Context Although increased intake of grain products has been
recommended to prevent cardiovascular disease (CVD), prospective data
examining the relation of whole grain intake to risk of ischemic stroke
are sparse, especially among women.
Objective To examine the hypothesis that higher whole grain intake
reduces the risk of ischemic stroke in women.
Design, Setting, and Participants A prospective cohort of
75,521 US women aged 38 to 63 years without previous diagnosis
of diabetes mellitus, coronary heart disease, stroke, or other CVDs in
1984, who completed detailed food frequency questionnaires (FFQs) in
1984, 1986, 1990, and 1994, and were followed up for 12 years as part
of the Nurses' Health Study.
Main Outcome Measure Incidence of ischemic stroke, confirmed by
medical records, by quintile of whole grain intake according to FFQ
responses.
Results During 861,900 person-years of follow-up, 352
confirmed incident cases of ischemic stroke occurred. We observed an
inverse association between whole grain intake and ischemic stroke
risk. The age-adjusted relative risks (RRs) from the lowest to highest
quintiles of whole grain intake were 1.00 (referent), 0.68 (95%
confidence interval [CI], 0.49-0.94), 0.69 (95% CI, 0.51-0.95), 0.49
(95% CI, 0.35-0.69), and 0.57 (95% CI, 0.42-0.78;
P = .003 for trend). Adjustment for
smoking modestly attenuated this association (RR comparing extreme
quintiles, 0.64; 95% CI, 0.47-0.89). This inverse
association remained essentially unchanged with further adjustment for
known CVD risk factors, including saturated fat and transfatty
acid intake (multivariate-adjusted RR comparing extreme quintiles,
0.69; 95% CI, 0.50-0.98). The inverse relation between whole
grain intake and risk of ischemic stroke was also consistently observed
among subgroups of women who never smoked, did not drink alcohol, did
not exercise regularly, or who did not use postmenopausal hormones. No
significant association was observed between total grain intake and
risk of ischemic stroke.
Conclusions In this cohort, higher intake of whole grain foods was
associated with a lower risk of ischemic stroke among women,
independent of known CVD risk factors. These prospective data support
the notion that higher intake of whole grains may reduce the risk of
ischemic stroke.
Although
stroke-related mortality has clearly declined since the mid-20th
century,1 incidence rates of stroke have been level since
the mid-1980s, and stroke remains a leading cause of serious disability
and death in women.2 In the United States, approximately
600,000 cases of stroke accounted for 160,000 deaths in
1997.2 At all ages, more women than men die of stroke. Many
of the approximately 4.4 million stroke survivors have permanent
disability, and the cost of stroke-related care amounts to $40 billion
each year.3 Because known risk factors for the development
of stroke, including hypercholesterolemia, hypertension, obesity, and
diabetes mellitus, can be changed through dietary modification, primary
prevention holds much promise.4 Few studies, however, have
specifically examined the relationship of diet to stroke risk,
especially among women.5,6 Moreover, previous studies have
often failed to distinguish stroke subtypes, although the pathologic
mechanisms for ischemic and hemorrhagic strokes are known to
differ.4
Several epidemiological studies have associated higher intakes of
specific nutrients, such as dietary fiber, potassium, and vitamin E,
with a lower risk of cardiovascular disease
(CVD).7-10 Few epidemiologic studies, however,
have
directly examined the relationship between foods
rich in such nutrients, particularly whole grains, fruits, and
vegetables, and risk of stroke, especially ischemic stroke. Such
studies are important because whole foods contain numerous other
beneficial phytochemicals—many of which are not documented in existing
databases11—and because the beneficial effects of specific
nutrients may not be apparent when examined individually because of
potentially important interactions between them. Recently, we and
others reported that a higher intake of whole grains was associated
with a lower risk of coronary morbidity12 and
mortality.13 For this report, we analyzed prospective data
from the Nurses' Health Study from 1984-1996 to evaluate the
hypothesis that greater whole grain intake reduces the risk of ischemic
stroke. A direct assessment of the association between whole grains and
ischemic stroke can provide not only important biological insights but
also practical dietary guidance as well.
