- Open Access
- Open Peer Review
Nut consumption and risk of atrial fibrillation in the Physicians' Health Study
Nutrition Journalvolume 11, Article number: 17 (2012)
Atrial Fibrillation is highly prevalent in clinical practice affecting approximately 2.3 million people in USA and 4.5 million people in European Union. The aim of the study was to examine the association between nut consumption and incident atrial fibrillation.
Prospective cohort of 21,054 male participants of Physicians' Health Study I. Nut consumption was estimated using food frequency questionnaire and incident atrial fibrillation was ascertained through yearly follow-up questionnaires. Cox regression was used to estimate relative risks of atrial fibrillation.
The average age was 54.6 ± 9.5 years (40.7-87.1). During a mean follow up of 20 years (median 24 years), 3,317 cases of atrial fibrillation occurred. The crude incidence rate was 7.6, 7.4, 8.2, 7.9, and 6.8 cases/1000 person-years for people reporting nut consumption of rarely/never, 1-3/month, 1/per week, 2-6/week, and ≥ 7/week, respectively. Multivariable adjusted hazard ratios (95% CI) for incident atrial fibrillation were 1.00 (ref), 1.00 (0.90-1.11), 1.09 (0.97-1.21), 1.07 (0.95-1.21), and 0.91 (0.70-1.17) for nut consumption from the lowest to the highest category of nut consumption (p for trend 0.26). No statistically significant association between nut consumption and atrial fibrillation was found when stratified by body mass index (BMI < 25 vs ≥ 25 kg/m2) or age (< 65 vs. ≥ 65 years).
Our data did not show an association between nut consumption and incident atrial fibrillation among US male physicians.
Atrial Fibrillation (AF) is highly prevalent in clinical practice affecting approximately 2.3 million people in USA and 4.5 million people in European Union [1, 2]. The incidence of AF increases by about 0.1%-0.2% per year after the age of 40 while AF prevalence ranges from 2%-4% in people over 60 years of age to 8% in people over 80 years of age [3–6]. Prevalence for age- adjusted AF is reported to be higher in men than in women [4, 7]. AF is associated with 2-7 fold increased risk of ischemic stroke [8–11] and is also associated with a higher rate of mortality [7, 10, 11]. Several risk factors of AF have been shown to be influenced by modifiable lifestyle factors. Among dietary factors, nuts are low in sodium and contain many important nutrients including mono- and polyunsaturated fatty acids, fiber, vitamins E, and B2 (riboflavin), folate, and essential minerals (magnesium, phosphorus, copper, selenium, and potassium), thereby making them an excellent nutrient source . Nut consumption has previously been associated with improved serum cholesterol , blood pressure , weight loss , risk of diabetes  and sudden death/coronary heart disease . Nuts are relatively cheap and widely available and thereby can serve as a cost-effective means to prevent AF. However, it is not known whether nut consumption is associated with the risk of incident AF. Therefore, the current study sought to prospectively assess whether nut consumption is associated with a lower risk of developing AF among US male physicians.
Data was obtained from the Physicians' Health Study (PHS) I cohort. The details of the PHS I have been described elsewhere . In short, PHS I was a randomized, double blind, placebo controlled trial, of 22,071 US male physicians 40-84 years of age with no history of myocardial infarction, stroke, transient ischemic events or cancer at the time of randomization, with a two-by-two factorial design to study the effects of low dose aspirin (ASA) and beta-carotene on cardiovascular disease and cancer among the US male physicians (1982 to 1995). Of the 22,071 subjects in the PHS, we excluded subjects who were lost to follow up (n = 7) at 12 month post-randomization, those with missing data on nut consumption (n = 612), and those with prevalent AF (n = 398) at 12 months post-randomization. Thus, a final sample of 21,054 participants was selected for current analyses.
Information on health status, risk factors for cardiovascular disease (CVD), dietary, and lifestyle factors was collected by questionnaires. Each participant gave written informed consent and the Institutional Review Board at Brigham and Women's Hospital approved the study protocol.
Information on nut consumption was self-reported using a simple abbreviated food frequency questionnaire at 12 months post-randomization (1983-1985). Participants were asked the following: "Please indicate how often, on average, you have eaten each of the following foods during the past year". "Nuts (small packet or 1 oz.)" Possible response categories included "rarely/never", "1-3/month", "1/week", "2-4/week", "5-6/week", "daily", and "2+/day". While the food frequency questionnaire was not validated in the Physicians' Health Study, it has been validated in several cohorts [19–21].
