Abstract
Selenium (Se) has been shown to act as a functional antagonist to mercury (Hg) and arsenic (As). Se may influence Hg and As toxicity by modulating redox homeostasis and inflammation. At the same time, the clinical significance of such interactions is questionable. Despite extensive experimental data, human studies on the interaction between these trace elements, as well as on the influence of such interaction on human health are limited. Current data are reviewed on how Hg and Se interplay impacts on cardiovascular diseases, neurotoxicity, neurodegeneration, diabetes and obesity. Studies also demonstrate that the interaction between Se and As significantly affects the development of certain cardiovascular diseases and cancer. This notion is further supported by the results of our analysis of 63,118 adults and 13,734 children from different regions of Russia indicating that the hair Se/Hg ratio is characterized by a tighter association with demographical indices (birth rate, mortality, life span, total morbidity) and morbidity than Hg or Se individually. It is proposed that modulation of the Se/As and Se/Hg ratios in humans may help to improve population health and demography.
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Skalny, A.V., Skalnaya, M.G., Nikonorov, A.A., Tinkov, A.A. (2016). Selenium Antagonism with Mercury and Arsenic: From Chemistry to Population Health and Demography. In: Hatfield, D., Schweizer, U., Tsuji, P., Gladyshev, V. (eds) Selenium. Springer, Cham. https://doi.org/10.1007/978-3-319-41283-2_34
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