Steady-state plasma levels of nortriptyline and its hydroxylated metabolites in Japanese patients: impact of CYP2D6 genotype on the hydroxylation of nortriptyline

• Published in: Journal of clinical psychopharmacology Vol. 20; no. 2; p. 141
• Main Authors: Morita, S, Shimoda, K, Someya, T, Yoshimura, Y, Kamijima, K, Kato, N
• Format: Journal Article
• Language: English
• Published: United States 01.04.2000
• Subjects: Adjustment Disorders - blood; Adjustment Disorders - drug therapy; Adjustment Disorders - genetics; Adolescent; Adult; Aged; Alleles; Bipolar Disorder - blood; Bipolar Disorder - drug therapy; Bipolar Disorder - genetics; Cytochrome P-450 CYP2D6 - genetics; Depressive Disorder, Major - blood; Depressive Disorder, Major - drug therapy; Depressive Disorder, Major - genetics; DNA Mutational Analysis; Ethnic Groups - genetics; Female; Genotype; Humans; Japan; Male; Middle Aged; Nortriptyline - analogs & derivatives; Nortriptyline - pharmacokinetics; Japan
• ISSN: 0271-0749
• DOI: 10.1097/00004714-200004000-00005

The authors investigated the impact of the CYP2D6 genotype on steady-state concentrations of nortriptyline (NT) and its metabolites, trans-10-hydroxynortriptyline (EHNT) and cis-10-hydroxynortriptyline in a Japanese population of psychiatric patients. Forty-one patients (20 men and 21 women) were orally administered nortriptyline hydrochloride. The allele frequencies of the CYP2D6*5 and CYP2D6*10 were 4.9% and 34.1%, respectively. Significant differences in NT concentrations corrected for dose and weight were observed between the subjects with no mutated alleles and those with one mutated allele (mean +/- SD for no mutated alleles vs. one mutated allele: 70.3 +/- 25.4 vs. 98.4 +/- 36.6 ng/mL x mg(-1) x kg(-1); t = 2.54, dcf = 33, p < 0.05) and between the subjects with no mutated alleles and two mutated alleles (no mutated alleles vs. two mutated alleles: 70.3 +/- 25.4 vs. 147 +/- 31.1 ng/mL x mg(-1) x kg(-1); t = 5.87, df = 19, p < 0.0001). Also, a significant difference in the NT/EHNT ratio, which is representative of the hydroxylation ratio of NT, was observed between the subjects with no mutated alleles and those with two mutated alleles (no mutated alleles vs. two mutated alleles: 0.82 +/- 0.30 vs. 2.71 +/- 0.84; t = 7.86, df = 19, p < 0.0001). Multiple regression analysis showed that the number of mutated alleles of CYP2D6, which was the only significant factor, accounted for 41% and 48% of the variability in log(NT corrected for dose and weight) and log(NT/EHNT), respectively.