Relationship Between Markers of Chronic Inflammation and Copper Nutritional Status in Obese Women

Biol Trace Elem Res. 2023 Jul;201(7):3133-3143. doi: 10.1007/s12011-022-03407-z. Epub 2022 Sep 14.

Abstract

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/m2) and control (18.5 > BMI > 24.9 kg/m2). 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-1β and tumor necrosis factor-alpha (TNF-α) 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-α and IL-10 and the SOD activity in the case group, suggesting a possible influence of chronic inflammation on copper distribution in obese individuals.

Keywords: Copper; Inflammation; Nutritional Status; Obesity.

MeSH terms

  • Copper*
  • Cross-Sectional Studies
  • Female
  • Humans
  • Inflammation / metabolism
  • Interleukin-10*
  • Interleukin-6
  • Nutritional Status
  • Obesity / metabolism
  • Superoxide Dismutase
  • Tumor Necrosis Factor-alpha

Substances

  • Interleukin-10
  • Copper
  • Tumor Necrosis Factor-alpha
  • Interleukin-6
  • Superoxide Dismutase