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Maternal cereal consumption and adequacy of micronutrient intake in the periconceptional period

Published online by Cambridge University Press:  01 August 2009

Meredith Snook Parrott
Affiliation:
Magee-Womens Research Institute, Pittsburgh, PA, USA Departments of Obstetrics and Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA
Lisa M Bodnar*
Affiliation:
Magee-Womens Research Institute, Pittsburgh, PA, USA Departments of Obstetrics and Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA Department of Epidemiology, University of Pittsburgh, A742 Crabtree Hall, 130 DeSoto Street, Pittsburgh, PA 15261, USA
Hyagriv N Simhan
Affiliation:
Magee-Womens Research Institute, Pittsburgh, PA, USA Departments of Obstetrics and Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA
Gail Harger
Affiliation:
Department of Epidemiology, University of Pittsburgh, A742 Crabtree Hall, 130 DeSoto Street, Pittsburgh, PA 15261, USA
Nina Markovic
Affiliation:
Department of Epidemiology, University of Pittsburgh, A742 Crabtree Hall, 130 DeSoto Street, Pittsburgh, PA 15261, USA
James M Roberts
Affiliation:
Magee-Womens Research Institute, Pittsburgh, PA, USA Departments of Obstetrics and Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA Department of Epidemiology, University of Pittsburgh, A742 Crabtree Hall, 130 DeSoto Street, Pittsburgh, PA 15261, USA
*
*Corresponding author: Email [email protected]
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Abstract

Objective

To assess the adequacy of periconceptional intake of key micronutrients for perinatal health in relation to regular cereal consumption of pregnant women.

Design, setting and subjects

Low-income pregnant women (n 596) in Pittsburgh, Pennsylvania, USA, who enrolled in a cohort study at <20 weeks’ gestation. These women reported usual dietary intake in the three months around conception on an FFQ. Cereal consumers were women who reported consuming any dry cereal at least three times per week. High risk for nutrient inadequacy was defined as intake less than the Estimated Average Requirement.

Results

About 31 % of the women regularly consumed cereal. After adjusting for energy intake, race/ethnicity, marital status, breakfast consumption and supplement use, cereal eaters had significantly higher intakes of folate, Fe, Zn, Ca, fibre and vitamins A, C, D and E (all P < 0·01) and were approximately two to six times more likely to have intakes in the highest third of the distribution for folate, Fe, Zn, Ca, vitamins A and D, and fibre (all P < 0·01) than cereal non-eaters. Cereal consumption was also associated with reductions of 65–90 % in the risk of nutrient inadequacies compared with non-consumption (all P < 0·01).

Conclusions

Encouraging cereal consumption may be a simple, safe and inexpensive nutrition intervention that could optimize periconceptional intake for successful placental and fetal development.

Type
Research Paper
Copyright
Copyright © The Authors 2008

The periconceptional period represents a specific stage in a woman’s life in which adequate nutrient intake is especially important for both her and her fetus. Optimal pregnancy outcomes rely on successful implantation and early placental and fetal development. Such physiological processes involve remodelling of the maternal arteries underlying the placenta, extensive cell division and differentiation, and well-regulated responses to increases in inflammation and generation of reactive oxygen species – all of which may be influenced by maternal nutritional status(Reference Cross, Werb and Fisher1Reference Jauniaux, Watson, Hempstock, Bao, Skepper and Burton3). Not surprisingly, inadequate periconceptional nutrition is associated with pregnancy complications such as congenital abnormalities(Reference Czeizel and Dudas4), preterm birth(Reference Bloomfield, Oliver, Hawkins, Campbell, Phillips, Gluckman, Challis and Harding5), fetal growth restriction(Reference MacLaughlin, Walker, Roberts, Kleemann and McMillen6, Reference Oliver, Hawkins and Harding7) and pre-eclampsia(Reference Roberts, Balk, Bodnar, Belizan, Bergel and Martinez8). Thus, ensuring that women receive adequate nutrition around the time of conception is essential. Nevertheless, many US women of reproductive age are at high risk of nutrient inadequacies(9, 10).