The Nurses' Health Study is a prospective cohort study of diet
and lifestyle factors in relation to chronic diseases among
121,700 female registered nurses aged 30 to 55 years at
enrollment. The cohort was initiated in 1976 when the participants
returned a mailed questionnaire about various dietary and lifestyle
risk factors for chronic diseases.14 In 1980, we assessed
diet with a 61-item semiquantitative food frequency questionnaire
(FFQ).14 In 1984, the FFQ was expanded to include
126 items. Because the expanded questionnaires contained numerous
additional food items that are important for assessing details of
carbohydrate intake, we considered 1984 as the baseline for the current
analysis. We excluded respondents with previously diagnosed diabetes
mellitus, angina, myocardial infarction, stroke, or other CVDs in 1984.
The final eligible baseline population for our analyses consisted of
75,521 women aged 38 to 63 years.
Measurements of whole grain and refined grain foods along with other
aspects of diet were repeated in 1986, 1990, and 1994 using FFQs
similar to the one used in 1984. For each food, a commonly used unit or
portion size (eg, 1 slice of bread) was specified, and the participant
was asked how often on average during the previous year she had
consumed that amount. Nine responses were possible, ranging from
"never" to "six or more times per day." The type and brand of
breakfast cereal were also assessed. The method used in classifying
whole and refined grains has been described
previously.12,13 Specifically, whole grain foods included
dark bread, whole grain breakfast cereal, popcorn, cooked oatmeal,
wheat germ, brown rice, bran, and other grains (eg, bulgur, kasha, and
couscous). Refined grain foods included sweet rolls and
cakes/desserts, white bread, pasta, English muffins, muffins or
biscuits, refined grain breakfast cereal, white rice, pancakes or
waffles, and pizza. The list of breakfast cereals reported in the FFQ
was evaluated for whole grain and bran content based on data provided
by the package labels, and breakfast cereals with 25% or more whole
grain or bran content by weight were classified as "whole grain." A
full description of the FFQs and data on reproducibility and validity
in this cohort have been previously reported.14,15 The
performance of the FFQ for assessing the individual grain products has
been documented to be high.16 For example, comparing the
FFQ with detailed diet records in a sample of the participants,
correlation coefficients were 0.75 for cold breakfast cereal, 0.71 for
white bread, and 0.77 for dark bread.
We confirmed incident cases of stroke by reviewing medical
records. When nonfatal stroke was reported on a follow-up
questionnaire, we obtained permission to review the pertinent medical
records and then classified stroke according to the criteria
recommended by the National Survey of Stroke.17Ischemic stroke was defined as a clinical syndrome, including
a constellation of neurological findings of sudden or rapid onset
persisting for 24 hours or more, and these findings were judged to be
from thrombotic or embolic occlusion of a cerebral artery, resulting in
infarction. "Silent" strokes were excluded, as were events
secondary to trauma, infection, or cancer. Deaths were reported by next
of kin or were obtained from postal authorities or the National Death
Index.18 Because the pathologic mechanisms for ischemic and
hemorrhagic strokes are known to differ,4 we focused on
ischemic stroke in our analyses to reduce end-point misclassification.
This is because the most likely plausible benefits of whole grains may
be associated with the etiology of arterosclerosis.
