Evidence map›Paper›PMID 31280309›Full record

ArticleBrain : a journal of neurology2019

Impaired reward-related learning signals in remitted unmedicated patients with recurrent depression.

Hanneke Geugies, Roel J T Mocking, Caroline A Figueroa, Paul F C Groot, Jan-Bernard C Marsman, Michelle N Servaas, J Douglas Steele, Aart H Schene, Henricus G Ruhé

Abstract read
In one paragraph

Article in Brain : a journal of neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  12. Neuropsychological Effects of Antidepressants: Translational Studies.Current topics in behavioral neurosciences · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Hanneke GeugiesUniversity Medical Center Groningen, University Center for Psychiatry, Mood and Anxiety Disorders, University of Groningen, The Netherlands.
Roel J T MockingDepartment of Psychiatry, Amsterdam University Medical Center, location AMC, University of Amsterdam, The Netherlands.
Caroline A FigueroaDepartment of Psychiatry, Amsterdam University Medical Center, location AMC, University of Amsterdam, The Netherlands.
Paul F C GrootDepartment of Radiology and Nuclear Medicine, Amsterdam University Medical Center, location AMC, University of Amsterdam, The Netherlands.
Jan-Bernard C MarsmanUniversity Medical Center Groningen, Department of Neuroscience, Neuroimaging Center, University of Groningen, The Netherlands.
Michelle N ServaasUniversity Medical Center Groningen, Department of Neuroscience, Neuroimaging Center, University of Groningen, The Netherlands.
J Douglas SteeleMedical School (Neuroscience), University of Dundee, Scotland, UK.
Aart H ScheneDonders Institute for Brain, Cognition and Behavior, Radboud University, Nijmegen, The Netherlands.
Henricus G RuhéUniversity Medical Center Groningen, University Center for Psychiatry, Mood and Anxiety Disorders, University of Groningen, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of the core symptoms of major depressive disorder is anhedonia, an inability to experience pleasure. In patients with major depressive disorder, a dysfunctional reward-system may exist, with blunted temporal difference reward-related learning signals in the ventral striatum and increased temporal difference-related (dopaminergic) activation in the ventral tegmental area. Anhedonia often remains as residual symptom during remission; however, it remains largely unknown whether the abovementioned reward systems are still dysfunctional when patients are in remission. We used a Pavlovian classical conditioning functional MRI task to explore the relationship between anhedonia and the temporal difference-related response of the ventral tegmental area and ventral striatum in medication-free remitted recurrent depression patients (n = 36) versus healthy control subjects (n = 27). Computational modelling was used to obtain the expected temporal difference errors during this task. Patients, compared to healthy controls, showed significantly increased temporal difference reward learning activation in the ventral tegmental area (PFWE,SVC = 0.028). No differences were observed between groups for ventral striatum activity. A group × anhedonia interaction [t(57) = -2.29, P = 0.026] indicated that in patients, higher anhedonia was associated with lower temporal difference activation in the ventral tegmental area, while in healthy controls higher anhedonia was associated with higher ventral tegmental area activation. These findings suggest impaired reward-related learning signals in the ventral tegmental area during remission in patients with depression. This merits further investigation to identify impaired reward-related learning as an endophenotype for recurrent depression. Moreover, the inverse association between reinforcement learning and anhedonia in patients implies an additional disturbing influence of anhedonia on reward-related learning or vice versa, suggesting that the level of anhedonia should be considered in behavioural treatments.

Indexed as

RewardAction PotentialsAdultAgedAnhedoniaConditioning, ClassicalCorpus StriatumDepressive DisorderDopaminergic NeuronsFemaleHumansLearningMagnetic Resonance ImagingMaleMiddle AgedPhotic Stimulationanhedoniaprediction-error codingrecurrent depressionreward-related learningtemporal difference model

Identifiers

PMID31280309
PMCPMC6734943

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.