The consumption of ready-to-eat breakfast cereals may help women meet the high nutrient requirements of pregnancy. Among non-pregnant individuals, breakfast eaters are less likely than breakfast skippers to have nutrient inadequacies(Reference Nicklas, O’Neil and Berenson11Reference Williams13), in part because of the typical intake of ready-to-eat breakfast cereals in the morning meal. Many ready-to-eat cereals are fortified with key nutrients, such as folic acid, Fe, Zn, Ca and vitamins A, C and D, all of which are linked to successful placental and fetal development. Among US adults, cereal is the top food source of folate, Fe and vitamin B6 and is among the top ten food sources for many other micronutrients(Reference Cotton, Subar, Friday and Cook14), trends also observed in pregnant women(Reference Siega-Riz, Bodnar and Savitz15). In fact, micronutrient fortification of cereals makes significant contributions to overall daily intakes, with a higher contribution in women than in men(Reference Galvin, Kiely and Flynn16). Indeed, children and non-pregnant adults who consume cereal regularly have higher intakes of most vitamins and minerals(Reference Nicklas, O’Neil and Berenson11, Reference Preziosi, Galan, Deheeger, Yacoub, Drewnowski and Hercberg12, Reference Galvin, Kiely and Flynn16Reference van den Boom, Serra-Majem, Ribas, Ngo, Perez-Rodrigo, Aranceta and Fletcher20) and lower prevalences of nutrient inadequacy than those who do not consume cereal(Reference Nicklas, O’Neil and Berenson11, Reference Williams13, Reference Galvin, Kiely and Flynn16, Reference Song, Chun, Kerver, Cho, Chung and Chung19, Reference van den Boom, Serra-Majem, Ribas, Ngo, Perez-Rodrigo, Aranceta and Fletcher20). Despite the importance of maternal micronutrient status around the time of conception, cereal intake has not been explored in relation to nutrient adequacy in pregnant women. As nutrient needs increase dramatically during pregnancy(21) and food preferences may change, studying the association between cereal intake and nutrient adequacy specifically during this stage of the woman’s life cycle is important.

Our objective was to assess the adequacy of periconceptional intake of key micronutrients for perinatal health in relation to regular cereal consumption. We hypothesized that pregnant women who ate cereal regularly in the periconceptional period would have higher absolute nutrient intakes and lower risk of nutrient inadequacies compared with women who did not eat cereal regularly.

Methods

Data came from two pregnancy cohort studies conducted at Magee-Womens Hospital in Pittsburgh, Pennsylvania, USA, from 2003 to 2005. The studies were designed to explore the effects of nutrition and other maternal factors on pregnancy outcomes. Both studies enrolled women at <20 weeks’ gestation (mean 17·6 (sd 3·9) weeks). Eligible women were aged 14 to 50 years, carrying singleton pregnancies, planning to deliver at Magee-Womens Hospital and without history of diabetes, hypertension, autoimmune disease or other pre-existing medical conditions. After providing informed, written consent, subjects in both studies completed an interviewer-administered questionnaire at enrolment to collect data on sociodemographics, medical history and health behaviours, including smoking, physical activity and television watching. At enrolment, women completed a self-administered FFQ assessing periconceptional dietary intake, supplement use and meal patterns (discussed below). The University of Pittsburgh Institutional Review Boards approved these studies. A total of 596 out of 829 (72 %) women had complete dietary data and were available for the current analysis.

Dietary assessment

Periconceptional dietary intake was assessed using a modified Block98 FFQ (approximately 120 food/beverage items)(Reference Block, Coyle, Hartman and Scoppa22, Reference Block, Hartman, Dresser, Carroll, Gannon and Gardner23). The questionnaire asks about usual dietary intake in the one month before and two months after conception. The food list for this questionnaire was developed from the dietary recall data of the third National Health and Nutrition Examination Survey. An individual portion size is asked for each food and pictures are provided to enhance accuracy of quantification. The FFQ has been validated in numerous samples(24Reference Block, Woods, Potosky and Clifford26) and is currently being validated in our own population. Slight modifications were made to the questionnaire to include a more extensive list of fish and seafood items, to focus on a three-month time period and to be specific for pregnancy. Because this FFQ is semi-quantitative, it provides a projection of the amount of nutrients consumed. The questionnaire also included an assessment of the type and frequency of dietary supplements used in the periconceptional period.

