Background Dietary fiber is part of a healthy diet and may exert a protective effect in the cardiovascular system. The effect of fiber intake on blood pressure (BP) has not yet been established.
Methods We performed a meta-analysis of randomized placebo-controlled trials to estimate the effect of fiber supplementation on BP overall and in population subgroups. Original articles published between January 1, 1966, and January 1, 2003, were retrieved for 24 trials that fulfilled criteria for meta-analysis. Data were abstracted on fiber dose, fiber type, BP changes, study design features, and study population characteristics. A random-effects model was used for meta-analysis.
Results Fiber supplementation (average dose, 11.5 g/d) changed systolic BP by –1.13 mm Hg (95% confidence interval: –2.49 to 0.23) and diastolic BP by –1.26 mm Hg (–2.04 to –0.48). Reductions in BP tended to be larger in older (>40 years) and in hypertensive populations than in younger and in normotensive ones.
Conclusion Increasing the intake of fiber in Western populations, where intake is far below recommended levels, may contribute to the prevention of hypertension.
Observational and experimental studies suggest a beneficial effect of dietary fiber intake on blood pressure (BP), in both normotensive and hypertensive subjects.1- 3 Subjects consuming a vegetarian diet are generally at lower risk of developing hypertension.1- 2 However, it is unknown whether this can be ascribed to the high fiber content of the diet because vegetarians—apart from differences in lifestyle—also have higher intakes of potassium, magnesium, and polyunsaturated fatty acids and a lower intake of saturated fat. Clinical trials of fiber supplementation have shown wide variation in BP response.3 In trials with purified fiber supplements, reductions in BP tend to be larger than in trials with fiber-rich foods. This difference in BP response might be explained by fiber dose, type of fiber consumed, or better compliance with dietary supplements than with high-fiber diets.3
Daily intake of fiber in the United States and many other Western countries is around 15 g/d, which is only half the amount recommended by the American Heart Association (25 to 30 g /d from foods).4- 6 Given this large population segment with inadequate fiber intake, the demonstration of beneficial effects of fiber on BP may impact public health policy. Many clinical trials of dietary fiber and BP have been conducted in the past decades, but most lacked power to detect small, potentially meaningful BP effects. We aggregated data from 24 randomized placebo-controlled trials of fiber supplementation and BP by conducting a comprehensive meta-analysis. It is unknown whether BP response to fiber intake is related to type of fiber and subject characteristics such as age, sex, and hypertensive status. Therefore, we also obtained BP estimates in these specific subgroups and took potential confounders into account.
A MEDLINE search (January 1, 1966, to January 1, 2003) was conducted using “(fiber OR fibre) AND (blood pressure OR hypertension) AND (trial OR intervention OR random* OR study)” as words in the title or abstract. In addition, we performed a manual search using reference lists of original research and review articles. The search was limited to studies in human subjects and English-language literature. For all trials, we retrieved the original publication, which in 2 cases were an abstract7 and a letter,8 respectively.
We selected any randomized controlled trial of fiber supplementation in human subjects with BP as a primary or secondary study outcome. Seventy-two trials were identified that met the inclusion criteria (Figure 1). Subsequently, 48 trials were excluded (reference list available from the authors) for the following reasons: lack of appropriate BP data (n = 7), intentional cointervention from which the effect of fiber supplementation could not be separated (n = 29), or lack of a concurrent placebo control group (n = 12). In 1 trial, BP response to fiber supplementation was reported for different sources of fiber, which yielded 2 treatment strata with an identical placebo control group.9 A total of 24 trials with 25 relevant strata remained for meta-analysis.7- 29 For 1 trial, data on diastolic BP were missing.25
Selection of randomized controlled trials (RCTs) for meta-analysis of fiber supplementation and blood pressure (BP).
The internal validity of trials included in this meta-analysis is largely guaranteed by random assignment of fiber supplementation. Quality of studies was additionally quantified by scoring of blinding toward the type of treatment (ie, open, single blind, and double blind).
Differences in systolic and diastolic BP and accessory variance measures were obtained for each trial according to a standardized procedure using a data abstraction form. In addition, data were collected on trial design (parallel vs crossover; double blind vs single blind or open); duration of the trial; type of fiber and fiber dose; and whether BP was a primary or secondary study outcome. Furthermore, we abstracted data on sample size and characteristics of the study population including mean age; sex (proportion of men); baseline BP; baseline body weight; baseline body mass index (BMI), calculated as weight in kilograms divided by the square of height in meters; change in body weight during intervention; use of antihypertensive drugs (percentage treated); and baseline (habitual) fiber intake.
