Evidence map›Paper›PMID 41999500›Full record

ArticlePsychopharmacology2026

From uniform pharmacotherapy to precision psychiatry: reinforcement sensitivity associations with SSRI outcomes.

Michal Piksa, Agata Cieslik-Starkiewicz, Rafal Rygula

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Article in Psychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Michal PiksaDepartment of Affective Cognitive Neuroscience, Maj Institute of Pharmacology Polish Academy of Sciences, 12 Smetna Street, Krakow, 31-343, Poland.
Agata Cieslik-StarkiewiczDepartment of Affective Cognitive Neuroscience, Maj Institute of Pharmacology Polish Academy of Sciences, 12 Smetna Street, Krakow, 31-343, Poland.
Rafal RygulaDepartment of Affective Cognitive Neuroscience, Maj Institute of Pharmacology Polish Academy of Sciences, 12 Smetna Street, Krakow, 31-343, Poland. rygula@gmail.com.

Funding

Narodowe Centrum Nauki 2021/43/B/HS6/02007
6 · The paper itself

Abstract

rationaleSelective serotonin reuptake inhibitors remain the first-line pharmacotherapy for depression and anxiety disorders, yet remission rates are low and variability in treatment outcomes is poorly understood. Reinforcement sensitivity, a trait-based dimension reflecting individual differences in responsiveness to reward and punishment, has been linked to affective vulnerability, but its association with SSRI outcomes has not been systematically examined in humans.

methodsWe conducted an online study recruiting over 3000 participants, of whom 1979 met strict inclusion criteria and were included in the analyses. Participants were taking citalopram, fluoxetine, or sertraline and provided standardized self-report data on anxiety and depressive-like symptoms. In addition, they completed experimental tasks assessing motivation and reinforcement sensitivity. Based on sensitivity to positive and negative reinforcement, participants were classified into four phenotypes (P-N-, P+N+, P-N+, P+N-). Symptom outcomes were analyzed in relation to treatment type, dose, and phenotype.

resultsAcross antidepressant groups, participants exhibited elevated anxiety and depressive-like symptoms relative to controls, consistent with residual symptomatology. Patterns of symptom differences varied across reinforcement sensitivity phenotypes: Lower insomnia levels were observed primarily in P-N- individuals receiving citalopram or fluoxetine, whereas comparable insomnia levels to controls were observed in P+N+ participants receiving sertraline. Genitourinary symptom levels were lower in P-N- and P-N+ phenotypes among citalopram users, and in P+N- individuals receiving fluoxetine or sertraline. Dose-dependent patterns were also observed.

conclusionsWe report exploratory associations between reinforcement sensitivity, residual symptom profiles, and antidepressant treatment characteristics, including SSRI type and dosage. These findings highlight reinforcement sensitivity as a potential descriptive framework for understanding heterogeneity in residual symptoms among SSRI users and underscore the value of large-scale online research.

Indexed as

Reinforcement SensitivityResidual SymptomsSSRI

Identifiers

PMID41999500

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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 Socratic graph.