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(Stroke. 2004;35:1538.)
© 2004 American Heart Association, Inc.
Original Contributions |
From the Department of Preventive Medicine (K.H., M.L.D., K.L., L.V.H., A.R.D., P.G.), Northwestern University Feinberg School of Medicine, Chicago, Ill; the Department of Nutrition (Y.S.), Harvard School of Public Health, Boston, Mass; and the Division of Epidemiology and Preventive Medicine (U.G.), Sackler Medical Faculty, Tel Aviv University, Tel Aviv, Israel.
Correspondence to Dr Ka He, Department of Preventive Medicine, The Feinberg School of Medicine, Northwestern University, 680 N Lake Shore Dr, Suite 1102, Chicago, IL 60611. E-mail kahe{at}northwestern.edu
| Abstract |
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Methods We searched the Medline and Embase databases (1966 through October 2003) and identified 9 independent cohorts (from 8 studies) that provided a relative risk (RR) and corresponding 95% CI for total or any type of stroke in relation to fish consumption. Pooled RR and 95% CI of stroke were estimated by variance-based meta-analysis.
Results Compared with those who never consumed fish or ate fish less than once per month, the pooled RRs for total stroke were 0.91 (95% CI, 0.79 to 1.06) for individuals with fish intake 1 to 3 times per month, 0.87 (95% CI, 0.77 to 0.98) for once per week, 0.82 (95% CI, 0.72 to 0.94) for 2 to 4 times per week, and 0.69 (95% CI, 0.54 to 0.88) for
5 times per week (P for trend=0.06). In stratified analyses of 3 large cohort studies with data on stroke subtypes, the pooled RRs across 5 categories of fish intake were 1.0, 0.69 (95% CI, 0.48 to 0.99), 0.68 (95% CI, 0.52 to 0.88), 0.66 (95% CI, 0.51 to 0.87), and 0.65 (95% CI, 0.46 to 0.93) for ischemic stroke (P for trend=0.24); and 1.0, 1.47 (95% CI, 0.81 to 2.69), 1.21 (95% CI, 0.78 to 1.85), 0.89 (95% CI, 0.56 to 1.40), and 0.80 (95% CI, 0.44 to 1.47) for hemorrhagic stroke (P for trend=0.31).
Conclusions These results suggest that intake of fish is inversely related to risk of stroke, particularly ischemic stroke. Fish consumption as seldom as 1 to 3 times per month may protect against the incidence of ischemic stroke.
Key Words: cerebrovascular accident fishes meta-analysis
| Introduction |
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A number of epidemiological studies have also examined the relationship between fish intake and risk of stroke. The preponderance of data derives from prospective cohort studies, but findings are conflicting. Some but not all cohort studies reported an inverse association between fish consumption and risk of stroke after adjustment for potential confounders.613 Differences in study populations, sample size, assessment of fish intake, and stroke end point, as well as adjustment for covariates, coupled with the fact that most studies did not separate ischemic from hemorrhagic stroke, may account for differences in assessing the effects of fish consumption on stroke risk. To provide a reliable quantitative assessment of the relationship of fish intake with stroke risk, we conducted a meta-analysis of all prospective cohort studies with relevant data. We also attempted to explore the major sources of heterogeneity among the reported studies.
| Materials and Methods |
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Data Extraction
The data we collected included the first authors name, year of publication, country of origin, duration of follow-up, range or mean of participants age, sample size, proportion of men, number of events, categories of fish intake, the amount of fish intake for each category, methods for measurement of fish intake, and adjusted covariates, as well as RRs and 95% CIs of total stroke and stroke subtypes in the corresponding categories. RRs transformed to their natural logarithms (ln), and the 95% CIs were used to calculate the corresponding SEs.
To standardize fish intake, we first converted frequency into grams per day. The amount of fish consumption (grams per day) was estimated by multiplying the frequency of consumption (servings per day) by the corresponding portion size (grams per serving). For example, the derived average portion size in the Health Professional Follow-Up Study was 105 g/serving. The range of fish consumption for 1 to 3 times per month was converted to 3.5 g/day (105/30) to 10.5 g/day. When the portion size of fish intake in an individual study was not available from the published article, the value was determined on the basis of data from the 2 largest cohort studies (the Nurses Health Study and the Health Professional Follow-Up Study), considering that the food frequency questionnaire (FFQ) used in these 2 studies has been validated.14,15 If the uppermost amount of the highest fish intake category was uncertain (eg, fish intake was
5 times per week), we assigned 1 daily serving of fish as the upper limit.
