Authors
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He, Y., Zhu, S., Zhang, Y., Tan, C.P., Zhang, J., Liu, Y., Xu, Y.-J. -More
Category
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Primary study
Journal»EUROPEAN JOURNAL OF CLINICAL NUTRITION
Year
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2024
Background: Despite the abundance of research examining the effects of coffee, tea, and alcohol on inflammatory diseases, there is a notable absence of conclusive evidence regarding their direct causal influence on circulating inflammatory cytokines. Previous studies have primarily concentrated on established cytokines, neglecting the potential impact of beverage consumption on lesser-studied but equally important cytokines.
Methods: Information regarding the consumption of coffee, tea, and alcohol was collected from the UK Biobank, with sample sizes of 428,860, 447,485, and 462,346 individuals, respectively. Data on 41 inflammatory cytokines were obtained from summary statistics of 8293 healthy participants from Finnish cohorts.
Results: The consumption of coffee was found to be potentially associated with decreased levels of Macrophage colony-stimulating factor (beta = -0.57, 95% CI -1.06 similar to -0.08; p = 0.022) and Stem cell growth factor beta (beta = -0.64, 95% CI -1.16 similar to -0.12; p = 0.016), as well as an increase in TNF-related apoptosis-inducing ligand (beta = 0.43, 95% CI 0.06 similar to 0.8; p = 0.023) levels. Conversely, tea intake was potentially correlated with a reduction in Interleukin-8 (beta = -0.45, 95% CI -0.9 similar to 0; p = 0.045) levels. Moreover, our results indicated an association between alcohol consumption and decreased levels of Regulated on Activation, Normal T Cell Expressed and Secreted (beta = -0.24, 95% CI -0.48 similar to 0; p = 0.047), as well as an increase in Stem cell factor (beta = 0.17, 95% CI 0.02 similar to 0.31; p = 0.023) and Stromal cell-derived factor-1 alpha (beta = 0.20, 95% CI 0.04 similar to 0.36; p = 0.013).
Conclusion: Revealing the interactions between beverage consumption and various inflammatory cytokines may lead to the discovery of novel therapeutic targets, thereby facilitating dietary interventions to complement clinical disease treatments.
Epistemonikos ID: fedb57884ddb91d8f8c00e83d873debb619d11ee
First added on: Feb 17, 2025