Hostname: page-component-cd9895bd7-hc48f Total loading time: 0 Render date: 2024-12-26T15:29:11.944Z Has data issue: false hasContentIssue false

Racial/ethnic and sociodemographic factors associated with micronutrient intakes and inadequacies among pregnant women in an urban US population

Published online by Cambridge University Press:  13 December 2013

Kelly J Brunst*
Affiliation:
Kravis Children's Hospital, Department of Pediatrics, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, Box 1198, New York, NY 10029, USA
Robert O Wright
Affiliation:
Kravis Children's Hospital, Department of Pediatrics, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, Box 1198, New York, NY 10029, USA Department of Preventive Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA
Kimberly DiGioia
Affiliation:
Channing Laboratory, Department of Medicine, Brigham and Women's Hospital and Harvard School of Public Health, Boston, MA, USA
Michelle Bosquet Enlow
Affiliation:
Department of Psychiatry, Boston Children's Hospital, Boston, MA, USA Department of Psychiatry, Harvard Medical School, Boston, MA, USA
Harriet Fernandez
Affiliation:
Channing Laboratory, Department of Medicine, Brigham and Women's Hospital and Harvard School of Public Health, Boston, MA, USA
Rosalind J Wright
Affiliation:
Kravis Children's Hospital, Department of Pediatrics, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, Box 1198, New York, NY 10029, USA Department of Preventive Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA
Srimathi Kannan
Affiliation:
Department of Animal Science, Food and Nutrition College of Agricultural Sciences, Southern Illinois University, Carbondale, IL, USA
*
*Corresponding author: Email kelly.brunst@mssm.edu
Rights & Permissions [Opens in a new window]

Abstract

Objective

To assess sociodemographic correlates of micronutrient intakes from food and dietary supplements in an urban, ethnically diverse sample of pregnant women in the USA.

Design

Cross-sectional analyses of data collected using a validated semi-quantitative FFQ. Associations between racial, ethnic and sociodemographic factors and micronutrient intakes were examined using logistic regression controlling for pre-pregnancy BMI, maternal age and smoking status.

Setting

Prenatal clinics, Boston, MA, USA.

Subjects

Analyses included pregnant women (n 274) in the PRogramming of Intergenerational Stress Mechanisms (PRISM) study, an urban longitudinal cohort designed to examine how stress influences respiratory health in children when controlling for other environmental exposures (chemical stressors, nutrition).

Results

High frequencies of vitamin E (52 %), Mg (38 %), Fe (57 %) and vitamin D (77 %) inadequacies as well as suboptimal intakes of choline (95 %) and K (99 %) were observed. Factors associated with multiple antioxidant inadequacies included being Hispanic or African American, lower education and self-reported economic-related food insecurity. Hispanics had a higher prevalence of multiple methyl-nutrient inadequacies compared with African Americans; both had suboptimal betaine intakes and higher odds for vitamin B6 and Fe inadequacies compared with Caucasians. Nearly all women (98 %) reported Na intakes above the tolerable upper limit; excessive intakes of Mg (35 %), folate (37 %) and niacin (38 %) were also observed. Women reporting excessive intakes of these nutrients were more likely Caucasian or Hispanic, more highly educated, US-born and did not report food insecurity.

Conclusions

Racial/ethnic and other sociodemographic factors should be considered when tailoring periconceptional dietary interventions for urban ethnic women in the USA.

Type
Research Papers
Copyright
Copyright © The Authors 2013 

Suboptimal environmental conditions during critical periods of development, including inadequate nutrition, may programme physiological mechanisms and contribute to chronic disease risk( Reference Barker, Osmond and Kajantie 1 ). Epidemiological research linking prenatal nutrition to children's health has focused largely on maternal macronutrient intakes such as energy and protein or correlates of nutritional status such as birth size and other indicators of fetal growth assessed retrospectively( Reference Barker 2 ). More recent evidence suggests the importance of specific micronutrients in prenatal programming of long-term health( Reference Monk, Georgieff and Osterholm 3 ). Moreover, various dietary components and inadequacies may mitigate or enhance the impact of chemical environmental exposures during early development as underscored by the National Advisory Environmental Health Sciences Council( 4 ). While epidemiological data are sparse for prenatal studies, dietary intake of antioxidants and methyl nutrients have been shown to reduce air pollution effects in non-pregnant adult samples( Reference Baccarelli, Cassano and Litonjua 5 , Reference Romieu, Castro-Giner and Kunzli 6 ). Interactions have also been observed for other physical (e.g. tobacco smoke) and social (e.g. psychological stress) environmental exposures( Reference Gallo, Renzi and Loizzo 7 , Reference Jiang, Yan and West 8 ). The methyl nutrient choline has recently been associated with alterations in the methylation state of genes influencing development of the fetal hypothalamic–pituitary–adrenal axis( Reference Jiang, Yan and West 8 ), which, in turn, has been linked to birth outcomes( Reference Baibazarova, van de Beek and Cohen-Kettenis 9 ) and respiratory and neurodevelopment during childhood( Reference Wright, Fisher and Chiu 10 ). Thus, understanding the correlates of inadequate dietary intakes may help inform effective intervention and prevention strategies in children's environmental health.

Studies from developing countries document dietary deficiencies in pregnancy as well as effects of micronutrient status on pregnancy outcomes( Reference Tulchinsky 11 ). A recent systematic review and meta-analysis demonstrates that pregnant women in developed countries, including the USA, are also at risk of suboptimal micronutrient intakes( Reference Blumfield, Hure and Macdonald-Wicks 12 ). It is also unlikely that pregnant and childbearing-aged women in developed countries have adequate intake of micronutrients, such as Fe and Ca, through foods alone( Reference Turner, Langkamp-Henken and Littell 13 ). Existing US studies have notable limitations, as most pre-date mandatory folic acid fortification, lack data on emerging essential micronutrients (i.e. choline, betaine) and few consider ethnic minorities. Of the three US studies including both African American and Hispanic women( Reference Lenders, Hediger and Scholl 14 Reference Swensen, Harnack and Ross 16 ), all examine a narrow range of micronutrients and lack assessments of choline and betaine intake, and only one considered both dietary and supplementation sources( Reference Blumfield, Hure and Macdonald-Wicks 12 ).

