Isomers of per- and polyfluoroalkyl substances and uric acid in adults: Isomers of C8 Health Project in China

https://doi.org/10.1016/j.envint.2019.105160Get rights and content
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Highlights

  • Per- and polyfluoroalkyl substances (PFAS) exposure in human is a global issue, particularly in developing countries.

  • No study explored the associations between isomeric PFASs and serum uric acid in human.

  • We reported novel results in which PFAS associations with uric acid varied according to isomer and adult kidney function.

  • The associations between PFAS and uric acid showed an inverted ‘U’ shaped pattern across kidney function stages.

Abstract

Background

Greater levels of serum per- and polyfluoroalkyl substances (PFAS) are known to be associated with higher uric acid which itself leads to a number of chronic diseases. However, whether this association varies across PFAS isomers which recently have been found to be associated with human health remains unknown.

Objectives

To address this research gap, we explored isomer-specific associations between serum PFAS and uric acid in Chinese adults.

Methods

We conducted a cross-sectional study of associations between serum PFAS isomer and serum uric acid in 1612 participants from the Isomer of C8 Health Project. We used multivariable linear and logistic regression models to analyze serum isomers of perfluorooctanoate (PFOA), perfluorooctane sulfonate (PFOS), and other PFASs as continuous and categorical predictors of uric acid, adjusted for confounders. The association was also stratified by kidney function stage based on estimated glomerular filtration rate (GF-1, GF-2, GF-3a, and GF-3b/4).

Results

We found positive associations between serum PFAS isomer concentrations and uric acid. Uric acid levels were greater for each log-unit increase in branched PFOA (β = 0.30, 95% CI: 0.21, 0.40), linear PFOA (β = 0.18, 95% CI: 0.09, 0.26), branched PFOS (β = 0.09, 95% CI: 0.02, 0.17) and linear PFOS (β = 0.06, 95% CI: −0.01, 0.14) concentration. The associations between PFAS and uric acid showed an inverted ‘U' shaped pattern across kidney function stages. For example, uric acid level was greater with each log-unit increase in total-PFOA among GF-1 (β = 0.21, 95% CI: 0.06, 0.37), this relationship was greater in GF-3a (β = 0.49, 95% CI: 0.09, 0.89) and decreased in GF-3b/4 (β = −0.22, 95% CI: −0.83, 0.39). We also found the odds of hyperuricemia increased linearly with increasing branched PFOA in quartiles (odds ratio = 2.67, 95% CI: 1.86, 3.85 at the highest quartile).

Conclusion

We report novel results in which PFAS associations with uric acid varied according to isomer and adult kidney function. Besides, our findings are consistent with previous epidemiologic studies in finding a positive association between serum PFAS concentrations and serum uric acid, especially for PFOA. Our results indicate that more research is needed to more clearly assess the impact of PFAS isomers on human health, which will help to refine regulation policies for PFAS.

Keywords

Per- and polyfluoroalkyl substances
Uric acid
Hyperuricemia
Adult
Isomers of C8 Health Project in China

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