Matches in SemOpenAlex for { <https://semopenalex.org/work/W2021193012> ?p ?o ?g. }
- W2021193012 endingPage "60" @default.
- W2021193012 startingPage "51" @default.
- W2021193012 abstract "Inflammatory phenomena at sites of atherosclerotic plaques are increasingly thought to be major determinants of the progression and clinical outcome of atherosclerotic disease. Therefore, attention is being paid to systemic markers/mediators which may reflect the inflammatory activity in the plaques. This study evaluates the pattern of the main proinflammatory cytokines tumor necrosis factor-alpha (TNFalpha), interleukin-1beta (IL-1beta), and interleukin-6 (IL-6), their soluble receptors/antagonist, and a variety of inflammatory markers, in patients with peripheral arterial disease (PAD). Eight patients with PAD suffering from claudicatio intermittens (CI), eight with critical limb ischemia (CLI) and eight controls (C) were studied. Blood samples were collected at baseline in all groups and. for C and CI, immediately after and 4 h after a 30-min treadmill test. Baseline: no differences in cytokine plasma levels were detected among the three groups. In contrast, soluble receptors of TNF (type I and II) and of IL-6, and IL-1beta receptor antagonist (IL-1ra) were increased in CI and CLI patients, as compared to C. Of note, IL-Ira correlated with the occurrence and stage of the disease in a highly significant proportion of the patients, reaching a predictive value for the disease of P < 0.0001. The opposite trend was observed for the soluble receptor of IL-1beta. Notably, in the patients no alterations could be found in white blood cell counts, expression of CD11c adherence molecule by circulating monocytes or, in vitro. O2- release from zymosan-activated neutrophils. Moreover, plasma levels of platelet activating factor (PAF), of neutrophil elastase and of the acute phase reactants C-reactive protein (CRP) and alpha1-acid glycoprotein were not found to be significantly altered. In contrast, the acute-phase proteins alpha1-antitrypsin (alpha1AT) and haptoglobin (HG) were found to be increased. Effect of treadmill: IL-1beta and TNFalpha remained at baseline levels following exercise, and IL-6 dropped to undetectable levels. Among cytokine antagonists, again the most relevant changes concerned the IL-1ra, which was significantly increased immediately after the treadmill test, both in CI and C, and returned to baseline levels after 4 h. In contrast, soluble TNFalpha, IL-1beta and IL-6 receptors, PAF, and the other markers of leukocyte activation were not found to be altered. Soluble TNFalpha and IL-6 receptors were shown to inhibit the biological effects of their ligands. Similarly, IL-1ra and the acute phase proteins alpha1AT and HG have been reported to exert anti-inflammatory functions. The increased plasma levels of these agents, together with low levels of inflammatory cytokines and other pro-inflammatory mediators such as PAF and alpha1-acid glycoprotein, appear to draw an undescribed picture, so far, of upregulation of a composite systemic anti-inflammatory mechanism in atherosclerotic patients. IL-1ra appears to be a reliable marker of the state of activation of this mechanism. These results may provide a basis for developing new insights into the pathogenesis of the atherosclerotic disease." @default.
- W2021193012 created "2016-06-24" @default.
- W2021193012 creator A5001254761 @default.
- W2021193012 creator A5019254291 @default.
- W2021193012 creator A5025489246 @default.
- W2021193012 creator A5040625595 @default.
- W2021193012 creator A5045242883 @default.
- W2021193012 creator A5048168718 @default.
- W2021193012 creator A5064530725 @default.
- W2021193012 creator A5091734057 @default.
- W2021193012 date "1999-07-01" @default.
- W2021193012 modified "2023-10-14" @default.
- W2021193012 title "Atherosclerosis and inflammation. Patterns of cytokine regulation in patients with peripheral arterial disease" @default.
- W2021193012 cites W1515994079 @default.
- W2021193012 cites W1902106965 @default.
- W2021193012 cites W1972613448 @default.
- W2021193012 cites W1983181818 @default.
- W2021193012 cites W1984420130 @default.
- W2021193012 cites W1985513210 @default.
- W2021193012 cites W1996862503 @default.
- W2021193012 cites W2001368390 @default.
- W2021193012 cites W2019023162 @default.
- W2021193012 cites W2033382588 @default.
