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1 Dept of Cardiology and Pulmonology, University of Goettingen, Goettingen, 3 Dept of Medical Biometry and Statistics, University Hospital of Freiburg, Freiburg, Germany, 2 Dept of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Austria, 4 Both authors contributed equally.
CORRESPONDENCE: S. Konstantinides, Dept of Cardiology and Pulmonology, University of Goettingen, D-37099 Goettingen, Germany. Fax: 49 5513914131. E-mail: skonstan{at}med.uni-goettingen.de
Keywords: Biomarkers, fatty acid-binding protein, prognosis, pulmonary hypertension
Received: August 3, 2007
Accepted January 15, 2008
Heart-type fatty acid-binding protein (H-FABP) is a reliable marker of myocardial injury and was recently identified as a predictor of outcome in acute pulmonary embolism. The aim of the present study was to investigate the prognostic value of H-FABP in chronic thromboembolic pulmonary hypertension (CTEPH).
In total, 93 consecutive patients with CTEPH were studied. During long-term follow-up (median duration 1,260 days, interquartile range (IQR) 708–2,460 days), 46 (49%) patients had an adverse outcome, defined as CTEPH-related death, lung transplantation or persistent pulmonary hypertension after pulmonary endarterectomy (PEA).
Baseline H-FABP levels in plasma ranged from 0.69–24.3 ng·mL–1 (median (IQR) 3.41 (2.28–4.86) ng·mL–1). Cox regression analysis revealed a hazard ratio of 1.10 (95% confidence interval 1.04–1.18) for each increase of H-FABP by 1 ng·mL–1, and continuous elevations of H-FABP emerged as an independent predictor of adverse outcome by multivariable analysis. PEA was performed in 52 patients and favourably affected the long-term outcome. Kaplan–Meier analysis revealed that patients with baseline H-FABP concentrations >2.7 ng·mL–1, the median value of the biomarker in the surgically treated population, had a lower probability of event-free survival after PEA.
Heart-type fatty acid-binding protein is a promising novel biomarker for risk stratification of patients with chronic thromboembolic pulmonary hypertension.
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