For 1 trial, the change in fiber intake during intervention was calculated using a compliance table.17 In 1 trial the intervention group received 2 different doses of fiber during the intervention period, which we averaged.11 Blood pressure measurements in the sitting position were abstracted. If those were not available, supine or awake ambulatory BP measurements were taken, in that order. For 2 trials, the change in BP had to be estimated from a graph in the article.13,23
For description of study populations, the baseline values of age, proportion of men, systolic and diastolic BP, body weight, BMI, and fiber intake in the intervention and control groups were averaged. In 3 trials, age was given as a range, and minimum and maximum values were averaged.9,22- 23 Baseline BMI of the study population was reported in 13 trials, change in body weight in 21 trials, baseline fiber intake in 11 trials, and use of antihypertensive drugs in 15 trials. Study populations were assumed to be not undergoing antihypertensive treatment in 5 trials where use of diuretics was defined as an exclusion criterion.21- 22,25- 26 In 1 trial, we imputed missing data on age (imputed value, 40 years, which was the median value for all other trials) and sex (imputed value, 50% male).8 Populations were considered hypertensive if more than 50% of the subjects were undergoing antihypertensive treatment or if mean BP at baseline was 140/90 mm Hg or higher.
For parallel trials, BP change from baseline in the intervention group was subtracted from that in the control group to yield the net change in BP due to fiber supplementation. For crossover trials, the net change in BP was calculated as the final BP in the intervention period minus the final BP in the control period. Standard errors (SEs) for the net changes in systolic and diastolic BP were obtained. If not given, SEs were derived from confidence intervals, P values, or individual SEs for BP changes in intervention and control groups or intervention and control periods (crossover design). For parallel trials in which SEs for paired BP differences were reported, the pooled SE for net BP change was calculated by using the following equation:
Grahic Jump Location
For parallel trials with lacking data on SEs for paired differences and for crossover trials, the pooled SE was estimated according to Follmann et al,30 assuming a correlation of 0.50 between baseline and final BP values or BP in intervention and control periods (crossover design), as follows:
If variance was only reported at baseline, we assumed similar variance at the end of follow-up. The SAS statistical package was used for data analysis (version 8; SAS Institute Inc, Cary, NC). We first tested homogeneity of effect size by Q statistics31 and found significant heterogeneity among trials (systolic χ224 = 24.7, P = .002; diastolic χ223 = 37.1, P = .03). We analyzed data according to Van Houwelingen et al,32 using a random-effects model that accounted for both within- and between-study variation (SAS PROC MIXED statement). Blood pressure estimates were reported with 95% confidence intervals (CIs). Two-sided P values lower than .05 were considered statistically significant.
We performed a number of predefined stratified meta-analyses to examine between-group differences in BP response to fiber supplementation.32 Subgroups were based on mean age (≤40 years vs >40 years), hypertensive status (no vs yes), sex (<50% male vs ≥50% male), BMI (≤28 kg/m2 vs >28 kg/m2), and type of fiber (soluble vs insoluble vs mixed). Analyses by age and BMI were based on the median of the frequency distribution of these variables. In addition, the associations of fiber dose and duration of intervention with BP response were examined by means of linear regression analysis, for which we reported intercepts and β regression coefficients with 2-sided P values. Analyses in subgroups were repeated using a multivariate model to adjust for the potential confounders of age, proportion of men, hypertensive status, study design (parallel vs crossover), duration of intervention, and fiber dose.
