Subjects with following cardiovascular diseases are also excluded: stroke, AMI, coronary artery disease (CAD), eye thrombus, angina pectoris, frequent arrhythmia, AOD, phlebitis, or rheumatic fever. The donors were between 18 and 65 years old, and their haemoglobin levels 135–195 and 125–175 g/l for men and women, respectively. All subjects gave their informed consent. The Local Ethics Committee at Helsinki University Central Hospital and the Finnish Red Cross, Oulu, Finland approved the study protocol. Sera were separated, divided into aliquots, and stored at −20 °C. Serum matrix metalloproteinase-8 (MMP-8), tissue inhibitor

of MMP-1 (TIMP-1), MPO, and HNE concentrations were determined both in the patients with arterial disease

and MG-132 molecular weight in the serum of the reference subjects. MMP-1 and MMP-13 concentrations were determined only in the patients. MMP-1, MMP-8, MMP-13, and TIMP-1 concentrations were determined using commercially available enzyme-linked immuno-sorbent assay (ELISA) kit according to the manufacturer’s instruction (Biotrak ELISA System; Amersham Biosciences, Buckinghamshire, UK) [15]. MPO (Immundiagnostik AG, Bensheim, Germany) and HNE (Alexis Biochemicals, Bender MedSystems, Vienna, Austria) concentrations were also analysed by ELISA. The absorbances were measured at 450 nm using Labsystems Multiskan RC (Thermo Bioanalysis Corporation, Santa Fe, USA), and the concentrations RAD001 were expressed as ng/ml. Serum concentrations of high-sensitive C-reactive protein (hsCRP), high- (HDL) and low-density (LDL) lipoprotein cholesterol, triglycerides, total cholesterol, Chlamydia pneumoniae markers (C. pneumonia IgA, IgG, and lipopolysaccharide),

antibody levels to Aggregatibacter actinomycetemcomitans (IgA, IgG), Porphyromonas gingivalis (IgA, IgG), and human heat-shock protein 60 (HSP60, IgA, and IgG), total lipopolysaccharide (LPS), LPS-binding protein (LBP), interleukin-6 (IL-6), and CD14 in the patients were measured as described previously [16]. Molar ratio of MMP-8 and TIMP-1 (indicated as MMP-8/TIMP-1) was determined by dividing the concentrations with the corresponding molecular weights, 65,000 Da click here and 28,000 Da, respectively [17]. The statistical significance of the differences between the groups was analysed by the student’s t-test. Correlation analyses of serum MMP and regulator levels were performed separately with in the patients and the healthy subjects by scatter plots and Pearson correlation analysis. Owing to the heterogeneous nature of the study population, the comparisons were done between the subgroups as well. Continuous variables are presented as median (interquartile range, IQR of 25–75%).