The Choice of Either Quetiapine or Aripiprazole as Augmentation Treatment in a European Naturalistic Sample of Patients With Major Depressive Disorder.


Journal

The international journal of neuropsychopharmacology
ISSN: 1469-5111
Titre abrégé: Int J Neuropsychopharmacol
Pays: England
ID NLM: 9815893

Informations de publication

Date de publication:
11 02 2022
Historique:
received: 11 07 2021
revised: 30 08 2021
accepted: 11 11 2021
pubmed: 13 10 2021
medline: 12 3 2022
entrez: 12 10 2021
Statut: ppublish

Résumé

Augmentation with second-generation antipsychotics (SGAs) represents an evidence-based psychopharmacotherapeutic strategy recommended in case of insufficient response to the first-line antidepressant (AD) treatment in major depressive disorder (MDD). Comparative evidence regarding efficacy and prescription preferences of the individual SGAs is scarce. In the scope of this European, multi-site, naturalistic cross-sectional investigation with retrospective assessment of treatment outcome, we compared sociodemographic and clinical characteristics of 187 MDD patients receiving either quetiapine (n = 150) or aripiprazole (n = 37) as augmentation of their first-line AD psychopharmacotherapy. Comorbid posttraumatic stress disorder and diabetes were significantly associated with aripiprazole augmentation in our primary and post-hoc binary logistic regression analyses. Furthermore, we identified an association between aripiprazole co-administration and the presence of additional psychotic features, higher rates of AD combination treatment, and a longer duration of psychiatric hospitalizations during the lifetime, which, however, lost significance after correcting for multiple comparisons. Regarding treatment outcome, we found a trend of higher response rates and greater reductions in severity of depressive symptoms in MDD patients dispensed quetiapine. Factors associated with a more chronic and severe profile of MDD seem to encourage clinicians to choose aripiprazole over quetiapine, that was, however, administered in the majority of our MDD patients, which might reflect the current approval situation allowing to prescribe exclusively quetiapine as on-label augmentation in MDD in Europe. Given the retrospective assessment of treatment response, the markedly smaller proportion of patients receiving aripiprazole augmentation generally showing an unfavorable disease profile, and the partially heterogeneous statistical robustness of our findings, further studies are required to elaborate on our observation and to generate unambiguous recommendations regarding the choice of first-line SGA augmentation in MDD.

Sections du résumé

BACKGROUND
Augmentation with second-generation antipsychotics (SGAs) represents an evidence-based psychopharmacotherapeutic strategy recommended in case of insufficient response to the first-line antidepressant (AD) treatment in major depressive disorder (MDD). Comparative evidence regarding efficacy and prescription preferences of the individual SGAs is scarce.
METHODS
In the scope of this European, multi-site, naturalistic cross-sectional investigation with retrospective assessment of treatment outcome, we compared sociodemographic and clinical characteristics of 187 MDD patients receiving either quetiapine (n = 150) or aripiprazole (n = 37) as augmentation of their first-line AD psychopharmacotherapy.
RESULTS
Comorbid posttraumatic stress disorder and diabetes were significantly associated with aripiprazole augmentation in our primary and post-hoc binary logistic regression analyses. Furthermore, we identified an association between aripiprazole co-administration and the presence of additional psychotic features, higher rates of AD combination treatment, and a longer duration of psychiatric hospitalizations during the lifetime, which, however, lost significance after correcting for multiple comparisons. Regarding treatment outcome, we found a trend of higher response rates and greater reductions in severity of depressive symptoms in MDD patients dispensed quetiapine.
CONCLUSIONS
Factors associated with a more chronic and severe profile of MDD seem to encourage clinicians to choose aripiprazole over quetiapine, that was, however, administered in the majority of our MDD patients, which might reflect the current approval situation allowing to prescribe exclusively quetiapine as on-label augmentation in MDD in Europe. Given the retrospective assessment of treatment response, the markedly smaller proportion of patients receiving aripiprazole augmentation generally showing an unfavorable disease profile, and the partially heterogeneous statistical robustness of our findings, further studies are required to elaborate on our observation and to generate unambiguous recommendations regarding the choice of first-line SGA augmentation in MDD.

Identifiants

pubmed: 34637516
pii: 6391496
doi: 10.1093/ijnp/pyab066
pmc: PMC8832223
doi:

Substances chimiques

Antidepressive Agents 0
Antipsychotic Agents 0
Quetiapine Fumarate 2S3PL1B6UJ
Aripiprazole 82VFR53I78

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

118-127

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of CINP.

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Auteurs

Lucie Bartova (L)

Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna,Austria.
Department of Biomedical and NeuroMotor Sciences, University of Bologna, Bologna,Italy.

Gernot Fugger (G)

Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna,Austria.
Department of Biomedical and NeuroMotor Sciences, University of Bologna, Bologna,Italy.

Markus Dold (M)

Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna,Austria.

Alexander Kautzky (A)

Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna,Austria.

Marleen Margret Mignon Swoboda (MMM)

Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna,Austria.

Dan Rujescu (D)

Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna,Austria.

Joseph Zohar (J)

Psychiatric Division, Chaim Sheba Medical Center , Tel Hashomer, Israel.

Daniel Souery (D)

School of Medicine, Free University of Brussels, Brussels,Belgium.
Psy Pluriel - European Centre of Psychological Medicine, Brussels,Belgium.

Julien Mendlewicz (J)

School of Medicine, Free University of Brussels, Brussels,Belgium.

Stuart Montgomery (S)

Imperial College School of Medicine, University of London, London,United Kingdom.

Chiara Fabbri (C)

Department of Biomedical and NeuroMotor Sciences, University of Bologna, Bologna,Italy.
Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London,United Kingdom.

Alessandro Serretti (A)

Department of Biomedical and NeuroMotor Sciences, University of Bologna, Bologna,Italy.

Siegfried Kasper (S)

Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna,Austria.
Center for Brain Research, Medical University of Vienna, Vienna,Austria.

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