Does Beef Increase Chances of Stroke

Introduction

High consumption of red meat has been associated with increased risk of total, cardiovascular, and cancer mortality,1 as well as with some types of cancers, including colorectal,2,3 pancreatic,4 esophageal, and stomach cancer.5,6 Moreover, results of studies indicated that processed meat consumption is connected with higher incidence of coronary heart disease7 and type 2 diabetes.1,7,8 Whether red meat consumption increases the risk of stroke is unclear. In a meta-analysis published by Micha et al,7 which was based on only 3 studies with a total of 2280 stroke cases, a positive relation between red meat consumption and stroke was observed in 1 study,9 but not in the other 2 studies.10,11 Furthermore, the authors presented results of combining the relative risk (RR) for different stroke subtypes (ischemic stroke, hemorrhagic stroke, and total stroke), which could have influenced the findings.

Clarifying the relationship between red meat consumption and stroke is relevant because of the high incidence of stroke, the high morbidity and mortality associated with the disease, and the widespread consumption of red meat. According to the American Heart Association report, each year ≈795 000 people experience a new or recurrent stroke and every 4 minutes someone dies from the disease.12 At the same time, in many countries red meat consumption is high and has remained at a stable level for several years. Nationally representative data collected for United States adults indicated that red meat consumption was approximately the same in surveys from 1988 to 1994 (45.5 g/d per person) and 1999 to 2004 (39.9 g/d per person), but it was lower in a survey conducted in 1994 to 1996 (32.3 g/d per person).13

Therefore, we conducted a systematic review and a meta-analysis of prospective studies to assess the relation between consumption of red meat (fresh red meat, processed meat, and total red meat) and the risk of total stroke and stroke subtypes. This meta-analysis includes 4.7-times more stroke cases and >2.2-times more participants compared with the previous meta-analysis.7 Moreover, this meta-analysis examines whether the association between red meat consumption and stroke risk differs by stroke subtypes, which could not be addressed in the previous meta-analysis.

Materials and Methods

Literature Search and Selection

We conducted a literature search through May 26, 2012, using the PubMed database (http://www.ncbi.nlm.nih.gov/pubmed) without language restrictions. The search term "stroke" was used in combination with "meat," "beef," "pork," "veal," "lamb," "steak," or "hamburger," and with the processed meat items "ham," "bacon," or "sausage." In addition, we reviewed the reference lists of retrieved articles to identify additional relevant studies.

Studies were included in the meta-analysis if the following criteria were met: (1) had a prospective design; (2) the exposure studied was fresh red meat, processed meat, and/or total red meat consumption; (3) the outcome of interest was stroke and stroke subtypes; and (4) reported RR with 95% confidence intervals (CI). If data were duplicated in >1 study, then we included the study with the largest number of stroke cases.

Data Extraction

The following data were extracted from each study: first author's last name, publication year, country where the study was performed, name of cohort study, study period, number of cases and cohort size, sex and age, type and categories of red meat consumption, stroke subtypes, covariates adjusted for in the analysis, and RR with 95% CI of total strokes and stroke subtypes for each category of meat consumption or for a 1 serving per day increase in consumption. Study selection and data extraction were conducted independently by 2 investigators (J.K. and S.C.L), with disagreements resolved by consensus.

Statistical Analysis

We transformed the reported RR and corresponding standard errors (derived from the CI) to their natural logarithms to stabilize the variances and to normalize the distributions. Because the majority of the studies provided results in servings (or frequency), rather than in grams, of red meat consumption, we used the results for servings per day. For 2 studies14,15 that provided results in grams per day, we used the original data to estimate the RR with 95% CI for a 1 serving per day increase in red meat consumption. We combined the results for a 1 serving per day increase in consumption of red meat using a random-effects model, which takes into account both within-study and between-study variabilities.16,17 If the study only provided results by categories of red meat consumption, then we estimated the RR with corresponding 95% CI for a 1 serving per day increase in red meat consumption using the method proposed by Greenland and Longnecker18 and Orsini et al.19 The median or mean level of red meat consumption for each consumption category was assigned to the corresponding RR. When the median or mean consumption per category was not reported, we assigned the midpoint of the upper and lower boundaries in each category as the average consumption. If the upper boundary of the highest category was not provided, then we assumed that it had the same amplitude as the previous category.

