15). Food fortification and vitamin supplementation were implemented as stopgap measures to address micronutrient deficiency in vulnerable groups, i.e. low socio-economic status children and adolescent girls, specifically deficiencies of vitamin A, B12, folate, iron and iodine(Reference Vijayaraghavan16). However, these approaches have been criticised for the lack of sustainability(Reference Locks, Shah and Bhaise17). The results of haematologic investigations in the Comprehensive National Nutrition Survey 2016–18(4) showed that iron deficiency anaemia was still prevalent in 40 % of adolescent girls in India(Reference Scott, Lahiri and Sethi18), and 24 % of adolescents were vitamin D deficient. The 2019–21 National Family Health Survey report has shown that more than half (51·5 %) of the adolescent girls in Delhi were anaemic, a further increase from the previous assessment in 2016.

The Government of India has now evolved its strategies to tackle the triple nutrition burden in adolescents through a package of interventions in the National Adolescent Health Program to be delivered in collaboration with other health agencies(1,19) . In addition to supply of fortified food in school lunches, approaches for adolescents to build an understanding of nutritious diet, make healthier choices and, avoid processed food are being implemented in Government schools but not in private schools. Policy-level action has been initiated to prohibit sale and marketing of unhealthy foods within and around schools(20). There are, however, no high-quality data on the level of intake of nutrients including sugars from local foods, and the existing reports are limited to intake of food groups(Reference Locks, Shah and Bhaise17) by adolescents. It is important to generate sub-national and national data on dietary intake to identify the level of any problem and inform the efforts to optimise eating behaviours.

Previous surveys of ten states of India of diet and nutrition status of rural(21) and urban(22) populations conducted in 2012 and 2017 respectively reported that the mean intakes of calcium, iron, folate, B12 and vitamin A in young adolescents did not meet the Recommended Dietary Allowance (RDA-the average daily dietary intake level that is sufficient to meet the nutrient requirement of nearly all (97–98 %) of healthy individuals). Since the publication of these reports, the reference values have been updated(23) and estimated average requirement (EAR) values were defined by the National Institute of Nutrition (NIN). For a given nutrient, the EAR represents the nutrient intake value that is estimated to meet the requirement of 50 % of the healthy individuals. The NIN-EAR was suggested for the first time as the appropriate reference value for assessing requirements and adequacy in healthy individuals. Since the update of dietary reference values in 2020, no data on dietary behaviour have been collected and compared with the initial EAR for E and nutrients.

Research shows that lockdown during the COVID-19 pandemic had a significant impact on diet and physical activity(Reference Stockwell, Trott and Tully24Reference Bennett, Young and Butler27). In adolescents, compared with pre-pandemic period, screen time and intake of all food groups increased with a notable decline in physical activity(Reference Martín-Rodríguez, Tornero-Aguilera and López-Pérez28,Reference Al Hourani, Alkhatib and Abdullah29) . In a study on young adolescents living in Mumbai, an increase in the intake of staple food and fruit, as well as foods high in sugar, fried food, sugar-sweetened beverages with a marked rise in snacking in between meals, was reported(Reference Moitra and Madan30). In Delhi, schools remained closed for two years due to the pandemic and reopened in 2022. In this post-pandemic context, an update on the nutrient intake would be useful to understand adolescent dietary behaviours.

Previous studies of dietary intake in India have relied on existing food composition databases and required researchers to manually analyse data(Reference Locks, Shah and Bhaise17) for the estimation of intake of nutrients from reported food intakes, and these were usually collected using 24 h recalls or food frequency questionnaires(21,22) . However, there are no comprehensive local food and recipe databases. Further, the challenge posed by the lack of software to link the intakes to national food compositional tables has been identified(Reference Locks, Shah and Bhaise17). Open-source and low-cost applications that facilitate assessment of dietary intake through the creation of a digital record of the food and drink intake are commonly used in high-income countries(Reference Ji, Plourde and Bouzo31,Reference Foster, Lee and Imamura32) . The application of such tools for dietary assessment in LMIC is limited or, as is the case with India, non-existent. The validity and reliability of one such tool ‘Intake24’ (https://intake24.org) has been tested(Reference Foster, Lee and Imamura32) and used in the national dietary surveys in other countries (e.g. the United Kingdom (UK) National Diet and Nutrition Survey)(Reference Foster, Lee and Imamura32Reference Simpson, Bradley and Poliakov34). An English Language South Asia Locale (2022 version) of this application has recently been developed (https://intake24.co.uk/info/localisation) but it has not previously been applied to populations in India.

The aim of this study was to determine the intake of E and nutrients in 11–13-year-old young adolescents attending private schools in Delhi using the South Asia locale of Intake24. The specific objectives were to (i) estimate the intake of E and macronutrients and the contribution of macronutrients to E, (ii) to estimate the intake of vitamins A, D, B12, folate and iron, calcium, zinc, iodine and (iii) compare the intakes with the NIN-EAR.

Methods

Ethical approval

This study was conducted according to the guidelines laid down in the Declaration of Helsinki, and all procedures involving research study participants were approved by The Human Research Ethics Committee at The University of Adelaide (H-2021-027, Date: 8 March 2022) and by the Institutional Ethics Committee, Centre for Chronic Disease Control, New Delhi, India (CCDC-IEC_14_2021 Date: 9 December 2021).

