Abstract
Background
Adequate nutrition during childhood and adolescence is essential to promote growth and development.
Objective
This study evaluated usual energy and nutrient intakes of Filipino schoolchildren and adolescents.
Design
Food and beverage intakes were collected from a nationally representative sample of schoolchildren aged 6–9 and 10–12 years (n = 3,594 and n = 2,971, respectively) and adolescents aged 13–18 years (n = 5,447) using 24-h dietary recalls. The distributions of usual energy and nutrient intakes and the prevalence of inadequate intakes, which is defined as the percent of children with intakes less than estimated average requirements or acceptable macronutrient distribution ranges, were estimated using the Personal Computer Software for Intake Distribution Estimation (PC-SIDE) program.
Results
The results showed that the mean energy intakes were 19–35% lower than estimated energy requirement. High prevalence of inadequate intakes was found for most macro- and micronutrients. Prevalence of inadequacies was as follows: protein 12–47%, total fat (as percentage of energy) 38–52%, calcium 92–94%, iron 75–90%, vitamin C 68–96%, folate 61–93%, vitamin A 58–81%, riboflavin 58–91%, thiamin 27–75%, and phosphorus 18–91%.
Conclusions
Generally, prevalence of inadequacy of key nutrients were relatively high among adolescents and schoolchildren, especially those from poor families and rural areas. This study demonstrated that nutrient intakes of Filipino schoolchildren and adolescents were highly inadequate, particularly among the poor and those living in rural areas.
Keywords: usual nutrient intakes, school-aged children, adolescents, the Philippines
Popular scientific summary
Adequate nutrition during childhood and adolescence is essential to promote growth and development.
This study evaluated usual energy and nutrient intakes of Filipino schoolchildren and adolescents.
The results demonstrated that intakes of many key nutrients in this population were highly inadequate, particularly among the poor and those living in rural areas.
The findings could be used by government agencies, non-profit organizations, and policy makers to develop intervention programs addressing the nutritional needs of this population.
Childhood and adolescence are both stages of physical, social, and cognitive growth and development (1, 2). Nutrient needs tend to parallel with rates of growth. Growth continues at a steady rate during childhood and then accelerates during adolescence; hence, there is a need for increase in nutrient intake. It is vital that children are provided with a diet containing sufficient quantities of macro- and micronutrients to allow them reach their growth and development potential (3). Inadequate intake of energy, protein, or certain micronutrients is reflected in slow growth rates, cognitive deficits, poorer school performance, and inadequate bone mass (4). However, little is known about the nutrition of adolescents, particularly in low-and middle-income countries. Dietary intake data for schoolchildren and adolescents are critical to guide appropriate intervention programs to improve their health and growth.
A number of studies have demonstrated that socioeconomic status (SES), usually measured as income, education, and occupation, contributes to inequalities in health and nutrition across all age groups (5). On average, a higher socioeconomic level has been associated with healthier dietary patterns in the developed countries (6), while persons of low SES are at risk of food insecurity and malnutrition (7, 8). Although most of these studies were focused on adults, however, low SES has been found to be associated with poor dietary patterns in children and adolescents (6). Apart from SES, place of residence may also affect nutritional status, as shown by the gaps in nutrient intakes observed between urban and rural areas (9). This is likely due to the accessibility and availability of a wide variety of food options in urban areas compared with rural areas (10).
In the Philippines, children and adolescents constitute almost one-third of the population (11). However, data from the latest Philippine National Nutrition Survey conducted in 2013 (2013 NNS) revealed that among children aged 5–10 years, 3 out of 10 were underweight and stunted, and among adolescents aged 10–19 years, 3 out of 10 were also stunted, and 12.4% were wasted. The highest prevalence of stunting, underweight, or wasting was found among those from poor families and rural areas (12). On the other hand, among the children aged 5–10 years from rich families, 1 in 4 was overweight or obese, and among 10–19-year-olds, 8.3% were overweight or obese, showing a 70% increase compared with the 4.9% in 2003. Furthermore, studies on worldwide trends in food consumption, including the Philippines, indicated that food consumption habits of Filipino children and adolescents have changed over the past few decades. These children and adolescents now consume more fat, especially saturated fats, and sweetened beverages and at the same time are not eating enough fruits or vegetables, thereby resulting in inadequate fiber consumption and inadequate intakes of other nutrients (13, 14).
Currently, a comprehensive assessment of usual intakes of energy and nutrients in a national representative sample of Filipino schoolchildren and adolescents is lacking. This knowledge can help understand the causes of malnutrition in this population and provide a direction to develop intervention strategies. The aims of this study were to evaluate the usual energy and nutrient intakes of Filipino schoolchildren and adolescents and also to look into how some socioeconomic factors, including place of residence and wealth status of families, affect their intakes.
Material and methods
Study population
The 2013 NNS is a cross-sectional and population-based survey conducted nationwide, covering all the 17 regions and 80 provinces in the Philippines. The survey used a multi-staged stratified sampling system. A total of 8,592 households were sampled for dietary survey, with a response rate of 87.7%. Individual dietary intake data from 12,012 schoolchildren aged 6–12 years (n = 6,565) and adolescents aged 13–18 years (n = 5,447) from the households were used in the current study. The Ethics Committee of the Food and Nutrition Research Institute (FNRI) approved the survey protocol. All surveyed households provided informed consent prior to participation.
Data collection
To estimate the day-to-day variation in energy and nutrient intakes, two 24-h dietary recalls were conducted by registered dietitians with the parents and children face-to-face using structured questionnaires. The first 24-h dietary recall was collected for all sampled households, and a second 24-h dietary recall was repeated in 50% of randomly selected households on a non-consecutive day. The second 24-h dietary recall was typically collected 2 days after the first 24-h recall. All food and beverages that the child consumed on the previous day were recorded during dietary recalls. The amount of each food item or beverage was estimated using common household measurements, such as cups, tablespoons, by size, or number of pieces. The information was then converted to grams using a portion to weight list for common foods compiled by FNRI or through actual weighing of food samples.
Socioeconomic and demographic data and anthropometric parameters of growth were taken from the 2013 NNS. The wealth status of families was classified by wealth quintiles, a composite measure of a household’s ownership of selected assets including televisions, bicycles, materials used for housing construction, and types of water access and sanitation facilities. Scores were generated for each household asset and were then used to define wealth quintiles as poorest, poor, middle, rich, and richest. Weight and height were measured using mechanical Detecto® platform beam balance scales (Detecto, Webb City, Missouri, USA) and Microtoise (SECA 206, Hamburg, Germany), respectively. Nutritional status indices such as stunting, wasting, and overweight were determined using the World Health Organization Child Growth Standards (15).
Data processing
A computer system called Individual Dietary Evaluation System developed by FNRI was used to evaluate the energy and nutrient content of foods consumed by each individual subject. This system contains the data of the expanded Filipino Food Composition Tables (FCT) created for this study (16). The expended FCT contains 27 nutrients from 1,359 foods.
Food coding and quantity recorded were reviewed to avoid misclassification and under- or overestimation. Energy and nutrients intakes obtained were also scanned to identify implausible values. Estimated energy requirements (EER) were calculated using the equations from the Institute of Medicine considering age, sex, body weight, height, and physical activity level (17). We assumed low physical activity for schoolchildren aged 6–9 years and active physical activity level for schoolchildren aged 10–12 years and adolescents aged 13–18 years. For the evaluation of energy intake, the ratio of daily energy intake to EER was calculated for each individual and transformed into a logarithmic scale to remove outliers below −3 standard deviations (SDs) and above +3 SDs (18). After the checking, 33 individuals were excluded from the analysis for energy intake. For the evaluation of micronutrient intakes, excessive micronutrient intakes were defined as those that exceed 1.5 times the 99th percentile of the observed intake distribution in the corresponding sex and age group. Intakes above this upper limit were substituted by a random value generated from a uniform distribution in the interval with lower bound equal to the 95th percentile of observed intake and an upper bound equal to 1.5 times the 99th percentile (18).
Statistical analysis
Participants of both sexes were grouped into three age groups: schoolchildren aged 6–9 years, schoolchildren aged 10–12 years, and adolescents aged 13–18 years. Mean and percentiles of usual intake distributions of nutrients were estimated by using the PC-SIDE software version 1.0 developed by Iowa State University (ISU) (Iowa State University, Ames, IA, USA). The ISU method adjusts daily intakes to remove the effect of intraindividual variability; therefore, the estimated distribution only reflects between-person variability in intake (19). This program also estimates the proportion below estimated average requirements (EARs) (20). In this study, The EARs used were from the Philippine Dietary Reference Intakes 2015 (21).