We conducted a sensitivity analysis in which 1 study at the time was removed and the rest were analyzed to assess the influence on single studies on the overall estimates. Furthermore, we conducted analyses stratified by geographic region and stroke subtypes (ischemic and hemorrhagic strokes). If the study presented results separately for intracerebral hemorrhage and subarachnoid hemorrhage, then we combined the results for the 2 subtypes. Statistical heterogeneity among studies was assessed using the I 2 statistics.20 We considered 2 cut points for the I 2 values: <30% (no or marginal between-study heterogeneity), 30% to 75% (mild heterogeneity), and >75% (notable heterogeneity). Test for publication bias was based on Egger test.17 All statistical analyses were performed with Stata (StataCorp). P values were 2-sided and P<0.05 was considered statistically significant.

Results

Study Characteristics

The detailed steps of our literature search are shown in Figure 1. Six studies were excluded for the following reasons: case-control study; review paper; assessing overall dietary pattern; or total meat included poultry. We identified 7 articles, based on 8 prospective studies, that investigated the relationship between fresh red meat, processed meat, and/or total red meat consumption and stroke risk.9–11,14,15,21,22 Two9,11 studies were excluded because data from those cohorts had been reanalyzed with longer follow-up and more stroke cases and published once again;21 only the latest publication21 was included in this meta-analysis. Hence, the present meta-analysis included results from 6 independent prospective studies (published in 5 articles).10,14,15,21,22

Figure 1.

Figure 1. Flow chart of study selection.

The eligible studies were published between 2003 and 2012, and included a total of 10 630 stroke cases and 329 495 participants (Supplementary Table 1). Data about subtypes of stroke were presented in 4 articles14,15,21,22 and contained 6420 cases of ischemic stroke and 1276 cases of hemorrhagic stroke. Two studies were conducted in Europe, 3 (published in 2 articles) were conducted in the United States, and 1 was conducted in Japan. Two studies provided results for red meat consumption in grams per day, 3 in servings per day, and 1 in frequency (how often). In 2 articles, stroke events were identified using The International Classification of Diseases 10th revision,14,15 in which strokes were classified as ischemic stroke (International Classification of Diseases 10th revision code I63), hemorrhagic strokes (International Classification of Diseases 10th revision codes I60 and I61), and unspecific strokes (I64). Bernstein et al21 classified strokes according to criteria in the National Survey of Stroke. Yaemsiri et al22 identified incident cases of ischemic stroke through self-reports; however, >95% of the cases were classified based on brain imaging and the Trial of ORG 10172 Acute Stroke Trial (TOAST) classification. In the study by Sauvaget et al,10 stroke deaths were ascertained by linkage to the nationwide family registration system of Japan and were coded according to the International Classification of Diseases 9th revision codes.

All studies provided RR and 95% CI that were adjusted for age, body mass index, and alcohol consumption. Moreover, almost all studies further controlled for smoking, physical activity, history of diabetes, history of hypertension, energy intake, and fruit and vegetable consumption.

Red Meat Consumption and Stroke

The RR (95% CI) of total stroke for an increment of 1 serving per day in red meat consumption are shown in Figure 2. The summary RR estimates showed that fresh red meat, processed meat, and total red meat consumption were associated with a statistically significant 11% to 13% increase in stroke risk, without heterogeneity among studies (all P for heterogeneity >0.16).

Figure 2.

Figure 2. Relative risks of total incident stroke and stroke mortality for a 1 serving per day increase in fresh red meat, processed meat, and total red meat consumption. One serving equals ≈50 g of processed meat and 100 to 120 g of fresh red meat and total red meat. Squares represent study-specific relative risk estimates (size of the square reflects the study-specific statistical weight, ie, the inverse of the variance). Horizontal lines represent 95% confidence interval (CI). Diamonds represent summary relative risk estimates with 95% CI. Tests for heterogeneity: fresh red meat, Q=3.35; P=0.65; I 2=0%; processed meat, Q=6.43; P=0.17; I 2=37.8%; and total red meat, Q=2.80; P=0.59; I 2=0%.

