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Development and validation of a ceramide- and phospholipid-based cardiovascular risk estimation score for coronary artery disease patients.
Hilvo, Mika; Meikle, Peter J; Pedersen, Eva Ringdal; Tell, Grethe S; Dhar, Indu; Brenner, Hermann; Schöttker, Ben; Lääperi, Mitja; Kauhanen, Dimple; Koistinen, Kaisa M; Jylhä, Antti; Huynh, Kevin; Mellett, Natalie A; Tonkin, Andrew M; Sullivan, David R; Simes, John; Nestel, Paul; Koenig, Wolfgang; Rothenbacher, Dietrich; Nygård, Ottar; Laaksonen, Reijo.
Afiliação
  • Hilvo M; Zora Biosciences Oy, Tietotie 2C, 02150 Espoo, Finland.
  • Meikle PJ; Metabolomics Laboratory, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne VIC 3004, Australia.
  • Pedersen ER; Department of Diabetes, Central Clinical School, Faculty of Medicine, Nursing and Health Sciences, Monash University, 99 Commercial Road, Melbourne VIC 3004, Australia.
  • Tell GS; Department of Heart Disease, Haukeland University Hospital, Jonas Lies veg 65, 5021 Bergen, Norway.
  • Dhar I; Department of Global Public Health and Primary Care, University of Bergen, Kalfarveien 31, 5020 Bergen, Norway.
  • Brenner H; Department of Clinical Science, University of Bergen, Jonas Lies veg 87, 5021 Bergen, Norway.
  • Schöttker B; Division of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 581, D-69120 Heidelberg, Germany.
  • Lääperi M; Network Ageing Research, University of Heidelberg, Bergheimer Straße 20, D-69115 Heidelberg, Germany.
  • Kauhanen D; Division of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 581, D-69120 Heidelberg, Germany.
  • Koistinen KM; Network Ageing Research, University of Heidelberg, Bergheimer Straße 20, D-69115 Heidelberg, Germany.
  • Jylhä A; Zora Biosciences Oy, Tietotie 2C, 02150 Espoo, Finland.
  • Huynh K; Zora Biosciences Oy, Tietotie 2C, 02150 Espoo, Finland.
  • Mellett NA; Zora Biosciences Oy, Tietotie 2C, 02150 Espoo, Finland.
  • Tonkin AM; Zora Biosciences Oy, Tietotie 2C, 02150 Espoo, Finland.
  • Sullivan DR; Metabolomics Laboratory, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne VIC 3004, Australia.
  • Simes J; Metabolomics Laboratory, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne VIC 3004, Australia.
  • Nestel P; School of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, Melbourne VIC 3004, Australia.
  • Koenig W; Department of Chemical Pathology, Royal Prince Alfred Hospital, 50 Missenden Road, Camperdown NSW 2050, Sydney, Australia.
  • Rothenbacher D; The NHMRC Clinical Trials Centre, University of Sydney, 92-94 Parramatta Rd, Camperdown NSW 2050, Sydney, Australia.
  • Nygård O; Heart Centre, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne VIC 3004, Australia.
  • Laaksonen R; Klinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technische Universität München, Lazarettstr. 36, D-80636 Munich, Germany.
Eur Heart J ; 41(3): 371-380, 2020 01 14.
Article em En | MEDLINE | ID: mdl-31209498
ABSTRACT

AIMS:

Distinct ceramide lipids have been shown to predict the risk for cardiovascular disease (CVD) events, especially cardiovascular death. As phospholipids have also been linked with CVD risk, we investigated whether the combination of ceramides with phosphatidylcholines (PCs) would be synergistic in the prediction of CVD events in patients with atherosclerotic coronary heart disease in three independent cohort studies. METHODS AND

RESULTS:

Ceramides and PCs were analysed using liquid chromatography-mass spectrometry (LC-MS) in three studies WECAC (The Western Norway Coronary Angiography Cohort) (N = 3789), LIPID (Long-Term Intervention with Pravastatin in Ischaemic Disease) trial (N = 5991), and KAROLA (Langzeiterfolge der KARdiOLogischen Anschlussheilbehandlung) (N = 1023). A simple risk score, based on the ceramides and PCs showing the best prognostic features, was developed in the WECAC study and validated in the two other cohorts. This score was highly significant in predicting CVD mortality [multiadjusted hazard ratios (HRs; 95% confidence interval) per standard deviation were 1.44 (1.28-1.63) in WECAC, 1.47 (1.34-1.61) in the LIPID trial, and 1.69 (1.31-2.17) in KAROLA]. In addition, a combination of the risk score with high-sensitivity troponin T increased the HRs to 1.63 (1.44-1.85) and 2.04 (1.57-2.64) in WECAC and KAROLA cohorts, respectively. The C-statistics in WECAC for the risk score combined with sex and age was 0.76 for CVD death. The ceramide-phospholipid risk score showed comparable and synergistic predictive performance with previously published CVD risk models for secondary prevention.

CONCLUSION:

A simple ceramide- and phospholipid-based risk score can efficiently predict residual CVD event risk in patients with coronary artery disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfolipídeos / Doença da Artéria Coronariana / Ceramidas / Medição de Risco / Aterosclerose Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfolipídeos / Doença da Artéria Coronariana / Ceramidas / Medição de Risco / Aterosclerose Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article