Search tips
Search criteria 


Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
Am J Lifestyle Med. Author manuscript; available in PMC 2010 July 1.
Published in final edited form as:
Am J Lifestyle Med. 2009 July; 3(1 Suppl): 39S–43S.
doi:  10.1177/1559827609332320
PMCID: PMC2847297

Functional Foods as Modifiers of Cardiovascular Disease


There is growing consensus that systemic inflammation is at the heart of cardiovascular disease (CVD). Inflammation is a key feature of the immune system, functioning to defend tissue integrity and function. However, chronic stimulation of inflammatory mediators leads to lasting vascular reactivity, insulin resistance, hyperlipidemia, and, subsequently, chronic disease. Dietary practices to minimize inflammatory stimuli and CVD risk include regular intakes of fatty fish rich in the eicosapentaenoic and docosahexaenoic acids that compete with the more pervasive membrane fatty acid, arachidonic acid, disrupting the metabolic cascades that stimulate inflammation. Another effective dietary strategy is to consume less arachidonic acid by reducing beef, poultry, fish, and eggs from the diet (e.g., adopting a vegetarian-like diet). Since oxidative stress plays a prominent role in immune system activation, regular ingestion of ample amounts of fruits and vegetables (8+ servings/d) rich in antioxidant compounds, the polyphenols, carotenoids, and vitamin C (e.g., citrus, tomatoes, berries, carrots, and greens), lowers inflammatory mediators and risk for chronic disease. Whole grains, legumes, and nuts have also been demonstrated in clinical trials to effectively reduce inflammatory mediators and risk for CVD. Hence, as proclaimed in antiquity, ‘let food be thy medicine and medicine be thy food’.

Keywords: functional foods, cardiovascular disease, inflammation


There is growing scientific consensus that arterial inflammation is at the heart of cardiovascular disease (CVD).1 Although research portrays inflammation as an instigator of CVD, in reality inflammation is a key feature of the immune system functioning to defend and preserve tissue integrity and function. Pathogen invasion damages vascular tissue initiating the production of oxygen ions and free radicals, collectively termed reactive oxygen species (ROS). These small molecules stimulate the production of eicosanoids from fatty acids located in the phospholipid bylayer of all cell membranes. Eicosanoids are cell signaling molecules that participate in a wide range of physiological processes including immune system activation and the ensuing inflammatory state.2 The activation of white blood cells by eicosanoids enables these cells to adhere to and activate endothelial cells. Both activated leukocytes and endothelial cells in turn release numerous cytokines, small hormone-like mediators with wide ranging effects for cellular metabolism. Collectively, this complex but integrated metabolic cascade results in a rapid and focused offensive to ensure pathogen destruction and the restoration of tissue function.

The inflammatory cytokines released during the immune response, including tumor necrosis factor alpha (TNF-α), interleukins 1 and 6 (IL-1 and IL-6), and C-reactive protein (CRP), promote glycogenolysis, insulin resistance, and muscle protein catabolism.3 These metabolic changes ensure a rapid supply of amino acids and glucose to fuel the immune response and enable rapid immune protein synthesis. In addition, inhibition of fat oxidation by inflammatory mediators leads to a state of hyperlipidemia which serves to neutralize viruses and inhibit pathogen infectivity. Once the pathogen is cleared from tissues, the immune system wanes and the inflammatory mediators dissipate leaving tissues healthy and free of infection. However, factors aside from foreign agents also stimulate immune responses such as elevated blood cholesterol or glucose concentrations, cigarette smoke and pollutants, chemical solvents, and even obesity or stress. Since these factors do not disappear or dissipate, the inflammatory mediators are chronically stimulated leading to lasting vascular reactivity, insulin resistance, and hyperlipidemia, and ironically, chronic disease. Individuals should focus on strategies to minimize these factors (e.g., smoking cessation, weight loss, and stress management) to reduce disease risk. In addition, there is substantial evidence that the adoption of certain dietary practices can help control chronic inflammation and minimize CVD disease risk.4,5

