Assessment of 1,3-butadiene exposure in polymer production workers using HPRT mutations in lymphocytes as a biomarker

被引:25
作者
Ammenheuser, MM
Bechtold, WE
Abdel-Rahman, SZ
Rosenblatt, JI
Hastings-Smith, DA
Ward, JB [1 ]
机构
[1] Univ Texas, Med Branch, Dept Prevent Med & Community Hlth, Div Environm Toxicol, Galveston, TX 77555 USA
[2] Lovelace Resp Res Inst, Albuquerque, NM USA
关键词
biological monitoring; butadiene; HPRT mutations; occupational health;
D O I
10.2307/3454747
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
1,3-Butadiene (BD), which is used to make styrene-butadiene rubber, is a potent carcinogen in mice and a probable carcinogen, associated with leukemia, in humans. We have previously used HPRT mutation as a biomarker to evaluate exposures to BD in a monomer production plant. We, now report on a study of 49 workers in a styrene-butadiene rubber plant in which we used them concentration of the BD metabolite 1,2-dihydroxy-4-(N-acetylcysteinyl-S)-butane (M1) in urine as a biomarker of exposure and the frequency of HPRT variant (mutant) lymphocytes (Vf) as a biomarker of effect. Workers were assigned to high- and low-exposure groups based on historical information about work areas and jobs. Personal exposure to BD for one work shift was measured using a passive badge dosimeter. Each participant provided a urine specimen and blood sample at the end of the work shift and completed a questionnaire providing information on lifestyle, health, and work activities. The average BD exposures in the high- and low-exposure groups were significantly different, even after excluding two extreme values, (high 1.48 ppm, low 0.15 ppm, p < 0.002). This study was done in 1994 and 1995 before them establishment, in 1996, of the new, permissible exposure limit of 1 ppm. Both the mean M 1 and the HPRT Vf were more than three times greater in the high-exposure group than in the low-exposure group (p < 0.00015). The three, end points correlated with each other, with sample correlation coefficients between 0.4 and 0.6. The correlations among BD exposure and the biomarkers of internal exposure and genotoxicity suggest that occupational exposure to BD, in the range of 1-3 ppm, may be associated with adverse biological effects.
引用
收藏
页码:1249 / 1255
页数:7
相关论文
共 44 条
[31]   Mutagenicity of 1,3-butadiene at the Hprt locus of T-lymphocytes following inhalation exposures of female mice and rats [J].
Meng, QX ;
Henderson, RF ;
Chen, T ;
Heflich, RH ;
Walker, DM ;
Bauer, MJ ;
Reilly, AA ;
Walker, VE .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1999, 429 (01) :107-125
[32]   REFINEMENT OF A LYMPHOCYTE-T CLONING ASSAY TO QUANTIFY THE INVIVO THIOGUANINE-RESISTANT MUTANT FREQUENCY IN HUMANS [J].
ONEILL, JP ;
MCGINNISS, MJ ;
BERMAN, JK ;
SULLIVAN, LM ;
NICKLAS, JA ;
ALBERTINI, RJ .
MUTAGENESIS, 1987, 2 (02) :87-94
[33]   INHALATION TOXICITY STUDIES WITH 1,3-BUTADIENE - 3 2 YEAR TOXICITY CARCINOGENICITY STUDY IN RATS [J].
OWEN, PE ;
GLAISTER, JR ;
GAUNT, IE ;
PULLINGER, DH .
AMERICAN INDUSTRIAL HYGIENE ASSOCIATION JOURNAL, 1987, 48 (05) :407-413
[34]   INCREASED FREQUENCY OF MUTATIONS AT A-T BASE-PAIRS IN THE BONE-MARROW OF B6C3F1 LACL TRANSGENIC MICE EXPOSED TO 1,3-BUTADIENE [J].
RECIO, L ;
MEYER, KG .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1995, 26 (01) :1-8
[35]   AN ANALYSIS OF IN-VIVO HPRT MUTANT FREQUENCY IN CIRCULATING T-LYMPHOCYTES IN THE NORMAL HUMAN-POPULATION - A COMPARISON OF 4 DATASETS [J].
ROBINSON, DR ;
GOODALL, K ;
ALBERTINI, RJ ;
ONEILL, JP ;
FINETTE, B ;
SALATREPAT, M ;
MOUSTACCHI, E ;
TATES, AD ;
BEARE, DM ;
GREEN, MHL ;
COLE, J .
MUTATION RESEARCH-ENVIRONMENTAL MUTAGENESIS AND RELATED SUBJECTS, 1994, 313 (2-3) :227-247
[36]   MOLECULAR ANALYSIS OF LACI MUTANTS FROM BONE-MARROW OF B6C3F1 TRANSGENIC MICE FOLLOWING INHALATION EXPOSURE TO 1,3-BUTADIENE [J].
SISK, SC ;
PLUTA, LJ ;
BOND, JA ;
RECIO, L .
CARCINOGENESIS, 1994, 15 (03) :471-477
[37]   Analysis of hprt mutations occurring in human TK6 lymphoblastoid cells following exposure to 1,2,3,4-diepoxybutane [J].
Steen, AM ;
Meyer, KG ;
Recio, L .
MUTAGENESIS, 1997, 12 (02) :61-67
[38]   Biological effect monitoring in industrial workers from the Czech Republic exposed to low levels of butadiene [J].
Tates, AD ;
vanDam, FJ ;
deZwart, FA ;
Darroudi, F ;
Natarajan, AT ;
Rossner, P ;
Peterkova, K ;
Peltonen, K ;
Demopoulos, NA ;
Stephanou, G ;
Vlachodimitropoulos, D ;
Sram, RJ .
TOXICOLOGY, 1996, 113 (1-3) :91-99
[39]   COMPARATIVE CYTOGENETIC ANALYSIS OF BONE-MARROW DAMAGE INDUCED IN MALE B6C3F1 MICE BY MULTIPLE EXPOSURES TO GASEOUS 1,3-BUTADIENE [J].
TICE, RR ;
BOUCHER, R ;
LUKE, CA ;
SHELBY, MD .
ENVIRONMENTAL MUTAGENESIS, 1987, 9 (03) :235-250
[40]  
Van Vunakis H, 1987, IARC Sci Publ, P317