Hostname: page-component-cd9895bd7-8ctnn Total loading time: 0 Render date: 2024-12-26T19:21:28.933Z Has data issue: false hasContentIssue false

Consumption of whole grains is associated with improved diet quality and nutrient intake in children and adolescents: the National Health and Nutrition Examination Survey 1999–2004

Published online by Cambridge University Press:  06 October 2010

Carol E O’Neil*
Affiliation:
Louisiana State University Agricultural Center, 261 Knapp Hall, Baton Rouge, LA 70803, USA
Theresa A Nicklas
Affiliation:
Department of Pediatrics, Baylor College of Medicine, Children’s Nutrition Research Center, Houston, TX, USA
Michael Zanovec
Affiliation:
Louisiana State University Agricultural Center, 261 Knapp Hall, Baton Rouge, LA 70803, USA
Susan S Cho
Affiliation:
NutraSource, Clarksville, MD, USA
Ronald Kleinman
Affiliation:
Department of Gastroenterology and Nutrition, Harvard Medical School, Boston, MA, USA
*
*Corresponding author: Email coneil1@lsu.edu
Rights & Permissions [Opens in a new window]

Abstract

Objective

To examine the association of consumption of whole grains (WG) with diet quality and nutrient intake in children and adolescents.

Design

Secondary analysis of cross-sectional data.

Setting

The 1999–2004 National Health and Nutrition Examination Survey.

Subjects

Children aged 2–5 years (n 2278) and 6–12 years (n 3868) and adolescents aged 13–18 years (n 4931). The participants were divided into four WG consumption groups: ≥0 to <0·6, ≥0·6 to <1·5, ≥1·5 to <3·0 and ≥3·0 servings/d. Nutrient intake and diet quality, using the Healthy Eating Index (HEI)-2005, were determined for each group from a single 24 h dietary recall.

Results

The mean number of servings of WG consumed was 0·45, 0·59 and 0·63 for children/adolescents at the age of 2–5, 6–12 and 13–18 years, respectively. In all groups, HEI and intakes of energy, fibre, vitamin B6, folate, magnesium, phosphorus and iron were significantly higher in those consuming ≥3·0 servings of WG/d; intakes of protein, total fat, SFA and MUFA and cholesterol levels were lower. Intakes of PUFA (6–12 years), vitamins B1 (2–5 and 13–18 years), B2 (13–18 years), A (2–5 and 13–18 years) and E (13–18 years) were higher in those groups consuming ≥3·0 servings of WG/d; intakes of added sugars (2–5 years), vitamin C (2–5 and 6–12 years), potassium and sodium (6–12 years) were lower.

Conclusions

Overall consumption of WG was low. Children and adolescents who consumed the most servings of WG had better diet quality and nutrient intake.

Type
Research paper
Copyright
Copyright © The Authors 2010

In the USA, the most commonly consumed grains are wheat, oats, rice, maize and barley, with wheat comprising 66–75 % of the total(Reference Slavin1, Reference Slavin, Jacobs and Marquart2). Whole grains (WG) are defined as cereal grains that are intact, or ground or cracked fruit with the endosperm, germ and bran present in the same relative proportions as the intact grain(3, 4). Endosperm (65–75 %) is composed of starch, NSP and small amounts of protein and lipids. Germ (4–17 %) is a rich source of proteins, lipids, B vitamins and vitamin E. Bran contains dietary fibre; protein; B vitamins, including thiamin, niacin, riboflavin and pantothenic acid; and minerals, including calcium, magnesium and potassium(Reference Slavin1, Reference Slavin, Jacobs and Marquart2, Reference Franz and Sampson5, Reference Jones, Reicks and Adams6). WG also have other health-protective compounds, including flavonoids, lignans, resistant starches and phenols. During processing, the majority of the nutritive value of WG is preserved(Reference Slavin, Jacobs and Marquart2).

Consumption of WG, unlike that of refined grains, is associated with a lower risk of CVD and stroke(Reference Jensen, Koh-Banerjee and Hu7, Reference Steffen, Jacobs and Stevens8), hypertension(Reference Steffen, Jacobs and Stevens8, Reference Wang, Gaziano and Liu9), type 2 diabetes(Reference de Munter, Hu and Spiegelman10) metabolic syndrome(Reference Steffen, Jacobs and Murtaugh11), obesity(Reference Good, Holschuh and Albertson12) and some cancers(Reference Larsson, Giovannucci and Bergkvist13, Reference Schatzkin, Mouw and Park14). The mechanisms of these beneficial effects are not clear and the components of WG may act synergistically(Reference Slavin1, Reference Jacobs and Steffen15). Most of these studies have been conducted in adults and little information is available for children or adolescents.

The 2005 Dietary Guidelines Advisory Committee recommended that at least half of the number of recommended grain servings be WG(16). Thus, the WG recommendation for children varies; children as young as 2 years need only 1·5 servings (ounce equivalents), whereas children at the age of 9 years and above need 3 servings/d(16, 17). These recommendations are supported by the American Academy of Pediatrics(Reference Gidding, Dennison and Birch18).

Intake of WG in children and adolescents is not well documented, but studies conducted before the release of the 2005 Dietary Guidelines for Americans (DGA) suggested that consumption was low. Using data from the 1989–1991 and 1994–1996 Continuing Survey of Food Intakes by Individuals (CSFII), it was shown that children and adolescents at the age of 2–19 years consumed a daily average of 0·9 servings of WG in 1989–1991 and 1·0 serving in 1994–1996(Reference Kantor, Variyam and Allshouse19). In all, 7 % and 9 % of children, respectively, consumed three servings of WG during the time frame of the study(Reference Kantor, Variyam and Allshouse19). Low intake of WG was confirmed in another study using the CSFII data(Reference Harnack, Walters and Jacobs20) and with data from the 1999–2002 National Health and Nutrition Examination Survey (NHANES). Data from the NHANES showed that children and adolescents at the age of 6–19 years consumed only 0·8–1·0 mean servings of WG/d(Reference Cook and Friday21). A smaller regional study of adolescents showed a slightly higher intake with female adolescents consuming 1·3 servings and male adolescents consuming 1·4 servings of WG/d(Reference Steffen, Jacobs and Murtaugh11).