Study location

Delhi is a Union Territory located in North India with a population of more than 16·7 million (2011 census)(35). New Delhi, the capital city of India, is located within Delhi. There are eleven civic administrative districts and three municipalities, divided broadly into rural and urban sectors. The municipal corporations of North, East, South and New Delhi constitute the urban sector and villages (n 112) located in different districts constitute the rural sector.(35).

Sample size and school selection

Young adolescents in the age group of interest (11–13 years) (hereafter referred to as adolescents in this paper) attend middle schools in Delhi, i.e. sixth to eighth Grade. Since the primary aim of the doctoral project was to determine the data on the level of intake, principal dietary sources and patterns of free sugars intake in this sample of 11–13-year-old schoolchildren in India, the sample size calculations were based on the number of participants needed to estimate the total sugars intake in grams per day with a margin of error of ± 5 g/d.

The calculations assumed 80 % power to estimate mean total sugar intake and two-sided α of 0·05. The target sample size was set at 450 which was inflated to allow for 20 % attrition. It was anticipated that by recording the food and drink data from at least 360 adolescents, considering the total number of 11–13-year-olds in Delhi, we would be able to calculate the sugars intake data with a margin of error of ± 5 g/d. Private schools constituted 40 % of the total school enrolment in 2022 and 95 % of the 11–14 age demographic attended a school in Delhi. The number of private schools and students is not uniform across the eleven districts in Delhi. Therefore, using the complete list of 1374 private schools provided by the Directorate of Education, Government of National Capital Territory Delhi, a statistician external to the research team generated a schedule containing the names of 150 random schools, stratified by district from across the eleven districts of Delhi. Using this schedule, schools were invited to participate, and recruitment continued until ten schools had consented.

School consent

Using the list of 150 schools, a researcher (AI) contacted the principal of each school through email and on telephone and explained the purpose of the study in plain language. The researcher made three attempts to connect with the school and explain the study information. If no response was obtained or if the school declined to take part, the researcher moved to the next school on the list for that specific district. This process was repeated until the researcher recruited at least one school from each district. Researchers collaborated with Health-Related Information Dissemination Amongst Youth, a nongovernmental organisation based in Delhi, for establishing initial contact with the principals of private schools. The researcher shared information about the study with those schools that expressed interest to take part in the research through email. Once a school agreed, a link to the school consent form was sent by email (Qualtrics XM Experience Management, North Sydney, Australia). Upon obtaining consent, the process for recruitment of participants was initiated.

Parent consent and participant assent

A template letter for inviting parents of the 11–13-year-old students to take part in the study was prepared by the researcher (AI) and provided to the school. Within each school, a dedicated teacher provided study information (prepared in plain language in both Hindi and English by the researcher AI) to the parents of the 11–13-year-old students through the school network on social media applications (WhatsApp) or through emails. Parents of interested students communicated their willingness to participate to the teachers. The teacher then created a list of all interested participants. Next, the teacher asked the parents to fill in and sign the online parent consent form by sharing a link to this form (hosted on Qualtrics) through the school’s social media network. Some schools requested the researcher to provide a brief orientation about the research to the group of participants who were selected by the school. This talk was organised by the school and held in the school’s auditorium or in a classroom. During this interaction, the researcher explained in detail the purpose of the study and the expected level of involvement of the participants. The researcher requested participants to share the study information with parents. Only after the researcher received a filled-in and signed consent form (made available in English and Hindi) from the parent(s), the student was recruited as a participant in the study. A participant information sheet was shared by the researcher for the participants to further understand the purpose of the study and the level of their involvement. Participants provided assent online (hosted on Qualtrics) before data collection commenced. The numbers of participating students from each school varied. This was based on the total number of 11–13-year-old students in the school, and the number of participants for whom parental consent has been obtained.

Collection of demographic data

Demographic data on participants were collected from their parents using an online questionnaire, using the Qualtrics survey tool. The variables included name, age and date of birth of the child, name and age of the parent and the area of residence. As part of this questionnaire, parents were asked to record at home or provide from previous records, the weight (in kilograms) and height (in inches or centimetres) of their child.

Dietary data collection

Dietary data were collected between May and October 2022. Participants recorded all foods and drinks consumed over three consecutive days in paper-based or online version of a purpose-designed food diary. The instructions for filling in the diary were provided in English and Hindi. Recording included two weekdays and one weekend day. This allowed estimation of the dietary intake during school days (Friday, Saturday, Monday and Tuesday) and non-school days (Sunday). Participants were asked to report all food and drink consumed including the time of consumption and the amount that was consumed using household measures (cups, bowls, spoons, glasses and plates etc.) After completing the diary, the researcher met each participant in a one-on-one online interview to discuss, clarify and enlarge on the information provided and to confirm the portion size of foods and drinks consumed using the library of 2500 food portion sizes available in the online dietary assessment tool Intake24 (South Asia Locale 2022 version)(Reference Foster, Lee and Imamura32,Reference Bradley, Simpson and Poliakov33) . During the interview, the researcher entered the dietary information into Intake24 which enabled the daily intake of E and sugars to be derived through integrated food composition tables. The Intake24 tool captures data on nutrient supplementation. However, these data were not analysed in this study as the intake of nutrients from foods was of interest.