Questionnaires were sent to Block Dietary Data Systems (Berkeley, CA, USA) for optical scanning and nutrient analysis using software originally developed at the National Cancer Institute. The software used for nutrient analysis produces estimates of usual intake for a wide array of nutrients. It calculates the frequency of daily intake and total daily grams of food consumed for each food item, and provides the gram weight for each serving size. Nutrient values were calculated by multiplying the nutrient content of the food by the gram weight and frequency, and summing across all food items. The nutrient values were updated based on the US Department of Agriculture (USDA) 1994–1996 Continuing Survey of Food Intake by Individuals for women aged 19–44 years and updated folate values for fortified foods from the USDA Nutrient Database for Standard Reference, Release 12 (USDA Agricultural Research Service, Beltsville, MD, USA). Folate values were adjusted for increased bioavailability of fortified folate. For foods without added folic acid, micrograms of dietary folate equivalents (DFE) were equal to the micrograms of naturally occurring food folate. For foods with added folic acid, DFE were calculated using the following formula(27): micrograms of naturally occurring food folate + (micrograms of added folic acid × 1·7).

The FFQ included three dry cereal line items: high-fibre cereals, highly fortified cereals and all other dry cereals. We summed the frequency reported for each cereal line item to obtain an overall frequency of any ready-to-eat cereal in the periconceptional period. We classified women as regular cereal eaters if they reported consuming cereal at least three times per week at any point throughout the day.

Women were defined as being at high risk for nutrient inadequacy if their nutrient intake was less than the Estimated Average Requirement (EAR) for pregnant women. The EAR is one of the Dietary Reference Intakes used to assess adequacy of a population’s intake(28). The EAR is the average daily nutrient intake to meet the requirements of half the healthy individuals for the specific life stage and gender group. We elected to assess periconceptional diets relative to the EAR for pregnant women because our definition of the three periconceptional months included two postconception months and one preconception month (a time when women should be preparing for pregnancy). To assess the likelihood of inadequacy for Fe, we used the cut-point approach rather than the full probability approach(29). Too few data were available for the Institute of Medicine to simulate an Fe requirement distribution for pregnant and lactating women. Because pregnant women have no menstrual losses, it is assumed that the requirements are normally distributed around the EAR (S. Murphy, personal communication, 2008). An EAR has not yet been established for Ca and vitamin D(30), so we did not calculate the risk of nutrient inadequacy for these micronutrients.

Covariates

Intake of breakfast was determined using a diet pattern questionnaire, which assessed the number, type and timing of meals and snacks consumed in a typical week around conception(Reference Siega-Riz, Herrmann, Savitz and Thorp31). The interpretation of what constituted a meal or snack was left up to the participants’ discretion. We defined breakfast consumption as a self-reported breakfast meal.

Sociodemographic and behavioural covariate information was acquired through interview-based self-report. Education (<12 years, 12 years, >12 years), pre-pregnancy smoking status (smoker, non-smoker), martial status (married, unmarried) and parity (0, 1 or more) were available. Race/ethnicity was self-reported and subsequently categorized as black or non-black because few women reported races other than black or white. Pre-pregnancy BMI (weight (kg)/height (m)2) was calculated from maternal self-report of pre-pregnancy weight and height measurement at initial visit. Women were asked to categorize their usual amount of time spent watching television in the year before the index pregnancy as 0–1, 2–3 or ≥4 h/d. At enrolment, subjects also self-reported their use of multivitamins or prenatal vitamins in the periconceptional period. Periconceptional supplement users were women who reported using a prenatal vitamin or multivitamin at least once per month in the three months around conception.