Moreover, while studies in non-pregnant samples link a number of sociodemographic characteristics and dietary inadequacies, these associations have not been well studied in pregnant women in the USA. Minority status( Reference Vaccaro and Huffman 17 ), lower education( Reference Aggarwal, Monsivais and Drewnowski 18 , Reference Kant and Graubard 19 ), food insecurity( Reference Kirkpatrick and Tarasuk 20 ) and lower income( Reference Aggarwal, Monsivais and Drewnowski 18 ) have all been linked to poorer nutrition in non-pregnant US adult samples. Other studies suggest nativity (US-born v. foreign-born)( Reference Harley, Eskenazi and Block 21 ) and acculturation status (e.g. years living in the USA)( Reference Perez-Escamilla 22 ) also contribute to dietary behaviours, although such data are even more limited. This is an important area of research because health inequalities may be attributed, in part, to disparities in micronutrient intakes across race/ethnicity and socio-economic status (SES)( Reference Vaccaro and Huffman 17 ).

In order to begin to address some of these gaps, the objectives of the present study were twofold: (i) to comprehensively assess a wide range of dietary micronutrient inadequacies (including choline and betaine) from food and dietary supplements, which post-dates the mandatory folic acid fortification; and (ii) to examine the sociodemographic correlates of micronutrient intakes in an urban US population comprised largely of African American and Hispanic pregnant women. Classes of micronutrients examined in these analyses were selected based on our current understanding of the mechanisms through which nutritional factors in pregnancy may impact fetal growth and development and exert more long-term effects( Reference Langley-Evans 23 ).

Experimental methods

Study population

Participants were from the PRogramming of Intergenerational Stress Mechanisms (PRISM) study, a prospective pregnancy cohort of 276 mother–child pairs originally designed to examine how perinatal stress influences respiratory health in children when controlling for other environmental exposures (chemical stressors, nutrition). Women were recruited from prenatal clinics at 26·9 (sd 8·1) weeks’ gestation from the Beth Israel Deaconess Medical Center and the East Boston Neighborhood Health Center from March 2011 to August 2012. Trained research staff approached women on selected clinic days. Recruitment sites were chosen given desired heterogeneity in sociodemographic and racial/ethnic characteristics. Eligibility criteria included: (i) English- or Spanish-speaking; (ii) age ≥18 years at enrolment; and (iii) singleton pregnancy. All women approached to participate completed a screener questionnaire including data on key variables including maternal age, race/ethnicity, education and nativity status. Procedures were approved by the human studies committee at the Brigham and Women's Hospital; written consent was obtained in the participant's primary language.

Nutrition assessment and processing

Maternal dietary intake was assessed at enrolment by trained interviewers using the modified Block98 (version 98·2; NutritionQuest, Berkeley, CA, USA) FFQ (Block 2006_Bodnar FFQ) consisting of approximately 120 food/beverage items( Reference Block, Hartman and Dresser 24 , Reference Snook Parrott, Bodnar and Simhan 25 ). The measure has been validated in multicultural populations( Reference Snook Parrott, Bodnar and Simhan 25 , Reference Volgyi, Carroll and Hare 26 ). Modifications were made to include a more extensive list of fish and seafood items( Reference Siega-Riz, Bodnar and Savitz 27 ). The FFQ asks about usual food and beverage intakes in the 3 months prior to pregnancy; women were not asked to differentiate their intake before v. during pregnancy. The food list was developed from National Health and Nutrition Examination Survey (NHANES) III dietary recall data; portion size pictures enhanced accuracy of quantification. For each item, women were asked how often (daily, weekly, monthly or rarely/never) and how much (small, medium or large serving sizes) they consumed. The FFQ also queried the type and frequency of dietary supplements, especially vitamins and minerals, used in the prenatal period.

FFQ were processed through the online Block Dietary Data Systems (Berkeley, CA, USA) using the US Department of Agriculture (USDA) Food and Nutrient Database for Dietary Surveys (FNDDS) utilizing software originally developed at the National Cancer Institute( Reference Block, Hartman and Dresser 24 ). Energy, macronutrient and micronutrient intakes were calculated per day by using nutrient values based on data from the third NHANES, the 1994–1996 Continuing Survey of Food Intakes by Individuals (CSFII) and the USDA Nutrient Database for Standard Reference( 28 ). Folate values were derived using the USDA 1998 nutrient database( 28 ). For foods with added folic acid, dietary folate equivalents (DFE) were calculated as: micrograms of naturally occurring food folate + (micrograms of added folic acid × 1·7)( 29 ). Nutrient calculations were provided by NutritionQuest using the USDA Nutrient Database for Standard Reference( 28 ) for the dietary variables and related nutrients of interest. Betaine and choline values were derived from the USDA Database for the Choline Content of Common Foods( 30 ) and the USDA Database for the Choline Content of Common Foods, Release 2( 31 ). Unlisted values were imputed using recipes or applying values from similar foods.

Nutrient intakes were compared with the recommended nutrient intakes of the Institute of Medicine (Estimated Average Requirement (EAR), Adequate Intake (AI), Upper Tolerable Limit (UL)) when available( 32 36 ). Pregnancy energy cut-off values recommended by Meltzer et al. ( Reference Meltzer, Brantsaeter and Ydersbond 37 ) and implemented by others( Reference Blumfield, Hure and Macdonald-Wicks 12 ) were used. Women were considered at risk for nutrient inadequacy if their total (food + supplement) nutrient intake was less than the EAR or AI for pregnant women as done previously( Reference Snook Parrott, Bodnar and Simhan 25 ). We calculated the likelihood of Fe inadequacy using the cut-point approach( 34 ).

Maternal characteristics

Information on race, maternal education, height and weight, smoking, nativity status and financial hardships was collected by interview-based questionnaire. Race/ethnicity was self-reported and categorized as Caucasian, Hispanic, African American, or other/mixed. Nativity status was defined as being US-born or foreign-born. Acculturation was considered based on age at immigration, length of time living in the USA and primary language spoken (Spanish, English or bilingual). Maternal education was categorized as high (some college or college degree) or low (high school/high-school diploma or less than high school). Perceived financial difficulties were assessed by the self-reported degree of difficulty (no difficulty v. at least some degree of difficulty) in living on the total household income and meeting monthly payments/bills( Reference Pearlin, Lieberman and Menaghan 38 ); these items were addressed independently in the analyses. Women reported smoking (yes/no) at baseline and in the third trimester; women were classified as smokers if they reported smoking at either visit. Maternal BMI was calculated from height and pre-pregnancy weight reported at enrolment and categorized as normal weight (BMI <25 kg/m2), overweight (BMI ≥25 to <30 kg/m2) or obese (BMI ≥30 kg/m2)( 39 ).

Ethnic identity

Ethnic identity was ascertained using the fourteen-item subscale assessing positive ethnic attitudes and sense of belonging, ethnic identity achievement and ethnic behaviour, from the Multigroup Ethnic Identity Measure (MEIM)( Reference Phinney 40 ). The MEIM has been used in Caucasian, African American and Hispanic populations with good validity and reliability( Reference Nguyen, Subramanian and Sorensen 41 ). Item responses, ranging from 1 (strongly disagree) to 4 (strongly agree), were summed (reverse scoring negatively worded items) and averaged over all items; the median split was used to index high and low ethnic identity scores.

