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Stroke. 2006;37:2430-2435
Published online before print July 27, 2006, doi: 10.1161/01.STR.0000236633.40160.ee
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(Stroke. 2006;37:2430.)
© 2006 American Heart Association, Inc.


Emerging Therapies

Nutrition and Stroke Prevention

Marc Fisher, MD; Kennedy Lees, MD, Section Editors: J. David Spence, MD, FRCPC

From the Stroke Prevention and Atherosclerosis Research Centre, Robarts Research Institute, London, Ontario, Canada.

Correspondence to Dr David Spence, Stroke Prevention and Atherosclerosis Research Centre, Robarts Research Institute, 1400 Western Rd, London, Ontario, Canada N6G 2V2. E-mail dspence{at}robarts.ca


*    Abstract
up arrowTop
*Abstract
down arrowIntroduction
down arrowCholesterol and Animal Fat
down arrowBenefits of a Mediterranean...
down arrowClinical Trials With the...
down arrowBeneficial Effects of...
down arrowB Vitamins for Lowering...
down arrowConclusion
down arrowReferences
 
Nutrition is much more important in prevention of stroke than is appreciated by most physicians. The powerful effects of statin drugs in lowering the levels of fasting cholesterol, combined with an unbalanced focus on fasting lipids (as opposed to postprandial fat and oxidative stress), have led many physicians and patients to believe that diet is relatively unimportant. Because the statins can lower fasting lipids by &50% to 60%, and a low-fat diet only lowers fasting cholesterol by &5% to 10%, this error is perhaps understandable. However, a Cretan Mediterranean diet, which is high in beneficial oils, whole grains, fruits, and vegetables and low in cholesterol and animal fat, has been shown to reduce stroke and myocardial infarction by 60% in 4 years compared with the American Heart Association diet. This effect is twice that of simvastatin in the Scandinavian Simvastatin Survival Study: a reduction of myocardial infarction by 40% in 6 years. Vitamins for lowering of homocysteine may yet be shown to be beneficial for reduction of stroke; a key issue is the high prevalence of unrecognized deficiency of vitamin B12, requiring higher doses of vitamin B12 than have been used in clinical trials to date. Efforts to duplicate with supplementation the evidence of benefit for vitamins E, C, and beta carotene have been largely fruitless. This may be related to the broad combination of antioxidants included in a healthy diet. A Cretan Mediterranean diet is probably more effective because it provides a wide range of antioxidants from fruits and vegetables of all colors.


Key Words: diet • nutrition • prevention • stroke • vitamins


*    Introduction
up arrowTop
up arrowAbstract
*Introduction
down arrowCholesterol and Animal Fat
down arrowBenefits of a Mediterranean...
down arrowClinical Trials With the...
down arrowBeneficial Effects of...
down arrowB Vitamins for Lowering...
down arrowConclusion
down arrowReferences
 
Nutrition is much more important in prevention of stroke than is appreciated by most physicians and, paradoxically, perhaps even by most nutritionists. Current issues that warrant discussion in this venue include the intake of animal fat and cholesterol, the Cretan Mediterranean diet, the failure of most studies to show benefit of supplements with antioxidant vitamins such as vitamins E and C, and the current controversy over failure of recent clinical trials to show reduction of stroke and other cardiovascular events by lowering plasma total homocysteine with folate, B6, and B12. A key issue is the recent recognition that vitamin B12 deficiency is much more common in the elderly than is commonly appreciated, and therefore higher doses of B12, and possibly additional therapies to lower homocysteine, may be required to achieve adequate reductions of total homocysteine.


*    Cholesterol and Animal Fat
up arrowTop
up arrowAbstract
up arrowIntroduction
*Cholesterol and Animal Fat
down arrowBenefits of a Mediterranean...
down arrowClinical Trials With the...
down arrowBeneficial Effects of...
down arrowB Vitamins for Lowering...
down arrowConclusion
down arrowReferences
 
The powerful effects of statin drugs in lowering of fasting cholesterol have seduced many patients and physicians into believing that diet is relatively unimportant: Why bother with a low-fat diet, which only lowers fasting cholesterol by &5% to 10%,1 when a pill can reduce fasting cholesterol by 50%2?

The reason that diet is still very important is that the blinkered focus on fasting lipids is inappropriate. Cholesterol is measured in the fasting state to minimize variability of the measurement; however, human beings are only in the fasting state for the last few hours of the night. What affects the endothelium for &18 hours of the day is the postprandial levels of lipids, cholesterol, oxidized cholesterol, and oxidative stress that follow meals containing trans fats, animal fat,3 or glucose.4 Diet is therefore much more important than would be predicted by effects on fasting lipids.5

A key problem with current dietary recommendations in North America is a failure to distinguish between kinds of fat and between red meat and poultry and fish. The mantra that "fat is bad" has led to a reduction of fat intake and a corresponding increase in carbohydrate intake, with harmful effects on cardiovascular disease and stroke risk.6 Willett and Stampfer7 indicate in an important review that standard dietary recommendations for low intake of fat arose from thin air, driven by a misplaced desire to simplify, and need to be corrected.

