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Juin 2006
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FMC Omega-3 fatty acids Their beneficial role in cardiovascular health Gerry Schwalfenberg, MD, CCFP
Dr Schwalfenberg is a family physician in full-time solo practice. He is a member of the Department of Family Practice at the Misericordia Hospital in Edmonton, Alta. During the last decade, the amount of research on omega-3 fatty acids has increased substantially. As a result, new guidelines recommend that patients at risk of cardiovascular (CV) disease increase their dietary intake of omega-3 fatty acids. This article looks at the role of omega-3 fatty acids of marine (eicosapentenoic acid [EPA], docosahexaenoic acid [DHA]) and plant (alpha-linolenic acid [ALA]) origin in CV health in order to bring family physicians up-to-date on current evidence. Quality of evidence Studies providing level I, II, and III evidence of the benefits of omega-3 fatty acids are reviewed in this article. MEDLINE was searched using the words “omega-3 fatty acids” and “fish oil” combined with “hypertension,” “coronary artery disease,” and “hypertriglyceridemia.” Trials involving humans were chosen.1-16 Omega-3 and omega-6 fatty acids The lipids essential for health are the omega-3 and omega-6 polyunsaturated fatty acids (PUFA).17 Interest in omega-3 fatty acids began in 1972. Studies by Bang and Dyerberg3 showed that Greenland Inuit who consumed a diet high in protein and fat (mainly from fish) had significantly lower total cholesterol (P < .005), low-density lipoprotein (LDL)(P < .02), and triglyceride (P < .005) levels than most other people had. Since then, much has been learned about the interaction of omega-6 and omega-3 fatty acids in CV disease and about the ratio between omega-6 and omega-3 fatty acids.18,19 Dietary intake of omega-3 fatty acids has decreased, and dietary intake of omega-6 fatty acids has substantially increased during the last 100 years due to greater use of vegetable oils high in omega-6 fatty acids.18,20 The ratio of omega-6 to omega-3 was about 1.5:1 as recently as 200 years ago and now is estimated at 16:1 in the average North American diet.18 This has resulted in a diet high in omega-6 fatty acids and deficient in omega-3 fatty acids.21
Hypertension
Trials are listed in Table 2.1-16 Geleijnse et al1 did a meta-analysis of 36 randomized trials (22 of which were double blind) carried out between 1966 and 2001 (level I evidence). The meta-analysis showed that consuming an average of 3.7 g/d of fish oil reduced systolic blood pressure (BP) by 2.1 mm Hg (P < .01) and diastolic BP by 1.6 mm Hg (P < .01). The BP-lowering effects were greater in people older than 45 years and in those whose BP was higher than 140/90 mm Hg. A meta-analysis (level I evidence) done by Appel et al2 found a significant reduction in BP (5.5 mm Hg systolic BP and 3.5 mm Hg diastolic BP) in untreated hypertensive patients taking supplements of more than 3 g/d of omega-3 PUFA. High doses were required to achieve these results, and patients’ acceptance of the fishy taste and subsequent belching was poor (P < .001). Most trials lasted less than 3 months, so the long-term benefits are unclear. Heart disease Bang and Dyerberg3 and Dyerberg et al4 did epidemiologic studies (level II evidence) to establish the cardioprotective effects of omega-3 fatty acids from marine sources in the Inuit people of Greenland in the 1970s. Despite a high-fat diet, the incidence of CV disease was exceptionally low among these people. A Canadian study5 looking at James Bay Cree people reported fewer CV risk factors and higher levels of plasma omega-3 fatty acids in adult Cree living along the coast than in those living inland (level II evidence). In September 1989, the Diet and Reinfarction Trial (DART)6 (level II evidence) was the first study to show that subjects who followed advice to eat fatty fish (high in omega-3 fatty acids) had a 29% reduction in 2-year all-cause mortality (P < .05). The study allocated 2033 men to 3 groups: group 1 reduced their fat intake and increased their intake of PUFA, group 2 increased their fatty fish intake, and group 3 increased their cereal fibre intake.