Economic-related food insecurity

Two items assessed economic-related food insecurity: (i) ‘How often do you not have enough money to afford the kind of food you and your family should have?’ (‘never’, ‘once in a while’, ‘often’ and ‘very often’; scores collapsed as never/ever), adapted from an economic strain measure( Reference Pearlin, Lieberman and Menaghan 38 ); and (ii) ‘In the past 6 months, did you go without food because you did not have the money to pay for it?’ (yes/no), from the Crisis in Family Systems-Revised measure( Reference Shalowitz, Berry and Rasinski 42 ). Women responding ‘ever’ and/or ‘yes’, respectively, were considered to be experiencing food insecurity from an economic perspective.

Statistical considerations

Nutrient intakes were energy adjusted using the residual method( Reference Willett, Howe and Kushi 43 ). Because residuals have a mean of zero and include negative values, they do not provide an intuitive sense of intakes. Therefore, the predicted nutrient intake for the mean energy intake of the sample (8354·6 kJ (1996·80 kcal)) was used as a constant. Supplemental intakes were then added to the energy-adjusted nutrients to provide the total energy-adjusted intakes of each micronutrient.

Logistic regression was performed for each micronutrient, with inadequate intake as the outcome. All models were adjusted for maternal age (years), pre-pregnancy BMI and prenatal smoking status( Reference Cuco, Fernandez-Ballart and Sala 44 Reference Padrao, Silva-Matos and Damasceno 46 ). Micronutrient inadequacies resulting in low cell counts unable to generate reliable odds ratios were assessed by using the median of the micronutrient distribution as a cut-point to index high and low intakes. Due to the small number of bilingual women, analyses including primary language compare English- with Spanish-speaking women only. Results are presented as odds ratios and corresponding 95 % confidence intervals. The χ 2 test was conducted to investigate possible differences in micronutrient intakes (dietary + supplements) above the UL( 29 , 32 36 ) by race, ethnic identity, food insecurity and other sociodemographic factors. Analyses assumed a two-sided alternative hypothesis, a 0·05 significance level and were conducted using the SAS statistical software package version 9·2.

Results

Characteristics of respondents

Of 389 eligible women approached, 276 agreed to participate (70·95 %). There were no significant differences based on age, race/ethnicity, education and nativity status when comparing eligible women who participated and those who declined participation. Two women with implausible energy intake (<2092 kJ (<500 kcal) or >20 920 kJ (>5000 kcal)) were excluded from analyses( Reference Meltzer, Brantsaeter and Ydersbond 37 ), resulting in 274 women participating in the study. Table 1 summarizes sample characteristics. Women were predominantly minorities (42·3 % Hispanic, 17·5 % African American, 9·9 % other/mixed). More than half the sample reported a low ethnic identity (54·1 %). Nearly half were foreign-born (47·8 %), with the majority moving to the USA as adults (67·7 %) and residing in the USA for longer than 5 years (78·5 %). Most women identified as English-speaking (63·6 %), almost one-third identified as primarily Spanish-speaking (31·2 %) and the remaining women identified as bilingual (5·2 %). One-third reported a high school education or less. More than half identified difficulty living on total household income (59·6 %) or meeting monthly payments (52·8 %). Food insecurity was reported by over a quarter of women (27·8 %). Additionally, the majority of women were overweight or obese (64·0 %), and 16·8 % smoked during pregnancy. Age at time of immigration and duration in the USA were not associated with micronutrient inadequacies, and thus are not considered further.

Table 1 Participants’ demographic and SES characteristics: pregnant women (n 274), PRISM study, Boston, MA, USA, March 2011–August 2012

PRISM, PRogramming of Intergenerational Stress Mechanisms; SES, socio-economic status; HS, high school; GED, General Educational Development; BA, Bachelor of Arts; MS, Masters; MD, Doctor of Medicine; PhD, Doctor of Philosophy.

Intake of antioxidants

Vitamin E and Mg were the most common inadequacies identified, with 51·5 % and 38·3 % of women consuming less than the EAR, respectively (Table 2). The prevalence of inadequacies of other antioxidants in descending order was Zn (15·3 %), vitamin A (10·2 %), vitamin C (7·3 %) and Se (1·1 %). When compared with Caucasians, African Americans and Hispanics had greater odds of inadequate intakes across all antioxidants except Mg and Zn (Table 3). Low ethnic identity was associated with inadequate intakes of Mg (OR = 2·19; 95 % CI 1·20, 3·99). Being foreign-born was a significant predictor of vitamin E (OR = 3·73; 95 % CI 2·04, 6·82) and Zn (OR = 2·51; 95 % CI 1·05, 6·00) inadequacies and β-carotene intakes below the median (OR = 2·15; 95 % CI 1·22, 3·80). Spanish-speaking women were also more likely to report suboptimal intakes of β-carotene, vitamin E, Se and Zn compared with those women whose primary language was English (Table 3).

Table 2 Frequencies of micronutrient inadequacies in the study participants: pregnant women (n 274), PRISM study, Boston, MA, USA, March 2011–August 2012

PRISM, PRogramming of Intergenerational Stress Mechanisms.

†Based on dietary intake only.

‡These nutrient intakes were compared with Adequate Intake (AI) levels; all other micronutrients were compared with the Estimated Average Requirement (EAR).

Table 3 Associations between race, ethnic identity and nativity and total (dietary + supplement) micronutrient inadequacy in the study participants: pregnant women (n 274), PRISM study, Boston, MA, USA, March 2011–August 2012

PRISM, PRogramming of Intergenerational Stress Mechanisms.

All analyses were adjusted for maternal age, BMI and smoking during pregnancy.

*Represents significance (P < 0·05).

†Women born in the USA are the reference group.

‡Caucasian women are the reference group. There were no significant findings among the other/mixed race category (data not shown).

§The median cut-point was used to define high and low total intake (vitamin A: 1133·62 μg; β-carotene: 4172·63 μg; Se: 111·36 μg; Zn: 13·58 mg; vitamin B12: 6·79 μg; riboflavin: 2·62 mg; methionine: 1·49 mg; choline: 311·47 mg; betaine: 159·89 mg; P: 1352·36 mg; K: 2·78 g; Na: 3·15 g; thiamin: 1·95 mg; niacin: 26·33 mg).

||Based on dietary intake only.