Dietary Patterns that Reduce Inflammatory Markers

Mediterranean diets

A diet rich in foods common to the Mediterranean region prior to the 1960's has been termed the ‘Mediterranean diet’. This diet is high in fruits, vegetables, cereals, beans, nuts and seeds, and olive oil; red meat is rarely eaten, and dairy products, fish and poultry are consumed in low to moderate amounts; and, wine is consumed in moderation. This diet plan gained scientific attention because numerous reports indicated that populations consuming these diets had extraordinary low rates of chronic disease.6,7 Clinical trials have confirmed the cardiovascular protective effects of this diet plan and that this diet effectively reduces markers of inflammation in high risk populations.8-10

In an early study, patients who survived a myocardial infarction within 6 months of enrollment adopted either a Mediterranean-like diet or the standard low-fat therapeutic diet according to random assignment.11 After a mean follow up of 27 months, overall cardiac mortality was significantly higher (16 versus 3), as was overall mortality (20 versus 8), in the control group versus the Mediterranean diet group. Thus, adoption of a Mediterranean-like diet may reduce inflammation in select populations at high risk for CVD and possibly delay disease progression and need for medical treatment. However, the beneficial effects of Mediterranean-like diets may not extend to patients with established CVD and receiving current standard medical treatments such as statins, betablockers and angiotensin-converting enzyme inhibitors.12 The mechanisms by which Mediterranean diets reduce inflammatory risk are not well understood but may relate to high intakes of fruits and vegetables which contain antioxidant nutrients and polyphenols that reduce ROS concentrations throughout tissues.

Vegetarian diets

Diets devoid of flesh foods also reduce risk for CVD and have been demonstrated to reverse coronary atherosclerosis.13,14 Risk for CVD among vegetarian populations is consistently 20-35% below that for omnivore populations.15 Much of this benefit is likely related to the low body weights and low blood cholesterol concentrations generally observed for vegetarians due to their lower intakes of saturated fats and calories. Additionally, survey data also indicate that vegetarians have reduced concentrations of inflammatory markers, particularly CRP.16 In fact, a modified vegetarian diet was demonstrated to reduce CRP concentrations to a greater extent than that achieved by pharmaceutical intervention with a statin drug.17 Moreover, randomized controlled trials in patients with inflammatory conditions such as atopic dermatitis or rheumatoid arthritis, have demonstrated that inflammatory markers are reduced and disease symptoms abate following the adoption of a vegetarian diet.18,19

Similar to Mediterranean diets, vegetarian diets are high in fruits, vegetables, and nuts, rich sources of the antioxidant nutrients and polyphenols that contribute to the anti-inflammatory potential of these diets. Additionally, fleshless diets are low in arachidonic acid, a fatty acid that rapidly incorporates into cell membrane phospholipids and subsequently becomes the precursor for the inflammatory eicosanoids. Adoption of a vegetarian diet reduces tissue arachidonic acid concentrations 6% after 3 months,19 and long-term vegetarians may have tissue arachidonic acid concentrations 10-15% lower than that of omnivores. Hence, vegetarian diets reduce risk for CVD by multiple mechanisms: reducing the initial insult in the atherosclerotic pathway (raised cholesterol concentrations), reducing ROS concentrations, reducing production of inflammatory eicosanoids, and reducing markers of inflammatory stress.

Functional Foods with Anti-Inflammatory Effects


Substantial evidence supports the anti-inflammatory benefits of regular fish consumption or fish oil ingestion.20 The long-chain fatty acids unique to marine foods (eicosapentaenoic acid [EPA] and docosahexaenoic acid [DHA]) compete with the more pervasive long-chain fatty acid, arachidonic acid, in cell membranes disrupting the metabolic cascades that stimulate immune responses; consequently the inflammatory sequel is stifled. The anti-inflammatory effects of daily fish oil ingestion are nearly identical to the anti-inflammatory effects demonstrated for low-arachidonic acid diets (i.e., vegetarian diets); and interestingly, the benefits of low-arachidonic acid diets are augmented by fish oil consumption.19

In addition to its anti-inflammatory properties, fish oil possesses antithrombotic, triglyceride lowering, and antiarrhythmic effects in patients with CVD.21 Moreover, fish and fish oil ingestion has been related to a reduced risk for myocardial infarction, which may relate to beneficial effects of EPA and DHA on plaque morphology and stability.22 In one trial, 188 patients awaiting carotid endarterectomy were randomly assigned to fish oil, sunflower oil, or control groups for a median of 42 days to examine effects on plaque stability.23 EPA and DHA were rapidly incorporated into carotid plaque in patients receiving fish oil compared to the other groups, and fewer plaques from these patients had signs of inflammation or thin fibrous caps, signs of plaque instability and myocardial infarction risk, compared to the other groups.

