T. Tateishi et al., Analysis of the C Upsilon P2D6 gene in relation to dextromethorphan O-demethylation capacity in a Japanese population, CLIN PHARM, 65(5), 1999, pp. 570-575
Objective: To analyze the CYP2D6 allele frequencies in a Japanese populatio
n and to evaluate the effects of CYP2D6 variants on in vivo CYP2D6 activity
as measured by the dextromethorphan metabolic ratio (MR).
Methods: Ninety-eight unrelated, healthy Japanese men were phenotyped with
dextromethorphan and genotyped by the polymerase chain reaction amplificati
on method for 7 CYP2D6 alleles.
Results:The CYP2D6*1, CYP2D6*10 CYP2D6*2 CYP2D6*5, CYP2D6*4, and CYP2D6*21
allele frequencies in our Japanese subjects were 0.423, 0.408, 0.092, 0.061
, 0.020, and 0.010, respectively. Thirty-three subjects (33.7%) were hetero
zygous for *10/*1, and 18 (18.4%) and 17 (17.3%) subjects were homozygous f
or *1 and *10 respectively. Subjects who were homozygous for *10 showed the
highest dextromethorphan MR among these 3 genotypes. Eighteen subjects (18
.3%) were heterozygous for *2 but their dextromethorphan MR values were not
greater than the MR values of subjects who were homozygous for *1. One sub
ject was a poor metabolizer phenotypically, and he was homozygous for *5.
Conclusions The CYP2D6 allele frequencies in our Japanese subjects differed
from those determined in previous studies of white subjects or mainland Ch
inese subjects. Individuals homozygous for *10 who have relatively low in v
ivo CYP2D6 activity represent almost 20% of the Japanese population. In add
ition, we did not identify any subjects with amplified *2 among our 98 Japa
nese men.