Intake of mercury from fish, lipid peroxidation, and the risk of myocardial infarction and coronary, cardiovascular, and any death in eastern Finnish men.

BACKGROUND Even though previous studies have suggested an association between high fish intake and reduced coronary heart disease (CHD) mortality, men in Eastern Finland, who have a high fish intake, have an exceptionally high CHD mortality. We hypothesized that this paradox could be in part explained by high mercury content in fish. METHODS AND RESULTS We studied the relation of the dietary intake of fish and mercury, as well as hair content and urinary excretion of mercury, to the risk of acute myocardial infarction (AMI) and death from CHD, cardiovascular disease (CVD), and any cause in 1833 men aged 42 to 60 years who were free of clinical CHD, stroke, claudication, and cancer. Of these, 73 experienced an AMI in 2 to 7 years. Of the 78 decreased men, 18 died of CHD and 24 died of CVD. Men who had consumed local nonfatty fish species had elevated hair mercury contents. In Cox models with the major cardiovascular risk factors as covariates, dietary intakes of fish and mercury were associated with significantly increased risk of AMI and death from CHD, CVD, and any death. Men in the highest tertile (> or = 2.0 micrograms/g) of hair mercury content had a 2.0-fold (95% confidence interval, 1.2 to 3.1; P = .005) age- and CHD-adjusted risk of AMI and a 2.9-fold (95% CI, 1.2 to 6.6; P = .014) adjusted risk of cardiovascular death compared with those with a lower hair mercury content. In a nested case-control subsample, the 24-hour urinary mercury excretion had a significant (P = .042) independent association with the risk of AMI. Both the hair and urinary mercury associated significantly with titers of immune complexes containing oxidized LDL. CONCLUSIONS These data suggest that a high intake of mercury from nonfatty freshwater fish and the consequent accumulation of mercury in the body are associated with an excess risk of AMI as well as death from CHD, CVD, and any cause in Eastern Finnish men and this increased risk may be due to the promotion of lipid peroxidation by mercury.

[1]  D Kromhout,et al.  The inverse relation between fish consumption and 20-year mortality from coronary heart disease. , 1985, The New England journal of medicine.

[2]  J. Salonen Selenium in ischaemic heart disease. , 1987, International journal of epidemiology.

[3]  D. Airey Mercury in human hair due to environment and diet: a review. , 1983, Environmental health perspectives.

[4]  M. Verta Mercury in Finnish forest lakes and reservoirs : anthropogenic contribution to the load and accumulation in fish , 1990 .

[5]  S. Rana,et al.  Antiperoxidative mechanisms offered by selenium against liver injury caused by cadmium and mercury in rat , 1992, Bulletin of environmental contamination and toxicology.

[6]  R. Rauramaa,et al.  Relationship of serum selenium and antioxidants to plasma lipoproteins, platelet aggregability and prevalent ischaemic heart disease in Eastern Finnish men. , 1988, Atherosclerosis.

[7]  J. Salonen,et al.  Socioeconomic conditions in childhood and ischaemic heart disease during middle age. , 1990, BMJ.

[8]  Heikki Korpela,et al.  High Stored Iron Levels Are Associated With Excess Risk of Myocardial Infarction in Eastern Finnish Men , 1992, Circulation.

[9]  J. Salonen The role of iron as a cardiovascular risk factor , 1993 .

[10]  J. Haines,et al.  International programme on chemical safety , 1996, The Lancet.

[11]  J. Salonen,et al.  Serum copper and the risk of acute myocardial infarction: a prospective population study in men in eastern Finland. , 1991, American journal of epidemiology.

[12]  T. Clarkson Mercury--an element of mystery. , 1990, The New England journal of medicine.

[13]  M. Nieminen,et al.  Association between dental health and acute myocardial infarction. , 1989, BMJ.

[14]  T. Lakka,et al.  Moderate to high intensity conditioning leisure time physical activity and high cardiorespiratory fitness are associated with reduced plasma fibrinogen in eastern Finnish men. , 1993, Journal of clinical epidemiology.

[15]  A. Hofman,et al.  Decreased selenium levels in acute myocardial infarction. , 1989, JAMA.

[16]  J M Venäläinen,et al.  Relation of leisure-time physical activity and cardiorespiratory fitness to the risk of acute myocardial infarction. , 1994, The New England journal of medicine.

[17]  C. Morris,et al.  Presence of foam cells containing oxidised low density lipoprotein in the synovial membrane from patients with rheumatoid arthritis. , 1993, Annals of the rheumatic diseases.

[18]  L. Benov,et al.  Thiol antidotes effect on lipid peroxidation in mercury-poisoned rats. , 1990, Chemico-biological interactions.

[19]  J. Salonen,et al.  An automated colorimetric assay for urine nicotine metabolites: a suitable alternative to cotinine assays for the assessment of smoking status. , 1987, Clinica chimica acta; international journal of clinical chemistry.

[20]  B. Halliwell,et al.  Free radicals in biology and medicine , 1985 .

[21]  J. Salonen,et al.  A method for routine assay of plasma ascorbic acid using high-performance liquid chromatography , 1986 .

[22]  A. Simopoulos,et al.  Summary of the conference on the health effects of polyunsaturated fatty acids in seafoods. , 1986, The Journal of nutrition.

