Journal
BIOLOGICAL TRACE ELEMENT RESEARCH
Volume 201, Issue 7, Pages 3133-3143Publisher
SPRINGERNATURE
DOI: 10.1007/s12011-022-03407-z
Keywords
Inflammation; Copper; Nutritional Status; Obesity
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This study aims to analyze the relationship between markers of chronic inflammation and copper nutritional status in obese women. The results showed that obese women had higher serum IL-6 concentrations, higher plasma copper concentrations, lower erythrocyte copper concentrations, and lower erythrocyte SOD activity compared to eutrophic women. Additionally, there was a significant negative correlation between TNF-alpha and IL-10 concentrations and SOD activity in the obese group.
Adipose tissue dysfunction causes the development of metabolic complications, such as low-grade chronic inflammation, which may to alter copper homeostasis in obese individuals. Thus, the objective of this study is to analyze the relationship between markers of chronic inflammation and copper nutritional status in obese women. Cross-sectional study involved women aged 20-50 years, divided into two groups: case (BMI > 35 kg/m(2)) and control (18.5 > BMI > 24.9 kg/m(2)). Plasma and erythrocyte copper concentrations were determined by inductively coupled plasma optical emission spectrometry (ICP-OES) method. Activity of superoxide dismutase (SOD) enzyme in the erythrocytes was determined with an automatic biochemical analyzer. Serum concentrations of interleukin (IL)-6, IL-8, IL-12, IL-10, and IL-1 beta and tumor necrosis factor-alpha (TNF-alpha) were determined by using flow cytometer. Serum IL-6 concentrations were 105% higher in the case group compared to eutrophic women. Plasma copper concentrations were 20.5% higher, and erythrocyte copper concentrations were 23.5% lower in patients with obesity. In addition, erythrocyte SOD activity was 20% lower in obese participants when compared to eutrophic women. Our study identified significant negative correlation between the cytokines TNF-alpha and IL-10 and the SOD activity in the case group, suggesting a possible influence of chronic inflammation on copper distribution in obese individuals.
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