Acceptable macronutrient distribution ranges (AMDRs) were used to evaluate carbohydrates, total fat, and protein intakes as a percentage of energy. The proportions of inadequate and excessive intakes were estimated as less than AMDR lower range and greater than AMDR upper range, respectively. Tolerable upper intake level (UL) was used to estimate the proportions of excessive nutrient intakes. For the inadequate intake of iron, a probability approach was used (22). Individual iron intakes were rescaled assuming 8% bioavailability (21), and then the risk of inadequacy was computed. The prevalence of inadequate iron intake was the average risk of inadequacy in the group.
Calculations for summary statistics and differences between groups were carried out using Stata (StataCorp 2017 Stata Statistical Software, release 15, College Station, TX, USA). T-tests were performed to examine the differences between rural and urban groups. Differences between wealth quintiles were analyzed using Analysis of variance (ANOVA) and Bonferroni multiple comparisons. All analyses accounted for the complex survey design and sampling to reflect nationally representative results.
Results
Demographic characteristics of the study population
Table 1 presents the characteristics of the study population. Of the total participants, 52% were boys, and the rest were girls. More than half of the schoolchildren and adolescents lived in urban areas (58%), while the rest lived in rural areas. Approximately, 51% of the respondents belonged to the poorest (28%) and poor (23%) wealth quintiles. Most mothers were unemployed (58%) and had an education of high school or vocational level. Among the study participants, the prevalence of stunting and wasting was 16.6 and 6.5% in schoolchildren aged 6–12 years and 13.7 and 5.2% in adolescents, respectively. In addition, overweight was 2.8% among schoolchildren aged 6–12 years and 2.3% among adolescents.
Table 1.
Characteristics of the study population
Respondents characteristics | Description | n | % |
---|---|---|---|
Sex | Boys | 6,264 | 52.1 |
Girls | 5,748 | 47.9 | |
Age | 6–9 years old (schoolchildren) | 3,594 | 29.9 |
10–12 years old (preteens) | 2,971 | 24.7 | |
13–18 years old (teenagers) | 5,447 | 45.3 | |
Wealth quintiles | Poorest | 3,238 | 27.7 |
Poor | 2,690 | 23.0 | |
Middle | 2,250 | 19.2 | |
Rich | 1,883 | 16.1 | |
Richest | 1,629 | 13.9 | |
Urbanity | Urban | 6,934 | 57.7 |
Rural | 5,078 | 42.2 | |
Stunting | 6–9 years old | 1,018 | 8.6 |
10–12 years old | 937 | 8.0 | |
13–18 years old | 1,607 | 13.7 | |
All | 3,562 | 30.3 | |
Wasting | 6–9 years old | 339 | 2.9 |
10–12 years old | 424 | 3.6 | |
13–15 years old | 607 | 5.2 | |
All | 1,370 | 11.6 | |
Overweight | 6–9 years old | 158 | 1.3 |
10–12 years old | 172 | 1.5 | |
13–15 years old | 267 | 2.3 | |
All | 597 | 5.1 | |
Body weight (kg) | 6–9 years old | 21.57 | 0.09 |
10–12 years old | 31.3 | 0.16 | |
13–18 years old | 45.6 | 0.13 | |
All | 34.8 | 0.12 | |
Height (cm) | 6–9 years old | 119.2 | 0.14 |
10–12 years old | 137.2 | 0.17 | |
13–18 years old | 154.5 | 0.12 | |
All | 139.6 | 0.16 | |
Mother’s education | No grades completed | 170 | 2 |
Elementary level | 1,350 | 16.1 | |
High school level | 2,993 | 35.7 | |
Vocational level | 2,240 | 26.7 | |
College level | 856 | 10.2 | |
Others (Special education (SPED), Arabic schooling, etc.) | 778 | 9.3 | |
Mother’s current work | No occupation | 4,803 | 58.6 |
With job/business | 3,389 | 41.4 |
Intakes of energy and nutrients
Inadequate intakes of energy and macronutrients were found in all age groups, and the extent of inadequacies increased with age. In the order of schoolchildren aged 6–9 years, schoolchildren aged 10–12 years, and adolescents, the mean energy intakes of these groups were 19, 29, and 35% lower than the estimated EERs, respectively. The prevalence of inadequate total fat intake, which is evaluated as the percentage of energy below the AMDR, was 38, 49, and 52%, respectively. The prevalence of inadequate protein intake was 12, 21, and 47%, respectively (Tables 2–4).
Table 2.
Usual energy and nutrient intakes from food and beverages for Filipino schoolchildren aged 6−9 years from 2013 NNS (n = 3,594)
Nutrients | Dietary reference intakes1 |
Mean/median intake percentiles |
Inadequate/excessive reported intake | ||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
EAR/AMDR | AI/RNI | UL | 10th | 25th | Median | Mean ± SE | 75th | 90th | % < EAR/AMDR | %>AMDR/>UL | |
Macronutrients | |||||||||||
Energy intake (kcal/d) | 1,474 (EER) | 762 | 941 | 1,184 | 1242.6 ± 7 | 1,479 | 1,798 | - | - | ||
Total fat (g/d) | - | - | - | 9.7 | 15 | 23.1 | 26.1 ± 0.3 | 33.7 | 46 | - | - |
Saturated fat (g/d) | - | - | - | 4 | 6 | 10 | 12.8 ± 0.2 | 15 | 24 | - | - |
Protein (g/d) | 24 | - | - | 23.2 | 29 | 36.8 | 38.8 ± 0.2 | 46.3 | 56.7 | 12 | - |
Carbohydrate (g/d) | - | - | - | 131 | 162 | 202 | 213.8 ± 1.3 | 253 | 310 | - | - |
Total sugar (g/d) | - | - | - | 9.3 | 15.1 | 23.6 | 27.1 ± 0.3 | 34.8 | 48.6 | - | - |
Dietary fiber (g/d) | - | 11–14 | - | 3.7 | 4.6 | 5.8 | 6.3 ± 0.04 | 7.5 | 9.4 | - | - |
As percentage of total energy | |||||||||||
Total fat (%) | 15–30a | - | - | 9.1 | 12.6 | 17.2 | 17.8 ± 0.1 | 22.3 | 27.2 | 38 | 5 |
Protein (%) | 6–15a | - | - | 10.4 | 11.3 | 12.4 | 12.6 ± 0.03 | 13.7 | 15.1 | 0 | 11 |
Carbohydrate (%) | 55–79a | - | - | 59.4 | 64.7 | 70.1 | 69.6 ± 0.1 | 75.1 | 79.1 | 4 | 10 |
Antioxidants | |||||||||||
Vitamin C (mg/d) | 22.5 | - | 1,200 | 6.4 | 10.4 | 17.1 | 19.6 ± 0.2 | 25.2 | 36.2 | 68 | 0 |
Vitamin E (mg/d) | 6 | - | 1 | 1.5 | 2.3 | 2.6 ± 0.03 | 3.3 | 4.5 | - | - | |
B vitamins | |||||||||||
Thiamine (mg/d) | 0.55 | - | - | 0.3 | 0.4 | 0.56 | 0.6 ± 0.004 | 0.76 | 0.97 | 48 | - |
Riboflavin (mg/d) | 0.55 | - | - | 0.3 | 0.4 | 0.5 | 0.6 ± 0.01 | 0.69 | 0.9 | 58 | - |
Niacin (mg/d) | 7 | - | 20 | 6.7 | 8.7 | 11.2 | 11.2 ± 0.1 | 14.3 | 17.6 | 11 | 4 |
Vitamin B6 (mg/d) | 0.65 | - | 60 | 0.5 | 0.6 | 0.9 | 1.5 ± 0.03 | 1.8 | 3.3 | 27 | 0 |
Folate (DFE μg/d) | 160 | - | 600 | 65 | 94 | 138 | 155.9 ± 1.5 | 197 | 268 | 61 | 0 |
Vitamin B12 (μg/d) | 1.15 | - | - | 1.4 | 1.8 | 2.5 | 2.9 ± 0.03 | 3.5 | 4.9 | 5 | - |
Bone-related nutrients | |||||||||||
Calcium (mg/d) | 440 | - | 2,500 | 132 | 173 | 232 | 250.8 ± 1.8 | 308 | 394 | 94 | 0 |
Phosphorus (mg/d) | 405 | - | 4,000 | 351 | 440 | 556 | 583.5 ± 3.4 | 697 | 849 | 18 | 0 |
Magnesium (mg/d) | - | 90 | - | 73 | 89 | 112 | 117.9 ± 0.7 | 140 | 171 | - | - |
Vitamin D (μg/d) | - | 5 | - | 1.1 | 1.5 | 2.1 | 2.4 ± 0.02 | 3 | 4.2 | - | - |
Other micronutrients | |||||||||||
Vitamin A (μg RE/d) | 271 | - | 1,700 | 117 | 168 | 243 | 304.9 ± 2.8 | 348 | 482 | 58 | <1 |
Iron (mg/d) | 8.2 | - | - | 3.5 | 4.6 | 6.2 | 6.8 ± 0.1 | 8.3 | 10.8 | 75 | - |
Zinc (mg/d) | 3.4 | - | 23 | 2.6 | 3.3 | 4.3 | 5.2 ± 0.1 | 5.8 | 8.1 | 28 | 1 |
Sodium (mg/d) | - | 400 | - | 329 | 497 | 748 | 834.2 ± 7.7 | 1,077 | 1,449 | - | - |
Potassium (mg/d) | - | 1,600 | - | 486 | 596 | 745 | 783 ± 4.3 | 931 | 1,131 | - | - |
Selenium (μg/d) | 15.4 | - | 280 | 39 | 49 | 64 | 67.9 ± 0.4 | 82 | 102 | <1 | 0 |
Philippine Dietary Reference Intakes 2015.