Person-time for each participant was calculated from the date of
return of the 1984 questionnaire to the date of confirmation of stroke,
death, or June 1, 1996, whichever came first. We initially examined
distributions of individual foods to create categories of consumption
with adequate person-time at risk in each category. Incidence rates
then were calculated by dividing the number of events by the
person-time in each category. The relative risks (RRs) were estimated
as the rate of ischemic strokes in a specific category of intake of
whole grain or refined grain divided by the rate in the lowest
category. We then conducted multivariate analyses adjusting for age
(5-year categories), body mass index (BMI; calculated as weight in
kilograms divided by the square of height in meters) (6 categories),
level of physical activity (hours per week in 5 categories), smoking
status (never, past, and current: 1-14, 15-24, and ≥25 cigarettes per
day), alcohol intake (4 categories: never, 0.1-4.9 g/d, 5.0-14.9 g/d,
and ≥15.0 g/d), parental history of myocardial infarction at age
younger than 60 years (yes or no), self-reported (asked as "doctor
diagnosed" in the questionnaire) hypertension (yes or no) and high
blood cholesterol level (yes or no), menopausal status (premenopausal,
postmenopausal without hormone replacement therapy, postmenopausal with
past hormone replacement therapy, or
postmenopausal with current hormone replacement
therapy), use of multivitamins or vitamin E supplements (yes or no),
saturated fat (quintiles), transfatty acids (quintiles), and
total energy intake (quintiles). Because fruit and vegetable
intake5 was inversely associated with risk of ischemic
stroke, we conducted a secondary analysis further adjusting for intake
of fruits and vegetables (in quintiles). To further minimize
residual confounding effects of smoking, alcohol consumption, physical
inactivity, and use of postmenopausal hormones, we examined the
association between whole grain intake and risk of ischemic stroke in 4
subgroups of women: never smokers, nondrinkers, inactive lifestyle, and
nonusers of postmenopausal hormones. Tests of linear trend across
increasing categories of grain intake were conducted by assigning the
medians of intakes in categories (servings per day) treated as a
continuous variable. All P values were 2-sided.
To reduce within-person variation and to best represent long-term diet,
we applied a cumulative average method that used repeated measures of
diet during the 12-year follow-up. Details of this method have been
reported elsewhere.19 Briefly, we used pooled logistic
regression20 to model the incident cases of ischemic stroke
using the cumulative average diet from all cycles of the FFQs up to the
beginning of each 2-year follow-up interval. For example, incidence of
ischemic stroke from 1984-1986 was related to the intake of whole grain
and other dietary variables assessed on the 1984 questionnaire,
incidence from 1986-1990 was related to the average intake reported in
1984 and 1986, and incidence from 1990-1994 was related to the average
intake reported in 1984, 1986, and 1990. Intermediate end points that
occurred during the follow-up, including angina, hypercholesterolemia,
diabetes mellitus, and hypertension, could have led to changes in diet
and therefore may have confounded the associations between diet and
disease. Hence, we stopped
updating information on diet at the beginning of the
interval during which those conditions were diagnosed in a participant.
At baseline in 1984, the mean daily intake of whole grain foods was
1.12 servings per day. The median intake of whole grain ranged from
virtually no consumption (0.13 servings/d) in the lowest quintile to
nearly 3 servings per day in the highest quintile (Table
1). Women with a high intake of
whole grains smoked less, exercised more, and were more likely to use
postmenopausal hormones or take multivitamins or vitamin E supplements.
Greater whole grain intake also was associated with higher intakes of
carbohydrates, fruits and vegetables, dietary fiber, and folate, but
lower intakes of fats, cholesterol, and alcohol (Table 1).
Body mass index and history of parental myocardial infarction at age
younger than 60 years did not vary appreciably across quintiles of
whole grain intake. In contrast, findings were generally reversed for
the associations between these lifestyle factors and the intake of
refined grains.
Intakes of both total grains and whole grains increased from 1984-1994,
while intake of refined grain remained fairly stable over time
(Table 2). The mean intake
of whole grains increased from 1.12 servings per day in 1984 to 1.36
servings per day in 1994. The Spearman correlation coefficients between
any 2 assessments of whole grain intakes reported from 1984-1994 ranged
from 0.44-0.61, depending on the closeness in the time of assessments.