As shown in Table 4, low maternal education was most consistently associated with antioxidant inadequacies (vitamins A, C and E, β-carotene, Mg, Zn and Se). Food insecurity was significantly associated with antioxidant inadequacies with the exception of β-carotene and Zn. The odds of vitamin E inadequacy was increased more than twofold among those experiencing difficulty living on their total household income or difficulty in meeting monthly payments/bills. While overall 7·3 % of participants had vitamin C inadequacy, it was significantly more prevalent among those experiencing difficulty with living on their total household income (OR = 4·20; 95 % CI 1·14, 15·56) and meeting monthly payments/bills (OR = 4·37; 95 % CI 1·31, 15·50). This was also the case for suboptimal β-carotene intakes. Difficulty meeting monthly payments/bills was also a predictor of lower Se intakes. Women with intakes above the UL for Mg (35 %) were more likely to be Caucasian or Hispanic (χ 2 = 7·96, P = 0·05), more highly educated (χ 2 = 14·77, P < 0·01) and less likely to report food insecurity (χ 2 = 10·19, P < 0·01) or difficulty living on their total household income (χ 2 = 3·86, P = 0·05) or meeting payments/bills (χ 2 = 6·02, P = 0·01). Women with vitamin A (4·7 %), vitamin C (0·36 %), vitamin E (0 %), Se (0 %) and Zn (1·8 %) intakes above the UL were infrequent.

Table 4 Associations between food insecurity and sociodemographic factors and total (dietary + supplement) micronutrient inadequacy in the study participants: pregnant women (n 274), PRISM study, Boston, MA, USA, March 2011–August 2012

PRISM, PRogramming of Intergenerational Stress Mechanisms.

All analyses were adjusted for maternal age, BMI and smoking during pregnancy.

*Represents significance (P < 0·05).

†Women with some college education or college degree are the reference group.

‡Women with no difficulty are the reference group.

§The median cut-point was used to define high and low intake (β-carotene: 4172·63 μg; Se: 111·36 μg; methionine: 1·49 mg; betaine: 159·89 mg; P: 1352·36 mg; K: 2·78 g; Na: 3·15 g);

||Based on dietary intake only.

Methyl/epigenetic-nutrient intake

The prevalence of Fe intakes below the EAR of 22–23 mg/d was 56·6 % (Table 2). Approximately 15 % of women had folate and vitamin B6 inadequacies below the EAR. Inadequate choline intake was documented in almost all participants, with over 95 % consuming less than the AI level. With respect to sociodemographic predictors of methyl-nutrient intakes, Hispanics had significantly lower intakes of vitamin B12 (OR = 2·76; 95 % CI 1·17, 4·43) and riboflavin (OR = 3·64; 95 % CI 1·83, 7·22) compared with Caucasians; both African Americans and Hispanics had increased odds for inadequacies in vitamin B6 and Fe and suboptimal intakes of betaine compared with Caucasians (Table 3). Foreign-born women had greater odds of suboptimal intakes of vitamin B6, Fe, methionine and betaine compared with those born in the USA. Spanish-speaking women also had greater odds of Fe, methionine and betaine suboptimal intakes compared with English-speaking women. Low ethnic identity was not associated with the intake of methyl/epigenetic nutrients.

Inadequacies in vitamin B6 (OR = 3·39; 95 % CI 1·51, 7·62), Fe (OR = 3·33; 95 % CI 1·74, 6·39) and betaine (OR = 7·60; 95 % CI 3·80, 15·20) were significantly associated with lower education (Table 4). Fe inadequacy and low intake of betaine were significantly more common among women experiencing food insecurity or difficulty living on total household income or meeting monthly bills. Folate inadequacy was also significantly associated with difficulty living on the family's total income (OR = 3·22; 95 % CI 1·24, 8·35).

Women having intakes above the UL for folate (n 102) were more likely to be Caucasian or Hispanic (χ 2 = 38·65, P<0·01), US-born (χ 2 = 7·27, P = 0·01), have a higher education (χ 2 = 24·45, P<0·01), and no report of food insecurity (χ 2 = 4·88, P = 0·03) or difficulty living on their total family income (χ 2 = 10·59, P<0·01) or meeting payments/bills (χ 2 = 10·36, P<0·01). Women with vitamin B6 (0 %) and Fe (5·8 %) intakes above the UL were infrequent.

Intake of bone-related micronutrients

More than 75 % of women had inadequate intakes of vitamin D (Table 2). Ca inadequacies were also prevalent (19·3 %). Only three women had P intake levels below the EAR. Being African American had a protective effect on vitamin D inadequacy (OR = 0·35; 95 % CI 0·14, 0·87) and a negative effect on Ca inadequacy (OR = 3·15; 95 % CI 1·07, 9·27) compared with being Caucasian. Foreign-born (OR = 2·85; 95 % CI 1·45, 5·59) and Spanish-speaking women (OR = 4·49; 95 % CI 1·78, 11·35) as well as those reporting low ethnic identity (OR = 1·93; 95 % CI 1·01, 3·68) had higher odds of vitamin D inadequacies (Table 3). Women with a low education level also had higher odds of vitamin D inadequacy (Table 4). Bone-related micronutrient intakes higher than the UL were not prevalent in this cohort (vitamin D (0 %), Ca (0·73 %), P (0 %)).

Intake status of electrolytes

With the exception of one participant, all women had K intakes below the AI level of 4·7 g/d (mean intake of 2·80 g/d). Thus, associations with race/ethnicity and SES factors were examined using the median to define high and low intakes. African American race (OR = 2·85; 95 % CI 1·19, 6·81) and low educational status (OR = 2·44; 95 % CI 1·32, 4·51) were the only correlates of low K intakes (Tables 3 and 4, respectively). Conversely, the amount of Na consumed by this cohort was much higher than the AI level of 1·5 g/d (mean intake of 3·19 g/d) with 98·9 % consuming more than the AI and 98·2 % having Na intakes above the UL of 2·3 g/d. Spanish-speaking women consumed less Na than those women whose primary language was English (OR = 2·15; 95 % CI 1·17, 3·97).

Intake of other nutrients

The frequency of thiamin (6·9 %) and niacin (5·8 %) inadequacies was relatively low and did not vary by nativity or ethnic identity (Table 3). However, African Americans and Hispanics and low maternal education were significantly associated with lower intakes of thiamin and niacin (Tables 3 and 4, respectively). Thiamin and niacin inadequacies were also associated with food insecurity (OR = 4·87; 95 % CI 1·61, 14·78) and speaking Spanish (OR = 4·43; 95 % CI 1·24, 15·75), respectively.

