Evidence map›Paper›PMID 40770189›Full record

ArticleSchizophrenia (Heidelberg, Germany)2025

Temporal characteristics of hemodynamic responses during active and passive hand movements in schizophrenia spectrum disorder.

Harun A Rashid, Tilo Kircher, Benjamin Straube

Abstract read
In one paragraph

Article in Schizophrenia (Heidelberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Harun A RashidDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany. arrashid@uni-marburg.de.ORCID http://orcid.org/0009-0004-8906-1826
Tilo KircherDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.
Benjamin StraubeDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.ORCID http://orcid.org/0000-0002-9837-0944

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) 222641018Deutsche Forschungsgemeinschaft (German Research Foundation) 286893149
6 · The paper itself

Abstract

In healthy individuals, active hand-movements typically elicit earlier neural processing than passive one, reflected by more positive contrast estimates of the first-order temporal derivative (TD) of hemodynamic response function (HRF) in functional MRI (fMRI) analyses. This temporal advantage might be due to prior movement-awareness and predictive mechanisms that support self-other distinction. However, it is unknown whether impaired predictive mechanisms in Schizophrenia Spectrum Disorder (SSD) influence earlier neural processing. Patients with SSD (n = 20) and healthy controls (HC; n = 20) performed active and passive hand movements, while detected delays in video feedback of their own or another person's hand. The recorded fMRI data were analysed applying TD to examine timing and second-order dispersion derivative (DD) to evaluate duration of neural responses. Compared to HC, patients with SSD exhibited delayed BOLD responses during active vs. passive movements in the right caudate nucleus, lobule VIII of right cerebellar hemisphere, left superior temporal gyrus, left postcentral gyrus, left thalamus, and left putamen/insula. Furthermore, during active movement with own hand feedback, patients with SSD showed delayed activation in the bilateral putamen and insula. Delayed insula/putamen responses' were associated with symptom severity. However, these exploratory findings remain not significant after correction for multiple comparisons and attenuated with Spearman's-rank correlations. Delayed BOLD responses in patients with SSD, particularly in the right cerebellar lobule VIII, left thalamus, and bilateral insula/putamen may contribute to disturbances in the sense of agency. Altered timing/duration of neural responses reflects new insight underlying deficits in predictive and feedback-monitoring mechanisms in SSD.

Identifiers

PMID40770189
PMCPMC12328563

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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.