Gm. Calvert et al., GENOTOXICITY IN WORKERS EXPOSED TO METHYL-BROMIDE, Mutation research. Genetic toxicology and environmental mutagenesis, 417(2-3), 1998, pp. 115-128
To address the genotoxicity of in vivo methyl bromide (CAS 74-83-9) ex
posure in humans, we collected blood and oropharyngeal cells as part o
f a cross-sectional morbidity study of methyl bromide-exposed fumigati
on workers and their referents. Micronuclei were measured in lymphocyt
es and oropharyngeal cells, and hypoxanthine-guanine phosphoribosyl tr
ansferase gene (hprt) mutations were measured in lymphocytes. A total
of 32 workers and 28 referents provided specimens. Among current non-s
mokers, mean hprt variant frequencies (Vfs) were found to be elevated
among workers compared to referents (geometric mean: workers = 4.49 x
10(-6), referents = 2.96 x 10(-6); two-sided p = 0.22); this differenc
e was more pronounced among workers with 4 h or more of recent methyl
bromide exposure compared to referents (geometric mean: workers = 6.56
x 10(-6), referents = 2.96 x 10(-6); two-sided p = 0.06). Mean oropha
ryngeal cell micronuclei were higher among workers compared to referen
ts (mean: workers = 2.00, referents = 1.31; two-sided p = 0.08); the r
esults were similar when workers with 4 h or more of recent methyl bro
mide exposure were compared to referents (mean: workers = 2.07, refere
nts = 1.31; two-sided p = 0.13). No consistent differences between wor
kers and referents were observed for frequencies of kinetochore-negati
ve lymphocyte micronuclei, or kinetochore-positive lymphocyte micronuc
lei. The study was limited by a sample size sufficient only for detect
ing relatively large differences, absence of a reliable method to meas
ure the intensity of workplace methyl bromide exposures, and relativel
y infrequent methyl bromide exposure (e.g., the median length of expos
ure to methyl bromide during the 2 weeks preceding the survey was 4 h)
. In conclusion, our findings provide some evidence that methyl bromid
e exposure may be associated with genotoxic effects in lymphocytes and
oropharyngeal cells. Further study on the genotoxicity of methyl brom
ide exposure in humans is warranted. (C) 1998 Elsevier Science B.V. Al
l rights reserved.