Saltar al contenido
Merck

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

Pharmacopsychiatry (1999-12-22)
E Haffen, P Vandel, F Broly, S Vandel, D Sechter, P Bizouard, P R Bechtel
RESUMEN

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.

MATERIALES
Referencia del producto
Marca
Descripción del producto

Supelco
N-Desmethylclomipramine hydrochloride solution, 1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®
Sigma-Aldrich
Norclomipramine hydrochloride, ≥98% (TLC), powder