Statistical analysis

We compared maternal characteristics by cereal intake using Pearson χ 2 statistics. Multivariable linear regression was used to assess differences in mean nutrient intake by cereal use after adjustment for confounders. Nutrients were log-transformed because nutrient intake was highly skewed. Mean micronutrient and fibre intakes were energy-adjusted by dividing the total amount of the nutrient by the number of calories, and then multiplying by 2000. These nutrient density values were then divided into thirds based on tertiles. We used χ 2 tests to compare the distribution of cereal eaters and cereal non-eaters among tertiles of nutrient intake. We then used multivariable logistic regression to assess the independent association between cereal intake and the odds of being in the upper tertile of nutrient intake compared with the lower two tertiles. Finally, we calculated the proportion of women who consumed less than the EAR for each micronutrient and used logistic regression to determine the odds of micronutrient inadequacy by regular cereal use. We also performed the aforementioned analyses excluding nineteen women who reported regular consumption of highly fortified cereals to ensure that the results were not driven by their intakes.

We fit parsimonious regression models by specifying a full model with potential confounding variables (energy intake, breakfast consumption, maternal age, race/ethnicity, parity, education, marital status, smoking, pre-pregnancy BMI, supplement use, pre-pregnancy television watching). Potential confounders were considered to not be influential and were removed from the model if their inclusion did not satisfy our a priori change-in-estimate criterion (a change in the coefficient of >10 %).

Results

About 31 % of women regularly consumed cereal. Cereal eaters were more likely than cereal non-eaters to be married, multiparous and users of dietary supplements (Table 1). Cereal users also tended to be leaner and more likely to consume a breakfast meal compared with cereal non-users, although not statistically significant.

Table 1 Subject characteristics by regular cereal consumptionFootnote *: low-income pregnant women (n 596), Pittsburgh, PA, USA, 2003–2005

* Regular cereal consumption defined as cereal intake ≥3 times/week.

Data missing on four women.

Energy intake was significantly greater among cereal eaters than cereal non-eaters (Table 2). After adjusting for energy intake, race/ethnicity, marital status, breakfast consumption and supplement use, women who regularly consumed cereal had significantly higher mean intakes of folate, Fe, Zn, Ca, vitamins A, C, D and E, and fibre (all P < 0·01; Table 2). Nutrient intakes were 14–83 % greater among users than non-users.

Table 2 AdjustedFootnote * mean nutrient intakes by regular cereal consumption: low-income pregnant women (n 596), Pittsburgh, PA, USA, 2003–2005

* Adjusted for daily energy intake, ethnicity, marital status, breakfast consumption and supplement use.

Derived from multivariable linear regression models with the log nutrient intake as the dependent variable and regular cereal consumption and covariates listed above as independent variables.

Compared with women who did not consume cereal regularly, regular consumers were significantly more likely to have folate, Fe, Zn, Ca, vitamin A, vitamin D and fibre intakes in the highest third of the distribution (Table 3). Notably, regular cereal consumers were about five and six times more likely to be in the highest tertile of periconceptional folate and Fe intake, respectively, than non-consumers after confounder adjustment.

Table 3 Association between regular cereal consumption and adjusted odds of nutrient intake in the highest third of the distribution: low-income pregnant women (n 596), Pittsburgh, PA, USA, 2003–2005

T1, lowest tertile; T2, middle tertile; T3, highest tertile of nutrient distribution; ref, referent category.

*Median energy-adjusted nutrient density for each tertile, calculated as (median nutrient intake/energy intake) × 2000.

†Based on Pearson χ 2 statistics when comparing proportions and logistic regression for odds ratios.

‡All odds ratios were adjusted for ethnicity, marital status, breakfast consumption and supplement use.

Compared with cereal users, a significantly higher proportion of non-users of cereal failed to achieve the EAR for folate, Fe, Zn and vitamins A, C and E (all P < 0·001; Table 4), and were therefore at high risk of nutrient inadequacy. For instance, about 27 % of cereal users and 71 % of non-users had folate intakes less than the EAR. After adjusting for energy intake, race/ethnicity, marital status, breakfast intake and supplement use, regular cereal consumption was associated with significant reductions in risk of nutrient inadequacies compared with cereal non-consumption (all P < 0·01). Women who regularly used cereal had approximately 90 % reductions in risk of inadequacy in folate and Fe, and 65–75 % reductions in risk of insufficiency in Zn, vitamin A, vitamin C and vitamin E.

