|
|
||||||||
ORIGINAL RESEARCH COMMUNICATION |
1 From the Department of Pediatrics, Boston University School of Medicine, Boston Medical Center, and the Department of Epidemiology, Boston University School of Public Health, Boston, MA (PKN); the Jean Mayer US Department of Agriculture Human Nutrition Research Center on Aging at Tufts University, Boston, MA (JM, PB, and KLT); the National Institute on Aging, National Institutes of Health, Baltimore, MD (DM and LF)
2 Supported by the USDA contract 58-1950-7-707; the Intramural Research Program of the NIH, National Institute on Aging; and General Mills Bell Institute of Health and Nutrition. Data for these analyses were obtained from the Baltimore Longitudinal Study of Aging, a study performed by the National Institute on Aging. 3 No reprints available. Address correspondence to PK Newby, Department of Pediatrics, Boston University School of Medicine, Boston, MA 02118. E-mail: pk.newby{at}bmc.org (pknewby{at}post.harvard.edu).
| ABSTRACT |
|---|
|
|
|---|
Objective: Our objective was to examine associations between whole grains, refined grains, and cereal fiber and chronic disease risk factors.
Design: In a cross-sectional analysis of participants in the Baltimore Longitudinal Study of Aging, associations between dietary intakes and risk factors were examined with multivariate linear regression analysis. Dietary intakes were assessed with 7-d dietary records and quantified in g/d.
Results: Compared with subjects in the lowest quintile (Q1) of whole-grain intake, subjects in the highest quintile (Q5) had lower body mass index (BMI; in kg/m2; Q1: 25.5; Q5: 24.8; P for trend <0.0001) and weight (Q1: 75.0 kg; Q5: 72.4 kg; P for trend = 0.004) and smaller waist circumference (Q1: 87.4 cm; Q5: 85.0 cm; P for trend = 0.002). Whole grains were also inversely associated with total cholesterol (P for trend = 0.02), LDL cholesterol (P for trend = 0.04), and 2-h glucose (P for trend = 0.0006). Associations between cereal fiber and anthropometrics and plasma lipids were similar. In subgroup analyses, refined grains were positively associated with fasting insulin among women (P for trend = 0.002).
Conclusions: Similar associations of whole grains and cereal fiber with weight, BMI, waist circumference, plasma cholesterol, and 2-h glucose were observed, suggesting that cereal fiber and its constituents may in part mediate these relations. Refined grains were associated with fasting insulin among women but not men. Additional research should explore potential interaction effects with BMI, sex, age, and genes.
Key Words: Whole grains refined grains fiber diet records risk factors
| INTRODUCTION |
|---|
|
|
|---|
Whole grains contain many bioactive components that might be responsible for their protective effect, including fiber, resistant starch, and oligosaccharides, as well as vitamins, minerals, phytate, phytoestrogens, and phytosterols (16). Research studies examining food groups such as whole grains are important, because they account for biological interactions that might otherwise be lost in an analysis of individual nutrients. However, studies examining single nutrients such as cereal fiber are also needed to increase our understanding of the mechanisms by which whole grains may be protective. Additional research is also needed to further examine whether intake of refined grains is associated with risk factors for chronic disease.
The objective of this study was to examine associations of the intakes of whole grains, refined grains, and cereal fiber measured with 7-d dietary records and quantified in gram weights with selected risk factors for chronic disease among adults participating in the Baltimore Longitudinal Study on Aging (BLSA). An additional goal was to explore whether associations with risk factors were modified by sex or body mass index (BMI; in kg/m2).
| SUBJECTS AND METHODS |
|---|
|
|
|---|
Initially, 1572 persons completed at least one 7-d diet record during the course of the study. Of those, we excluded subjects who had not completed
4 d of the record, as well as those with implausible energy intakes or statistical outliers for total energy intake (<2510 or >16 736 kJ/d for women; <3347 and >17 572 kJ/d for men) or who were missing information on age (n = 53). Our baseline population therefore included 1516 participants. Because of the limited number of persons with both repeated dietary data and outcome measures, this analysis only included participants from the first visit at which participants had complete dietary and outcome data. Thus, for each outcome, our sample size varied somewhat, as follows: BMI and weight (n = 1502), waist circumference (n = 1404), total cholesterol (n = 1444), HDL cholesterol (n = 1029), LDL cholesterol (n = 1025), triacylglycerols (n = 1430), diastolic and systolic blood pressures (n = 1464), fasting glucose (n = 1324), 2-h glucose (n = 882), fasting insulin (n = 460), and 2-h insulin (n = 455).
