Evidence map›Paper›PMID 38051397›Full record

ArticleEuropean archives of psychiatry and clinical neuroscience2024

Global reward processing deficits predict negative symptoms transdiagnostically and transphasically in a severe mental illness-spectrum sample.

Lauren Luther, Sierra A Jarvis, Michael J Spilka, Gregory P Strauss

Abstract read
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In one paragraph

Article in European archives of psychiatry and clinical neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. The antipsychotic potential ofIBRO neuroscience reports · 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

4 authors at 1 institution in 1 country.

Lauren LutherDepartment of Psychology, University of Georgia, 125 Baldwin St., Athens, GA, 30602, USA. lauren.luther@uga.edu.
Sierra A JarvisDepartment of Psychology, University of Georgia, 125 Baldwin St., Athens, GA, 30602, USA.
Michael J SpilkaDepartment of Psychology, University of Georgia, 125 Baldwin St., Athens, GA, 30602, USA.
Gregory P StraussDepartment of Psychology, University of Georgia, 125 Baldwin St., Athens, GA, 30602, USA. gstrauss@uga.edu.
University of Georgia · US

Funding

Modeling Anhedonia in Schizophrenia: A Stochastic Dynamical Systems ApproachR21MH112925 · NIMH · UNIVERSITY OF GEORGIA · PI STRAUSS, GREGORY P · 2017 to 2018
$417k
NIMH NIH HHS R21-MH112925
6 · The paper itself

Abstract

Reward processing impairments are a key factor associated with negative symptoms in those with severe mental illnesses. However, past findings are inconsistent regarding which reward processing components are impaired and most strongly linked to negative symptoms. The current study examined the hypothesis that these mixed findings may be the result of multiple reward processing pathways (i.e., equifinality) to negative symptoms that cut across diagnostic boundaries and phases of illness. Participants included healthy controls (n = 100) who served as a reference sample and a severe mental illness-spectrum sample (n = 92) that included psychotic-like experiences, clinical high-risk for psychosis, bipolar disorder, and schizophrenia participants. All participants completed tasks measuring four RDoC Positive Valence System constructs: value representation, reinforcement learning, effort-cost computation, and hedonic reactivity. A k-means cluster analysis of the severe mental illness-spectrum samples identified three clusters with differential reward processing profiles that were characterized by: (1) global reward processing deficits (22.8%), (2) selective impairments in hedonic reactivity alone (40.2%), and (3) preserved reward processing (37%). Elevated negative symptoms were only observed in the global reward processing cluster. All clusters contained participants from each clinical group, and the distribution of these groups did not significantly differ among the clusters. Findings identified one pathway contributing to negative symptoms that was transdiagnostic and transphasic. Future work further characterizing divergent pathways to negative symptoms may help to improve symptom trajectories and personalized treatments.

Indexed as

Bipolar DisorderPsychotic DisordersRewardAdolescentAdultFemaleHumansMaleMiddle AgedSchizophreniaYoung AdultEffortHedonic reactivityMood disorderPsychosisReinforcement learningSerious mental illnessUltra-high riskValue representation

Identifiers

PMID38051397
OpenAlexW4389330892

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.