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Use of central nervous system drugs in combination with selective serotonin reuptake inhibitor treatment: A Bayesian screening study for risk of suicidal behavior

BACKGROUND: Using other central nervous system (CNS) medications in combination with selective serotonin reuptake inhibitor (SSRI) treatment is common. Despite this, there is limited evidence on the impact on suicidal behavior of combining specific medications. We aim to provide evidence on signals...

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Autores principales: Lagerberg, Tyra, Sjölander, Arvid, Gibbons, Robert D., Quinn, Patrick D., D’Onofrio, Brian M., Hellner, Clara, Lichtenstein, Paul, Fazel, Seena, Chang, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682954/
https://www.ncbi.nlm.nih.gov/pubmed/36440412
http://dx.doi.org/10.3389/fpsyt.2022.1012650
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author Lagerberg, Tyra
Sjölander, Arvid
Gibbons, Robert D.
Quinn, Patrick D.
D’Onofrio, Brian M.
Hellner, Clara
Lichtenstein, Paul
Fazel, Seena
Chang, Zheng
author_facet Lagerberg, Tyra
Sjölander, Arvid
Gibbons, Robert D.
Quinn, Patrick D.
D’Onofrio, Brian M.
Hellner, Clara
Lichtenstein, Paul
Fazel, Seena
Chang, Zheng
author_sort Lagerberg, Tyra
collection PubMed
description BACKGROUND: Using other central nervous system (CNS) medications in combination with selective serotonin reuptake inhibitor (SSRI) treatment is common. Despite this, there is limited evidence on the impact on suicidal behavior of combining specific medications. We aim to provide evidence on signals for suicidal behavior risk when initiating CNS drugs during and outside of SSRI treatment. MATERIALS AND METHODS: Using a linkage of Swedish national registers, we identified a national cohort of SSRI users aged 6–59 years residing in Sweden 2006–2013. We used a two-stage Bayesian Poisson model to estimate the incidence rate ratio (IRR) of suicidal behavior in periods up to 90 days before and after a CNS drug initiation during SSRI treatment, while accounting for multiple testing. For comparison, and to assess whether there were interactions between SSRIs and other CNS drugs, we also estimated the IRR of initiating the CNS drug without SSRI treatment. RESULTS: We identified 53 common CNS drugs initiated during SSRI treatment, dispensed to 262,721 individuals. We found 20 CNS drugs with statistically significant IRRs. Of these, two showed a greater risk of suicidal behavior after versus before initiating the CNS drug (alprazolam, IRR = 1.39; flunitrazepam, IRR = 1.83). We found several novel signals of drugs that were statistically significantly associated with a reduction in the suicidal behavior risk. We did not find evidence of harmful interactions between SSRIs and the selected CNS drugs. CONCLUSION: Several of the detected signals for reduced risk correspond to drugs where there is previous evidence of benefit for antidepressant augmentation (e.g., olanzapine, quetiapine, lithium, buspirone, and mirtazapine). Novel signals of reduced suicidal behavior risk, including for lamotrigine, valproic acid, risperidone, and melatonin, warrant further investigation.
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spelling pubmed-96829542022-11-24 Use of central nervous system drugs in combination with selective serotonin reuptake inhibitor treatment: A Bayesian screening study for risk of suicidal behavior Lagerberg, Tyra Sjölander, Arvid Gibbons, Robert D. Quinn, Patrick D. D’Onofrio, Brian M. Hellner, Clara Lichtenstein, Paul Fazel, Seena Chang, Zheng Front Psychiatry Psychiatry BACKGROUND: Using other central nervous system (CNS) medications in combination with selective serotonin reuptake inhibitor (SSRI) treatment is common. Despite this, there is limited evidence on the impact on suicidal behavior of combining specific medications. We aim to provide evidence on signals for suicidal behavior risk when initiating CNS drugs during and outside of SSRI treatment. MATERIALS AND METHODS: Using a linkage of Swedish national registers, we identified a national cohort of SSRI users aged 6–59 years residing in Sweden 2006–2013. We used a two-stage Bayesian Poisson model to estimate the incidence rate ratio (IRR) of suicidal behavior in periods up to 90 days before and after a CNS drug initiation during SSRI treatment, while accounting for multiple testing. For comparison, and to assess whether there were interactions between SSRIs and other CNS drugs, we also estimated the IRR of initiating the CNS drug without SSRI treatment. RESULTS: We identified 53 common CNS drugs initiated during SSRI treatment, dispensed to 262,721 individuals. We found 20 CNS drugs with statistically significant IRRs. Of these, two showed a greater risk of suicidal behavior after versus before initiating the CNS drug (alprazolam, IRR = 1.39; flunitrazepam, IRR = 1.83). We found several novel signals of drugs that were statistically significantly associated with a reduction in the suicidal behavior risk. We did not find evidence of harmful interactions between SSRIs and the selected CNS drugs. CONCLUSION: Several of the detected signals for reduced risk correspond to drugs where there is previous evidence of benefit for antidepressant augmentation (e.g., olanzapine, quetiapine, lithium, buspirone, and mirtazapine). Novel signals of reduced suicidal behavior risk, including for lamotrigine, valproic acid, risperidone, and melatonin, warrant further investigation. Frontiers Media S.A. 2022-11-09 /pmc/articles/PMC9682954/ /pubmed/36440412 http://dx.doi.org/10.3389/fpsyt.2022.1012650 Text en Copyright © 2022 Lagerberg, Sjölander, Gibbons, Quinn, D’Onofrio, Hellner, Lichtenstein, Fazel and Chang. https://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
Lagerberg, Tyra
Sjölander, Arvid
Gibbons, Robert D.
Quinn, Patrick D.
D’Onofrio, Brian M.
Hellner, Clara
Lichtenstein, Paul
Fazel, Seena
Chang, Zheng
Use of central nervous system drugs in combination with selective serotonin reuptake inhibitor treatment: A Bayesian screening study for risk of suicidal behavior
title Use of central nervous system drugs in combination with selective serotonin reuptake inhibitor treatment: A Bayesian screening study for risk of suicidal behavior
title_full Use of central nervous system drugs in combination with selective serotonin reuptake inhibitor treatment: A Bayesian screening study for risk of suicidal behavior
title_fullStr Use of central nervous system drugs in combination with selective serotonin reuptake inhibitor treatment: A Bayesian screening study for risk of suicidal behavior
title_full_unstemmed Use of central nervous system drugs in combination with selective serotonin reuptake inhibitor treatment: A Bayesian screening study for risk of suicidal behavior
title_short Use of central nervous system drugs in combination with selective serotonin reuptake inhibitor treatment: A Bayesian screening study for risk of suicidal behavior
title_sort use of central nervous system drugs in combination with selective serotonin reuptake inhibitor treatment: a bayesian screening study for risk of suicidal behavior
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682954/
https://www.ncbi.nlm.nih.gov/pubmed/36440412
http://dx.doi.org/10.3389/fpsyt.2022.1012650
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