During 12 years of follow-up (861,900 person-years), 352
confirmed incident cases of ischemic stroke occurred. We observed a
strong inverse association between whole grain intake and risk of
ischemic stroke but no significant association between refined grain
intake and ischemic stroke risk (Table
3). Comparing women in the
highest with the lowest quintiles of intake, the age-adjusted RRs of
ischemic stroke were 0.57 for whole grain intake (95% confidence
interval [CI], 0.42-0.78; P = .003 for trend)
and 0.90 for refined grain intake (95% CI, 0.64-1.26;
P = .30 for trend). In multivariate
models of whole grain intake and ischemic stroke risk, smoking was the
strongest confounding factor. While adjustment for smoking attenuated
the inverse relation between whole grain intake and risk of ischemic
stroke, it remained strong and significant (RR, 0.64; 95% CI,
0.47-0.89, when comparing the 2 extreme quintiles;
P = .04 for trend). In a multivariate
model adjusting for known CVD risk factors, including saturated fat and
transfatty acids, the inverse relation between whole grain
intake and risk of ischemic stroke remained essentially unchanged (RR,
0.69; 95% CI, 0.50-0.98, when comparing the 2 extreme quintiles;
P = .08 for trend) (Table 3).
Additional adjustment for intake of fruits and vegetables did not
materially change the inverse relation between whole grain intake and
risk of ischemic stroke (RRs across increasing quintiles of whole grain
intake were 1.00, 0.73, 0.78, 0.61, and 0.70;
P = .09 for trend).
To further minimize residual confounding effects of smoking, alcohol
consumption, physical inactivity, and use of postmenopausal hormones,
we examined the stratified models of whole grain intake and risk of
ischemic stroke in 4 subgroups of women: never smokers, nondrinkers,
inactive lifestyle, and nonusers of postmenopausal hormones. The
reduction in risk of ischemic stroke associated with a high intake of
whole grain was even stronger among never smokers (RR, 0.50; 95% CI,
0.34-0.76; P = .006 for trend), while it
remained essentially unchanged from the overall results among
nondrinkers, women who did not engage in vigorous physical activity, or
nonusers of postmenopausal hormones (Table
4). In addition, we found that
the inverse relation of whole grain intake to risk of ischemic stroke
was similar regardless of levels of intake of saturated fat or
transfatty acids, BMI, or physical activity levels.
To determine whether the effects of whole grains exceed their potential
known mediators, we examined whether the inverse relation of whole
grain intake to ischemic stroke risk could be attributed to increased
intakes of dietary fiber, folate, potassium, magnesium, and vitamin E.
After these constituents of whole grains were simultaneously included
in a multivariate model, the association of whole grain intake with
risk of ischemic stroke was somewhat attenuated (RR, 0.76; 95% CI,
0.51-1.15, when comparing the highest vs the lowest quintiles;
P = .38 for trend).
We also examined the relations of whole grain intake to risk of total
stroke. An inverse association was found for total stroke
(multivariate-adjusted RRs across increasing quintiles of whole grain
intake were 1.00, 0.90, 0.92, 0.79, and 0.77;
P = .06 for trend). Relatively few
cases of hemorrhagic stroke (n = 76) occurred among the
participants of the
Nurses' Health Study between 1984 and 1996, so
the power to detect an association between whole grain intake and risk
of hemorrhagic stroke was limited. Whole grain intake did not appear to
reduce the risk of hemorrhagic stroke, with an age- and smoking-adjusted RR for hemorrhagic stroke of 1.01 (95% CI, 0.44-2.32,
when comparing the 2 extreme quintiles of whole grain intake;
P = .98 for trend) and a multivariate-adjusted
RR of 1.15 (95% CI, 0.51-2.58; P = .90 for
trend). The number of incident fatal strokes was also small
(n = 91), and the multivariate-adjusted RR was 0.91 (95%
CI, 0.37-2.20; P = .33 for trend) when comparing
the 2 extreme quintiles of whole grain intake.
In this large prospective study, the higher the consumption of whole
grain foods the lower the risk of ischemic stroke, independent of a
variety of CVD risk factors. Because whole grain intake was reported
through a self-administered FFQ, measurement errors were inevitable.
However, assessment of whole grain foods by the questionnaires used in
this study had relatively high validity (r>0.70 for most
whole grain foods when compared with a 7-day dietary record).