There is increasing evidence that postprandial fats and oxidative stress are as important or more important than fasting lipids.8,9 A high-fat meal impairs endothelial function for several hours,10 and this effect can be mitigated by pretreatment with vitamins C and E,11 indicating that oxidative stress from free radicals is an important contributor to the endothelial dysfunction from high-fat meals.

Carluccio et al12 found a direct antiatherosclerotic effect of oleic acid in endothelial cells. Tsimikas et al13 showed that subjects consuming an American diet had monocyte adhesion and chemotaxis induced by LDL, in contrast to subjects on a normal Greek diet. This effect could be reversed by oleic acid supplementation in subjects on the American diet.

Dietary intake of cholesterol probably is important. The National Cholesterol Education Program (NCEP) dietary guidelines specified a daily cholesterol intake <300 mg/d for low-risk and <200 mg/d for high-risk vascular disease candidates.14 A single egg yolk contains 275 mg of cholesterol, as much as an 8-ounce steak, and therefore it is difficult to understand how dieticians in our vascular wards can continue to advise patients that an intake of 3 eggs per week is acceptable. There is evidence that egg yolks should not be consumed by patients at risk of vascular disease.

Ginsberg et al15showed a dose-response relationship between intake of eggs and increases in plasma cholesterol. Hu et al found that in diabetics, a group with a level of vascular risk equivalent to that of coronary survivors,16 consumption of 1 egg per day was associated with a doubling of coronary risk compared with <1 egg per week.17 It may be that this relates to dietary intake of oxidized cholesterol. Levy et al18 showed that an egg per day only raises levels of LDL cholesterol by 10% but increased LDL oxidation by 34%.

In the Indo-Mediterranean Diet Study, discussed below, the intake of cholesterol in the intervention arm was only 125 mg/d. A single egg yolk thus contains more than twice the daily intake of cholesterol achieved in that diet; so does an 8-ounce steak. A diet suitable for patients with vascular disease should therefore include no egg yolks and much less animal flesh, of any color, than North Americans are used to consuming. (The cholesterol content of all kinds of animal flesh is very similar; the emphasis on avoidance of red meat is based on the effects on fasting lipids of saturated fat, which is higher in red meat.)


*    Benefits of a Mediterranean Diet
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowCholesterol and Animal Fat
*Benefits of a Mediterranean...
down arrowClinical Trials With the...
down arrowBeneficial Effects of...
down arrowB Vitamins for Lowering...
down arrowConclusion
down arrowReferences
 
The Ornish regression diet, together with other lifestyle changes, has been shown to regress coronary disease.19 However, it is very difficult for patients to persist with it. Among >16 000 patients with vascular disease that I have followed, only 2 were able to persist with the Ornish diet. A more palatable and acceptable diet is a Mediterranean diet, which is high in beneficial oils (from olive, canola, and fish), high in vitamins and antioxidants, and low in cholesterol, trans fats, and harmful animal fat. A recent Japanese prospective study with 477 325 person-years of follow-up showed a 37% reduction of coronary disease when the highest versus lowest quartiles of fish intake were compared.20

A Mediterranean diet has been shown to improve endothelial function in hyperlipidemic men,21 perhaps in part because it reduces plasma lipid peroxidation.22 Vogel et al23 found that the components of a Mediterranean diet that were responsible for this benefit appeared to be antioxidant-rich foods, including vegetables, fruits, balsamic vinegar, and omega-3–rich fish and canola oil.

There is epidemiological evidence that people who follow a Mediterranean diet are at much lower risk of cardiovascular events.24,25 A Mediterranean diet has also been shown to improve endothelial function and reduce insulin resistance.26

More importantly, there is strong evidence from randomized clinical trials that a Cretan Mediterranean diet is much more effective at reducing vascular events than the diet recommended by the NCEP and the American Heart Association.


*    Clinical Trials With the Cretan Mediterranean Diet
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowCholesterol and Animal Fat
up arrowBenefits of a Mediterranean...
*Clinical Trials With the...
down arrowBeneficial Effects of...
down arrowB Vitamins for Lowering...
down arrowConclusion
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Two important studies have shown that a Mediterranean diet significantly reduced vascular events compared with a usual Western diet.

In the Lyon Diet Heart Study, 423 survivors of myocardial infarction (MI) were randomized to a "prudent Western diet" amounting to a Step 1 NCEP diet14 or to a Mediterranean diet from Crete. This diet was low in cholesterol, low in animal fat, and high in olive oil, canola oil, fruits, and vegetables; canola margarine was substituted for butter. The proportion of calories from fat was the same (&30%) in the 2 diets, but the Mediterranean diet provided a significant reduction in dietary cholesterol and a significant increase of beneficial oils such as {alpha}-linolenic acid as opposed to the animal fats of the prudent Western diet. The patients assigned to the Mediterranean diet27 had a 60% reduction in cardiac death and MI over 4 years (P=0.0001) compared with the prudent Western diet. Importantly, there was no difference in alcohol consumption between the 2 diets.

