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Merck

Pharmacogenetics of olanzapine metabolism.

Pharmacogenomics (2013-08-13)
Mao Mao Söderberg, Marja-Liisa Dahl
ABSTRACT

The pharmacokinetics of the atypical antipsychotic, olanzapine, display large interindividual variation leading to multiple-fold differences in drug exposure between patients at a given dose. This variation in turn gives rise to the need for individualized dosing in order to avoid concentration-dependent adverse effects or therapeutic failure. Genetically determined differences in olanzapine metabolism represent a less studied source of variability in comparison to environmental and physiological factors. In this review, we summarize available in vitro and in vivo data addressing the influence of polymorphisms in drug-metabolizing enzymes on olanzapine serum exposure. The polymorphic CYP2D6 enzyme appears to have no significant influence on olanzapine steady-state serum concentrations. The formation of the various olanzapine metabolites is influenced by polymorphisms in the genes coding for CYP1A2, CYP1A expression regulator AHR, UGT1A4 and UGT2B10, as well as FMO3. An impact on steady-state olanzapine serum concentrations has been suggested for variants of CYP1A2 and UGT1A4, with somewhat conflicting findings. The potential involvement of FMO1 and CYP3A43 in olanzapine disposition has also been suggested but needs future validation.

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Sigma-Aldrich
Olanzapine, ≥98% (HPLC)
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Supelco
Olanzapine solution, 1.0 mg/mL in acetonitrile, ampule of 1 mL, certified reference material, Cerilliant®
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USP
Olanzapine, United States Pharmacopeia (USP) Reference Standard
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Olanzapine, European Pharmacopoeia (EP) Reference Standard
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Olanzapine for system suitability, European Pharmacopoeia (EP) Reference Standard
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