Why the study?
To evaluate the combined impact of D-dimer, hs-CRP, and Lp(a) on long-term cardiovascular outcomes addressing thrombosis, inflammation, and lipid risk in patients after PCI.
Does the combined elevation of D-dimer, hs-CRP, and Lp(a) increase the risk of adverse clinical outcomes in patients after percutaneous coronary intervention?
Does the combined elevation of D-dimer, hs-CRP, and Lp(a) increase the risk of adverse clinical outcomes in patients after percutaneous coronary intervention?
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Simultaneous assessment of D-dimer, hs-CRP, and Lp(a) provides incremental prognostic value beyond traditional risk factors for identifying high-risk patients after PCI.
To reduce cardiovascular risk in patients with established coronary heart disease, the present study investigated the combined effect of D-dimer, high-sensitivity C-reactive protein (hs-CRP), and lipoprotein(a) [Lp(a)] on long-term cardiovascular outcomes from the perspectives of thrombosis, inflammation, and lipid risk simultaneously. Consecutive 10,724 patients with percutaneous coronary intervention (PCI) were enrolled throughout 2013. Over a median follow-up of 5.1 years, each individual elevation of D-dimer, hs-CRP, and Lp(a) was associated with poor ischemic outcomes but not bleeding. Concurrent high D-dimer, hs-CRP, and Lp(a) had even greater risks of all-cause death (hazard ratio [HR] 2.714, 95% confidence interval [CI] 1.742-4.231) and cardiac death (HR 4.152, 95% CI 2.207-7.812) and had incremental value beyond the traditional risk factors model. Concurrent high D-dimer, hs-CRP, and Lp(a) levels had a synergistic effect on adverse 5-year ischemic outcomes, highlighting that the potential utility of simultaneous assessment of multiple cardiovascular risk biomarkers may help to identify high-risk patients after PCI.
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Li et al. (2023) studied this question.
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