2Adequate Intake (AI in italic text), Recommended Nutrient Intake (RNI in bold text).
Table 4.
Usual energy and nutrient intakes from food and beverages for Filipino adolescents aged 13−18 years from 2013 NNS (n = 5,447).
Nutrients | Dietary reference intakes1 |
Mean/median intake percentiles |
Inadequate/excessive reported intake |
||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
EAR/AMDR | AI/RNI | UL | 10th | 25th | Median | Mean ± SE | 75th | 90th | % < EAR/AMDR | %>AMDR/>UL | |
Macronutrients | |||||||||||
Energy intake (kcal/d) | 2,326 (EER) | 1,076 | 1,334 | 1,680 | 1,756.5 ± 8 | 2,092 | 2,529 | - | - | ||
Total fat (g/d) | - | - | - | 12 | 18 | 28 | 31.74 ± 0.25 | 41 | 56 | - | - |
Saturated fat (g/d) | - | - | - | 5 | 8 | 12 | 14.1 ± 0.1 | 18 | 26 | - | - |
Protein (g/d) | 54 | - | - | 35 | 44 | 55 | 58.16 ± 0.3 | 69 | 84 | 47 | - |
Carbohydrate (g/d) | - | - | - | 186 | 233 | 296 | 312.25 ± 1.5 | 374 | 459 | - | - |
Total sugars (g/d) | - | - | - | 10 | 15 | 23 | 26.16 ± 0.2 | 33 | 46 | - | - |
Dietary fiber (g/d) | - | 20–23 | - | 5 | 6.3 | 8.1 | 8.69 ± 0.05 | 10.4 | 13 | - | - |
As percentage of total energy | |||||||||||
Total fat (%) | 15–30a | - | - | 8 | 11 | 15 | 15.59 ± 0.1 | 20 | 25 | 52 | 3 |
Protein (%) | 6–15a | - | - | 10.5 | 11.3 | 12.4 | 12.60 ± 0.04 | 13.7 | 14.9 | 0 | 10 |
Carbohydrate (%) | 55–79a | - | - | 62 | 67 | 73 | 71.78 ± 0.1 | 77 | 81 | 3 | 17 |
Antioxidants | |||||||||||
Vitamin C (mg/d) | 54.5 | - | 1,800 | 8.9 | 13.8 | 21.5 | 24.28 ± 0.3 | 31.1 | 43.5 | 96 | 0 |
Vitamin E (mg/d) | 10.5 | - | 1.3 | 1.8 | 2.7 | 2.9 ± 0.03 | 3.7 | 5 | - | - | |
B vitamins | |||||||||||
Thiamine (mg/d) | 1 | - | - | 0.5 | 0.6 | 0.8 | 0.83 ± 0.01 | 1 | 1.3 | 75 | - |
Riboflavin (mg/d) | 1.05 | - | - | 0.39 | 0.49 | 0.63 | 0.68 ± 0.01 | 0.82 | 1.03 | 91 | - |
Niacin (mg/d) | 12.5 | - | 30 | 10.9 | 13.8 | 17.7 | 18.44 ± 0.1 | 22.2 | 27 | 17 | 5 |
Vitamin B6 (mg/d) | 1.15 | - | 80 | 0.8 | 1 | 1.3 | 1.6 ± 0.01 | 1.9 | 2.6 | 38 | 0 |
Folate (DFE μg/d) | 330 | - | 800 | 80 | 112 | 163 | 179.8 ± 1.2 | 229 | 303 | 93 | 0 |
Vitamin B12 (μg/d) | 21.5 | - | - | 1.8 | 2.4 | 3.3 | 3.6 ± 0.02 | 4.4 | 5.6 | 18 | - |
Bone-related nutrients | |||||||||||
Calcium (mg/d) | 440 | - | 2,500 | 179 | 220 | 276 | 290.67 ± 1.3 | 345 | 421 | 92 | 0 |
Phosphorus (mg/d) | 1,055 | - | 4,000 | 503 | 626 | 787 | 818.19 ± 3.6 | 975 | 1,173 | 82 | 0 |
Magnesium (mg/d) | - | 495 | - | 105 | 129 | 160 | 167.8 ± 0.7 | 199 | 241 | - | - |
Vitamin D (μg/d) | - | 5 | - | 1.2 | 1.8 | 2.6 | 3 ± 0.03 | 3.8 | 5.3 | - | - |
Other micronutrients | |||||||||||
Vitamin A (μg RE/d) | 495 | - | 2,800 | 175 | 239 | 334 | 364.60 ± 2.3 | 456 | 593 | 81 | 0 |
Iron (mg/d) | 14.2 | - | - | 4.9 | 6.2 | 8 | 8.52 ± 0.04 | 10.2 | 12.8 | 90 | - |
Zinc (mg/d) | 5.4 | - | 34 | 3.2 | 4.1 | 5.4 | 6.5 ± 0.1 | 7.6 | 11 | 50 | 0 |
Sodium (mg/d) | - | 500 | - | 405 | 580 | 833 | 896.85 ± 5.7 | 1,147 | 1,478 | - | - |
Potassium (mg/d) | - | 2,000 | - | 685 | 842 | 1,052 | 1096.2 ± 4.8 | 1,301 | 1,564 | - | - |
Selenium (μg/d) | 27.6 | - | 400 | 62 | 78 | 101 | 106.1 ± 0.5 | 128 | 157 | <1 | 0 |
Philippine Dietary Reference Intakes 2015.
2Adequate Intake (AI in italic text), Recommended Nutrient Intake (RNI in bold text).
Table 3.
