This study demonstrates that, in the case of diagnostic image quality, contrast-enhanced MDCT permits an accurate identification of coronary plaques and that computed tomography density values measured within plaques reflect echogenity and plaque composition.

Background Hemodynamic load regulates myocardial function and gene expression. We tested the hypothesis that afterload and preload despite similar average load result in different phenotypes. Methods and Results Afterload and preload were compared in mice with transversal aortic constriction (TAC) and aorto-caval shunt (Shunt). When compared to sham mice, six hours after surgery, systolic wall stress (afterload) was increased in TAC (+40%, P<0.05), diastolic wall stress (preload) was increased in Shunt (+277%, P<0.05) and TAC (+74%, P<0.05) and mean total wall stress was similarly increased in TAC (69%) and Shunt (67%) (TAC vs. Shunt: not significant (n.s.), each P<0.05 vs. Sham). At 1 week, left ventricular weight/tibia length was significantly increased by 22% in TAC and 29% in Shunt (n.s. TAC vs. Shunt). After 24 hours and 1 week, calcium/calmodulin dependent protein kinase II (CaMKII) signaling was increased in TAC. This resulted in altered calcium cycling, including increased L-type calcium current, calcium transients, fractional SR release and calcium spark frequency. In Shunt, Akt phosphorylation was increased. TAC was associated with inflammation, fibrosis and cardiomyocyte apoptosis. The latter was significantly reduced in CaMKIIδ-KO TAC mice. 157 mRNAs and 13 microRNAs were differentially regulated in TAC vs. Shunt. After 8 weeks, fractional shortening was lower and mortality higher in TAC Conclusions Afterload results in maladaptive fibrotic hypertrophy with CaMKII-dependent altered calcium cycling and apoptosis. Preload is associated with Akt activation without fibrosis, little apoptosis, better function and lower mortality. This indicates that different loads result in distinct phenotype differences which may require specific pharmacological interventions.

We conclude that 64-slice CT reveals encouraging results to noninvasively detect different types of coronary plaques located in the proximal coronary system. The ability to determine plaque burden currently is hampered by mainly an insufficient reproducibility.

Calcium screening with EBCT is a highly sensitive and moderately specific test to predict stenotic disease. Exclusion of coronary calcium defines a substantial subgroup of patients, albeit symptomatic, with a very low probability of significant stenoses.

Objectives-Pericardial fat as a visceral fat depot may be involved in the pathogenesis of coronary atherosclerosis. To gain evidence for that concept we sought to investigate the relation of pericardial fat volumes to risk factors, serum adiponectin levels, inflammatory biomarkers, and the quantity and morphology of coronary atherosclerosis. PϾ0.001). No association was found between BMI and coronary atherosclerosis. PAT volumes Ͼ300 cm 3 were the strongest independent risk factor for coronary atherosclerosis (odds ratio 4.1; CI 3.63 to 4.33) also significantly stronger compared to the Framingham score. We furthermore demonstrated that elevated PAT volumes are significantly associated with low adiponectin levels, low HDL levels, elevated TNF-␣ levels, and hsCRP. Conclusion-In the present study we demonstrated that elevated PAT volumes are associated with coronary atherosclerosis, hypoadiponectinemia, and inflammation and represent the strongest risk factor for the presence of atherosclerosis and may be important for risk stratification and monitoring. Key Words: cardiac CT Ⅲ pericardial fat Ⅲ obesity Ⅲ adiponectin Ⅲ plaque imaging T here is growing evidence that regional visceral fat distribution may contribute to an unfavorable metabolic and cardiovascular risk profile. 1,2 In patients with obesity, insulin resistance, diabetes, and hyperlipidemia visceral fat hypertrophies and transforms into a multifunctional organ that produces and secretes multiple endocrine and paracrine factors promoting inflammation, neovascularization, and oxidative stress, features that also characterize atherosclerosis. 3 Pericardial fat as a local visceral fat depot with close proximity to coronary arteries may serve as a source of inflammatory cytokines and cells that may locally enhance systemic proatherogenic effects via outside to inside signaling. 4,5 Thus it may be a specific parameter indicating an unfavorable cardio-metabolic state and may be used for risk stratification. To date, however, only little attention has focused on this regional fat depot located around the heart and its relation to cardiovascular risk factors, and the quantity and composition of coronary atherosclerosis is not well studied yet. Methods and Results-UsingMulti-slice CT is a noninvasive tool that allows to reliably assess both obstructive and nonobstructive subclinical coronary artery disease in an earlier stage than invasive angiography. 6 -9 Based on density measurements, plaques can be further characterized in noncalcified, mixed, and calcified plaques. 7 By using the same scan data this tool furthermore allows to quantify the exact pericardial fat volume. 9 We thus sought to assess the relation of pericardial fat volume to cardiovascular risk factors, levels of inflammatory cytokines, adiponectin, and to the extent and the phenotype of coronary atherosclerosis.

Objectives: Chemerin is a recently discovered adipokine that regulates adipocyte differentiation and modulates chemotaxis and activation of dendritic cells and macrophages. Given the convergence of adipocyte and macrophage function, chemerin may provide an interesting link between obesity, inflammation and atherosclerosis in humans. We sought to examine the relationship of i) chemerin and markers of inflammation, ii) chemerin and components of the metabolic syndrome, and iii) chemerin and coronary atherosclerotic plaque burden and morphology. Design: Serum chemerin levels were determined in 303 patients with stable typical or atypical chest pain who underwent dual-source multi-slice CT-angiography to exclude coronary artery stenosis. Atherosclerotic plaques were classified as calcified, mixed, or non-calcified. Results: Chemerin levels were highly correlated with high sensitivity C-reactive protein (rZ0.44, P!0.0001), interleukin-6 (rZ0.18, PZ0.002), tumor necrosis factor-a (rZ0.24, P!0.0001), resistin (rZ0.28, P!0.0001), and leptin (rZ0.36, P!0.0001) concentrations. Furthermore, chemerin was associated with components of the metabolic syndrome including body mass index (rZ0.23, PZ0.0002), triglycerides (rZ0.29, P!0.0001), HDL-cholesterol (rZK0.18, PZ0.003), and hypertension (P!0.0001). In bivariate analysis, chemerin levels were weakly correlated with coronary plaque burden (rZ0.16, PZ0.006) and the number of non-calcified plaques (rZ0.14, PZ0.02). These associations, however, were lost after adjusting for established cardiovascular risk factors (odds ratio, OR 1.17, 95% confidence interval (CI) 0.97-1.41, PZ0.11 for coronary plaque burden; OR 1.06, 95% CI 0.96-1.17, PZ0.22 for non-calcified plaques). Conclusions: Chemerin is strongly associated with markers of inflammation and components of the metabolic syndrome. However, chemerin does not predict coronary atherosclerosis.

Dynamic CT-based stress myocardial perfusion imaging may allow detection of hemodynamically significant coronary artery stenosis.

The cuticules (shells) of the woodlice Porcellio scaber and Armadillidium vulgare were analysed with respect to their content of inorganic material. It was found that the cuticles consist of crystalline magnesium calcite, amorphous calcium carbonate (ACC), and amorphous calcium phosphate (ACP), besides small amounts of water and an organic matrix. It is concluded that the cuticle, which constitutes a mineralized protective organ, is chemically adapted to the biological requirements by this combination of different materials.