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. 2013 Jan 1;5(1):205–210. doi: 10.4161/derm.24389

The effectiveness of a short food frequency questionnaire in determining vitamin D intake in children

Anita M Nucci 1,*, Caitlin Sundby Russell 2, Ruiyan Luo 3, Vijay Ganji 1, Flora Olabopo 4, Barbara Hopkins 1, Michael F Holick 5, Kumaravel Rajakumar 6
PMCID: PMC3897592  PMID: 24494056

Abstract

Previous studies have found a high prevalence of vitamin D deficiency in children, yet few validated dietary vitamin D assessment tools are available for use in children. Our objective was to determine whether a short food frequency questionnaire (SFFQ) can effectively assess vitamin D intake in children. Vitamin D intake ascertained by a SFFQ was compared with assessments by a previously validated long food frequency questionnaire (LFFQ) in a population of 296 healthy 6- to 14-y-old children (54% male, 60% African American) from Pittsburgh, PA. The questionnaires were completed at two points 6 mo apart. Median reported daily vitamin D intake from the SFFQ (baseline: 380 IU, follow-up: 363 IU) was higher than the LFFQ (255 IU and 254 IU, respectively). Reported median dairy intake, including milk, cheese, and yogurt, was 3.7 cups/day, which meets the USDA recommendation for children. Vitamin D intake reported by the 2 questionnaires was modestly correlated at baseline and follow-up (r = 0.35 and r = 0.37, respectively; p < 0.001). These associations were stronger in Caucasians (r = 0.48 and r = 0.49, p < 0.001) than in African Americans (r = 0.27 and r = 0.31; p = 0.001). The sensitivity of the SFFQ for predicting daily vitamin D intake, defined as intake of ≥ 400 IU on both the SFFQ and LFFQ, was 65%. Specificity, defined as intake of < 400 IU on both questionnaires, was 42%. Vitamin D requirements may not be met despite adequate consumption of dairy products. The SFFQ was found to be a modestly valid and sensitive tool for dietary assessment of vitamin D intake in children.

Keywords: nutrition assessment, food frequency questionnaire, children, adolescents, vitamin D, validity

Introduction

The primary role of vitamin D in humans is to maintain serum calcium and phosphorus concentrations at levels that support metabolic cellular function and bone mineralization.1,2 When humans become deficient in vitamin D, calcium absorption is impaired, resulting in secondary hyperparathyroidism, with a potential for reduced peak bone mass in children and risk of osteoporosis and fragility fractures earlier in life.3 Function of vitamin D also extend beyond calcium homeostasis; maintaining the adequacy of vitamin D status has the potential to improve immune function and cardiovascular health and reduce the risk of cancer and diabetes.2,4-6 Vitamin D status is affected by dietary intake, skin pigmentation, season, and latitude of residence.5,7 Low serum 25-hydroxyvitamin D [25(OH)D], a marker of vitamin D status, is associated with African American race, obesity, inadequate sun exposure, topical sunblock lotions, and insufficient consumption of vitamin D-rich foods.8,9

Because vitamin D is found in few foods, fortified foods and beverages provide the US population with most of its dietary vitamin D. Fish liver oil, fatty fish, and mushrooms exposed to sunlight are natural sources of vitamin D.6,7 Multiple studies have reported a high prevalence of hypovitaminosis D,8,10-19 yet there are limited data on the validity of dietary assessment tools for children and adolescents.20-23 The food frequency questionnaire (FFQ) has been shown to provide reasonable estimates of intake in children when compared with food records,24,25 24-h dietary recalls,26 and observed food intake.27 Fumagalli et al.,28 however, have reported that the FFQ appears to overestimate usual energy and nutrient intakes in children and portion sizes need to be adjusted before adoption of this instrument for children. Thus, there is a need to validate a FFQ for the assessment of vitamin D intake in children. Therefore, this study was designed to determine if a short food frequency questionnaire (SFFQ) can effectively assess vitamin D intake in children when compared with a previously validated long food frequency questionnaire (LFFQ).

Results

Our sample comprised 296 healthy 6- to 14-y-old children (54% boys), with a median age of 10.0 y at baseline. The 6 mo follow-up dietary assessments were missing for 46 subjects (37 subjects were lost to follow-up and 9 subjects failed to complete the exit dietary assessments). Approximately 20% of the subjects were obese, and majority of them were African American (60%) and the remaining where Caucasian. There were no significant differences in median weight, height, or BMI values by race (Table 1).