Usual energy and nutrient intakes from food and beverages for Filipino schoolchildren aged 10–12 years from 2013 NNS (n = 2,971)
Nutrients | Dietary reference intakes1 |
Mean/median intake percentiles |
Inadequate/excessive reported intake |
||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
EAR/AMDR | AI/RNI | UL | 10th | 25th | Median | Mean ± SE | 75th | 90th | % <EAR/AMDR | % >AMDR/>UL | |
Macronutrients | |||||||||||
Energy intake (kcal/d) | 1,967 (EER) | 934 | 1,125 | 1,456 | 1,526.2 ± 9.5 | 1,818 | 2,207 | - | - | ||
Total fat (g/d) | - | - | - | 10.2 | 16 | 25 | 28.8 ± 0.3 | 37.6 | 52.5 | - | - |
Saturated fat (g/d) | - | - | - | 4 | 7 | 11 | 14.8 ± 0.3 | 17 | 28 | - | - |
Protein (g/d) | 34.5 | - | - | 28.7 | 35.7 | 45.2 | 47.4 ± 0.3 | 56.6 | 69 | 21 | - |
Carbohydrate (g/d) | - | - | - | 164 | 203 | 256 | 269.7 ± 1.7 | 321 | 393 | - | - |
Total sugars (g/d) | - | - | - | 9.9 | 15.4 | 23.7 | 26.4 ± 0.3 | 34.3 | 46.2 | - | - |
Dietary fiber (g/d) | - | 15–17 | - | 4.5 | 5.6 | 7.2 | 7.8 ± 0.1 | 9.2 | 11.8 | - | - |
As percentage of total energy | |||||||||||
Total fat (%) | 15–30a | - | - | 7.7 | 10.8 | 15.2 | 16 ± 0.1 | 20.2 | 25.2 | 49 | 3 |
Protein (%) | 6–15a | - | - | 10.7 | 11.47 | 12.4 | 12.6 ± 0.03 | 13.6 | 14.71 | 0 | 8 |
Carbohydrate (%) | 55–79a | - | - | 61.4 | 66.8 | 72.2 | 71.5 ± 0.1 | 76.9 | 80.6 | 3 | 16 |
Antioxidants | |||||||||||
Vitamin C (mg/d) | 34.5 | - | 1,200 | 6.8 | 10.9 | 17.3 | 19.6 ± 0.2 | 25.6 | 35.4 | 89 | 0 |
Vitamin E (mg/d) | 8 | - | 1.2 | 1.7 | 2.6 | 2.9 ± 0.03 | 3.8 | 5.3 | - | - | |
B vitamins | |||||||||||
Thiamine (mg/d) | 0.75 | - | - | 0.37 | 0.48 | 0.6 | 0.7 ± 0.01 | 0.9 | 1.1 | 63 | - |
Riboflavin (mg/d) | 0.8 | - | - | 0.3 | 0.4 | 0.5 | 0.6 ± 0.01 | 0.7 | 0.97 | 81 | - |
Niacin (mg/d) | 9.5 | - | 20 | 8.5 | 11 | 14 | 14.7 ± 0.1 | 17.7 | 21.6 | 16 | 15 |
Vitamin B6 (mg/d) | 0.9 | - | 60 | 0.7 | 0.8 | 1.1 | 1.7 ± 0.03 | 2 | 3.8 | 35 | 0 |
Folate (DFE μg/d) | 250 | - | 600 | 70 | 103 | 154 | 174.5 ± 1.8 | 223 | 307 | 81 | 0 |
Vitamin B12 (μg/d) | 1.6 | - | - | 1.6 | 2.2 | 2.9 | 3.4 ± 0.03 | 4.2 | 5.7 | 9 | - |
Bone-related nutrients | |||||||||||
Calcium (mg/d) | 440 | - | 2,500 | 157 | 200 | 260 | 278.3 ± 2 | 337 | 422 | 92 | 0 |
Phosphorus (mg/d) | 1,055 | - | 4,000 | 431 | 542 | 688 | 718.3 ± 4.5 | 862 | 1,044 | 91 | 0 |
Magnesium (mg/d) | - | 155 | - | 90 | 111 | 138 | 146 ± 0.9 | 173 | 211 | - | - |
Vitamin D (μg/d) | - | 5 | - | 1.3 | 1.8 | 2.5 | 2.9 ± 0.03 | 3.5 | 4.6 | - | - |
Other micronutrients | |||||||||||
Vitamin A (μg RE/d) | 369.5 | - | 1,700 | 143 | 198 | 285 | 345.9 ± 3.3 | 414 | 543 | 68 | 0 |
Iron (mg/d) | 13.4 | - | - | 4.2 | 5.4 | 7.2 | 7.8 ± 0.1 | 9.4 | 12 | 90 | - |
Zinc (mg/d) | 4.25 | - | 23 | 2.8 | 3.6 | 4.8 | 5.6 ± 0.1 | 6.8 | 9.5 | 40 | 0 |
Sodium (mg/d) | - | 500 | - | 363 | 542 | 810 | 893.3 ± 8.7 | 1,156 | 1,536 | - | - |
Potassium (mg/d) | - | 2,000 | - | 592 | 726 | 909 | 953.8 ± 5.8 | 1,134 | 1,376 | - | - |
Selenium (μg/d) | 17.2 | - | 280 | 48 | 62 | 80 | 83.4 ± 0.6 | 101 | 124 | <1 | 0 |
Philippine Dietary Reference Intakes 2015.
2Adequate Intake (AI in italic text), Recommended Nutrient Intake (RNI in bold text).
Inadequate intakes were found for all micronutrients except selenium in all age groups. Again, the extent of inadequacies increased with age. The highest inadequacies were for calcium (92–94%), iron (75–90%), vitamin C (68–96%), folate (61–93%), riboflavin (58–91%), and vitamin A (58–81%). In addition, among the schoolchildren aged 10–12 years and adolescents, a high prevalence of inadequacies was also found for thiamin (81–91%) and phosphorus (82–91%). The mean intakes of vitamin E, vitamin D, and potassium in all groups were far below the Adequate Intakes (AIs). Mean sodium intakes were, however, above the AIs (Tables 2–4).
Intakes of energy and nutrients in relation to place of residence
In all age groups, the mean intakes of energy, total fat, saturated fat, protein, carbohydrate, and total sugar were significantly lower in rural than in urban areas. Mean fiber intakes appeared to be slightly higher in rural than in urban areas but were not statistically significant (Supplementary Table 1). In addition, in all groups, the mean intakes of most micronutrients were significantly lower in rural than in urban areas, including vitamin E, calcium, phosphorus, magnesium, vitamin A, zinc, iron, selenium, potassium, and sodium. Mean intakes of thiamin and riboflavin among schoolchildren aged 6–9 years and adolescents were significantly lower in rural areas compared with those in urban areas, while the mean intakes of these two nutrients among schoolchildren aged 10–12 years were significantly lower in urban areas compared with those in rural areas. On the contrary, in all age groups, the mean intakes of vitamin C and vitamin D, however, were significantly lower in urban than in rural areas (Table 5).
Table 5.
Prevalence of inadequate nutrient intakes among schoolchildren and adolescents by place of residence
Nutrients | Prevalence of inadequacy (%) ± SE |
|||||
---|---|---|---|---|---|---|
6–9 years old |
10–12 years old |
13–18 years old |
||||
Rural (n = 2,060) | Urban (n = 1,534) | Rural (n = 1,764) | Urban (n = 885) | Rural (n = 3,109) | Urban (n = 2,337) | |
Protein (g/d) | 56 ± 0.01* | 37 ± 0.01 | 18 ± 0.02* | 6 ± 0.01 | 33 ± 0.02* | 11 ± 0.02 |
Total fat (%) | 69 ± 0.01* | 37 ± 0.02 | 55 ± 0.01* | 21 ± 0.02 | 66 ± 0.02* | 31 ± 0.02 |
Protein (%) | 0 | 0 | 0 | 0 | 0 | 0 |
Carbohydrate (%) | 1 ± 0.001* | 4 ± 0.01 | <1 ± 0.01* | 6 ± 0.01 | 1 ± 0.004* | 4 ± 0.01 |
Vitamin C (mg/d) | 95 ± 0.02NS | 96 ± 0.02 | 63 ± 0.02* | 73 ± 0.04 | 88 ± 0.03NS | 89 ± 0.04 |
Thiamine (mg/d) | 82 ± 0.01* | 67 ± 0.02 | 62 ± 0.01* | 33 ± 0.02 | 75 ± 0.02* | 51 ± 0.02 |
Riboflavin (mg/d) | 94 ± 0.01* | 89 ± 0.02 | 71 ± 0.01* | 45 ± 0.02 | 89 ± 0.02* | 71 ± 0.02 |
Niacin (mg/d) | 26 ± 0.01* | 8 ± 0.02 | 19 ± 0.01* | 5 ± 0.01 | 24 ± 0.02* | 7 ± 0.02 |
Vitamin B6 (mg/d) | 42 ± 0.01* | 33 ± 0.02 | 29 ± 0.02* | 23 ± 0.02 | 42 ± 0.02* | 26 ± 0.03 |
Vitamin B12 (mg/d) | 18 ± 0.03NS | 16 ± 0.03 | 6 ± 0.02* | 4 ± 0.02 | 9 ± 0.03NS | 8 ± 0.04 |
Folate DFE (μg/d) | 91 ± 0.01* | 96 ± 0.02 | 64 ± 4.1* | 57 ± 0.02 | 80 ± 0.02* | 84 ± 0.03 |
Calcium (mg/d) | 93 ± 0.02NS | 92 ± 0.02 | 95 ± 0.01* | 93 ± 0.02 | 93 ± 0.02NS | 91 ± 0.02 |
Phosphorus (mg/d) | 85 ± 0.01* | 80 ± 0.02 | 25 ± 0.01* | 13 ± 0.02 | 93 ± 0.01* | 88 ± 0.02 |
Vitamin A (μg RE/d) | 80 ± 0.03* | 83 ± 0.04 | 56 ± 0.01* | 44 ± 0.02 | 68 ± 0.02* | 60 ± 0.03 |
Zinc (mg/d) | 59. ± 0.01* | 38 ± 0.01 | 39 ± 0.01* | 16 ± 0.02 | 50 ± 0.01* | 27 ± 0.02 |
Iron (mg/d) | 98 ± 0.01* | 96 ± 0.01 | 87 ± 0.01* | 76 ± 0.01 | 97 ± 0.01* | 89 ± 0.01 |
Selenium (μg/d) | <1 | 0 | 0 | 0 | 0 | 0 |
Significantly different from urban, P < 0.05, by using hypothesis testing to compare two population proportion with Bonferroni error correction.