Primary outcome was the development of AF in the study population. As presented in the ACC/AHA ESC guidelines for the management of patients with first detected episode of AF it can be classified into: Paroxysmal (self terminating usually lasting < 7 days) and Persistent (non- self terminating usually lasting > 7 days). Recurrent if two or more episodes of AF and permanent AF if Persistent AF is long lasting . All types of AF cases were assessed annually via follow-up questionnaires from 12 months forward. These self- reports of AF have been validated in another study conducted in the same cohort using a more detailed questionnaire on the diagnosis of AF and the review of medical records .
Data on demographics, anthropometrics, randomization to ASA, randomization to beta-carotene, diabetes mellitus (DM), hypertension (HTN), hypercholesterolemia, coronary heart disease (CHD), congestive heart failure (CHF) physical activity, smoking as well as cereal, fruit, vegetable, and alcohol consumption were assessed at the baseline (1982-1983). Age was categorized in 5 year categories (< 45, 45-49, 50-54, 55-59, 60-64, 65-69, 70-74, and 75+ y), body mass index (BMI) was classified as lean, overweight, and obese i.e. < 25, 25-29.9, and ≥ 30 kg/m2, respectively. Randomization to both ASA and beta-carotene was categorized as yes versus no. For physical activity, participants were asked how often they exercised to sweat; for current analysis, physical activity was dichotomized into exercise to sweat ≥ 1 versus < 1 per week. Smoking was classified as never, past, and current smokers. Alcohol consumption was classified as none, monthly, weekly, and daily. Cereal consumption was classified as ≤ 1, 2-6, and ≥ 7 servings per week. Fruit/vegetable consumption was categorized as servings per week and used as a continuous variable. Diagnosis of DM was made on self-reports via questionnaires mailed to each participant every 6 months during the first year and annually thereafter. HTN was defined as anyone who self reported the diagnosis, BP > 140/90 mm Hg per JNC7 guidelines or on the basis of medication list provided by the study participants. Diagnosis of hypercholesterolemia was also made on self-report as well as on the basis of available blood cholesterol levels. Diagnosis of CHD was made by including patients with self reported history of myocardial infarction (MI) and coronary artery bypass grafting (CABG). CHF diagnosis was again self reported and was verified and validated by detailed review of the medical record .
We classified each subject into one of the following categories of nut consumption: rarely/never, 1-3 per month, 1 per week, 2-6 per week, and 7+ per week as described previously in this cohort [36, 37]. We computed person-time of follow up from exposure assessment (12 months post-randomization) until the first occurrence of a) AF, b) death, or c) censoring date i.e. the date of last available follow up. Baseline demographic variables were recorded and compared with respect to each category of nut consumption.
We used Cox proportional hazard models to compute multivariable adjusted hazard ratios (HR) with corresponding 95% confidence intervals (CI) using participants in the lowest category of nut consumption as the reference group. Potential confounding was assessed for established risk factors of AF. The basic model only adjusted for age in 5-year categories. Model 1 was a multivariable model and controlled for age in 5-year categories, BMI randomization to ASA, randomization to beta-carotene, physical activity, smoking, cereal consumption, fruit/vegetable consumption, alcohol consumption, history of HTN, history of hypercholesterolemia, and DM.
In a secondary analysis using BMI of 25 kg/m2 as cut point, we assessed if adiposity modified the relation between nut consumption and AF. We then conducted stratified analyses by BMI < 25 or ≥ 25 kg/m2 and tested statistical interaction using a product term of nut consumption and adiposity variable in a hierarchical model. We also conducted stratified analyses by age using 65 years as cut point to assess if aging modified the relation between nut consumption and AF.
Since information on nut exposure does not describe peanut butter, a relatively large source across the U.S. it was separately queried using the same multivariable model as for nut consumption. We classified each subject into one of the following categories of peanut butter consumption: None, 1-3 per month, 1 per week, 2-6 per week, and 7+ per week. In an additional analysis using the same multivariable model we dichotomized nut consumption into ≥ weekly versus < weekly to see if it modified the relation between nut consumption and AF.
A sensitivity analysis by excluding those who developed any chronic disease such as any cancer, DM, or CVD and consequently might have changed their dietary patterns during the follow-up was also conducted. Assumptions for proportional hazard models were tested (by including main effects and product terms of nut consumption and logarithmic-transformed time factor) and were met (all P values > 0.05). All analyses were conducted using SAS, version 9.2 (SAS Institute, NC). Significance level was set at 0.05.
