Multiple biomarkers for the prediction of first major cardiovascular events and death
- PMID: 17182988
- DOI: 10.1056/NEJMoa055373
Multiple biomarkers for the prediction of first major cardiovascular events and death
Abstract
Background: Few investigations have evaluated the incremental usefulness of multiple biomarkers from distinct biologic pathways for predicting the risk of cardiovascular events.
Methods: We measured 10 biomarkers in 3209 participants attending a routine examination cycle of the Framingham Heart Study: the levels of C-reactive protein, B-type natriuretic peptide, N-terminal pro-atrial natriuretic peptide, aldosterone, renin, fibrinogen, D-dimer, plasminogen-activator inhibitor type 1, and homocysteine; and the urinary albumin-to-creatinine ratio.
Results: During follow-up (median, 7.4 years), 207 participants died and 169 had a first major cardiovascular event. In Cox proportional-hazards models adjusting for conventional risk factors, the following biomarkers most strongly predicted the risk of death (each biomarker is followed by the adjusted hazard ratio per 1 SD increment in the log values): B-type natriuretic peptide level (1.40), C-reactive protein level (1.39), the urinary albumin-to-creatinine ratio (1.22), homocysteine level (1.20), and renin level (1.17). The biomarkers that most strongly predicted major cardiovascular events were B-type natriuretic peptide level (adjusted hazard ratio, 1.25 per 1 SD increment in the log values) and the urinary albumin-to-creatinine ratio (1.20). Persons with "multimarker" scores (based on regression coefficients of significant biomarkers) in the highest quintile as compared with those with scores in the lowest two quintiles had elevated risks of death (adjusted hazard ratio, 4.08; P<0.001) and major cardiovascular events (adjusted hazard ratio, 1.84; P=0.02). However, the addition of multimarker scores to conventional risk factors resulted in only small increases in the ability to classify risk, as measured by the C statistic.
Conclusions: For assessing risk in individual persons, the use of the 10 contemporary biomarkers that we studied adds only moderately to standard risk factors.
Copyright 2006 Massachusetts Medical Society.
Comment in
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The limitations of risk factors as prognostic tools.N Engl J Med. 2006 Dec 21;355(25):2615-7. doi: 10.1056/NEJMp068249. N Engl J Med. 2006. PMID: 17182986 No abstract available.
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Biomarkers for prediction of cardiovascular events.N Engl J Med. 2007 Apr 5;356(14):1472; author reply 1474-5. doi: 10.1056/NEJMc070079. N Engl J Med. 2007. PMID: 17409333 No abstract available.
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Biomarkers for prediction of cardiovascular events.N Engl J Med. 2007 Apr 5;356(14):1472-3; author reply 1474-5. N Engl J Med. 2007. PMID: 17415901 No abstract available.
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Biomarkers for prediction of cardiovascular events.N Engl J Med. 2007 Apr 5;356(14):1473; author reply 1474-5. N Engl J Med. 2007. PMID: 17415902 No abstract available.
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Biomarkers for prediction of cardiovascular events.N Engl J Med. 2007 Apr 5;356(14):1473; author reply 1474-5. N Engl J Med. 2007. PMID: 17415903 No abstract available.
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New biomarkers add little to current predictors for CAD.J Fam Pract. 2007 Mar;56(3):178. J Fam Pract. 2007. PMID: 17607830 No abstract available.
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