Table 1. Median anthropometric measures and obesity rate by visit and race.

Initial Visit Total
(n = 293)
African American
(n = 178)
Caucasian
(n = 115)
Weight (kg) 37.8 (30.9, 49.1) 37.8 (30.4, 49.6) 37.8 (31.3, 48.9)
Height (cm) 140.1 (130.9, 150.8) 139.9 (130.6, 154.2) 141.0 (131.0, 149.3)
BMI (kg/m2) 19.1 (16.8, 22.5) 19.1 (16.9, 22.9) 19.1 (16.6, 22.1)
Obesity (BMI ≥ 95th percentile) Rate (%) 20 29.8 6.8
6 Month Visit Total
(n = 252)
African American
(n = 144)
Caucasian
(n = 107)
Weight (kg) 40.5 (32.2, 52.9) 41.2 (32.6, 54.5) 39.8 (31.9, 51.6)
Height (cm) 142.6 (134.0, 155.3) 142.5 (133.9, 157.3) 143.1 (134.0, 153.2)
BMI (kg/m2) 19.5 (16.9, 22.9) 19.8 (17.0, 23.5) 18.9 (16.9, 22.4)
Obesity (BMI ≥ 95th percentile) Rate (%) 19.5 28.1 6.8

Weight, height and BMI values are reported as median (25%, 75%)

While median intake of regular cow’s milk was reported to be 2 cups/day (interquartile range, 1–2.5 cups/day), intake of other vitamin D-fortified dairy products (e.g., soy milk, Lactaid® and chocolate milk) or vitamin D-fortified orange juice was minimal (interquartile range 0–1 cup/day) at baseline and follow-up (Table 2). Median intake of cheese was reported at 1 ounce/day (interquartile range, 1–2 ounces/day), and intake of yogurt at 0.5 cup/day (interquartile range 0–1 cup/day). Median dairy intake, including all milk, cheese, and yogurt was 3.7 cups/day (interquartile range 2.2–5.3 cups/day). Few subjects reported consuming fish or dried mushrooms. Vitamin D intake as reported on the LFFQ was significantly lower than that reported on the SFFQ at both time points for the total population (p < 0.001) and after stratification by race (Baseline: p < 0.001 for both races; Follow-up: Caucasian p = 0.043, African American p < 0.001). Vitamin D intake assessed by the SFFQ at the 6 mo visit differed significantly between racial groups (p = 0.003). No racial differences in milk or dairy intake were observed.

Table 2. Dietary vitamin D intake by type of questionnaire, visit and racea.

  Total African American Caucasian
Initial Visit (n = 296) (n = 178) (n = 118)
Dietary vitamin D (IU)
LFFQ 255 (150, 408)* 255 (152, 404)* 251 (144, 417)*
SFFQ 380 (236, 625) 408 (229, 662) 351 (236, 505)
SFFQ Dietary data      
Combined milk intake (cups/day)b 2 (1, 4) 2 (1, 4) 2 (1, 3.5)
Dairy intake (cups/day)c 3.7 (2.3, 5.3) 3.7 (2.2, 5.5) 3.6 (2.4, 5.0)
6 Month Visit (n = 252) (n = 144) (n = 107)
Dietary Vitamin D (IU)
LFFQ 254 (154, 420)* 252 (155, 439)* 287 (150, 414)**
SFFQ 363 (249, 558) 395 (290,602)‡ 315 (201, 464)
SFFQ Dietary Data
Combined milk intake (cups/day)b 2 (1.5, 3.4) 2 (1.4, 3.6) 2 (1.5, 3.0)
Dairy intake (cups/day)c 3.7 (2.7, 5.3) 3.7 (2.7, 6.2) 3.7 (2.5, 5.3)

LFFQ, long food frequency questionnaire; SFFQ, short food frequency questionnaire. aMedian (25%,75%); bCombination of regular cow’s milk, fortified soy milk, Lactaid® milk and chocolate milk; cAll milk, cheese and yogurt. Comparison between LFFQ and SFFQ: *p < 0.001, **p = 0.043. Comparison by race: ‡p = 0.003

Validity test statistics revealed that the degree of association between the two questionnaires (SFFQ and LFFQ) was modest overall at baseline and follow-up (r = 0.35 and r = 0.37, respectively; p < 0.001), but was stronger in Caucasians (r = 0.48 and r = 0.49, respectively; p < 0.001) than the African American subgroups (r = 0.27 and r = 0.31, respectively; p < 0.001). Outliers did not affect the results. Therefore, only participants with missing observations at the 6 mo visit were removed from the validity analysis.