Following the completion of all interviews, the resulting data file was downloaded as an Excel spreadsheet from Intake24. The dietary data were imported into STATA 17·0 (Stata Statistical Software: Release 17. College Station, TX: Stata Corp LLC). In the dataset, the daily dietary data for each participant for each of the three days were organised into eating occasions. The pre-defined eating occasions in Intake24 included the following: (1) early snack or drink; (2) breakfast; (3) morning snack or drink; (4) lunch; (5) afternoon snack or drink; (6) evening meal and (7) late snack or drink. Water intake was recorded at the end of each day as daily water intake. In the spreadsheet, the data were identified through user ID which included name of the school and the numeric participant ID (1 to n for each school). Indexing variables were created for the school, the participant, the day and the eating occasion. The total intake of E (megajoules), grams of carbohydrates, protein, fat, saturated fat and fibre and vitamins A, B12, folate and D, and minerals iron, calcium, zinc, iodine and selenium for each of the three days of recording was derived and then averaged to get the daily intake of E and nutrients for each participant.

Validation of energy intake

The estimation of physical activity level (PAL) was used to validate the reported E and identify the proportion of participants who may have over- or under-reported E. The PAL was calculated by dividing the reported E by the basal metabolic rate. Schofield equation(Reference Schofield36) was used to predict the basal metabolic rate from gender, age, height and weight information provided by the participants.

Statistical analyses

The distribution of variables was assessed. Descriptive statistics for continuous variables that were normally distributed included mean, SD and 95 % CI and for variables with non-Gaussian distribution median and interquartile range (IQR) were reported. Between gender differences for E, macronutrient and micronutrient intake and percentage E obtained from macronutrients were explored through Wilcoxon rank-sum tests. A two-sided significance level of 0·05 was used in all analyses.

Results

Participation rate

During the school recruitment process, twenty-seven schools declined to participate, and fifteen schools could not be contacted. In total, fifty-two schools were approached before the required sample of ten was achieved. Between June and October 2022, students from each school consented. Of the 514 participants in total who provided consent, 393 (169 girls, 224 boys) completed the diary on all three days and attended the interview (76·4 %) (Fig. 1). The mean age of the participants was 11·4 (sd 1·8) years.

Fig. 1. Participation rate from ten private schools in Delhi, India.

Energy intake and physical activity level ratios

The distribution of the E, macronutrient and micronutrient intake data was skewed, and therefore, the data have been summarised as medians and IQR. The median IQR daily E intake was 2580 (2139·3–2989·8) kcal (10·8 (9·0 − 12·5) MJ) for girls and 2941·5 (2466·7–3599·3) kcal (12·3 (10·3–15·2) MJ) for boys (Table 1). The PAL ratios derived for those 241 participants who provided height and weight were 2·0 for girls and 2·1 for boys. The median weight of the ninety-seven (57·4 %) girls who provided anthropometric data was forty-five (IQR 38; 51) kg and of the 144 (67·3 %) boys who provided data was 44·1 (IQR 37; 52·5) kg. The median weight for the study population was above the reference weight for Indian 10 to 12 years old (34·9 kg for boys and 36·4 kg for girls) (23).

Table 1. Energy, macronutrient intake and percentage contributions of macronutrients to energy for 393 11–13-year-old adolescents (224 boys and 169 girls) attending private schools in Delhi, India

(Median values and IQR values)

IQR, interquartile range; EAR, estimated average requirement; NIN, National Institute of Nutrition

Macronutrient intakes

The information on the median daily intakes of carbohydrate, fat, saturated fat and protein is detailed in Table 1. There were no significant between-gender differences in percentage E from protein: median 10·2 (IQR 9·2–11·4); boys 10·1 (9·2–11·4) v. girls 10·4 (IQR 9·2–11·5), or carbohydrate: median 52·4 (IQR 48·7–56·7); boys 51·9 (48·4–56·3) v. girls 52·9 (49·5–57·5). A comparison of the macronutrient intake (g) of the study population with NIN-EAR for Indian 10–12-year-olds(23) and the percentage E contributed by macronutrients with the FAO recommended ranges(37) is also presented in Table 1. The absolute intakes of macronutrients (g/d) were above the India NIN-EAR for 10–12-year-old population. The percentage E contributed by carbohydrate and protein was within the recommended FAO ranges but the contribution of saturated fat to E was considerably above the recommended threshold of no more than 10 %(37). Girls obtained less percentage E from saturated fat (16·1 % (IQR 11·0–18·2) compared with boys 16·3 % (IQR 14·2–19·1) (P < 0·05).

Micronutrient intakes

The median intakes of micronutrients are summarised in Table 2, along with the percentage of participants achieving NIN-EAR for the intake of micronutrients.

Table 2. Micronutrient intake by 393 11–13-year-old adolescents (224 boys and 169 girls) attending private schools in Delhi, India

(Median values and IQR values)

IQR, interquartile range; EAR, estimated average requirement; NIN, National Institute of Nutrition, RDA Recommended Dietary Allowance.

Nearly all the participants (95 %) achieved the EAR for daily vitamin A intake. In contrast, only 7 % of boys and 4 % of girls achieved the NIN-EAR for Vitamin D. The median daily intakes of Iodine in girls iron, selenium and vitamin D in both girls and boys were below the NIN-EAR. Less than 40 % of girls achieved the NIN-EAR for daily iron intake.

