Evidence map›Paper›PMID 40816655›Full record

ArticleBiological psychiatry. Cognitive neuroscience and neuroimaging2026

Cerebellar-Prefrontal Connectivity Predicts Negative Symptom Severity Across the Psychosis Spectrum.

Sean A Yarrell, Sophia H Blyth, Alexandra B Moussa-Tooks, Baxter P Rogers, Anna Huang, Neil D Woodward, Stephan Heckers, Roscoe O Brady, Heather Burrell Ward

Abstract read
In one paragraph

Article in Biological psychiatry. Cognitive neuroscience and neuroimaging, 2026. 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. Review
  2. Article
  3. Cerebellar Connectivity Addresses Gaps in Cognitive Deficits and Negative Symptoms in Psychosis.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Sean A YarrellDepartment of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, Tennessee.
Sophia H BlythDepartment of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, Tennessee.
Alexandra B Moussa-TooksDepartment of Psychological and Brain Sciences, Indiana University, Bloomington, Indiana; Department of Psychiatry, Indiana University School of Medicine, Indianapolis, Indiana.
Baxter P RogersDepartment of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, Tennessee.
Anna HuangDepartment of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, Tennessee.
Neil D WoodwardDepartment of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, Tennessee.
Stephan HeckersDepartment of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, Tennessee.
Roscoe O BradyDepartment of Psychiatry, Beth Israel Deaconess Medical Center, McLean Hospital, and Harvard Medical School, Boston, Massachusetts.
Heather Burrell WardDepartment of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, Tennessee. Electronic address: heather.b.ward@vumc.org.

Funding

Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at VanderbiltP50HD103537 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Jeffrey L Neul · 2020 to 2026
$10.3M
Imaging Hippocampal Function in PsychosisR01MH070560 · NIMH · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HECKERS, STEPHAN · 2005 to 2025
$7.2M
Network Mediation of Experiential and Expressive Deficits in Psychotic DisordersR01MH116170 · NIMH · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Roscoe O. Brady, KATHRYN Eve LEWANDOWSKI · 2019 to 2026
$5.4M
Thalamocortical Networks in PsychosisR01MH102266 · NIMH · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WOODWARD, NEIL D. · 2014 to 2018
$2.3M
Replacement and Upgrade of a 3T MR Scanner for ResearchS10OD021771 · OD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GORE, JOHN C · 2016 to 2016
$2.0M
Longitudinal Assessment of Distinct Motor Learning Processes to Inform Mechanistic Models of Sensorimotor Function in PsychosisK23MH135215 · NIMH · TRUSTEES OF INDIANA UNIVERSITY · PI MOUSSA-TOOKS, ALEXANDRA · 2024 to 2025
$1.0M
Network-Targeted Neuromodulation for Nicotine Dependence in SchizophreniaK23DA059690 · NIDA · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Heather Burrell Ward · 2024 to 2026
$557k
NICHD NIH HHS P50 HD103537NIDA NIH HHS K23 DA059690NIH HHS S10 OD021771NIMH NIH HHS K23 MH135215NIMH NIH HHS R01 MH070560NIMH NIH HHS R01 MH102266NIMH NIH HHS R01 MH116170
6 · The paper itself

Abstract

backgroundNegative symptom severity predicts functional outcomes and quality of life in people with psychosis. However, negative symptoms respond poorly to medication, and existing literature has not converged on their neurobiological basis. Previous work in small schizophrenia samples has observed that lower cerebellar-dorsolateral prefrontal cortex (DLPFC) connectivity is associated with higher negative symptom severity and that increasing cerebellar-DLPFC connectivity with neuromodulation reduces negative symptoms. We extended this finding by testing associations between cerebellar-DLPFC connectivity, negative symptoms, and cognitive performance in a large sample of individuals with psychosis.

methodsIndividuals with psychosis spectrum disorders (N = 260) underwent resting-state functional magnetic resonance imaging and clinical characterization using the Positive and Negative Syndrome Scale and the Screen for Cognitive Impairment in Psychiatry. Using a previously identified cerebellar region as a seed, we measured connectivity to the DLPFC and regressed connectivity against negative symptom severity, covarying for age, sex, and scanner. Then, we tested whether cognitive performance indirectly affected the relationship between connectivity and negative symptom severity.

resultsAcross the psychosis spectrum, higher cerebellar-DLPFC connectivity was associated with lower negative symptom severity (r = -0.17, p = .007). This connectivity-negative symptom relationship was not affected by psychosis subtype or duration of illness. Better delayed verbal learning was associated with higher cerebellar-DLPFC connectivity (r = 0.13, p = .034) and had a significant indirect effect on the relationship between connectivity and negative symptoms.

conclusionsOur results extend relationships between cerebellar-DLPFC connectivity, negative symptom severity, and cognitive performance across the psychosis spectrum. Larger neuromodulation studies should test whether increasing cerebellar-DLPFC connectivity reduces negative symptoms in psychotic disorders.

Indexed as

CerebellumDorsolateral Prefrontal CortexPrefrontal CortexPsychotic DisordersSchizophreniaAdultFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedNeural PathwaysSeverity of Illness IndexYoung AdultCerebellumCognitive performanceDorsolateral prefrontal cortexNegative symptomsPsychosis spectrum disordersResting-state functional connectivity

Identifiers

PMID40816655
PMCPMC12861324

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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.