Dietary assessment
Dietary intake was assessed by 7-d dietary records, and subjects were instructed by trained dietitians how to assess portion size, weigh foods, and complete the records. Reports that detail the dietary collection methods and dietary intake in the BLSA population were published previously (18, 19). Food records were completed at home by the participant and sent back to the study center. Before 1993, subjects were given food models and a booklet of food pictures to help them assess portion size. Since 1993, subjects were given a portable scale to weigh food portions. Participants were contacted by telephone with any questions about their records.
Dietary records were originally coded and entered into a nutrient database maintained by the BLSA, whereas diet records completed since 1993 were coded and entered into the Minnesota Nutrient Database at Tufts University. Dietary data collected before 1993 were then reentered in the Minnesota Nutrient Database, and nutrient intakes were back adjusted to correct for changes in the food supply (eg, nutrient content because of fortification of cereals) with data from the US Department of Agriculture to correspond to appropriate time intervals (20, 21).
Measurements of whole grains, refined grains, and cereal fiber
For this study, we used all available dietary data from the BLSA to create a whole-grains database. In brief, all foods containing grains or mixed dishes with foods containing grains, either whole or refined, were identified and then assigned the best-matched pyramid code from the Pyramid Servings Database, a reference database of servings per 100 g from 30 food groups, including 3 grain groups (total grain, whole grain, and nonwhole grain). We then used the Continuing Survey of Food Intakes by Individuals 1994–1996 recipe database to disaggregate mixed dishes that contained grains (either whole or refined) to obtain gram weights of individual ingredients. Some foods could not be disaggregated to the ingredient level, in which case the reference gram amount of grains was determined by multiplying by the pyramid definition of a serving (eg, a grain serving of one slice of bread contains 16 g of flour and a grain serving of one serving of cereal contains 28 g of flour). Once the reference database was completed, we calculated the absolute amount of grains consumed by multiplying the gram amount eaten by the reference values/100 for each day of the dietary record, and values for all days were summed and divided by the total number of days of dietary records to obtain an average intake.
Cereal fiber was measured by summing the fiber content from cereal foods, which includes the starchy grains produced from grass plants. Thus, our quantification of cereal fiber included fiber from whole grains (eg, wheat, rice, corn, oats, etc) and all foods made from grains, including ready-to-eat and hot cereals, bread, pasta, crackers, sweet baked goods, and salty snacks. Whole grains, refined grains, and cereal fiber were adjusted for total energy intake with the nutrient residual method.
Outcome assessment
Our outcome variables included various risk factors for chronic disease. Anthropometric and clinical measurements were obtained by following standardized procedures (22) that have been fully described elsewhere (23). In summary, weight and height were measured for each subject at each visit, from which BMI was calculated. Waist circumference was measured with the use of an inelastic tape at the narrowest part of the torso at the end of expiration (23), roughly equivalent to the bottom of the ribcage for most persons. Blood pressure was measured from a sitting position with the use of a standard protocol (24).
For lipid measurements, an antecubital venous blood sample was drawn from study subjects after an overnight fast. As previously described (25, 26), concentrations of triacylglycerols and total cholesterol were measured by enzymatic method (Abbott Laboratories ABA-200 ATC Biochromatic Analyzer; Irving, TX). HDL cholesterol was measured by the dextran sulfate–magnesium precipitation procedure (27), and LDL cholesterol was estimated by the Friedewald formula (28).
As described previously, fasting plasma glucose and 2-h glucose concentrations were obtained with the use of an oral glucose tolerance test after overnight fasting, in which the glucose dose was 40 g/m2 body surface area, corresponding to an average dose of 78 g in men and 68 g in women (29). Plasma glucose was measured by the glucose oxidase method (Beckman Instruments, Fullerton, CA). Plasma insulin was measured in duplicate by radioimmunoassay (30).
Covariate assessment
Race-ethnicity, physical activity, smoking, education, and vitamin supplement use were determined by questionnaire at the time dietary records were collected. Physical activity was measured by an adapted version of the Harvard Alumni questionnaire, which asked participants about all daily activities (eg, activities at home, work, and during recreation or sports). The amount of time spent for each activity was summed across all activities to determine the daily energy output per body weight (in kJ/kg) and was described previously (18, 32).
