Oxidative stress is associated with C-reactive protein in non-diabetic postmenopausal women, independent of obesity and insulin resistanceYear: 2012
Type: Journal Article
Abstract: OBJECTIVE: Oxidative stress is associated with obesity, metabolic syndrome, and inflammation, suggesting it could be an early event in the pathology of chronic diseases. We tested the hypothesis that elevated levels of oxidative stress markers are associated with increased C-reactive protein (CRP) and that this is independent of obesity and insulin resistance. RESEARCH DESIGN AND METHODS: This study was cross-sectional designed and non-diabetic postmenopausal women (n=1821) with CRP levels =10 mg/L was enrolled. The CRP levels were categorized into quartiles from the lowest to the highest concentrations (Q1-Q4). The degree of insulin resistance was determined using the homeostasis model assessment of insulin resistance (HOMA-IR). We measured oxidative stress using urinary 8-epi-prostaglandin F(2alpha) (8-epi-PGF(2alpha) ) and plasma oxidized low-density lipoprotein (ox-LDL). RESULTS: After adjustments for age and lifestyle habits, including smoking and drinking, we found higher body mass index (BMI) and HOMA-IR scores in Q2 and Q3 versus Q1. The Q4 BMI and HOMA-IR scores were higher than all other quartiles. The plasma ox-LDL was higher in Q4 than in Q1. Urinary 8-epi-PGF(2alpha) was higher in Q3 and Q4 than in Q1 or Q2. Urinary 8-epi-PGF(2alpha) positively correlated with CRP (r=0.235, P<0.001) whereas no correlation was found between ox-LDL and CRP. Multiple linear regression analyses of BMI and HOMA-IR showed that the association between urinary 8-epi-PGF(2alpha) and CRP levels remained significant (P<0.001). CONCLUSIONS: Oxidative stress measured by increased concentration of urine 8-epi-PGF(2alpha) is strongly associated with CRP levels. This finding was independent of obesity and insulin resistance in non-diabetic postmenopausal women. (c) 2012 Blackwell Publishing Ltd.
Authors: Park, S. Kim, M. Paik, J. K. Jang, Y. J. Lee, S. H. Lee, J. H.
Journal: Clin Endocrinol (Oxf)
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