D-Dimer Predicts Long-Term Cause-Specific Mortality, Cardiovascular Events, and Cancer in Patients With Stable Coronary Heart Disease: LIPID Study
- PMID: 29367425
- DOI: 10.1161/CIRCULATIONAHA.117.029901
D-Dimer Predicts Long-Term Cause-Specific Mortality, Cardiovascular Events, and Cancer in Patients With Stable Coronary Heart Disease: LIPID Study
Abstract
Background: D-dimer, a degradation product of cross-linked fibrin, is a marker for hypercoagulability and thrombotic events. Moderately elevated levels of D-dimer are associated with the risk of venous and arterial events in patients with vascular disease. We assessed the role of D-dimer levels in predicting long-term vascular outcomes, cause-specific mortality, and new cancers in the LIPID trial (Long-Term Intervention with Pravastatin in Ischaemic Disease) in the context of other risk factors.
Methods: LIPID randomized patients to placebo or pravastatin 40 mg/d 5 to 38 months after myocardial infarction or unstable angina. D-dimer levels were measured at baseline and at 1 year. Median follow-up was 6.0 years during the trial and 16 years in total.
Results: Baseline D-dimer levels for 7863 patients were grouped by quartile (≤112, 112-173, 173-273, >273 ng/mL). Higher levels were associated with older age, female sex, history of hypertension, poor renal function, and elevated levels of B-natriuretic peptide, high-sensitivity C-reactive protein, and sensitive troponin I (each P<0.001). During the first 6 years, after adjustment for up to 30 additional risk factors, higher D-dimer was associated with a significantly increased risk of a major coronary event (quartile 4 versus 1: hazard ratio [HR], 1.45; 95% confidence interval, 1.21-1.74), major cardiovascular disease (CVD) event (HR, 1.45; 95% confidence interval, 1.23-1.71) and venous thromboembolism (HR, 4.03; 95% confidence interval, 2.31-7.03; each P<0.001). During the 16 years overall, higher D-dimer was an independent predictor of all-cause mortality (HR, 1.59), CVD mortality (HR, 1.61), cancer mortality (HR, 1.54), and non-CVD noncancer mortality (HR, 1.57; each P<0.001), remaining significant for deaths resulting from each cause occurring beyond 10 years of follow-up (each P≤0.01). Higher D-dimer also independently predicted an increase in cancer incidence (HR, 1.16; P=0.02).The D-dimer level increased the net reclassification index for all-cause mortality by 4.0 and venous thromboembolism by 13.6.
Conclusions: D-dimer levels predict long-term risk of arterial and venous events, CVD mortality, and non-CVD noncancer mortality independent of other risk factors. D-dimer is also a significant predictor of cancer incidence and mortality. These results support an association of D-dimer with fatal events across multiple diseases and demonstrate that this link extends beyond 10 years' follow-up.
Keywords: biomarkers; cardiovascular diseases; cholesterol; coronary disease; fibrin fragment D; hydroxymethylglutaryl-CoA reductase inhibitors; lipids; risk assessment.
Comment in
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Biomarkers: Extended predictive value of d-dimer.Nat Rev Cardiol. 2018 Apr;15(4):198. doi: 10.1038/nrcardio.2018.13. Epub 2018 Feb 15. Nat Rev Cardiol. 2018. PMID: 29446770 No abstract available.
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D-Dimer for Long-Term Risk Prediction in Patients After Acute Coronary Syndrome: Jack of All Trades, or Master of None?Circulation. 2018 Aug 14;138(7):724-726. doi: 10.1161/CIRCULATIONAHA.118.033670. Circulation. 2018. PMID: 30359138 No abstract available.
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Letter by Mehta and Mandawat Regarding Article, "D-Dimer Predicts Long-Term Cause-Specific Mortality, Cardiovascular Events, and Cancer in Patients With Stable Coronary Heart Disease".Circulation. 2019 Feb 26;139(9):1243-1244. doi: 10.1161/CIRCULATIONAHA.118.037677. Circulation. 2019. PMID: 30802171 No abstract available.
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Response by Simes et al to Letter Regarding Article, "D-Dimer Predicts Long-Term Cause-Specific Mortality, Cardiovascular Events, and Cancer in Patients With Stable Coronary Heart Disease".Circulation. 2019 Feb 26;139(9):1245-1246. doi: 10.1161/CIRCULATIONAHA.118.038480. Circulation. 2019. PMID: 30857403 No abstract available.
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