Determining WG consumption has been difficult since the definition of WG has been unclear. The vast majority of studies(Reference De Moura, Lewis and Falk22) that have assessed WG intake were not based on the current definition of WG, but on the classification scheme proposed by Jacobs et al.(Reference Jacobs, Meyer and Kushi23) in 1998, with WG defined as foods containing ≥25 % WG or bran by weight. The current definition of WG was adopted by the Food and Drug Administration (FDA) in 2006(4). Currently, the FDA allows health claims for WG foods that contain ≥51 % WG ingredient(s) by weight per reference amount customarily consumed(24). The new FDA definition excludes bran and pearled barley as WG(24). The US Department of Agriculture (USDA) MyPyramid Equivalents Database (MPED) versions 1(Reference Friday and Bowman25) and 2(Reference Bowman, Friday and Mosfegh26) provides quantified measures of WG foods, and it provides information with and without bran (old and new definitions) respectively.

There are no recent studies using nationally representative data looking at the consumption of WG or the relationship of WG consumption with diet quality and nutrient intake of children and adolescents. The purpose of the present study was to examine the association of WG consumption, using the FDA definition of WG, with diet quality and nutrient intake in a recent, nationally representative sample of children and adolescents.

Methods

NHANES is a continuous programme that collects information about the nutrition and health status of the US population using a complex, multi-stage, stratified probability sample of the non-institutionalized civilian US population, aged 2 years and above(27). As recommended, the NHANES data sets from 1999–2000, 2001–2002 and 2003–2004 were concatenated(28).

Dietary assessment method

For data collection years, 1999–2002, a single multiple-pass 24 h dietary recall was conducted during an interview using computer-assisted software to record dietary intake data(Reference Jonnalagadda, Mitchell and Smiciklas-Wright29). In 2003–2004, 2 d intakes were collected; however, for the present study, only the first day interview-administered recalls were used to assure consistency with the 1999–2002 dietary data. Parents of children 2–5 years of age provided the recalls; children (6–11 years) were assisted by an adult; and older children and adolescents (12–18 years) provided their own recall. Descriptions of these methods are provided in the NHANES Dietary Interviewer’s Procedures Manual(30).

Participants and whole grains consumption categories

NHANES data collected from 1999 to 2004 were used to compare diet quality and nutrient intake of children at the age of 2–5 years (n 2278), 6–12 years (n 3868) and adolescents at the age of 13–18 years (n 4931). Pregnant and lactating female adolescents were excluded. In addition, there were six foods, principally breakfast cereals or bars, introduced in 2003 that could contain WG; however, there was no information available to calculate their WG content and the individuals (n 11) who consumed at least one of these products were also excluded. As this was a secondary data analysis with no personal identifiers, the present study was exempted by the Institutional Review Board of the LSU AgCenter.

The participants were categorized into one of four WG consumption categories: ≥0 to <0·6, ≥0·6 to <1·5, ≥1·5 to <3·0 and ≥3·0 servings/d. This categorization was chosen since the recommendation for most children and adolescents is 3 servings/d; 1·5 servings represents one-half of the recommendation; and the average number of servings was approximately 0·6 servings. WG intake was calculated using the new definition for WG (excluding bran) as outlined by the MPED(Reference Friday and Bowman25, Reference Bowman, Friday and Mosfegh26). The MPED food data files contain the number of MyPyramid equivalents/100 g of food by thirty-two MyPyramid food groups.

Nutrient analysis

The USDA 1994–98 Survey Nutrient Database(Reference Cook, Friday and Subar31) was used to process the dietary interview data in NHANES 1999–2000, whereas the USDA Food and Nutrient Database for Dietary Studies (FNDDS), versions 1(32) and 2(33), were used in NHANES 2001–2002 and 2003–2004, respectively. In the original release of NHANES 1999–2000, data on vitamin A intake were only available in μg retinol equivalents (μg RE), vitamin E intake data were only available in mg α-tocopherol equivalents (mg ATE), only total folate (μg) intake data, and no vitamin K (μg) or sugar (g) intake data were available as well. Currently, Dietary Reference Intakes (DRI) for vitamins A and E and folate are expressed as μg RAE, mg AT and dietary folate equivalents (DFE), respectively(34, 35). The special database released by the USDA to determine vitamin A as μg RAE and vitamin E as mg AT was used(36). The FNDDS was used to append the intake of folate (DFE), vitamin K (μg) and total sugars (g) to the NHANES 1999–2000 database. The food composition data of added sugars were obtained from the MPED for USDA Survey Food Codes version 1·0(Reference Friday and Bowman25).

The Healthy Eating Index (HEI)-2005 score was used to determine the diet quality(Reference Guenther, Reedy and Krebs-Smith37). The HEI contains twelve food components that reflect the recommendations of the DGA 2005. Dietary intake is expressed per 4184 kJ (1000 kcal) for all components except SFA and sodium, which are fixed recommendations. The maximum possible score on the index is 100. The first six components (i.e. total fruit, whole fruit, total vegetable, dark green/orange vegetables and legumes, total grain and WG) are scored from 0 to 5 points. The next five components (i.e. milk, meat and beans, oil, SFA and sodium) are scored from 0 to 10 points; and the last component of solid fat, alcohol and added sugar is scored from 0 to 20 points. Scores were calculated proportionally, except for SFA and sodium; for these components, the scores were pro-rated linearly between 0–8 and 8–10 points (8 and 10 points represented acceptable and optimal levels, respectively)(Reference Guenther, Reedy and Krebs-Smith37). To calculate HEI, ‘discretionary solid fat’ and ‘discretionary oil’ were needed. The MPED (version 2) only provides ‘Total Discretionary Fats’ as a single group. To overcome this problem, a ratio of ‘Discretionary Oil to Discretionary Solid Fat’ was created for each food using the MPED (version 1), which had these fats separated. The SAS code used to calculate HEI scores was downloaded from the Center for Nutrition Policy and Promotion website(38).