The SFFQ was tested against the gold standard LFFQ for sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) using daily intake of vitamin D reported by each participant at baseline (n = 294 pairs). The sensitivity statistic evaluated whether the SFFQ was as likely as the LFFQ to identify a subject who met the AAP or IOM and Endocrine Society recommendations for vitamin D intake (≥ 400 IU/day and ≥ 600 IU/day, respectively).29 The SFFQ identified 65% of participants who met the AAP recommendation and 63% who met the IOM and Endocrine Society recommendation, as determined by the LFFQ. The specificity statistic evaluated whether the SFFQ was as likely as the LFFQ to identify a subject who did not meet the recommended intakes for vitamin D. Our SFFQ identified 42% of participants who did not meet the AAP guideline and 23% who did not meet the IOM and Endocrine Society guidelines, as determined by the LFFQ. The predictive value statistics examined the accuracy of the sensitivity and specificity predictions. The probabilities that subjects actually consumed ≥ 400 IU/day or ≥ 600 IU/day (PPV) were 0.37 and 0.15, respectively. Therefore, while the SFFQ appeared to be a very sensitive tool, the probability of accuracy of the result was modest at best. The probabilities that these participants did not actually consume < 400 IU/day or < 600 IU/day (NPV) were 0.82 and 0.97, respectively. Thus, among those who were identified as not consuming recommended levels, the likelihood that this result was true was very good.

Discussion

We have demonstrated that an SFFQ is a valid and reproducible tool for assessing vitamin D intake in children as compared with a previously validated LFFQ. Adolescents’ level of independence and their caretakers’ unawareness of the foods they consume complicate assessment of dietary consumption.30 The development of a valid and easy to administer tool that accurately measures vitamin D consumption in children is important in order to assess factors that optimize vitamin D status in this vulnerable subgroup.

In our sample, the daily median intake of vitamin D reported by the SFFQ was higher than the assessment by the LFFQ. This finding is not surprising because the primary focus of the SFFQ is on vitamin-D-rich foods, while the LFFQ assesses all foods eaten over a 1 y period. Despite these differences, associations between the short and long FFQs were modest to good. We found a weaker association between the LFFQ and SFFQ for African Americans. Kaaks et al.31 have reported that obese adults usually underreport food intake regardless of dietary assessment technique used. Similarly, Bandini et al.32 found that obese adolescents underreported food intake significantly more than non-obese adolescents. These findings may explain our results, as a high proportion of African American adolescents in our study were obese.

The USDA recommends an intake of 3 cups of dairy foods per day for girls and boys between 9 and 13 y of age.33 One cup of dairy food is equivalent to 1 cup of milk or calcium fortified soy milk, 1 cup of yogurt, or 1.5 ounces of hard cheese. The reported median daily intake of dairy products in our sample was ~3.7 cups at both visits, which meets the USDA guideline. However, not all brands of cheese and yogurt are vitamin D-fortified. In our sample, consumption of vitamin D-fortified orange juice was minimal. Although the children in our sample reportedly consumed dairy servings in excess of the USDA daily recommendation, the amount of vitamin D consumed did not meet daily requirements. In November 2010, the IOM revised the Dietary Reference Intakes for vitamin D and set the estimated average requirement (EAR) as 400 IU/day for all age groups and the Recommended Dietary Allowance (RDA) as 600 IU for persons aged 1–70 y.34,35 In 2008, the AAP revised its recommended intake of vitamin D for infants, children, and adolescents upward, from 200 IU to 400 IU/day.29 Using average daily vitamin D intake as determined by the LFFQ, only 27% of our population consumed ≥ 400 IU and only 6% consumed ≥ 600 IU/day. The Endocrine Society recently reported that children and adolescents at high risk for vitamin D deficiency may require as much as 1000 IU/day of vitamin D to raise the blood level of 25(OH)D consistently above > 30 ng/ml, the level considered to be sufficient.35 Only 1% of our sample consumed > 1000 IU vitamin D/day.