[23]  J. Salonen,et al.  Autoantibody against oxidised LDL and progression of carotid atherosclerosis , 1992, The Lancet.

[24]  V. Salomaa,et al.  Acute myocardial infarction (AMI) in Finland--baseline data from the FINMONICA AMI register in 1983-1985. , 1992, European heart journal.

[25]  Ivar Heuch,et al.  Fish consumption and mortality from coronary heart disease. , 1985, The New England journal of medicine.

[26]  J. Salonen,et al.  Effects of antioxidant supplementation on platelet function: a randomized pair-matched, placebo-controlled, double-blind trial in men with low antioxidant status. , 1991, The American journal of clinical nutrition.

[27]  J. S. Woods,et al.  Reactivity of Hg(II) with superoxide: evidence for the catalytic dismutation of superoxide by Hg(II). , 1991, Journal of biochemical toxicology.

[28]  M. Harms-Ringdahl,et al.  Stimulating effects of mercuric- and silver ions on the superoxide anion production in human polymorphonuclear leukocytes. , 1993, Free radical research communications.

[29]  Christoph Hohenemser,et al.  Mercury. . . Measuring and Managing the Risk. , 1978 .

[30]  C. Hohenemser,et al.  Power plant performance , 1978 .

[31]  Lu Kun-Ping,et al.  The stimulatory effect of heavy metal cations on proliferation of aortic smooth muscle cells. , 1990 .

[32]  H. Hein,et al.  Serum selenium concentration and risk of ischaemic heart disease in a prospective cohort study of 3000 males. , 1992, Atherosclerosis.

[33]  Salonen Jt Is there a continuing need for longitudinal epidemiologic research? The Kuopio Ischaemic Heart Disease Risk Factor Study. , 1988 .

[34]  H. Ganther,et al.  Selenium: Relation to Decreased Toxicity of Methylmercury Added to Diets Containing Tuna , 1972, Science.

[35]  J L Witztum,et al.  Beyond cholesterol. Modifications of low-density lipoprotein that increase its atherogenicity. , 1989, The New England journal of medicine.

[36]  J. Salonen,et al.  Nutrition data collection in the Kuopio Ischaemic Heart Disease Risk Factor Study: Nutrient intake of middle-aged eastern finnish men , 1989 .

[37]  T. Dolecek,et al.  Dietary polyunsaturated fatty acids and mortality in the Multiple Risk Factor Intervention Trial (MRFIT). , 1991, World review of nutrition and dietetics.

[38]  F. Sunderman Metals and lipid peroxidation. , 2009, Acta pharmacologica et toxicologica.

[39]  R. Furness,et al.  Mercury and selenium interaction: a review. , 1991, Ecotoxicology and environmental safety.

[40]  D. Williamson,et al.  Dental disease and risk of coronary heart disease and mortality. , 1993, BMJ.

[41]  J. S. Woods,et al.  Studies on Hg(II)-induced H2O2 formation and oxidative stress in vivo and in vitro in rat kidney mitochondria. , 1993, Biochemical pharmacology.

[42]  S. Welsh,et al.  The protective effect of vitamin E and N,N'-diphenyl-p-phenylenediamine (DPPD) against methyl mercury toxicity in the rat. , 1979, The Journal of nutrition.

[43]  J. Salonen,et al.  Coping with inner feelings and stress: heavy alcohol use in the context of alexithymia. , 1992, Behavioral medicine.

[44]  H. Ganther INTERACTIONS OF VITAMIN E AND SELENIUM WITH MERCURY AND SILVER , 1980, Annals of the New York Academy of Sciences.

[45]  H. Blackburn,et al.  Cardiovascular survey methods. , 1969, Monograph series. World Health Organization.

[46]  D. Cox Regression Models and Life-Tables , 1972 .

[47]  Who Monica WHO MONICA Project: Assessing CHD Mortality and Morbidity , 1989 .

[48]  K. Ingold,et al.  The relative contributions of vitamin E, urate, ascorbate and proteins to the total peroxyl radical-trapping antioxidant activity of human blood plasma. , 1987, Biochimica et biophysica acta.

[49]  J. Salonen,et al.  Interactions of serum copper, selenium, and low density lipoprotein cholesterol in atherogenesis. , 1991, BMJ.

[50]  H. DeLuca THE CONTROL OF CALCIUM AND PHOSPHORUS METABOLISM BY THE VITAMIN D ENDOCRINE SYSTEM* , 1980, Annals of the New York Academy of Sciences.

[51]  A. Naganuma,et al.  Behavior of methylmercury in mammalian erythrocytes. , 1980, Toxicology and applied pharmacology.

[52]  P. Puska,et al.  ASSOCIATION BETWEEN CARDIOVASCULAR DEATH AND MYOCARDIAL INFARCTION AND SERUM SELENIUM IN A MATCHED-PAIR LONGITUDINAL STUDY , 1982, The Lancet.

[53]  A. Ahlbom,et al.  Fish consumption and mortality from coronary heart disease. , 1986, British medical journal.

[54]  R. Rauramaa,et al.  HDL, HDL2, and HDL3 Subfractions, and the Risk of Acute Myocardial Infarction: A Prospective Population Study in Eastern Finnish Men , 1991, Circulation.

[55]  B. Kostka Potentiation of ADP-induced platelet aggregation by mercury compounds. , 1990, Thrombosis research.