Modulation of environmental exposures by host genetic factors may expl
ain interindividual variation in susceptibility to carcinogenesis. One
determinant of susceptibility is mutagen sensitivity measured by the
frequency of bleomycin-induced breaks in an in vitro lymphocyte assay.
Mutagen sensitivity is a significant predictor of aerodigestive tract
cancer risk. In this case-control study of lung-cancer susceptibility
markers, 54% of 132 lung-cancer cases had mutagen-sensitivity scores
greater than or equal to 1 break/cell, compared with only 22% of 232 c
ontrols. The mean breaks/cell value (+/-SE) for the 88 African-America
n cases was 1.11 (+/-0.60), compared with 0.82 (+/-0.49) for the 121 c
ontrols (P < 0.001). For the 44 Mexican-American cases and 111 control
s, the comparable values were 1.11 (+/-0.52) and 0.76 (+/-0.38), respe
ctively. The overall odds ratio (OR) for mutagen sensitivity (dichotom
ized at greater than or equal to 1 break/cell), after adjusting for et
hnicity and smoking status, was 3.62 (95% confidence limits [CL] = 2.2
, 5.9). For current smokers the adjusted risk associated with mutagen
sensitivity was 2.52 (1.2, 5.3). For former smokers, the comparable OR
(95% CL) was 6.19 (2.7, 14.1). The risk estimate for those under 61 y
ears of age was 4.85 (2.3, 10.4), compared with 2.85 (1.5, 5.6) for ol
der subjects. The risk also appeared to be higher for lighter smokers
(<20 cigarettes daily) than heavier smokers (ORs = 5.72 and 3.20, resp
ectively). The ethnicity-adjusted ORs by quartile of breaks/cell were
1.0, 1.40, 2.46, and 4.80; the trend test was significant at P < 0.001
. The joint effects of mutagen sensitivity and former smoking, current
smoking, or heavy smoking were greater than additive, although the in
teraction terms were not statistically significant in the logistic mod
el. Mutagen sensitivity may therefore be a useful member of a panel of
susceptibility markers for defining high-risk subgroups for chemoprev
ention trials. (C) 1997 Wiley-Liss, Inc.