Statistical Analysis
Fish consumption was categorized into 5 standardized intervals: "never or less than once per month," "1 to 3 times per month," "once per week," "2 to 4 times per week," and "
5 times per week." We created a data set by assigning each RR extracted from each individual study into its corresponding standardized interval according to the range or median amount of fish intake in the category. If the median amount of fish consumption from more than 1 category in a single study fell into the same standardized category of fish intake in our meta-analysis, we pooled these RRs and used the combined estimate for that category. Also, if the range of fish intake covered more than 1 standardized category, we allocated RR on the basis of the median fish intake. We estimated the pooled RRs and 95% CIs of stroke for each standardized category of fish consumption compared with the lowest category using both fixed- and random-effects models. In the fixed-effects model, the pooled RR was obtained by averaging the ln RRs weighted by the inverses of their variances.16 In the random-effects model, DerSimonian and Lairds method was used to further incorporate the between-study variability.17 We reported the pooled estimate from the random-effects model if the test for heterogeneity was significant. Formal tests of between-study heterogeneity were performed using a
2 test. To test for linear trend, a weighted linear regression was used to model the ln RR for stroke as a function of continuous fish intake derived from the median intake of each category using the inverse of the variance as the study weight.
In stratified meta-analyses, we examined potential sources of heterogeneity, including gender, methods of dietary assessment (FFQ versus in-person interview), and subtypes of stroke (ischemic and hemorrhagic).16 All analyses were performed using STATA statistical software (Version 7.0; STATA Corp).
| Results |
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Compared with those who never consumed fish or ate fish less than once per month, individuals with higher fish intake had lower risk of total stroke (Table 2). The reduction in risk of total stroke was statistically significant for fish intake once per week (RR, 0.87; 95% CI, 0.77 to 0.98). Beneficial effects on stroke risk appeared to increase with greater fish intake. For individuals who ate fish
5 times per week, the risk of stroke was lower by 31% (RR, 0.69; 95% CI, 0.54 to 0.88). However, the test for linear trend was statistically nonsignificant (P for trend=0.06). In addition, there was no evidence for the presence of significant heterogeneity among the 9 cohorts (
28=12.5; P=0.13; see Figure).
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In the stratified analyses, the inverse association between fish intake and risk of stroke was slightly attenuated among men. Also, this association was somewhat weaker in studies using in-person interviews (Table 2). On the basis of 3 large studies that provided data on stroke subtypes, we found an inverse threshold association between fish intake and ischemic stroke. The risk of ischemic stroke was reduced significantly by eating fish 1 to 3 times per month. For hemorrhagic stroke, we did not observe any significant association with fish intake (Table 2). Given the nonlinear relations between fish consumption and stroke risk, we further dichotomized fish intake as less than once per month versus at least once per month. The pooled RR for those who consumed fish at least once per month were 0.85 (95% CI, 0.79 to 0.91) for total stroke, 0.67 (95% CI, 0.58 to 0.78) for ischemic stroke, and 1.06 (95% CI, 0.82 to 1.37) for hemorrhagic stroke.
| Discussion |
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Most studies included in our meta-analysis had a large sample size and long-term follow-up periods that increased the statistical power to examine the overall associations of fish intake and incidence of stroke. The prospective study designs also minimized selection bias and recall bias. Although randomized placebo-controlled trials are the most definitive tool for evaluation of the causality of diet-disease relations, it would be difficult to conduct a long-term, large-scale, randomized trial on fish consumption and stroke because of feasibility considerations such as long-term compliance.
The study also has limitations. One concern is that most studies did not separate ischemic from hemorrhagic stroke. Therefore, our capacity to examine fish intake in relation to stroke subtypes was limited. Because of the distinct pathogeneses of these 2 types of stroke, the underlying relationship between fish intake and stroke risk may be somewhat attenuated by combining ischemic and hemorrhagic stroke in the analysis. Alternatively, our pooled results of total stroke would mostly reflect the relationship between fish consumption and risk of ischemic stroke because most studies were conducted in western countries, where ischemic stroke is the major type of stroke. Of note, 1 of the included studies10 was conducted in China, where one third or more cases might be hemorrhagic stroke.18 In addition, 1 study in a Japanese population found that high intake of fish was inversely associated with death caused by intracerebral hemorrhage but not with death caused by cerebral infarction.