Statistical analysis

Sample-weighted data were used in all statistical analyses, and all analyses were performed using SUDAAN Release 9·0·1 (Research Triangle Institute, Research Triangle Park, NC, USA) using a modified 6-year weight sample. A 6-year weight variable was created by assigning two-thirds of the 4-year weight for 1999–2002 if the person was sampled in 1999–2002 or assigning one-third of the 2-year weight for 2003–2004 if the person was sampled in 2003–2004. The unadjusted mean WG intake and counts and percentages of children and adolescents in WG consumption groups were calculated using SUDAAN. Nutrient intake was based on all foods consumed. Least-squares mean diet quality (HEI), total energy intake and macro- and micronutrient intakes were obtained by regressing intake variables on WG consumption groups. The models were adjusted for age, gender, ethnicity and total energy (kJ (kcal)). P for trend was calculated using SUDAAN with WG intake as a linear independent variable in place of the WG categories. A probability of ≤0·05 was considered significant.

Results

Servings of the whole grains consumed by children and adolescents

Table 1 shows the mean number of WG consumed by each of the three age groups. Children aged 2–5 years consumed an average of 0·45 servings of WG/d, whereas children aged 6–12 years and adolescents of 13–18 years of age consumed 0·59 and 0·63 servings, respectively. Only 1·49 %, 4·00 % and 4·34 % of children aged 2–5, 6–12 years and adolescents aged 13–18 years, respectively, consumed ≥3 servings of WG/d.

Table 1 Mean number of servings of WG consumed and number (%) of consumers for the three age groups by WG consumption group

WG, whole grains.

Healthy Eating Index, energy and nutrient intakes for children aged 2–5 years

HEI scores were significantly higher when more servings of WG were consumed (P < 0·001; Table 2). Intakes of energy (P < 0·001), carbohydrates (P < 0·001), fibre (P < 0·001), vitamins A (P = 0·05), B1 (P = 0·04) and B6 (P < 0·001), folate (P < 0·001), magnesium (P < 0·001), phosphorus (P = 0·0015) and iron (P < 0·001) were significantly higher when an increased number of servings of WG was consumed. Intakes of protein (P = 0·05), added sugars (P = 0·04), total fat (P = 0·01), SFA (P < 0·001), MUFA (P < 0·001), cholesterol (P < 0·001) and vitamin C (P = 0·01) were significantly lower when an increased number of servings of WG was consumed.

Table 2 Diet quality, daily total energy and nutrient intakes by WG consumption groups, US children aged 2–5 years, NHANES 1999–2004Footnote *

WG, whole grains; NHANES, National Health and Nutrition Examination Survey; HEI, Healthy Eating Index; RAE, retinol activity equivalents; AT, α-tocopherol.

* Estimates were adjusted for age, gender, ethnicity and total energy intake. Models for total energy did not include total energy intake.

WG was defined according to the new definition that excludes bran.

Healthy Eating Index, energy and nutrient intakes for children aged 6–12 years

HEI scores were significantly higher when an increased number of servings of WG was consumed (P < 0·001; Table 3). Energy (P < 0·001), carbohydrates (P < 0·001), fibre (P < 0·001), PUFA (P = 0·01), vitamin B6 (P = 0·0037), folate (P = 0·04), magnesium (P < 0·001), phosphorus (P < 0·001) and iron (P < 0·001) intakes were higher when more servings of WG were consumed. Intakes of protein (P = 0·01), total fat (P = 0·05), SFA (P < 0·001), MUFA (P = 0·01), cholesterol (P < 0·001), vitamin C (P < 0·001), potassium (P = 0·05) and sodium (P = 0·05) were lower when more servings of WG were consumed.

Table 3 Diet quality, daily total energy and nutrient intakes by WG consumption groups, US children aged 6–12 years, NHANES 1999–2004Footnote *

WG, whole grains; NHANES, National Health and Nutrition Examination Survey; HEI, Healthy Eating Index; RAE, retinol activity equivalents; AT, α-tocopherol.

* Estimates were adjusted for age, gender, ethnicity and total energy intake. Models for total energy did not include total energy intake.

WG were defined according to the new definition that excludes bran.

Healthy Eating Index, energy and nutrient intakes for adolescents aged 13–18 years

HEI scores were significantly higher when more servings of WG were consumed (P < 0·001; Table 4). Energy (P < 0·001), carbohydrates (P < 0·001), fibre (P < 0·001), vitamins A (P = 0·04), E (P = 0·03), B1 (P = 0·03), B2 (P < 0·001) and B6 (P < 0·001), folate (P < 0·001), magnesium (P < 0·001), phosphorus (P = 0·03) and iron (P < 0·001) intakes were significantly higher when more servings of WG were consumed. Intakes of protein (P < 0·001), total fat (P < 0·001), SFA (P < 0·001), MUFA (P = 0·05) and cholesterol (P < 0·001) were significantly lower when more servings of WG were consumed.

Table 4 Diet quality, daily total energy and nutrient intakes by WG consumption groups, US adolescents aged 13–18 years, NHANES 1999–2004Footnote *

WG, whole grains; NHANES, National Health and Nutrition Examination Survey; HEI, Healthy Eating Index; RAE, retinol activity equivalents; AT, α-tocopherol.