Vitamin K intakes below the AI level were prevalent in over 20 % of the study population (Table 2). Hispanics (OR = 3·67; 95 % CI 1·35, 10·03) and African Americans (OR = 5·67; 95 % CI 1·82, 17·67) were more likely to have lower vitamin K intake than Caucasians. Low vitamin K intake was significantly more common among women with a lower level of education or more difficulty living on their total family income or meeting monthly payments/bills (Table 4).

Discussion

These analyses, considering both dietary and supplemental intakes, identify a range of micronutrient intake inadequacies in a multi-ethnic, primarily urban US population of pregnant women that may have implications for perinatal and more long-term child health. These analyses expand prior research involving pregnant US samples that pre-dated changes in folic acid awareness and its widespread fortification or more narrowly considered multivitamin use. We also identified vulnerable groups of women with distinct differences in dietary micronutrient composition related to sociodemographic factors that may inform tailored intervention strategies going forward.

Of the antioxidant inadequacies identified, vitamin E and Mg were most striking. Notably, the EAR for vitamin E is the same (12 mg/d) in pregnant and non-pregnant women; Mg requirements increase slightly during pregnancy (255 mg/d preconception to 290 mg/d in pregnancy). Although Mg intake exceeded the UL in some women, the prevalence of intake below the EAR was over 30 %. Hispanics and African Americans were more likely to report antioxidant inadequacies compared with Caucasians, with the exception of Mg. African Americans were most likely to have inadequate vitamin E intake. As other studies suggest that African Americans are less likely to select from food groups rich in α-tocopherol and Mg, such as nuts, seeds, whole grains, green leafy vegetables and vegetable oils( Reference Kant, Graubard and Kumanyika 47 ), this may represent a unique target for dietary intervention among this group. A recent pilot study demonstrated the feasibility and acceptability of a food-exchange-based intervention to optimize prenatal dietary vitamin E intake( Reference Clark, Craig and McNeill 48 ). Such studies should be expanded to include ethnic minority, urban populations.

Nearly all women reported choline intakes lower than the recommended AI. This is concerning since choline plays an important role in placental function and fetal development (birth defects, brain development), possibly by influencing DNA methylation status( Reference Jiang, Yan and West 8 , Reference Boeke, Baccarelli and Kleinman 49 ). As prenatal vitamins do not contain an adequate source of choline, some have proposed that women with low intakes of milk, meat, eggs or other choline-rich foods should consider a prenatal dietary supplement containing this micronutrient. Similar to findings in a number of developed countries (e.g. Japan, Australia, Europe, UK)( Reference Blumfield, Hure and Macdonald-Wicks 12 ), Fe inadequacy, which may also influence epigenetic modifications( Reference Cyr and Domann 50 Reference Zhang, Zhang and Clark 52 ), was common in these women. Pregnant women are particularly vulnerable to Fe deficiency given that the EAR for Fe increases by approximately 15 mg/d in pregnancy( 34 ). However, even after considering supplementation in our sample, 57 % of women had inadequate Fe intakes and reported insufficient intakes of relevant food sources, which include red meats, fish, poultry, beans, lentils and fortified foods( 53 ). African American, Hispanic and foreign-born women consumed less Fe and other methyl nutrients, including vitamin B6 and betaine, compared with Caucasians and US-born women, respectively. While disparities in Fe intake among pregnant African Americans and Hispanics have been reported( Reference Mei, Cogswell and Looker 54 ), nativity status has been less well studied. One study found that pregnant Hispanic immigrants consumed more folate, vitamin C, Fe and Zn than US-born Hispanics( Reference Schaffer, Velie and Shaw 55 ). Longer duration of US residence has been attributed to lower energy intake( Reference Harley, Eskenazi and Block 21 ). Our study showed decreases in antioxidant and methyl-nutrient intakes among Hispanics and foreign-born women. Dissimilarities in micronutrient intakes by race and nativity could partly be explained by differences in the use of supplements, as previously shown with Fe( Reference Cogswell, Parvanta and Ickes 56 ). The complex relationships among race, nativity status and prenatal micronutrient intakes warrant further investigation.

Inadequate vitamin D intake was present in over 75 % of these women from the north-eastern USA, where vitamin D status is also likely influenced by season given the importance of sun exposure and consequent conversion to 25-hydroxyvitamin D( Reference Wuertz, Gilbert and Baier 57 ). Even moderately decreased levels of 25-hydroxyvitamin D have been associated with poor fetal and infant skeletal growth and tooth mineralization( Reference Marshall, Mehta and Petrova 58 ). Therefore, inadequate dietary intake of vitamin D may be more relevant in populations, such as this cohort, affected by seasonal climates where sun exposure, as a source of vitamin D, is limited. In our study, foreign-born women and those with low ethnic identity were most likely to have bone-related micronutrient inadequacies. Immigrant groups perceiving that their American identity is being challenged( Reference Cheryan and Monin 59 ) may abandon their ethnic identity and conform to an American identity, in part, by embracing poor dietary behaviours( Reference Guendelman, Cheryan and Monin 60 ). Thus, ethnic identity may be another important factor to consider when identifying vulnerable populations at risk for suboptimal nutrient status.

Low maternal education consistently predicted inadequate antioxidant and suboptimal or inadequate methyl-nutrient intakes. Data from non-pregnant US samples similarly report that education is an important predictor of diet quality( Reference Kant and Graubard 19 ). When micronutrient intakes, including vitamins A, C, D, E and B12, β-carotene, folate, Fe, Ca and Mg, were examined in relation to diet cost and SES (indexed by education and income), researchers found that lower-cost/quality diets were also consumed more frequently by lower-SES groups in the USA( Reference Aggarwal, Monsivais and Drewnowski 18 ). Taken together, these findings suggest that both maternal education and SES play a role in dietary intake.

Food insecurity was also significantly associated with antioxidant inadequacies (except Zn and β-carotene) and the methyl nutrients Fe and betaine. Food insecurity, characterized by limited and/or uncertain availability or access to nutritionally adequate foods( Reference Kendall and Kennedy 61 ), affected nearly 30 % of this population. Some have proposed that food insecurity could impact fetal development through physiological and psychological changes due to micronutrient deficiencies or the stress experienced as a result of limited access to nutritionally adequate food, respectively( Reference Ramsey, Giskes and Turrell 62 ). US and Canadian studies suggest that individuals experiencing food insecurity have lower intakes of fruits and vegetables( Reference Kirkpatrick and Tarasuk 20 , Reference Kaiser, Melgar-Quinonez and Townsend 63 , Reference Tingay, Tan and Tan 64 ), in part due to the perception that nutrient-dense food groups are expensive( Reference Tanumihardjo, Anderson and Kaufer-Horwitz 65 ). Our findings highlight the need for an enhanced elucidation of the impact of food insecurity on micronutrient intakes in multi-ethnic US pregnant women.