Because our analyses are based on observational studies, certain limitations of such studies may have affected our findings. For example, the individual RR estimate included in the meta-analysis was adjusted for different covariates in the different studies. Thus, the possibility of residual confounding resulting from inclusion of different factors or bias attributable to measurement errors cannot be excluded. Alternatively, a meta-analysis on the basis of individual data with subsequent adjustment for identified covariates may provide a more powerful approach. In addition, differences in follow-up period, dietary assessment method, and measurement of the stroke end point, coupled with the fact that most studies enrolled only men, might lead to difficulties in estimating true effects of fish intake on stroke risk. However, our stratified analyses did not support the presence of substantial effect modification by gender or dietary assessment method. Moreover, misclassification of fish intake was still possible when we standardized fish consumption, although most studies provided data on portion size and the range of fish intake for each exposure category.
Fish intake may also be a surrogate for some other underlying healthy lifestyle factors that protect against stroke.1921 For example, individuals with higher fish consumption generally tended to exercise more, smoke less, and were less likely to be overweight. Although most of the included studies were well designed and adjusted for major dietary and lifestyle variables, we could not exclude completely the possibility that the inverse association between fish intake and stroke is partly explained by undefined healthy lifestyle factors.
The possibility of publication bias is always a concern in a meta-analysis. Although we do not have enough statistical power to formally test for publication bias, there was no apparent tendency for the smaller cohorts to report much larger effect estimates compared with the larger studies. More importantly, the inverse associations between fish intake and risk of stroke appeared to be consistent across most studies. Thus, the likelihood that these findings are largely a result of selective publication seems to be minimal. However, a potential bias resulting from excluding studies published in other languages (if any) is possible.
Beneficial effects of fish intake on ischemic stroke are biologically plausible. Fish is the main dietary source of long-chain omega-3 PUFAs. Such marine-derived long-chain omega-3 PUFAs have been shown to have multiple favorable effects on blood pressure, arrhythmias, lipid profile, platelet aggregation, and endothelial function2224 that may reduce the risk of ischemic stroke. Conversely, the antiplatelet effect and the observation of high incidence of hemorrhage in Eskimos, who consume large amounts of fish, have raised concerns about possible adverse effects of high fish intake on risk of hemorrhagic stroke. In the present meta-analysis, we did not observe any significant association between fish intake and hemorrhagic stroke. One possible explanation is that the risk of hemorrhage with high fish consumption is somehow balanced by other benefits of fish intake such as lowering blood pressure. Presumably, the overall effect of fish intake on hemorrhagic stroke may be minor.
Numerous experimental studies have indicated protective effects from the use of fish oil supplements on cardiovascular diseases. However, the dose of long-chain omega-3 PUFAs used in the experimental studies is much higher than the amount typically found in the diet. It is not clear how much intake of long-chain omega-3 PUFAs may be required to significantly reduce risk of stroke. In addition, whether fish consumption provides other beneficial nutrients not present in pure fish oil remains uncertain. Because a small amount of fish intake was associated with significantly lower risk of ischemic stroke,12 the possibility of interactions between long-chain omega-3 PUFAs and some unknown constituents in fish providing synergistic effects cannot be ruled out. Accordingly, one should be cautious when advising people to use fish oil supplements instead of eating whole fish. Moreover, considering the different amounts of long-chain omega-3 PUFAs in different types of fish, one would expect to observe more benefit by eating fatty fish rich in long-chain omega-3 PUFAs if any beneficial effect of fish intake on risk of stroke is largely attributable to its content of long-chain omega-3 PUFAs. However, data are very limited regarding the effect of intake of different types of fish on stroke risk. Finally, some potentially important issues, such as how fish is cooked might modify benefits of fish consumption and what is the optimal way to cook fish, remain unanswered and call for future research.
In summary, our meta-analysis of all relevant cohort studies indicated an inverse association between fish consumption and stroke, particularly ischemic stroke. The incidence of ischemic stroke might be significantly reduced by consuming fish as seldom as 1 to 3 times per month. Because of scarce data, the effect of fish intake on the risk of hemorrhagic stroke remains equivocal. Further studies are required to better understand the potentially different effects of fish consumption on risk of stroke subtypes by gender and in different ethnic groups.
| Acknowledgments |
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Received January 6, 2004; revision received March 25, 2004; accepted March 26, 2004.
| References |
|---|
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|
|---|
2. Bjerregaard P, Dyerberg J. Mortality from ischaemic heart disease and cerebrovascular disease in Greenland. Int J Epidemiol. 1988; 17: 514519.