* Estimates were adjusted for age, gender, ethnicity and total energy intake. Models for total energy did not include total energy intake.

WG was defined according to the new definition that excludes bran.

Discussion

The present study showed that although the overall consumption of WG was low, increasing consumption of WG was associated with improved diet quality and nutrient intake in children and adolescents. The number of servings increased slightly in each of the age groups, suggesting that older children and adolescents were more likely to consume WG than younger ones. In children aged 2–5 years, only 1·5 % consumed three or more servings of WG/d; in this age group the consumption of 1·5–2·99 servings, which more closely matches the recommendations(17), was approximately 7 %. The number of WG servings consumed by children and adolescents in the present study was lower than previously reported(Reference Kantor, Variyam and Allshouse19Reference Cook and Friday21), but this is likely the result of the definition of WG used. When the current definition of WG was used(Reference Bowman, Friday and Mosfegh26, 27), there were fewer servings consumed than when the older definition was used (data not shown).

The low consumption of WG by adults is a reason for children not consuming WG(Reference Steffen, Jacobs and Stevens8, Reference Good, Holschuh and Albertson12, Reference Cleveland, Moshfegh and Albertson39Reference Newby, Maras and Bakun41). Interestingly, adults living with children in the household consumed fewer servings of WG than those who did not(Reference Lin and Yen40). Thus, WG foods are not available to children. Parents influence what children eat by determining home food availability and accessibility(Reference Baranowski, Watson and Missaghian42Reference Hanson, Neumark-Sztainer and Eisenberg44); parenting style or practices(Reference Faith, Scanlon and Birch45, Reference Patrick, Nicklas and Hughes46), role modelling(Reference Hanson, Neumark-Sztainer and Eisenberg44, Reference Burgess-Champoux, Rosen and Marquart47, Reference Patrick and Nicklas48) and the level to which they are influenced by their children’s food preferences(Reference Burgess-Champoux, Marquart and Vickers49) affect what foods are consumed. Adolescents show increasing control over their food choices(Reference Befort, Kaur and Nollen50). For adolescents, some(Reference Befort, Kaur and Nollen50), but not all studies(Reference Hanson, Neumark-Sztainer and Eisenberg44, Reference Larson, Story and Wall51) suggest home availability and parenting style are less important than in younger children. Taste and personal health beliefs are important influences on an adolescent’s choice of foods(Reference Larson, Story and Wall51). Influences on consumption of WG in children and adolescents are understudied(Reference Burgess-Champoux, Rosen and Marquart47, Reference Burgess-Champoux, Marquart and Vickers49).

Little is known about barriers to WG consumption in children, but taste, texture and appearance were important in one study, with children preferring refined, sweetened grain products(Reference Burgess-Champoux, Marquart and Vickers49). Younger children did not cite health as a reason for consuming WG and they were unable to identify WG foods, whereas older children could identify them and relate some of their health benefits(Reference Burgess-Champoux, Marquart and Vickers49).

The eating habits developed in childhood can track into adulthood(Reference Li and Wang52Reference Singer, Moore and Garrahie54); thus, it is important to encourage healthy eating habits early in life. Recently, it was shown that a school-based intervention could increase WG consumption by one serving and decrease refined grain consumption by one serving in fourth and fifth grade students(Reference Burgess-Champoux, Chan and Rosen55). School is an appropriate venue for improving WG consumption in children. This is important, since few WG were served at school(Reference Kantor, Variyam and Allshouse19). Although the USDA has issued a policy encouraging adherence to the DGA in the National School Lunch Program(56), the law requires only that sponsors must offer grains, which can be either enriched or WG(57). An Institute of Medicine Report(58) has called for industry and schools to work together to increase availability of WG in child nutrition programmes.

Consumption of WG improved diet quality as indicated by the increasing HEI scores(Reference Guenther, Reedy and Krebs-Smith37, Reference Kennedy59) across the WG consumption groups. The HEI-2005 is designed to reflect the 2005 DGA(Reference Guenther, Reedy and Krebs-Smith37). That version of the HEI includes a WG component, and includes energy from solid fat, alcohol and added sugars. Inclusion of the last three components should assuage concerns about the use of the HEI with children(Reference Kennedy59). The HEI scores are presented as the total score, which is appropriate for studying populations(Reference Guenther, Reedy and Krebs-Smith37). Although HEI scores improved with increasing levels of WG consumption, the mean score of those consuming ≥3 servings of WG/d ranged from 54 to 58 out of a maximum of 100 in the different age groups suggesting that overall diet quality of both children and adolescents could be improved(Reference Feskanich, Rockett and Colditz60). The impact of WG may be small because of the low consumption levels.

Intakes of many macro- and micronutrients also improved with increased consumption of WG. The focus of this discussion will be on the shortfall nutrients in the diets of children (fibre, magnesium, vitamin E, calcium and potassium)(16). These shortfall nutrients are found naturally in WG(Reference Slavin1).

The majority of children do not meet the daily fibre requirement, with mean intake approximately half of the recommendation(61) for Adequate Intake(62). The present study showed that increased WG consumption was associated with increased fibre intake; however, mean intake fell below recommendations for all age groups. In children and adolescents, fibre intake is inversely associated with serum cholesterol levels(Reference Williams and Strobino63) and constipation(Reference Lee, Ip and Chan64), which is a major cause of morbidity in children(Reference Loening-Baucke65). Fruit, vegetable and WG intake should be encouraged in children and adolescents to help them meet the fibre requirement.

All age groups showed a significant increase in magnesium with the consumption of WG. Magnesium is an essential cofactor for over 300 metabolic reactions. In adults, higher intake is associated with an inverse risk of type 2 diabetes(Reference Song, Manson and Buring66) and metabolic syndrome(Reference McKeown, Jacques and Zhang67). One of the few studies conducted in children suggested that magnesium deficiency is associated with insulin resistance in obese children(Reference Huerta, Roemmich and Kington68). Adolescents appear at greatest risk for low magnesium intake(Reference Lee, Ip and Chan64) . In the present study, mean intake by adolescents failed to reach the DRI (separate data by gender not shown).

