P-616 Abstract: Health effects associated with chronic, low-level exposures to arsenic in drinking water (<100 μg/L) remain unclear, in part due to uncertainties in assessing exposure. Drinking water and toenail arsenic concentrations have been used to assess past exposure to arsenic in epidemiological studies, under the assumption that a single measurement can be used to estimate historical exposure. Using data from a population-based case-control study of arsenic exposure and bladder cancer in Michigan, this study aims to better understand variability in drinking water and toenail arsenic concentrations. Drinking water samples were collected an average of fourteen months apart for 261 participants whose drinking water sources included private wells (n= 215), public water supply systems (n=33), and bottled water supplies (n = 13). Samples were collected from the primary drinking water source, which often included a point-of-use (POU) treatment system such as a home water softener or filter. Untreated samples were also collected from participants on private wells. Up to three toenail samples were obtained from participants. The first and second sample were clipped an average of fourteen months apart, while the second and third samples were collected an average of one month apart. All samples were analyzed for total arsenic using an Inductively Coupled Plasma Mass Spectrometer (ICP-MS). Pearson correlation coefficients reveal strong relationships between the two drinking water measurements collected from untreated private wells (r= 0.91, p<0.0001, n=197). The correlation was also high for samples collected from the primary source of drinking water (r=0.88, p<0.0001, n=196), suggesting that a single measurement may be effective in estimating past exposure. While POU treatment devices did not differentially affect measurement reproducibility, use of these systems affected arsenic concentrations. Toenail samples collected an average of fourteen months apart were positively correlated (r=0.43, p<0.0001, n=236); less variability is apparent for samples clipped consecutively (r=0.77, p<0.0001, n=189). The influence of arsenic concentration, drinking water source, and other variables on reproducibility of the toenail arsenic measurement will be discussed. In conclusion, both exposure measurements may be effective in monitoring past exposures in a stable population; exposure misclassification may be reduced by accounting for consistency of drinking water source, POU treatments, and drinking water concentration over time.
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