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Vol. 28, Issue 6, 617-619, June 2000
Laboratoire du Centre de We studied the influence of drinking and smoking habits on CYP2D6
metabolic capacity measured by the use of debrisoquine as a substance
test. We did not find any significant differences in the frequency of
subjects with CYP2D6 deficiency (poor metabolizers) among four groups
of healthy individuals: nonsmokers/nondrinkers, smokers/drinkers,
nondrinkers/smokers, and nonsmokers/drinkers. We demonstrated that,
among poor metabolizers, alcohol and tobacco consumption was associated
with higher metabolic ratios than it was with the control group, but
the differences were not statistically significant. Among extensive
metabolizers, the lowest metabolic ratio (highest enzyme activity) was
detected for nondrinkers/smokers, intermediate values for
smokers/drinkers, and the highest metabolic ratio (lowest enzyme
activity) for nonsmokers/drinkers. These variations were slight but
statistically significant when logarithmic ratio values were applied.
These results show that smoking and drinking habits do not need to be
taken into account when humans are phenotyped for CYP2D6.
Médecine Préventive
(M.V.-V., M.M.G.),
Département Statistiques
du Centre
de Médecine
Préventive (B.F.),
54501
Vandoeuvre-lès-Nancy
Cédex, France,
EA 3117 Université
Henri Poincaré Nancy 1 (M.M.G.),
Centre
du Médicament,
54000 Nancy, France
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