Vitamin E, calcium and potassium are the remaining shortfall nutrients in the diets of children. Vitamin E is found in WG; however, only 5 %(Reference Liu69) to 21 %(Reference Truswell70) of vitamin E is retained when wheat is processed. Adolescents were the only group that showed improved vitamin E intake with increased WG consumption and their mean intake did not approach the DRI of 15 mg/d for male and female adolescents aged 14–18 years(35). Increased consumption of WG by adults was associated with increased intake of vitamin E(Reference Koh-Banerjee, Franz and Sampson71); however, that study included dietary supplements in the nutrient analysis. Of the other shortfall nutrients, only potassium showed a marginal increase with increased consumption of WG in children aged 6–12 years. It may have been that WG consumption was not high enough to influence intake of vitamin E, calcium and potassium, since WG are not good sources of these nutrients. Foods such as low-fat dairy, fruit, vegetables, nuts and oils should be encouraged along with WG in the diet to improve the intake of these micronutrients.

The present study had several limitations. NHANES collects cross-sectional data and, therefore, causal inferences cannot be drawn. Twenty-four-hour dietary recalls are subject to under- or over-reporting of energy and examiner effects(Reference Johnson, Driscoll and Goran72); single 24 h dietary recalls may not accurately reflect the usual dietary intake patterns of participants. Although 2 d recalls are now available from NHANES, only one day was used from the 2003–2004 data set; therefore, data from that reporting period would be comparable with data from the other survey years (1999–2002). Parents reported or assisted with the 24 h recalls of children aged 2–11 years; parents can often report accurately what children eat in the home(Reference Basch, Shea and Arliss73), but may not know what their children eat outside the home(Reference Baranowski, Sprague and Baranowski74), which could result in reporting errors(Reference Schoeller75). With a large sample size, 24 h recalls produce reasonably accurate group estimates of nutrient intake(Reference Hennekens and Buring76). The strengths of the study included a nationally representative sample with a large sample size and use of the new definition of WG.

Overall consumption of WG in children and adolescents was low; however, diet quality and nutrient intake were significantly improved with increasing consumption of WG. WG consumption for children, adolescents and their parents should be encouraged by health professionals, especially registered dietitians.

There is a paucity of published research looking at WG consumption in children. Recommendations for WG intake are based on findings in adults, which have been extrapolated to children and adolescents. Few studies have looked at ethnic and socio-economic influences on WG consumption in these age groups(35). Barriers to WG intake in children and adolescents have not been widely studied(Reference Faith, Scanlon and Birch45), and only recently have results from interventions to increase consumption of WG in children been published(Reference Burgess-Champoux, Chan and Rosen55). Nutrition education programmes that increase awareness, health benefits and consumption of WG should be made more widely available. Finally, it is important to quantify the effect that WG consumption has on health parameters, such as weight, in children.

Acknowledgements

This research was supported by funds from the Kellogg’s Corporate Citizenship Fund. Partial support was received from the US Department of Agriculture (USDA) Hatch Projects 940-36-3104 Project no. 93673 and LAB 93676 no. 0199070 and a USDA/ARS (Agricultural Research Service)-specific Cooperative Agreement no. 58-6250-6-003. This work is a publication of the USDA/ARS Children’s Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine in Houston, TX, USA, and was also funded in part with federal funds from the USDA/ARS under Cooperative Agreement no. 58-6250-6-003. The contents of this publication do not necessarily reflect the views or policies of the USDA, nor does the mention of trade names, commercial products, or organizations imply endorsement from the US government. The sponsors had no role in the design and conduct of the study; the collection, management, analysis and interpretation of the data; or the preparation and approval of the manuscript. The authors have no conflicts of interest to declare. C.E.O’N. directed implementation and was the principal author. T.A.N. conceptualized the study; helped with the editing and interpretation of the results. M.Z. and R.K. helped with the editing. S.S.C. conducted the statistical analyses. The authors thank Bee Wong for help with the literature and Pamelia Harris for formatting the manuscript.

