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No Effect of Dose Adjustment to the CYP2D6 Genotype in Patients With Severe Mental Illness
Background: The CYP2D6 enzyme is involved in the metabolism of numerous psychopharmacological drugs. Guidelines recommend how to adjust the dose of medication based on the CYP2D6 genotype. Aims: To evaluate the effect of dose adjustment to the CYP2D6 genotype and phenotype, in patients with severe m...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090167/ https://www.ncbi.nlm.nih.gov/pubmed/30131727 http://dx.doi.org/10.3389/fpsyt.2018.00349 |
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author | Koopmans, Anne B. Vinkers, David J. Poulina, Igmar T. Gelan, Petra J. A. van Schaik, Ron H. N. Hoek, Hans W. van Harten, Peter N. |
author_facet | Koopmans, Anne B. Vinkers, David J. Poulina, Igmar T. Gelan, Petra J. A. van Schaik, Ron H. N. Hoek, Hans W. van Harten, Peter N. |
author_sort | Koopmans, Anne B. |
collection | PubMed |
description | Background: The CYP2D6 enzyme is involved in the metabolism of numerous psychopharmacological drugs. Guidelines recommend how to adjust the dose of medication based on the CYP2D6 genotype. Aims: To evaluate the effect of dose adjustment to the CYP2D6 genotype and phenotype, in patients with severe mental illness (SMI) already receiving psychopharmacological treatment. Methods: A total of 269 psychiatric patients (on the island Curaçao) receiving antipsychotic treatment were genotyped for CYP2D6. Of these, 45 patients were included for dose adjustment according to the clinical guideline of the Royal Dutch Association for the Advancement of Pharmacy, i.e., 17 CYP2D6 poor metabolizers, 26 intermediate metabolizers, and 2 ultrarapid metabolizers. These 45 patients were matched for age, gender, and type of medication with a control group of 41 patients who were CYP2D6 extensive metabolizers (i.e., with a normal CYP2D6 function). At baseline and at 4 months after dose adjustment, subjective experience, psychopathology, extrapyramidal side-effects, quality of life, and global functioning were assessed in these two groups. Results: At baseline, there were no differences between the groups regarding the prescribed dosage of antipsychotics, the number of side-effects, psychiatric symptoms, global functioning, or quality of life. After dose adjustment, no significant improvement in these parameters was reported. Conclusion: In psychiatric patients with SMI already receiving antipsychotic treatment, dose adjustment to the CYP2D6 genotype or phenotype according to the guidelines showed no beneficial effect. This suggests that dose adjustment guidelines are currently not applicable for patients already using antipsychotics. ClinicalTrials.gov: Cost-effectiveness of CYP2D6 and CYP2C19 Genotyping in Psychiatric Patients in Curacao; Identifier: NCT02713672; https://clinicaltrials.gov/ct2/show/NCT02713672?term=CYP2D6&rank=5 |
format | Online Article Text |
id | pubmed-6090167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60901672018-08-21 No Effect of Dose Adjustment to the CYP2D6 Genotype in Patients With Severe Mental Illness Koopmans, Anne B. Vinkers, David J. Poulina, Igmar T. Gelan, Petra J. A. van Schaik, Ron H. N. Hoek, Hans W. van Harten, Peter N. Front Psychiatry Psychiatry Background: The CYP2D6 enzyme is involved in the metabolism of numerous psychopharmacological drugs. Guidelines recommend how to adjust the dose of medication based on the CYP2D6 genotype. Aims: To evaluate the effect of dose adjustment to the CYP2D6 genotype and phenotype, in patients with severe mental illness (SMI) already receiving psychopharmacological treatment. Methods: A total of 269 psychiatric patients (on the island Curaçao) receiving antipsychotic treatment were genotyped for CYP2D6. Of these, 45 patients were included for dose adjustment according to the clinical guideline of the Royal Dutch Association for the Advancement of Pharmacy, i.e., 17 CYP2D6 poor metabolizers, 26 intermediate metabolizers, and 2 ultrarapid metabolizers. These 45 patients were matched for age, gender, and type of medication with a control group of 41 patients who were CYP2D6 extensive metabolizers (i.e., with a normal CYP2D6 function). At baseline and at 4 months after dose adjustment, subjective experience, psychopathology, extrapyramidal side-effects, quality of life, and global functioning were assessed in these two groups. Results: At baseline, there were no differences between the groups regarding the prescribed dosage of antipsychotics, the number of side-effects, psychiatric symptoms, global functioning, or quality of life. After dose adjustment, no significant improvement in these parameters was reported. Conclusion: In psychiatric patients with SMI already receiving antipsychotic treatment, dose adjustment to the CYP2D6 genotype or phenotype according to the guidelines showed no beneficial effect. This suggests that dose adjustment guidelines are currently not applicable for patients already using antipsychotics. ClinicalTrials.gov: Cost-effectiveness of CYP2D6 and CYP2C19 Genotyping in Psychiatric Patients in Curacao; Identifier: NCT02713672; https://clinicaltrials.gov/ct2/show/NCT02713672?term=CYP2D6&rank=5 Frontiers Media S.A. 2018-08-07 /pmc/articles/PMC6090167/ /pubmed/30131727 http://dx.doi.org/10.3389/fpsyt.2018.00349 Text en Copyright © 2018 Koopmans, Vinkers, Poulina, Gelan, van Schaik, Hoek and van Harten. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Psychiatry Koopmans, Anne B. Vinkers, David J. Poulina, Igmar T. Gelan, Petra J. A. van Schaik, Ron H. N. Hoek, Hans W. van Harten, Peter N. No Effect of Dose Adjustment to the CYP2D6 Genotype in Patients With Severe Mental Illness |
title | No Effect of Dose Adjustment to the CYP2D6 Genotype in Patients With Severe Mental Illness |
title_full | No Effect of Dose Adjustment to the CYP2D6 Genotype in Patients With Severe Mental Illness |
title_fullStr | No Effect of Dose Adjustment to the CYP2D6 Genotype in Patients With Severe Mental Illness |
title_full_unstemmed | No Effect of Dose Adjustment to the CYP2D6 Genotype in Patients With Severe Mental Illness |
title_short | No Effect of Dose Adjustment to the CYP2D6 Genotype in Patients With Severe Mental Illness |
title_sort | no effect of dose adjustment to the cyp2d6 genotype in patients with severe mental illness |
topic | Psychiatry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090167/ https://www.ncbi.nlm.nih.gov/pubmed/30131727 http://dx.doi.org/10.3389/fpsyt.2018.00349 |
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