Not significantly different.
From the above discussion, it can be stated that the prevalence of inadequate intakes of most macro- and micronutrients was higher in rural than in urban areas. Among schoolchildren aged 6–9 years, the prevalence of inadequate intakes of protein, total fat, thiamin, riboflavin, niacin, vitamin B6, calcium, phosphorus, vitamin A, zinc, and iron was significantly higher in rural than in urban areas, while the inadequacies of folate and vitamin A were higher in urban than in rural areas. Among schoolchildren aged 10–12 years, the prevalence of inadequate intakes of protein, total fat, thiamin, riboflavin, niacin, vitamin B6, folate, calcium, phosphorus, vitamin A, zinc, and iron was higher in rural areas compared with those in urban areas, whereas the inadequacy of vitamin C was significantly higher in urban areas compared with those in rural areas. Among adolescents, the inadequacy of protein, total fat, thiamin, riboflavin, niacin, vitamin B6, calcium, phosphorus, vitamin A, zinc, and iron was significantly higher in rural than in urban areas; however, the inadequacy of folate was significantly higher in urban than in rural areas (Table 5).
Intakes of energy and nutrients in relation to wealth status
In all age groups, the mean intakes of energy and most macro- and micronutrients increased with wealth quintile moving up (Tables 6–8 and Supplementary Tables 1–4). Because of this, an overall higher prevalence of inadequate intakes was found among the poor and poorest schoolchildren and adolescents. For example, the prevalence of inadequate protein intake among the poorest was 25–69% compared to 1–20% among the richest. The prevalence of inadequate total fat intake as percentage of energy among the poorest was very high (77–84%), whereas those among the richest it was 1–20%. For most micronutrients, large to modest differences in the prevalence of inadequacies between wealth quintiles were found, including thiamin, riboflavin, niacin, calcium, iron, and zinc.
Table 6.
Prevalence of inadequate nutrient intakes among schoolchildren aged 6–9 years from the 2013 NNS by wealth quintile
Nutrients | Prevalence of inadequacy ± SE (%) |
||||
---|---|---|---|---|---|
Poorest (n = 1,021) | Poor (n = 791) | Middle (n = 649) | Rich (n = 562) | Richest (n = 468) | |
Protein (g/d) | 25 ± 0.02b,c,d,e | 15 ± 0.02a,c,d,e | 7 ± 0.03a,b,e | 5 ± 0.02a,b,e | 1 ± 0.01a,b,c,d |
Total fat (%) | 77 ± 0.03b,c,d,e | 48 ± 0.03a,c,d,e | 27 ± 0.04ab,d,e | 13 ± 0.04a,b,c,e | 4 ± 0.04a,b,c,d |
Protein (%) | 0NS | 0NS | 0NS | 0NS | 0NS |
Carbohydrate (%) | <1 ± 0.002b,c,d,e | 1 ± 0.01a,d,e | 1 ± 0.02a,d,e | 3 ± 0.02a,b,c,e | 12 ± 0.04a,b,c,d |
Vitamin C (mg/d) | 63 ± 0.04b,c,d,e | 77 ± 0.04a,c,d,e | 69 ± 0.06a,b,e | 70 ± 0.06a,b,e | 59 ± 0.04a,b,c,d |
Thiamine (mg/d) | 74 ± 0.02b,c,d,e | 55 ± 0.02a,c,d,e | 48 ± 0.03a,b,d,e | 30 ± 0.04a,b,c,e | 12 ± 0.06a,b,c,d |
Riboflavin (mg/d) | 85 ± 0.02b,c,d,e | 69 ± 0.02a,c,d,e | 55 ± 0.03a,b,d,e | 40 ± 0.03a,b,c,e | 18 ± 0.04a,b,c,d |
Niacin (mg/d) | 23 ± 0.02b,c,d,e | 15 ± 0.02a,c,d,e | 9 ± 0.02a,b,d,e | 6 ± 0.02a,b,c,e | 1 ± 0.01a,b,c,d |
Vitamin B6 (mg/d) | 31 ± 0.03c,d,e | 35 ± 0.02c,d,e | 20 ± 0.06a,b,e | 18 ± 0.04a,b,e | 7 ± 0.04a,b,c,d |
Vitamin B12 (mg/d) | 10 ± 0.04c,d,e | 10 ± 0.03c,d,e | 2 ± 0.03a,b,d,e | <1 ± 0.01a,b,c | <1 ± 0.02a,b,c |
Folate DFE (μg/d) | 67 ± 0.02c,e | 65 ± 0.03c,e | 59 ± 0.03a,b,d,e | 65 ± 0.04c,e | 42 ± 0.03a,b,c,d |
Calcium (mg/d) | 97 ± 0.01d,e | 96 ± 0.02d,e | 97 ± 0.02d,e | 92 ± 0.03a,b,c,e | 85 ± 0.04a,b,c,d |
Phosphorus (mg/d) | 34 ± 0.02b,c,d,e | 22 ± 0.02a,c,d,e | 15 ± 0.03a,b,d,e | 11 ± 0.03a,b,c,e | 3 ± 0.02a,b,c,d |
Vitamin A (μg RE/d) | 66 ± 0.03c,d,e | 58 ± 0.03a,c,d,e | 48 ± 0.03a,b,d,e | 36 ± 0.03a,b,c,e | 25 ± 0.06a,b,c,d |
Zinc (mg/d) | 50 ± 0.02b,c,d,e | 33 ± 0.02a,c,d,e | 29 ± 0.03a,b,d,e | 13 ± 0.04a,b,c,e | 1 ± 0.02a,b,c,d |
Iron (mg/d) | 92 ± 0.01b,c,d,e | 86 ± 0.02a,c,d,e | 80 ± 0.02a,b,e | 80 ± 0.01a,b,e | 66 ± 0.02a,b,c,d |
Selenium (μg/d) | <1NS | 0NS | 0NS | 0NS | 0NS |
Significantly different from apoorest, bpoor, cmiddle, drich, and erichest, P < 0.05, by using hypothesis testing to compare two population proportion with Bonferroni error correction.
Not significantly different.
Table 8.
