Loading…

An ERP study of multidimensional source retrieval in depression

[Display omitted] •Depressed adults benefit from deep encoding followed by deep retrieval.•The influence of depression on source retrieval is reflected in left parietal ERPs.•Chronic sleep disruption may contribute to poor episodic memory in depression. We collected event-related potentials (ERPs) f...

Full description

Saved in:
Bibliographic Details
Published in:Biological psychology 2018-02, Vol.132, p.176-191
Main Authors: Barrick, Elyssa M., Dillon, Daniel G.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:[Display omitted] •Depressed adults benefit from deep encoding followed by deep retrieval.•The influence of depression on source retrieval is reflected in left parietal ERPs.•Chronic sleep disruption may contribute to poor episodic memory in depression. We collected event-related potentials (ERPs) from 24 unmedicated adults with Major Depressive Disorder (MDD) and 24 controls during source memory retrieval. Words were encoded on the left or right during animacy and mobility judgments. Mobility judgments were slower than animacy judgments, suggesting deeper encoding. Participants then recalled the encoding judgment (Question cue) and position (Side cue) for each word. Depressed adults, but not controls, showed better accuracy for words from the mobility task presented under the Question vs. Side Cue. Furthermore, depressed adults showed larger left parietal ERPs to words from the mobility task presented under the Question vs. the Side Cue from 400 to 800 ms and 800–1400 ms. This ERP effect was negatively correlated with sleep quality. Thus, deep encoding followed by retrieval of the encoding judgment supported memory in MDD and augmented left parietal ERPs that have been linked to recollection and that appear sensitive to sleep disturbance.
ISSN:0301-0511
1873-6246
DOI:10.1016/j.biopsycho.2018.01.001