Evidence map›Paper›PMID 39487160›Full record

ArticleScientific reports2024

Good vision without peripheries: behavioral and fMRI evidence.

M Ninghetto, A Kozak, T Gałecki, K Szulborski, J P Szaflik, M Ołdak, A Marchewka, K Burnat

Abstract read
In one paragraph

Article in Scientific reports, 2024. 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

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

2 citing papers in PubMed.

  1. Cortical response to transient and long-term visual field loss.Cerebral cortex (New York, N.Y. : 1991) · 2025
    Article
  2. A Task-Based Functional MRI Double Dissociation of Visual Language and Feature Processing in Healthy Adults.Journal of neuroimaging : official journal of the American Society of Neuroimaging
    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

8 authors.

M NinghettoLaboratory of Brain Imaging, Neurobiology Center, Nencki Institute of Experimental Biology, Warsaw, Poland.
A KozakLaboratory of Brain Imaging, Neurobiology Center, Nencki Institute of Experimental Biology, Warsaw, Poland.
T GałeckiDepartment of Ophthalmology, Medical University of Warsaw, Warsaw, Poland.
K SzulborskiDepartment of Ophthalmology, Medical University of Warsaw, Warsaw, Poland.
J P SzaflikDepartment of Ophthalmology, Medical University of Warsaw, Warsaw, Poland.
M OłdakDepartment of Histology and Embryology, Medical University of Warsaw, Warsaw, Poland.
A MarchewkaLaboratory of Brain Imaging, Neurobiology Center, Nencki Institute of Experimental Biology, Warsaw, Poland.
K BurnatLaboratory of Brain Imaging, Neurobiology Center, Nencki Institute of Experimental Biology, Warsaw, Poland. k.burnat@nencki.edu.pl.

Funding

National Science Centre, Poland 2018/29/B/NZ4/02435
6 · The paper itself

Abstract

In healthy vision, bright slow-motion stimuli are processed primarily by the regions of the visual system that receive input from the central part of the scene, whereas processing of dark fast-motion stimuli is more dependent on peripheral visual input. We tested 31 retinitis pigmentosa (RP) patients with long-term loss of peripheral photoreceptors and healthy controls with temporarily limited peripheral vision. We measured motion-based acuity using random-dot kinematograms, establishing individual thresholds for differentiating a circle from an ellipse. Participants subsequently performed a functional magnetic resonance imaging (fMRI) task set at a constant level of difficulty. The results showed that limiting vision did not affect motion-acuity thresholds in control participants but did cause different brain activations than those in RP patients, indicating prompt implementation of the strategy that would be perceptually successful. Compared with controls with both full and limited vision, impaired motion acuity in RP patients led to decreased brain activation, particularly in the primary peripheral visual areas V1-3. Importantly, compared with controls in full vision, matched decreased activation in MT+/V5, salience-processing cortices and the superior temporal cortex were detected in RP patients and in controls with limited peripheral vision, revealing brain networks that compensate for the loss of peripheral vision.

Indexed as

Magnetic Resonance ImagingRetinitis PigmentosaAdultBrainBrain MappingCase-Control StudiesFemaleHumansMaleMiddle AgedMotion PerceptionPhotic StimulationVision, OcularVisual AcuityVisual CortexYoung Adult

Identifiers

PMID39487160
PMCPMC11530436

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.