Prevalence of inadequate nutrient intakes among adolescents from the 2013 NNS by wealth quintile
Nutrients | Prevalence of inadequacy ± SE (%) |
||||
---|---|---|---|---|---|
Poorest (n =1,333) | Poor (n = 1,203) | Middle (n = 1,082) | Rich (n = 903) | Richest (n = 781) | |
Protein (g/d) | 69 ± 0.02b,c,d,e | 56 ± 0.02a,c,d,e | 43 ± 0.02a,b,d,e | 35 ± 0.02a,b,c,e | 20 ± 0.04a,b,c,d |
Total fat (%) | 84 ± 0.03b,c,d,e | 70 ± 0.03a,c,d,e | 57 ± 0.02a,b,d,e | 30 ± 0.03a,b,c,e | 9 ± 0.04a,b,c,d |
Protein (%) | 0NS | 0NS | 0NS | 0NS | 0NS |
Carbohydrate (%) | <1 ± 0.03c,d,e | <1 ± 0.01c,d,e | 1 ± 0.01a,b,d,e | 3 ± 0.02a,b,c,e | 9 ± 0.03a,b,c,d |
Vitamin C (mg/d) | 93 ± 0.03b,c,e | 98 ± 0.02a,d | 97 ± 0.03a | 95 ± 0.03b,e | 98 ± 0.05a,d |
Thiamine (mg/d) | 90 ± 0.02b,c,d,e | 86 ± 0.03a,c,d,e | 75 ± 0.03a,b,d,e | 64 ± 0.03a,b,c,e | 52 ± 0.03a,b,c,d |
Riboflavin (mg/d) | 98 ± 0.01b,c,d,e | 96 ± 0.01a,c,d,e | 92 ± 0.03a,b,d,e | 88 ± 0.04a,b,c,e | 81 ± 0.06a,b,c,d |
Niacin (mg/d) | 35 ± 0.02b,c,d,e | 22 ± 0.02a,c,d,e | 12 ± 0.03a,b,e | 9 ± 0.03a,b,e | 2 ± 0.02a,b,c,d |
Vitamin B6 (mg/d) | 52 ± 0.02c,d,e | 47 ± 0.02c,d,e | 29 ± 0.04a,b,e | 30 ± 0.03a,b,e | 8 ± 0.07a,b,c,d |
Vitamin B12 (mg/d) | 21 ± 0.04e | 24 ± 0.03d,e | 21 ± 0.06e | 17 ± 0.04b,e | 3 ± 0.06a,b,c,d |
Folate DFE (μg/d) | 87 ± 0.02b,c,d,e | 94 ± 0.02a,d | 94 ± 0.02a,d | 98 ± 0.02a,b,c,e | 95 ± 0.03a,d |
Calcium (mg/d) | 94 ± 0.04e | 96 ± 0.02c,d,e | 93 ± 0.03b,e | 91 ± 0.03b,e | 87 ± 0.05a,b,c,d |
Phosphorus (mg/d) | 90 ± 0.02b,c,d,e | 86 ± 0.02a,c,d,e | 80 ± 0.02a,b | 79 ± 0.03a,b | 76 ± 0.03a,b |
Vitamin A (μg RE/d) | 82 ± 0.04NS | 86 ± 0.06d,e | 83 ± 0.07 | 79 ± 0.05b | 78 ± 0.09b |
Zinc (mg/d) | 99 ± 0.01d,e | 99 ± 0.01d,e | 98 ± 0.01e | 96 ± 0.01a,b | 95 ± 0.01a,b,c |
Iron (mg/d) | 70 ± 0.02b,c,d,e | 57 ± 0.02a,c,d,e | 50 ± 0.02a,b,d,e | 33 ± 0.03a,b,c,e | 19 ± 0.04a,b,c,d |
Selenium (μg/d) | 1b,c,d | <1NS | 0NS | 0NS | 0NS |
Significantly different from apoorest, bpoor, cmiddle, drich, and erichest, P < 0.05, by using hypothesis testing to compare two population proportion with Bonferroni error correction.
Not significantly different.
Table 7.
Prevalence of inadequate nutrient intakes among schoolchildren aged 10–12 years from the 2013 NNS by wealth quintile
Nutrients | Prevalence of inadequacy ± SE (%) |
||||
---|---|---|---|---|---|
Poorest (n = 885) | Poor (n = 696) | Middle (n = 519) | Rich (n = 418) | Richest (n = 380) | |
Protein (g/d) | 43 ± 0.02b,c,d,e | 27 ± 0.03a,c,d,e | 19 ± 0.03a,b,d,e | 7 ± 0.04a,b,c,e | 2 ± 0.02a,b,c,d |
Total fat (%) | 84 ± 0.03b,c,d,e | 63 ± 0.03a,c,d,e | 40 ± 0.04a,b,d,e | 20 ± 0.05a,b,c,e | 6 ± 0.04a,b,c,d |
Protein (%) | 0NS | 0NS | 0NS | 0NS | 0NS |
Carbohydrate (%) | <1 ± 0.01c,d,e | <1 ± 0.01c,d,e | 1 ± 0.01a,b,e | 1 ± 0.02a,b,e | 3 ± 0.04a,b,c,d |
Vitamin C (mg/d) | 88 ± 0.04b,c,e | 93 ± 0.05a,c,e | 98 ± 0.06a,b,d,e | 92 ± 0.07c,e | 81 ± 0.1a,b,c,d |
Thiamine (mg/d) | 86 ± 0.02b,c,d,e | 74 ± 0.03a,c,d,e | 60 ± 0.03a,b,d,e | 50 ± 0.03a,b,c,e | 26 ± 0.04a,b,c,d |
Riboflavin (mg/d) | 97 ± 0.01b,c,d,e | 89 ± 0.03a,c,d,e | 81 ± 0.04a,b,d,e | 72 ± 0.04a,b,c,e | 42 ± 0.04a,b,c,d |
Niacin (mg/d) | 32 ± 0.02b,c,d,e | 17 ± 0.03a,d,e | 13 ± 0.03a,d,e | 5 ± 0.03a,b,c,e | 2 ± 0.02a,b,c,d |
Vitamin B6 (mg/d) | 47 ± 0.02b,c,d,e | 39 ± 0.03a,d,e | 35 ± 0.01a,d,e | 21 ± 0.06a.b.c.e | 12 ± 0.05a,b,c,d |
Vitamin B12 (mg/d) | 14 ± 0.05c,d,e | 19 ± 0.04c,d,e | <1 ± 0.03a,b | <1 ± 0.03a,b | <1 ± 0.04a,b |
Folate DFE (μg/d) | 80 ± 0.02d | 83 ± 0.04NS | 82 ± 0.05d | 87 ± 0.06a,c,e | 80 ± 0.1d |
Calcium (mg/d) | 96 ± 0.02d,e | 94 ± 0.02e | 95 ± 0.03d,e | 91 ± 0.04a,c | 75 ± 0.05a,b,c,d |
Phosphorus (mg/d) | 95 ± 0.01d,e | 92 ± 0.02e | 94 ± 0.02d,e | 88 ± 0.03a,c | 81 ± 0.05a,b,c |
Vitamin A (μg RE/d) | 74 ± 0.04d,e | 70 ± 0.03d,e | 70 ± 0.1d,e | 59 ± 0.1a,b,c,e | 37 ± 0.06a,b,c,d |
Zinc (mg/d) | 64 ± 0.02b,c,d,e | 48 ± 0.02a,c,d,e | 7 ± 0.04a,b,d | 20 ± 0.06a,b,c,e | 5 ± 0.04a,b,d |
Iron (mg/d) | 98 ± 0.01b,c,d,e | 95 ± 0.01a,d | 93 ± 0.01a,e | 91 ± 0.01a,e | 84 ± 0.02a.b,c,d |
Selenium (μg/d) | 0NS | 0NS | 0NS | 0NS | 0NS |
Significantly different from apoorest, bpoor, cmiddle, drich, and erichest, P < 0.05, by using hypothesis testing to compare two population proportion with Bonferroni error correction.
Not significantly different.
However, the above patterns were not found for vitamin C and folate. The mean vitamin C intake among the poorest adolescents was higher than that in other wealth quintiles; hence, the prevalence of inadequacy was lower (Table 8 and Supplementary Tables 2–4). However, it is worth mentioning that in any case the prevalence of inadequate vitamin C intake among adolescents across all wealth quintiles were high (93 to 98%) (Table 8). Furthermore, the mean folate intake among the poorest adolescents was higher than that from other wealth quintiles, hence a lower prevalence of inadequacy (Table 8 and Supplementary Table 4).
Discussion
Inadequate energy and nutrient intakes
This study provides estimates of usual energy and nutrients from the food and beverages consumed by a representative sample of Filipino schoolchildren and adolescents and the prevalence of inadequacy. The results indicate marked inadequacies in the intakes of energy, fat, and most micronutrients. The high inadequacies of calcium, iron, vitamins A and C, and folate should be a cause of concern, as these are the key nutrients required for growth and development in this population (4). The prevalence of inadequacies was worse among the adolescents, the poor segments of all age groups, and those living in rural areas. The data also imply that despite the steady economic growth of the country over the past few decades (23), large shortfall in the diets of Filipinos is still a pressing issue. Indeed, our findings are supported by recent reports, which revealed that about seven out of 10 Filipino households are still experiencing food insecurity (24), and the current diets of a majority of Filipinos are monotonous, comprising mostly of cereals, in fact, predominately refined rice (14, 25).
The results of this study are in conformity with studies conducted in other developing countries, in which the researchers found that the intakes of most micronutrients among children were suboptimal and the diets consumed by the children and adolescents in those developing countries were generally inadequate for energy and fats (2, 26).