A recent meta-analysis of ten qualifying randomized controlled trials, encompassing 14,727 patients, reported that daily fish oil consumption reduced incidence of death due to myocardial infarction by 24% and all cause mortality by 16%.24 In 2002, the American Heart Association recommended fish consumption (specifically fatty fish: salmon, tuna, herring, halibut, and mackerel) at least twice weekly to reduce risk for heart disease.25 However, for patients with CVD, or those needing to lower serum triglyceride concentrations, the American Heart Association recommends up to 4 g EPA+DHA daily in supplemental form in consultation with a physician.

Fruit and vegetables

Oxidative stress plays a prominent role in immune system activation and inflammatory conditions. Individuals consuming diets rich in fruits and vegetables have increased tissue concentrations of the antioxidant nutrients, particularly vitamin C, carotenoids, and polyphenols, and a lower risk for CVD.26,27 In randomized clinical trials, vitamin C lowered concentrations of the inflammatory mediator CRP 25-35%,28,29 and this vitamin C induced reduction in CRP was related to clinical improvements in cardiac patients.29 Citrus, red and yellow peppers, Brussels sprouts, melons, and strawberries are rich sources of vitamin C. The powerful extracellular and intracellular antioxidant functions of vitamin C serve to reduce tissue ROS concentrations, which in the atherosclerotic condition helps prevent endothelial dysfunction, inhibit vascular smooth muscle proliferation, and reduce oxidized low density lipoprotein (LDL) cholesterol.30

The carotenoids, particularly lycopene and beta-carotene concentrated in deeply colored items such as carrots, tomatoes, and dark green vegetables, are other dietary antioxidants that function to reduce oxidative stress in vivo and blood markers of inflammation. In healthy adults, the incorporation of tomato juice into their typical diets (2 cups per day for 2 weeks) significantly reduced plasma concentrations of CRP (-17%) and TNF-α (-43%).31 In patients with grade-1 hypertension, LDL cholesterol oxidation levels in plasma and systolic and diastolic blood pressure measures were significantly reduced following four weeks of daily tomato extract consumption as compared to placebo treatment.32 Many fruits and vegetables (particularly berries and grapes) are rich sources of another category of antioxidants known as the polyphenols, which includes tannins, lignins, and flavonoids. After an overnight fast, patients with CVD were randomly assigned to receive a red grape extract or placebo, and postprandial endothelial cell function was assessed for a 2-hour period by measuring flow-mediated dilation of the brachial artery.33 At 60 to 120 minutes post-treatment, flow-mediated dilation was enhanced 70% for the red grape extract versus placebo. In healthy adults, raisin consumption (1 cup per day for 6 weeks), but not placebo, significantly reduced TNF-α and intra-cellular adhesion molecules.34 Interestingly, tea, coffee and chocolate are also rich sources of polyphenols and have been demonstrated in randomized feeding trials to reduce markers of oxidative stress.

Fruits and vegetables are ranked by their antioxidant capacity, known as the Oxygen Radical Absorbance Capacity (ORAC) score, which reflects the combined antioxidant effects of vitamin C, carotenoids, polyphenols, and other constituents. Fruit with high ORAC scores include blueberries, plums, blackberries, strawberries, raspberries, sweet cherries, avocados, navel oranges, and red grapes; vegetables with high ORAC scores include artichokes, asparagus, red cabbage, spinach, and Russet potatoes.35 Foods from these lists should be regularly included in the diet to maximize the heart-protective potential of fruit and vegetables consumption.

