Citalopram: an interaction study with clomipramine in a patient heterozygous for CYP2D6 genotype

被引:13
作者
Haffen, E
Vandel, P
Broly, F
Vandel, S
Sechter, D
Bizouard, P
Bechtel, PR
机构
[1] Univ Hosp Besancon, Dept Clin Psychiat & Med Psychol, Besancon, France
[2] Univ Hosp Besancon, Dept Clin Pharmacol, Besancon, France
[3] Univ Hosp Lille, Biochem & Mol Biol Lab, Lille, France
关键词
D O I
10.1055/s-1999-7960
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A pharmacokinetic interaction between the selective serotonin reuptake inhibitor citalopram and a tricyclic antidepressant, clomipramine, was noted in a patient treated for major depression and obsessive-compulsive disorder. After the addition of citalopram, a desmethylclomipramine plasma level increase and an 8-hydroacy-desmethylclomipramine plasma level decrease were observed. The CYP2D6 phenotype, determined when the patient received the antidepressant comedication, characterized a poor metabolizer status (dextromethorphan metabolic ratio > 0.3), despite a heterozygous genotype containing a wild-type allele with extensive metabolic capacity and a mutant non-functional allele (CYP2D6*1A/CYP2D6*4A). This case seems to be one of the first descriptions of the clinical relevance of a CYP2D6 heterozygous genotype in a patient treated with antidepressant.
引用
收藏
页码:232 / 234
页数:3
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