It is well established that not only nutrient deficiencies but also excesses can have adverse effects on perinatal outcomes and fetal development( Reference Mao, Liu and Li 66 ). As the majority of pregnant women in the USA take a dietary supplement, most frequently a multivitamin/mineral product, they may be more likely to exceed the UL. When considering food intakes combined with supplements, more than 35 % of the women in the present study reported Mg, folate and niacin intakes higher than the UL. In addition, nearly the entire study population (98 %) had Na intakes above the UL. Women reporting excessive intakes of Mg, folate and niacin were more likely to be Caucasian or Hispanic, of higher SES, US-born and not reporting food insecurity. These findings highlight the importance of including supplement use when examining dietary intakes during pregnancy and identifying excessive intakes as well as inadequacies.

Interpretation of our findings should be considered in light of our study's limitations. Food and supplemental intakes were based on participant recall and therefore subjected to under- or overestimation. For example, the multiple food items and choices in an FFQ may result in overestimation for some nutrients, and the retrospective nature of the questionnaire may influence recall. However, FFQ are useful for obtaining estimates of usual intake over time (e.g. months), including during pregnancy( Reference Blumfield, Hure and Macdonald-Wicks 12 ). Misclassification of nutrient intake is likely random and therefore would be expected to result in an underestimation of associations. Nevertheless, future research would be enhanced through the incorporation of food records and 24 h dietary recalls. Second, the median was used as the cut-point to define high and low micronutrient intakes when an EAR or AI was not available. This may not represent a true inadequacy. Thus, the results are best viewed as estimates rather than absolute levels of intake because FFQ may contain measurement error. We acknowledge that the assessment of food insecurity was not comprehensive. Nevertheless, our findings concerning economically related food insecurity are interesting and warrant further investigation. The approximately 70 % rate of participation at enrolment may reduce generalizability; however, women who were eligible and agreed to participate did not differ on key covariates when compared with those who declined.

Conclusions

The present study provides a thorough examination of the influence of race/ethnicity, SES and other sociodemographic factors, including nativity status and ethnic identity, on micronutrient intakes in a sociodemographically diverse sample of pregnant women in the USA. These data highlight the high prevalence of inadequate intakes of specific micronutrients (e.g. antioxidants, methyl nutrients, electrolytes, bone-related micronutrients) that have been implicated in the prenatal programming of developmental diseases, including allergies and asthma( Reference Erkkola, Nwaru and Kaila 67 ), obesity( Reference Yang and Huffman 68 ) and neurodevelopment( Reference Monk, Georgieff and Osterholm 3 ). Moreover, in utero micronutrient inadequacies may enhance fetal vulnerability to other environmental exposures (e.g. air pollution, stress)( Reference Monk, Georgieff and Osterholm 3 , Reference Kannan, Misra and Dvonch 69 ). Prenatal nutritional interventions may be enhanced in urban ethnic-minority populations if tailored to account for the specific sociodemographic determinants of prenatal dietary patterns.

Acknowledgements

Sources of funding: This work was supported by the National Institute of Environmental Health Sciences (NIEHS; grant number R21ES021318-01). NIEHS had no role in the design, analysis or writing of this article. Conflicts of interest: The authors report no conflict of interest. Authors’ contributions: R.J.W. and S.K. are co-senior authors. K.J.B. drafted the manuscript, contributed to the concept and design of the analyses, and led the analyses, interpretation of data and writing of the manuscript; R.O.W. contributed significantly to analyses and interpretation of data and provided critical review and revisions of the manuscript; K.D. contributed to the interpretation of data analyses and provided critical review and revisions of the manuscript; M.B.E. contributed to the interpretation of data analyses and provided critical review and revisions of the manuscript; H.F. contributed to the interpretation of data analyses and provided critical review and revisions of the manuscript; R.J.W. contributed to conception and design of the cohort, data acquisition, analyses and interpretation of data, and provided critical review and revisions of the manuscript; S.K. contributed to dietary data acquisition, analyses and interpretation of data, and provided critical review and revisions of the manuscript.

Footnotes

Co-senior authors.