Table 1 shows the baseline demographics of 21,054 US male according to the categories of nut consumption. Mean age of the study participants was 54.6 ± 9.5 years (range 40.7 to 87.1 years). Among the total participants reporting nut consumption, there were 20%, 36%, 24%, 17%, and 3% people in the rarely/never, 1-3 per month, 1 per week, 2-6 per week, and ≥ 7 per week categories respectively. Frequent nut consumption was associated with a lower prevalence of current smoking and HTN while a higher prevalence of physical activity, fruit/vegetable intake, and cereal intake. During an average follow up of 20 years (median 24 years), 3,317 new cases of AF were reported. The crude incidence rates of AF were 7.6, 7.4, 8.2, 7.9, and 6.8 cases/1,000 person-years, from the lowest to the highest category of nut consumption (Table 2). There was no statistically significant association between nut consumption and incident AF. Multivariable adjusted hazard ratios (95% CI) for incident AF were 1.00 (ref), 1.00 (0.90-1.11), 1.09 (0.97-1.21), 1.07 (0.95-1.21), and 0.91 (0.70-1.17) for nut consumption of rarely/never, 1-3 per month, 1 per week, 2-6 per week, and ≥ 7 per week with p for linear trend of 0.26 (Table 2).
In a secondary analysis, nut consumption was not associated with incident AF among lean subjects (BMI < 25 kg/m2) [multivariable adjusted hazard ratios (95% CI) of 1.0 (reference), 1.07 (0.92-1.23), 1.16 (0.99-1.36), 1.16 (0.98-1.37), and 0.97 (0.70-1.34) from the lowest to the highest category of nut consumption, respectively (p for trend 0.11)]. Corresponding values for individuals that were overweight/obese were 1.0 (reference), 0.95 (0.82-1.09), 1.02 (0.87-1.19), 0.98 (0.82-1.18), and 0.84 (0.54-1.29), respectively (p for trend 0.95)].
Similarly, nut consumption was not associated with incident AF among younger (age < 65 years) physicians [multivariable adjusted hazard ratios (95% CI) of 1.0 (reference), 0.99 (0.88-1.11), 1.06 (0.94-1.20), 1.07 (0.94-1.23), and 0.92 (0.69-1.22) across consecutive categories of nut consumption, respectively (p for trend 0.30)]. Corresponding values for older participants (≥ 65 y) were 1.0 (reference), 1.06 (0.84-1.34), 1.20 (0.93-1.53), 1.04 (0.78-1.37), and 0.88 (0.48-1.60), respectively (p for trend 0.71)].
In a separate analysis multivariable adjusted hazard ratios (95% CI) for incident AF for peanut butter consumption were 1.00 (ref), 1.01 (0.91-1.11), 1.13 (1.02-1.25), 1.01 (0.90-1.12), and 1.00 (0.80-1.25) from the lowest to the highest category, respectively (overall p = 0.41). The multivariable adjusted hazard ratios (95% CI) for incident AF using nut consumption as ≥ weekly versus < weekly was 1.07 (0.99-1.15).
Results of sensitivity analysis excluding those who developed any chronic disease such as any cancer, DM, or CVD did not alter the results either [hazard ratios (95% CI) of 1.0 (reference), 1.00 (0.89-1.14), 1.07 (0.94-1.23), 1.10 (0.95-1.27), and 0.94 (0.70-1.26) from the lowest to the highest category of nut consumption, respectively, p for trend 0.22].
Our findings do not support a meaningful association between the consumption of nuts and incident AF among apparently healthy US male physicians. In addition, adiposity or advancing age did not modify the relation between nut intake and AF risk. To the best of our knowledge, this is the first large prospective study to assess the association between nut consumption and the incidence of AF.
Several factors could have lead to this null association between nut consumption and incident AF. We did not have any data on the type of nuts consumed. We were also unable to characterize different types of nut preparations like salted, roasted, etc to study their effects on the incident AF. Perhaps in 1980s, nut intake was not necessarily low in sodium and this could have lead to a higher prevalence of HTN, an important risk factor for AF. However, lower prevalence of HTN with increased nut consumption argues against it as a possible explanation. Each of the different types of nut (i.e. walnut, pistachio, hazelnut, etc) has been demonstrated to have a specific nutrient profile. Another important limitation was a single assessment of nut consumption during the study period. The results indicate that although the power was limited at the levels of nut consumption that would be most likely to influence AF risk, there was a non-statistically significant increase in AF risk among all consumers of nuts weekly or more. As a post hoc analysis, this would therefore be an interesting analysis for other data sets. We did not have information on family history of hypertension, hypercholesterolemia, or diabetes and therefore were unable to adjust for it. The crude way of assessing physical activity was also a potential limitation in our analysis and could have lead to residual confounding. Lastly our population consisted of only male physicians, who might have a higher consumption of nuts due to being aware of their health benefits making it difficult to generalize our findings to the general population.
