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J Am Coll Cardiol, 2009; 54:601-608, doi:10.1016/j.jacc.2009.05.022
© 2009 by the American College of Cardiology Foundation
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CLINICAL RESEARCH: BIOMARKERS

Significance of a Multiple Biomarkers Strategy Including Endothelial Dysfunction to Improve Risk Stratification for Cardiovascular Events in Patients at High Risk for Coronary Heart Disease

Toshimitsu Nozaki, MD*, Seigo Sugiyama, MD, PhD*,*, Hidenobu Koga, MD, PhD*, Koichi Sugamura, MD*, Keisuke Ohba, MD*, Yasushi Matsuzawa, MD*, Hitoshi Sumida, MD, PhD{dagger}, Kunihiko Matsui, MD, PhD{ddagger}, Hideaki Jinnouchi, MD, PhD§ and Hisao Ogawa, MD, PhD*

* Department of Cardiovascular Medicine, Graduate School of Medical Science, Kumamoto University, Kumamoto, Japan
{dagger} Department of Interventional Cardiology, Graduate School of Medical Science, Kumamoto University, Kumamoto, Japan
{ddagger} Department of General Medicine, Graduate School of Medical Science, Kumamoto University, Kumamoto, Japan
§ Jinnouchi Hospital, Kumamoto, Japan

Manuscript received January 5, 2009; revised manuscript received May 21, 2009, accepted May 25, 2009.

* Reprint requests and correspondence: Dr. Seigo Sugiyama, Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto City 860-8556, Japan (Email: ssugiyam{at}gpo.kumamoto-u.ac.jp).

Objectives: We investigated whether a multiple biomarkers strategy that includes plasma levels of endothelium-derived microparticles (EMP), reflecting endothelial dysfunction, can improve prediction of future cardiovascular events in patients at high risk for coronary heart disease (CHD).

Background: Detailed risk stratification using multiple biomarkers can provide clinical benefits in high-risk patients. Endothelial dysfunction has been described as a predictor of cardiovascular complications.

Methods: We measured 3 biomarkers in 488 consecutive patients with various CHD risks: B-type natriuretic peptide (BNP), high-sensitivity C-reactive protein (hsCRP), and EMP. We followed 387 stable patients at high risk for CHD and examined future cardiovascular events.

Results: During a mean follow-up of 36 months, 55 patients developed cardiovascular events. Multivariate Cox proportional hazards analysis adjusted for established risk factors identified age, BNP, hsCRP, and EMP as significant and independent predictors of future cardiovascular events (age: hazard ratio [HR]: 1.042, 95% confidence interval [CI]: 1.007 to 1.080, p = 0.02; BNP: HR: 1.242, 95% CI: 1.004 to 1.536, p = 0.046; hsCRP: HR: 1.468, 95% CI: 1.150 to 1.875, p = 0.002; EMP: HR: 1.345, 95% CI: 1.094 to 1.652, p = 0.005). The C statistics for cardiovascular events increased when each biomarker or combinations of biomarkers were added to the Framingham risk model (C statistics: Framingham risk model alone 0.636, Framingham risk + BNP 0.695, Framingham risk + hsCRP 0.696, Framingham risk + EMP 0.682, and Framingham risk + BNP + hsCRP + EMP 0.763).

Conclusions: The assessment of endothelial dysfunction by plasma levels of EMP can independently predict future cardiovascular events in patients at high risk for CHD. A multiple biomarkers strategy that includes endothelial dysfunction assessed by EMP can identify patients vulnerable to cardiovascular disease. (University Hospital Medical Information Network number: UMIN000000876)

Key Words: biomarkers • endothelium • microparticles • follow-up studies • coronary heart disease

Abbreviations and Acronyms
  ACS = acute coronary syndromes
  BNP = B-type natriuretic peptide
  CAD = coronary artery disease
  CHD = coronary heart disease
  CI = confidence interval
  DM = diabetes mellitus
  eGFR = estimated glomerular filtration rate
  EMP = endothelium-derived microparticle(s)
  HDL = high-density lipoprotein
  HR = hazard ratio
  hsCRP = high-sensitivity C-reactive protein
  LDL = low-density lipoprotein


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