Emotional Blunting in Depression in the PREDDICT Clinical Trial: Inflammation-Stratified Augmentation of Vortioxetine With Celecoxib

Author:

Sampson Emma1ORCID,Kavakbasi Erhan2ORCID,Mills Natalie T1ORCID,Hori Hikaru3ORCID,Schubert K Oliver145ORCID,Fourrier Célia1ORCID,Baune Bernhard T1267ORCID

Affiliation:

1. Discipline of Psychiatry, Adelaide Medical School, University of Adelaide , Adelaide , Australia

2. Department of Psychiatry, University Hospital Münster, University of Münster , Münster , Germany

3. Department of Psychiatry, Faculty of Medicine, Fukuoka University , Fukuoka City , Japan

4. Northern Adelaide Mental Health Service , Salisbury , Australia

5. Headspace Adelaide Early Psychosis, Sonder , Adelaide , Australia

6. Department of Psychiatry, Melbourne Medical School, The University of Melbourne , Melbourne , Australia

7. The Florey Institute of Neuroscience and Mental Health, The University of Melbourne , Parkville, VIC , Australia

Abstract

Abstract Background Emotional symptoms are recognized as a key feature in individuals with major depressive disorder. Previously, emotional blunting has been described both as a side effect of antidepressant treatment and as a symptom of depression. Little is known about the change of emotional blunting during antidepressant treatment. Methods The PREDDICT trial is a randomized, placebo-controlled, 6-week trial on the augmentation of vortioxetine with the anti-inflammatory agent celecoxib or placebo. Presently we report on exploratory secondary outcomes of changes in emotional blunting in depression assessed with the Oxford Depression Questionnaire (ODQ) total score and subscores from baseline to 8-week, 3-month, and 6-month follow-up assessments. Results In the whole group, there was a significant improvement in the ODQ total score and all subscores after 8 weeks. After stratification of participants into the treatment groups, the ODQ total score as well as subscores related to emotional blunting as a symptom of depression (reduction in positive emotions, not caring) improved between baseline and all follow-up time points in both treatment groups. Changes in subscores considered as a side effect of antidepressants (general reduction in emotions, emotional detachment) were inconclusive in both treatment groups. Overall, the placebo-augmented group showed slightly better results in changes of emotional blunting scores than the celecoxib group as did those with elevated inflammation at screening, regardless of treatment group. Conclusions This analysis suggests favorable effects of vortioxetine on emotional blunting in both short- and long-term course. The beneficial impact of vortioxetine on emotional blunting was weaker in celecoxib-augmented patients compared with placebo, possibly due to pharmacokinetic interactions. Clinical Trials Registration: Australian New Zealand Clinical Trials Registry (ANZCTR), ACTRN12617000527369p. Registered on 11 April 2017, http://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?ACTRN=12617000527369p.

Publisher

Oxford University Press (OUP)

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