This reduction in MI and death was twice that achieved by simvastatin in the Scandinavian Simvastatin Survival Study (a reduction of coronary risk by 40% over 6 years).28 Importantly, this benefit was achieved without any difference in fasting lipids between the 2 groups. It seems very likely that the benefit was attributable to reduction of postprandial fat, as well as the increased intake of antioxidants and other beneficial constituents of the Mediterranean diet. Whole grains, in addition to antioxidants and fiber, contain phytoestrogens, which may have beneficial effects on arteries.29 Flax lignans, for example, are potent phytoestrogens.30

These results have been replicated in a study of 1000 patients with coronary artery disease in India. Even though 60% of patients were already vegetarian, a Mediterranean version of the Indian diet reduced coronary and stroke events by half in 2 years, compared with an Indian version of a NCEP Step II diet.31 This was achieved by substituting beneficial oils such as mustard oil or soya oil for harmful fats, with an increase of fruits, vegetables, walnuts, almonds, and whole grains, and a reduction of cholesterol intake to 125 mg/d. Although there has been some concern about the validity of the Indo-Mediterranean diet study,32 an investigation by Berry indicated that despite some problems with record keeping, the results did not appear to be fabricated.33


*    Beneficial Effects of Antioxidant Vitamins?
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowCholesterol and Animal Fat
up arrowBenefits of a Mediterranean...
up arrowClinical Trials With the...
*Beneficial Effects of...
down arrowB Vitamins for Lowering...
down arrowConclusion
down arrowReferences
 
A single high-fat meal has been shown to impair endothelial function for several hours,10 and this effect can be reduced by pretreatment with vitamins C and E.11 A Mediterranean diet has been shown to improve endothelial function in hyperlipidemic men.21 A Mediterranean diet has a higher content of antioxidants and significantly lower indices of plasma lipid peroxidation.22 Vogel et al23 studied the effect of components of the Mediterranean diet on endothelial function and found that the beneficial components appeared to be antioxidant-rich foods, including vegetables, fruits, balsamic vinegar, and omega-3–rich fish and canola oil.

Antioxidant vitamins may reduce vascular disease by reducing harmful effects of free radicals.34,35 Oxidation of LDL is thought to be important in atherosclerosis because oxidized LDL is chemotactic to monocytes, stimulates binding of monocytes to the endothelium, traps monocytes in the subendothelial space, and is cytotoxic to vascular cells; it is actively taken up by scavenger receptors on macrophages in the subintima to form foam cells.36 Antioxidants such as probucol and various dietary antioxidants are antiatherosclerotic in animal models and human angiographic studies,37 and epidemiological evidence indicates that high intake and high blood levels of antioxidants, particularly vitamin E, may be protective.36,38

A clinical trial in coronary patients showed reduced vascular death and nonfatal coronary events, although cardiovascular mortality was not reduced.39 In the Womens’ Health Initiative study, vitamin E had no beneficial effects.40 Meta-analysis showed no benefit, and possible harm, from high-dose supplements of vitamin E.41 In the Heart Outcomes Prevention Evaluation (HOPE) trial, vitamin E had no beneficial effects and appeared to increase the risk of heart failure.42 A recent pooled analysis of vitamins and antioxidants showed a small cardiovascular benefit of vitamin C.43 Confusion in this area may result from the need to combine vitamins: vitamin E forms the tocopheryl radical, which may require detoxification by other antioxidants such as vitamin C; Salonen et al44 hypothesized that this effect accounted for their finding of reduced progression of intima-media thickness by combined vitamin E and slow-release vitamin C.

This point raises a general principle that a diet high in antioxidant vitamins may be more beneficial than taking supplementary vitamins and antioxidants because of the combined effects of antioxidants.45 Fruits and vegetables often get their color and flavor from antioxidants: beta carotene in carrots; lycopene in tomatoes, strawberries, and watermelon; resveratrol in grape juice and red wine; and anthocyanins in blueberries. Naringin is the color and flavor of grapefruit; naringin is similar to hesperitin from orange juice and genistein from soy; all of these have beneficial anticancer effects and potential cardiovascular benefits.46–48 A useful slogan in this regard is that "we should eat fruits and vegetables of all colors."

An exception to this principle may be the use of B vitamins for lowering of homocysteine.


*    B Vitamins for Lowering of Homocysteine
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowCholesterol and Animal Fat
up arrowBenefits of a Mediterranean...
up arrowClinical Trials With the...
up arrowBeneficial Effects of...
*B Vitamins for Lowering...
down arrowConclusion
down arrowReferences
 
Despite recent reports of studies showing no reduction of stroke or MI by vitamin therapy for lowering of plasma total homocysteine,49–51 it may be too early to discard the hypothesis that treatment with folate, vitamin B6, and vitamin B12 may reduce stroke and other cardiovascular events. Indeed, the HOPE-2 trial showed a significant reduction of stroke and acute coronary syndrome. There is a strong, independent, and graded risk of elevated total homocysteine,52,53 and many mechanisms provide a strong rationale for lowering of homocysteine: High levels of total homocysteine increase thrombosis,54 impair endothelial function,55–57 and increase oxidative stress.58–60 Treatment to lower total homocysteine with folate, B6, and B12 reverses many of these effects and has other benefits, including reducing Lp(a) and fibrinogen,61 halting the progression of carotid plaque in patients whose plaque was progressing despite treatment of traditional risk factors,62,63 reducing progression of peripheral vascular disease,64 and, in 1 study, reducing restenosis in coronary angioplasty.65 A contrary study, which did not show benefit of vitamin therapy in coronary angioplasty, used a much smaller dose of B12 (40 versus 400 ìg/d).66