Despite a lack of association between nut consumption and AF, beneficial effects of nuts have been reported on numerous outcomes considered to be important risk factors for developing AF. Nuts have been shown to improve serum cholesterol levels , lower blood pressure [14, 24–28], lower the risk of DM , improve weight loss , improve inflammation , and lower the risk of cardiovascular mortality . Our study has several strengths, including a large sample size, 20 years follow up, use of a standardized questionnaires, and a homogeneous group of male physicians able to recognize signs and symptoms of AF than the general population.
In summary, our study does not provide evidence in support of a significant association between nut consumption and incident AF among US male physicians.
ACC/AHA/ESC: Guidelines for the Management of Patients with Atrial Fibrillation: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the European Society of Cardiology Committee for Practice Guidelines (Writing Committee to Revise the 2001 Guidelines for the Management of Patients With Atrial Fibrillation): developed in collaboration with the European Heart Rhythm Association and the Heart Rhythm Society. Circulation. 2006, 2006 (114): e257-354.
Go AS, Hylek EM, Phillips KA, Chang Y, Henault LE, Selby JV, Singer DE: Prevalence of diagnosed atrial fibrillation in adults: national implications for rhythm management and stroke prevention: the AnTicoagulation and Risk Factors in Atrial Fibrillation (ATRIA) Study. JAMA. 2001, 285: 2370-2375. 10.1001/jama.285.18.2370.
Kannel WB, Abbott RD, Savage DD, McNamara PM: Epidemiologic features of chronic atrial fibrillation: the Framingham study. N Engl J Med. 1982, 306: 1018-1022. 10.1056/NEJM198204293061703.
Furberg CD, Psaty BM, Manolio TA, Gardin JM, Smith VE, Rautaharju PM: Prevalence of atrial fibrillation in elderly subjects (the Cardiovascular Health Study). Am J Cardiol. 1994, 74: 236-241. 10.1016/0002-9149(94)90363-8.
Petersen P, Godtfredsen J: Atrial fibrillation: a review of course and prognosis. Acta Med Scand. 1984, 216: 5-9.
Godtfredsen J: Atrial Fibrillation: Etiology, Course and Prognosis: A Follow-up Study of 1212 Cases. 1975, Copenhagen, Denmark: Munksgaard
Kannel WB, Abbott RD, Savage DD: McNamara PM Coronary heart disease and atrial fibrillation: the Framingham Study. Am Heart J. 1983, 106: 389-396. 10.1016/0002-8703(83)90208-9.
Wolf PA, Abbott RD, Kannel WB: Atrial fibrillation: a major contributor to stroke in the elderly: the Framingham Study. Arch Intern Med. 1987, 147: 1561-1564. 10.1001/archinte.1987.00370090041008.
Wolf PA, Abbott RD, Kannel WB: Atrial fibrillation as an independent risk factor for stroke: the Framingham Study. Stroke. 1991, 22: 983-988. 10.1161/01.STR.22.8.983.
Flegel KM, Shipley MJ, Rose G: Risk of stroke in non-rheumatic atrial fibrillation [published erratum appears in Lancet 1987;1:878]. Lancet. 1987, 1: 526-529.
Krahn AD, Manfreda J, Tate RB, Mathewson FA, Cuddy TE: The natural history of atrial fibrillation: incidence, risk factors, and prognosis in the Manitoba Follow-Up Study. Am J Med. 1995, 98: 476-484. 10.1016/S0002-9343(99)80348-9.
Kris-Etherton PM, Yu-Poth S, Sabaté J, Ratcliffe HE, Zhao G, Etherton TD: Nuts and their bioactive constituents: effects on serum lipids and other factors that affect disease risk. Am J Clin Nutr. 1999, 70 (3 Suppl): 504S-511S.
Sabaté J, Oda K, Ros E: Nut consumption and blood lipid levels: a pooled analysis of 25 intervention trials. Arch Intern Med. 2010, 170: 821-827. 10.1001/archinternmed.2010.79.
Djousse L, Rudich T, Gaziano JM: Nut consumption and risk of hypertension in US male physicians. Clin Nutr. 2009, 28: 10-14. 10.1016/j.clnu.2008.08.005.
Bes-Rastrollo M, Sabate J, Gomez-Gracia E, Alonso A, Martinez JA, Martinez-Gonzalez MA: Nut consumption and weight gain in a Mediterranean cohort: the SUN study. Obesity (Silver Spring). 2007, 15: 107-116. 10.1038/oby.2007.507.
Jiang R, Manson JE, Stampfer MJ, Liu S, Willett WC, Hu FB: Nut and peanut butter consumption and risk of type 2 diabetes in women. JAMA. 2002, 288: 2554-2560. 10.1001/jama.288.20.2554.
