The copper/zinc ratio correlates with markers of disease activity in patients with inflammatory bowel disease

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Abstract

Background Zinc (Zn) and copper (Cu) are trace elements that serve as cofactors in catalytic processes with impact on immune responses. In patients with inflammatory bowel disease (IBD), decreased levels of serum Zn and Cu have been observed. Here, we investigated the effect of inflammation on serum concentrations of these trace elements in patients with IBD. Methods In this cross-sectional study, 98 patients with Crohn disease (CD) and 56 with ulcerative colitis (UC) were prospectively enrolled. Disease activity parameters, such as C-reactive protein (CRP) and fecal calprotectin (FC) were compared to serum Zn, Cu, and Cu/Zn ratio. Results Zinc insufficiency was observed in 11.2% of patients with CD and 14.3% with UC, Cu insufficiency in 20.4% with CD and 7.1% with UC. Anemia, hypoalbuminemia, increased FC, and elevated CRP were more frequently present in Zn-insufficient patients with IBD. In contrast, lower serum CRP values and a trend to lower FC were observed in Cu-insufficient patients. In multiple linear regression models adjusted for age, gender, and serum albumin, CRP positively correlated with serum Cu (P < 0.001) and the Cu/Zn ratio in both CD and UC (P < 0.001) but not with serum Zn concentrations. FC levels correlated only with the Cu/Zn ratio in patients with UC (P < 0.038). Conclusion Systemic inflammation inversely affected the serum Zn and Cu concentrations and, consequently, resulted in an increased Cu/Zn ratio. Lay Summary We found that zinc (Zn) and copper (Cu) insufficiency occurred in patients with inflammatory bowel disease and that systemic inflammation decreased serum Zn and increased Cu concentrations. This resulted in an increased Cu/Zn ratio. It may represent a novel parameter to assess disease activity.

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Schneider, T., Caviezel, D., Korcan Ayata, C., Kiss, C., Niess, J. H., & Hruz, P. (2020). The copper/zinc ratio correlates with markers of disease activity in patients with inflammatory bowel disease. Crohn’s and Colitis 360, 2(1). https://doi.org/10.1093/crocol/otaa001

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