Table 4 Association between regular cereal consumption and risk of nutrient inadequacy: low-income pregnant women (n 596), Pittsburgh, PA, USA, 2003–2005

EAR, Estimated Average Requirements; ref, referent category.

*Based on χ 2 tests when comparing proportions and logistic regression for odds ratios.

†EAR of specified nutrient for pregnant women >18 years. EAR is the average daily energy intake to meet the requirements of half the healthy individuals for the specific life stage and gender group. Intakes lower than the EAR suggest high risk for nutritional inadequacy.

‡All odds ratios are adjusted for daily energy intake, ethnicity, marital status, breakfast consumption and supplement use.

The exclusion of the nineteen cereal users who reported regular consumption of highly fortified cereals did not meaningfully influence the findings (data not shown). Further adjustment for age, education, smoking status, parity, pre-pregnancy BMI and television watching did not considerably alter any of the results (data not shown).

Discussion

We observed that pregnant women who ate cereal at least three times per week around the time of conception had significantly higher intakes of key micronutrients compared with women who did not eat cereal regularly, even after controlling for confounders such as energy and breakfast intake. Moreover, regular cereal users had significant reductions in risk of periconceptional micronutrient inadequacies, including that of folate and Fe, compared with non-users. These results are meaningful as these micronutrients have been highlighted as shortfall nutrients in women of reproductive age(10). In addition, the positive effects of eating cereal were not limited to women who regularly consumed highly fortified cereals.

To our knowledge, the present study is the first one to explore the association between cereal intake and micronutrient adequacy in pregnant women. Our findings are consistent with numerous studies relating cereal intake to nutritional status among children and non-pregnant adults(Reference Nicklas, O’Neil and Berenson11, Reference Galvin, Kiely and Flynn16, Reference Song, Chun, Kerver, Cho, Chung and Chung19). For example, in a nationally representative US sample of individuals aged 9 years and older, nutrient intakes were 14–63 % higher in cereal consumers than non-consumers as defined by self-report on 24 h dietary recalls(Reference Song, Chun, Kerver, Cho, Chung and Chung19). Additionally, another study of children and young adults in the USA found that cereal eaters were significantly more likely to meet at least two-thirds of the Recommended Dietary Allowance for folate, Fe, Ca, Zn and vitamins A, C and D(Reference Nicklas, O’Neil and Berenson11). Similarly, in 717 non-pregnant Irish women aged 18–64 years, it was reported that cereal consumption was associated with lower prevalence of inadequate intakes of folate, Fe, Ca, Zn and vitamin C according to European Average Requirements. Moreover, the proportion of women with nutrient inadequacies decreased as cereal consumption increased(Reference Galvin, Kiely and Flynn16).

We used an FFQ to assess cereal intake, while most previous studies used dietary recalls or records. Nevertheless, the percentage of pregnant women regularly consuming cereal in our study was comparable to that previously reported in women of reproductive age(Reference Barton, Eldridge, Thompson, Affenito, Striegel-Moore, Franko, Albertson and Crockett17, Reference Song, Chun, Kerver, Cho, Chung and Chung19, Reference Siega-Riz, Popkin and Carson32, Reference Song, Chun, Obayashi, Cho and Chung33). Although investigators of past studies tended to focus on cereal intake at breakfast, we included cereal intake throughout the day because a sizeable proportion (36 %) of regular cereal eaters in our study reported not usually consuming breakfast. This suggests that cereal was often consumed as a snack or part of another meal. This finding is consistent with a study of US children and young adults, which found that about 40 % of cereal eaters consumed cereal as lunch, dinner or a snack and that those who consumed cereal at any time of day had higher micronutrient intakes(Reference Nicklas, O’Neil and Berenson11). Taken together, these data highlight that cereal intake may not need to be part of breakfast to have a positive impact on diet quality.

