J. Cole et al., BIOMONITORING OF POSSIBLE HUMAN EXPOSURE TO ENVIRONMENTAL GENOTOXIC CHEMICALS - LESSONS FROM A STUDY FOLLOWING THE WRECK OF THE OIL TANKER BRAER, Environmental and molecular mutagenesis, 30(2), 1997, pp. 97-111
In January 1993 the oil tanker Braer ran aground in the Shetland islan
ds, Scotland. Approximately 80,000 ions of crude oil were released. Ex
ceptionally high winds caused extensive pollution and exposure of the
local population to crude oil. We describe the study which was immedia
tely set in place to examine the exposed population for evidence of ge
notoxic exposure. Brood samples were token and primary DNA damage was
measured in the mononuclear cell fraction by the butanol modification
of the P-32-postlabelling method. Mutation was measured at the hprt lo
cus in T lymphocytes. No evidence of genotoxicity was obtained for eit
her end point, but nevertheless, we believe that useful lessons were l
earnt, which should be incorporated into the design of future studies:
(1) A rapid response is essential, and even if sufficient funds are n
ot immediately available, it is still worth attempting to obtain sampl
es quickly and use cryopreservation, also to attempt to estimate expos
ure. (2) Adequate numbers of volunteers must be sought, together with
enough controls, not just to allow meaningful analysis but to overcome
toss of samples and failure of things to go according to plan. (3) Po
ints concerning laboratory practice include: (i) samples should be cod
ed, (ii) clearly defined and proven protocols should be used, (iii) ir
replaceable samples should not be used for method development, (iv) sh
ould a problem become apparent during the study, work on such samples
should cease immediately until the problem is solved, (v) all critical
experimental components should be pretested against a laboratory stan
dard. (4) The study design should include replicate experiments to mon
itor experimental variability and reproducibility, as well os internal
standards and cryopreserved ''in house'' samples. Care must be token
that samples from any one exposure group are spread between a number o
f independent experiments and that each experiment includes samples fr
om a number of exposure groups. (5) A computerised data base should be
maintained with full details of experimental variables, donor attribu
tes, and raw data so that any contribution of experimental artefacts t
o ''outlier'' results can be monitored. (6) Because of the nature of t
he statistical variation for many environmental genotoxicity end point
s, only a large-scale study is likely to be capable of yielding useful
information. (C) 1997 Wiley-Liss, Inc.