The GISSI-Prevenzione trial (level I evidence)9,10 randomly assigned 11 324 patients surviving a recent MI into 4 groups: one took a capsule containing 850 mg/d of omega-3 fatty acids each day, another took 300 IU of vitamin E daily, a third group took both each day, and the control group took nothing. After 3.5 years, overall mortality was reduced by 20% and CV mortality was reduced by 30% in the group taking capsules of omega-3 fatty acids. No benefit was apparent from taking vitamin E alone. A 45% reduction in sudden cardiac death (P = .01) accounted for most of the benefit. Omega-3 fatty acids seem to be able to stabilize contractile heart cells electrically and thus prevent ventricular arrhythmias.23 A meta-analysis by Bucher et al11 (level I evidence) identified 11 trials published between 1966 and 1999 with a total of 7951 patients in intervention groups and 7855 in control groups. They found that intake of fish or fish oil reduced rates of overall mortality (P < .001), fatal MI (P < .001), and sudden cardiac death (P < .01). Mortality from coronary artery disease was reduced by 40% to 60% with consumption of 40 to 60 g of fish daily. Several studies, including the Cardiovascular Health Study,37 the Family Heart Study,38 the Health Professionals Follow-up Study,39 the Multiple Risk Factor Intervention Trial,40 and the Nurses’ Health Study,41 showed benefit of ALA in CV disease. The Zutphen Elderly Study,42 however, found a modest link between ALA and increased risk of CV disease. Excessive consumption of trans fatty acids might have contributed to this.
Severe familial hypertriglyceridemia Supplementation with omega-3 fatty acids has been shown to be of benefit in severe familial hypertriglyceridemia. Richter et al13 (level II evidence) demonstrated that adding 4.32 g/d of omega-3 fatty acids to the diet for 8 weeks reduced serum triglycerides from 18.29 to 10.1 mmol/L. Pschierer et al14 (level II evidence) showed that serum triglycerides had decreased significantly from 16.9 to 11.2 mmol/L after 1 month, and further decreased after 11 months to 10.1 mmol/L on average with supplementation with omega-3 fatty acids. Fish oil and HMG-CoA reductase inhibitors The effectiveness of statins can be improved by adding omega-3 fatty acids to the diet.43,44 A small study looked at combining statins and fish oil (level II evidence).15 Adding 900 to 1800 mg of EPA to the diet of patients already taking HMG-CoA reductase inhibitors resulted in a further decrease in total cholesterol from 5.63 to 5.02 mmol/L (P < .05) and in triglycerides from 2.07 to 1.08 mmol/L (P < .01). Serum HDL increased significantly from 1.23 to 1.34 mmol/L (P < .01). Cardiovascular surgery In a study done by Eritsland et al16 (level I evidence), 610 patients who underwent coronary artery bypass grafting were assigned to a fish-oil group (4 g/d of fish oil) or to a control group. The end point was patency of the graft at 1 year. A year later, vein graft occlusion was 27% in the experimental group and 33% in the control group (P = .034). Vein graft occlusion was inversely related to the relative change in serum omega-3 fatty acid levels. Initial studies done on coronary angioplasty patients45 showed that fish oil had promise for reducing recurring stenosis, but later studies using higher doses did not show any statistically significant reduction.46
