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Circulation. 2006;114:550-557
Published online before print July 31, 2006, doi: 10.1161/CIRCULATIONAHA.106.641936
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(Circulation. 2006;114:550-557.)
© 2006 American Heart Association, Inc.


Coronary Heart Disease

Prognostic Utility of Heart-Type Fatty Acid Binding Protein in Patients With Acute Coronary Syndromes

Michelle O’Donoghue, MD; James A. de Lemos, MD; David A. Morrow, MD, MPH; Sabina A. Murphy, MPH; Jacqueline L. Buros, AB; Christopher P. Cannon, MD; Marc S. Sabatine, MD, MPH

From the TIMI Study Group (M.O., D.A.M., S.A.M., J.L.B., C.P.C., M.S.S.), Cardiovascular Division, Brigham and Women’s Hospital, Boston, Mass, and Division of Cardiology (J.A.d.L.), Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas.

Correspondence to Marc S. Sabatine, MD, MPH, Brigham and Women’s Hospital, TIMI Study Group, 350 Longwood Ave, First Floor, Boston, MA 02115. E-mail msabatine{at}partners.org

Received April 26, 2006; revision received May 30, 2006; accepted June 8, 2006.

Background— Heart-type fatty acid binding protein (H-FABP) is a cytosolic protein that is released rapidly from the cardiomyocyte in response to myocardial injury. Although it has been investigated as an early marker of acute myocardial infarction, its prognostic utility in acute coronary syndromes has not been established.

Methods and Results— We measured H-FABP in 2287 patients with acute coronary syndromes from the OPUS-TIMI 16 trial. H-FABP was elevated (>8 ng/mL) in 332 patients (14.5%). Patients with an elevated H-FABP were more likely to suffer death (hazard ratio [HR], 4.1; 95% CI, 2.6 to 6.5), recurrent myocardial infarction (HR, 1.6; 95% CI, 1.0 to 2.5), congestive heart failure (HR, 4.5; 95% CI, 2.6 to 7.8), or the composite of these end points (HR, 2.6; 95% CI, 1.9 to 3.5) through the 10-month follow-up period. H-FABP predicted the risk of the composite end point both in patients who were troponin I negative (HR, 2.1; 95% CI, 1.3 to 3.4) and in those who were troponin I positive (HR, 3.3; 95% CI, 2.0 to 5.3). In a Cox proportional-hazards model that adjusted for baseline variables, including demographics, clinical characteristics, creatinine clearance, ST deviation, index diagnosis, and troponin I, elevated H-FABP remained a significant predictor of the composite end point (HR, 1.9; 95% CI, 1.3 to 2.7), as well as the individual end points of death (HR, 2.7; 95% CI, 1.5 to 4.9) and CHF (HR, 2.4; 95% CI, 1.2 to 5.0). In a multimarker approach, H-FABP, troponin I, and B-type natriuretic peptide provided complementary information.

Conclusions— Elevation of H-FABP is associated with an increased risk of death and major cardiac events in patients presenting across the spectrum of acute coronary syndromes and is independent of other established clinical risk predictors and biomarkers.


 

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