Evidence map›Paper›PMID 40279794›Full record

ArticleJournal of psychiatric research2025

Pretreatment anhedonia as a predictor of exposure-based anxiety treatment outcomes.

Matthew Mattoni, Iris Ka-Yi Chat, Lily A Brown, Marin Kautz

Abstract read
In one paragraph

Article in Journal of psychiatric research, 2025. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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.

Matthew MattoniTemple University, Department of Psychology and Neuroscience, 1801 N Broad St., Philadelphia, PA, USA. Electronic address: matt.mattoni@temple.edu.
Iris Ka-Yi ChatTemple University, Department of Psychology and Neuroscience, 1801 N Broad St., Philadelphia, PA, USA.
Lily A BrownUniversity of Pennsylvania, Department of Psychiatry, 3535 Market St., Philadelphia, PA, USA.
Marin KautzUniversity of Pennsylvania, Department of Psychiatry, 3535 Market St., Philadelphia, PA, USA.

Funding

Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI A. Clementina Mesaros · 2006 to 2026
$35.3M
Penn Mental Health AIDS Research CenterP30MH097488 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI Karine Dube, Kelly L Jordan-Sciutto · 2013 to 2026
$23.5M
Signature ProjectP50MH127511 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI MANDELL, DAVID S · 2021 to 2025
$14.4M
A mechanistic trial of the neurobiology of extinction learning and intraparietal sulcus stimulationR01MH132740 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI Lily A Brown · 2024 to 2026
$2.4M
Between- and Within-Person Heterogeneity in Adolescent Resting State Networks: Associations with Internalizing PsychopathologyF31MH134533 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI MATTONI, MATTHEW · 2023 to 2024
$75k
The Relationships of Peripheral Inflammation and Reward-Related Brain Function with Anhedonia, Somatic Symptoms and Functional Impairment in AdolescenceF31MH132230 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI CHAT, KA-YI · 2022 to 2023
$66k
NIEHS NIH HHS P30 ES013508NIMH NIH HHS F31 MH132230NIMH NIH HHS F31 MH134533NIMH NIH HHS P30 MH097488NIMH NIH HHS P50 MH127511NIMH NIH HHS R01 MH132740
6 · The paper itself

Abstract

Reward processes can reinforce extinction learning and aide cognitive processes involved with inhibitory learning. Anhedonia, characterized by deficits in reward incentivization, hedonic response, and learning, may therefore predict worse treatment outcomes. The current study examined associations between pretreatment self-reported anhedonia and several measures of anxiety symptom severity and treatment outcomes in a naturalistic exposure-based treatment setting. We used multilevel models to examine the relationship between pretreatment anhedonia with change in general treatment response and disorder-specific symptoms for obsessive compulsive disorder (OCD), post-traumatic stress disorder (PTSD), generalized anxiety disorder (GAD), social anxiety disorder (SAD), and panic disorder (PD). Consistent with hypotheses, pretreatment anhedonia severity was associated with higher pretreatment anxiety symptom severity across all measures. However, inconsistent with hypotheses, higher anhedonia scores were associated with greater symptom improvement across treatment for OCD, GAD, and PD, and had no significant relationships with diagnosis-general outcome measures, PTSD symptoms, or SAD symptoms. In sensitivity analyses including number of sessions, higher anhedonia was associated with more sessions across treatment and anhedonia no longer significantly predicted OCD or GAD treatment outcomes when controlling for treatment dose. Together, findings suggest that individuals with higher pretreatment anhedonia still respond to exposure therapy for anxiety disorders, but may require more sessions. More broadly, results highlight challenges in translating laboratory research to naturalistic clinical settings and the need for intensive longitudinal studies that can assess the role of reward processes in exposure therapy.

Indexed as

AnhedoniaAnxiety DisordersImplosive TherapyAdultFemaleHumansMaleMiddle AgedStress Disorders, Post-TraumaticTreatment OutcomeYoung AdultAnhedoniaAnxiety disordersOCDPTSDTreatment outcomesTreatment prediction

Identifiers

PMID40279794
PMCPMC12068967

What Socratic holds

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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 Socratic graph.