Dietary suggestions, discussion, and recommendations In 1990, Canada was the first country to provide separate dietary recommendations for omega-6 and omega-3 fatty acids for people of all ages.47 For adults between 25 and 49 years old, Health Canada suggests 1500 mg of omega-3 and 9000 mg of omega-6 polyunsaturates daily for men and 1100 mg of omega-3 and 7000 mg of omega-6 fatty acids daily for women. This results in an omega-6–to–omega-3 ratio of 6:1. It is thought that most Canadians do not have this modest daily intake of omega-3 fatty acids. Dietary sources of omega-3 fatty acids and some instructions for making them palatable are shown in Table 3.48 Side effects and interactions associated with consumption of fish oil are listed in Table 4.49-53 The American Heart Association issued new recommendations on consumption of omega-3 fatty acids in 2003.48 These are listed in Table 548,54 along with recommendations from an expert round-table discussion at the 34th Annual Scientific Meeting of the European Society for Clinical Investigation.54
Conclusion There is now solid evidence that omega-3 fatty acids favourably modulate disease processes, such as hypertension, coronary artery disease, and hypertriglyceridemia. Increasing dietary intake of omega-3 fatty acids and bringing the ratio of omega-3 to omega-6 fatty acids into a healthy balance would improve Canadians’ cardiovascular health. Competing interests None declared Correspondence to: Dr G. Schwalfenberg, 9509—156 St, Suite 301, Edmonton AB T5P 4J5; telephone 780 484-1433; fax 780 489-1211; e-mail gschwals@telus.net
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Hu FB, Stampfer MA, Manson JE, Rimm EB, Wolk A, Colditz GA, et al. Dietary intake of alpha-linolenic acid and risk of fatal ischemic heart disease among women. Am J Clin Nutr 1999;69(5):890-7. 42. Oomen CM, Ocke MC, Feskens EJ, Kok FJ, Kromhout D. Alpha-Linolenic acid intake is not beneficially associated with 10-y risk of coronary artery disease incidence: the Zutphen Elderly Study. Am J Clin Nutr 2001;74(4):457-63. 43. Das UN. Essential fatty acids as possible mediators of the actions of statins. Prostaglandins Leukot Essent Fatty Acids 2001;65(1):37-40. 44. Nakamura N, Hamazaki T, Jokaji H, Minami S, Kobayashi M. Effect of HMG-CoA reductase inhibitors on plasma polyunsaturated fatty acid concentrations in patients with hyperlipidemia. Int J Clin Lab Res 1998;28(3):192-5. 45. Dehmer GJ, Popma JJ, van den Berg EK, Eichhom EJ, Prewitt JB, Campbell WB, et al. Reduction in the rate of early restenosis after coronary angioplasty by a diet supplemented with n-3 fatty acids. N Engl J Med 1988;319(12):733-40. 46. Johansen O, Brekke M, Seljeflot I, Abdelnoor M, Arnesen H. N-3 fatty acids do not prevent restenosis after coronary angioplasty: results from the CART study. Coronary Angioplasty Restenosis Trial. J Am Coll Cardiol 1999;33(6):1619-26. 47. Scientific Review Committee. Nutritional recommendations. (Document H49-42/1990E). Ottawa, Ont: National Health and Welfare Canada; 1990. 48. Kris-Etherton PM, Harris WS, Appel LJ. Fish consumption, fish oil, omega-3 fatty acids, and cardiovascular disease. Arterioscler Thromb Vasc Biol 2003;23(2):e20-30. 49. Buckley MS, Goff AD, Knapp WE. Fish oil interaction with warfarin. Ann Pharmacother 2004;38(1):50-2. 50. Bernard M, Gerbi A, Barbey O, Jamme I, Cozzone PJ, Maixent JM. Dietary fish oil promotes positive inotropy and efficiency of digitalis. Lipids 1999;34(Suppl):S195. 51. Eritsland J, Arnesen H, Seljeflot I, Kierulf P. Long-term effects of n-3 polyunsaturated fatty acids on haemostatic variables and bleeding episodes in patients with coronary artery disease. Blood Coagul Fibrinolysis 1995;6(1):17-22. 52. Lezaun A, Fraj J, Colas C, Duce F, Dominguez MA, Cuevas M, et al. Anaphylaxis from linseed. Allergy 1998;53(1):105-6. 53. Foran SE, Flood JG, Lewandrowski KB. Measurement of mercury levels in concentrated over-the-counter fish oil preparations: is fish oil healthier than fish? Arch Pathol Lab Med 2003;127(12):1603-5. 54. Nordoy A, Marchioli R, Arnesen H, Videbaek J. n-3 polyunsaturated fatty acids and cardiovascular diseases. Lipids 2001;36(Suppl):S127-9. |
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