- W2021193012 cites W2047616703 @default.
- W2021193012 cites W2048340136 @default.
- W2021193012 cites W2053706055 @default.
- W2021193012 cites W2058312167 @default.
- W2021193012 cites W2062889364 @default.
- W2021193012 cites W2065181541 @default.
- W2021193012 cites W2065581832 @default.
- W2021193012 cites W2066397836 @default.
- W2021193012 cites W2071104427 @default.
- W2021193012 cites W2083955105 @default.
- W2021193012 cites W2089520473 @default.
- W2021193012 cites W2093664978 @default.
- W2021193012 cites W2118606452 @default.
- W2021193012 cites W2120549911 @default.
- W2021193012 cites W2127539832 @default.
- W2021193012 cites W2137570167 @default.
- W2021193012 cites W2140712394 @default.
- W2021193012 cites W2148068424 @default.
- W2021193012 cites W2159750628 @default.
- W2021193012 cites W2171609051 @default.
- W2021193012 cites W2266911869 @default.
- W2021193012 cites W2315575691 @default.
- W2021193012 cites W2316376271 @default.
- W2021193012 cites W2322377611 @default.
- W2021193012 cites W2396341425 @default.
- W2021193012 cites W38793834 @default.
- W2021193012 cites W70458992 @default.
- W2021193012 doi "https://doi.org/10.1016/s0021-9150(99)00013-1" @default.
- W2021193012 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/10428295" @default.
- W2021193012 hasPublicationYear "1999" @default.
- W2021193012 type Work @default.
- W2021193012 sameAs 2021193012 @default.
- W2021193012 citedByCount "123" @default.
- W2021193012 countsByYear W20211930122012 @default.
- W2021193012 countsByYear W20211930122013 @default.
- W2021193012 countsByYear W20211930122014 @default.
- W2021193012 countsByYear W20211930122015 @default.
- W2021193012 countsByYear W20211930122016 @default.
- W2021193012 countsByYear W20211930122017 @default.
- W2021193012 countsByYear W20211930122018 @default.
- W2021193012 countsByYear W20211930122019 @default.
- W2021193012 countsByYear W20211930122020 @default.
- W2021193012 countsByYear W20211930122022 @default.
- W2021193012 countsByYear W20211930122023 @default.
- W2021193012 crossrefType "journal-article" @default.
- W2021193012 hasAuthorship W2021193012A5001254761 @default.
- W2021193012 hasAuthorship W2021193012A5019254291 @default.
- W2021193012 hasAuthorship W2021193012A5025489246 @default.
- W2021193012 hasAuthorship W2021193012A5040625595 @default.
- W2021193012 hasAuthorship W2021193012A5045242883 @default.
- W2021193012 hasAuthorship W2021193012A5048168718 @default.
- W2021193012 hasAuthorship W2021193012A5064530725 @default.
- W2021193012 hasAuthorship W2021193012A5091734057 @default.
- W2021193012 hasConcept C11988809 @default.
- W2021193012 hasConcept C126322002 @default.
- W2021193012 hasConcept C134018914 @default.
- W2021193012 hasConcept C164027704 @default.
- W2021193012 hasConcept C170493617 @default.
- W2021193012 hasConcept C17991360 @default.
- W2021193012 hasConcept C203014093 @default.
- W2021193012 hasConcept C2776252253 @default.
- W2021193012 hasConcept C2776885963 @default.
- W2021193012 hasConcept C2776914184 @default.
- W2021193012 hasConcept C2778122271 @default.
- W2021193012 hasConcept C2778690821 @default.
- W2021193012 hasConcept C71924100 @default.
- W2021193012 hasConcept C74172505 @default.
- W2021193012 hasConceptScore W2021193012C11988809 @default.
- W2021193012 hasConceptScore W2021193012C126322002 @default.
- W2021193012 hasConceptScore W2021193012C134018914 @default.
- W2021193012 hasConceptScore W2021193012C164027704 @default.
- W2021193012 hasConceptScore W2021193012C170493617 @default.
- W2021193012 hasConceptScore W2021193012C17991360 @default.
- W2021193012 hasConceptScore W2021193012C203014093 @default.
- W2021193012 hasConceptScore W2021193012C2776252253 @default.