4.7 Article

Human health risks estimations from polycyclic aromatic hydrocarbons in serum and their hydroxylated metabolites in paired urine samples*

期刊

ENVIRONMENTAL POLLUTION
卷 290, 期 -, 页码 -

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ELSEVIER SCI LTD
DOI: 10.1016/j.envpol.2021.117975

关键词

Health risk assessment; Human exposure; Polycyclic aromatic hydrocarbons; Serum; Urine

资金

  1. National Natural Science Foundation of China [41991311, 41977303]
  2. National Key R&D Program of China [2018YFC1801105]
  3. Guangdong-Hong Kong-Macao Joint Laboratory for Contaminants Exposure and Health [2020B1212030008]
  4. Guangzhou Center for Disease Control and Prevention
  5. 100 Talents Program of Guangdong University of Technology

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The study found that while PAH levels in serum were lower than OH-PAH levels in urine, there was no significant correlation between the concentrations of parent PAHs in serum and their metabolites in urine. This suggests that estimates based solely on urine sampling may substantially understate health risks due to PAH exposure.
Polycyclic aromatic hydrocarbons (PAHs) are compounds with two or more benzene rings whose hydroxylated metabolites (OH-PAHs) are excreted in urine. Human PAH exposure is therefore commonly estimated based on urinary OH-PAH concentrations. However, no study has compared PAH exposure estimates based on urinary OHPAHs to measurements of PAH levels in blood samples. Estimates of PAH exposure based solely on urinary OHPAHs may thus be subject to substantial error. To test this hypothesis, paired measurements of parent PAHs in serum and OH-PAHs in urine samples from 480 participants in Guangzhou, a typical developed city in southern China, were used to investigate differences in the estimates of human PAH exposure obtained by sampling different biological matrices. The median PAH concentration in serum was 4.05 ng mL-1, which was lower than that of OH-PAHs in urine (8.33 ng mL-1). However, serum pyrene levels were significantly higher than urinary levels of its metabolite 1-hydroxypyrene. Concentrations of parent PAHs in serum were not significantly correlated with those of their metabolites in urine with the exception of phenanthrene, which exhibited a significant negative correlation. Over 28% of the participants had carcinogenic risk values above the acceptable cancer risk level of 10-6. Overall, estimated human exposure and health risks based on urinary 1-hydroxypyrene levels were only 13.6% of those based on serum pyrene measurements, indicating that estimates based solely on urine sampling may substantially understate health risks due to PAH exposure.

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