In a sensitivity analysis in which 1 study at the time was excluded and the rest were analyzed, the RR of stroke for each 1 serving per day increment of total red meat consumption ranged from 1.10 (95% CI, 1.04–1.15) when excluding the Swedish Mammography Cohort14 to 1.14 (95% CI, 1.07–1.22) when excluding the Cohort of Swedish Men.15 For fresh red meat, the corresponding RR ranged from 1.09 (95% CI, 1.00–1.19) when excluding the Nurses' Health Study21 to 1.16 (95% CI, 1.04–1.28) when excluding the Cohort of Swedish Men.15 For processed red meat, excluding 1 of the studies at a time resulted in RR that ranged from 1.09 (95% CI, 1.03–1.15) when excluding the Health Professionals Follow-Up Study21 to 1.18 (95% CI, 1.02–1.37) when excluding the Cohort of Swedish Men.15 Hence, none of the individual studies alone accounted for the observed associations. Excluding the Japanese study,10 which was the only study with stroke mortality as the outcome and the only that did not adjust for physical activity and fruit and vegetable consumption, did not change the results materially (RR, 1.11 and 95% CI, 1.02–1.21 for fresh red meat; RR, 1.14 and 95% CI, 1.03–1.28 for processed meat).

When we stratified the analysis by geographic region, positive associations of fresh red meat, processed meat, and total red meat consumption with risk of stroke were observed in studies conducted in Europe (Sweden) and in the United States, but not in Japan (only 1 study). For example, for total red meat, the RR of stroke for an increase of 1 serving per day in consumption were 1.11 (95% CI, 1.00–1.24) for the 2 studies in Sweden and 1.13 (95% CI, 1.06–1.21) for the 3 United States studies.

In analyses by stroke subtypes, the risk of ischemic stroke was significantly increased for each serving per day increase in fresh red meat (RR, 1.13; 95% CI, 1.00–1.27), processed meat (RR, 1.15; 95% CI, 1.06–1.24), and total red meat consumption (RR, 1.12; 95% CI, 1.05–1.19), without heterogeneity among studies (P>0.34). There was no significant association between hemorrhagic stroke and consumption of fresh red meat (RR, 1.08; 95% CI, 0.84–1.39), processed meat (RR, 1.16; 95% CI, 0.92–1.46), or total red meat (RR, 1.13; 95% CI, 0.94–1.35).

We found no evidence of publication bias. The P values based on Egger test were 0.76 for fresh red meat, 0.26 for processed meat, and 0.09 for total red meat.

Discussion

This meta-analysis of 6 prospective studies, including a large number of stroke cases, showed that fresh red meat, processed meat, and total red meat consumption are significantly positively associated with risk of total stroke and ischemic stroke. Increased consumptions of 1 serving per day of fresh red meat, processed meat, and total red meat were associated with 11%, 13%, and 11% higher risk of total stroke, respectively.

There are several potential mechanisms by which red meat consumption may increase the risk of stroke. Red meat is a source of saturated fatty acids and cholesterol. Some studies have indicated that a high intake of saturated fatty acids increases plasma total cholesterol levels and low-density lipoprotein cholesterol and triglycerides,23–25 which could increase the risk of stroke. Moreover, red meat is a source of heme iron. It is well-known that iron is a redox-active metal that catalyzes the formation of hydroxyl free radicals in the Fenton reaction. High doses of iron may lead to oxidative stress, a state with increased peroxidation of lipids,26–28 protein modification, and DNA damage.28–30 If continued for a long time, oxidative stress induced by iron may lead to the development of many diseases, such as cardiovascular disease,31,32 type 2 diabetes,33–35 atherosclerosis,36,37 neurological disorders,38,39 and chronic inflammation.40 According to Liang et al,41 intake of high amounts of iron (>161 mg/wk vs <100 mg/wk) was related to higher risk of ischemic stroke. Moreover, processed meat contains sodium and nitrite preservatives, which can contribute to increased risk of cardiovascular disease, type 2 diabetes, and other diseases. Dietary sodium significantly increases blood pressure42 and may also lead to impaired arterial compliance and cause vascular stiffness.43 Results from a meta-analysis of 10 prospective studies showed that high dietary sodium (salt) intake was associated with a significant 23% increased risk of stroke.44 Nitrites and their products promote atherosclerosis and vascular dysfunction,45 and they also reduced and impaired insulin secretion.46,47 A stronger association between red meat consumption and stroke risk is expected for processed meat than for fresh red meat because processed meat is a source of sodium and nitrite preservatives. It should be noted that the serving size for processed meat is usually smaller than for fresh red meat, which is eaten as a main dish. This may explain the similar risk estimates for 1 serving per day of processed meat and fresh red meat consumption.