To our knowledge, this study is one of only a few to evaluate a FFQ designed specifically to measure vitamin D consumption in youth. Taylor et al.36 evaluated a 40-item FFQ for determining calcium and vitamin D intake in adolescent girls (12–18 y) with and without anorexia nervosa compared with 4-d food records. The researchers reported greater subject compliance with completion of the FFQ (99%) than the food record (71%). They found a strong correlation between the dietary assessment methods for calcium and vitamin D in girls with anorexia nervosa (r = 0.65 and r = 0.78, respectively; P < 0.0001). In controls, the relation was somewhat weaker for calcium (r = 0.45, p = 0.004) and vitamin D (r = 0.47, p = 0.003).

Using a 3-d diary as a reference, Marshall et al.24 investigated the relative validities of the Iowa Fluoride Study questionnaire and the Block Kids’ Food Questionnaire in assessing vitamin D intake. Associations between vitamin D intakes estimated from 3-d diaries and the 2 questionnaires were modest and virtually identical to our findings. The study authors concluded that a dietary assessment method that targets specific foods or nutrients can be as effective in estimating intake as a more comprehensive assessment tool. An earlier study by Marshall et al.,37 which evaluated the validity of a beverage frequency questionnaire in assessing calcium and vitamin D intake in young children, found that the questionnaire could provide a relative estimate of vitamin D intake. The authors noted that as beverage intake patterns change, with decreased milk intake and increased soft drink and energy drink intake, fewer beverages contribute vital nutrients such as calcium and vitamin D to the total diet; thus beverage intake is less useful in assessing vitamin D intake. Araujo et al.,25 who examined the validity of dietary intake data from an FFQ designed for adolescents living in Brazil, concluded that their FFQ was a suitable tool for ranking adolescents’ energy and nutrient intake. The authors stated that food models and photographs should be used to reduce bias when reporting food intake portions.

Recently, Diffey (2013) proposed a complex mathematical model for estimating serum 25(OH)D concentrations based on oral intake of vitamin D and sun exposure in British white adults.38 Based on this model, it is reasonable to conclude that one could estimate the serum 25(OH)D concentrations given the availability of data on vitamin D intake and sun exposure. However, Diffey’s (2013) model has several limitations. These include variabilities in endogenous production of vitamin D in the skin based on skin pigmentation within the individual and between 2 individuals, age (decreased production of vitamin D as person ages) and body composition (decreased synthesis of vitamin D with adiposity and bioavailability of oral vitamin D.) Given these serious shortcomings, the use of Diffey’s model has limited application in estimating circulating 25(OHD concentrations.

Our study had a few limitations. We were unable to adjust our analyses for energy intake because energy intake could not be calculated from the SFFQ. However, no significant association was found between caloric intake and vitamin D intake with the LFFQ, and therefore, we don’t anticipate energy to be a confounder. The LFFQ was validated with youth who were 9 y or older while our sample included youth as young as 6 y of age.39 A small proportion of participants (15%) reported taking multivitamin supplements. If the supplement brand was not reported, a generic children’s vitamin product with 400 IU vitamin D was used in the nutrient analysis. Given the variation in vitamin D content of multivitamin products, some with 800 or 1000 IU, the calculated vitamin D intake for those who took supplements may have been underestimated. Our questionnaire was designed to document intake of dried mushrooms. However, the vitamin D content of artificially dried mushrooms (10–100 IU/100 g) is considerably less than the vitamin D content of sun-dried mushrooms (350+ IU/100 g). Future versions of the questionnaire should therefore specify the method of drying. We also assumed that the soy milk consumed by participants was vitamin D-fortified. Future versions of the questionnaire should specify fortified soy milk in the question as unfortified varieties are still available. Also, the sunlight exposure questions should obtain information regarding timing of exposure (before 10 a.m.; between 10 a.m.–3PM; after 3 p.m.) and incorporate chest and abdomen in the list of parts of the body that are usually exposed to sunlight under question #19. Although our sunlight exposure questions provide a surrogate estimate of the dose (duration and area of exposure) and quality of sunlight (timing of exposure), which are relevant determinants of vitamin D photoproduction, variations in human skin color make it hard for these questions to estimate the amount of vitamin D photosynthesized in the skin.

