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  4. Antidepressant responses in direct comparisons of melancholic and non-melancholic depression
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Antidepressant responses in direct comparisons of melancholic and non-melancholic depression

Journal
Journal of Psychopharmacology
ISSN
0269-8811
1461-7285
Date Issued
2020
Author(s)
Juan Undurraga  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Gustavo H Vázquez
Leonardo Tondo
Ross J Baldessarini
Type
Resource Types::text::journal::journal article
Scopus ID
2-s2.0-85090464477
WoS ID
WOS:000567996500001
DOI
10.1177/0269881120953983
URL
https://investigadores.udd.cl/handle/123456789/3675
URL Institutional Repository
http://hdl.handle.net/11447/4247
Abstract
<jats:sec><jats:title>Background:</jats:title><jats:p> Efforts to develop less heterogeneous, more clinically useful diagnostic categories for depressive disorders include renewed interest in the concept of melancholia (Mel). However, clinical or biological differentiation of Mel from other (nonMel) episodes of depression has been questioned, and it remains unclear whether pharmacological responses proposed to be characteristic of Mel are supported by available research. </jats:p></jats:sec><jats:sec><jats:title>Methods:</jats:title><jats:p> We carried out a systematic review seeking treatment trials reports comparing Mel and nonMel depressed subjects for meta-analyses of their differences in responses (a) to antidepressants overall, (b) to tricyclic (TCAs) or serotonin-enhancing agents (serotonin reuptake inhibitors/serotonin–norepinephrine reuptake inhibitors) and (c) with placebo treatment. </jats:p></jats:sec><jats:sec><jats:title>Results:</jats:title><jats:p> We identified 25 trials in 16 reports comparing 2597 Mel with 5016 nonMel subjects. Overall, responses to antidepressant treatment did not differ between Mel (39.4%) and nonMel (42.2%) subjects. However, all subjects responded better to TCAs (50.6%) than SRIs (30.0%; p<0.0001). Mel subjects also responded less well with placebo, but also were significantly more severely depressed at intake. </jats:p></jats:sec><jats:sec><jats:title>Conclusions:</jats:title><jats:p> Antidepressant responses were similar in Mel and nonMel depressed patients. Mel subjects responded 25% less with placebo but were more severely depressed initially, and there was preferential response to TCAs in both Mel and nonMel subjects. The findings provide little support for proposed differences in responses to particular treatments among Mel versus nonMel depressed patients, and underscore the need to match for illness severity in making such comparisons. </jats:p></jats:sec>
Project(s)
Development of novel imaging techniques to study the brain in severe mental health disorders  
Subjects
antidepressants

; 

melancholia

; 

serotonin-reuptake inhibitors

; 

tricyclic antidepressants

; 

antidepressive agents, tricyclic

; 

depressive disorder

; 

humans

; 

outcome assessment, health care

; 

serotonin and noradrenaline reuptake inhibitors

; 

serotonin uptake inhibitors

; 

citalopram

; 

clomipramine

; 

desipramine

; 

duloxetine

; 

escitalopram

; 

fluoxetine

; 

imipramine

; 

lamotrigine

; 

mirtazapine

; 

moclobemide

; 

nefazodone

; 

nortriptyline

; 

paroxetine

; 

serotonin noradrenalin reuptake inhibitor

; 

serotonin uptake inhibitor

; 

sertraline

; 

tricyclic antidepressant agent

; 

venlafaxine

; 

serotonin noradrenalin reuptake inhibitor

; 

serotonin uptake inhibitor

; 

tricyclic antidepressant agent

; 

antidepressant activity

; 

article

; 

clinical feature

; 

depression

; 

disease severity

; 

drug efficacy

; 

drug safety

; 

hamilton depression rating scale

; 

human

; 

melancholia

; 

montgomery asberg depression rating scale

; 

outcome assessment

; 

priority journal

; 

systematic review

; 

comparative study

; 

depression
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