Albert CM, Gaziano J, Willett WC, Manson JE: Nut consumption and decreased risk of sudden cardiac death in the Physicians' Health Study. Arch Intern Med. 2002, 162: 1382-1387. 10.1001/archinte.162.12.1382.
The Steering Committee of the Physicians' Health Study Research Group: Final report in the aspirin component of the ongoing Physicians' Health Study. N Engl J Med. 1989, 321: 129-335.
Rimm EB, Giovannucci E, Stampfer MJ, Colditz GA, Litin LB, Willett WC: Reproducibility and validity of an expanded self-administered semiquantitative food frequency questionnaire among male health professionals. Am J Epidemiol. 1992, 135: 1114-1126.
Willett WC, Sampson L, Stampfer MJ, Rosner B, Bain C, Witschi J, Hennekens CH, Speizer FE: Reproducibility and validity of a semiquantitative food frequency questionnaire. Am J Epidemiol. 1985, 122: 51-65.
Stein AD, Shea S, Basch CE, Contento IR, Zybert P: Consistency of the Willett semiquantitative food frequency questionnaire and 24-hour dietary recalls in estimating nutrient intakes of preschool children. Am J Epidemiol. 1992, 135: 667-677.
Aizer A, Gaziano J, Cook NR, Manson JE, Buring JE, Albert CM: Relation of Vigorous Exercise to Risk of Atrial Fibrillation. Am J Cardiol. 2009, 103: 1572-1577. 10.1016/j.amjcard.2009.01.374.
Djoussé L, Driver JA, Gaziano JM: Relation between modifiable lifestyle factors and lifetime risk of heart failure. JAMA. 2009, 302: 394-400. 10.1001/jama.2009.1062.
Ferrara L, Raimondi S, d'Episcopo L, Guida L, Dello Russo A, Marotta T: Olive oil and reduced need for antihypertensive medications. Arch Intern Med. 2000, 160: 837-842. 10.1001/archinte.160.6.837.
Brancati FL, Appel LJ, Seidler AJ, Whelton PK: Effect of potassium supplementation on blood pressure in African Americans on a low-potassium diet. a randomized, double-blind, placebocontrolled trial. Arch Intern Med. 1996, 156: 61-67. 10.1001/archinte.1996.00440010079010.
Myers VH, Champagne CM: Nutritional effects on blood pressure. Curr Opin Lipidol. 2007, 18: 20-24. 10.1097/MOL.0b013e328012d911.
Estruch R, Martinez-Gonzalez MA, Corella D, Salas-Salvadó J, Ruiz-Gutiérrez V, Covas MI, Fiol M, Gómez-Gracia E, López-Sabater MC, Vinyoles E, Arós F, Conde M, Lahoz C, Lapetra J, Sáez G, Ros E: PREDIMED Study Investigators: Effects of a Mediterranean-style diet on cardiovascular risk factors: a randomized trial. Ann Intern Med. 2006, 145: 1-11.
Welty FK, Lee KS, Lew NS, Zhou JR: Effect of soy nuts on blood pressure and lipid levels in hypertensive, prehypertensive, and normotensive postmenopausal women. Arch Intern Med. 2007, 167: 1060-1067. 10.1001/archinte.167.10.1060.
Jiang R, Jacobs DR, Mayer-Davis E, Szklo M, Herrington D, Jenny NS, Kronmal R, Barr RG: Nut and seed consumption and inflammatory markers in the multi-ethnic study of atherosclerosis. Am J Epidemiol. 2006, 163: 222-231.
We are indebted to the participants in the PHS for their outstanding commitment and cooperation and to the entire PHS staff for their expert and unfailing assistance.
Grants funding and role of the funding source. The Physicians' Health Study is supported by grants CA-34944, CA-40360 and CA-097193 from the National Cancer Institute and grants HL-26490, and HL-34595, from the National Heart, Lung and Blood Institute of Health, Bethesda, MD. Funding agencies play no role in the data collection, analysis and manuscript preparation.
Acknowledgement to all contributors who do not meet the criteria for authorship N/A.
The authors declare that they have no competing interests.
Each author has participated sufficiently, intellectually or practically, in the work to take public responsibility for the content of the article, including the conception, design, and conduct of the experiment and for data interpretation. OK participated in study design, carried out collection of data, data analyses and drafted the manuscript. JG helped in drafting the manuscript along with providing significant advice and consultation. LD conceived of the study, participated in study design, helped in drafting the manuscript and provided significant advice and consultation. All authors read and approved the final manuscript.