Prediction of Residual Risk by Ceramide‐Phospholipid Score in Patients With Stable Coronary Heart Disease on Optimal Medical Therapy

Author:

Hilvo Mika1,Wallentin Lars23,Ghukasyan Lakic Tatevik3,Held Claes23,Kauhanen Dimple1,Jylhä Antti1,Lindbäck Johan3,Siegbahn Agneta23,Granger Christopher B.4,Koenig Wolfgang56,Stewart Ralph A. H.7,White Harvey7,Laaksonen Reijo189,

Affiliation:

1. Zora Biosciences Oy Espoo Finland

2. Department of Medical Sciences Uppsala University Uppsala Sweden

3. Uppsala Clinical Research Center Uppsala Sweden

4. Medical Center Duke University Durham NC

5. Deutsches Herzzentrum München Technische Universität München München Germany and DZHK (German Centre for Cardiovascular Research), partner site Munich Heart Alliance Munich Germany

6. Institute of Epidemiology and Medical Biometry University of Ulm Germany

7. N Green Lane Cardiovascular Service Auckland City Hospital and University of Auckland New Zealand

8. Finnish Cardiovascular Research Center University of Tampere Finland

9. Finnish Clinical Biobank Tampere Tampere University Hospital Tampere Finland

Abstract

Background Identification of patients with stable coronary heart disease who are at significant residual risk could be helpful for targeted prevention. Our aim was to determine the prognostic value of the recently introduced ceramide‐ and phospholipid‐based risk score, the Cardiovascular Event Risk Test ( CERT 2), in patients with stable coronary heart disease on optimal medical therapy and to identify biological processes that contribute to the CERT 2 score. Methods and Results Plasma samples (n=11 222) obtained from the STABILITY (Stabilization of Atherosclerotic Plaque by Initiation of Darapladib Therapy) trial were analyzed using a tandem liquid chromatography‐mass spectrometry method. STABILITY was a trial in patients with stable coronary heart disease randomized to the lipoprotein‐associated phospholipase A2 inhibitor darapladib or placebo on optimized medical therapy at baseline, with a median follow‐up of 3.7 years. Hazard ratios per SD for the CERT 2 risk score were 1.32 (95% CI, 1.25–1.39) for major adverse cardiovascular event, 1.47 (95% CI, 1.35–1.59) for cardiovascular death, 1.32 (95% CI, 1.16–1.49) for stroke, 1.23 (95% CI, 1.14–1.33) for myocardial infarction, and 1.56 (95% CI, 1.39–1.76) for hospitalization due to heart failure, when adjusted for traditional cardiovascular risk factors. CERT 2 showed correlation ( P <0.001, r >0.2) with inflammatory markers high‐sensitivity C‐reactive protein, interleukin 6, the heart failure marker N‐terminal pro‐B‐type natriuretic peptide, and low‐density lipoprotein cholesterol. After also adjusting for levels of other prognostic biomarkers, the CERT 2 score was still independently related to the risk of cardiovascular death but not to nonfatal events. Conclusions The CERT 2 risk score can detect residual risk in patients with stable coronary heart disease and is associated with biomarkers indicating inflammation, myocardial necrosis, myocardial dysfunction, renal dysfunction, and dyslipidemia. REGISTRATION URL : https://www.clini​caltr​ials.gov . Unique identifier: NCT 00799903.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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