This discrepancy raises the issue of unrecognized deficiency of vitamin B12 in the elderly and its relationship to failure of B vitamin therapy in lowering of homocysteine. The Vitamin Intervention for Stroke Prevention (VISP) trial, which showed no reduction of stroke, coronary events, or vascular death in a comparison of high-dose vitamins with low-dose vitamins, faced a number of challenges. Folate fortification of grain products in North America coincided with the start of the trial, and in the face of folate fortification, the key determinant of plasma homocysteine is vitamin B12.67 Both treatment arms received a multiple vitamin tablet containing the usual doses of many vitamins, with either a low or high dose of folate, B6, and B12. Unfortunately, the low-dose arm received the recommended daily intake of B12 (6 ìg), and the high-dose arm received only 400 ìg of B12. We thought that we were using a generous dose of B12 in the high-dose arm, but a subsequent dose-response study in people aged >65 years with serum B12 <212 pmol/L showed that elderly subjects require much higher doses, of 1000 µg/d or more.68 In both treatment arms, patients with low levels of B12 received injections of B12 to avoid subacute combined degeneration of the spinal cord.

In a recent efficacy analysis of the VISP trial, patients capable of responding to the study vitamin were found to have a significant reduction of stroke, death, and coronary disease, and B12 status at the beginning of the trial was a significant determinant of response.69

Vitamin B12 deficiency is much more common in the elderly than is usually recognized because many factors are involved in absorption of B12, all of which may go wrong. The conceptual problem for many physicians is the meaning of the word normal. Most biochemistry laboratories report a "normal" or "reference" range based on the mean ±2 SD. Thus, by definition, only the top 2.5% and the bottom 2.5% of the population are abnormal. This statistical definition of normality results in a "normal" range for serum B12 of &160 to 600 pmol/L, and most physicians think that if the serum B12 level is in the normal range, then it is adequate. However, when adequacy of B12 is assessed in metabolic terms, ie, the level of B12 sufficient to prevent an elevation of methylmalonic acid >271 nmol/L or homocysteine >14 ìmol/L in folate-replete patients, then a much higher proportion of the population is identified as deficient in B12. In the Framingham Study, 40% of the elderly had B12 levels <258 pmol/L, and 12% were B12 deficient. Andres et al70 found that 20% of the elderly are B12 deficient. In my Stroke Prevention Clinic, the "normal" range is substantially lower than in a general population (Figure). A previously unpublished analysis of the database used for the study by Robertson et al67 from our clinic revealed a prevalence of B12 deficiency defined metabolically as above, by tertiles of age, of 12% below age 50 years, 13% between ages 50 and 71 years, and 30% at age 71 years or older.


Figure 1
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Serum B12 levels in a stroke prevention clinic.

To successfully reduce total homocysteine to sufficiently low targets may, in the future, require higher doses of B12. As suggested by Loscalzo,71 it may also require other therapies. Promising candidates include betaine72 and thiols.73–75


*    Conclusion
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowCholesterol and Animal Fat
up arrowBenefits of a Mediterranean...
up arrowClinical Trials With the...
up arrowBeneficial Effects of...
up arrowB Vitamins for Lowering...
*Conclusion
down arrowReferences
 
Diet is much more important for stroke prevention and B12 deficiency is much more common in the elderly than is commonly realized. Patients at risk of stroke should consume a Cretan Mediterranean diet, avoid egg yolks, eat less animal flesh than do most North Americans, and require higher doses of B12, and in the future they may benefit from improved therapies to lower levels of total homocysteine.


*    Acknowledgments
 
Disclosures

None.

Received May 26, 2006; accepted June 5, 2006.


*    References
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowCholesterol and Animal Fat
up arrowBenefits of a Mediterranean...
up arrowClinical Trials With the...
up arrowBeneficial Effects of...
up arrowB Vitamins for Lowering...
up arrowConclusion
*References
 
1. Ginsberg HN, Barr SL, Gilbert A, Karmally W, Deckelbaum R, Kaplan K, Ramakrishnan R, Holleran S, Dell RB. Reduction of plasma cholesterol levels in normal men on an American Heart Association Step 1 diet or a Step 1 diet with added monounsaturated fat. N Engl J Med. 1990; 322: 574–579.[Abstract]

2. Nissen SE, Nicholls SJ, Sipahi I, Libby P, Raichlen JS, Ballantyne CM, Davignon J, Erbel R, Fruchart JC, Tardif JC, Schoenhagen P, Crowe T, Cain V, Wolski K, Goormastic M, Tuzcu EM, for the ASTEROID Investigators. Effect of very high-intensity statin therapy on regression of coronary atherosclerosis: the ASTEROID trial. JAMA. 2006; 295: 1556–1565.[Abstract/Free Full Text]

3. Dandona P, Mohanty P, Ghanim H, Aljada A, Browne R, Hamouda W, Prabhala A, Afzal A, Garg R. The suppressive effect of dietary restriction and weight loss in the obese on the generation of reactive oxygen species by leukocytes, lipid peroxidation, and protein carbonylation. J Clin Endocrinol Metab. 2001; 86: 355–362.[Abstract/Free Full Text]

