Metabolic, genetic, and pharmacokinetic parameters for the prediction of olanzapine efficacy

•There are individual differences in the clinical use of olanzapine.•The polymorphism of the GABA-T gene has an impact on the metabolism of 5-hydroxytryptamine.•The polymorphism of the GABA-T gene is related to the pharmacokinetics of olanzapine.•Lysophosphatidylethanolamine (0:0/18:3), lysophosphat...

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Veröffentlicht in:European journal of pharmaceutical sciences 2022-10, Vol.177, p.106277-106277, Article 106277
Hauptverfasser: Cong, Ling, Wan, Zirui, Li, Pengfei, Liu, Dan, He, Jiuming, An, Zhuoling, Liu, Lihong
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Sprache:eng
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Zusammenfassung:•There are individual differences in the clinical use of olanzapine.•The polymorphism of the GABA-T gene has an impact on the metabolism of 5-hydroxytryptamine.•The polymorphism of the GABA-T gene is related to the pharmacokinetics of olanzapine.•Lysophosphatidylethanolamine (0:0/18:3), lysophosphatidylethanolamine (0:0/22:5), and octadecatrienoic acid can distinguish subjects with high and low olanzapine drug oral clearance rate.•The study provides an important basis for individualized medication of olanzapine. Clinical use of the a olanzapine has significantly different individual-to-individual outcomes. Accordingly, this study aimed to develop a means of predicting response to olanzapine using a combined approach based on pharmacokinetics, pharmacometabonomics, and genetic polymorphism. The olanzapine pharmacokinetics of 19 healthy volunteers treated with orally disintegrating tablets were determined using high-performance liquid chromatography–tandem mass spectrometry. Metabolic profiling and phenotyping were performed on the blood samples that remained after pharmacokinetic analysis using ultrahigh-performance liquid chromatography coupled with high-resolution mass spectrometry. Uridine diphosphate-glucuronosyltransferase (UGT), tyrosine hydroxylase (TH), γ-aminobutyric acid transaminase (GABA-T), and succinic semialdehyde dehydrogenase (SSADH) were identified as key genes. The single nucleotide polymorphism genotypes most related to drug metabolism were investigated by polymerase chain reaction and Sanger sequencing. Forty-one metabolites (p < 0.05) are increased or decreased after treatment with olanzapine. Tryptophan metabolism, norepinephrine metabolism, and γ-aminobutyric acid metabolism were identified as being related to the effects of olanzapine. Subjects carrying rs1641031 AC and CC exhibited a 59.2% increase in the mean peak concentration (Cmax) value and a 25.33% decrease in the mean oral clearance rate (CL/F) value, compared to that in subjects with the GABA-T rs1641031 AA genotype (p < 0.05). Moreover, polymorphism of the GABA-T gene has an impact on the metabolism of 5-hydroxytryptamine. Lysophosphatidylethanolamine (0:0/18:3), lysophosphatidylethanolamine (0:0/22:5), and octadecatrienoic acid distinguish subjects with high and low olanzapine drug oral clearance and are thus identified as biomarkers for predicting its efficacy. [Display omitted]
ISSN:0928-0987
1879-0720
DOI:10.1016/j.ejps.2022.106277