High-dose venlafaxine treatment in a depressed patient with a genetic CYP2D6 deficiency

被引:6
作者
Haller-Gloor, F
Eap, CB
Turgeon, J
Baumann, P
机构
[1] Ctr Neurosci Psychiat, Dept Univ Psychiat Adulte, Unite Biochim & Psychopharmacol Clin, CH-1008 Prilly, Switzerland
[2] Univ Montreal, Fac Pharm, Montreal, PQ H3C 3J7, Canada
关键词
CYP2D6; pharmacogenetics; depression; venlafaxine; enantiomers; plasma concentrations; non-response; lithium;
D O I
10.1080/13651500410005559
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
A female patient ( 47 years) who suffered from a severe episode of a recurrent depression with psychotic symptoms (F33.3) firstly underwent several unsuccessful treatments. She was then submitted to a combined treatment with 2 x 300 mg/day extended-release venlafaxine (VEN) and lithium (0.7 mmol/l). She responded within 7 weeks and, after 9 weeks, she showed full remission. Moreover, she tolerated this medication well. Steady-state plasma concentrations of VEN and its metabolites and their enantiomers were measured. The concentrations of VEN and its metabolite O-demethyl-VEN (ODV) were 1024 and 234 ng/ml, respectively. The unusually high concentration of the parent compound in comparison to the metabolite is mainly explained by an impaired metabolism of R-VEN in this patient, who by genotyping was shown to have a genetic deficiency of CYP2D6. In conclusion, in patients suffering from non-response to an antidepressant treatment, an individualised treatment strategy should be developed, and stereoselective therapeutic drug monitoring and genotyping may be recommended.
引用
收藏
页码:191 / 195
页数:5
相关论文
共 22 条
  • [1] Béïque JC, 1999, SYNAPSE, V32, P198, DOI 10.1002/(SICI)1098-2396(19990601)32:3<198::AID-SYN6>3.0.CO
  • [2] 2-2
  • [3] Briley M, 1998, HUM PSYCHOPHARM CLIN, V13, P99, DOI 10.1002/(SICI)1099-1077(199803)13:2<99::AID-HUP954>3.0.CO
  • [4] 2-2
  • [5] Comparative affinity of duloxetine and venlafaxine for serotonin and norepinephrine transporters in vitro and in vivo, human serotonin receptor subtypes, and other neuronal receptors
    Bymaster, FP
    Dreshfield-Ahmad, LJ
    Threlkeld, PG
    Shaw, JL
    Thompson, L
    Nelson, DL
    Hemrick-Luecke, SK
    Wong, DT
    [J]. NEUROPSYCHOPHARMACOLOGY, 2001, 25 (06) : 871 - 880
  • [6] CIUSANI E, 2004, IN PRESS J PSYCHOPHA
  • [7] Marked increase of venlafaxine enantiomer concentrations as a consequence of metabolic interactions: A case report
    Eap, CB
    Bertel-Laubscher, R
    Zullino, D
    Amey, M
    Baumann, P
    [J]. PHARMACOPSYCHIATRY, 2000, 33 (03) : 112 - 115
  • [8] Role of CYP2D6 in the stereoselective disposition of venlafaxine in humans
    Eap, CB
    Lessard, E
    Baumann, P
    Brawand-Amey, M
    Yessine, MA
    O'Hara, G
    Turgeon, J
    [J]. PHARMACOGENETICS, 2003, 13 (01): : 39 - 47
  • [9] O- and N-demethylation of venlafaxine in vitro by human liver microsomes and by microsomes from cDNA-transfected cells:: Effect of metabolic inhibitors and SSRI antidepressants
    Fogelman, SM
    Schmider, J
    Venkatakrishnan, K
    von Moltke, LL
    Harmatz, JS
    Shader, RI
    Greenblatt, DJ
    [J]. NEUROPSYCHOPHARMACOLOGY, 1999, 20 (05) : 480 - 490
  • [10] Assessment of the predictive power of genotypes for the in-vivo catalytic function of CYP2D6 in a German population
    Griese, EU
    Zanger, UM
    Brudermanns, U
    Gaedigk, A
    Mikus, G
    Morike, K
    Stuven, T
    Eichelbaum, M
    [J]. PHARMACOGENETICS, 1998, 8 (01): : 15 - 26