Dose-Response Modeling of Occupational Exposure to Polycyclic Aromatic Hydrocarbons with Biomarkers of Exposure and Effect

• Published in: Cancer epidemiology, biomarkers & prevention biomarkers & prevention, 2007-09, Vol.16 (9), p.1863-1873
• Main Authors: PESCH, Beate, KAPPLER, Martin, SCHERENBERG, Michael, ADAMS, Ansgar, UDO KÄFFERLEIN, Heiko, ANGERER, Jürgen, WILHELM, Michael, SEIDEL, Albrecht, BRÜNING, Thomas, STRAIF, Kurt, MARCZYNSKI, Boleslaw, PREUSS, Ralf, ROSBACH, Bernd, RIHS, Hans-Peter, WEISS, Tobias, RABSTEIN, Sylvia, PIERL, Christiane
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Biomarker; Biomarkers; Carcinogenesis, carcinogens and anticarcinogens; Carcinogens, Environmental - toxicity; Chemical agents; Chemical compounds (mineral, organic); Chemical, physic and infectious diseases; Comet Assay; Computer Simulation; DNA Damage; dose-response modeling; Dose-Response Relationship, Drug; exposure assessment; genotoxicity; Humans; Industry; Male; Medical sciences; Models, Statistical; Occupational Exposure; Occupational medicine; Olea; polycyclic aromatic hydrocarbons; Polycyclic Aromatic Hydrocarbons - toxicity; Public health. Hygiene-occupational medicine; Tumors
• ISSN: 1055-9965; 1538-7755
• DOI: 10.1158/1055-9965.EPI-07-0033

In regulatory toxicology, the dose-response relationship between occupational exposure and biomarkers is of importance in setting threshold values. We analyzed the relationships between occupational exposure to polycyclic aromatic hydrocarbons (PAH) and various biomarkers of internal exposure and DNA damage with data from 284 highly exposed male workers. Personal exposure to phenanthrene and other PAHs was measured during shift and correlated with the sum of 1−, 2+9−, 3−, and 4-hydroxyphenanthrenes in post-shift urine. PAHs and hydroxyphenanthrenes were associated with DNA damage assessed in WBC as 8-oxo-7,8-dihydro-2′-deoxyguanosine/10 6 dGuo and strand breaks by Comet assay as Olive tail moment. Hydroxyphenanthrenes correlated with phenanthrene (Spearman r s = 0.70; P < 0.0001). No correlations could be found between strand breaks and exposure ( r s = 0.01, P < 0.0001 for PAHs; r s = −0.03, P = 0.68 for hydroxyphenanthrenes). Correlations with 8-oxo-7,8-dihydro-2′-deoxyguanosine/10 6 dGuo were weakly negative ( r s = −0.22, P = 0.004 for PAHs) or flat ( r s = −0.08, P = 0.31 for hydroxyphenanthrenes). Linear splines were applied to assess the relationships between the log-transformed variables. All regression models were adjusted for smoking and type of industry. For hydroxyphenanthrenes, 51.7% of the variance could be explained by phenanthrene and other predictors. Up to 0.77 μg/m 3 phenanthrene, no association could be found with hydroxyphenanthrenes. Above that point, hydroxyphenanthrenes increased by a factor of 1.47 under a doubling of phenanthrene exposure (slope, 0.56; 95% confidence interval, 0.47-0.64). Hydroxyphenanthrenes may be recommended as biomarker of occupational PAH exposure, whereas biomarkers of DNA damage in blood did not show a dose-response relation to PAH exposure. (Cancer Epidemiol Biomarkers Prev 2007;16(9):1863–73)