Nuts and legumes

Nuts and peanuts have been demonstrated to reduce risk for CVD in numerous large prospective cohort studies,36,37 and the substitution of a serving of nuts for equivalent energy from carbohydrates or saturated fat in the typical diet theoretically reduces risk for CVD by over 30%.37 Nuts are complex foods containing cholesterol lowering mono- and poly-unsaturated fatty acids, arginine (a precursor to the vasodilator nitric oxide), soluble fiber, and several antioxidant polyphenols. In a randomized trial with olive oil as the control treatment, a single portion of walnuts (3 oz) as part of a high saturated fat meal (salami and cheese sandwich with high fat yogurt) reduced postprandial vascular reactivity, an emerging risk factor for CVD, in patients with hypercholesterolemia.38 Postprandial vascular reactivity is characterized by decreased bioavailability of nitric oxide and increased expression of proinflammatory cytokines and cellular adhesion molecules. Over a longer term, the daily consumption of walnuts (8-13 nuts daily for four weeks) by hypercholesterolemic adults improved endothelial function to a greater degree than the adoption of a Mediterranean-type diet.39

It is not surprising that the evidence supporting the cardio-protective effects of diets high in nuts is robust as multiple mechanisms work together to reduce risk; yet many are hesitant to add nuts to their diet regularly due to their high caloric value. Recent trials specifically examining weight gain in populations adhering to daily nut consumption (1.5 to 3 servings daily for 8-27 weeks) did not report significant weight gains.40 It is likely that a portion of the energy in nuts is not assimilated due to poor digestibility and that individuals successfully compensate for the calories in nuts due to their high satiety value.

Legumes are also complex foods rich in soluble fibers and polyphenols, as well as folic acid, a B vitamin that reduces blood homocysteine concentrations, a risk factor for CVD. Despite this favorable nutrient profile, and the fact that legumes are a dietary staple in Mediterranean-like diets, randomized controlled trials examining the potential of legumes to reduce CVD risk are not available. However, a large incident case-control study in Costa Rica concluded that the consumption of 1 serving of legumes daily was associated with a 40% lower risk of myocardial infarction.41 Interestingly, legumes were the only food group predictive of survival among five long-lived elderly cohorts in Japan, Sweden, Greece, and Australia.42

Whole grains

Whole grain products contain intact grain kernels rich in fiber and trace nutrients. Since grains are predominant in American diets comprising 30-50% total energy, the regular consumption of whole grains markedly improves dietary nutrient and fiber profiles, and there is consistent evidence from epidemiological surveys that whole grain consumption reduces risk for CVD. In a cohort of 14,153 African-American and white adults from the Atherosclerosis Risk in Communities (ARIC) Study, whole grain consumption, but not fruit and vegetable or nut consumption, was associated with a 7% lower risk for heart failure over a 13-year period.43 A recent meta-analysis based on seven qualifying prospective cohort studies focused on whole grain consumption and cardiovascular outcomes reported that the inverse association between dietary whole grains and incident CVD was strong and consistent across trials.44

In a 12-week intervention trial, fifty individuals at risk for CVD were instructed to follow a therapeutic, hypo-caloric diet for weight loss (5 servings fruits and vegetables, 3 servings low-fat dairy products, 2 servings lean meats, and 4-7 servings grains as based on energy needs); one-half of participants were instructed to consume only refined grains and the remainder consumed only whole grain products.45 At the end of the trial, both groups of participants lost similar amounts of weight (4-5 kg), but there was a greater degree of abdominal body fat loss in the whole grain group versus the refined grain group. Moreover, CRP concentrations decreased in the whole grain group (-38%) but were unchanged in the refined grain group. Although the anti-inflammatory mechanism is not clear, the reduction in CRP noted in this trial may be related to higher intakes of antioxidant nutrients present in the germ of whole grains. Also, as compared to refined grains, whole grains have a reduced glycemic response following ingestion (i.e., the postprandial rise in blood glucose is lessened), and reductions in postprandial glucose surges have been associated with reduced ROS generation after a meal and reduced postprandial inflammation and CVD risk.46


Diet plans rich in fruits and vegetables, nuts and legumes, whole grains, and fish, and low in red and processed meats, refined grains, high fat dairy, and sweets, have consistently been shown to reduce risk of CVD and total mortality. The low morbidity and mortality attributed to populations that adhere to Mediterranean-type diets or vegetarian diets further substantiate the benefits of a plant-based diet. It is now evident, based on the extensive scientific evidence, that constituents in these foods have broad ranging physiologic effects in vivo that lessen inflammatory cascades and vascular reactivity. In many cases, these effects are as powerful as pharmaceutical interventions, albeit much safer. As proclaimed in antiquity: ‘let food be thy medicine and medicine be thy food’.