3. Zhang J, Sasaki S, Amano K, Kesteloot H. Fish consumption and mortality from all causes, ischemic heart disease, and stroke: an ecological study. Prev Med. 1999; 28: 520529.[CrossRef][Medline] [Order article via Infotrieve]
4. Yamori Y, Nara Y, Iritani N, Workman RJ, Inagami T. Comparison of serum phospholipid fatty acids among fishing and farming Japanese populations and American inlanders. J Nutr Sci Vitaminol (Tokyo). 1985; 31: 417422.[Medline] [Order article via Infotrieve]
5. Kristensen SD, Schmidt EB, Dyerberg J. Dietary supplementation with n-3 polyunsaturated fatty acids and human platelet function: a review with particular emphasis on implications for cardiovascular disease. J Intern Med Suppl. 1989; 225: 141150.
6. Keli SO, Feskens EJ, Kromhout D. Fish consumption and risk of stroke. The Zutphen Study. Stroke. 1994; 25: 328332.[Abstract]
7. Morris MC, Manson JE, Rosner B, Buring JE, Willett WC, Hennekens CH. Fish consumption and cardiovascular disease in the physicians health study: a prospective study. Am J Epidemiol. 1995; 142: 166175.
8. Orencia AJ, Daviglus ML, Dyer AR, Shekelle RB, Stamler J. Fish consumption and stroke in men. 30-year findings of the Chicago Western Electric Study. Stroke. 1996; 27: 204209.
9. Gillum RF, Mussolino ME, Madans JH. The relationship between fish consumption and stroke incidence. The NHANES I Epidemiologic Follow-up Study (National Health and Nutrition Examination Survey). Arch Intern Med. 1996; 156: 537542.
10. Yuan JM, Ross RK, Gao YT, Yu MC. Fish and shellfish consumption in relation to death from myocardial infarction among men in Shanghai, China. Am J Epidemiol. 2001; 154: 809816.
11. Iso H, Rexrode KM, Stampfer MJ, Manson JE, Colditz GA, Speizer FE, Hennekens CH, Willett WC. Intake of fish and omega-3 fatty acids and risk of stroke in women. JAMA. 2001; 285: 304312.
12. He K, Rimm EB, Merchant A, Rosner BA, Stampfer MJ, Willett WC, Ascherio A. Fish consumption and risk of stroke in men. JAMA. 2002; 288: 31303136.
13. Sauvaget C, Nagano J, Allen N, Grant EJ, Beral V. Intake of animal products and stroke mortality in the Hiroshima/Nagasaki Life Span Study. Int J Epidemiol. 2003; 32: 536543.
14. 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: 5165.
15. Feskanich D, Rimm EB, Giovannucci EL, Colditz GA, Stampfer MJ, Litin LB, Willett WC. Reproducibility and validity of food intake measurements from a semiquantitative food frequency questionnaire. J Am Diet Assoc. 1993; 93: 790796.[CrossRef][Medline] [Order article via Infotrieve]
16. Petitti DB. Statistical methods in meta-analysis. In: Petitti DB, ed. Meta-Analysis, Decision Analysis, and Cost-Effectiveness Analysis. 2nd ed. New York, NY: Oxford University Press; 2000: 94118.
17. DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986; 7: 177188.[CrossRef][Medline] [Order article via Infotrieve]
18. Zhang LF, Yang J, Hong Z, Yuan GG, Zhou BF, Zhao LC, Huang YN, Chen J, Wu YF. Proportion of different subtypes of stroke in China. Stroke. 2003; 34: 20912096.
19. Lee CD, Folsom AR, Blair SN. Physical activity and stroke risk: a meta-analysis. Stroke. 2003; 34: 24752481.
20. Kurth T, Kase CS, Berger K, Schaeffner ES, Buring JE, Gaziano JM. Smoking and the risk of hemorrhagic stroke in men. Stroke. 2003; 34: 11511155.
21. Suk SH, Sacco RL, Boden-Albala B, Cheun JF, Pittman JG, Elkind MS, Paik MC; Northern Manhattan Stroke Study. Abdominal obesity and risk of ischemic stroke: the Northern Manhattan Stroke Study. Stroke. 2003; 34: 15861592.
22. Nestel PJ. Effects of n-3 fatty acids on lipid metabolism. Annu Rev Nutr. 1990; 10: 149167.[CrossRef][Medline] [Order article via Infotrieve]
23. Harris WS. n-3 fatty acids and serum lipoproteins: human studies. Am J Clin Nutr. 1997; 65 (suppl 5): 1645S1654S.
24. Dyerberg J, Bang HO, Stoffersen E, Moncada S, Vane JR. Eicosapentaenoic acid and prevention of thrombosis and atherosclerosis? Lancet. 1978; 2: 117119.[CrossRef][Medline] [Order article via Infotrieve]
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