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Review
. 2023 Mar:248:114115.
doi: 10.1016/j.ijheh.2023.114115. Epub 2023 Jan 21.

Human urinary arsenic species, associated exposure determinants and potential health risks assessed in the HBM4EU Aligned Studies

Jurgen Buekers  1 , Kirsten Baken  2 , Eva Govarts  2 , Laura Rodriguez Martin  2 , Nina Vogel  3 , Marike Kolossa-Gehring  3 , Zdenka Šlejkovec  4 , Ingrid Falnoga  4 , Milena Horvat  4 , Sanna Lignell  5 , Anna Karin Lindroos  5 , Loïc Rambaud  6 , Margaux Riou  6 , Susana Pedraza-Diaz  7 , Marta Esteban-Lopez  7 , Argelia Castaño  7 , Elly Den Hond  8 , Willy Baeyens  9 , Tiina Santonen  10 , Greet Schoeters  11
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Free article
Review

Human urinary arsenic species, associated exposure determinants and potential health risks assessed in the HBM4EU Aligned Studies

Jurgen Buekers et al. Int J Hyg Environ Health. 2023 Mar.
Free article

Abstract

The European Joint Programme HBM4EU coordinated and advanced human biomonitoring (HBM) in Europe in order to provide science-based evidence for chemical policy development and improve chemical management. Arsenic (As) was selected as a priority substance under the HBM4EU initiative for which open, policy relevant questions like the status of exposure had to be answered. Internal exposure to inorganic arsenic (iAs), measured as Toxic Relevant Arsenic (TRA) (the sum of As(III), As(V), MMA, DMA) in urine samples of teenagers differed among the sampling sites (BEA (Spain) > Riksmaten adolescents (Sweden), ESTEBAN (France) > FLEHS IV (Belgium), SLO CRP (Slovenia)) with geometric means between 3.84 and 8.47 μg/L. The ratio TRA to TRA + arsenobetaine or the ratio TRA to total arsenic varied between 0.22 and 0.49. Main exposure determinants for TRA were the consumption of rice and seafood. When all studies were combined, Pearson correlation analysis showed significant associations between all considered As species. Higher concentrations of DMA, quantitatively a major constituent of TRA, were found with increasing arsenobetaine concentrations, a marker for organic As intake, e.g. through seafood, indicating that other sources of DMA than metabolism of inorganic As exist, e.g. direct intake of DMA or via the intake of arsenosugars or -lipids. Given the lower toxicity of DMA(V) versus iAs, estimating the amount of DMA not originating from iAs, or normalizing TRA for arsenobetaine intake could be useful for estimating iAs exposure and risk. Comparing urinary TRA concentrations with formerly derived biomonitoring equivalent (BE) for non-carcinogenic effects (6.4 μg/L) clearly shows that all 95th percentile exposure values in the different studies exceeded this BE. This together with the fact that cancer risk may not be excluded even at lower iAs levels, suggests a possible health concern for the general population of Europe.

Keywords: Arsenic; DMA; EU; Exposure; HBM; HBM4EU; TRA.

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