Paper presented at the Building Healthy Lifestyles Conference, Arizona State University, Mesa, AZ on February 28-29, 2008


1. Libby P. Inflammatory mechanisms: the molecular basis of inflammation and disease. Nutr Rev. 2007;65:S140–S146. [PubMed]
2. Balboa MA, Balsinde J. Oxidative stress and arachidonic acid mobilization. Biochim Biophys Acta. 2006;1761:385–391. [PubMed]
3. Klasing KC. Nutritional aspects of leukocytic cytokines. J Nutr. 1988;118:1436–1446. [PubMed]
4. Heidemann C, Schulze MB, Franco OH, van Dam RM, Mantzoros CS, Hu FB. Dietary patterns and risk of mortality from cardiovascular disease, cancer, and all causes in a prospective cohort of women. Circulation. 2008;118:230–237. [PMC free article] [PubMed]
5. O'Keefe JH, Gheewala NM, O'Keefe JO. Dietary strategies for improving post-prandial glucose, lipids, inflammation, and cardiovascular health. J Am Coll Cardiol. 2008;51:249–255. [PubMed]
6. Keys A, Menotti A, Karvonen MJ, Aravanis C, Blackburn H, Buzina R, Djordjevic BS, Dontas AS, Fidanza F, Keys MH, et al. The diet and 15-year death rate in the seven countries study. Am J Epidemiol. 1986;124:903–915. [PubMed]
7. Kushi LH, Lenart EB, Willett WC. Health implications of Mediterranean diets in light of contemporary knowledge. 1. Plant foods and dairy products. Am J Clin Nutr. 1995;61(6 Suppl):1407S–1415S. [PubMed]
8. Huang CL, Sumpio BE. Olive oil, the mediterranean diet, and cardiovascular health. J Am Coll Surg. 2008;207:407–416. [PubMed]
9. Esposito K, Ciotola M, Giugliano D. Mediterranean diet, endothelial function and vascular inflammatory markers. Public Health Nutr. 2006;9:1073–1076. [PubMed]
10. Esposito K, Marfella R, Ciotola M, Di Palo C, Giugliano F, Giugliano G, D'Armiento M, D'Andrea F, Giugliano D. Effect of a mediterranean-style diet on endothelial dysfunction and markers of vascular inflammation in the metabolic syndrome: a randomized trial. JAMA. 2004;292:1440–1446. [PubMed]
11. de Lorgeril M, Renaud S, Mamelle N, Salen P, Martin JL, Monjaud I, Guidollet J, Touboul P, Delaye J. Mediterranean alpha-linolenic acid-rich diet in secondary prevention of coronary heart disease. Lancet. 1994;343:1454–1459. [PubMed]
12. Michalsen A, Lehmann N, Pithan C, Knoblauch NT, Moebus S, Kannenberg F, Binder L, Budde T, Dobos GJ. Mediterranean diet has no effect on markers of inflammation and metabolic risk factors in patients with coronary artery disease. Eur J Clin Nutr. 2006;60:478–485. [PubMed]
13. Ornish D, Scherwitz LW, Billings JH, Brown SE, Gould KL, Merritt TA, Sparler S, Armstrong WT, Ports TA, Kirkeeide RL, Hogeboom C, Brand RJ. Intensive lifestyle changes for reversal of coronary heart disease. JAMA. 1998;280:2001–2007. [PubMed]
14. Aldana SG, Greenlaw R, Salberg A, Merrill RM, Hager R, Jorgensen RB. The effects of an intensive lifestyle modification program on carotid artery intima-media thickness: a randomized trial. Am J Health Promot. 2007;21:510–516. [PubMed]
15. Key TJ, Fraser GE, Thorogood M, Appleby PN, Beral V, Reeves G, Burr ML, Chang-Claude J, Frentzel-Beyme R, Kuzma JW, Mann J, McPherson K. Mortality in vegetarians and non-vegetarians: a collaborative analysis of 8300 deaths among 76,000 men and women in five prospective studies. Public Health Nutr. 1998;1:33–41. [PubMed]
16. Krajcovicova-Kudlackova M, Blazicek P. C-reactive protein and nutrition. Bratisl Lek Listy. 2005;106:345–347. [PubMed]