Our FFQ was designed to minimize day-to-day variation by assessing an
average long-term dietary intake. More importantly, it can clearly
discriminate participants' dietary patterns and rank them
accordingly.21,22 For example, in a sample of nurses
without diabetes mellitus or coronary heart disease who
provided fasting blood samples, we observed a
positive dose-response relation between fasting plasma levels of
triglycerides and dietary carbohydrate that was consistent with
findings from controlled metabolic experiments.23,24
Furthermore, any measurement error in assessing whole grain intake
should not be related to stroke end point because dietary assessments
were completed before the end points occurred. This kind of
nondifferential misclassification would tend to weaken the association
between whole grain intake and ischemic stroke risk and would not
explain the significant 40% lower risk rate for ischemic stroke
associated with a high intake of whole grain.
Several potential alternative explanations need to be
considered when interpreting our findings. First, the association
between whole grain intake and ischemic stroke may be because of other
potential confounding factors. As expected, a higher intake of whole
grains was correlated with a generally healthy lifestyle. However, the
apparent protective effect of whole grain consumption persisted in
multivariate models that accounted for known CVD risk factors.
Furthermore, the apparent inverse relation between whole grain intake
and risk of ischemic stroke was remarkably consistent among subgroups
of women who were never smokers, did not drink alcohol, did not report
regular vigorous physical activity, or did not use postmenopausal
hormones. This argues against the possibility of residual confounding
from these known risk factors.
Because women with a high background risk of ischemic stroke, such as
those with diabetes mellitus, hypertension, or hypercholesterolemia,
may change their diet after being diagnosed with these conditions, the
associations between whole grain intake and ischemic stroke may be
confounded by these indications. In addition, intermediate end points
that occurred during the follow-up, including angina,
hypercholesterolemia, diabetes mellitus, and hypertension, also could
have led to changes in diet and therefore may have confounded the
associations between diet and disease. To account for this, we stopped
updating information on diet at the beginning of the interval during
which those conditions were diagnosed in a participant. Although we
could not entirely exclude the possibility of confounding by
indication, it seemed more likely that the protective effect of whole
grain intake would be underestimated because women who perceived
themselves to be at increased risk of ischemic stroke would tend to
increase their intake of whole grain foods. Similar findings were
observed when women with those conditions at baseline in 1984 were
excluded from the main analysis. Also, these results are internally
consistent with our previous report of an inverse association between
whole grain consumption and risk of coronary heart disease in this
cohort of female nurses.12 Because of the differences in
etiologic mechanisms between hemorrhagic and ischemic stroke, the
finding that consumption of whole grains was not associated with risk
of hemorrhagic stroke indirectly strengthens the interpretation that
the inverse relation between whole grain and ischemic stroke that we
observed may be mechanistic rather than because of chance or bias.
The protective effect of whole grains against ischemic
stroke may involve multiple biological pathways,11 and the
active ingredients in whole grains that may impart this risk reduction
are not completely understood. Whole grains contain an abundance of
antioxidants, minerals, phytochemicals, and fibers in both the
outer (bran) and inner (germ) layers, both of which are removed during
processing. Of the myriad compounds found in whole grains, folate,
vitamin E, magnesium, potassium, and fibers have received much
attention. Folate can lower homocysteine blood levels by converting
homocysteine to methionine, and a high intake of folate has been
associated with a lower risk of coronary events.25
High serum homocysteine and low serum folate levels also have
been associated with carotid artery stenosis.26 Greater
intake of potassium, magnesium, and vitamin E also has been
independently associated with reduced risks of coronary events or
ischemic stroke.7-10,27 Finally, intake of cereal fiber has
been consistently associated with lower risk of coronary events in
prospective cohort studies,9,28 which also may explain the
protective effects of whole grains. Because our primary objective was
to evaluate the total impact of whole grains on risk of ischemic
stroke, we did not control for the effects of these whole grain
constituents in our primary analyses. In our secondary analyses,
however, we examined whether the protective effects of whole grains are
limited to these known constituents or go beyond them. Adjustment for
these components of whole grain foods attenuated the inverse relation
of whole grain intake with ischemic stroke, suggesting that the
apparent protective effect of whole grains can be partially attributed
to these protective constituents. However, the inverse relation
remained (although it was not statistically significant), indicating
that other constituents may contribute to additional protection. Before
generalizing our findings to the other populations, it is important to
consider that our study cohort was approximately 98% white. Because
nonwhite women are underrepresented, when findings are expected to
differ significantly according to underlying biological differences
between ethnic groups, studies in other populations will be desirable
to confirm our findings.