Publication bias was visually examined after construction of a funnel graph, in which weight factors (1/SE2) were plotted against net changes in BP.33 In addition, a nonparametric “trim and fill” method was used to adjust for publication bias.34
An overview of the 24 randomized controlled trials of fiber and BP included in our meta-analysis is given in Table 1. A total of 1404 subjects were included, and sample sizes ranged from 12 to 201 subjects. Trials had a mean duration of 9.0 weeks (median, 8 weeks; range, 2-24 weeks). Sixteen trials were double-blind, and 15 had BP as a primary study outcome. The mean age of trial populations was 42 years (median, 40 years; range, 23-63 years). Three trials included only men, 6 trials only women, and the remainder both men and women. Average baseline BP was 133/82 mm Hg, and populations in 8 trials were considered hypertensive. Baseline BMI was reported for 12 trial populations, 11 (92%) of which appeared to be overweight (ie, BMI ≥25 kg/m2). Net mean change in body weight during fiber supplementation was available for 21 trials and ranged from –2.5 kg to +1.0 kg (mean, –0.39 kg; P = .13). Baseline fiber intake was reported in 11 trials and ranged from 12.8 to 44.1 g/d (mean, 24.8 g/d). Soluble fiber was given in 11 trials, insoluble fiber in 7 trials, and a mixture of soluble and insoluble fiber in the remaining trials. In 4 trials, fiber intake was increased by dietary intervention.14,16- 18 Fiber doses varied between 3.5 and 42.6 g/d, with a mean dose of 11.5 g/d (median dose, 7 g/d). The unweighted average BP change in all trials combined for systolic BP was –1.54 mm Hg (95% CI, –3.48 to 0.39) and for diastolic BP, –1.34 mm Hg (95% CI, –2.41 to –0.27).
Meta-analysis yielded a weighted overall effect of fiber supplementation on systolic BP of –1.13 mm Hg (95% CI, –2.49 to 0.23) and on diastolic BP, –1.26 mm Hg (95% CI, −2.04 to −0.48) (Figure 2). Blood pressure responses to fiber supplementation in strata of population characteristics are summarized in Table 2. Blood pressure reductions were larger in older populations (mean age, >40 years) than in younger populations, but the difference was only statistically significant for systolic BP (P = .001). Hypertensive populations had significantly larger BP reductions than normotensive populations, both systolic (P<.001) and diastolic (P = .019). Sex and BMI of trial populations did not significantly modify BP response to fiber supplementation.
Blood pressure (BP) response to fiber supplementation in randomized controlled trials. Effects on systolic BP (A) and diastolic BP (B) in individual trials are depicted as open squares; error bars indicate 95% confidence intervals. Meta-analysis yielded pooled estimates of –1.13 mm Hg (–2.49 to 0.23) for systolic BP and –1.26 mm Hg (−2.04 to −0.48) for diastolic BP, which are depicted as black diamonds. Data on diastolic BP were missing for the trial by Ryttig et al.25
Changes in BP became less pronounced with increasing fiber dose in linear regression analysis, but β coefficients were small and not statistically significant (regression equation for systolic BP, –1.55 + 0.032 mm Hg /g of fiber, P = .60; diastolic BP, –1.89 + 0.047 mm Hg/g of fiber, P = .16). Blood pressure reponse was also not related to duration of intervention (regression equation for systolic BP, −0.77 – 0.046 mm Hg /wk, P = .73; diastolic BP, –1.15 – 0.013 mm Hg /wk, P = .88). With regard to type of intervention, soluble fiber changed BP by –1.32 mm Hg systolic (95% CI, –3.19 to 0.55) and −0.82 mm Hg diastolic (95% CI, –1.83 to 0.18); insoluble fiber by −0.23 mm Hg systolic (95% CI, –2.88 to 2.42) and −0.57 mm Hg diastolic (95% CI, –1.86 to 0.72); and the mixture of soluble and insoluble fiber by –1.74 mm Hg systolic (95% CI, −4.49 to 1.02) and –2.22 mm Hg diastolic (95% CI, –3.40 to –1.03).
Results from multivariate, stratified meta-analyses with adjustment for age, hypertensive status, proportion of men, duration of intervention, study design, and fiber dose are also summarized in Table 2. Change in body weight during intervention appeared not to be significantly associated with systolic and diastolic BP (P = .65 and P = .38, respectively) and was therefore left out of the multivariate model. Again, age was a significant modifier of the effect on systolic BP. The reduction in systolic BP remained significantly larger in older than in younger populations (P = .04). Blood pressure effects were also larger in hypertensive than normotensive populations after adjustment for confounders, but the difference was no longer statistically significant (Table 2).
Exclusion of 8 nonblinded trials yielded essentially similar effects of fiber on systolic BP (–1.14 mm Hg [95% CI, –2.37 to 0.08]) but a larger effect on diastolic BP (–1.71 mm Hg [95% CI, −2.61 to −0.81]). Exclusion of the trial by Fehily et al14 with a relatively large sample size (n = 201) did not change the overall BP estimates (data not presented). Exclusion of 4 dietary trials did not change the estimate for systolic BP (–1.06 mm Hg [95% CI, –2.80 to 0.67]) but yielded a larger effect of fiber supplementation on diastolic BP (–1.43 mm Hg diastolic BP [95% CI, −2.36 to −0.50]).
