Background: Microparticles (MP) are vesicles released from activated or apoptotic cells. Endothelial MP (EMP) are derived from injured endothelium, platelet MP (PMP) from activated platelets, and Annexin V positive MP (AMP) from apoptotic endothelial cells. The aim was to assess the release of MP and its association with inflammation and atherosclerotic burden. Methods and Results:AMP, EMP and PMP were measured on admission (Day 0) in 33 patients with stable angina (SA) and 43 patients with acute coronary syndrome (ACS) undergoing percutaneous coronary interventions (PCI). In SA, peripheral artery disease (PAD) was assessed by ultrasound examination. In 30 of the 76 patients (20 ACS and 10 SA), MP, high-sensitivity-C-reactive protein (hs-CRP), and troponin T (TnT) levels were also assessed 24 h (Day 1) and 48 h (Day 2) after PCI. AMP, EMP, and PMP were higher in ACS than in SA (all P<0.01). In the SA group, AMP, PMP, and EMP were similar in patients with or without PAD. In the ACS group, AMP increased until Day 2 (P=0.001), while EMP and PMP peaked on Day 1 (P<0.01) then decreased to baseline values. Day 2 AMP correlated with Day 2 TnT levels (r=0.43, P=0.01) while Day 1 EMP and PMP correlated with Day 1 hs-CRP (r=0.37, P=0.04 and r=0.33, P=0.05; respectively). Conclusions:Higher MP levels were observed in ACS than in SA. Atherosclerotic burden did not affect MP levels in stable patients. (Circ J 2012; 76: 2174 - 2182
Background and Purpose-Osteoprotegerin (OPG) is a secretory glycoprotein which belongs to the tumor necrosis factor receptor family. Various mechanisms have been suggested by which calcification might alter atherosclerotic plaque stability, but the significance of this intimal calcification is controversial. High concentrations of OPG have been associated with the presence of vascular and cardiovascular diseases. This study was designed to assess the association between gene polymorphisms of the OPG gene (TNFRSF11B), the serum OPG level, and plaque stability in patients with carotid atherosclerosis. Methods-We studied 177 patients with internal carotid artery stenosis who underwent carotid endarterectomy and also 303 controls. Carotid endarterectomy samples removed from patients were assessed by immunohistochemistry. Concentrations of OPG were measured and gene polymorphisms were examined by polymerase chain reaction and restriction enzyme analysis and were compared, initially between patients with carotid atherosclerosis and controls, and subsequently between stable and unstable carotid plaques. Results-We found that the GG genotype of the T245G polymorphism, the CC genotype of the T950C polymorphism, and the CC genotype of the G1181C polymorphism were significantly higher in patients with carotid plaque than in controls (21.5% versus 10.9% , PϽ0.01; 15.8% versus 7.6%, PϽ0.01; and 20.3% versus 10.9%, PϽ0.01, respectively) and that these polymorphisms were associated with high serum OPG levels (4. A therosclerosis is a disease of the elastic and large muscular arteries in which atheroma is the characteristic lesion. The lesions of atherosclerosis enlarge the arterial intima with variable amounts and types of lipids, connective tissues, inflammatory cells, and a variety of extracellular components including matrix proteins, enzymes, and calcium deposits. 1 In the past, calcification of normal tissue has been recognized as a common component of atherosclerotic lesions. 2 Some evidence suggests that calcification of atherosclerotic arteries is an organized, regulated process, rather than being a passive phenomenon of aging. 3,4 Several factors related to bone and mineral formation have been demonstrated within atherosclerotic plaques; these include osteocalcin, osteopontin, osteonectin, osteoprotegerin (OPG), and bone morphogenetic proteins. 5,6 The presence of these factors indicates the potential of arterial wall cells to promote Received March 3, 2011; accepted June 10, 2011 The human OPG gene (8q24; TNFRSF11B) consists of 5 exons and 4 introns and is transcribed into 4 transcripts (2.4 kb, 3.0 kb, 4.2 kb, and 6.5 kb lengths). The gene encoding for OPG is affected by common, functionally important genetic polymorphisms that have been associated with osteoporosis 13 and are considered early predictors of cardiovascular disease 14 ; among the most important are the T245G (rs 3134069), located in the promoter region, the T950C (rs 2073617) located in the 5Ј untranslated region, and the G1181C (rs 2073618) located ...
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