Survey data indicate that most of the grains consumed in the United
States are processed and refined,29 with the average
consumption of whole grain products at approximately one-half serving
per day.30 In this cohort of female nurses, whole grains
accounted for only one third of the servings of total grains, and
median consumption of whole grain foods was 1 serving per day. Even the
women in the top quintile of whole grain intake barely approached the 3
servings per day that are generally
recommended.31 Given that the inverse
relation we observed between whole grain intake and ischemic stroke
risk in this cohort of women was continuous, although risk reduction
seemed to level off at the fourth quintile (about a 30%-40% lower
risk rate of ischemic stroke associated with 1.3 servings per day),
replacing refined grains with whole grains by even 1 serving a day may
have significant benefits in reducing the risk of ischemic stroke.
In conclusion, higher intakes of whole grain foods were
associated with a lower risk of ischemic stroke, independent of known
CVD risk factors, in this large population of women. These findings
support the hypothesis that increasing intake of whole grains may help
reduce the incidence of ischemic stroke.
1. Achievements in public health, 1990-1999:
decline in deaths from heart disease and stroke—United States: 1900-1999
MMWR Morb Mortal Wkly Rep.1999;48:649-656.Google Scholar 2.American Heart Association. 2000 Heart and Stroke Statistical Update. Dallas, Tex: American Heart Association; 2000.
3.Taylor TN, Davis PH, Torner JC, Holmes J, Meyer JW, Jacobson MF. Lifetime cost of stroke in the United States.
Stroke.1996;27:1459-1466.Google Scholar 4.Bronner LL, Kanter DS, Manson JE. Primary
prevention of stroke.
N Engl J Med.1995;333:1392-1400.Google Scholar 5.Joshipura KJ, Ascherio A, Manson JE.
et al. Fruit and
vegetable intake in relation to risk of ischemic stroke.
JAMA.1999;282:1233-1239.Google Scholar 6.Ness AR, Powles JW. The role of diet, fruit and
vegetables and antioxidants in the aetiology of stroke.
J
Cardiovasc Risk.1999;6:229-234.Google Scholar 7.Khaw KT, Barrett-Connor E. Dietary potassium and
stroke-associated mortality: a 12-year prospective population study.
N Engl J Med.1987;316:235-240.Google Scholar 8.Rimm EB, Stampfer MJ, Ascherio A, Giovannucci E, Colditz GA, Willett WC. Dietary antioxidant intake and risk of coronary heart
disease among men.
N Engl J Med.1993;328:1450-1456.Google Scholar 9.Rimm EB, Ascherio A, Giovannucci E, Spiegelman D, Stampfer MJ, Willett WC. Vegetable, fruit, and cereal fiber intake and
risk of coronary heart disease among men.
JAMA.1996;275:447-451.Google Scholar 10.Knekt P, Jarvinen R, Reunanen A, Maatela J. Flavonoid
intake and coronary mortality in Finland: a cohort study.
BMJ.1996;312:478-481.Google Scholar 11.Slavin J, Jacobs D, Marquart L. Whole-grain consumption
and chronic disease: protective mechanism.
Nutr Cancer.1997;27:14-21.Google Scholar 12.Liu S, Stampfer MJ, Hu FB.
et al. Whole grain
consumption and risk of coronary heart disease: results from the
Nurses' Health Study.