Place of residence and nutrient intakes
We found the proportions of schoolchildren and adolescents not meeting the recommendations for energy and nutrients were higher in rural areas than those in urban areas. This is in line with the findings of studies conducted in both developing and developed countries (8, 26). The reasons are likely to be multifactorial. First, these inequalities might be driven by poverty. Among the Filipino households residing in rural areas, where the population is generally engaged in agriculture, more than half (58.4%) were classified as poor (27). Many Filipinos in rural areas suffer from lack of food or poor diets because of inadequate access to food or food rich in nutrients (28). This is indeed the situation observed in many other low- and middle-income countries, where children living in rural areas experience lower dietary diversity and lower intakes of important nutrients, whereas those in urban areas have higher intakes of calories, protein, total fat, and micronutrients (10). Second, unavailability of healthy foods could be another reason behind the differences between rural and urban areas. Food variety is often much greater in urban communities since food markets are better supplied and more accessible, whereas this is not the case in rural areas (29). In addition, a low income not only restricts the ability of households to buy foods rich in nutrients but also limits their access to food retailers. Few of the poor families have access to a private vehicle; therefore, they have to shop in local markets, where food can be more expensive than in supermarkets (30).
Unlike other nutrients, the prevalence of inadequacy for vitamin C and folate was lower in rural than in urban groups. A lower prevalence of inadequacy for folate and a higher fiber intake was also observed among the rural groups. This may be a result from a higher vegetable intake among rural households as reported by the 2013 NNS (14). In a review on global fruit and vegetable consumption, a higher vegetable consumption was reported in rural versus urban areas, but the overall fruit and vegetable consumption in Philippine population was considered low (31).
Wealth status and nutrient intakes
The influence of SES on dietary intakes has been reported in many studies around the world (7, 8, 32–34). In our study, the effect of wealth status on dietary intake was illustrated by the clear income gradient with respect to energy and nutrient intakes in all age groups. The mean intakes of energy and most macro- and micronutrients increased with increasing wealth quintile. Hence, schoolchildren and adolescents of the poorest quintile had the highest and the richest quintile had the lowest prevalence of inadequacies. This finding is indeed supported by the higher prevalence of stunting and wasting among the poor segments of the population reported by the 2013 NNS (12).
The low mean intakes of all vitamins and most minerals, as well as the large proportion of poor schoolchildren and adolescents with these nutrients below the EAR, indicate poor food variety. The diets of the lower wealth quintile groups comprised of mainly rice, with little intake of meat, fruit, vegetables, and milk (14), and hence very low in essential nutrients. The low fat intake among the schoolchildren and adolescents with low wealth quintile compared with those with high wealth quintile indicated a low fat consumption among the poor. Coconut oil, which is the main source of cooking oil, may not always be available to families with low wealth quintile due to lack of money (14).
It is worth mentioning that unlike most nutrients, the mean intake of calcium and the prevalence of inadequacy between rural and urban areas and between wealth quintiles were small. The prevalence of inadequate calcium intakes was high in all groups (75–97%). Low calcium intake had been reported in Filipino children before (35). It is well known that milk and dairy products are the primary source of calcium, and the low intake of calcium can be attributed to the high price of milk and dairy products (30) and social isolation, which makes access to supermarkets more difficult. Another nutrient is iron. Iron inadequacy increased as age increased, with a slight increase between 10–12-year-olds and 13–18-year-olds. Most importantly, the inadequacy was consistently high among all quintiles in these two age groups. The possible reason for this could be that the diets consumed lack iron but EARs are set high for these age groups in order to meet their rapid growth (21).
Limitation of the study
This study has a number of limitations. First, the study did not take into account the potential intake of vitamin and mineral supplements of the children that were additional to their diets; therefore, this could result in a potential underestimation of micronutrient intakes in this study population. Second, as with all national surveys regarding food and beverage intake of children, the study results rely on self-reported dietary intake by the parents and children; hence, there lies the risk of overestimation and underestimation of the food intake. Another limitation of this study was that the updated Philippine food composition tables used in this study were expanded by adopting some data from the food composition tables of different countries. Food composition from other countries may not reflect the foods in Philippine population, especially for the mixed dishes prepared at home.
Conclusions
This study evaluated the usual energy and nutrient intakes of Filipino schoolchildren and adolescents and demonstrated that the intakes of energy, fat, and most key micronutrients were markedly inadequate. The inadequacies were more common among the poor and those living in rural areas. The results reinforce the need to focus on effective implementation of programs among the populations that are at high risk of nutrient deficiencies. The findings of this study could be used by government agencies, non-profit organizations, local government units, and other policy makers in the Philippines for developing programs, intervention policies, and advocacy initiatives addressing the needs of these age groups specifically. In addition, the knowledge from this study will also enable food industry to formulate food products that could target the nutritional needs of this population. Further studies to understand food sources energy and nutrients among the schoolchildren and adolescents are currently underway.
Supplementary Material
Acknowledgments
The research presented in this article is a collaboration of two organizations: the Department of Science and Technology- Food and Nutrition Research Institute and Nestle Research, Lausanne. The authors would like to acknowledge Kristine T. Biona, Glen Melvin Gironella, Regina R. Rodriguez, Royce Ann D. Octavio, Mark Lester C. Cayadong, and Patricia Gaya Amita for their contribution to this study.
Conflicts of interest and funding
The authors declare no conflicts of interest. L.D. and E.J. are employees of Nestlé Research, Vers-chez-les-Blanc, Lausanne, Switzerland. This research was funded by Nestlé Research, Lausanne, Switzerland.
Authors’ contributions
I.A.A. and L.D. conceptualized and designed the study, interpreted the data, and drafted the manuscript. M.B.T. and V.A.O. contributed to the data collection and data analysis, interpreted the data, and revised the initial manuscript. A.L.C. contributed to the data analysis, review, and interpretation. E.J. contributed to data interpretation, critical review, and editing of the manuscript, and M.V.C reviewed the draft of the manuscript. All authors proofread and approved the final manuscript.
References
- 1.United Nations Children’s Fund (US) The state of the world’s children 2011. New York: United Nations Children’s Fund; 2011, p. 148 Available from: https://www.unicef.org/adolescence/files/SOWC_2011_Main_Report_EN_02092011.pdf [cited 6 January 2018]. [Google Scholar]
- 2.Ochola S, Masibo PK. Dietary intake of schoolchildren and adolescents in developing countries. Ann Nutr Metab 2014; 64 Suppl 2: 24–40.doi: 10.1159/000365125 [DOI] [PubMed] [Google Scholar]
- 3.Story M, Stang J. Nutrition needs of adolescents. 2005; p. 34 Available from: https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=1&cad=rja&uact=8&ved=2ahUKEwjlxZOD7OXfAhUK2LwKHZBwCGsQFjAAegQIChAB&url=http%3A%2F%2Fenvisionnm.unm.edu%2Fxcalendar%2Fviewfile%2F640%2F&usg=AOvVaw2O-5si01Lsjjvnb20kN3Lj [cited 11 September 2018].
