Hostname: page-component-78c5997874-8bhkd Total loading time: 0 Render date: 2024-11-18T04:25:59.416Z Has data issue: false hasContentIssue false

Self-reported Rumination as Trait Marker for Depression: Evidence from Functional Neuroimaging [P02-20]

Published online by Cambridge University Press:  16 April 2020

D. Arnone
Affiliation:
Neuroscience & Psychiatry Unit, University of Manchester, Manchester, UK
E. Pegg
Affiliation:
Neuroscience & Psychiatry Unit, University of Manchester, Manchester, UK
S. Mckie
Affiliation:
Neuroscience & Psychiatry Unit, University of Manchester, Manchester, UK
D. Downey
Affiliation:
Neuroscience & Psychiatry Unit, University of Manchester, Manchester, UK
R. Elliott
Affiliation:
Neuroscience & Psychiatry Unit, University of Manchester, Manchester, UK
J.F.K. Deakin
Affiliation:
Neuroscience & Psychiatry Unit, University of Manchester, Manchester, UK
I.M. Anderson
Affiliation:
Neuroscience & Psychiatry Unit, University of Manchester, Manchester, UK

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Background:

Research using fMRI indicates that sustained limbic activity is linked to processing negative words and self-reported rumination in currently depressed individuals. It is unknown whether this is also present in remitted depressed individuals. We tested the hypothesis that a tendency to ruminate constitutes a trait for depression by using a standard covert fMRI emotional task face in previously and never depressed volunteers and postulated that high rumination scores would correlate with activity in brain areas previously associated with depression.

Methods:

37 controls (25 female) and 30 remitted depressed (RD, 22 female) were enrolled. Volunteers completed the Ruminative Responses Scale (RRS) and underwent fMRI scanning using a standard covert fMRI emotional task faces. Significance level was set at p < 0.05 (FWE).

Results:

With RRS score controlled for RD showed reduced subcortical and limbic activity to sad and fearful faces compared to controls. Correlations between RRS scores and neural activity in all participants and control participants alone were very limited. However, in RD, RRS score was negatively correlated with neural response to happy faces and positively correlated with neural response to sad and fearful faces, in cortical and limbic regions associated with depression (hippocampus, thalamus, caudate, insula and cingulate gyrus).

Conclusion:

The results suggest that reduced limbic activity is associated with remission, possibly as a maintenance mechanism. However, within the remitted group the more ruminative participants show greater response in these areas to negative stimuli, and less to positive stimuli. This could be a neurobiological marker for risk of relapse.

Type
P02-20
Copyright
Copyright © European Psychiatric Association 2009
Submit a response

Comments

No Comments have been published for this article.