Conclusion

The SFFQ is a reasonably valid and reliable tool that can be used to assess vitamin D intake in preadolescent and adolescent children. The SFFQ can serve well as a tool for studies with large populations to monitor vitamin D intake in at risk populations because it is easy to administer, low cost, and takes little time to analyze. Additionally, validated FFQs can provide nutrient intake information more accurately for any micronutrient policy initiatives.

Subjects and Methods

Participants

Our study population comprised 296 healthy 6- to14-y-old African American and Caucasian children residing in Pittsburgh, PA. Subjects were participants in Dr. Rajakumar’s National Institutes of Health-funded (R03 and K23 grants) vitamin D clinical research protocols designed to assess the seasonal and racial differences in vitamin D status of African American and Caucasian children (short longitudinal observational study, n = 140) and refine the serum 25(OH)D thresholds for defining vitamin D insufficiency in children [randomized controlled trial (RCT) of 1000 IU of vitamin D3 vs. placebo for 6 mo, n = 156]. Subjects were enrolled between June 2006 and March 2011. Children with hepatic or renal disease, disorders of vitamin D or calcium metabolism, malabsorptive disorders, or cancer, and those on treatment with anticonvulsants or systemic glucocorticoids were excluded from participation in the observational study and the clinical trial. Children enrolled in the clinical trial were not taking oral contraceptives, depot medoroxyprogesterone, vitamin D containing multivitamins, or vitamin D supplements. The University of Pittsburgh Institutional Review Board approved the vitamin D research protocols, and signed parental informed consent and participants’ assent were obtained prior to enrollment. The Institutional Review Board at Georgia State University approved the dietary analysis done for the study reported here.

Study Measurements

Subjects’ height and weight were measured at baseline and at the 6 mo follow-up visit; BMI was calculated. Subjects were classified as obese if age and gender based BMI was ≥ 95th percentile.40,41 Dietary intake was recorded by participants at both time points using the SFFQ and the LFFQ. The SFFQ was adapted from a questionnaire developed by Dr. Michael Holick (Boston University Medical Center) for assessment of vitamin D intake and sunlight exposure in adults. The SFFQ has 21 questions and is designed for completion by the participant or the parent. Seventeen of the questions focus on vitamin D and calcium rich foods, since Dr. Rajakumar’s initial study was designed to assess the intake of these nutrients (Supplemental Data). The LFFQ is a semi-quantitative FFQ designed by the Harvard Medical School (copyright ©1995 Brigham and Women’s Hospital) that addresses intake of 7 food groups with 152 questions requesting information on dietary intake over the past year. Completed SFFQs were analyzed using the Food Processor SQL (version 10.4.0, ESHA Research). LFFQ data forms were analyzed at Brigham and Women’s Hospital. Nutrient intake data comprised 17 nutrients, including total energy, dietary calcium, and dietary vitamin D.

Statistical Analysis

The Mann-Whitney U test was used to determine if there was a significant difference between anthropometric and nutrition variables by race at each time point since the distribution of these variables was skewed in our population. Internal validity was determined by comparing vitamin D intake reported on the LFFQ with that reported on the SFFQ at each time point using the Spearman rank correlation statistic. Correlations were interpreted using the following guidelines: r = 0.0–0.3 weak, r = 0.3–0.6 modest, and r = 0.6–1.0 good. Using a 2 x 2 contingency table, external validity of the SFFQ was evaluated using sensitivity, specificity, PPV, and NPV equations. The table cell values were determined by whether or not subjects met the AAP recommendation for vitamin D of 400 IU/day (30) and the IOM and Endocrine Society Clinical Practice Guideline recommendation of 600 IU/day,34,35 as reported by the LFFQ (x) and SFFQ (y). Statistical analyses were conducted using SPSS® (version 18, 2010, IBM Corp).

Supplementary Material

Additional material
de-5-205-s01.pdf (133.4KB, pdf)

Glossary

Abbreviations:

25(OH)D

25-hydroxyvitamin D

AAP

American Academy of Pediatrics

BMI

body mass index

cm

centimeter

EAR

estimated average requirement

FFQ

food frequency questionnaire

IOM

Institute of Medicine

IU

international units

kg

kilogram

LFFQ

long food frequency questionnaire

NHANES

National Health and Nutrition Examination Survey

NPV

negative predictive value

OJ

orange juice

PPV

positive predictive value

RCT

randomized controlled trial

RDA

recommended dietary allowance

SFFQ

short food frequency questionnaire

UPMC

University of Pittsburgh Medical Center

USDA

United States Department of Agriculture

Funding

The author(s) disclosed receipt of the following financial support for the research and/or authorship of this article: This project was supported by the following National Institutes of Health grants: R03HD053479 (Kumaravel Rajakumar) and K23HD052550 (Kumaravel Rajakumar) from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

Disclosure of Potential Conflicts of Interest

No potential conflicts of interest were disclosed.