This meta-analysis was based on data from large cohort studies. The prospective design minimizes the potential concern of differential recall bias, which could be a problem in case-control studies with retrospective information about exposures. By combining the results from several studies with a large number of cases, we had higher statistical power in our analyses and could detect weaker relations than in the individual studies. A limitation of any meta-analysis of observational studies is that confounding from other risk factors may have affected the results. The 5 studies from Sweden and the United States, which all observed a positive association between total red meat consumption and stroke risk, adjusted for major potential confounders such as age, smoking, body mass index, physical activity, history of diabetes, history of hypertension, total energy intake, and alcohol, fruit, and vegetable consumption. However, the possibility that residual confounding may have influenced the findings cannot be entirely excluded. Another limitation is that red meat consumption was self-reported through questionnaires, which will inevitably lead to some misclassification of exposure. Nevertheless, because information about red meat consumption was obtained before the diagnosis of stroke, any misclassification is most likely to lead to an attenuation of the true association between red meat consumption and stroke risk. The serving sizes for red meat and processed meat consumption may differ between studies and between individuals, which could have influenced the results. As a meta-analysis of published studies, we cannot rule out that publication bias may have affected our results, although we found no evidence of such bias in the present meta-analysis. Moreover, it should be emphasized that the structure of red meat consumption, ie, quantity, frequency, and dietary patterns in the United States, Sweden and Japan, is different. According to Food and Agriculture Organization of the United Nations statistics, annual consumption (in kg per person per year) of beef in the Americans and Swedes compared with the Japanese is higher, ≈4.8-times and ≈2.7-times, respectively, and consumption of pork is higher 2.2-times and 1.7 times,48 which may have resulted in the difference in intake of some nutrients such as heme iron, saturated fatty acids, and cholesterol. With regard to dietary patterns, studies among United States and Swedish women have shown that red meat consumption is correlated with consumption of refined grains, full-fat dairy products, and sweets or soft drinks.9,49 In a Japanese population, meat consumption correlated with consumption of fish and deep-fried foods or tempura.50

In conclusion, results from this meta-analysis indicate that both fresh red meat and processed meat consumption may increase the risk of stroke. This finding is of great public health importance because of the widespread consumption of red meat and the high morbidity and mortality associated with stroke. Whether the association between red meat consumption and stroke risk is limited to ischemic stroke warrants further study.

Sources of Funding

This study was supported by a research grant from the Swedish Council for Working Life and Social Research (FAS). The funder had no role in the design and conduct of the study; collection, management, analysis, or interpretation of the data; or preparation, review, or approval of the manuscript.

Disclosures

None.

Footnotes

The online-only Data Supplement is available at http://stroke.ahajournals.org/lookup/suppl/doi:10.1161/STROKEAHA.112.663286/-/DC1.

Larsson had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: Kaluza, Wolk, and Larsson. Acquisition of data: Kaluza and Larsson. Analysis and interpretation of data: Larsson and Kaluza. Drafting of the manuscript: Kaluza and Larsson. Critical revision of the manuscript for important intellectual content: Kaluza, Wolk, and Larsson. Statistical analysis: Larsson. Study supervision: Wolk and Larsson.