Some health-care professionals may wonder about the negative aspects of promoting cereal intake, such as excessive weight gain, high sugar intakes and/or micronutrient intakes above tolerable levels. Nevertheless, cross-sectional studies have shown that cereal eaters are often leaner(Reference Barton, Eldridge, Thompson, Affenito, Striegel-Moore, Franko, Albertson and Crockett17, Reference Song, Chun, Obayashi, Cho and Chung33, Reference Cho, Dietrich, Brown, Clark and Block34) and also have lower daily intakes of fat and cholesterol(Reference Galvin, Kiely and Flynn16Reference Song, Chun, Kerver, Cho, Chung and Chung19, Reference Song, Chun, Obayashi, Cho and Chung33) than cereal non-eaters. We also found that cereal users tended (P = 0·07) to have lower BMI values than cereal non-users. Moreover, ready-to-eat breakfast cereals contribute minimally to overall daily sugar intake(Reference Williams13). Cereal consumption should, however, be encouraged in moderation, with attention paid to serving size, and in the context of a healthy diet.

The positive effect we observed of cereal intake on micronutrient intake may not have been due to the cereal itself, but rather to foods commonly eaten by cereal users or healthy eating behaviours. For example, the higher intakes of Ca and vitamin D seen among cereal users may be due to the use of milk on cereal. We could not separate these effects because 85 % of the cereal consumers reported regularly using milk on their cereal. In addition, there is unfortunately no gold standard for assessing usual dietary intake. FFQ are limited by a restricted, culture-specific food list; their representation of a person’s perceived intake rather than actual intake; and their limited ability to estimate absolute energy intake(Reference Willet35). However, FFQ have the advantages of capturing usual past intake of micronutrients, having a low respondent burden, and ranking individuals relative to one another (i.e. high v. low consumers)(Reference Willet35). We performed our analyses assessing both tertiles of nutrient intake (to capture a ranking of subjects) and micronutrient intakes less than the EAR (an absolute measure of intake) and came to comparable conclusions. Another limitation was the time lapse between the period of recall (periconceptional period) and completion of the FFQ (mid-pregnancy). A study to validate the FFQ in our population is currently underway. Finally, our small sample size prohibited us from studying whether cereal intake protected against adverse pregnancy outcomes. Future investigations should explore this intriguing research question.

Our results suggest that regularly consuming cereal in the periconceptional period may help reduce the prevalence of deficiencies in essential micronutrients, including folate and Fe. Inquiring about regular intake of cereal could be used as an instant assessment of micronutrient inadequacies in pregnant women. Encouraging cereal consumption as part of a healthy lifestyle around conception may be a simple, safe and inexpensive nutrition intervention that could optimize maternal periconceptional intake for successful placental and fetal development.

Acknowledgements

Sources of funding:The study was partially supported by National Institutes of Health Grants R01 HD041663, P01 HD030367 and M01 RR000056. L.M.B. was supported by K01 MH074092. M.S.P. was supported by a Clinical Scientist Training Program scholarship from the University of Pittsburgh School of Medicine.

Conflict of interest declaration:None declared.

Authorship responsibilities:L.M.B. originated the idea for this project. H.N.S. and J.M.R. secured the funding for the studies. G.H. and N.M. aided with data collection. M.S.P. conducted analyses with input from L.M.B. All authors contributed to the interpretation of the data. M.S.P. and L.M.B. wrote the manuscript while all authors gave final approval.

