RELATIONSHIP BETWEEN SPHINGOMYELINASE, CERAMIDE AND CLINICAL PRESENTATION, EXTENT AND SEVERITY OF ATHEROSCLEROTIC CORONARY ARTERY DISEASE

Objectives Background and objective Matrix metalloproteinases (MMPs) and Tissue Inhibitor of Matrix Metalloproteinases (TIMPs) associated with atherogenesis and plaque rupture. Sphingomyelinase has a potential regulator role in the activation of MMP via induced ceramide formation. So we evaluated the relationship between sphingomyelinase, ceramide levels and presentation, extent and severity of atherosclerotic coronary artery disease (CAD). Methods Consecutive patients who underwent coronary angiography were randomly included. The serum concentrations of sphingomyelinase, ceramide, MMP-2, MMP-9 and TIMP-1 were analysed with ELISA method in 274 patients. Participants were divided into 5 groups; stable angina pectoris (SAP; n=64), unstable angina pectoris (USAP; n=67), non-ST elevation myocardial infarction (NSTEMI; n=56), acute ST elevation myocardial infarction (STEMI; n=55) and controls (n=30). Coronary angiographic Gensini score was calculated, and the correlation between sphingomyelinase, ceramide, MMP-2, MMP-9 and clinical presentation, extent and severity of atherosclerotic coronary artery disease were analysed. Results sphingomyelinase, ceramide, MMP-2 levels were higher in STEMI and NSTEMI groups compared with USAP, SAP and control groups (STEMI vs USAP p=0.001; STEMI vs SAP p=0.001; STEMI vs control p