Footnotes

References

  • 1.Shils ME, Shike M, Ross C, Caballero B, Cousins R. Modern Nutrition in Health and Disease. 10th ed. Baltimore, MD: Lippincot Williams & Wilkins; 2005. [Google Scholar]
  • 2.Linus Pauling Institute Micronutrient Research for Optimum Health. Vitamin D. http://lpi.oregonstate.edu/infocenter/vitamins/vitaminD/ Updated November 7, 2008. Accessed November 22, 2009.
  • 3.Misra M, Pacaud D, Petryk A, Collett-Solberg PF, Kappy M, Drug and Therapeutics Committee of the Lawson Wilkins Pediatric Endocrine Society Vitamin D deficiency in children and its management: review of current knowledge and recommendations. Pediatrics. 2008;122:398–417. doi: 10.1542/peds.2007-1894. [DOI] [PubMed] [Google Scholar]
  • 4.Wagner CL, Greer FR, American Academy of Pediatrics Section on Breastfeeding. American Academy of Pediatrics Committee on Nutrition Prevention of rickets and vitamin D deficiency in infants, children, and adolescents. Pediatrics. 2008;122:1142–52. doi: 10.1542/peds.2008-1862. [DOI] [PubMed] [Google Scholar]
  • 5.Holick MF. Vitamin D deficiency. N Engl J Med. 2007;357:266–81. doi: 10.1056/NEJMra070553. [DOI] [PubMed] [Google Scholar]
  • 6.Holick MF. Vitamin D: importance in the prevention of cancers, type 1 diabetes, heart disease, and osteoporosis. Am J Clin Nutr. 2004;79:362–71. doi: 10.1093/ajcn/79.3.362. [DOI] [PubMed] [Google Scholar]
  • 7.National Institutes of Health. Dietary Supplement Fact Sheet: Vitamin D. http://dietary-supplements.info.nih.gov/factsheets/vitamind.asp#h3 Updated November 13, 2009. Accessed November 22, 2009.
  • 8.Gordon CM, Feldman HA, Sinclair L, Williams AL, Kleinman PK, Perez-Rossello J, et al. Prevalence of vitamin D deficiency among healthy infants and toddlers. Arch Pediatr Adolesc Med. 2008;162:505–12. doi: 10.1001/archpedi.162.6.505. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Moore CE, Murphy MM, Holick MF. Vitamin D intakes by children and adults in the United States differ among ethnic groups. J Nutr. 2005;135:2478–85. doi: 10.1093/jn/135.10.2478. [DOI] [PubMed] [Google Scholar]
  • 10.Rajakumar K, Holick MF, Jeong K, Moore CG, Chen TC, Olabopo F, et al. Impact of season and diet on vitamin D status of African American and Caucasian children. Clin Pediatr (Phila) 2011;50:493–502. doi: 10.1177/0009922810397334. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Kumar J, Muntner P, Kaskel FJ, Hailpern SM, Melamed ML. Prevalence and associations of 25-hydroxyvitamin D deficiency in US children: NHANES 2001-2004. Pediatrics. 2009;124:e362–70. doi: 10.1542/peds.2009-0051. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Rajakumar K, Fernstrom JD, Janosky JE, Greenspan SL. Vitamin D insufficiency in preadolescent African-American children. Clin Pediatr (Phila) 2005;44:683–92. doi: 10.1177/000992280504400806. [DOI] [PubMed] [Google Scholar]
  • 13.Gordon CM, DePeter KC, Feldman HA, Grace E, Emans SJ. Prevalence of vitamin D deficiency among healthy adolescents. Arch Pediatr Adolesc Med. 2004;158:531–7. doi: 10.1001/archpedi.158.6.531. [DOI] [PubMed] [Google Scholar]
  • 14.Dong Y, Pollock N, Stallmann-Jorgensen IS, Gutin B, Lan L, Chen TC, et al. Low 25-hydroxyvitamin D levels in adolescents: race, season, adiposity, physical activity, and fitness. Pediatrics. 2010;125:1104–11. doi: 10.1542/peds.2009-2055. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Looker AC, Dawson-Hughes B, Calvo MS, Gunter EW, Sahyoun NR. Serum 25-hydroxyvitamin D status of adolescents and adults in two seasonal subpopulations from NHANES III. Bone. 2002;30:771–7. doi: 10.1016/S8756-3282(02)00692-0. [DOI] [PubMed] [Google Scholar]