From visual examination of the funnel plot it was concluded that small trials with large systolic BP reductions are possibly overrepresented in meta-analysis (Figure 3). A nonparametric “trim and fill” method revealed that 1 trial might have been missing. After adjustment for putative missing data, the overall effect on systolic BP was attenuated to −0.94 mm Hg (95% CI, –2.34 to 0.46).
Funnel plot of trial weights against change in systolic blood pressure (BP). Blood pressure effects in individual trials are depicted as squares scattered around the pooled BP estimate of –1.13 mm Hg. A nonparametric “trim and fill” method34 indicated that 1 trial might have been missing owing to publication bias. After adjustment for putative missing data, the overall effect on systolic BP was attenuated to −0.94 mm Hg (95% confidence interval, –2.34 to 0.46).
In this meta-analysis of 24 randomized controlled trials, fiber supplementation (mean dose, 11.5 g/d) caused a nonsignificant change in systolic BP of –1.13 mm Hg (95% CI, –2.49 to 0.23) and a significant change in diastolic BP of –1.26 mm Hg (95% CI, –2.04 to −0.48). The effects of fiber supplementation on BP were larger in older (>40 years) than in younger populations in multivariate analysis, although this was only statistically significant for systolic BP. Furthermore, BP reductions tended to be larger in hypertensive populations, but after adjustment for the older age of hypertensive populations (mean age, 52 years vs 37 years in normotensive populations), this difference lost statistical significance. Body weight and sex did not modify the effect of fiber supplementation on BP.
The effect of fiber on BP was estimated only from randomized placebo-controlled trials that had a high internal validity. Studies in which other dietary factors were modulated at the same time were excluded, and the BP effects are therefore likely to be causal and primarily attributable to changes in fiber intake. An advanced statistical approach for meta-analysis of continuous outcomes was used that accounted for both within- and between-study variability, which yielded accurate BP estimates and confidence intervals.32
This meta-analysis also has several limitations. First, we might not have been able to completely rule out BP effects by magnesium and potassium in the studies of fiber supplementation that we examined. A meta-analysis by Jee et al35 showed a small, nonsignificant change in BP of −0.6 mm Hg systolic (95% CI, –2.2 to 1.0) and −0.8 mm Hg diastolic (95% CI, –1.9 to 0.4) after magnesium supplementation. A meta-analysis by Whelton et al36 showed a significant BP change of –3.11 mm Hg systolic (95% CI, –1.91 to –4.31) and –1.97 mm Hg diastolic (95% CI, –0.52 to –3.42) after potassium supplementation. In 1 of the 4 dietary intervention trials in our meta-analysis, a concomitant increase in magnesium and potassium intake occurred.18 Moreover, fiber supplementation may also increase magnesium intake, as reported in 2 other trials,9,19 and potassium intake, as reported in 1 trial.9 For the remaining trials, no data on magnesium or potassium intake were available.
Second, publication bias could have occurred in that trials with large systolic BP reductions might be somewhat overrepresented. However, these trials had small weights in meta-analysis, and adjustment for putative missing data caused only a small attenuation of the effect on systolic BP. Sutton et al37 empirically assessed the effect of publication bias on meta-analyses, which is a common phenomenon in systematic reviews, and found that the impact of publication bias on final conclusions is generally small.
Dietary fiber or nonstarch polysaccharide is a collective term for a variety of plant substances that are resistant to digestion by human gastrointestinal enzymes. The structural fibers (cellulose, lignin, and hemicelluloses) are insoluble, whereas the natural gel-forming fibers (pectins, gums, and mucilages) are soluble.38 In the human diet, insoluble fiber is mainly derived from whole-grain products and soluble fiber from fruits, vegetables, pulses, and oats.38 Little is known about the potential mechanisms through which dietary fiber might lower BP. Dietary fiber reduces the glycemic index of foods, thereby attenuating insulin response.39 Insulin may play a role in BP regulation,40 and dietary fiber has been shown to enhance insulin sensitivity and improve vascular endothelial function.39,41 Furthermore, there is evidence that fiber, especially soluble types, improves mineral absorption in the gastrointestinal system,42- 43 which may have an indirect favorable effect on BP. In the Dietary Approaches to Stop Hypertension (DASH) trial,44 the effect of dietary patterns on BP was assessed. The fruits-and-vegetables diet provided potassium, magnesium, and high amounts of fiber and resulted in BP reductions of 2.8/1.1 mm Hg compared with a typical US diet. Data from our meta-analysis provide some support for a larger effect of soluble than insoluble fiber on BP.