4. Mohanty P, Hamouda W, Garg R, Aljada A, Ghanim H, Dandona P. Glucose challenge stimulates reactive oxygen species (ROS) generation by leucocytes. J Clin Endocrinol Metab. 2000; 85: 2970–2973.[Abstract/Free Full Text]

5. Spence JD. Fasting lipids: the carrot in the snowman. Can J Cardiol. 2003; 19: 890–892.[Medline] [Order article via Infotrieve]

6. Oh K, Hu FB, Cho E, Rexrode KM, Stampfer MJ, Manson JE, Liu S, Willett WC. Carbohydrate intake, glycemic index, glycemic load, and dietary fiber in relation to risk of stroke in women. Am J Epidemiol. 2005; 161: 161–169.[Abstract/Free Full Text]

7. Willett WC, Stampfer MJ. Rebuilding the food pyramid. Sci Am. 2003; 288: 64–71.[Medline] [Order article via Infotrieve]

8. Steiner G. Triglyceride-rich lipoproteins and atherosclerosis, from fast to feast. Ann Med. 1993; 25: 431–435.[Medline] [Order article via Infotrieve]

9. Gronholdt ML, Nordestgaard BG, Nielsen TG, Sillesen H. Echolucent carotid artery plaques are associated with elevated levels of fasting and postprandial triglyceride-rich lipoproteins. Stroke. 1996; 27: 2166–2172.[Abstract/Free Full Text]

10. Vogel RA, Corretti MC, Plotnick GD. Effect of a single high-fat meal on endothelial function in healthy subjects. Am J Cardiol. 1997; 79: 350–354.[CrossRef][Medline] [Order article via Infotrieve]

11. Plotnick GD, Corretti MC, Vogel RA. Effect of antioxidant vitamins on the transient impairment of endothelium-dependent brachial artery vasoactivity following a single high-fat meal. JAMA. 1997; 278: 1682–1686.[Abstract/Free Full Text]

12. Carluccio MA, Massaro M, Bonfrate C, Siculella L, Maffia M, Nicolardi G, Distante A, Storelli C, De Caterina R. Oleic acid inhibits endothelial activation: a direct vascular antiatherogenic mechanism of a nutritional component in the Mediterranean diet. Arterioscler Thromb Vasc Biol. 1999; 19: 220–228.[Abstract/Free Full Text]

13. Tsimikas S, Philis-Tsimikas A, Alexopoulos S, Sigari F, Lee C, Reaven PD. LDL isolated from Greek subjects on a typical diet or from American subjects on an oleate-supplemented diet induces less monocyte chemotaxis and adhesion when exposed to oxidative stress. Arterioscler Thromb Vasc Biol. 1999; 19: 122–130.[Abstract/Free Full Text]

14. Adult Treatment Panel III. Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III): final report. Circulation. 2002; 106: 3143–3421.[Free Full Text]

15. Ginsberg HN, Karmally W, Siddiqui M, Holleran S, Tall AR, Rumsey SC, Deckelbaum RJ, Blaner WS, Ramakrishnan R. A dose-response study of the effects of dietary cholesterol on fasting and postprandial lipid and lipoprotein metabolism in healthy young men. Arterioscler Thromb. 1994; 14: 576–586.[Abstract/Free Full Text]

16. Haffner SM, Lehto S, Ronnemaa T, Pyorala K, Laakso M. Mortality from coronary heart disease in subjects with type 2 diabetes and in nondiabetic subjects with and without prior myocardial infarction. N Engl J Med. 1998; 339: 229–234.[Abstract/Free Full Text]

17. Hu FB, Stampfer MJ, Rimm EB, Manson JE, Ascherio A, Colditz GA, Rosner BA, Spiegelman D, Speizer FE, Sacks FM, Hennekens CH, Willett WC. A prospective study of egg consumption and risk of cardiovascular disease in men and women. JAMA. 1999; 281: 1387–1394.[Abstract/Free Full Text]

18. Levy Y, Maor I, Presser D, Aviram M. Consumption of eggs with meals increases the susceptibility of human plasma and low-density lipoprotein to lipid peroxidation. Ann Nutr Metab. 1996; 40: 243–251.[Medline] [Order article via Infotrieve]

19. Ornish d, Schwerwitz 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.[Abstract/Free Full Text]

20. Iso H, Kobayashi M, Ishihara J, Sasaki S, Okada K, Kita Y, Kokubo Y, Tsugane S, for the JPHC Study Group. Intake of fish and n3 fatty acids and risk of coronary heart disease among Japanese: the Japan Public Health Center-Based (JPHC) Study Cohort I. Circulation. 2006; 113: 195–202.[Abstract/Free Full Text]

21. Fuentes F, Lopez-Miranda J, Sanchez E, Sanchez F, Paez J, Paz-Rojas E, Marin C, Gomez P, Jimenez-Pereperez J, Ordovas JM, Perez-Jimenez F. Mediterranean and low-fat diets improve endothelial function in hypercholesterolemic men. Ann Intern Med. 2001; 134: 1115–1119.[Abstract/Free Full Text]

