Co-exposure to environmental cadmium and arsenic leads to kidney damage even at lower concentrations.

backgroundWhile many studies have examined the effects of single heavy metal exposure, the impact of combined exposure to multiple heavy metals on kidney health remains underexplored.

objectiveThis study aims to assess the risk of kidney damage associated with relatively low concentrations of Cd and As, below established reference levels, and to investigate whether simultaneous exposure leads to synergistic or additive harmful effects.

methodsIn this cross-sectional study of 1948 non-occupationally exposed individuals, we explored the relationship between environmental exposure to heavy metals at sub-occupational levels and the prevalence of kidney damage in this population.

resultsThe risk of kidney damage was increased proportionally to urinary cadmium (uCd) and urinary arsenic (uAs) levels. Co-exposure to Cd and As at Co3 (both metals were above the 3rd tertile) resulted in a 2.65-fold increase in β2-microglobulin (MG) and a 4.41-fold increase in urinary total protein compared to those at Co1 (both metals were below the 3rd tertile). N-acetyl-beta-D-glucosaminidase (NAG) level was 7.42-fold higher at Co3 than at Co1. Subgroup analysis showed that the odds ratio of NAG level elevation increased by 2.74 folds when uCd level was >0.96 μg/g Creatinine (Cr) and uAs level was >8.17 μg/g Cr, and by 3.04-fold when uCd level was >1.86 μg/g Cr (3rd tertile) and uAs level was >4.71 μg/g Cr (2nd tertile). This suggests that co-exposure to both metals can cause kidney damage at concentrations lower than the reference level and even lower than the single metal concentration (uCd 1.86 μg/g Cr) that caused kidney damage. SIGNIFICANCE: In this study, combined exposure to cadmium and arsenic causes kidney damage even at levels below reference thresholds. The findings highlight synergistic effects, with significant increases in biomarkers like β2-microglobulin and NAG. IMPACT: This study demonstrates that environmental cadmium and arsenic exposure can lead to kidney damage in the general population, even at levels significantly below established reference thresholds. These findings highlight the need to reconsider and potentially lower the biological exposure index for combined heavy metal exposure. Additionally, NAG was identified as a highly sensitive biomarker for detecting kidney damage caused by low-level exposure to heavy metals. Unlike previous studies, this research provides specific concentration thresholds, offering a clearer understanding of exposure risks and advancing the assessment of combined heavy metal toxicity on kidney health.