References

1.Slavin, J (2004) Whole grains and human health. Nutr Res Rev 17, 99110.CrossRefGoogle ScholarPubMed
2.Slavin, JL, Jacobs, D, Marquart, L et al. (2001) The role of whole grains in disease prevention. J Am Diet Assoc 101, 780785.CrossRefGoogle ScholarPubMed
3.American Association of Cereal Chemists (1999) International definition of whole grain. http://www.aaccnet.org/definitions/wholegrain.asp (accessed October 2009).Google Scholar
4.US Food and Drug Administration (2006) Guidance for industry and FDA staff: whole grain label statements (draft guidance). http://www.fda.gov/Food/GuidanceComplianceRegulatoryInformation/GuidanceDocuments/FoodLabelingNutrition/ucm059088.htm (accessed October 2009).Google Scholar
5.Franz, M & Sampson, L (2006) Challenges in developing a whole grain database: definitions, methods, and quantification. J Food Compost Anal 19, S38S44.CrossRefGoogle Scholar
6.Jones, JM, Reicks, M, Adams, J et al. (2002) The importance of promoting a whole grain foods message. J Am Coll Nutr 21, 293297.CrossRefGoogle ScholarPubMed
7.Jensen, MK, Koh-Banerjee, P, Hu, FB et al. (2004) Intakes of whole grains, bran, and germ and the risk of coronary heart disease in men. Am J Clin Nutr 80, 14921499.CrossRefGoogle ScholarPubMed
8.Steffen, LM, Jacobs, DR Jr, Stevens, J et al. (2003) Associations of whole-grain, refined-grain, and fruit and vegetable consumption with risks of all-cause mortality and incident coronary artery disease and ischemic stroke: the Atherosclerosis Risk in Communities (ARIC) Study. Am J Clin Nutr 78, 383390.CrossRefGoogle ScholarPubMed
9.Wang, L, Gaziano, JM, Liu, S et al. (2007) Whole- and refined-grain intakes and the risk of hypertension in women. Am J Clin Nutr 86, 472479.CrossRefGoogle ScholarPubMed
10.de Munter, JS, Hu, FB, Spiegelman, D et al. (2007) Whole grain, bran, and germ intake and risk of type 2 diabetes: a prospective cohort study and systematic review. PLoS Med 4, e261.CrossRefGoogle ScholarPubMed
11.Steffen, LM, Jacobs, DR Jr, Murtaugh, MA et al. (2003) Whole grain intake is associated with lower body mass and greater insulin sensitivity among adolescents. Am J Epidemiol 158, 243250.CrossRefGoogle ScholarPubMed
12.Good, CK, Holschuh, N, Albertson, AM et al. (2008) Whole grain consumption and body mass index in adult women: an analysis of NHANES 1999–2000 and the USDA pyramid servings database. J Am Coll Nutr 27, 8087.CrossRefGoogle ScholarPubMed
13.Larsson, SC, Giovannucci, E, Bergkvist, L et al. (2005) Whole grain consumption and risk of colorectal cancer: a population-based cohort of 60,000 women. Br J Cancer 92, 18031807.CrossRefGoogle Scholar
14.Schatzkin, A, Mouw, T, Park, Y et al. (2007) Dietary fiber and whole-grain consumption in relation to colorectal cancer in the NIH-AARP Diet and Health Study. Am J Clin Nutr 85, 13531360.CrossRefGoogle ScholarPubMed
15.Jacobs, DR Jr & Steffen, LM (2003) Nutrients, foods, and dietary patterns as exposures in research: a framework for food synergy. Am J Clin Nutr 78, Suppl. 3, 508S513S.CrossRefGoogle ScholarPubMed
16.United States Department of Agriculture, Dietary Guidelines Advisory Committee, Agricultural Research Service (2005) Report of the Dietary Guidelines Advisory Committee on the Dietary Guidelines for Americans 2005: To the Secretary of Health and Human Services and the Secretary of Agriculture. http://www.health.gov/DietaryGuidelines/dga2005/report/default.htm (accessed July 2008).Google Scholar
17.United States Department of Agriculture (modified 2010) MyPyramid Website. http://www.mypyramid.gov (accessed July 2008).Google Scholar
18.Gidding, SS, Dennison, BA, Birch, LL et al. (2005) Dietary recommendations for children and adolescents: a guide for practitioners: consensus statement from the American Heart Association. Circulation 112, 20612075.CrossRefGoogle ScholarPubMed
19.Kantor, LS, Variyam, JN, Allshouse, JE et al. (2001) Choose a variety of grains daily, especially whole grains: a challenge for consumers. J Nutr 131, Suppl., S473S486.CrossRefGoogle ScholarPubMed
20.Harnack, L, Walters, SA & Jacobs, DR Jr (2003) Dietary intake and food sources of whole grains among US children and adolescents: data from the 1994–1996 Continuing Survey of Food Intakes by Individuals. J Am Diet Assoc 103, 10151019.CrossRefGoogle ScholarPubMed
21.Cook, AJ & Friday, JE (2005) CNRG Table Set 3.0: Pyramid Servings Intakes in the United States 1999–2002, 1 Day. Beltsville, MD: US Department of Agriculture, Agricultural Research Service; available at http://www.ba.ars.usda.gov/cnrgGoogle Scholar
22.De Moura, FF, Lewis, KD & Falk, MC (2009) Applying the FDA definition of whole grains to the evidence for cardiovascular disease health claims. J Nutr 139, Suppl., S2220S2226.CrossRefGoogle Scholar
23.Jacobs, DR Jr, Meyer, KA, Kushi, LH et al. (1998) Whole-grain intake may reduce the risk of ischemic heart disease death in postmenopausal women: the Iowa Women’s Health Study. Am J Clin Nutr 68, 248257.CrossRefGoogle ScholarPubMed
24.US Food and Drug Administration (1999) Health claim notification for whole grain foods. http://www.fda.gov/ohrms/dockets/dailys/01/Sep01/091901/let0003.pdf (accessed July 2008).Google Scholar
25.Friday, JE & Bowman, SA (2006) MyPyramid Equivalents Database for USDA Survey Food Codes, 1994–2002, version 1.0. Beltsville, MD: US Department of Agriculture, Agricultural Research Service; available at http://www.ars.usda.gov/ba/bhnrc/fsrg/Google Scholar