Discussion

In this sample of adolescents living in Delhi, the intakes (g/d) of protein, carbohydrate and fat were above the NIN-EAR. The median E intake 2761 (2348·4–3358·1) Kcal/d (11·6 (9·9–14·1) MJ/d) was higher than that previously reported for similar aged adolescents living in some high-income countries in the WHO European(Reference Samuelson38), American(Reference Sullivan, Childs and O’Connell3,Reference Aljaraedah, Takruri and Tayyem39) , Eastern Mediterranean(Reference Al-Jawaldeh, Taktouk and Nasreddine40), Western Pacific Regions(Reference Dutch, Golley and Johnson41) and LMIC like Libya(Reference Huew, Maguire and Waterhouse42) but is similar to intakes reported for adolescents in the African and South East Asian regions; e.g. 9·7 MJ/d in Cameroon(Reference Dapi, Hörnell and Janlert43) and approximately 12·3 MJ/d in Bangladesh(Reference Ali, Scheelbeek and Sanin44). The E intake in the current study was validated against the estimation of PAL using data provided by a sub-sample (n 241). The PAL for this sub-sample falls in the ‘vigorous activity’ category of the FAO classification; however, the higher than desirable median weight (45 kgs) and high median E intake is suggestive of overeating. Hence, there is a need to control E intake in order to prevent obesity. However, it is possible that participants may have overestimated portion sizes for social desirability. Moreover, Intake24 sometimes relies on best-match foods from the UK food compositional database when data on the composition of local foods are unavailable. Further development of the SE Asian version of Intake24 to include more specific compositional data is desirable for future surveys.

Macronutrient intake

Of concern is the percentage contribution of saturated fat to E (median 16·3 %), which is above the 10 % E threshold for intake of saturated fats recommended by the WHO FAO and other authoritative agencies(23,37) . More than 90 % of the current study sample consumed above 10 % E as saturated fat and dietary fat contributed more than 35 % to total E in 75 % of the boys and 65 % of girls. This figure is higher than the reported contribution of saturated fat to E in the diets of 11–18-year-olds living in the UK (median 12·6 %)(45) and 13–18-year-olds in Europe (14·0 %)(Reference Samuelson38) and the Middle East (15·0 %)(Reference Al-Jawaldeh, Taktouk and Nasreddine40). Due to the known association between a diet high in saturated fat and risk for noncommunicable diseases(46), strategies to lower the intake of saturated fat to less than 10 % E in adolescents need consideration. The intake of the ready-to-eat and prepackaged foods reported by the current study sample as ‘snacks’ probably contributed to the high-fat intake(Reference Kaushik, Narang and Parakh47). Such foods are widely available within private schools in the cafeteria and in school food environments(Reference Gupta, Shah and Kumar48). It is important to find means and strategies to support and promote the intake of nutrient-dense food and reduce the consumption of high-fat energy-dense food.

The percentage E from carbohydrates and fat in the current study was lower than that in diets of adolescents in the UK(45) and many high-income countries in Europe(Reference Samuelson38) and Middle East(Reference Al-Jawaldeh, Taktouk and Nasreddine40) and in LMIC such as Lebanon, Libya and Morocco(Reference Al-Jawaldeh, Taktouk and Nasreddine40). The balance of carbohydrate, fat, saturated fat and protein in the diets of adolescents should be investigated further to inform strategies that promote healthy eating by this population. The intake of energy-dense and nutrient-poor prepackaged snacks especially by schoolchildren is driven by the ubiquitous sale and marketing of such foods. A lack of policy in India that calls for limiting the use of saturated fats in the manufacture or preparation of snack foods compounds the scenario around snack food intake.

The median percentage E contributed by protein in the current study sample (10 %) is lower than the contribution of protein (approximately 15 %) in the diets of adolescents aged between 11 and 18 years in the UK(45) and between 13 and 18 years in Europe(Reference Cruz49) and Middle East(Reference Al-Jawaldeh, Taktouk and Nasreddine40) but is similar to the reported intake of protein for similar aged adolescents attending schools in LMIC, for instance Cameroon (10 %)(Reference Dapi, Hörnell and Janlert43) and Bangladesh (9 %)(Reference Ali, Scheelbeek and Sanin44). The 2017 survey on urban populations in India has reported that the intake of protein is low when compared with the recommended dietary allowance(22). Further, results from a survey that compared Indian diet with the Lancet EAT-reference diet indicate that the intake of plant and animal-based protein is low across all sectors, regions and income groups in India(Reference Sharma, Kishore and Roy50). The sources of protein, saturated fat and carbohydrates in the diet of this population should be investigated further to inform strategies to promote a balanced diet. While large sections of the populations consume a carbohydrate-based vegetarian diet during the week and limit intake of meat-based protein sources to weekends and special occasions, it would be useful to investigate the factors that drive the protein intake patterns of adolescents to improve intake.

Micronutrient intake

The intake of micronutrients was compared with the NIN-EAR, except for selenium. The India NIN provides the recommended dietary allowance for daily selenium intake but no EAR. Median intakes below the NIN-EAR were observed for the intake of vitamin D, folate, iron and zinc.

The finding that the intake of Vitamin A was above the NIN-EAR in nearly all participants (95 %) contrasts with the findings for school-age adolescents in developing countries which have reported the status of Vitamin A to be inadequate in > 85 % of adolescents in Ethiopia and > 80 % of adolescents in Cameroon and Uganda(Reference Ochola and Masibo51). The current study figure is also unlike the 2012 and 2017 survey findings(21) which showed that vitamin A intake was inadequate in 52–85 % of adolescents. However, these previous reports compared the intake with the recommended dietary allowance for vitamin A (600 µg/d). In addition to the difference in methodology to report the adequacy of intake, it is also likely that the results are different due to the reported change in diet with a shift towards intake of raw vegetables and in some participants, supplementation.