Correspondence to Joanna Kaluza, PhD,

Department of Human Nutrition, Warsaw University of Life Sciences–SGGW, 159C Nowoursynowska Str, 02-776 Warsaw, Poland

. E-mail [email protected] pl

References

  • 1. Pan A, Sun Q, Bernstein AM, Schulze MB, Manson JE, Stampfer MJ , et al. . Red meat consumption and mortality: results from 2 prospective cohort studies. Arch Intern Med . 2012; 172:555–563.CrossrefMedlineGoogle Scholar
  • 2. Larsson SC, Wolk A. Meat consumption and risk of colorectal cancer: a meta-analysis of prospective studies. Int J Cancer . 2006; 119:2657–2664.CrossrefMedlineGoogle Scholar
  • 3. Smolinska K, Paluszkiewicz P. Risk of colorectal cancer in relation to frequency and total amount of red meat consumption. Systematic review and meta-analysis. Arch Med Sci . 2010; 6:605–610.CrossrefMedlineGoogle Scholar
  • 4. Larsson SC, Wolk A. Red and processed meat consumption and risk of pancreatic cancer: meta-analysis of prospective studies. Br J Cancer . 2012; 106:603–607.CrossrefMedlineGoogle Scholar
  • 5. Larsson SC, Bergkvist L, Wolk A. Processed meat consumption, dietary nitrosamines and stomach cancer risk in a cohort of Swedish women. Int J Cancer . 2006; 119:915–919.CrossrefMedlineGoogle Scholar
  • 6. Cross AJ, Freedman ND, Ren J, Ward MH, Hollenbeck AR, Schatzkin A , et al. . Meat consumption and risk of esophageal and gastric cancer in a large prospective study. Am J Gastroenterol . 2011; 106:432–442.CrossrefMedlineGoogle Scholar
  • 7. Micha R, Wallace SK, Mozaffarian D. Red and processed meat consumption and risk of incident coronary heart disease, stroke, and diabetes mellitus: a systematic review and meta-analysis. Circulation . 2010; 121:2271–2283.LinkGoogle Scholar
  • 8. Pan A, Sun Q, Bernstein AM, Schulze MB, Manson JE, Willett WC , et al. . Red meat consumption and risk of type 2 diabetes: 3 cohorts of US adults and an updated meta-analysis. Am J Clin Nutr . 2011; 94:1088–1096.CrossrefMedlineGoogle Scholar
  • 9. Fung TT, Stampfer MJ, Manson JE, Rexrode KM, Willett WC, Hu FB. Prospective study of major dietary patterns and stroke risk in women. Stroke . 2004; 35:2014–2019.LinkGoogle Scholar
  • 10. 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; 32:536–543.CrossrefMedlineGoogle Scholar
  • 11. He K, Merchant A, Rimm EB, Rosner BA, Stampfer MJ, Willett WC , et al. . Dietary fat intake and risk of stroke in male US healthcare professionals: 14 year prospective cohort study. BMJ . 2003; 327:777–782.CrossrefMedlineGoogle Scholar
  • 12. Roger VL, Go AS, Lloyd-Jones DM, Benjamin EJ, Berry JD, Borden WB , et al. . Heart disease and stroke statistics–2012 update: a report from the American Heart Association. Circulation . 2012; 125:e2–e220.LinkGoogle Scholar
  • 13. Wang Y, Beydoun MA, Caballero B, Gary TL, Lawrence R. Trends and correlates in meat consumption patterns in the US adult population. Public Health Nutr . 2010; 13:1333–1345.CrossrefMedlineGoogle Scholar
  • 14. Larsson SC, Virtamo J, Wolk A. Red meat consumption and risk of stroke in Swedish women. Stroke . 2011; 42:324–329.LinkGoogle Scholar
  • 15. Larsson SC, Virtamo J, Wolk A. Red meat consumption and risk of stroke in Swedish men. Am J Clin Nutr . 2011; 94:417–421.CrossrefMedlineGoogle Scholar
  • 16. DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials . 1986; 7:177–188.CrossrefMedlineGoogle Scholar
  • 17. Egger M, Davey Smith G, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ . 1997; 315:629–634.CrossrefMedlineGoogle Scholar
