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Relationship of obesity and visceral adiposity with serum concentrations of CRP, TNF-alpha and IL-6. Diabetes research and clinical practice. [Diabetes Res Clin Pract] Journal article

 
TitleRelationship of obesity and visceral adiposity with serum concentrations of CRP, TNF-alpha and IL-6.
Author(s)Park HS, Park JY, Yu R 
InstitutionDepartment of Family Medicine, Asan Medical Center, University of Ulsan College of Medicine, 388-1 Pungnap-dong, Songpa-gu, Seoul 138-736, South Korea. hyesoon@amc.seoul.kr
SourceDiabetes Res Clin Pract 2005 Jul; 69(1):29-35.
MeSHAbdomen
Adipose Tissue
Adult
Biological Markers
Body Mass Index
C-Reactive Protein
Cross-Sectional Studies
Female
Humans
Interleukin-6
Korea
Male
Obesity
Regression Analysis
Research Support, Non-U.S. Gov't
Tumor Necrosis Factor-alpha
AbstractOBJECTIVE: To investigate the relationship between serum concentrations of the cytokines C-reactive protein (CRP), tumor necrosis factor (TNF)-alpha, and interleukin (IL)-6, and obesity and visceral adiposity.
METHODS: A cross-sectional study of 100 Korean adults free from pre-existing inflammatory disease or cancer was performed. Body mass index (BMI), waist circumference, and serum concentrations of CRP, TNF-alpha and IL-6 were measured. In 46 obese subjects, fat mass was assessed by bioimpedance analysis and abdominal fat distribution was determined by computerized tomography scan.
RESULTS: Overall, serum concentrations of CRP, TNF-alpha and IL-6 were significantly correlated with weight, BMI, waist circumference, hip circumference, and waist-hip ratio. In obese subjects, CRP and IL-6 were significantly correlated with BMI, waist circumference and visceral adipose tissue. Multiple regression analysis showed that CRP was significantly associated with BMI, whereas IL-6 was significantly related with visceral adiposity in obese subjects.
CONCLUSIONS: The positive associations of obesity and visceral adiposity with elevated cytokine levels suggest the importance of reducing obesity and visceral adiposity to prevent elevations in cytokine levels.
Languageeng
Pub Type(s)Journal Article
PubMed ID15955385
  
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