The low intake of Vitamin D in the current study population is similar to that reported for adolescents in UK (1·8 µg/d)(45). Dietary sources of Vitamin D are few; however, it is likely that the study population benefited from subcutaneous synthesis of vitamin D. According to the serologic investigations conducted as a part of the 2016–18 Comprehensive National Nutrition Survey,(4) nearly half of the (47·1 %) adolescents in Delhi were found to be deficient in Vitamin D. Information of the serum concentrations of 25(OH)D (25-hydroxy cholecalciferol) would provide more comprehensive information on Vitamin D status. Possible changes in the exposure to sunlight due to the confinement of participants indoors because of the pandemic may have affected the vitamin D status.

The median daily intake of folate by girls in the present study (254 µg/d (IQR 203–304)) is considerably higher than the previously reported intake (165 µg/d) for south Indian adolescent girls(Reference Gupta, Noronha and Shobha52). Of concern, however, are the relatively low intakes of iron by girls found in the current study. Inadequate status of iron in adolescent girls has previously been reported for several developing countries in Africa, Southeast Asia and Middle East(Reference Ochola and Masibo51,Reference Arsenault, Moursi and Olney53) . More than 60 % of the girls in the current study did not achieve the NIN-EAR for iron intake. The figure is much higher with 73 % of boys achieving the NIN-EAR. Information on menarche was not collected in the current study which may have provided clarity on the demand for iron and folate in girls. Both the 2012 and 2017 surveys in India(21) showed that adolescent girls and boys are unable to achieve adequate iron intake. Girls have poorer dietary intake in general compared with boys. The information on the sources of iron in food and the pattern of intake of iron by girls and boys could be investigated further to understand the factors that inform the differences in percentage of boys and girls achieving the NIN-EAR for Iron.

Furthermore, more than half of anaemia cases are estimated to be due to iron deficiency(54). In India, anaemia is a recognised public health problem. One priority of the National Adolescent Health Program(19) is weekly micronutrient supplementation through the provision of iron and folic acid tablets. However, only adolescents in government, government-aided and municipal schools are covered(7,19) . The current study results suggest the need to improve iron intake by girls. The fact that the current study sample of adolescents attending private schools does not have access to the fortified food supply through school lunches suggests that there is a need to explore the feasibility of expanding the weekly supplementation to adolescent girls in all schools.

Compared with intakes reported for adolescents in previous studies conducted in LMIC in Africa(Reference Ochola and Masibo51,Reference Arsenault, Moursi and Olney53) and Middle East(Reference Ochola and Masibo51), median zinc intake (8·6 mg/d) was high with 72 % of girls achieving the NIN-EAR. Participants in the present study reported intake of zinc-containing foods as a part of main meals, e.g. dal, and pulses like chickpeas, soybeans, rajma beans, etc., which may have contributed to adequate zinc intake. Compared with previously reported intake for adolescent girls in India,(Reference Gupta, Noronha and Shobha52,Reference Awasthi, Kumar and Mahdi55,Reference Kawade56) the zinc intake is high.

The proportion of the study population which achieved the NIN-EAR for iodine (75 %) is higher compared with previous estimates(Reference Gonmei and Toteja57). Salt fortification with iodine was a crucial component of a national programme that aimed to prevent and control the endemic iodine deficiency disorders in India which also lead to a ban on the sale of non-iodised salt. Although information on the intake of iodised salt was not specifically obtained in the current study, this is likely to have contributed to adequacy of iodine intake. Thirty percentage of girls and 37 % of boys achieved the NIN-recommended dietary allowance for selenium intake (40 µg/d, EAR not defined). There are few comparative data on selenium intake available although the intake was comparable with that reported for UK adolescents(45). However, recently available data from the estimation of serum selenium levels showed that 10 % of urban young adolescents in India and a majority of adolescents in LMIC in Africa have inadequate serum selenium(Reference Awasthi, Kumar and Mahdi55,Reference Amare, Moges and Fantahun58) .

Strengths and limitations

Revised nutrient recommendations for intake of E and nutrients in the Indian population at different ages were proposed in the year 2020. To the authors’ knowledge, this is the first assessment of dietary intake reported since then. The data on nutrient intake are the first to be collected using the Intake24 South Asia Locale and the results provide an update on the status of nutrient intake in schoolchildren since the pandemic. This research study serves as an example for application of a validated digital tool for assessment of nutrient intake in school settings and provides the opportunity to discuss the scope of further research through localisation of the tool for dietary surveys in India.

Nonetheless, there are some limitations which need to be acknowledged. First, participant-reported and not researcher-measured height and weight were used to derive PAL. The height and weight data were available for only 61·3 % of the sample which may have impacted the accuracy of the PAL ratios. Second, Intake24 is designed to be a self-completed multiple pass 24 h recall dietary analysis tool. However, the South Asia locale is available only in the English language which was not the first language for many participants. Therefore, the food and drink intake data were collected using a 3d dietary diary and the researcher transferred this information to Intake24 which was used to ascertain the portion size (during a participant-researcher interview) and to translate recorded food intake into the intake of nutrients. Although the participants did not directly enter dietary data, the library of portion size photographs enabled portion size estimation. Third, despite Intake24 South Asia locale being the most comprehensive dietary assessment tool designed to be used in all the Southeast Asian countries, the nutrient composition of every Southeast Asian food and drink item is not available. Therefore, the system finds a best match from the UK food composition tables which may introduce some inaccuracies. Fourth, the study was conducted between May and December 2022, a time during which participants were transitioning back into in-person learning at schools after the COVID-19 lockdown led to school closures. The changes to diet reported by participants, i.e. increase in the intake of raw vegetables, citrus fruit juices and whole fruits(Reference Motiwala, Khan and Ahmad25,Reference Bennett, Young and Butler27) which persisted even after schools reopened, could have influenced the nutrient intakes. Finally, it is possible that the data were subject to bias of social desirability so that unhealthy food or drink items may have been under-reported, and participants may have overestimated the portion sizes during the interview with the researcher(Reference Miller, Abdel-Maksoud and Crane59,Reference Kelly, Doty and Guidinger60) .

