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Electrophysiological evidence of mal-adaptation to error in remitted depression
Lilian Y Li1, James E Glazer1, Fiona Helgren1
1Department of Psychiatry and Behavioral Sciences, Northwestern University, Chicago, IL, USA.
Abstract:
Identifying risk markers for major depressive disorder (MDD) that persist into remission is key to address MDD's high rate of recurrence. Central to MDD recurrence are the disorder's negative information processing biases, such as heightened responses to errors, which may subsequently impair abilities to monitor performance and adjust behaviors based on environmental demands. However, little is known regarding the neurophysiological correlates of post-error adaptation in depression. The current study investigated event-related potentials (ERPs) and behavioral performance following errors from a flanker task in 58 participants with remitted MDD (rMDD) and 118 healthy controls (HC). Specifically, using trial-level data, we tested: (a) the impact of errors on response-locked ERPs of the current and post-error trials (error-related negativity [ERN] and correct response negativity [CRN]) and (b) longer-term adaptation to errors (ERN/CRN) over the course of the task. Compared to HC, rMDD participants showed a larger ERN to the current trial and smaller habituation in ERN over time. On trials immediately following errors, rMDD participants showed slower reaction times that were predicted by the previous-trial ERN amplitude but comparable accuracy to HC, suggesting a deficient ability to disengage from errors and/or a compensatory effort to mitigate accuracy decrements. Critically, this pattern of responding: (a) was concurrently associated with greater levels of anhedonia symptoms, more severe MDD history, and interpersonal impairment (but lower impairment in life activities) and (b) predicted more anhedonia symptoms at one-year follow-up. Collectively, a hyperactive performance monitoring system may be a useful risk marker for future MDD recurrence.
Insights
Individuals with remitted major depressive disorder (MDD) exhibit heightened error-related negativity (ERN) and impaired post-error adaptation, suggesting a hyperactive performance monitoring system as a risk marker for recurrence.
Area of Science:
- Neuroscience
- Psychiatry
- Cognitive Psychology
Background:
- Major depressive disorder (MDD) has a high recurrence rate, necessitating identification of persistent risk markers.
- Negative information processing biases, particularly heightened responses to errors, are implicated in MDD recurrence.
- Neurophysiological underpinnings of post-error adaptation in depression remain underexplored.
Purpose of the Study:
- To investigate event-related potentials (ERPs) and behavioral performance following errors in individuals with remitted MDD (rMDD) compared to healthy controls (HC).
- To examine the impact of errors on current and post-error trial ERPs (error-related negativity [ERN] and correct response negativity [CRN]).
- To assess longer-term adaptation to errors over the course of a task in rMDD participants.
Main Methods:
- Utilized a flanker task to assess behavioral performance and response-locked ERPs.
- Included 58 participants with rMDD and 118 HC.
- Analyzed trial-level data to examine ERN/CRN amplitudes and habituation patterns.
Main Results:
- rMDD participants displayed a larger ERN on error trials and reduced ERN habituation over time compared to HC.
- Following errors, rMDD participants exhibited slower reaction times, predicted by prior ERN amplitude, but maintained comparable accuracy.
- This pattern was associated with greater anhedonia, MDD history, and interpersonal impairment, and predicted future anhedonia symptoms.
Conclusions:
- A hyperactive performance monitoring system, indicated by enhanced ERN and impaired adaptation, may serve as a risk marker for MDD recurrence.
- Deficient error disengagement or compensatory strategies may underlie the observed behavioral differences in rMDD.
- Findings highlight the link between neurophysiological responses to errors, symptom severity, and long-term recurrence risk in MDD.
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