Accuracy in recognising happy facial expressions is associated with antidepressant response to a NOP receptor antagonist but not placebo treatment.
Adult
Biomarkers
Depressive Disorder, Major
/ drug therapy
Double-Blind Method
Emotions
/ drug effects
Facial Expression
Facial Recognition
/ drug effects
Female
Humans
Male
Middle Aged
Narcotic Antagonists
/ administration & dosage
Outcome Assessment, Health Care
Pyrans
/ administration & dosage
Receptors, Opioid
/ drug effects
Spiro Compounds
/ administration & dosage
Nociceptin Receptor
Depression
FERT
LY2940094
antidepressant
biomarker
emotional recognition
Journal
Journal of psychopharmacology (Oxford, England)
ISSN: 1461-7285
Titre abrégé: J Psychopharmacol
Pays: United States
ID NLM: 8907828
Informations de publication
Date de publication:
12 2021
12 2021
Historique:
pubmed:
6
10
2021
medline:
22
2
2022
entrez:
5
10
2021
Statut:
ppublish
Résumé
Clinical trials with putative antidepressants can be difficult to execute as it can take up to 8 weeks before differences emerge between drug and placebo, and long expensive trials often fail. Implementation of early response biomarkers could aid this process significantly with potential to identify new treatments. In a secondary analysis, we examined the association of early effects on emotional processing with later clinical outcome following treatment with the novel NOP antagonist LY2940094 versus placebo. We hypothesised that early induction of positive bias would be associated with reduced severity of depression after 8 weeks of treatment. This was a multicentre, randomised, double-blind, parallel-group, fixed-dose, placebo-controlled, 8 week study to assess sensitivity of the facial emotional recognition task (FERT) to early changes in emotional bias induced by LY2940094. Patients who met diagnostic criteria for major depression were randomised to receive LY2940094 ( Patients identified happy faces with higher accuracy (Wald χ These data suggest that emotional processing biomarkers may be sensitive to early effects of antidepressant treatment indicative of later clinical response. Further studies in this area may be useful in developing new treatments and clinical trial designs for predicting antidepressant response.
Sections du résumé
BACKGROUND
Clinical trials with putative antidepressants can be difficult to execute as it can take up to 8 weeks before differences emerge between drug and placebo, and long expensive trials often fail. Implementation of early response biomarkers could aid this process significantly with potential to identify new treatments.
AIMS
In a secondary analysis, we examined the association of early effects on emotional processing with later clinical outcome following treatment with the novel NOP antagonist LY2940094 versus placebo. We hypothesised that early induction of positive bias would be associated with reduced severity of depression after 8 weeks of treatment.
METHODS
This was a multicentre, randomised, double-blind, parallel-group, fixed-dose, placebo-controlled, 8 week study to assess sensitivity of the facial emotional recognition task (FERT) to early changes in emotional bias induced by LY2940094. Patients who met diagnostic criteria for major depression were randomised to receive LY2940094 (
RESULTS
Patients identified happy faces with higher accuracy (Wald χ
CONCLUSION
These data suggest that emotional processing biomarkers may be sensitive to early effects of antidepressant treatment indicative of later clinical response. Further studies in this area may be useful in developing new treatments and clinical trial designs for predicting antidepressant response.
Identifiants
pubmed: 34608842
doi: 10.1177/02698811211044684
doi:
Substances chimiques
Biomarkers
0
LY2940094
0
Narcotic Antagonists
0
Pyrans
0
Receptors, Opioid
0
Spiro Compounds
0
Nociceptin Receptor
0
OPRL1 protein, human
0
Types de publication
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM