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Effects of fatty and lean fish intake on stroke risk: a meta-analysis of prospective cohort studies

Lipids in Health and Disease volume 17, Article number: 264 (2018) Cite this article

Abstract

Background

Fish intake has been postulated to reduce the risk of stroke. However, whether the beneficial effect of fish are mainly linked to fat content, as a source of omega-3 polyunsaturated fatty acids, remains unclear. We conducted a meta-analysis to compare the effect of fatty and lean fish intake on stroke risk.

Methods

We performed a literature search on four database (PubMed, Embase, Scopus, and Cochrane Library) through February 1, 2018 to identify prospective studies of fatty and lean fish in relation to stroke risk. A random-effects model was used to calculate the summary estimates.

Results

We identified five prospective studies, including 7 comparisons for fatty fish intake and 5 comparisons for lean fish intake. Compared with the highest category of intake with lowest category, the summary relative risk was 0.88 [95% confidence interval (CI), 0.74–1.04] for fatty fish intake and 0.81 (95% CI, 0.67–0.99) for lean fish intake. No heterogeneity across studies and publication bias were observed.

Conclusion

Our findings demonstrated that fatty and lean fish intake has beneficial effects on stroke risk, especially lean fish intake. Additional prospective studies are necessary to confirm these observations.

Background

Stroke is the major cause of morbidity and mortality. In 2013, stroke was the second most common cause of deaths (11.8% of all deaths) worldwide, and the third most common cause of disability (4.5% of disability-adjusted life-years from all cause) [1]. The risk factors for stroke include family history and genetic backgrounds, improper nutrition, physical inactivity, smoking/tobacco use, and some associated diseases such as hypertension [2].

In 2002, the American Heart Association (AHA) published a scientific statement, “Fish Consumption, Fish Oil, Omega-3 Fatty Acids, and Cardiovascular Disease” [3]. Recently, AHA science advisory further addressed the specific effect of omega-3 polyunsaturated fatty acids (PUFAs) from seafood supplementation on clinical cardiovascular events [4]. Agencies and organizations in different countries advise that at least two servings of fish, especially fatty fish, per week are needed to promote cardiovascular health in the general population [4, 5]. However, evidence was mainly derived from the studies which focus on the beneficial effects of omega-3 PUFAs, not from fatty fish rich in these fatty acids.

Previous meta-analyses showed that fish intake has a protective effect against stroke, especially in ischemic stroke [6, 7]. However, a recently systematic assessment indicated that increasing omega-3 PUFAs has no effect on stroke risk [RR = 1.06, 95% confidence interval (95% CI): 0.96–1.16] [8]. The content of omega-3 PUFAs ranged widely in different kinds of seafood. Fatty fish such as anchovies and herring [eicosapentenoic acid (EPA) + docosahexaenoic acid (DHA): 2300–2400 mg/4 oz], tuna (1700 mg/4 oz), and salmon (1200–2400 mg/4 oz) have higher levels of omega-3 PUFAs. In contrast, lean fish including shrimp (100 mg/4 oz), lobster, scallops, and cod (200 mg/4 oz) have lower levels [9]. In addition, seafood contains other nutrients, which varied greatly in the lean and fatty fish. Hengeveld et al. also demonstrated that the association of fatty fish and lean fish with stroke is likely to be independent from one another [10]. With the accumulation of epidemical studies [11,12,13,14,15,16,17,18,19] as well as the above converging evidence, we performed a meta-analysis to elucidate whether the effects of fatty and lean fish intake on stroke risk might be different. Findings from this study might provide theoretical guidance for fatty and lean fish intake for general population.

Methods

Four database (PubMed, Embase, Scopus, and Cochrane Library) were search through February 1, 2018 using the key words fish and stroke without restrictions. Furthermore, we reviewed the reference list of retrieved articles. Prospective studies were included if they reported hazard ratio (HR)/relative risk (RR) with a corresponding 95% CI of stroke relating to fatty or lean fish intake in the healthy population. The data that we collected included the last name of the first author, year of publication, country of origin, study name, number of participants and cases, range or mean of participants’ age, duration of follow-up, covariate adjustments, and maximally adjusted risk estimates and 95% CI of lean and fatty fish intake. We used the Newcastle-Ottawa Quality Assessment Scale (NOS), with the highest scale is nine, to evaluate the quality of each cohort [20]. Study selection and date extraction were conducted independently by two authors (Q-ZZ and X-JY), with any disagreements resolved by consensus.

We estimated the summary risk estimates of stroke for fatty and lean fish intake compared the highest with the lowest category using a random-effects model [21]. Heterogeneity test was performed using Q and I2 statistics [22]. For the Q statistics, P < 0.1 was considered statistically significant; and for the I2 statistics, the following conventional cutoff points were used: < 25% (low heterogeneity), 25–50% (moderate heterogeneity), and > 75% (severe heterogeneity). We conducted a sensitivity analysis to investigate the influence of a single study on the overall risk estimates by omitting one study in each turn. To assess the potential publication bias, we performed Begg’s and Egger’s tests, and inspected the funnel plots as well [23]. All statistical analyses were performed using STATA software, version 11.0 (STATACorp, College Station, TX, USA). Except where otherwise specified, a P value < 0.05 was considered to be statistically significant.

Results

The systematic literature search yielded 821 potentially relevant records. After the exclusion of clearly irrelevant publications by reading titles and abstracts, we obtained 41 full articles of potentially relevant studies for further evaluation. After full-text reviews, 29 articles were excluded because of lack of subtype of fish intake. Three studies were excluded because of meta-analysis of total fish intake and stroke risk [6, 7, 24]. Other three studies were excluded because of case-control design [11,12,13]. One article was further excluded because the participants were patients with type 2 diabetes [14]. Finally, five independent prospective cohort studies with 7 comparisons for fatty fish intake [15,16,17,18,19] and four studies with 5 comparisons for lean fish intake [15,16,17,18] were included (Fig. 1).

Fig. 1
figure1

Flow diagram of systematic literature search

Full size image

Characteristics of the included studies are reported in Table 1. Five studies were conducted in the UK (n = 2), Italy (n = 1), Spain (n = 1) and Sweden (n = 1). Numbers of participants ranged from 2710 to 41,020. The number of stroke events ranged from 66 to 1680. Except Atkinson’s study [17], other 4 studies excluded participants with a history of cardiovascular disease (CVD) or stroke at baseline. All studies included ischemic and hemorrhagic stroke cases, and the former was the majority of stroke type. The follow-up duration ranged from 4.3 to 18 years. Fish intake was measured by food frequency questionnaire in all studies. Three studies reported fish intake as times/week [15, 18, 19]. One study reported it as grams/day [16], and the last one did not provide the data of fish amounts [17]. Fish intake in the highest category varied largely across each study. Quality scores based on the NOS ranged from 6 to 9.

Table 1 Characteristics of the studies included in the meta-analysis
Full size table

Five studies with 7 comparisons were included in the highest versus lowest analysis of fatty fish intake and stroke. The summary RR was 0.88 (95% CI, 0.74–1.04, P = 0.124), with low heterogeneity across studies (I2 = 26.2%, Pheterogeneity = 0.229) (Fig. 2). The sensitivity analyses showed a range from 0.83 (95% CI, 0.71–0.96) to 0.93 (95% CI, 0.79–1.10). When Amiano’s study [16] on women was excluded, the inverse association of fatty fish intake with stroke risk became significant.

Fig. 2
figure2

Meta-analysis of the highest versus lowest fatty fish intake and stroke risk

Full size image

Four studies with 5 comparisons were included for lean fish intake and stroke risk. The summary RR was 0.81 (95% CI, 0.67–0.99, P = 0.042), without heterogeneity across studies (I2 = 0%, Pheterogeneity = 0.609) (Fig. 3). The sensitivity analyses showed a range from 0.77 (95% CI, 0.62–0.96) to 0.92 (95% CI, 0.79–1.19). The summary effect size became non-significant when Larsson’s study [18] was excluded.

Fig. 3
figure3

Meta-analysis of the highest versus lowest lean fish intake and stroke risk

Full size image

There was no obvious dissymmetry in the shape of funnel plots for both analyses of fatty and lean fish intake. Publication bias was also not found using Begg’s test (P = 0.764 for fatty fish, P = 0.462 for lean fish) and Egger’s tests (P = 0.891 for fatty fish, P = 0.324 for lean fish).

Discussion

Our meta-analysis was the first to analyze the effect of fatty and lean fish intake on stroke risk. A significantly beneficial association was observed between lean fish intake and stroke risk. A lower stroke risk by fatty fish intake did not obtain statistical significance.

Our findings were somewhat opposite to the general knowledge that fatty fish is “better” than lean fish. The health benefits of fish intake have traditionally been attributed to the effect of PUFAs, such as EPA and DHA [6, 13, 17, 19]. However, a meta-analysis including 9 randomized controlled trials (RCTs) showed that no statistically significant association was observed with stroke when combined studies supplemented PUFAs [25]. In fact, advantages associated with PUFAs were mainly observed for high amounts, often not within the range of dietary intake of fish [15]. Thus, a recent science advisory from the AHA demonstrated that there is no proven benefit of PUFA supplementation as a means to reduce the risk of stroke [4]. Aside from a variety of nutrients, fish in some cases contains noxious agents. Environmental pollutants, such as persistent organic pollutants and organic mercury, are fat soluble and therefore found mainly in fatty fish. Fish intake was positively correlated with erythrocyte mercury content and EPA + DHA [11]. Both persistent organic pollutants and organic mercury are potential risk factors for CVD and stroke [26, 27]. Daneshmand even found that higher serum omega-3 PUFA concentration was associated with an increased risk of ischaemic stroke among participants with hair mercury content above the median [28].

Lean fish, which contains relatively low amounts of PUFAs, is considered a superior source of proteins. Fish proteins are easy to digest and rich in essential amino acids. Aadland performed an RCT to compare the effect of different protein sources on cardiovascular lipid risk factors in healthy subjects. They found that lean seafood reduced serum triacylglycerol and prevented an elevation in medium-sized, very low-density lipoprotein particle concentrations relative to those of non-seafood intervention [29]. Compared with fatty fish, lean fish contains more iodine, selenium and less energy, which are beneficial to human health [30, 31]. Moreover, lean fish intake significantly decreased circulating soluble intercellular cell adhesion molecule-1 concentrations in patients with ischemic heart disease, but fatty fish intake had no effect [32]. Dietary advice in these recommendations emphasize intake of fatty fish due to its high levels of omega-3 PUFA. However, lean fish contains numerous nutrients that may be beneficial in the prevention of CVD, indicating that also lean fish should be included in the diet when targeting the modifiable risk factors of CVD [31].

Some case-control studies observing the effect of fatty and lean fish on stroke risk also deserve consideration. In a nested case-control study, stroke risk in men increased with fatty and lean fish intake [11]. Using the same cohorts with a larger population and a more extensive questionnaire dataset, they found that previous association between high lean fish intake and stroke risk in men could not be repeated [12]. A relatively high proportion of male with high intake of lean fish were single men, who consumed more semi-finished products. In Sweden, semi-finished lean fish product is commonly fried with relatively large quantities of fat. In another case-control study, ischemic stroke risk decreased with fatty fish intake. However, lean fish intake had no effect on ischemic stroke risk in men and increased risk in women [13].

At the human population level, fish consumption could positively affect plasma lipid profiles, consequently decreasing stoke risk. In a Norwegian cross-sectional study, increased intake of fatty and lean fish was associated with decreased serum triglyceride and increased high-density lipoprotein cholesterol [30]. A RCT also indicated that omega-3 PUFA supplementation reduced plasma triglyceride in pre-menopausal women [33]. Circulating omega-3 PUFA are considered as possible biomarker for intake of fatty acids. Saber measured circulating fatty acids at baseline in 3 separate US cohorts and found that higher circulating levels of DHA were inversely associated with incident atherothrombotic stroke and DPA with cardioembolic stroke [34]. Arachidonic acid (AA), a chief source of omega-6 PUFAs, is a source of mediators that cause inflammation in vessels. High serum ratio of EPA to AA (EPA/AA) levels may be a good biomarker for the risk of CVD [35]. In a population-based prospective cohort study, a lower serum EPA/AA ratio was significantly increased the risk of coronary heart disease, but there was no evidence of an association with stroke [36].

Although there were no animal studies investigating the effect of fish intake on stroke risk, some stroke-related animal models were used to observe the role of omega-3 PUFA. When rats were intraperitoneally pretreated with DHA before being subjected to focal cerebral cerebral ischemia/reperfusion injury, brain infarction was obviously alleviated with the decrease in blood-brain barrier disruption, brain edema, and inflammatory cell infiltration [37]. However, EPA + DHA intervention for 5 weeks aggravated the edema and bleeding, and oxidative damage in the brain of rats with intracerebral hemorrhagic stroke [38].

A major strength of our study is that the included studies used a prospective cohort design, which eliminates the possibility of reverse causation and minimizes selection bias. Several limitations should be acknowledged. First, residual confounding remains a concern. Although a wide range of potential confounders related to stroke were adjusted for in the multivariate models, the possibility of residual confounding could not be ruled out. Second, misclassification bias may have weakened the strength of the association. Given that dietary assessment was based on self-administered questionnaires, misclassification of dietary intake is inevitable. Third, fatty and lean fish are in a heterogeneous group. The number and proportion of the types of fish consumed varied among countries. For example, the most commonly consumed fish were cod (29.9%), tuna (16.4%) and salmon (14.2) in the UK. Meanwhile, hake/burbot (35.0%), tuna (15.2%) and cod (12.3) were typically consumed in Spain [39]. In addition, some methods of fish preparation, which have not been considered in this study, may differently affect the stroke risk. For example, fatty fish is commonly eaten salted, and lean fish is usually eaten cooked, roasted, or fried in Sweden [18]. Fourth, Then, the data of plasma fatty acid pattern in fatty and lean fish were unavailable, therefore whether the differential effects of fatty and lean fish on stroke risk might be associated plasma fatty acid pattern remain unclear. Fifth, the sensitivity analyses showed that the results were less stable when Amiano’s study in women on fatty fish intake [16] or Larsson’s study on lean fish intake [18] was excluded. The exact explanation was unclear, but possibly was related to only women included in these two cohorts. In general, women were inclined to suffer from milder strokes than men [19]. Finally, the limited number of included studies made the subgroup analysis impossible. We were not able to assess the potential effect modification of variables, including geographic region, gender and stroke type, on stroke risk. Also, a dose-response analysis was not performed. We could not determine whether the relationship between fatty and lean fish intake and stroke risk had a threshold or be was U- or J-shaped.

Conclusion

Our findings demonstrated that fatty and lean fish intake had beneficial effects on stroke risk, especially lean fish intake. Considering the limited number of included studies and limitations mentioned above, additional prospective studies with improved methods of estimating the intake of different kinds of fish is warranted to investigate whether fatty and lean fish intake has different effects on stroke risk among the general populations.

Abbreviations

AHA:

American Heart Association

CI:

Confidence interval

CVD:

Cardiovascular disease

DHA:

Docosahexaenoic acid

EPA:

Eicosapentenoic acid

HR:

Hazard ratio

NOS:

Newcastle-Ottawa Quality Assessment Scale

PUFA:

Omega-3 polyunsaturated fatty acid

RCT:

Randomized controlled trial

RR:

Relative risk

References

  1. 1.

    Feigin VL, Norrving B, Mensah GA. Global burden of stroke. Circ Res. 2017;120(3):439–48.

  2. 2.