References

1.Cross, JC, Werb, Z & Fisher, SJ (1994) Implantation and the placenta: key pieces of the development puzzle. Science 266, 15081518.Google Scholar
2.Goodger, AM & Rogers, PA (1993) Uterine endothelial cell proliferation before and after embryo implantation in rats. J Reprod Fertil 99, 451457.CrossRefGoogle ScholarPubMed
3.Jauniaux, E, Watson, AL, Hempstock, J, Bao, YP, Skepper, JN & Burton, GJ (2000) Onset of maternal arterial blood flow and placental oxidative stress. A possible factor in human early pregnancy failure. Am J Pathol 157, 21112122.Google Scholar
4.Czeizel, AE & Dudas, I (1992) Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation. N Engl J Med 327, 18321835.CrossRefGoogle ScholarPubMed
5.Bloomfield, FH, Oliver, MH, Hawkins, P, Campbell, M, Phillips, DJ, Gluckman, PD, Challis, JR & Harding, JE (2003) A periconceptional nutritional origin for noninfectious preterm birth. Science 300, 606.Google Scholar
6.MacLaughlin, SM, Walker, SK, Roberts, CT, Kleemann, DO & McMillen, IC (2005) Periconceptional nutrition and the relationship between maternal body weight changes in the periconceptional period and feto-placental growth in the sheep. J Physiol 565, 111124.Google Scholar
7.Oliver, MH, Hawkins, P & Harding, JE (2005) Periconceptional undernutrition alters growth trajectory and metabolic and endocrine responses to fasting in late-gestation fetal sheep. Pediatr Res 57, 591598.Google Scholar
8.Roberts, JM, Balk, JL, Bodnar, LM, Belizan, JM, Bergel, E & Martinez, A (2003) Nutrient involvement in preeclampsia. J Nutr 133, 1684S1692S.CrossRefGoogle ScholarPubMed
9. US Department of Health and Human Services (2000) Healthy People 2010: National Health Promotion and Disease Prevention Objectives. Washington, DC: DHHS.Google Scholar
10. US Department of Health and Human Services and US Department of Agriculture (2005) The Report of the Dietary Guidelines Advisory Committee on Dietary Guidelines for Americans, 2005, 6th ed. Washington, DC: DHHS and USDA.Google Scholar
11.Nicklas, TA, O’Neil, CE & Berenson, GS (1998) Nutrient contribution of breakfast, secular trends, and the role of ready-to-eat cereals: a review of data from the Bogalusa Heart Study. Am J Clin Nutr 67, 757S763S.Google Scholar
12.Preziosi, P, Galan, P, Deheeger, M, Yacoub, N, Drewnowski, A & Hercberg, S (1999) Breakfast type, daily nutrient intakes and vitamin and mineral status of French children, adolescents, and adults. J Am Coll Nutr 18, 171178.Google Scholar
13.Williams, P (2005) Breakfast and the diets of Australian adults: an analysis of data from the 1995 National Nutrition Survey. Int J Food Sci Nutr 56, 6579.CrossRefGoogle ScholarPubMed
14.Cotton, PA, Subar, AF, Friday, JE & Cook, A (2004) Dietary sources of nutrients among US adults, 1994 to 1996. J Am Diet Assoc 104, 921930.Google Scholar
15.Siega-Riz, AM, Bodnar, LM & Savitz, DA (2002) What are pregnant women eating? Nutrient and food group differences by race. Am J Obstet Gynecol 186, 480486.CrossRefGoogle ScholarPubMed
16.Galvin, MA, Kiely, M & Flynn, A (2003) Impact of ready-to-eat breakfast cereal (RTEBC) consumption on adequacy of micronutrient intakes and compliance with dietary recommendations in Irish adults. Public Health Nutr 6, 351363.CrossRefGoogle ScholarPubMed
17.Barton, BA, Eldridge, AL, Thompson, D, Affenito, SG, Striegel-Moore, RH, Franko, DL, Albertson, AM & Crockett, SJ (2005) The relationship of breakfast and cereal consumption to nutrient intake and body mass index: the National Heart, Lung, and Blood Institute Growth and Health Study. J Am Diet Assoc 105, 13831389.CrossRefGoogle ScholarPubMed
18.Gibson, S (2003) Micronutrient intakes, micronutrient status and lipid profiles among young people consuming different amounts of breakfast cereals: further analysis of data from the National Diet and Nutrition Survey of Young People aged 4 to 18 years. Public Health Nutr 6, 815820.Google Scholar