Am J Clin Nutr.1999;70:412-419.Google Scholar 13.Jacobs Jr DR, Meyer KA, Kushi LH, Folsom AR. Whole-grain intake may reduce the risk of ischemic heart disease death
in postmenopausal women: the Iowa Women's Health Study.
Am J Clin
Nutr.1998;68:248-257.Google Scholar 14.Willett WC, Sampson L, Stampfer MJ.
et al. Reproducibility and validity of a semiquantitative food frequency
questionnaire.
Am J Epidemiol.1985;122:51-65.Google Scholar 15.Willett WC. Nutritional epidemiology. In: Rothman KJ,
Greenland S, eds. Modern Epidemiology. 2nd ed. Philadelphia,
Pa: Lippincott-Raven Publishers; 1998:623-642.
16.Salvini S, Hunter DJ, Sampson L.
et al. Food-based
validation of a dietary questionnaire: the effects of week-to-week
variation in food consumption.
Int J Epidemiol.1989;18:858-867.Google Scholar 17.Walker AE, Robins M, Weinfeld FD. The National Survey
of Stroke: clinical findings.
Stroke.1981;12:I13-I44.Google Scholar 18.Stampfer MJ, Willett WC, Speizer FE.
et al. Test of the
National Death Index.
Am J Epidemiol.1984;119:837-839.Google Scholar 19.Hu F, Stampfer M, Rimm E.
et al. Dietary fat and
coronary heart disease: a comparison of approaches for adjusting for
total energy intake and modeling repeated dietary measurements.
Am
J Epidemiol.1999;149:531-540.Google Scholar 20.Cupples LA, D'Agostino RB, Anderson K, Kannel WB. Comparison of baseline and repeated measure covariate techniques in the
Framingham Heart Study.
Stat Med.1988;7:205-222.Google Scholar 21.Willett WC. Nutritional Epidemiology. 2nd ed.
New York, NY: Oxford University Press; 1998.
22.Hu FB, Rimm E, Smith-Warner SA.
et al. Reproducibility
and validity of dietary patterns assessed with a food-frequency
questionnaire.
Am J Clin Nutr.1999;69:243-249.Google Scholar 23.Grundy S, Denke M. Dietary influences on serum lipids
and lipoproteins.
J Lipid Res.1990;31:1149-1172.Google Scholar 24.Liu S, Manson JE, Stampfer M.
et al. Dietary glycemic
load assessed by food frequency questionnaire in relation to plasma
high-density lipoprotein cholesterol and fasting triglycerides among
postmenopausal women.
Am J Clin Nutr.In press.Google Scholar 25.Rimm EB, Willett WC, Hu FB.
et al. Folate and vitamin
B
6 from diet and supplements in relation to risk of
coronary heart disease among women.
JAMA.1998;279:359-364.Google Scholar 26.Selhub J, Jacques PF, Bostom AG.
et al. Relationship between plasma homocysteine, vitamin status and
extracranial carotid-artery stenosis in the Framingham Study
population.
J Nutr.1996;126:1258S-1265S.Google Scholar 27.Ascherio A, Rimm EB, Hernan MA.
et al. Intake of
potassium, magnesium, calcium, and fiber and risk of stroke among US
men.
Circulation.1998;98:1198-1204.Google Scholar 28.Wolk AM, Stampfer MJ, Hu FB.
et al. Long-term intake of
dietary fiber and decreased risk of coronary heart disease among women.
BMJ.In press.Google Scholar 29.Anderson GH. Dietary patterns vs dietary
recommendations: identifying the gaps for complex carbohydrate.
Crit Rev Food Sci Nutr.1994;34:435-440.Google Scholar 30.Albertson A, Tobelmann R. Consumption of grain and
whole-grain foods by an American population during the years 1990-1992.
J Am Diet Assoc.1995;95:703-704.Google Scholar 31.USDA. Nutrition and Your Health: Dietary
Guidelines for Americans. 5th ed. Washington, DC: US Dept of
Agriculture, US Dept of Health and Human Services; 2000.