    Benjamin EJ, Virani SS, Callaway CW, Chamberlain AM, Chang AR, Cheng S, Chiuve SE, Cushman M, Delling FN, Deo R, et al. Heart disease and stroke Statistics-2018 update: a report from the American Heart Association. Circulation. 2018;137(12):e67–e492.

  3. 3.

    Kris-Etherton PM, Harris WS, Appel LJ. Fish consumption, fish oil, omega-3 fatty acids, and cardiovascular disease. Circulation. 2002;106(2):2747–57.

  4. 4.

    Siscovick DS, Barringer TA, Fretts AM, Wu JH, Lichtenstein AH, Costello RB, Kris-Etherton PM, Jacobson TA, Engler MB, Alger HM, et al. Omega-3 polyunsaturated fatty acid (fish oil) supplementation and the prevention of clinical cardiovascular disease: a science advisory from the American Heart Association. Circulation. 2017;135:e867–84.

  5. 5.

    National Food Agency, Sweden. Food habits, health and environment: fish and shellfish. https://www.livsmedelsverket.se/en/food-habits-health-and-environment/dietary-guidelines/adults/fisk-och-skaldjur--rad. Accessed 17 Nov 2018.

  6. 6.

    Xun P, Qin B, Song Y, Nakamura Y, Kurth T, Yaemsiri S, Djousse L, He K. Fish consumption and risk of stroke and its subtypes: accumulative evidence from a meta-analysis of prospective cohort studies. Eur J Clin Nutr. 2012;66(11):1199–207.

  7. 7.

    Larsson SC, Orsini N. Fish consumption and the risk of stroke: a dose-response meta-analysis. Stroke. 2011;42(12):3621–3.

  8. 8.

    Abdelhamid AS, Brown TJ, Brainard JS, Biswas P, Thorpe GC, Moore HJ, Deane KH, AlAbdulghafoor FK, Summerbell CD, Worthington HV, et al. Omega-3 fatty acids for the primary and secondary prevention of cardiovascular disease. Cochrane Database Syst Rev. 2018;7:CD003177.

  9. 9.

    US Department of Agriculture and US Department of Health and Human Services. Dietary Guidelines for Americans, 2010. 7th ed. Washington, DC: US Government Printing Office. p. 2010.

  10. 10.

    Hengeveld LM, Praagman J, Beulens JWJ, Brouwer IA, van der Schouw YT, Sluijs I. Fish consumption and risk of stroke, coronary heart disease, and cardiovascular mortality in a Dutch population with low fish intake. Eur J Clin Nutr. 2018;72(7):942–50.

  11. 11.

    Wennberg M, Bergdahl IA, Stegmayr B, Hallmans G, Lundh T, Skerfving S, Strömberg U, Vessby B, Jansson JH. Fish intake, mercury, long-chain n-3 polyunsaturated fatty acids and risk of stroke in northern Sweden. Br J Nutr. 2007;98(5):1038–45.

  12. 12.

    Wennberg M, Jansson JH, Norberg M, Skerfving S, Strömberg U, Wiklund PG, Bergdahl IA. Fish consumption and risk of stroke: a second prospective case-control study from northern Sweden. Nutr J. 2016;15(1):98.

  13. 13.

    Oudin A, Wennberg M. Fish consumption and ischemic stroke in southern Sweden. Nutr J. 2011;10:109.

  14. 14.

    Wallin A, Orsini N, Forouhi NG, Wolk A. Fish consumption in relation to myocardial infarction, stroke and mortality among women and men with type 2 diabetes: a prospective cohort study. Clin Nutr. 2018;37(2):590–6.

  15. 15.

    Bonaccio M, Ruggiero E, Di Castelnuovo A, Costanzo S, Persichillo M, De Curtis A, Cerletti C, Donati MB, de Gaetano G, Iacoviello L. Fish intake is associated with lower cardiovascular risk in a Mediterranean population: prospective results from the Moli-sani study. Nutr Metab Cardiovasc Dis. 2017;27(10):865–73.

  16. 16.

