Matches in SemOpenAlex for { <https://semopenalex.org/work/W2113177621> ?p ?o ?g. }
- W2113177621 endingPage "2889" @default.
- W2113177621 startingPage "2883" @default.
- W2113177621 abstract "Leptin and tumor necrosis factor (TNF)-alpha are associated with insulin resistance and cardiovascular disease. In vitro studies suggested that these effects may be mediated via overproduction of monocyte chemoattracting protein (MCP)-1/CCL2, which is a chemokine involved in the pathogenesis of atherosclerosis.In this study, fasting plasma leptin, soluble TNF-alpha receptor 2 (TNF-alpha-R2), and MCP-1/CCL2 concentrations were measured in 207 middle-aged women (age 61 +/- 12 years, BMI 30.1 +/- 6.6 kg/m(2)), including 53 patients with type 2 diabetes, 42 with impaired glucose tolerance, and 112 with normal glucose tolerance, to assess cross-sectionally their relationship with markers of atherosclerosis and, longitudinally over 7 years, whether their circulating levels were associated with cardiovascular disease (CVD) mortality.At baseline, leptin and TNF-alpha-R2 were not different among groups; meanwhile, MCP-1/CCL2 was increased in type 2 diabetes (P < 0.05). All showed significant associations with biochemical risk markers of atherosclerosis. In a univariate analysis, age, fasting insulin, leptin, and MCP-1/CCL2 were associated with CVD mortality at 7 years. When a multivariate analysis was performed, only age, leptin, and insulin retained an independent association with CVD mortality, with leptin showing a protective effect (hazard ratio 0.88; P < 0.02).In middle-aged women, MCP-1/CCL2, leptin, and TNF-alpha-R2 were all related to biochemical risk markers of atherosclerosis. MCP-1/CCL2 concentration was the only one to be increased in type 2 diabetes with respect to nondiabetic women and the only one to be associated with increased risk of CVD mortality after a 7-year follow-up period in the univariate analysis. In the multivariate analysis, neither MCP-1/CCL2 nor TNF-alpha-R2 was associated with CVD mortality, and inspection of the data showed that leptin, in both the univariate and multivariate analysis, was associated with a protective effect." @default.
- W2113177621 created "2016-06-24" @default.
- W2113177621 creator A5005129014 @default.
- W2113177621 creator A5012414650 @default.
- W2113177621 creator A5032653514 @default.
- W2113177621 creator A5033698326 @default.
- W2113177621 creator A5034353445 @default.
- W2113177621 creator A5067743960 @default.
- W2113177621 creator A5072631239 @default.
- W2113177621 creator A5078824497 @default.
- W2113177621 creator A5080880936 @default.
- W2113177621 creator A5084865475 @default.
- W2113177621 date "2003-10-01" @default.
- W2113177621 modified "2023-10-16" @default.
- W2113177621 title "Fasting Plasma Leptin, Tumor Necrosis Factor-α Receptor 2, and Monocyte Chemoattracting Protein 1 Concentration in a Population of Glucose-Tolerant and Glucose-Intolerant Women" @default.
- W2113177621 cites W1536347913 @default.
- W2113177621 cites W1969605153 @default.
- W2113177621 cites W1970022980 @default.
- W2113177621 cites W1971770296 @default.
- W2113177621 cites W1976651776 @default.
- W2113177621 cites W1980079027 @default.
- W2113177621 cites W1986610158 @default.
- W2113177621 cites W2004916319 @default.
- W2113177621 cites W2008699478 @default.
- W2113177621 cites W2013844800 @default.
- W2113177621 cites W2016542625 @default.
- W2113177621 cites W2025587336 @default.
- W2113177621 cites W2068491028 @default.
- W2113177621 cites W2068649426 @default.
- W2113177621 cites W2077762036 @default.
- W2113177621 cites W2079793296 @default.
- W2113177621 cites W2080101101 @default.
- W2113177621 cites W2096345851 @default.
- W2113177621 cites W2103302057 @default.
- W2113177621 cites W2115163080 @default.
- W2113177621 cites W2126426760 @default.
- W2113177621 cites W2136961309 @default.
- W2113177621 cites W2140372161 @default.
- W2113177621 cites W2141600407 @default.
- W2113177621 cites W2142031401 @default.
- W2113177621 cites W2148562280 @default.
- W2113177621 cites W2155191102 @default.
- W2113177621 cites W2156667932 @default.
- W2113177621 cites W2158181279 @default.
- W2113177621 cites W2166933182 @default.
- W2113177621 cites W2167474616 @default.
- W2113177621 cites W2318151031 @default.
- W2113177621 cites W2324841714 @default.
- W2113177621 cites W4230870013 @default.
- W2113177621 cites W4232427403 @default.
- W2113177621 cites W4245839389 @default.
- W2113177621 doi "https://doi.org/10.2337/diacare.26.10.2883" @default.
- W2113177621 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/14514596" @default.
- W2113177621 hasPublicationYear "2003" @default.
- W2113177621 type Work @default.
- W2113177621 sameAs 2113177621 @default.
- W2113177621 citedByCount "124" @default.
- W2113177621 countsByYear W21131776212012 @default.
- W2113177621 countsByYear W21131776212013 @default.
- W2113177621 countsByYear W21131776212014 @default.
- W2113177621 countsByYear W21131776212015 @default.
- W2113177621 countsByYear W21131776212016 @default.
- W2113177621 countsByYear W21131776212017 @default.
- W2113177621 countsByYear W21131776212018 @default.
- W2113177621 countsByYear W21131776212020 @default.
- W2113177621 countsByYear W21131776212021 @default.
- W2113177621 countsByYear W21131776212023 @default.
- W2113177621 crossrefType "journal-article" @default.
- W2113177621 hasAuthorship W2113177621A5005129014 @default.
- W2113177621 hasAuthorship W2113177621A5012414650 @default.
- W2113177621 hasAuthorship W2113177621A5032653514 @default.
- W2113177621 hasAuthorship W2113177621A5033698326 @default.
- W2113177621 hasAuthorship W2113177621A5034353445 @default.
- W2113177621 hasAuthorship W2113177621A5067743960 @default.
- W2113177621 hasAuthorship W2113177621A5072631239 @default.
- W2113177621 hasAuthorship W2113177621A5078824497 @default.
- W2113177621 hasAuthorship W2113177621A5080880936 @default.
- W2113177621 hasAuthorship W2113177621A5084865475 @default.
- W2113177621 hasBestOaLocation W21131776211 @default.
- W2113177621 hasConcept C126322002 @default.
- W2113177621 hasConcept C134018914 @default.
- W2113177621 hasConcept C14372207 @default.
- W2113177621 hasConcept C17991360 @default.
- W2113177621 hasConcept C194832188 @default.
- W2113177621 hasConcept C2777180221 @default.
- W2113177621 hasConcept C2777391703 @default.
- W2113177621 hasConcept C2779306644 @default.
- W2113177621 hasConcept C2780613262 @default.
- W2113177621 hasConcept C511355011 @default.
- W2113177621 hasConcept C555293320 @default.
- W2113177621 hasConcept C71924100 @default.
- W2113177621 hasConceptScore W2113177621C126322002 @default.
- W2113177621 hasConceptScore W2113177621C134018914 @default.
- W2113177621 hasConceptScore W2113177621C14372207 @default.
- W2113177621 hasConceptScore W2113177621C17991360 @default.
- W2113177621 hasConceptScore W2113177621C194832188 @default.
- W2113177621 hasConceptScore W2113177621C2777180221 @default.
- W2113177621 hasConceptScore W2113177621C2777391703 @default.