Future directions

The results show that it is possible to obtain individual and population-level data including the daily intake of E and nutrients through the use of Intake24. The capture of data using Intake24 reduced research burden by translating reported food intake into daily intake of nutrients. Intake24 should be further developed into local languages and expanded to include a more comprehensive coverage of foods and dishes that are part of the food culture of India.

The findings of this study pertaining to the intake of E and macronutrients suggest that interventions including policy measures are needed to prevent excess E intake provided by fat, especially saturated fat. The results relating to the intake of iron in girls suggest targeted strategies to reduce the risk of anaemia in adolescence by improving dietary intake through measures such as food fortification may be required. Further research should be undertaken to understand the balance of fat intakes and patterns of protein intake by adolescents in India to underpin the strategies to lower exposure of schoolchildren to deep-fried snack foods and encourage healthy eating.

Conclusion

The E intake in this sample of young adolescents attending private schools in Delhi, India, was above the level recommended by FAO and the India NIN-EAR. The intake of saturated fat was above the <10 % E threshold, with higher intakes in boys compared with girls. The majority of the girls did not achieve the NIN-EAR for iron. Strategies to optimise dietary behaviours in young adolescents attending private schools in India should focus on preventing excess energy intakes, reducing the intake of saturated fat and promoting increased intake of iron in girls.

Acknowledgements

The authors thank the school principals, teachers, participants and parents for their cooperation for the study. The authors are grateful to the Intake24 team for setting up Intake24-South Asia Locale 2022 version for use in this study to analyse the dietary data. Intake24 is an open-source web-based dietary assessment research tool based on the 24-hour recall method, primarily designed for self-completion. Intake24 was created by Newcastle University (UK), funded by Food Standards Agency, Scotland, and is now maintained and developed through a collaboration between Cambridge University (UK), Monash University (Australia) and Newcastle University (UK). The authors are thankful to the Health-Related Information Dissemination Amongst Youth team for support during the fieldwork.

AI’s Ph.D. was funded through the University of Adelaide-Colgate-Betty Fanning Scholarship.

The study was conceptualised by P. M., A. I., L. G., L. D., funding acquisition: P. M. Data acquisition, initial analysis, software, methodology and interpretation: A. I., P. M., L. G. and L. D. Statistical analyses: L. G, A. I., P. M and L. D. Writing: original draft: A. I. as a part of her PhD studies with contributions from, P. M., L. G., L. D. Writing – review and editing: all authors.

The authors have declared no competing interests.