  • 16.Willis CM, Laing EM, Hall DB, Hausman DB, Lewis RD. A prospective analysis of plasma 25-hydroxyvitamin D concentrations in white and black prepubertal females in the southeastern United States. Am J Clin Nutr. 2007;85:124–30. doi: 10.1093/ajcn/85.1.124. [DOI] [PubMed] [Google Scholar]
  • 17.Cole CR, Grant FK, Tangpricha V, Swaby-Ellis ED, Smith JL, Jacques A, et al. 25-hydroxyvitamin D status of healthy, low-income, minority children in Atlanta, Georgia. Pediatrics. 2010;125:633–9. doi: 10.1542/peds.2009-1928. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Weng FL, Shults J, Leonard MB, Stallings VA, Zemel BS. Risk factors for low serum 25-hydroxyvitamin D concentrations in otherwise healthy children and adolescents. Am J Clin Nutr. 2007;86:150–8. doi: 10.1093/ajcn/86.1.150. [DOI] [PubMed] [Google Scholar]
  • 19.Ganji V, Zhang X, Tangpricha V. Serum 25-hydroxyvitamin D concentrations and prevalence estimates of hypovitaminosis D in the U.S. population based on assay-adjusted data. J Nutr. 2012;142:498–507. doi: 10.3945/jn.111.151977. [DOI] [PubMed] [Google Scholar]
  • 20.Willet W. Nutritional Epidemiology 2nd ed. New York, NY: Oxford University Press; 1998. [Google Scholar]
  • 21.Rockett HR, Berkey CS, Colditz GA. Evaluation of dietary assessment instruments in adolescents. Curr Opin Clin Nutr Metab Care. 2003;6:557–62. doi: 10.1097/00075197-200309000-00009. [DOI] [PubMed] [Google Scholar]
  • 22.Rockett HR, Wolf AM, Colditz GA. Development and reproducibility of a food frequency questionnaire to assess diets of older children and adolescents. J Am Diet Assoc. 1995;95:336–40. doi: 10.1016/S0002-8223(95)00086-0. [DOI] [PubMed] [Google Scholar]
  • 23.Rockett HR, Berkey CS, Colditz GA. Comparison of a short food frequency questionnaire with the Youth/Adolescent Questionnaire in the Growing Up Today Study. Int J Pediatr Obes. 2007;2:31–9. doi: 10.1080/17477160601095417. [DOI] [PubMed] [Google Scholar]
  • 24.Marshall TA, Eichenberger Gilmore JM, Broffitt B, Stumbo PJ, Levy SM. Relative validity of the Iowa Fluoride Study targeted nutrient semi-quantitative questionnaire and the block kids’ food questionnaire for estimating beverage, calcium, and vitamin D intakes by children. J Am Diet Assoc. 2008;108:465–72. doi: 10.1016/j.jada.2007.12.002. [DOI] [PubMed] [Google Scholar]
  • 25.Araujo MC, Yokoo EM, Pereira RA. Validation and calibration of a semiquantitative food frequency questionnaire designed for adolescents. J Am Diet Assoc. 2010;110:1170–7. doi: 10.1016/j.jada.2010.05.008. [DOI] [PubMed] [Google Scholar]
  • 26.Harnack LJ, Lytle LA, Story M, Galuska DA, Schmitz K, Jacobs DR, Jr., et al. Reliability and validity of a brief questionnaire to assess calcium intake of middle-school-aged children. J Am Diet Assoc. 2006;106:1790–5. doi: 10.1016/j.jada.2006.08.014. [DOI] [PubMed] [Google Scholar]
  • 27.de Assis MAA, Kupek E, Guimarães D, Calvo MCM, de Andrade DF, Bellisle F. Test-retest reliability and external validity of the previous day food questionnaire for 7-10-year-old school children. Appetite. 2008;51:187–93. doi: 10.1016/j.appet.2008.02.014. [DOI] [PubMed] [Google Scholar]
