Nonfasting triglycerides and risk of myocardial infarction, ischemic heart disease, and death in men and women - PubMed (original) (raw)
. 2007 Jul 18;298(3):299-308.
doi: 10.1001/jama.298.3.299.
Affiliations
- PMID: 17635890
- DOI: 10.1001/jama.298.3.299
Nonfasting triglycerides and risk of myocardial infarction, ischemic heart disease, and death in men and women
Børge G Nordestgaard et al. JAMA. 2007.
Abstract
Context: Elevated nonfasting triglycerides indicate the presence of remnant lipoproteins, which may promote atherosclerosis.
Objective: To test the hypothesis that very high levels of nonfasting triglycerides predict myocardial infarction (MI), ischemic heart disease (IHD), and death.
Design, setting, and participants: A prospective cohort study of 7587 women and 6394 men from the general population of Copenhagen, Denmark, aged 20 to 93 years, followed up from baseline (1976-1978) until 2004.
Main outcome measures: Hazard ratios (HRs) for incident MI, IHD, and total death according to baseline nonfasting triglyceride level categories of 1 to 1.99 mmol/L (88.5-176.1 mg/dL), 2 to 2.99 mmol/L (177.0-264.6 mg/dL), 3 to 3.99 mmol/L (265.5-353.0 mg/dL), 4 to 4.99 mmol/L (354.0-441.6 mg/dL), and 5 mmol/L or more (> or =442.5 mg/dL) vs triglyceride levels of less than 1 mmol/L (<88.5 mg/dL).
Results: With increasing levels of nonfasting triglycerides, levels of remnant lipoprotein cholesterol increased. During a mean follow-up of 26 years, 1793 participants (691 women and 1102 men) developed MI, 3479 (1567 women and 1912 men) developed IHD, and 7818 (3731 women and 4087 men) died. For MI, among women, the age-adjusted HRs and multifactorially adjusted HRs (aHRs) for each respective category per 1-mmol/L increase in nonfasting triglyceride levels were 2.2 (aHR, 1.7), 4.4 (aHR, 2.5), 3.9 (aHR, 2.1), 5.1 (aHR, 2.4), and 16.8 (aHR, 5.4); for both, P for trend < .001. For MI, among men, the values were 1.6 (aHR, 1.4), 2.3 (aHR, 1.6), 3.6 (aHR, 2.3), 3.3 (aHR, 1.9), and 4.6 (aHR, 2.4); for both, P for trend < .001. For IHD, among women, the values were 1.7 (aHR, 1.4), 2.8 (aHR, 1.8), 3.0 (aHR, 1.8), 2.1 (aHR, 1.2), and 5.9 (aHR, 2.6); for both, P for trend < .001. For IHD, among men, the values were 1.3 (aHR, 1.1), 1.7 (aHR, 1.3), 2.1 (aHR, 1.3), 2.0 (aHR, 1.2), and 2.9 (aHR, 1.5); P for trend < .001 for age-adjusted and P for trend = .03 for multifactorially adjusted. For total death, among women, the values were 1.3 (aHR, 1.3), 1.7 (aHR, 1.6), 2.2 (aHR, 2.2), 2.2 (aHR, 1.9), and 4.3 (aHR, 3.3); for both, P for trend < .001. For total death, among men, the values were 1.3 (aHR, 1.2), 1.4 (aHR, 1.4), 1.7 (aHR, 1.5), 1.8 (aHR, 1.6), and 2.0 (aHR, 1.8); for both, P for trend < .001.
Conclusion: In this general population cohort, elevated nonfasting triglyceride levels were associated with increased risk of MI, IHD, and death in men and women.
Republished in
- [Non-fasting triglycerides and risk of for myocardial infarction and death among women and men].
Nordestgaard BG, Benn M, Schnohr P, Tybjaerg-Hansen A. Nordestgaard BG, et al. Ugeskr Laeger. 2007 Nov 5;169(45):3865-8. Ugeskr Laeger. 2007. PMID: 18031660 Danish.
Comment in
- Triglycerides and risk for coronary heart disease.
McBride PE. McBride PE. JAMA. 2007 Jul 18;298(3):336-8. doi: 10.1001/jama.298.3.336. JAMA. 2007. PMID: 17635897 No abstract available. - Nonfasting triglycerides and cardiovascular risk.
Yancy WS Jr, Volek JS, Westman EC. Yancy WS Jr, et al. JAMA. 2007 Nov 7;298(17):2004; author reply 2005-6. doi: 10.1001/jama.298.17.2004-a. JAMA. 2007. PMID: 17986691 No abstract available. - Fasting versus nonfasting triglycerides and the prediction of cardiovascular risk: do we need to revisit the oral triglyceride tolerance test?
Ridker PM. Ridker PM. Clin Chem. 2008 Jan;54(1):11-3. doi: 10.1373/clinchem.2007.097907. Epub 2007 Nov 12. Clin Chem. 2008. PMID: 17998265 No abstract available. - Fasting versus nonfasting triglycerides: implications for laboratory measurements.
Warnick GR, Nakajima K. Warnick GR, et al. Clin Chem. 2008 Jan;54(1):14-6. doi: 10.1373/clinchem.2007.098863. Epub 2007 Nov 26. Clin Chem. 2008. PMID: 18039717 No abstract available.
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