An evaluation of styrene genotoxicity using several biomarkers in a 3-year follow-up study of hand-lamination workers
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
10575431
DOI
10.1016/s1383-5718(99)00127-8
PII: S1383-5718(99)00127-8
Knihovny.cz E-zdroje
- MeSH
- adukty DNA krev MeSH
- biologické markery analýza MeSH
- dechové testy MeSH
- dospělí MeSH
- hemoglobiny účinky léků MeSH
- hypoxanthinfosforibosyltransferasa genetika MeSH
- jednovláknová DNA účinky léků MeSH
- kometový test MeSH
- kyseliny mandlové moč MeSH
- látky znečišťující vzduch v pracovním prostředí škodlivé účinky analýza MeSH
- lidé středního věku MeSH
- lidé MeSH
- mutace MeSH
- následné studie MeSH
- plastické hmoty MeSH
- poškození DNA * MeSH
- pracovní expozice škodlivé účinky analýza MeSH
- regresní analýza MeSH
- styren škodlivé účinky analýza chemie MeSH
- T-lymfocyty účinky léků enzymologie MeSH
- valin analogy a deriváty analýza účinky léků MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adukty DNA MeSH
- biologické markery MeSH
- hemoglobiny MeSH
- hypoxanthinfosforibosyltransferasa MeSH
- jednovláknová DNA MeSH
- kyseliny mandlové MeSH
- látky znečišťující vzduch v pracovním prostředí MeSH
- mandelic acid MeSH Prohlížeč
- plastické hmoty MeSH
- styren MeSH
- valin MeSH
A study employing several biomarkers of styrene exposure and genotoxicity was carried out in a group of lamination (reinforced plastic) workers and controls, who had been repeatedly sampled during a 3-year period. Special attention will be paid to the last sampling (S.VI), reported here for the first time. Styrene concentration in the breathing zone, monitored by personal dosimeters, and urinary mandelic acid (MA) were measured as indicators of external exposure. Blood samples were assayed for styrene-specific O6-guanine adducts in DNA, N-terminal valine adducts of styrene in haemoglobin, DNA single-strand breaks (SSB), determined by use of the single cell gel electrophoresis (Comet) assay), and hypoxanthine guanine phosphoribosyl transferase (HPRT) mutant frequencies (MF) in T-lymphocytes. O6-styrene guanine adduct levels were significantly higher in the exposed group (5.9 +/- 4.9 adducts/10(8) dNp) as compared to laboratory controls (0.7 +/- 0.8 adducts/10(8) dNp; P = 0.001). DNA adduct levels significantly correlated with haemoglobin adducts, SSB parameters and years of employment. Styrene-induced N-terminal valine adducts were detected in the lamination workers (1.7 +/- 1.1 pmol/g globin), but not in the control group (detection limit 0.1 pmol/g globin). N-terminal valine adducts correlated strongly with external exposure indicators, DNA adducts and HPRT MF. No significant correlation was found with SSB parameters. A statistically significant difference in HPRT MF was observed between the laminators (22.3 +/- 10.6/10(6)) and laboratory controls (14.2 +/- 6.5/10(6), P = 0.039). HPRT MF in the laminators significantly correlated with styrene concentration in air, MA and haemoglobin adducts, as well as with years of employment and age of the employees. No significant difference (P = 0.450) in MF between the laminators and the factory controls was observed. Surprisingly, we detected differences in MF between sexes. When data from all measurements were combined, women showed higher MF (geometric mean 15.4 vs. 11.2 in men, P = 0.020). The styrene-exposed group exhibited significantly higher SSB parameters (tail moment (TM), tail length (TL) and the percentage of DNA in the tail (TP)) than the control group (P < 0.001). SSB parameters correlated with indicators of external exposure and with O6-styrene guanine adducts. No significant correlation was found between SSB parameters and haemoglobin adducts or HPRT MF. The data encompassing biomarkers from repeated measurements of the same population over a 3-year period are discussed with respect to the mechanisms of genotoxic effects of styrene and the interrelationship of individual biomarkers.
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