  • 28.Fumagalli F, Pontes Monteiro J, Sartorelli DS, Vieira MN, de Lourdes Pires Bianchi M. Validation of a food frequency questionnaire for assessing dietary nutrients in Brazilian children 5 to 10 years of age. Nutrition. 2008;24:427–32. doi: 10.1016/j.nut.2008.01.008. [DOI] [PubMed] [Google Scholar]
  • 29.Wagner CL, Greer FR, American Academy of Pediatrics Section on Breastfeeding. American Academy of Pediatrics Committee on Nutrition Prevention of rickets and vitamin D deficiency in infants, children, and adolescents. Pediatrics. 2008;122:1142–52. doi: 10.1542/peds.2008-1862. [DOI] [PubMed] [Google Scholar]
  • 30.Zemel BS, Carey LB, Paulhamus DR, Stallings VA, Ittenbach RF. Quantifying calcium intake in school age children: development and validation of the Calcium Counts! food frequency questionnaire. Am J Hum Biol. 2010;22:180–6. doi: 10.1002/ajhb.20975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Kaaks R, Ferrari P, Ciampi A, Plummer M, Riboli E, Part H. Uses and limitations of statistical accounting for random error correlations, in the validation of dietary questionnaire assessments. Public Health Nutr. 2002;5(6A):969–76. doi: 10.1079/PHN2002380. [DOI] [PubMed] [Google Scholar]
  • 32.Bandini LG, Schoeller DA, Cyr HN, Dietz WH. Validity of reported energy intake in obese and nonobese adolescents. Am J Clin Nutr. 1990;52:421–5. doi: 10.1093/ajcn/52.3.421. [DOI] [PubMed] [Google Scholar]
  • 33.United States Department of Agriculture. MyPlate.gov. How much food from the Dairy Group is needed daily? http://www.choosemyplate.gov/foodgroups/dairy_amount.aspx Updated June 4, 2011. Accessed October 30, 2012.
  • 34.Institute of Medicine of the National Academies. Dietary Reference Intakes for Calcium and Vitamin D. Washington, DC. National Academy of Sciences, November 2010.
  • 35.Holick MF, Binkley NC, Bischoff-Ferrari HA, Gordon CM, Hanley DA, Heaney RP, et al. Endocrine Society Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2011;96:1911–30. doi: 10.1210/jc.2011-0385. [DOI] [PubMed] [Google Scholar]
  • 36.Taylor C, Lamparello B, Kruczek K, Anderson EJ, Hubbard J, Misra M. Validation of a food frequency questionnaire for determining calcium and vitamin D intake by adolescent girls with anorexia nervosa. J Am Diet Assoc. 2009;109:479–485.e3. doi: 10.1016/j.jada.2008.11.025. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Marshall TA, Eichenberger Gilmore JM, Broffitt B, Levy SM, Stumbo PJ. Relative validation of a beverage frequency questionnaire in children ages 6 months through 5 years using 3-day food and beverage diaries. J Am Diet Assoc. 2003;103:714–20, discussion 720. doi: 10.1053/jada.2003.50137. [DOI] [PubMed] [Google Scholar]
  • 38.Diffey BL. Modelling vitamin D status due to oral intake and sun exposure in an adult British population. Br J Nutr. 2013;23:1–9. doi: 10.1017/S0007114512005466. [DOI] [PubMed] [Google Scholar]
  • 39.Rockett HR, Breitenbach MA, Frazier AL, Witschi J, Wolf AM, Field AE, et al. Validation of a youth/adolescent food frequency questionnaire. Prev Med. 1997;26:808–16. doi: 10.1006/pmed.1997.0200. [DOI] [PubMed] [Google Scholar]
  • 40.Centers for Disease Control and Prevention. Overweight and Obesity. Defining Childhood Overweight and Obesity. http://www.cdc.gov/obesity/childhood/defining.html Updated October 20, 2009. Accessed October 12, 2010.
  • 41.Centers for Disease Control and Prevention. Clinical Growth Charts. http://www.cdc.gov/growthcharts/clinical_charts.htm#Set1 Updated August 4, 2009. Accessed October 12, 2010.

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