Few prospective studies have examined the relationship between fiber intake and the risk of hypertension. In the Health Professionals’ Follow-up Study45 of 30 681 US male subjects, dietary fiber was independently associated with a reduced risk of hypertension. In the Nurses’ Health Study46 of 41 541 predominantly white US women, a significant inverse association of fiber intake with self-reported BP was found although not with risk of hypertension.
Dietary fiber may, apart from its effect on BP, also favorably influence other cardiovascular risk factors. A meta-analysis by Brown et al47 showed that soluble fiber had a favorable effect on blood lipids: for each gram increase in dietary fiber, the concentration of blood low-density lipoprotein cholesterol was lowered by about 2 mg/dL (about 0.052 mmol/L). Furthermore, high intake of fiber, although mainly insoluble types from cereals, has been associated with lower risk of diabetes mellitus type 2.48- 49
In the Cardiovascular Health Study,50 a population-based multicenter study among 3588 elderly men and women, an inverse association between the consumption of fiber from cereal sources (insoluble fiber) and the risk of incident cardiovascular disease has recently been reported. As a biologically plausible mechanism for the beneficial effects of cereal fiber intake on cardiovascular risk in the elderly, the authors suggested a BP lowering effect of dietary fiber. In the large National Health and Nutrition Examination Survey I (NHANES I) Epidemiologic Follow-up Study,51 a higher intake of dietary fiber appeared to be associated with a reduced risk of coronary heart disease. Beneficial effects in NHANES I were related to water-soluble types of fiber rather than insoluble fiber, as was also the case in our meta-analysis of BP trials.
Intake of fiber in Western countries is low, with less than half of the US population meeting the recommended levels.4- 6,51 The present meta-analysis shows that dietary fiber has a small BP-lowering effect. Increasing fiber intake in the general population may contribute to the prevention of hypertension.
Correspondence: Johanna M. Geleijnse, PhD, Wageningen University, Division of Human Nutrition, PO Box 8129, 6700 EV Wageningen, the Netherlands (marianne.geleijnse@wur.nl).
Accepted for Publication: August 17, 2004.
Financial Disclosure: None.
Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature
Use interactive graphics and maps to view and sort country-specific infant and early dhildhood mortality and growth failure data and their association with maternal
Instructions
Thank you for submitting a comment on this article. It will be reviewed by JAMA Internal Medicine editors. You will be notified when your comment has been published. Comments should not exceed 500 words of text and 10 references.
Do not submit personal medical questions or information that could identify a specific patient, questions about a particular case, or general inquiries to an author. Only content that has not been published, posted, or submitted elsewhere should be submitted. By submitting this Comment, you and any coauthors transfer copyright to the journal if your Comment is posted.
* = Required Field
Disclosure of Any Conflicts of Interest* Indicate all relevant conflicts of interest of each author below, including all relevant financial interests, activities, and relationships within the past 3 years including, but not limited to, employment, affiliation, grants or funding, consultancies, honoraria or payment, speakers’ bureaus, stock ownership or options, expert testimony, royalties, donation of medical equipment, or patents planned, pending, or issued. If all authors have none, check "No potential conflicts or relevant financial interests" in the box below. Please also indicate any funding received in support of this work. The information will be posted with your response.
Register and get free email Table of Contents alerts, saved searches, PowerPoint downloads, CME quizzes, and more
Subscribe for full-text access to content from 1998 forward and a host of useful features
Activate your current subscription (AMA members and current subscribers)
Purchase Online Access to this article for 24 hours
Some tools below are only available to our subscribers or users with an online account.
Download citation file:
Web of Science® Times Cited: 79
Customize your page view by dragging & repositioning the boxes below.
and access these and other features:
Register Now
Enter your username and email address. We'll send you a link to reset your password.
Enter your username and email address. We'll send instructions on how to reset your password to the email address we have on record.
Need assistance?
Athens and Shibboleth are access management services that provide single sign-on to protected resources. They replace the multiple user names and passwords necessary to access subscription-based content with a single user name and password that can be entered once per session. It operates independently of a user's location or IP address. If your institution uses Athens or Shibboleth authentication, please contact your site administrator to receive your user name and password.