- 4.World Health Organization (CH) WHO Discussion papers on adolescence: nutrition in adolescents-issues and challenges for the health sector. Geneva: WHO Library Cataloguing-in-Publication Data; 2005, p. 115 Available from: http://apps.who.int/iris/bitstream/handle/10665/43342/9241593660_eng.pdf;jsessionid=D02E4E49AECD73195D500E426BAC4BC9?sequence=1WHO Library Cataloguing-in-Publication Data ISBN 92 4 159366 0 ISBN 92 4 159366 0 [cited 11 September 2018]. [Google Scholar]
- 5.Galobardes B, Shaw M, Lawlor DA, Lynch JW, Smith GD. Indicators of socioeconomic position (part 1). J Epidemiol Community Health 2006; 60(1): 7–12. doi: 10.1136/jech.2004.023531 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Ranjit N, Wilkinson AV, Lytle LM, Evans AE, Saxton D, Hoelscher DM. Socioeconomic inequalities in children's diet: the role of the home food environment. Int J Behav Nutr Phys Act. 201; 12 Suppl: S4. doi: 10.1186/1479-5868-12-S1-S4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Manyanga T, Tremblay MS, Chaput JP, Katzmarzyk PT, Fogelholm M, Hu G, et al. Socioeconomic status and dietary patterns in children from around the world: different associations by levels of country human development? BMC Public Health 2017; 17(457): 1–11. doi: 10.1186/s12889-017-4383-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Casey PH, Szeto K, Lensing S, Bogle M, Weber J. Children in food-insufficient low-income families. Arch Pediatr Adolesc Med 2001; 155(4): 508–14. doi: 10.1001/archpedi.155.4.508 [DOI] [PubMed] [Google Scholar]
- 9.Rodriguez-Ramirez S, Mundo-Rosas V, Shamah-Levy T, Ponce-Martinez X, Jimenez-Aguilar A, Gonzalez-de Cossio T. Energy and nutrient intake in Mexican adolescents: analysis of the Mexican national health and nutrition survey 2006. Salud Publica Mex 2009; 51 Suppl 4: S551–S561. Available from: https://bit.ly/2DbQRzr: [cited 8 August 2018]. [DOI] [PubMed] [Google Scholar]
- 10.Mayen AL, Marques-vidal P, Paccaud F, Bovet P, Stringhini S. Socioeconomic determinants of dietary patterns in low-and middle-income countries: a systematic review 1–4. Am J Clin Nutr 2014; 100: 1520–31. doi: 10.3945/ajcn.114.089029 [DOI] [PubMed] [Google Scholar]
- 11.Philippines Statistical Authority Philippine Statistical Yearbook. Quezon City (PH): Philippine Statistic Authority; 2017, p. 667 Available from: https://www.psa.gov.ph/tags/philippine-statistical-yearbook [cited 10 August 2018]. [Google Scholar]
- 12.Food and Nutrition Research Institute Facts and figures 2013: 8th National Nutrition Survey Anthropometric Survey. Taguig, the Philippines: Department of Science and Technology; 2015. [Google Scholar]
- 13.Pedro MR, Benavides RC, Barba CV. Dietary changes and their health implications in the Philippines. In: The double burden of malnutrition: case studies from six developing countries, FAO Food and Nutrition Paper 84. FAO; 2006. Available from: http://www.fao.org/tempref/docrep/fao/009/a0442e/a0442e02.pdf [cited 18 July 2018]. [PubMed] [Google Scholar]
- 14.Food and Nutrition Research Institute Facts and figures 2013: 8th National Nutrition Survey Dietary Survey. Taguig, the Philippines: Department of Science and Technology; 2015. [Google Scholar]
- 15.World Health Organization, Department of Nutrition for Health WHO child growth standards. Geneva: WHO Library Cataloguing-in-Publication Data; 2006, p. 307 Available from: https://www.who.int/childgrowth/standards/Technical_report.pdf [cited 19 July 2018]. [Google Scholar]
- 16.Denney L, Angeles-Agdeppa I, Capanzana MV, Toledo M, Donohue, Carriquiry AL. Nutrition intakes and food sources of Filipino infants, toddlers and young children are inadequate: findings from the national nutrition survey 2013. Nutrients 2018; 10(1730): 1–19. doi: 10.2290/nu10111730 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Institute of Medicine (US) Dietary reference intakes for energy, carbohydrate, fiber, fat, fatty acids, cholesterol, protein, and amino acids. Washington, DC: National Academies Press; 2005, p. 3313 Available from: https://www.nal.usda.gov/sites/default/files/fnic_uploads/energy_full_report.pdf [cited 18 September 2018]. [Google Scholar]
- 18.Lopez-Olmedo N, Carriquiry AL, Rodriguez-Ramirez S, Ramirez-Silva I, Espinosa-Montero J, Hernandez-Barrera L, et al. Usual intake of added sugars and saturated fats is high while dietary fiber is low in the Mexican population. J Nutr 2016;146 (9): 1856S–65S. doi: 10.3945/jn.115.218214 [DOI] [PubMed] [Google Scholar]
- 19.Nusser SM, Carriquiry AL, Fuller WA. A semi parametric transformation approach to estimating usual daily intake distributions CARD Working Papers 138. J Am Stat Assoc 1992; 138: 1–33. doi: 10.1080/01621459.1996.10476712 [DOI] [Google Scholar]
- 20.Carriquiry AL. Assessing the prevalence of nutrient inadequacy. Public Health Nutr 1999; 2(1): 23–33. doi: 10.1017/S1368980099000038 [DOI] [PubMed] [Google Scholar]
- 21.Food and Nutrition Research Institute Philippine Dietary Reference Intakes 2015. Taguig, the Philippines: Department of Science and Technology; 2015. Available from: http://www.fnri.dost.gov.ph/index.php/159-fnri-launches-the-philippine-dietary-reference-intakes-pdri-2015 [cited 10 March 2018]. [Google Scholar]
- 22.National Research Council (US) Nutrient adequacy: assessment using food consumption survey. Washington, DC: National Academy Press; 1986, p. 143 Available from: https://www.ncbi.nlm.nih.gov/books/NBK217533/pdf/Bookshelf_NBK217533.pdf [cited 27 July 2018]. [PubMed] [Google Scholar]
- 23.World Bank (US) Philippines economic update: investing in the future. Washington, DC: the World Bank; 2018, p. 63 Available from:http://pubdocs.worldbank.org/en/280741523838376587/Philippines-Economic-Update-April-15-2018-final.pdf [cited 18 October 2018]. [Google Scholar]
- 24.Food and Nutrition Research Institute Facts and figures 2013: 8th National Nutrition Survey Food Security Survey. Taguig, the Philippines: Department of Science and Technology; 2015. [Google Scholar]
- 25.Food and Agriculture Organization of the United Nations (FAO) Philippines-food and nutrition security profiles. 2014. Available from: http://www.fao.org/3/a-at701e.pdf [cited 10 May 2018]. [Google Scholar]
- 26.Mitchikpe CE, Dossa RA, Ategbo EA, Van Raaij JM, Kok FJ. Seasonal variation in food pattern but not in energy and nutrient intakes of rural Beninese school-aged children. Public Health Nutr 2009; 12(3): 414–22. doi: 10.1017/S1368980008002929 [DOI] [PubMed] [Google Scholar]
- 27.Food and Nutrition Research Institute Facts and figures 2013: 8th National Nutrition Survey Overview. Taguig, the Philippines: Department of Science and Technology; 2015. [Google Scholar]
- 28.Brain Trust Inc (PH) Strategic review: food security and nutrition in the Philippines. An independent review commissioned by the World Food Pregame Brain Trust, Inc; Pasig City; 2017, p. 111 Available from: https://docs.wfp.org/api/documents/WFP-0000015508/download/ [cited 21 March 2018]. [Google Scholar]
- 29.Global Panel (GB) Urban diets and nutrition: trends, challenges and opportunities for policy action, policy brief no. 9. Global Panel on Agriculture and Food Systems for Nutrition; London; 2017, p. 32 Available from: http://glopan.org/sites/default/files/Downloads/GlobalPanelUrbanizationPolicyBrief.pdf [cited 6 August 2018]. [Google Scholar]
- 30.James WP, Nelson M, Ralph A, Leather S. Socioeconomic determinants of health: the contribution of nutrition to inequalities in health. BMJ 1997; 314: 1545–49. doi: 10.1136/bmj.314.7093.1545 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Hall JN, Moore S, Harper SB, Lynch JW. Global variability in fruit and vegetable consumption. Am J Prev Med 2009; 36(5): 402–09e5. doi: 10.1016/j.amepre.2009.01.029 [DOI] [PubMed] [Google Scholar]
- 32.Shafiee S, Mesgarani M, Begum K. Assessment of nutritional status among adolescent boys in an urban population of South India. Glob J Health Sci 2015; 7(3): 335–44. doi: 10.5539/gjhs.v7n3p335 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Dapi LN, Hornell A, Janlert U, Stenlund H, Larsson C. Energy and nutrient intakes in relation to sex and socio-economic status among school adolescents in urban Cameroon, Africa. Public Health Nutr 2011; 14(5): 904–13. doi: 10.1017/S1368980010003150 [DOI] [PubMed] [Google Scholar]
- 34.Richter A, Heidemann C, Schulze MB, Roosen J, Thiele S, Mensink GB. Dietary patterns of adolescents in Germany-Associations with nutrient intake and other health related lifestyle characteristics. BMC Pediatr 2012; 12(35): 1–14. doi: 10.1186/1471-2431-12-35 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Angeles-Agdeppa I, Gironella G, Constantino M. Evaluation of calcium intakes of young children in the Philippines as a result of the 2008 national nutrition survey. Philipp J Sci 2016; 145(2): 165–7474 Available from: http://philjournalsci.dost.gov.ph/images/pdf/pjs_pdf/vol145no2/evaluation-of-calcium-intakes-of-young-children-in-the-Phils.pdf [cited 23 January 2018]. [Google Scholar]
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