References

UNICEF (2023) Adolescent Development and Participation. New York: UNICEF.Google Scholar
Kupka, R, Siekmans, K & Beal, T (2020) The diets of children: overview of available data for children and adolescents. Global Food Secur 27, 100442.CrossRefGoogle Scholar
Sullivan, CJ, Childs, KK & O’Connell, D (2010) Adolescent risk behavior subgroups: an empirical assessment. J Youth Adolescence 39, 541562.CrossRefGoogle ScholarPubMed
Ministry of Health and Family Welfare (MoHFW), Government of India, UNICEF & Population Council (2019) Comprehensive National Nutrition Survey (CNNS) National Report. New Delhi: MoHFW, UNICEF.Google Scholar
Pandurangi, R, Mummadi, MK, Challa, S, et al. (2022) Burden and predictors of malnutrition among Indian adolescents (10–19 Years): insights from comprehensive national nutrition survey data. Front Public Health 10, 877073.CrossRefGoogle ScholarPubMed
Meenakshi, JV (2016) Trends and patterns in the triple burden of malnutrition in India. Agric Econ 47, 115134.CrossRefGoogle Scholar
Ministry of Education, Governemnt of India (2023) Pradhan Mantri Poshan Shakti Nirman (PM POSHAN). New Delhi: Ministry of Education, Governemnt of India.Google Scholar
Verma, M, Aditi, A, Kapoor, N, et al. (2023) Childhood obesity and essential micronutrients: insights from India’s comprehensive national nutrition survey (2016–18). Diabetes Ther 14, 12671283.CrossRefGoogle ScholarPubMed
Hollis, JL, Collins, CE, DeClerck, F, et al. (2020) Defining healthy and sustainable diets for infants, children and adolescents. Global Food Secur 27, 100401.CrossRefGoogle Scholar
Shetty, PS (2002) Nutrition transition in India. Public Health Nutr 5, 175182.CrossRefGoogle ScholarPubMed
Popkin, BM (2014) Nutrition, agriculture and the global food system in low and middle income countries. Food Policy 47, 9196.CrossRefGoogle ScholarPubMed
Sawyer, ADM, van Lenthe, F, Kamphuis, CBM, et al. (2021) Dynamics of the complex food environment underlying dietary intake in low-income groups: a systems map of associations extracted from a systematic umbrella literature review. Int J Behav Nutr Physical Activity 18, 96.CrossRefGoogle ScholarPubMed
Bassi, S, Bahl, D, Arora, M, et al. (2021) Food environment in and around schools and colleges of Delhi and National Capital Region (NCR) in India. BMC Public Health 21, 1767.CrossRefGoogle ScholarPubMed
Ranjani, H, Mehreen, TS, Pradeepa, R, et al. (2016) Epidemiology of childhood overweight & obesity in India: a systematic review. Indian J Med Res 143, 160174.Google Scholar
Sankar, R & van den Briel, T (2014) Prospects for better nutrition in India. Asia Pac J Clin Nutr 23, S13.Google ScholarPubMed
Vijayaraghavan, K (2002) Control of micronutrient deficiencies in India: obstacles and strategies. Nutr Rev 60, S7376.CrossRefGoogle Scholar
Locks, LM, Shah, M, Bhaise, S, et al. (2022) Assessing the diets of young children and adolescents in India: challenges and opportunities. Front Pediatr 10, 725812.CrossRefGoogle ScholarPubMed
Scott, S, Lahiri, A, Sethi, V, et al. (2022) Anaemia in Indians aged 10–19 years: prevalence, burden and associated factors at national and regional levels. Maternal Child Nutr 18, e13391.CrossRefGoogle ScholarPubMed
National Health Mission (2023) Rashtriya Kishor Swasthya Karyakram (RKSK). New Delhi: Government of India.Google Scholar
Food Safety and Standards Authority of India (2020) Ministry of Health and Family Welfare. New Delhi: Government of India.Google Scholar
National Nutrition Monitoring Bureau (2012) Diet and Nutrition Status of Rural Population, Prevalence of Hypertension and Diabetes among Adults; Infant and Young Child Feeding Practices- Report of the Third Repeat Survey. Hyderabad: ICMR- National Institute of Nutrition.Google Scholar
National Nutrition Monitoring Bureau (2017) Diet and Nutritional Status of Urban Population in India. Hyderabad: NNMB.Google Scholar
National Institute of Nutrition (2020) Nutrient Requirements and Recommended Dietary Allowances for Indians. Hyderabad: National Institute of Nutrition.Google Scholar
Stockwell, S, Trott, M, Tully, M, et al. (2021) Changes in physical activity and sedentary behaviours from before to during the COVID-19 pandemic lockdown: a systematic review. BMJ Open Sport Exerc Med 7, e000960.CrossRefGoogle ScholarPubMed
Motiwala, ZY, Khan, IR, Ahmad, S, et al. (2023) Dietary changes among the Indian population during the covid-19 pandemic: a cross-sectional study. Indian J Community Med 48, 137141.CrossRefGoogle ScholarPubMed
Gavaravarapu, SM, Seal, A, Banerjee, P, et al. (2022) Impact of ‘infodemic in pandemic’ on food and nutrition related perceptions and practices of Indian internet users. PLoS One 17, e0266705.CrossRefGoogle ScholarPubMed
Bennett, G, Young, E, Butler, I, et al. (2021) The impact of lockdown during the COVID-19 outbreak on dietary habits in various population groups: a scoping review. Front Nutr 8, 626432.CrossRefGoogle Scholar
Martín-Rodríguez, A, Tornero-Aguilera, JF, López-Pérez, PJ, et al. (2022) Dietary patterns of adolescent students during the COVID-19 pandemic lockdown. Physiol Behav 249, 113764.CrossRefGoogle Scholar
Al Hourani, H, Alkhatib, B & Abdullah, M (2022) Impact of COVID-19 lockdown on body weight, eating habits, and physical activity of Jordanian children and adolescents. Disaster Med Public Health Prep 16, 18551863.CrossRefGoogle Scholar
Moitra, P & Madan, J (2022) Impact of screen time during COVID-19 on eating habits, physical activity, sleep, and depression symptoms: a cross-sectional study in Indian adolescents. PLoS One 17, e0264951.CrossRefGoogle ScholarPubMed
Ji, Y, Plourde, H, Bouzo, V, et al. (2020) Validity and usability of a smartphone image-based dietary assessment app compared to 3-day food diaries in assessing dietary intake among Canadian adults: randomized controlled trial. JMIR Mhealth Uhealth 8, e16953.CrossRefGoogle ScholarPubMed