26.Bowman, SA, Friday, JE & Mosfegh, A (2008) MyPyramid Equivalents Database, 2.0 for USDA Survey Foods, 2003–2004. Beltsville, MD: US Department of Agriculture, Agricultural Research Service; available at http://www.ars.usda.gov/ba/bhnrc/fsrg/Google Scholar
27.Centers for Disease Control and Prevention (2008) National Health and Nutrition Examination Survey. http://www.cdc.gov/nchs/nhanes.htm (accessed July 2009).Google Scholar
28.Centers for Disease Control and Prevention (2004) NHANES analytical guidelines. http://www.cdc.gov/nchs/data/nhanes/nhanes_03_04/nhanes_analytic_guidelines_dec_2005.pdf (accessed July 2008).Google Scholar
29.Jonnalagadda, SS, Mitchell, DC, Smiciklas-Wright, H et al. (2000) Accuracy of energy intake data estimated by a multiple-pass, 24-hour dietary recall technique. J Am Diet Assoc 100, 303308.CrossRefGoogle ScholarPubMed
30.National Center for Health Statistics (2004) NHANES MEC In-Person Dietary Interviewers Procedures Manual. http://www.cdc.gov/nchs/data/nhanes/nhanes_03_04/DIETARY_MEC.pdf (accessed July 2008).Google Scholar
31.Cook, A, Friday, JE & Subar, AF (2004) Dietary Source Nutrient Database for USDA Food Codes. Beltsville, MD: US Department of Agriculture, Agricultural Research Service; available at http://www.ars.usda.gov/ba/bhnrc/fsrg/Google Scholar
32.US Department of Agriculture (2004) USDA Food and Nutrient Database for Dietary Studies, 1.0. Beltsville, MD: Agricultural Research Service, Food Surveys Research Group.Google Scholar
33.US Department of Agriculture (2006) USDA Food and Nutrient Database for Dietary Studies, 2.0. Beltsville, MD: Agricultural Research Service, Food Surveys Research Group.Google Scholar
34.Institute of Medicine (2001) Dietary Reference Intakes for Vitamin A, Vitamin K, Arsenic, Boron, Chromium, Copper, Iodine, Iron, Manganese, Molybdenum, Nickel, Silicon, Vanadium, and Zinc. Washington, DC: National Academy Press.Google Scholar
35.Institute of Medicine (2000) Dietary Reference Intakes for Vitamin C, Vitamin E, Selenium, and Carotenoids. Washington, DC: National Academy Press.Google Scholar
36.US Department of Agriculture (2006) USDA Database of Vitamin A (mcg RAE) and Vitamin E (mg AT) for National Health and Nutrition Examination Survey 1999–2000. Beltsville, MD: Agricultural Research Service, Food Surveys Research Group.Google Scholar
37.Guenther, PM, Reedy, J, Krebs-Smith, SM et al. (2007) Development and evaluation of the Healthy Eating Index-2005: technical report. http://www.cnpp.usda.gov/HealthyEatingIndex.htm (accessed July 2008).CrossRefGoogle Scholar
38.US Department of Agriculture, Center for Nutrition Policy and Promotion (2009) Healthy Eating Index-2005. Development and evaluation: technical report support files. http://www.cnpp.usda.gov/HealthyEatingIndex-2005report.htm (accessed July 2009).Google Scholar
39.Cleveland, LE, Moshfegh, AJ, Albertson, AM et al. (2000) Dietary intake of whole grains. J Am Coll Nutr 19, Suppl. 3, S331S338.CrossRefGoogle ScholarPubMed
40.Lin, BH & Yen, ST (2007) The US Grain Consumption Landscape: Who Eats Grain, in What Form, Where, and How Much? Economic Research Report no. ERR-50. Washington, DC: USDA Economic Research Service; available at http://www.ers.usda.gov/Publications/ERR50/Google Scholar
41.Newby, PK, Maras, J, Bakun, P et al. (2007) Intake of whole grains, refined grains, and cereal fiber measured with 7-d diet records and associations with risk factors for chronic disease. Am J Clin Nutr 86, 17451753.CrossRefGoogle ScholarPubMed
42.Baranowski, T, Watson, K, Missaghian, M et al. (2008) Social support is a primary influence on home fruit, 100% juice, and vegetable availability. J Am Diet Assoc 108, 12311235.CrossRefGoogle ScholarPubMed
43.Haerens, L, Craeynest, M, Deforche, B et al. (2008) The contribution of psychosocial and home environmental factors in explaining eating behaviours in adolescents. Eur J Clin Nutr 62, 5159.CrossRefGoogle ScholarPubMed
44.Hanson, NI, Neumark-Sztainer, D, Eisenberg, ME et al. (2005) Associations between parental report of the home food environment and adolescent intakes of fruits, vegetables and dairy foods. Public Health Nutr 8, 7785.CrossRefGoogle ScholarPubMed
45.Faith, MS, Scanlon, KS, Birch, LL et al. (2004) Parent-child feeding strategies and their relationships to child eating and weight status. Obes Res 12, 17111722.CrossRefGoogle ScholarPubMed
46.Patrick, H, Nicklas, TA, Hughes, SO et al. (2005) The benefits of authoritative feeding style: caregiver feeding styles and children’s food consumption patterns. Appetite 44, 243249.CrossRefGoogle ScholarPubMed
47.Burgess-Champoux, TL, Rosen, R, Marquart, L et al. (2008) The development of psychosocial measures for whole-grain intake among children and their parents. J Am Diet Assoc 108, 714717.CrossRefGoogle ScholarPubMed
48.Patrick, H & Nicklas, TA (2005) A review of family and social determinants of children’s eating patterns and diet quality. J Am Coll Nutr 24, 8392.CrossRefGoogle ScholarPubMed
49.Burgess-Champoux, T, Marquart, L, Vickers, Z et al. (2006) Perceptions of children, parents, and teachers regarding whole-grain foods, and implications for a school-based intervention. J Nutr Educ Behav 38, 230237.CrossRefGoogle ScholarPubMed
50.Befort, C, Kaur, H, Nollen, N et al. (2006) Fruit, vegetable, and fat intake among non-Hispanic black and non-Hispanic white adolescents: associations with home availability and food consumption settings. J Am Diet Assoc 106, 367373.CrossRefGoogle ScholarPubMed