22. Mancini M, Parfitt VJ, Rubba P. Antioxidants in the Mediterranean diet. Can J Cardiol. 1995; 11 (suppl G): 105G–109G.[Medline] [Order article via Infotrieve]

23. Vogel RA, Corretti MC, Plotnick GD. The postprandial effect of components of the Mediterranean diet on endothelial function. J Am Coll Cardiol. 2000; 36: 1455–1460.[Abstract/Free Full Text]

24. Knoops KT, de Groot LC, Kromhout D, Perrin AE, Moreiras-Varela O, Menotti A, van Staveren WA. Mediterranean diet, lifestyle factors, and 10-year mortality in elderly European men and women: the HALE project. JAMA. 2004; 292: 1433–1439.[Abstract/Free Full Text]

25. Rimm EB, Stampfer MJ. Diet, lifestyle, and longevity: the next steps? JAMA. 2004; 292: 1490–1492.[Free Full Text]

26. 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.[Abstract/Free Full Text]

27. de Lorgeril M, Salen P, Martin JL, Monjaud I, Delaye J, Mamelle N. Mediterranean diet, traditional risk factors, and the rate of cardiovascular complications after myocardial infarction: final report of the Lyon Diet Heart Study. Circulation. 1999; 99: 779–785.[Abstract/Free Full Text]

28. Scandinavian Simvastatin Survival Study Group. Randomized trial of cholesterol lowering in 4,444 patients with coronary heart disease: the Scandinavian Simvastatin Survival Study (4S). Lancet. 1994; 344: 1383–1389.[CrossRef][Medline] [Order article via Infotrieve]

29. Flight I, Clifton P. Cereal grains and legumes in the prevention of coronary heart disease and stroke: a review of the literature. Eur J Clin Nutr. 2006; May 3 [Epub ahead of print].

30. Spence JD, Thornton T, Muir AD, Westcott ND. The effect of flax seed cultivars with differing content of alpha-linolenic acid and lignans on responses to mental stress. J Am Coll Nutr. 2003; 22: 494–501.[Abstract/Free Full Text]

31. Singh RB, Dubnov G, Niaz MA, Ghosh S, Singh R, Rastogi SS, Manor O, Pella D, Berry EM. Effect of an Indo-Mediterranean diet on progression of coronary artery disease in high-risk patients (Indo-Mediterranean Diet Heart Study): a randomized single-blind trial. Lancet. 2002; 360: 1455–1461.[CrossRef][Medline] [Order article via Infotrieve]

32. Horton R. Expression of concern: Indo-Mediterranean Diet Heart Study. Lancet. 2005; 366: 354–356.[CrossRef][Medline] [Order article via Infotrieve]

33. Berry EM. Indo-Mediterranean diet and progression of coronary artery disease. Lancet. 2005; 366: 367.[CrossRef][Medline] [Order article via Infotrieve]

34. Spence JD. Vitamins and antioxidants. In: Bogousslavsky J, ed. Drug Therapy for Stroke Prevention. New York, NY: Taylor & Francis; 2001: 231–252.

35. Brody T. Nutritional Chemistry. 2nd ed. San Diego, Calif: Academic Press; 1999.

36. Diaz MN, Frei B, Vita JA, Keaney JF Jr. Antioxidants and atherosclerotic heart disease. N Engl J Med. 1997; 337: 408–416.[Free Full Text]

37. Tardif JC, Cote G, Lesperance J, Bourassa M, Lambert J, Doucet S, Bilodeau L, Nattel S, de Guise P, for the Multivitamins and Probucol Study Group. Probucol and multivitamins in the prevention of restenosis after coronary angioplasty. N Engl J Med. 1997; 337: 365–372.[Abstract/Free Full Text]

38. Gaziano JM. Vitamin E and cardiovascular disease: observational studies. Ann N Y Acad Sci. 2004; 1031: 280–291.[CrossRef][Medline] [Order article via Infotrieve]

39. Stephens NG, Parsons A, Schofield PM, Kelly F, Cheeseman K, Mitchinson MJ. Randomised controlled trial of vitamin E in patients with coronary disease: Cambridge Heart Antioxidant Study (CHAOS). Lancet. 1996; 347: 781–786.[CrossRef][Medline] [Order article via Infotrieve]

40. Lee IM, Cook NR, Gaziano JM, Gordon D, Ridker PM, Manson JE, Hennekens CH, Buring JE. Vitamin E in the primary prevention of cardiovascular disease and cancer: the Women’s Health Study: a randomized controlled trial. JAMA. 2005; 294: 56–65.[Abstract/Free Full Text]

41. Miller ER III, Pastor-Barriuso R, Dalal D, Riemersma RA, Appel LJ, Guallar E. Meta-analysis: high-dosage vitamin E supplementation may increase all-cause mortality. Ann Intern Med. 2005; 142: 37–46.[Abstract/Free Full Text]

42. Lonn E, Bosch J, Yusuf S, Sheridan P, Pogue J, Arnold JM, Ross C, Arnold A, Sleight P, Probstfield J, Dagenais GR, for the HOPE and HOPE-TOO Trial Investigators. Effects of long-term vitamin E supplementation on cardiovascular events and cancer: a randomized controlled trial. JAMA. 2005; 293: 1338–1347.[Abstract/Free Full Text]

