Personality as a basis for antidepressant selection for patients with depression: A two-point outcome study at 4 and 8 weeks.


Journal

Journal of affective disorders
ISSN: 1573-2517
Titre abrégé: J Affect Disord
Pays: Netherlands
ID NLM: 7906073

Informations de publication

Date de publication:
01 10 2022
Historique:
received: 09 01 2022
revised: 29 06 2022
accepted: 01 07 2022
pubmed: 8 7 2022
medline: 11 8 2022
entrez: 7 7 2022
Statut: ppublish

Résumé

The treatment course for depression is multifactorial, and the gold standard method for antidepressant selection remains unclear. Therefore, we focused on patients' personality as a possible indicator of the treatment response to mirtazapine and selective serotonin reuptake inhibitors (SSRIs) and whether it can contribute to antidepressant selection. One hundred one patients with major depressive disorder were randomized at baseline to receive either mirtazapine or SSRI treatment. Their personality was measured using the NEO Five-Factor Inventory at baseline, and depressive symptoms were evaluated using the Hamilton Rating Scale for Depression at baseline and 4 and 8 weeks. Stepwise multivariable logistic regression and receiver operating characteristic analyses were performed to determine the association of personality traits with remission and better antidepressant selection. Neuroticism had the substantial influence on remission at 4 and 8 weeks among the entire sample. The cutoff T-score of neuroticism for predicting remission at 4 weeks was 62.5. The patients with moderate neuroticism (scores below the cutoff) were more likely to experience remission after 4-week mirtazapine treatment (remission rate: 73.7 %) than after SSRI treatment (40.0 %); those with high neuroticism (scores above the cutoff) were more likely to experience remission after 8-week SSRI treatment (74.1 %) than after mirtazapine treatment (35.7 %). The small sample size increased the confidence intervals. The treatment response of the patients with depression differed according to the type of antidepressants and degree of neuroticism. Measuring personality traits at treatment initiation may help in selecting better antidepressants and predicting the time to remission.

Sections du résumé

BACKGROUND
The treatment course for depression is multifactorial, and the gold standard method for antidepressant selection remains unclear. Therefore, we focused on patients' personality as a possible indicator of the treatment response to mirtazapine and selective serotonin reuptake inhibitors (SSRIs) and whether it can contribute to antidepressant selection.
METHODS
One hundred one patients with major depressive disorder were randomized at baseline to receive either mirtazapine or SSRI treatment. Their personality was measured using the NEO Five-Factor Inventory at baseline, and depressive symptoms were evaluated using the Hamilton Rating Scale for Depression at baseline and 4 and 8 weeks. Stepwise multivariable logistic regression and receiver operating characteristic analyses were performed to determine the association of personality traits with remission and better antidepressant selection.
RESULTS
Neuroticism had the substantial influence on remission at 4 and 8 weeks among the entire sample. The cutoff T-score of neuroticism for predicting remission at 4 weeks was 62.5. The patients with moderate neuroticism (scores below the cutoff) were more likely to experience remission after 4-week mirtazapine treatment (remission rate: 73.7 %) than after SSRI treatment (40.0 %); those with high neuroticism (scores above the cutoff) were more likely to experience remission after 8-week SSRI treatment (74.1 %) than after mirtazapine treatment (35.7 %).
LIMITATIONS
The small sample size increased the confidence intervals.
CONCLUSIONS
The treatment response of the patients with depression differed according to the type of antidepressants and degree of neuroticism. Measuring personality traits at treatment initiation may help in selecting better antidepressants and predicting the time to remission.

Identifiants

pubmed: 35798178
pii: S0165-0327(22)00759-5
doi: 10.1016/j.jad.2022.07.001
pii:
doi:

Substances chimiques

Antidepressive Agents 0
Serotonin Uptake Inhibitors 0
Mirtazapine A051Q2099Q

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

27-33

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Auteurs

Minami Naito (M)

Department of Neuropsychiatry, Kansai Medical University, 10-15 Fumizono-cho Moriguchi-city, Osaka 570-8506, Japan.

Masaki Kato (M)

Department of Neuropsychiatry, Kansai Medical University, 10-15 Fumizono-cho Moriguchi-city, Osaka 570-8506, Japan. Electronic address: katom@takii.kmu.ac.jp.

Yosuke Koshikawa (Y)

Department of Neuropsychiatry, Kansai Medical University, 10-15 Fumizono-cho Moriguchi-city, Osaka 570-8506, Japan.

Hiroki Bandou (H)

Seishokai Sephiroth Hospital, Shiga, Japan.

Shiho Sakai (S)

Kamehiro Memorial Medical Society, Kansai Kinen Hospital, Hirakata, Osaka, Japan.

Yoshiteru Takekita (Y)

Department of Neuropsychiatry, Kansai Medical University, 10-15 Fumizono-cho Moriguchi-city, Osaka 570-8506, Japan.

Keiichiro Nishida (K)

Department of Neuropsychiatry, Kansai Medical University, 10-15 Fumizono-cho Moriguchi-city, Osaka 570-8506, Japan.

Toshihiko Kinoshita (T)

Department of Neuropsychiatry, Kansai Medical University, 10-15 Fumizono-cho Moriguchi-city, Osaka 570-8506, Japan.

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