    Amiano P, Chamosa S, Etxezarreta N, Arriola L, Moreno-Iribas C, Huerta JM, Egües N, Guevara M, Navarro C, Chirlaque MD, et al. No association between fish consumption and risk of stroke in the Spanish cohort of the European prospective investigation into Cancer and nutrition (EPIC-Spain): a 13·8-year follow-up study. Public Health Nutr. 2016;19(4):674–81.

  17. 17.

    Atkinson C, Whitley E, Ness A, Baker I. Associations between types of dietary fat and fish intake and risk of stroke in the Caerphilly prospective study (CaPS). Public Health. 2011;125(6):345–8.

  18. 18.

    Larsson SC, Virtamo J, Wolk A. Fish consumption and risk of stroke in Swedish women. Am J Clin Nutr. 2011;93(3):487–93.

  19. 19.

    Myint PK, Welch AA, Bingham SA, Luben RN, Wareham NJ, Day NE, Khaw KT. Habitual fish consumption and risk of incident stroke: the European prospective investigation into Cancer (EPIC)-Norfolk prospective population study. Public Health Nutr. 2006;9(7):882–8.

  20. 20.

    Wells GA, Shea B, O’Connell D, Peterson J, Welch V, Losos M, Tugwell P. The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp. Accessed 16 Nov 2018.

  21. 21.

    DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7(3):177–88.

  22. 22.

    Higgins JP, Thompson SG. Quantifying heterogeneity in a meta-analysis. Stat Med. 2002;21(11):1539–58.

  23. 23.

    Egger M, Davey Smith G, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997;315:629–34.

  24. 24.

    He K, Song Y, Daviglus ML, Liu K, Van Horn L, Dyer AR, et al. Fish consumption and incidence of stroke: a meta-analysis of cohort studies. Stroke. 2004;35:1538–42.

  25. 25.

    Rizos EC, Ntzani EE, Bika E, Kostapanos MS, Elisaf MS. Association between omega-3 fatty acid supplementation and risk of major cardiovascular disease events: a systematic review and meta-analysis. JAMA. 2012;308:1024–33. https://doi.org/10.1001/2012.jama.11374.

  26. 26.

    Lind L, Lind PM. Can persistent organic pollutants and plastic-associated chemicals cause cardiovascular disease? J Intern Med. 2012;271(6):537–53.

  27. 27.

    Houston MC. Role of mercury toxicity in hypertension, cardiovascular disease, and stroke. J Clin Hypertens (Greenwich). 2011;13(8):621–7.

  28. 28.

    Daneshmand R, Kurl S, Tuomainen TP, Virtanen JK. Associations of serum n-3 and n-6 PUFA and hair mercury with the risk of incident stroke in men: the Kuopio Ischaemic heart disease risk factor study (KIHD). Br J Nutr. 2016;115(10):1851–9.

  29. 29.

    Aadland EK, Lavigne C, Graff IE, Eng Ø, Paquette M, Holthe A, Mellgren G, Jacques H, Liaset B. Lean-seafood intake reduces cardiovascular lipid risk factors in healthy subjects: results from a randomized controlled trial with a crossover design. Am J Clin Nutr. 2015;102(3):582–92.

  30. 30.

    Tørris C, Molin M, Cvancarova MS. Lean fish consumption is associated with lower risk of metabolic syndrome: a Norwegian cross sectional study. BMC Public Health. 2016;16:347.

  31. 31.

    Tørris C, Småstuen MC, Molin M. Nutrients in fish and possible associations with cardiovascular disease risk factors in metabolic syndrome. Nutrients. 2018;10(7).

  32. 32.

    de Mello VD, Erkkila AT, Schwab US, Pulkkinen L, Kolehmainen M, Atalay M, et al. The effect of fatty or lean fish intake on inflammatory gene expression in peripheral blood mononuclear cells of patients with coronary heart disease. Eur J Nutr. 2009;48:447–55. https://doi.org/10.1007/s00394-009-0033-y.

  33. 33.