  • 18. Greenland S, Longnecker MP. Methods for trend estimation from summarized dose-response data, with applications to meta-analysis. Am J Epidemiol . 1992; 135:1301–1309.CrossrefMedlineGoogle Scholar
  • 19. Orsini N, Bellocco R, Greenland S. Generalized least squares for tend estimation of summarized dose-response data. Stata J . 2006; 6:40–57.Google Scholar
  • 20. Higgins JP, Thompson SG. Quantifying heterogeneity in a meta-analysis. Stat Med . 2002; 21:1539–1558.CrossrefMedlineGoogle Scholar
  • 21. Bernstein AM, Pan A, Rexrode KM, Stampfer M, Hu FB, Mozaffarian D , et al. . Dietary protein sources and the risk of stroke in men and women. Stroke . 2012; 43:637–644.LinkGoogle Scholar
  • 22. Yaemsiri S, Sen S, Tinker L, Rosamond W, Wassertheil-Smoller S, He K. Trans fat, aspirin, and ischemic stroke in postmenopausal women. Ann Neurol . 2012;In press.CrossrefMedlineGoogle Scholar
  • 23. Gascon A, Jacques H, Moorjani S, Deshaies Y, Brun LD, Julien P. Plasma lipoprotein profile and lipolytic activities in response to the substitution of lean white fish for other animal protein sources in premenopausal women. Am J Clin Nutr . 1996; 63:315–321.CrossrefMedlineGoogle Scholar
  • 24. Hodson L, Skeaff CM, Chisholm WA. The effect of replacing dietary saturated fat with polyunsaturated or monounsaturated fat on plasma lipids in free-living young adults. Eur J Clin Nutr . 2001; 55:908–915.CrossrefMedlineGoogle Scholar
  • 25. Wolmarans P, Benade AJ, Kotze TJ, Daubitzer AK, Marais MP, Laubscher R. Plasma lipoprotein response to substituting fish for red meat in the diet. Am J Clin Nutr . 1991; 53:1171–1176.CrossrefMedlineGoogle Scholar
  • 26. Lasheras C, Gonzalez S, Huerta JM, Braga S, Patterson AM, Fernandez S. Plasma iron is associated with lipid peroxidation in an elderly population. J Trace Elem Med Biol . 2003; 17:171–176.CrossrefMedlineGoogle Scholar
  • 27. King SM, Donangelo CM, Knutson MD, Walter PB, Ames BN, Viteri FE , et al. . Daily supplementation with iron increases lipid peroxidation in young women with low iron stores. Exp Biol Med (Maywood) . 2008; 233:701–707.CrossrefMedlineGoogle Scholar
  • 28. Zago MP, Verstraeten SV, Oteiza PI. Zinc in the prevention of Fe2+-initiated lipid and protein oxidation. Biol Res . 2000; 33:143–150.CrossrefMedlineGoogle Scholar
  • 29. Walter PB, Knutson MD, Paler-Martinez A, Lee S, Xu Y, Viteri FE , et al. . Iron deficiency and iron excess damage mitochondria and mitochondrial DNA in rats. Proc Natl Acad Sci U S A . 2002; 99:2264–2269.CrossrefMedlineGoogle Scholar
  • 30. Hori A, Mizoue T, Kasai H, Kawai K, Matsushita Y, Nanri A , et al. . Body iron store as a predictor of oxidative DNA damage in healthy men and women. Cancer Sci . 2010; 101:517–522.CrossrefMedlineGoogle Scholar
  • 31. van der A DL, Peeters PH, Grobbee DE, Marx JJ, van der Schouw YT. Dietary haem iron and coronary heart disease in women. Eur Heart J . 2005; 26:257–262.CrossrefMedlineGoogle Scholar
  • 32. Qi L, van Dam RM, Rexrode K, Hu FB. Heme iron from diet as a risk factor for coronary heart disease in women with type 2 diabetes. Diabetes Care . 2007; 30:101–106.CrossrefMedlineGoogle Scholar
  • 33. Lee DH, Liu DY, Jacobs DR, Shin HR, Song K, Lee IK , et al. . Common presence of non-transferrin-bound iron among patients with type 2 diabetes. Diabetes Care . 2006; 29:1090–1095.CrossrefMedlineGoogle Scholar
  • 34. Swaminathan S, Fonseca VA, Alam MG, Shah SV. The role of iron in diabetes and its complications. Diabetes Care . 2007; 30:1926–1933.CrossrefMedlineGoogle Scholar