Statistical analysis
We first examined the relations between the intakes of whole grains, refined grains, and cereal fiber and the sample characteristics at the time of the first visit, as well as associations with nutrient intakes. We also explored associations between the 3 dietary variables with the use of Spearman correlation coefficients. Our main analyses used multivariate linear regression to estimate separately the relation between whole grains, refined grains, and cereal fiber with each of our outcome variables. As such, we built separate regression models for each dietary variable, and each was divided into quintiles of intake. For example, we fit models estimating the relation between whole grains (in quintiles) and each risk factor (BMI, weight, waist circumference, total cholesterol, HDL cholesterol, LDL cholesterol, diastolic blood pressure, systolic blood pressure, fasting glucose, 2-h glucose, fasting insulin, and 2-h insulin). Similar models were fit for refined grains and cereal fiber. We used a generalized linear model to estimate the least-squares means for each outcome, and each model was adjusted for age, sex, race, education, decade of visit, vitamin supplement use, total energy, percentage of energy from saturated fat, and alcohol. The whole-grain models were further adjusted for intakes of refined grains, and the refined-grain models were further adjusted for intakes of whole grains.
Models that predicted lipid outcomes were further adjusted for BMI, use of lipid-lowering medication, and diagnosis of hypercholesterolemia. Models that predicted blood pressure were further adjusted for BMI, use of blood pressure–lowering medication, and diagnosis of hypertension. Models that predicted glucose and insulin outcomes were further adjusted for BMI, use of oral hypoglycemic medication, and diagnosis of diabetes. We also repeated the analyses for the above outcomes excluding subjects rather than adjusting for these variables in the analysis (ie, subjects with a diagnosis of diabetes were excluded from the glucose and insulin analyses) to remove the possibility of residual confounding. We created interaction terms to test whether the effects of the intakes of whole grains, refined grains, and cereal fiber on risk factors were modified by sex in all models and whether the effects were modified by BMI in our models that estimated fasting glucose, 2-h glucose, fasting insulin, and 2-h insulin.
We performed a number of additional analyses to test the robustness of our models. First, we tested models for each relation with further adjustment for physical activity on a limited subset of subjects for whom such data were available. In addition, we tested all associations limiting our dataset to subjects entering the study in 1980 or later to reduce the potential of a cohort effect. We also added a quadratic term for age to our models to determine whether it improved model fit. All analyses were performed with the use of SAS for WINDOWS, version 9.1 (SAS Institute, Cary, NC).
| RESULTS |
|---|
|
|
|---|
|
|
|
|
|
| DISCUSSION |
|---|
|
|
|---|
Several other studies have shown similar inverse associations with anthropometric variables for whole grains (11, 12, 39) and cereal fiber (40, 41). Fiber contributes to satiation, satiety, and the secretion of gut hormones (9), thereby affecting body weight and body composition through its effect on energy intake. McKeown et al (10) also observed comparable associations for whole grains (odds ratio: 0.67; 95% CI: 0.48, 0.91) and cereal fiber (odds ratio: 0.62; 95% CI: 0.45, 0.86) with risk of metabolic syndrome. Unlike other studies (11, 39, 41), our study showed significant inverse associations between whole grains and cereal fibers with total cholesterol, and whole grains were also inversely associated with LDL cholesterol. Jensen et al (42) also reported a significant inverse association between whole grains and total cholesterol (P = 0.02). The relation between dietary fiber and cholesterol is thought to be mainly due to soluble fibers rather than insoluble fibers (43, 44), but phytosterols (16) and phytoestrogens (35) may also affect cholesterol metabolism. No significant associations were observed between whole grains and blood pressure in our study, as seen in 2 other cross-sectional studies (11, 39), but a small intervention study observed a decline in blood pressure after a whole-grain diet (45). Cereal fiber intake was also unrelated to blood pressure in our study. Although 2 meta-analyses reported a small but significant inverse association between total fiber and blood pressure (46, 47), neither specifically addressed the role of cereal fiber, so whether cereal fiber specifically is associated with blood pressure requires more research.