51.Larson, NI, Story, M, Wall, M et al. (2006) Calcium and dairy intakes of adolescents are associated with their home environment, taste preferences, personal health beliefs, and meal patterns. J Am Diet Assoc 106, 18161824.CrossRefGoogle ScholarPubMed
52.Li, J & Wang, Y (2008) Tracking of dietary intake patterns is associated with baseline characteristics of urban low-income African-American adolescents. J Nutr 138, 94100.CrossRefGoogle ScholarPubMed
53.Nicklas, TA (1995) Dietary studies of children: the Bogalusa Heart Study experience. J Am Diet Assoc 95, 11271133.CrossRefGoogle ScholarPubMed
54.Singer, MR, Moore, LL, Garrahie, EJ et al. (1995) The tracking of nutrient intake in young children: the Framingham Children’s Study. Am J Public Health 85, 16731677.CrossRefGoogle ScholarPubMed
55.Burgess-Champoux, TL, Chan, HW, Rosen, R et al. (2008) Healthy whole-grain choices for children and parents: a multi-component school-based pilot intervention. Public Health Nutr 11, 849859.CrossRefGoogle ScholarPubMed
56.US Department of Agriculture, Food and Nutrition Service (2007) Incorporating the 2005 Dietary Guidelines for Americans into school meals. http://www.fns.usda.gov/cnd/Governance/Policy-Memos/2008/SP_04-2008-OS.pdf (accessed July 2008).Google Scholar
57.US Department of Agriculture, Food and Nutrition Service (2000) Menu Planning for the National School Lunch Program. http://www.fns.usda.gov/cnd/menu/menu_planning.doc (accessed July 2008).Google Scholar
58.Institute of Medicine (2007) Nutrition standards for foods in schools: leading the way toward healthier youth. http://www.iom.edu/Object.File/Master/42/628/fact%20sheet.pdf (accessed July 2008).Google Scholar
59.Kennedy, E (2008) Putting the pyramid into action: the Healthy Eating Index and Food Quality Score. Asia Pac J Clin Nutr 17, Suppl. 1, 7074.Google ScholarPubMed
60.Feskanich, D, Rockett, HR & Colditz, GA (2004) Modifying the Healthy Eating Index to assess diet quality in children and adolescents. J Am Diet Assoc 104, 13751383.CrossRefGoogle ScholarPubMed
61.US Department of Agriculture, Agricultural Research Service (2004) Nutrient intakes: mean amounts consumed per individual, one day, 2003–2004. http://www.ars.usda.gov/SP2UserFiles/Place/12355000/pdf/0304/Table_1_NIF.pdf (accessed July 2008).Google Scholar
62.Institute of Medicine (2005) Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids (Macronutrients). Washington, DC: National Academy Press; available at http://www.nap.edu/books/0309085373/htmlGoogle Scholar
63.Williams, CL & Strobino, BA (2008) Childhood diet, overweight, and CVD risk factors: the Healthy Start project. Prev Cardiol 11, 1120.CrossRefGoogle ScholarPubMed
64.Lee, WT, Ip, KS, Chan, JS et al. (2008) Increased prevalence of constipation in pre-school children is attributable to under-consumption of plant foods: a community-based study. J Paediatr Child Health 44, 170175.CrossRefGoogle Scholar
65.Loening-Baucke, V (1995) Functional constipation. Semin Pediatr Surg 4, 2634.Google ScholarPubMed
66.Song, Y, Manson, JE, Buring, JE et al. (2004) Dietary magnesium intake in relation to plasma insulin levels and risk of type 2 diabetes in women. Diabetes Care 27, 5965.CrossRefGoogle ScholarPubMed
67.McKeown, NM, Jacques, PF, Zhang, XL et al. (2008) Dietary magnesium intake is related to metabolic syndrome in older Americans. Eur J Nutr 47, 210216.CrossRefGoogle ScholarPubMed
68.Huerta, MG, Roemmich, JN, Kington, ML et al. (2005) Magnesium deficiency is associated with insulin resistance in obese children. Diabetes Care 28, 11751181.CrossRefGoogle ScholarPubMed
69.Liu, S (2002) Intake of refined carbohydrates and whole grain foods in relation to risk of type 2 diabetes mellitus and coronary heart disease. J Am Coll Nutr 21, 298306.CrossRefGoogle ScholarPubMed
70.Truswell, AS (2002) Cereal grains and coronary heart disease. Eur J Clin Nutr 56, 114.CrossRefGoogle ScholarPubMed
71.Koh-Banerjee, P, Franz, M, Sampson, L et al. (2004) Changes in whole-grain, bran, and cereal fiber consumption in relation to 8-y weight gain among men. Am J Clin Nutr 80, 12371245.CrossRefGoogle ScholarPubMed
72.Johnson, RK, Driscoll, P & Goran, MI (1996) Comparison of multiple-pass 24-hour recall estimates of energy intake with total energy expenditure determined by the doubly labeled water method in young children. J Am Diet Assoc 96, 11401144.CrossRefGoogle ScholarPubMed
73.Basch, CE, Shea, S, Arliss, R et al. (1990) Validation of mothers’ reports of dietary intake by four to seven year-old children. Am J Public Health 80, 13141317.CrossRefGoogle ScholarPubMed
74.Baranowski, T, Sprague, D, Baranowski, JH et al. (1991) Accuracy of maternal dietary recall for preschool children. J Am Diet Assoc 91, 669674.CrossRefGoogle ScholarPubMed
75.Schoeller, DA (1990) How accurate is self-reported dietary energy intake? Nutr Rev 48, 373379.CrossRefGoogle ScholarPubMed
76.Hennekens, CH & Buring, J (1987) Epidemiology in Medicine. Baltimore, MD: Lippincott, Williams & Wilkins.Google Scholar
Figure 0

Table 1 Mean number of servings of WG consumed and number (%) of consumers for the three age groups by WG consumption group

Figure 1

Table 2 Diet quality, daily total energy and nutrient intakes by WG consumption groups, US children aged 2–5 years, NHANES 1999–2004*

Figure 2

Table 3 Diet quality, daily total energy and nutrient intakes by WG consumption groups, US children aged 6–12 years, NHANES 1999–2004*

Figure 3

Table 4 Diet quality, daily total energy and nutrient intakes by WG consumption groups, US adolescents aged 13–18 years, NHANES 1999–2004*