  • 35. Le Blanc S, Villarroel P, Candia V, Gavilan N, Soto N, Perez-Bravo F , et al. . Type 2 diabetic patients and their offspring show altered parameters of iron status, oxidative stress and genes related to mitochondrial activity. Biometals . 2012; 25:725–735.CrossrefMedlineGoogle Scholar
  • 36. Stadler N, Lindner RA, Davies MJ. Direct detection and quantification of transition metal ions in human atherosclerotic plaques: evidence for the presence of elevated levels of iron and copper. Arterioscler Thromb Vasc Biol . 2004; 24:949–954.LinkGoogle Scholar
  • 37. Syrovatka P, Kraml P, Hulikova K, Fialova L, Vejrazka M, Crkovska J , et al. . Iron stores are associated with asymptomatic atherosclerosis in healthy men of primary prevention. Eur J Clin Invest . 2011; 41:846–853.CrossrefMedlineGoogle Scholar
  • 38. Levenson CW. Iron and Parkinson's disease: chelators to the rescue? Nutr Rev . 2003; 61:311–313.CrossrefMedlineGoogle Scholar
  • 39. Bush AI, Curtain CC. Twenty years of metallo-neurobiology: where to now? Eur Biophys J . 2008; 37:241–245.CrossrefMedlineGoogle Scholar
  • 40. Depalma RG, Hayes VW, Chow BK, Shamayeva G, May PE, Zacharski LR. Ferritin levels, inflammatory biomarkers, and mortality in peripheral arterial disease: a substudy of the Iron (Fe) and Atherosclerosis Study (FeAST) Trial. J Vasc Surg . 2010; 51:1498–1503.CrossrefMedlineGoogle Scholar
  • 41. Liang W, Lee AH, Binns CW. Dietary intake of minerals and the risk of ischemic stroke in Guangdong Province, China, 2007–2008. Prev Chronic Dis . 2011; 8:A38.MedlineGoogle Scholar
  • 42. He FJ, MacGregor GA. Effect of modest salt reduction on blood pressure: a meta-analysis of randomized trials. Implications for public health. J Hum Hypertens . 2002; 16:761–770.CrossrefMedlineGoogle Scholar
  • 43. Sanders PW. Vascular consequences of dietary salt intake. Am J Physiol Renal Physiol . 2009; 297:F237–F243.CrossrefMedlineGoogle Scholar
  • 44. Strazzullo P, D'Elia L, Kandala NB, Cappuccio FP. Salt intake, stroke, and cardiovascular disease: meta-analysis of prospective studies. BMJ . 2009; 339:b4567.CrossrefMedlineGoogle Scholar
  • 45. Forstermann U. Oxidative stress in vascular disease: causes, defense mechanisms and potential therapies. Nat Clin Pract Cardiovasc Med . 2008; 5:338–349.CrossrefMedlineGoogle Scholar
  • 46. Portha B, Giroix MH, Cros JC, Picon L. Diabetogenic effect of N-nitrosomethylurea and N-nitrosomethylurethane in the adult rat. Ann Nutr Aliment . 1980; 34:1143–1151.MedlineGoogle Scholar
  • 47. McGrowder D, Ragoobirsingh D, Dasgupta T. Effects of S-nitroso-N-acetyl-penicillamine administration on glucose tolerance and plasma levels of insulin and glucagon in the dog. Nitric Oxide . 2001; 5:402–412.CrossrefMedlineGoogle Scholar
  • 48. The State of Food and Agriculture 2009: Livestock in the Balance . Rome, Italy: Food and Agriculture Organization of the United Nations; 2009.Google Scholar
  • 49. Rashidkhani B, Akesson A, Lindblad P, Wolk A. Major dietary patterns and risk of renal cell carcinoma in a prospective cohort of Swedish women. J Nutr . 2005; 135:1757–1762.CrossrefMedlineGoogle Scholar
  • 50. Maruyama K, Iso H, Date C, Kikuchi S, Watanabe Y, Wada Y, Inaba Y, Tamakoshi A: Dietary patterns and risk of cardiovascular deaths among middle-aged Japanese: JACC Study. Nutr Metab Cardiovasc Dis . 2012;In press.MedlineGoogle Scholar

millersayindons.blogspot.com

Source: https://www.ahajournals.org/doi/10.1161/strokeaha.112.663286

0 Response to "Does Beef Increase Chances of Stroke"

Post a Comment

Iklan Atas Artikel

Iklan Tengah Artikel 1

Iklan Tengah Artikel 2

Iklan Bawah Artikel