Foster, E, Lee, C, Imamura, F, et al. (2019) Validity and reliability of an online self-report 24-h dietary recall method (intake24): a doubly labelled water study and repeated-measures analysis. J Nutr Sci 8, e29.CrossRefGoogle ScholarPubMed
Bradley, J, Simpson, E, Poliakov, I, et al. (2016) Comparison of INTAKE24 (an online 24-h dietary recall tool) with interviewer-Led 24-h recall in 11–24 year-old. Nutrients 8, 358.CrossRefGoogle Scholar
Simpson, E, Bradley, J, Poliakov, I, et al. (2017) Iterative development of an online dietary recall tool: INTAKE24. Nutrients 9, 118.CrossRefGoogle ScholarPubMed
Census of India (2014) District Census Handbook. Directorate of Census Operations, NCT of Delhi. New Delhi: Census of India.Google Scholar
Schofield, WN (1981) Predicting basal metabolic rate, new standards and review of previous work. Hum Nutr Clin Nutr 39, 541.Google Scholar
FAO (2001) Energy Requirements of Children and Adolescents. Rome: FAO.Google Scholar
Samuelson, G (2000) Dietary habits and nutritional status in adolescents over Europe. An overview of current studies in the Nordic countries. Eur J Clin Nutr 54, S21S28.CrossRefGoogle ScholarPubMed
Aljaraedah, TY, Takruri, HR & Tayyem, RF (2019) Dietary practices and nutrient intake among adolescents: a general review. Obesity Med 16, 100145.CrossRefGoogle Scholar
Al-Jawaldeh, A, Taktouk, M & Nasreddine, L (2020) Food consumption patterns and nutrient intakes of children and adolescents in the eastern Mediterranean region: a call for policy action. Nutrients 12, 3345.CrossRefGoogle Scholar
Dutch, DC, Golley, RK & Johnson, BJ (2021) Diet quality of Australian children and adolescents on weekdays versus weekend days: a secondary analysis of the national nutrition and physical activity survey 2011–2012. Nutrients 13, 4128.CrossRefGoogle Scholar
Huew, R, Maguire, A, Waterhouse, P, et al. (2014) Nutrient intake and dietary patterns of relevance to dental health of 12-year-old Libyan children. Public Health Nutr 17, 11071113.CrossRefGoogle ScholarPubMed
Dapi, LN, Hörnell, A, Janlert, U, et al. (2011) Energy and nutrient intakes in relation to sex and socio-economic status among school adolescents in urban Cameroon, Africa. Public Health Nutr 14, 904913.CrossRefGoogle ScholarPubMed
Ali, Z, Scheelbeek, PFD, Sanin, KI, et al. (2021) Characteristics of distinct dietary patterns in rural Bangladesh: nutrient adequacy and vulnerability to shocks. Nutrients 13, 2049.CrossRefGoogle ScholarPubMed
Public Health England (2020) NDNS: Results from Years 9–11 (2016–2017 and 2018–2019). New Delhi: Official Statistics.Google Scholar
World Health Organization (2023) The Global Health Observatory. Indicator Metadata Registry List: Fat Intake. Geneva: World Health Organization.Google Scholar
Kaushik, JS, Narang, M & Parakh, A (2011) Fast food consumption in children. Indian Pediatrics 48, 97.CrossRefGoogle ScholarPubMed
Gupta, P, Shah, D, Kumar, P, et al. (2019) Indian academy of pediatrics guidelines on the fast and junk foods, sugar sweetened beverages, fruit juices, and energy drinks. Indian Pediatr 56, 849863.CrossRefGoogle Scholar
Cruz, JA (2000) Dietary habits and nutritional status in adolescents over Europe--Southern Europe. Eur J Clin Nutr 54, S2935.CrossRefGoogle ScholarPubMed
Sharma, M, Kishore, A, Roy, D, et al. (2020) A comparison of the Indian diet with the EAT-Lancet reference diet. BMC Public Health 20, 812.CrossRefGoogle ScholarPubMed
Ochola, S & Masibo, PK (2014) Dietary intake of schoolchildren and adolescents in developing countries. Ann Nutr Metab 64, 2440.CrossRefGoogle Scholar
Gupta, A, Noronha, JA, Shobha, K, et al. (2018) Dietary intake of macronutrients and micronutrients among adolescent girls: a cross sectional study. Clin Epidemiol Global Health 6, 192197.CrossRefGoogle Scholar
Arsenault, JE, Moursi, M, Olney, DK, et al. (2020) Validation of 24-h dietary recall for estimating nutrient intakes and adequacy in adolescents in Burkina Faso. Matern Child Nutr 16, e13014.CrossRefGoogle ScholarPubMed
World Health Organization (2006) Adolescent Nutrition: A Review of the Situation in Selected South-East Asian Countries. New Delhi: WHO Regional Office for Southeast Asia.Google Scholar
Awasthi, S, Kumar, D, Mahdi, AA, et al. (2022) Prevalence of specific micronutrient deficiencies in urban school going children and adolescence of India: a multicenter cross-sectional study. PLoS One 17, e0267003.CrossRefGoogle ScholarPubMed
Kawade, R (2012) Zinc status and its association with the health of adolescents: a review of studies in India. Global Health Action 5, 7353.CrossRefGoogle ScholarPubMed
Gonmei, Z & Toteja, GS (2018) Micronutrient status of Indian population. Indian J Med Res 148, 511521.Google ScholarPubMed
Amare, B, Moges, B, Fantahun, B, et al. (2012) Micronutrient levels and nutritional status of school children living in Northwest Ethiopia. Nutr J 11, 108.CrossRefGoogle ScholarPubMed
Miller, TM, Abdel-Maksoud, MF, Crane, LA, et al. (2008) Effects of social approval bias on self-reported fruit and vegetable consumption: a randomized controlled trial. Nutr J 7, 18.CrossRefGoogle ScholarPubMed
Kelly, NR, Doty, KJ, Guidinger, C, et al. (2024) Social desirability bias is related to children’s energy intake in a laboratory test meal paradigm. Appetite 195, 107235.CrossRefGoogle Scholar
Figure 0

Fig. 1. Participation rate from ten private schools in Delhi, India.

Figure 1

Table 1. Energy, macronutrient intake and percentage contributions of macronutrients to energy for 393 11–13-year-old adolescents (224 boys and 169 girls) attending private schools in Delhi, India(Median values and IQR values)

Figure 2

Table 2. Micronutrient intake by 393 11–13-year-old adolescents (224 boys and 169 girls) attending private schools in Delhi, India(Median values and IQR values)