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High stored iron levels are associated with excess risk of myocardial infarction in eastern Finnish men
Abstract
BACKGROUND: Iron can induce lipid peroxidation in vitro and in vivo in humans and has promoted ischemic myocardial injury in experimental animals. We tested the hypothesis that high serum ferritin concentration and high dietary iron intake are associated with an excess risk of acute myocardial infarction. METHODS AND RESULTS: Randomly selected men (n = 1,931), aged 42, 48, 54, or 60 years, who had no symptomatic coronary heart disease at entry, were examined in the Kuopio Ischaemic Heart Disease Risk Factor Study (KIHD) in Eastern Finland between 1984 and 1989. Fifty-one of these men experienced an acute myocardial infarction during an average follow-up of 3 years. On the basis of a Cox proportional hazards model adjusting for age, examination year, cigarette pack-years, ischemic ECG in exercise test, maximal oxygen uptake, systolic blood pressure, blood glucose, serum copper, blood leukocyte count, and serum high density lipoprotein cholesterol, apolipoprotein B, and triglyceride concentrations, men with serum ferritin greater than or equal to 200 micrograms/l had a 2.2-fold (95% CI, 1.2-4.0; p less than 0.01) risk factor-adjusted risk of acute myocardial infarction compared with men with a lower serum ferritin. An elevated serum ferritin was a strong risk factor for acute myocardial infarction in all multivariate models. This association was stronger in men with serum low density lipoprotein cholesterol concentration of 5.0 mmol/l (193 mg/dl) or more than in others. Also, dietary iron intake had a significant association with the disease risk in a Cox model with the same covariates. CONCLUSIONS: Our data suggest that a high stored iron level, as assessed by elevated serum ferritin concentration, is a risk factor for coronary heart disease.
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“Cell activation can occur via receptor-mediated generation of ROS through both mitochondrial and cytosolic pathways involving the electron transport chain and NAD(P)H oxidase, respectively (472,473) .”
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“all of which could aid in weight loss/maintenance, enhance glycemic control and insulin regulation, improve lipid profile, reduce blood pressure, improve vascular health, decrease inflammation, and foster more favorable diet- gut microbiome interactions (e.g. through lowered levels of trimethylamine N-oxide), thereby lowering CHD risk.”
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“The mechanisms through which hPDI could reduce CHD risk are likely shared with the mechanisms for type 2 diabetes risk reduction.(2, 24–32)”
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Metadata
- Authors
- Salonen, J. T., Nyyssönen, K., Korpela, H., Tuomilehto, J., Seppänen, R., & Salonen, R.
- Affiliations
- University of Eastern Finland (FI)
- Venue
- Circulation
- Published
- 1992-09
- Volume
- 86
- Issue
- 3
- Pages
- 803-811
- ISSN
- 0009-7322 (ISSN-L)
- 1524-4539
- OpenAlex
- W2065303599
- Cited by
- 1,284
- References
- 38
- Citations by year
- 2026: 8 · 2025: 15 · 2024: 16 · 2023: 17 · 2022: 43 · 2021: 32 · 2020: 27 · 2019: 33 · 2018: 36 · 2017: 42 · 2016: 47 · 2015: 35 · 2014: 38 · 2013: 40 · 2012: 48
- FWCI
- 34.96
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Circulation (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Acute Myocardial Infarction Research
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Health and Risk Factors
- Keywords
- serum ferritin, stored iron, acute myocardial infarction, coronary heart disease risk, iron intake, lipid peroxidation, LDL cholesterol, men, Eastern Finland
- MeSH terms
- Adult, Aging, Diet, Dose-Response Relationship, Drug, Ferritins, Finland, Hemoglobins, Humans, Iron, Cholesterol, LDL, Male, Middle Aged, Myocardial Infarction, Risk Factors, Smoking, Proportional Hazards Models
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