    Sparkes C, Gibson R, Sinclair A, Else PL, Meyer BJ. Effect of low dose docosahexaenoic acid-rich fish oil on plasma lipids and lipoproteins in pre-menopausal women: a dose-response randomized placebocontrolled trial. Nutrients. 2018;10(10).

  34. 34.

    Saber H, Yakoob MY, Shi P, Longstreth WT Jr, Lemaitre RN, Siscovick D, Rexrode KM, Willett WC, Mozaffarian D. Omega-3 fatty acids and incident ischemic stroke and its atherothrombotic and cardioembolic subtypes in 3 US cohorts. Stroke. 2017;48(10):2678–85.

  35. 35.

    Itakura H, Yokoyama M, Matsuzaki M, Saito Y, Origasa H, Ishikawa Y, Oikawa S, Sasaki J, Hishida H, Kita T, et al. Relationships between plasma fatty acid composition and coronary artery disease. J Atheroscler Thromb. 2011;18(2):99–107.

  36. 36.

    Ninomiya T, Nagata M, Hata J, Hirakawa Y, Ozawa M, Yoshida D, Ohara T, Kishimoto H, Mukai N, Fukuhara M, et al. Association between ratio of serum eicosapentaenoic acid to arachidonic acid and risk of cardiovascular disease: the Hisayama study. Atherosclerosis. 2013;231(2):261–7.

  37. 37.

    Pan HC, Kao TK, Ou YC, Yang DY, Yen YJ, Wang CC, Chuang YH, Liao SL, Raung SL, Wu CW, et al. Protective effect of docosahexaenoic acid against brain injury in ischemic rats. J Nutr Biochem. 2009;20(9):715–25.

  38. 38.

    Park Y, Nam S, Yi HJ, Hong HJ, Lee M. Dietary n-3 polyunsaturated fatty acids increase oxidative stress in rats with intracerebral hemorrhagic stroke. Nutr Res. 2009;29(11):812–8.

  39. 39.

    Welch AA, Lund E, Amiano P, Dorronsoro M, Brustad M, Kumle M, Rodriguez M, Lasheras C, Janzon L, Jansson J, et al. Variability of fish consumption within the 10 European countries participating in the European investigation into Cancer and nutrition (EPIC) study. Public Health Nutr. 2002;5(6B):1273–85.

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Acknowledgements

Not applicable.

Funding

This research was supported by National Natural Science Foundation of China (No. 81874264; 81472974).

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All data generated or analysed during this study are included in this published article.

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Affiliations

  1. School of Public Health, Hebei Medical University, 361 East Zhongshan Road, Shijiazhuang, 050017, Hebei Province, China
    • Zhi-Zhen Qin
    •  & Yu-Xia Ma
  2. State Key Laboratory of Radiation Medicine and Protection, School of Radiation Medicine and Protection, Soochow University, 199 Ren’ai Road, Suzhou, 215123, Jiangsu Province, China
    • Jia-Ying Xu
    •  & Li-Qiang Qin
  3. Department of Nutrition and Food Hygiene, School of Public Health, Soochow University, 199 Ren’ai Road, Suzhou, 215123, Jiangsu Province, China
    • Guo-Chong Chen
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Contributions

LQQ and YXM were responsible for the study concept and design. ZZQ performed the literature searches and selected available articles. ZZ Q and JYX extracted data from these available reports and did the analyses. ZZ Q and LQQ was responsible for the article writing. GCC and YXM revised the manuscript. All authors reviewed and approved the final manuscript.

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Correspondence to Yu-Xia Ma or Li-Qiang Qin.

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Qin, Z., Xu, J., Chen, G. et al. Effects of fatty and lean fish intake on stroke risk: a meta-analysis of prospective cohort studies. Lipids Health Dis 17, 264 (2018). https://doi.org/10.1186/s12944-018-0897-z

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Keywords

  • Fatty fish
  • Lean fish
  • Stroke risk
  • Meta-analysis

Lipids in Health and Disease

ISSN: 1476-511X