43. Knekt P, Ritz J, Pereira MA, O’Reilly EJ, Augustsson K, Fraser GE, Goldbourt U, Heitmann BL, Hallmans G, Liu S, Pietinen P, Spiegelman D, Stevens J, Virtamo J, Willett WC, Rimm EB, Ascherio A. Antioxidant vitamins and coronary heart disease risk: a pooled analysis of 9 cohorts. Am J Clin Nutr. 2004; 80: 1508–1520.[Abstract/Free Full Text]

44. Salonen RM, Nyyssonen K, Kaikkonen J, Porkkala-Sarataho E, Voutilainen S, Rissanen TH, Tuomainen TP, Valkonen VP, Ristonmaa U, Lakka HM, Vanharanta M, Salonen JT, Poulsen HE. Six-year effect of combined vitamin C and E supplementation on atherosclerotic progression: the Antioxidant Supplementation in Atherosclerosis Prevention (ASAP) Study. Circulation. 2003; 107: 947–953.[Abstract/Free Full Text]

45. Woodside JV, McCall D, McGartland C, Young IS. Micronutrients: dietary intake v. supplement use. Proc Nutr Soc. 2005; 64: 543–553.[CrossRef][Medline] [Order article via Infotrieve]

46. Kurowska EM, Spence JD, Jordan J, Wetmore S, Freeman DJ, Piche LA, Serratore P. HDL-cholesterol-raising effect of orange juice in subjects with hypercholesterolemia. Am J Clin Nutr. 2000; 72: 1095–1100.[Abstract/Free Full Text]

47. Borradaile NM, de Dreu LE, Barrett PH, Behrsin CD, Huff MW. Hepatocyte apoB-containing lipoprotein secretion is decreased by the grapefruit flavonoid, naringenin, via inhibition of MTP-mediated microsomal triglyceride accumulation. Biochemistry. 2003; 42: 1283–1291.[CrossRef][Medline] [Order article via Infotrieve]

48. Borradaile NM, Carroll KK, Kurowska EM. Regulation of HepG2 cell apolipoprotein B metabolism by the citrus flavanones hesperetin and naringenin. Lipids. 1999; 34: 591–598.[Medline] [Order article via Infotrieve]

49. Toole JF, Malinow MR, Chambless LE, Spence JD, Pettigrew LC, Howard VJ, Sides EG, Wang CH, Stampfer M. Lowering homocysteine in patients with ischemic stroke to prevent recurrent stroke, myocardial infarction, and death: the Vitamin Intervention for Stroke Prevention (VISP) randomized controlled trial. JAMA. 2004; 291: 565–575.[Abstract/Free Full Text]

50. Lonn E, Yusuf S, Arnold MJ, Sheridan P, Pogue J, Micks M, McQueen MJ, Probstfield J, Fodor G, Held C, Genest J Jr, for the Heart Outcomes Prevention Evaluation (HOPE) 2 Investigators. Homocysteine lowering with folic acid and B vitamins in vascular disease. N Engl J Med. 2006; 354: 1567–1577.[Abstract/Free Full Text]

51. Bonaa KH, Njolstad I, Ueland PM, Schirmer H, Tverdal A, Steigen T, Wang H, Nordrehaug JE, Arnesen E, Rasmussen K, for the NORVIT Trial Investigators. Homocysteine lowering and cardiovascular events after acute myocardial infarction. N Engl J Med. 2006; 354: 1578–1588.[Abstract/Free Full Text]

52. Clarke R, Daly L, Robinson K, Naughten E, Cahalane S, Fowler B, Graham I. Hyperhomocysteinemia: an independent risk factor for vascular disease. N Engl J Med. 1991; 324: 1149–1155.[Abstract]

53. Nygård O, Nordrehaug JE, Refsum H, Ueland PM, Farstad M, Vollset SE. Plasma homocysteine levels and mortality in patients with coronary artery disease. N Engl J Med. 1997; 337: 230–236.[Abstract/Free Full Text]

54. den Heijer M, Rosendaal FR, Blom HJ, Gerrits WB, Bos GM. Hyperhomocysteinemia and venous thrombosis: a meta-analysis. Thromb Haemost. 1998; 80: 874–877.[Medline] [Order article via Infotrieve]

55. Bellamy MF, McDowell IF, Ramsey MW, Brownlee M, Bones C, Newcombe RG, Lewis MJ. Hyperhomocysteinemia after an oral methionine load acutely impairs endothelial function in healthy adults. Circulation. 1998; 98: 1848–1852.[Abstract/Free Full Text]

56. Chambers JC, McGregor A, Jean-Marie J, Kooner JS. Acute hyperhomocysteinaemia and endothelial dysfunction. Lancet. 1998; 351: 36–37.[Medline] [Order article via Infotrieve]

57. Stamler JS, Osborne JA, Jaraki O, Rabbani LE, Mullins M, Singel D, Loscalzo J. Adverse vascular effects of homocysteine are modulated by endothelium-derived relaxing factor and related oxides of nitrogen. J Clin Invest. 1993; 91: 308–318.[Medline] [Order article via Infotrieve]

