<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>19(12)</volume><submitter>Toth K</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The shortcomings of clonazepam therapy include tolerance, withdrawal symptoms, and adverse effects such as drowsiness, dizziness, and confusion leading to increased risk of falls. Inter-individual variability in the incidence of adverse events in patients partly originates from the differences in clonazepam metabolism due to genetic and nongenetic factors.&lt;h4>Methods&lt;/h4>Since the prominent role in clonazepam nitro-reduction and acetylation of 7-amino-clonazepam is assigned to CYP3A and N-acetyl transferase 2 enzymes, respectively, the association between the patients' CYP3A status (CYP3A5 genotype, CYP3A4 expression) or N-acetyl transferase 2 acetylator phenotype and clonazepam metabolism (plasma concentrations of clonazepam and 7-amino-clonazepam) was evaluated in 98 psychiatric patients suffering from schizophrenia or bipolar disorders.&lt;h4>Results&lt;/h4>The patients' CYP3A4 expression was found to be the major determinant of clonazepam plasma concentrations normalized by the dose and bodyweight (1263.5±482.9 and 558.5±202.4ng/mL per mg/kg bodyweight in low and normal expressers, respectively, P&lt;.0001). Consequently, the dose requirement for the therapeutic concentration of clonazepam was substantially lower in low-CYP3A4 expresser patients than in normal expressers (0.029±0.011 vs 0.058±0.024mg/kg bodyweight, P&lt;.0001). Furthermore, significantly higher (about 2-fold) plasma concentration ratio of 7-amino-clonazepam and clonazepam was observed in the patients displaying normal CYP3A4 expression and slower N-acetylation than all the others.&lt;h4>Conclusion&lt;/h4>Prospective assaying of CYP3A4 expression and N-acetyl transferase 2 acetylator phenotype can better identify the patients with higher risk of adverse reactions and can facilitate the improvement of personalized clonazepam therapy and withdrawal regimen.</pubmed_abstract><journal>The international journal of neuropsychopharmacology</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5203763</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Optimization of Clonazepam Therapy Adjusted to Patient's CYP3A Status and NAT2 Genotype.</pubmed_title><pmcid>PMC5203763</pmcid><pubmed_authors>Sirok D</pubmed_authors><pubmed_authors>Monostory K</pubmed_authors><pubmed_authors>Toth K</pubmed_authors><pubmed_authors>Csukly G</pubmed_authors><pubmed_authors>Belic A</pubmed_authors><pubmed_authors>Kiss A</pubmed_authors><pubmed_authors>Hafra E</pubmed_authors><pubmed_authors>Deri M</pubmed_authors><pubmed_authors>Menus A</pubmed_authors><pubmed_authors>Bitter I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Optimization of Clonazepam Therapy Adjusted to Patient's CYP3A Status and NAT2 Genotype.</name><description>&lt;h4>Background&lt;/h4>The shortcomings of clonazepam therapy include tolerance, withdrawal symptoms, and adverse effects such as drowsiness, dizziness, and confusion leading to increased risk of falls. Inter-individual variability in the incidence of adverse events in patients partly originates from the differences in clonazepam metabolism due to genetic and nongenetic factors.&lt;h4>Methods&lt;/h4>Since the prominent role in clonazepam nitro-reduction and acetylation of 7-amino-clonazepam is assigned to CYP3A and N-acetyl transferase 2 enzymes, respectively, the association between the patients' CYP3A status (CYP3A5 genotype, CYP3A4 expression) or N-acetyl transferase 2 acetylator phenotype and clonazepam metabolism (plasma concentrations of clonazepam and 7-amino-clonazepam) was evaluated in 98 psychiatric patients suffering from schizophrenia or bipolar disorders.&lt;h4>Results&lt;/h4>The patients' CYP3A4 expression was found to be the major determinant of clonazepam plasma concentrations normalized by the dose and bodyweight (1263.5±482.9 and 558.5±202.4ng/mL per mg/kg bodyweight in low and normal expressers, respectively, P&lt;.0001). Consequently, the dose requirement for the therapeutic concentration of clonazepam was substantially lower in low-CYP3A4 expresser patients than in normal expressers (0.029±0.011 vs 0.058±0.024mg/kg bodyweight, P&lt;.0001). Furthermore, significantly higher (about 2-fold) plasma concentration ratio of 7-amino-clonazepam and clonazepam was observed in the patients displaying normal CYP3A4 expression and slower N-acetylation than all the others.&lt;h4>Conclusion&lt;/h4>Prospective assaying of CYP3A4 expression and N-acetyl transferase 2 acetylator phenotype can better identify the patients with higher risk of adverse reactions and can facilitate the improvement of personalized clonazepam therapy and withdrawal regimen.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Dec</publication><modification>2021-03-18T09:14:55Z</modification><creation>2019-03-27T02:32:53Z</creation></dates><accession>S-EPMC5203763</accession><cross_references><pubmed>27639091</pubmed><doi>10.1093/ijnp/pyw083</doi></cross_references></HashMap>