References

1. Barker, DJ, Osmond, C, Kajantie, E et al. (2009) Growth and chronic disease: findings in the Helsinki Birth Cohort. Ann Hum Biol 36, 445458.CrossRefGoogle ScholarPubMed
2. Barker, DJP (1998) Mothers, Babies, and Health in Later Life, 2nd ed. Edinburgh: Churchill Livingstone.Google Scholar
3. Monk, C, Georgieff, MK & Osterholm, EA (2013) Research review: maternal prenatal distress and poor nutrition – mutually influencing risk factors affecting infant neurocognitive development. J Child Psychol Psychiatry 54, 115130.CrossRefGoogle ScholarPubMed
4. National Advisory Environmental Health Sciences Council (2010) Dietary influences on the human health effects of environmental exposures. http://www.niehs.nih.gov/about/boards/naehsc/agenda/may2010/dietary_influences_on_the_human_health_effects_of_environmental_exposures.pdf (accessed May 2013).Google Scholar
5. Baccarelli, A, Cassano, PA, Litonjua, A et al. (2008) Cardiac autonomic dysfunction: effects from particulate air pollution and protection by dietary methyl nutrients and metabolic polymorphisms. Circulation 117, 18021809.CrossRefGoogle ScholarPubMed
6. Romieu, I, Castro-Giner, F, Kunzli, N et al. (2008) Air pollution, oxidative stress and dietary supplementation: a review. Eur Res J 31, 179197.Google Scholar
7. Gallo, C, Renzi, P, Loizzo, S et al. (2010) Potential therapeutic effects of vitamin E and C on placental oxidative stress induced by nicotine: an in vitro evidence. Open Biochem J 4, 7782.CrossRefGoogle Scholar
8. Jiang, X, Yan, J, West, AA et al. (2012) Maternal choline intake alters the epigenetic state of fetal cortisol-regulating genes in humans. FASEB J 26, 35633574.CrossRefGoogle ScholarPubMed
9. Baibazarova, E, van de Beek, C, Cohen-Kettenis, PT et al. (2013) Influence of prenatal maternal stress, maternal plasma cortisol and cortisol in the amniotic fluid on birth outcomes and child temperament at 3 months. Psychoneuroendocrinology 38, 907915.Google Scholar
10. Wright, RJ, Fisher, K, Chiu, YH et al. (2013) Disrupted prenatal maternal cortisol, maternal obesity, and childhood wheeze: insights into prenatal programming. Am J Respir Crit Care Med 187, 11861193.CrossRefGoogle ScholarPubMed
11. Tulchinsky, TH (2010) Micronutrient deficiency conditions: global health issues. Public Health Rev 32, 12.CrossRefGoogle Scholar
12. Blumfield, ML, Hure, AJ, Macdonald-Wicks, L et al. (2013) A systematic review and meta-analysis of micronutrient intakes during pregnancy in developed countries. Nutr Rev 71, 118132.Google Scholar
13. Turner, RE, Langkamp-Henken, B, Littell, RC et al. (2003) Comparing nutrient intake from food to the estimated average requirements shows middle- to upper-income pregnant women lack iron and possibly magnesium. J Am Diet Assoc 103, 461466.Google Scholar
14. Lenders, CM, Hediger, ML, Scholl, TO et al. (1997) Gestational age and infant size at birth are associated with dietary sugar intake among pregnant adolescents. J Nutr 127, 11131117.CrossRefGoogle ScholarPubMed
15. Rifas-Shiman, SL, Rich-Edwards, JW, Willett, WC et al. (2006) Changes in dietary intake from the first to the second trimester of pregnancy. Paediatr Perinat Epidemiol 20, 3542.Google Scholar
16. Swensen, AR, Harnack, LJ & Ross, JA (2001) Nutritional assessment of pregnant women enrolled in the Special Supplemental Program for Women, Infants, and Children (WIC). J Am Diet Assoc 101, 903908.Google Scholar
17. Vaccaro, JA & Huffman, FG (2013) Race/ethnicity-, gender- and age-specific differences in micronutrient intakes of US adults with and without diabetes. Int J Food Sci Nutr 64, 175184.Google Scholar
18. Aggarwal, A, Monsivais, P & Drewnowski, A (2012) Nutrient intakes linked to better health outcomes are associated with higher diet costs in the US. PLoS One 7, e37533.CrossRefGoogle ScholarPubMed
19. Kant, AK & Graubard, BI (2007) Secular trends in the association of socio-economic position with self-reported dietary attributes and biomarkers in the US population: National Health and Nutrition Examination Survey (NHANES) 1971–1975 to NHANES 1999–2002. Public Health Nutr 10, 158167.Google Scholar
20. Kirkpatrick, SI & Tarasuk, V (2008) Food insecurity is associated with nutrient inadequacies among Canadian adults and adolescents. J Nutr 138, 604612.Google Scholar
21. Harley, K, Eskenazi, B & Block, G (2005) The association of time in the US and diet during pregnancy in low-income women of Mexican descent. Paediatr Perinat Epidemiol 19, 125134.CrossRefGoogle ScholarPubMed
22. Perez-Escamilla, R (2011) Acculturation, nutrition, and health disparities in Latinos. Am J Clin Nutr 93, issue 5, 1163S1167S.Google Scholar
23. Langley-Evans, SC (2013) Fetal programming of CVD and renal disease: animal models and mechanistic considerations. Proc Nutr Soc 72, 317325.Google Scholar
24. Block, G, Hartman, AM, Dresser, CM et al. (1986) A data-based approach to diet questionnaire design and testing. Am J Epidemiol 124, 453469.Google Scholar
25. Snook Parrott, M, Bodnar, LM, Simhan, HN et al. (2009) Maternal cereal consumption and adequacy of micronutrient intake in the periconceptional period. Public Health Nutr 12, 12761283.Google Scholar
26. Volgyi, E, Carroll, KN, Hare, ME et al. (2013) Dietary patterns in pregnancy and effects on nutrient intake in the Mid-South: the Conditions Affecting Neurocognitive Development and Learning in Early Childhood (CANDLE) Study. Nutrients 5, 15111530.CrossRefGoogle ScholarPubMed
27. 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.Google Scholar
28. US Department of Agriculture, Nutrient Data Laboratory (1998) USDA National Nutrient Database for Standard Reference. http://www.ars.usda.gov/nutrientdata (accessed January 2013).Google Scholar
29. Institute of Medicine (2000) Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline. Washington, DC: The National Academies Press.Google Scholar
30. US Department of Agriculture, Beltsville Human Nutrition Research Center (2004) USDA Database for the Choline Content of Common Foods. http://www.algry.com/ing/6/doc/08.pdf (accessed May 2013).Google Scholar
31. US Department of Agriculture, Beltsville Human Nutrition Research Center (2008) USDA Database for the Choline Content of Common Foods, Release 2. http://www.ars.usda.gov/SP2UserFiles/Place/12354500/Data/Choline/Choln02.pdf (accessed May 2013).Google Scholar
32. Institute of Medicine (1997) Dietary Reference Intakes for Calcium, Phosphorus, Magnesium, Vitamin D, and Fluoride. Washington, DC: The National Academies Press.Google Scholar
33. Institute of Medicine (2000) Dietary Reference Intakes for Vitamin C, Vitamin E, Selenium, and Carotenoids. Washington, DC: The National Academies Press.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: The National Academies Press.Google Scholar
35. Institute of Medicine (2002) Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids. Washington, DC: The National Academies Press.Google Scholar
36. Institute of Medicine (2011) Dietary Reference Intakes for Calcium and Vitamin D. Washington, DC: The National Academies Press.Google Scholar