17. Jenkins DJ, Kendall CW, Marchie A, Faulkner DA, Josse AR, Wong JM, de Souza R, Emam A, Parker TL, Li TJ, Josse RG, Leiter LA, Singer W, Connelly PW. Direct comparison of dietary portfolio vs statin on C-reactive protein. Eur J Clin Nutr. 2005;59:851–60. [PubMed]
18. Tanaka T, Kouda K, Kotani M, Takeuchi A, Tabei T, Masamoto Y, Nakamura H, Takigawa M, Suemura M, Takeuchi H, Kouda M. Vegetarian diet ameliorates symptoms of atopic dermatitis through reduction of the number of peripheral eosinophils and of PGE2 synthesis by monocytes. J Physiol Anthropol Appl Human Sci. 2001;20:353–361. [PubMed]
19. Adam O, Beringer C, Kless T, Lemmen C, Adam A, Wiseman M, Adam P, Klimmek R, Forth W. Anti-inflammatory effects of a low arachidonic acid diet and fish oil in patients with rheumatoid arthritis. Rheumatol Int. 2003;23:27–36. [PubMed]
20. Fritsche K. Fatty acids as modulators of the immune response. Annu Rev Nutr. 2006;26:45–73. [PubMed]
21. Mozaffarian D. Fish and n–3 fatty acids for the prevention of fatal coronary heart disease and sudden cardiac death. Am J Clin Nutr. 2008;87:1991S–1996S. [PubMed]
22. Ueeda M, Doumei T, Takaya Y, Shinohata R, Katayama Y, Ohnishi N, Takaishi A, Miyoshi T, Hirohata S, Kusachi S. Serum N-3 polyunsaturated Fatty Acid levels correlate with the extent of coronary plaques and calcifications in patients with acute myocardial infarction. Circ J. 2008;72:1836–1843. [PubMed]
23. Thies F, Garry JM, Yaqoob P, Rerkasem K, Williams J, Shearman CP, Gallagher PJ, Calder PC, Grimble RF. Association of n-3 polyunsaturated fatty acids with stability of atherosclerotic plaques: a randomised controlled trial. Lancet. 2003;361:477–485. [PubMed]
24. Yzebe D, Lievre M. Fish oils in the care of coronary heart disease patients: a meta-analysis of randomized controlled trials. Fundam Clin Pharmacol. 2004;18:581–592. [PubMed]
25. Kris-Etherton PM, Harris WS, Appel LJ, American Heart Association. Nutrition Committee Fish consumption, fish oil, omega-3 fatty acids, and cardiovascular disease. Circulation. 2002;106:2747–2757. [PubMed]
26. Liu S, Manson JE, Lee IM, Cole SR, Hennekens CH, Willett WC, Buring JE. Fruit and vegetable intake and risk of cardiovascular disease: the Women's Health Study. Am J Clin Nutr. 2000;72:922–928. [PubMed]
27. Rissanen TH, Voutilainen S, Virtanen JK, Venho B, Vanharanta M, Mursu J, Salonen JT. Low intake of fruits, berries and vegetables is associated with excess mortality in men: the Kuopio Ischaemic Heart Disease Risk Factor (KIHD) Study. J Nutr. 2003;133:199–204. [PubMed]
28. Block G, Jensen CD, Dalvi TB, Norkus EP, Hudes M, Crawford PB, Holland N, Fung EB, Schumacher L, Harmatz P. Vitamin C treatment reduces elevated C-reactive protein. Free Radic Biol Med. 2008 Oct 10; Epub ahead of print. [PMC free article] [PubMed]
29. Korantzopoulos P, Kolettis TM, Kountouris E, Dimitroula V, Karanikis P, Pappa E, Siogas K, Goudevenos JA. Oral vitamin C administration reduces early recurrence rates after electrical cardioversion of persistent atrial fibrillation and attenuates associated inflammation. Int J Cardiol. 2005;102:321–326. [PubMed]
30. Aguirre R, May JM. Inflammation in the vascular bed: importance of vitamin C. Pharmacol Ther. 2008;119:96–103. [PMC free article] [PubMed]