58. Dudman NP, Wilcken DE, Stocker R. Circulating lipid hydroperoxide levels in human hyperhomocysteinemia: relevance to development of arteriosclerosis. Arterioscler Thromb. 1993; 13: 512–516.[Abstract/Free Full Text]

59. Voutilainen S, Morrow JD, Roberts LJ, Alfthan G, Alho H, Nyyssonen K, Salonen JT. Enhanced in vivo lipid peroxidation at elevated plasma total homocysteine levels. Arterioscler Thromb Vasc Biol. 1999; 19: 1263–1266.[Abstract/Free Full Text]

60. Zhang F, Slungaard A, Vercellotti GM, Iadecola C. Superoxide-dependent cerebrovascular effects of homocysteine. Am J Physiol. 1998; 274 (pt 2): R1704–R1711.[Medline] [Order article via Infotrieve]

61. Naruszewicz M, Klinke M, Dziewanowski K, Staniewicz A, Bukowska H. Homocysteine, fibrinogen, and lipoprotein(a) levels are simultaneously reduced in patients with chronic renal failure treated with folic acid, pyridoxine, and cyanocobalamin. Metabolism. 2001; 50: 131–134.[CrossRef][Medline] [Order article via Infotrieve]

62. Peterson JC, Spence JD. Vitamins and progression of atherosclerosis in patients with hyper-homocyst(e)inemia. Lancet. 1998; 351: 263.[Medline] [Order article via Infotrieve]

63. Hackam DG, Peterson JC, Spence JD. What level of plasma homocyst(e)ine should be treated? Effects of vitamin therapy on progression of carotid atherosclerosis in patients with homocyst(e)ine levels above and below 14mol/L. Am J Hypertens. 2000; 13: 105–110.[CrossRef][Medline] [Order article via Infotrieve]

64. Taylor LM Jr, Moneta GL, Sexton GJ, Schuff RA, Porter JM. Prospective blinded study of the relationship between plasma homocysteine and progression of symptomatic peripheral arterial disease. J Vasc Surg. 1999; 29: 8–19.[CrossRef][Medline] [Order article via Infotrieve]

65. Schnyder G, Roffi M, Pin R, Flammer Y, Lange H, Eberli FR, Meier B, Turi ZG, Hess OM. Decreased rate of coronary restenosis after lowering of plasma homocysteine levels. N Engl J Med. 2001; 345: 1593–1600.[Abstract/Free Full Text]

66. Lange H, Suryapranata H, De Luca G, Borner C, Dille J, Kallmayer K, Pasalary MN, Scherer E, Dambrink JH. Folate therapy and in-stent restenosis after coronary stenting. N Engl J Med. 2004; 350: 2673–2681.[Abstract/Free Full Text]

67. Robertson J, Iemolo F, Stabler SP, Allen RH, Spence JD. Increased importance of vitamin B12 for total homocysteine and carotid plaque in the era of folate fortification of the grain supply. CMAJ. 2005; 172: 1569–1573.[Abstract/Free Full Text]

68. Rajan S, Wallace JI, Brodkin KI, Beresford SA, Allen RH, Stabler SP. Response of elevated methylmalonic acid to three dose levels of oral cobalamin in older adults. J Am Geriatr Soc. 2002; 50: 1789–1795.[CrossRef][Medline] [Order article via Infotrieve]

69. Spence JD, Bang H, Chambless LE, Stampfer MJ. Vitamin Intervention for Stroke Prevention Trial: an efficacy analysis. Stroke. 2005; 36: 2404–2409.[Abstract/Free Full Text]

70. Andres E, Loukili NH, Noel E, Kaltenbach G, Abdelgheni MB, Perrin AE, Noblet-Dick M, Maloisel F, Schlienger JL, Blickle JF. Vitamin B12 (cobalamin) deficiency in elderly patients. CMAJ. 2004; 171: 251–259.[Abstract/Free Full Text]

71. Loscalzo J. Homocysteine trials: clear outcomes for complex reasons. N Engl J Med. 2006; 354: 1629–1632.[Free Full Text]

72. Olthof MR, van VT, Boelsma E, Verhoef P. Low dose betaine supplementation leads to immediate and long term lowering of plasma homocysteine in healthy men and women. J Nutr. 2003; 133: 4135–4138.[Abstract/Free Full Text]

73. House AA, Eliasziw M, Urquhart BL, Freeman DJ, Spence JD. Dimercaptosuccinic acid for the treatment of hyperhomocysteinemia in hemodialysis patients: a placebo-controlled, double-blind, randomized trial. Am J Kidney Dis. 2004; 44: 689–694.[CrossRef][Medline] [Order article via Infotrieve]

74. Urquhart BL, House AA, Cutler MJ, Spence JD, Freeman DJ. Thiol exchange: an in vitro assay that predicts the efficacy of novel homocysteine lowering therapies J Pharm Sci. 2006; Jun 22 [Epub ahead of print].

75. Pendyala L, Schwartz G, Smith P, Zdanowicz J, Murphy M, Hausheer F. Modulation of plasma thiols and mixed disulfides by BNP7787 in patients receiving paclitaxel/cisplatin therapy. Cancer Chemother Pharmacol. 2003; 51: 376–384.[Medline] [Order article via Infotrieve]




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