37. Meltzer, HM, Brantsaeter, AL, Ydersbond, TA et al. (2008) Methodological challenges when monitoring the diet of pregnant women in a large study: experiences from the Norwegian Mother and Child Cohort Study (MoBa). Matern Child Nutr 4, 1427.Google Scholar
38. Pearlin, LI, Lieberman, MA, Menaghan, EG et al. (1981) The stress process. J Health Soc Behav 22, 337356.CrossRefGoogle ScholarPubMed
39. World Health Organization (2006) Global database on BMI classification. http://www.who.int/bmi/index.Jsp?Intropage-intro_3.html (accessed May 2013).Google Scholar
40. Phinney, JS (1992) The Multigroup Ethnic Identity Measure: a new scale for use with diverse groups. J Adolesc Res 7, 20.Google Scholar
41. Nguyen, KH, Subramanian, SV, Sorensen, G et al. (2012) Influence of experiences of racial discrimination and ethnic identity on prenatal smoking among urban black and Hispanic women. J Epidemiol Community Health 66, 315321.CrossRefGoogle ScholarPubMed
42. Shalowitz, MU, Berry, CA, Rasinski, KA et al. (1998) A new measure of contemporary life stress: development, validation, and reliability of the CRISYS. Health Serv Res 33, 13811402.Google Scholar
43. Willett, WC, Howe, GR & Kushi, LH (1997) Adjustment for total energy intake in epidemiological studies. Am J Clin Nutr 65, 4 Suppl., 1220S1228S.CrossRefGoogle Scholar
44. Cuco, G, Fernandez-Ballart, J, Sala, J et al. (2006) Dietary patterns and associated lifestyles in preconception, pregnancy and postpartum. Eur J Clin Nutr 60, 364371.CrossRefGoogle ScholarPubMed
45. Olinto, MT, Willett, WC, Gigante, DP et al. (2011) Sociodemographic and lifestyle characteristics in relation to dietary patterns among young Brazilian adults. Public Health Nutr 14, 150159.CrossRefGoogle ScholarPubMed
46. Padrao, P, Silva-Matos, C, Damasceno, A et al. (2011) Association between tobacco consumption and alcohol, vegetable and fruit intake across urban and rural areas in Mozambique. J Epidemiol Community Health 65, 445453.Google Scholar
47. Kant, AK, Graubard, BI & Kumanyika, SK (2007) Trends in black–white differentials in dietary intakes of US adults, 1971–2002. Am J Prev Med 32, 264272.Google Scholar
48. Clark, J, Craig, L, McNeill, G et al. (2012) A novel dietary intervention to optimize vitamin E intake of pregnant women to 15 mg/day. J Acad Nutr Diet 112, 297301.Google Scholar
49. Boeke, CE, Baccarelli, A, Kleinman, KP et al. (2012) Gestational intake of methyl donors and global LINE-1 DNA methylation in maternal and cord blood: prospective results from a folate-replete population. Epigenetics 7, 253260.Google Scholar
50. Cyr, AR & Domann, FE (2011) The redox basis of epigenetic modifications: from mechanisms to functional consequences. Antioxid Redox Signal 15, 551589.CrossRefGoogle ScholarPubMed
51. Yi, CQ, Yang, CG & He, C (2009) A non-heme iron-mediated chemical demethylation in DNA and RNA. Acc Chem Res 42, 519529.Google Scholar
52. Zhang, HK, Zhang, X, Clark, E et al. (2010) TET1 is a DNA-binding protein that modulates DNA methylation and gene transcription via hydroxylation of 5-methylcytosine. Cell Res 20, 13901393.Google Scholar
53. Office of Dietary Supplements & National Center for Complementary and Alternative Medicine, National Institutes of Health (2013) Home page. http://ods.od.nih.gov/ (accessed January 2013).Google Scholar
54. Mei, Z, Cogswell, ME, Looker, AC et al. (2011) Assessment of iron status in US pregnant women from the National Health and Nutrition Examination Survey (NHANES), 1999–2006. Am J Clin Nutr 93, 13121320.CrossRefGoogle ScholarPubMed
55. Schaffer, DM, Velie, EM, Shaw, GM et al. (1998) Energy and nutrient intakes and health practices of Latinas and white non-Latinas in the 3 months before pregnancy. J Am Diet Assoc 98, 876884.Google Scholar
56. Cogswell, ME, Parvanta, I, Ickes, L et al. (2003) Iron supplementation during pregnancy, anemia, and birth weight: a randomized controlled trial. Am J Clin Nutr 78, 773781.Google Scholar
57. Wuertz, C, Gilbert, P, Baier, W et al. (2013) Cross-sectional study of factors that influence the 25-hydroxyvitamin D status in pregnant women and in cord blood in Germany. Br J Nutr 110, 18951902.Google Scholar
58. Marshall, I, Mehta, R & Petrova, A (2013) Vitamin D in the maternal–fetal–neonatal interface: clinical implications and requirements for supplementation. J Matern Fetal Neonatal Med 26, 633638.Google Scholar
59. Cheryan, S & Monin, B (2005) ‘Where are you really from?’: Asian Americans and identity denial. J Pers Soc Psychol 89, 717730.Google Scholar
60. Guendelman, MD, Cheryan, S & Monin, B (2011) Fitting in but getting fat: identity threat and dietary choices among US immigrant groups. Psychol Sci 22, 959967.CrossRefGoogle ScholarPubMed
61. Kendall, A & Kennedy, E (1998) Position of the American Dietetic Association: domestic food and nutrition security. J Am Diet Assoc 98, 337342.Google Scholar
62. Ramsey, R, Giskes, K, Turrell, G et al. (2012) Food insecurity among adults residing in disadvantaged urban areas: potential health and dietary consequences. Public Health Nutr 15, 227237.CrossRefGoogle ScholarPubMed
63. Kaiser, LL, Melgar-Quinonez, H, Townsend, MS et al. (2003) Food insecurity and food supplies in Latino households with young children. J Nutr Educ Behav 35, 148153.Google Scholar
64. Tingay, RS, Tan, CJ, Tan, NC et al. (2003) Food insecurity and low income in an English inner city. J Public Health Med 25, 156159.Google Scholar
65. Tanumihardjo, SA, Anderson, C, Kaufer-Horwitz, M et al. (2007) Poverty, obesity, and malnutrition: an international perspective recognizing the paradox. J Am Diet Assoc 107, 19661972.Google Scholar
66. Mao, C, Liu, R, Li, S et al. (2013) High salt diets during pregnancy affected fetal and offspring renal renin–angiotensin system. J Endocrinol 218, 6173.Google Scholar
67. Erkkola, M, Nwaru, BI, Kaila, M et al. (2012) Risk of asthma and allergic outcomes in the offspring in relation to maternal food consumption during pregnancy: a Finnish birth cohort study. Pediatr Allergy Immunol 23, 186194.Google Scholar
68. Yang, Z & Huffman, SL (2013) Nutrition in pregnancy and early childhood and associations with obesity in developing countries. Matern Child Nutr 9, Suppl. 1, 105119.CrossRefGoogle ScholarPubMed
69. Kannan, S, Misra, DP, Dvonch, JT et al. (2006) Exposures to airborne particulate matter and adverse perinatal outcomes: a biologically plausible mechanistic framework for exploring potential effect modification by nutrition. Environ Health Perspect 114, 16361642.Google Scholar
Figure 0

Table 1 Participants’ demographic and SES characteristics: pregnant women (n 274), PRISM study, Boston, MA, USA, March 2011–August 2012

Figure 1

Table 2 Frequencies of micronutrient inadequacies in the study participants: pregnant women (n 274), PRISM study, Boston, MA, USA, March 2011–August 2012

Figure 2

Table 3 Associations between race, ethnic identity and nativity and total (dietary + supplement) micronutrient inadequacy in the study participants: pregnant women (n 274), PRISM study, Boston, MA, USA, March 2011–August 2012

Figure 3

Table 4 Associations between food insecurity and sociodemographic factors and total (dietary + supplement) micronutrient inadequacy in the study participants: pregnant women (n 274), PRISM study, Boston, MA, USA, March 2011–August 2012