Plasma ceramides predict cardiovascular death in patients with stable coronary artery disease and acute coronary syndromes beyond LDL-cholesterol

Reijo Laaksonen(Zora Biosciences (Finland)), Kim Ekroos(Zora Biosciences (Finland)), Marko Sysi‐Aho(Zora Biosciences (Finland)), Mika Hilvo(Zora Biosciences (Finland)), Terhi Vihervaara(Zora Biosciences (Finland)), Dimple Kauhanen(Zora Biosciences (Finland)), Matti Suoniemi(Zora Biosciences (Finland)), Reini Hurme(Zora Biosciences (Finland)), Winfried März(University Hospital Heidelberg), Hubert Scharnagl(Medical University of Graz), Tatjana Stojaković(Medical University of Graz), Efthymia Vlachopoulou(University of Helsinki), Marja‐Liisa Lokki(University of Helsinki), Markku S. Nieminen(Helsinki University Hospital), Roland Klingenberg(University Hospital of Zurich), Christian M. Matter(University of Zurich), Thorsten Hornemann(University Hospital of Zurich), Peter Jüni(University of Toronto), Nicolas Rodondi(University of Lausanne), Lorenz Räber(University Hospital of Bern), Stephan Windecker(University Hospital of Bern), Bariş Gencer(University Hospital of Geneva), Eva Ringdal Pedersen(University of Bergen), Grethe S. Tell(University of Bergen), Ottar Nygård(Haukeland University Hospital), François Mach(University Hospital of Geneva), Juha Sinisalo(University of Helsinki), Thomas F. Lüscher(University Hospital of Zurich)
European Heart Journal
April 28, 2016
Cited by 679Open Access
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Abstract

AIMS: The aim was to study the prognostic value of plasma ceramides (Cer) as cardiovascular death (CV death) markers in three independent coronary artery disease (CAD) cohorts. METHODS AND RESULTS: Corogene study is a prospective Finnish cohort including stable CAD patients (n = 160). Multiple lipid biomarkers and C-reactive protein were measured in addition to plasma Cer(d18:1/16:0), Cer(d18:1/18:0), Cer(d18:1/24:0), and Cer(d18:1/24:1). Subsequently, the association between high-risk ceramides and CV mortality was investigated in the prospective Special Program University Medicine-Inflammation in Acute Coronary Syndromes (SPUM-ACS) cohort (n = 1637), conducted in four Swiss university hospitals. Finally, the results were validated in Bergen Coronary Angiography Cohort (BECAC), a prospective Norwegian cohort study of stable CAD patients. Ceramides, especially when used in ratios, were significantly associated with CV death in all studies, independent of other lipid markers and C-reactive protein. Adjusted odds ratios per standard deviation for the Cer(d18:1/16:0)/Cer(d18:1/24:0) ratio were 4.49 (95% CI, 2.24-8.98), 1.64 (1.29-2.08), and 1.77 (1.41-2.23) in the Corogene, SPUM-ACS, and BECAC studies, respectively. The Cer(d18:1/16:0)/Cer(d18:1/24:0) ratio improved the predictive value of the GRACE score (net reclassification improvement, NRI = 0.17 and ΔAUC = 0.09) in ACS and the predictive value of the Marschner score in stable CAD (NRI = 0.15 and ΔAUC = 0.02). CONCLUSIONS: Distinct plasma ceramide ratios are significant predictors of CV death both in patients with stable CAD and ACS, over and above currently used lipid markers. This may improve the identification of high-risk patients in need of more aggressive therapeutic interventions.


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