31. Jacob K, Periago MJ, Böhm V, Berruezo GR. Influence of lycopene and vitamin C from tomato juice on biomarkers of oxidative stress and inflammation. Br J Nutr. 2008;99:137–146. [PubMed]
32. Engelhard YN, Gazer B, Paran E. Natural antioxidants from tomato extract reduce blood pressure in patients with grade-1 hypertension: a double-blind, placebo-controlled pilot study. Am Heart J. 2006;151:100.e6–100.e1. [PubMed]
33. Lekakis J, Rallidis LS, Andreadou I, Vamvakou G, Kazantzoglou G, Magiatis P, Skaltsounis AL, Kremastinos DT. Polyphenolic compounds from red grapes acutely improve endothelial function in patients with coronary heart disease. Eur J Cardiovasc Prev Rehabil. 2005;12:596–600. [PubMed]
34. Puglisi MJ, Vaishnav U, Shrestha S, Torres-Gonzalez M, Wood RJ, Volek JS, Fernandez ML. Raisins and additional walking have distinct effects on plasma lipids and inflammatory cytokines. Lipids Health Dis. 2008;7:14. [PMC free article] [PubMed]
35. Wu X, Beecher GR, Holden JM, Haytowitz DB, Gebhardt SE, Prior RL. Lipophilic and hydrophilic antioxidant capacities of common foods in the United States. J Agric Food Chem. 2004;52:4026–4037. [PubMed]
36. Fraser GE. Nut consumption, lipids, and risk of a coronary event. Clin Cardiol. 1999;22(7 Suppl):III11–15. [PubMed]
37. Hu FB, Stampfer MJ. Nut consumption and risk of coronary heart disease: a review of epidemiologic evidence. Curr Atheroscler Rep. 1999;1:204–209. [PubMed]
38. Cortés B, Núñez I, Cofán M, Gilabert R, Pérez-Heras A, Casals E, Deulofeu R, Ros E. Acute effects of high-fat meals enriched with walnuts or olive oil on postprandial endothelial function. J Am Coll Cardiol. 2006;48:1666–1671. [PubMed]
39. Ros E, Núñez I, Pérez-Heras A, Serra M, Gilabert R, Casals E, Deulofeu R. A walnut diet improves endothelial function in hypercholesterolemic subjects: a randomized crossover trial. Circulation. 2004;109:1609–1614. [PubMed]
40. Mattes RD, Kris-Etherton PM, Foster GD. Impact of peanuts and tree nuts on body weight and healthy weight loss in adults. J Nutr. 2008;138:1741S–1745S. [PubMed]
41. Kabagambe EK, Baylin A, Ruiz-Narvarez E, Siles X, Campos H. Decreased consumption of dried mature beans is positively associated with urbanization and nonfatal acute myocardial infarction. J Nutr. 2005;135:1770–1775. [PubMed]
42. Darmadi-Blackberry I, Wahlqvist ML, Kouris-Blazos A, Steen B, Lukito W, Horie Y, Horie K. Legumes: the most important dietary predictor of survival in older people of different ethnicities. Asia Pac J Clin Nutr. 2004;13:217–220. [PubMed]
43. Nettleton JA, Steffen LM, Loehr LR, Rosamond WD, Folsom AR. Incident heart failure is associated with lower whole-grain intake and greater high-fat dairy and egg intake in the Atherosclerosis Risk in Communities (ARIC) study. J Am Diet Assoc. 2008;108:1881–1887. [PMC free article] [PubMed]
44. Mellen PB, Walsh TF, Herrington DM. Whole grain intake and cardiovascular disease: a meta-analysis. Nutr Metab Cardiovasc Dis. 2008;18:283–290. [PubMed]
45. Katcher HI, Legro RS, Kunselman AR, Gillies PJ, Demers LM, Bagshaw DM, Kris-Etherton PM. The effects of a whole grain-enriched hypocaloric diet on cardiovascular disease risk factors in men and women with metabolic syndrome. Am J Clin Nutr. 2008;87:79–90. [PubMed]
46. Brand-Miller J, Dickinson S, Barclay A, Celermajer D. The glycemic index and cardiovascular disease risk. Curr Atheroscler Rep. 2007;9:479–485. [PubMed]