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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2009-7-6
pubmed:abstractText
We tested the hypothesis that concentrations of adipocytokines are altered in SLE and associated with coronary atherosclerosis, insulin resistance and inflammation. Concentrations of resistin, leptin, adiponectin and visfatin were measured in 109 patients with SLE and 78 control subjects. Coronary calcification was measured using electron beam-computed tomography, and insulin resistance was defined by the homeostasis model assessment index. Concentrations of adiponectin (28.7 +/- 17.9 vs 22.0 +/- 15.3 microg/mL, P = 0.003), leptin (41.1 +/- 49.9 vs 19.8 +/- 24.6 ng/mL, P < 0.001) and visfatin (7.5 +/- 10.5 vs 4.5 +/- 2.8 ng/mL, P < 0.001) were higher in patients with SLE than in controls. These differences remained significant after adjustment for age, race, sex and body mass index (BMI; all P values < 0.02). Concentrations of resistin (10.7 +/- 7.6 vs 9.1 +/- 5.1 ng/mL, P = 0.41) did not differ in patients and controls. In patients with SLE, leptin was positively associated with BMI (rho = 0.80, P < 0.001), insulin resistance (rho = 0.46, P < 0.001) and C-reactive protein (CRP) (rho = 0.30, P = 0.002), whereas adiponectin was negatively associated with the same factors (rho = -0.40, P < 0.001; rho = -0.38, P < 0.001; rho = -0.22, P = 0.02, respectively). None of the adipocytokines were associated with coronary atherosclerosis in SLE. In conclusion, patients with SLE have increased concentrations of adiponectin, leptin and visfatin. Lower concentrations of adiponectin and higher concentrations of leptin are associated with insulin resistance, BMI and CRP in patients with SLE.
pubmed:grant
pubmed:commentsCorrections
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pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0961-2033
pubmed:author
pubmed:issnType
Print
pubmed:volume
18
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
799-806
pubmed:dateRevised
2010-9-27
pubmed:meshHeading
pubmed-meshheading:19578104-Adipokines, pubmed-meshheading:19578104-Adiponectin, pubmed-meshheading:19578104-Adult, pubmed-meshheading:19578104-Body Mass Index, pubmed-meshheading:19578104-C-Reactive Protein, pubmed-meshheading:19578104-Case-Control Studies, pubmed-meshheading:19578104-Coronary Artery Disease, pubmed-meshheading:19578104-Cross-Sectional Studies, pubmed-meshheading:19578104-Female, pubmed-meshheading:19578104-Humans, pubmed-meshheading:19578104-Inflammation, pubmed-meshheading:19578104-Insulin Resistance, pubmed-meshheading:19578104-Leptin, pubmed-meshheading:19578104-Lupus Erythematosus, Systemic, pubmed-meshheading:19578104-Male, pubmed-meshheading:19578104-Metabolic Syndrome X, pubmed-meshheading:19578104-Middle Aged, pubmed-meshheading:19578104-Nicotinamide Phosphoribosyltransferase, pubmed-meshheading:19578104-Resistin, pubmed-meshheading:19578104-Risk Factors
pubmed:year
2009
pubmed:articleTitle
Adipocytokines in systemic lupus erythematosus: relationship to inflammation, insulin resistance and coronary atherosclerosis.
pubmed:affiliation
Department of Medicine, Vanderbilt University, Nashville, Tennessee 37232-6602, USA.
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