19.Song, WO, Chun, OK, Kerver, J, Cho, S, Chung, CE & Chung, SJ (2006) Ready-to-eat breakfast cereal consumption enhances milk and calcium intake in the US population. J Am Diet Assoc 106, 17831789.CrossRefGoogle ScholarPubMed
20.van den Boom, A, Serra-Majem, L, Ribas, L, Ngo, J, Perez-Rodrigo, C, Aranceta, J & Fletcher, R (2006) The contribution of ready-to-eat cereals to daily nutrient intake and breakfast quality in a Mediterranean setting. J Am Coll Nutr 25, 135143.CrossRefGoogle Scholar
21.Institute of Medicine, Food and Nutrition Board (2006) Dietary Reference Intakes: The Essential Guide to Nutrient Requirements. Washington, DC: National Academies Press.Google Scholar
22.Block, G, Coyle, LM, Hartman, AM & Scoppa, SM (1994) Revision of dietary analysis software for the Health Habits and History Questionnaire. Am J Epidemiol 139, 11901196.CrossRefGoogle ScholarPubMed
23.Block, G, Hartman, AM, Dresser, CM, Carroll, MD, Gannon, J & Gardner, L (1986) A data-based approach to diet questionnaire design and testing. Am J Epidemiol 124, 453469.CrossRefGoogle ScholarPubMed
24. Block G & DiSogra C (1994) WIC Dietary Assessment Validation Study. Final Report. Alexandria, VA: US Department of Agriculture, Food and Nutrition Service.Google Scholar
25.Block, G, Thompson, FE, Hartman, AM, Larkin, FA & Guire, KE (1992) Comparison of two dietary questionnaires validated against multiple dietary records collected during a 1-year period. J Am Diet Assoc 92, 686693.CrossRefGoogle ScholarPubMed
26.Block, G, Woods, M, Potosky, A & Clifford, C (1990) Validation of a self-administered diet history questionnaire using multiple diet records. J Clin Epidemiol 43, 13271335.Google Scholar
27.Institute of Medicine, Food and Nutrition Board (2000) Folate. In Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline. Washington, DC: National Academies Press.Google Scholar
28.Institute of Medicine, Food and Nutrition Board (2002) Dietary Reference Intakes (DRIs): Estimated Average Requirements for Groups. Washington, DC: National Academies Press.Google Scholar
29.Institute of Medicine, Food and Nutrition Board (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 Academies Press.Google Scholar
30.Institute of Medicine, Food and Nutrition Board (1997) Dietary Reference Intakes for Calcium, Phosphorus, Magnesium, Vitamin D, and Fluoride. Washington, DC: National Academies Press.Google Scholar
31.Siega-Riz, AM, Herrmann, TS, Savitz, DA & Thorp, JM (2001) Frequency of eating during pregnancy and its effect on preterm delivery. Am J Epidemiol 153, 647652.Google Scholar
32.Siega-Riz, AM, Popkin, BM & Carson, T (2000) Differences in food patterns at breakfast by sociodemographic characteristics among a nationally representative sample of adults in the United States. Prev Med 30, 415424.Google Scholar
33.Song, WO, Chun, OK, Obayashi, S, Cho, S & Chung, CE (2005) Is consumption of breakfast associated with body mass index in US adults? J Am Diet Assoc 105, 13731382.Google Scholar
34.Cho, S, Dietrich, M, Brown, CJ, Clark, CA & Block, G (2003) The effect of breakfast type on total daily energy intake and body mass index: results from the Third National Health and Nutrition Examination Survey (NHANES III). J Am Coll Nutr 22, 296302.CrossRefGoogle ScholarPubMed
35.Willet, WC (1998) Nutritional Epidemiology, 2nd ed.New York: Oxford University Press.Google Scholar
Figure 0

Table 1 Subject characteristics by regular cereal consumption*: low-income pregnant women (n 596), Pittsburgh, PA, USA, 2003–2005

Figure 1

Table 2 Adjusted* mean nutrient intakes by regular cereal consumption: low-income pregnant women (n 596), Pittsburgh, PA, USA, 2003–2005

Figure 2

Table 3 Association between regular cereal consumption and adjusted odds of nutrient intake in the highest third of the distribution: low-income pregnant women (n 596), Pittsburgh, PA, USA, 2003–2005

Figure 3

Table 4 Association between regular cereal consumption and risk of nutrient inadequacy: low-income pregnant women (n 596), Pittsburgh, PA, USA, 2003–2005