Antioxidants and minerals present in whole grains and cereal fiber may contribute to insulin sensitivity (9, 48), and fiber may also be related to insulin sensitivity through effects on delayed gastric emptying. We observed a significant inverse association between whole grains and cereal fiber and 2-h glucose, and the magnitude of the effects was quite similar for both variables. McKeown et al (39) observed null associations between whole grains and 2-h glucose and 2-h insulin in a cross-sectional study of persons in the Framingham Offspring Study, and whole grains were also unrelated to fasting insulin in 2 large cohort studies (42). Although Lairon et al (41) saw no significant association between whole grains and fasting glucose, Sahyoun et al (11) showed an inverse dose-response relation (P for trend = 0.01). A small crossover study among overweight persons reported improved insulin sensitivity after an intervention with cereal fiber (49), and several other studies have shown significant associations between whole grains and plasma glucose (39) and insulin sensitivity (50, 51) among subjects with higher BMI, suggesting effect modification. Inconsistent findings on associations of whole grains or cereal fiber in relation to insulin or glucose measures may be due to differences in study design and dietary assessment methods, inadequate testing of interaction effects, or chance.
We observed a significant positive association between refined grains and fasting insulin among women but not men. Interaction effects are more likely to occur by chance and often are not reproducible (52), so our findings need to be interpreted with caution. However, our result is supported by recent results from the Hypertension Genetic Epidemiology Network study, which found a quantitative trait locus influencing fasting insulin in female, but not male, subjects (53). Refined grains are major contributors to glycemic load, and several reviews support a positive association between glycemic load and insulin resistance or glycemic control (54-56). That the percentage of energy from total carbohydrate in the highest quintile of refined grains (50.5%) and whole grains (51.7%) is so similar underscores the importance of differentiating between whole and refined foods when making dietary choices. Indeed, a small randomized crossover feeding study among overweight subjects with hyperinsulinemia observed 10% lower fasting insulin when consumption with refined grains were replaced with whole grains (57), as seen in a trial that included a reduction in refined grains as part of a comprehensive dietary intervention (58, 59). Note also that we observed a significant interaction between refined grains and sex in relation to 2-h insulin. Although the observed effects were in the expected direction, we likely had inadequate power to achieve statistical significance in stratified analyses.
Refined grains were not significantly associated with any other risk factor in this study. As mentioned, findings about refined grains and risk factors for chronic disease are inconsistent. Decreasing intake of refined grains was associated with a smaller weight change in one study (12), whereas increasing intake of refined-grain breakfast cereals was inversely related to weight gain and BMI in another (13). Refined grains were positively associated with fasting glucose among older adults (11) and hypertriglyceridemic waist phenotype (60). Refined grains were also positively associated with risk of metabolic syndrome in 2 cross-sectional studies (10, 11), but neither showed associations with individual risk factors. Those results and ours suggest that the effect of refined grains on measures of insulin and glucose may be modified by age (11), BMI (4, 33), and sex, probably due to differences in glucose tolerance and insulin sensitivity.
There are several limitations to our study. First, our study is cross-sectional; thus, our results do not allow us to make inferences about the directions of our associations and may be obfuscated by reverse causation. Although a longitudinal study would be stronger, our data are limited by the small numbers of subjects who have repeated measures of both dietary and risk factor data. An additional limitation is that our study sample, which is selected from an open cohort study, includes subjects across several decades. However, a cohort effect was not observed in an earlier study in this population (19). In addition, our models were adjusted for decade of the visit, and results remained similar when we limited our study to data from 1980 or later. Our study has a small sample size for some of our outcome variables; thus, we probably had insufficient power to detect and explore potential interactions. Finally, our study did not include markers of genetic variability, which are increasingly understood to modify the effect of diet on disease risk factors such as plasma lipids (61).
In conclusion, our study shows significant and similar associations of whole grains and cereal fiber with weight, BMI, waist circumference, and total cholesterol. Refined grains were positively associated with fasting insulin among women but not men. Longitudinal studies are needed to reproduce these findings, and special attention should be dedicated to exploring potential interactions with BMI, sex, age, and genes.
| ACKNOWLEDGMENTS |
|---|
The author's responsibilities were as follows—PKN: was responsible for the design and analysis for this report and drafted the manuscript; JM and PB: created the database for this study; DM and LF: contributed to data collection for the Baltimore Longitudinal Study of Aging; KLT: contributed to the database development and oversaw the HNRCA collaboration with the BLSA. All authors made critical comments during the preparation of the manuscript and fully accept responsibility for the work. None of the authors had a financial interest or professional or personal affiliation that compromises the scientific integrity of this work.
| REFERENCES |
|---|
|
|
|---|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |