OSCR

Increased Attentive Use Is Linked to More Idiosyncratic Functional Connections.

Overview

Authors: Pinar Demirayak1,2, Leland L. Fleming3, Pauline Stewart1,2, Rachel Chua1,2, Kristina M. Visscher1,2
  1. Civitan International Research Center, University of Alabama at Birmingham, Birmingham, Alabama 35294
  2. Department of Neurobiology, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama 35233
  3. Department of Psychiatry, McLean Hospital/Harvard Medical School, Boston, Massachusetts 02478
Institutions: Civitan International (United States); University of Alabama at Birmingham (United States); UAB Medicine; Harvard University (United States); McLean Hospital (United States)
Dates: received 26 November 2025; accepted 28 July 2026; published online 9 September 2026; in print 9 September 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1523/jneurosci.2178-25.2026 · PMID 42562649 · PMCID PMC13560913 · OpenAlex W7196954788
Open access: hybrid, a free copy (OpenAlex)
Status: empty repository
Categories: fMRI (modality), human (organism), other condition (population)
Methods: Connectivity, Smoothing, state filtering, decompositions, Statistics, fMRI & imaging, Physiology & signal measures
Keywords: fMRI, functional connectivity, lesion projection zone, macular degeneration, plasticity, preferred retinal locus, resting state
MeSH: Attention*, Brain*, Nerve Net*, Adult, Brain Mapping, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged (* major topic)
Journal subjects: Development/Plasticity/Repair
Topic: Functional Brain Connectivity Studies (Cognitive Neuroscience, Neuroscience), according to OpenAlex
Funding: HHS | NIH | National Eye Institute (NEI) (U01 EY025858-01A1, R01EY031589); UAB Center for Clinical and Translational Science (UL1 TR000165); Vision Science Research Center (P30 EY003039); Civitan International Research Center; McKnight Brain Research Foundation; Edward R. Roybal Center for Translational Research on Aging and Mobility (P30 AG022838); UAB Comprehensive Center for Healthy Aging
Citations: not cited yet (Europe PMC); 83 references in the paper

Abstract

Experience is thought to modify neural connections to adapt the network to be more optimal for the environment. Given the brain's complexity, multiple network changes could each move the system toward optimality. Standard approaches examine each connection independently; these studies have often shown considerable interindividual variability and modest effects (Marek et al., 2022). Here, we take a different strategy, determining how a whole-brain connection pattern differs from the typical pattern, that is, how “idiosyncratic” the pattern is. We examined how the idiosyncrasy of whole-brain connection patterns varies with frequency of the use of that part of cortex for attention-demanding tasks, focusing on central versus peripheral vision in healthy individuals (who use central vision more frequently for attention-demanding tasks). We found that the whole-brain pattern of functional connections to the cortical representations of central vision is idiosyncratic, whereas patterns of connections to representations of peripheral vision were very similar person to person in healthy vision controls (14 females, 9 males). In a second set of analyses, we examined the brains of people with central vision loss (11 females, 10 males) who use a portion of peripheral vision [the preferred retinal locus (PRL)] more frequently for attention-demanding tasks in their daily lives. The cortical representation of the PRL exhibits more idiosyncratic connections, compared with a control brain region or compared with the same brain region in matched healthy vision controls. These results are consistent with the hypothesis that increased attentive use of a brain area results in idiosyncratic patterns of whole-brain connections.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

No file of the authors' code could be read here: it is described below, and read at its source.

OSF g42yd

License: none: the authors keep all their rights
State: the link answers, verified on 26 September 2026
Evidence: files inventoried
Size: 1 file, 0 scripts
Software Heritage: not checked
Found in: the references
Not found: README, license file, CITATION.cff, environment file, tests, continuous integration, documentation
Availability: 1 check, the latest on 26 September 2026: the link answers (HTTP 200)
  • 26 September 2026: the link answers (HTTP 200)
At the source: osf.io/g42yd/

Tracing map

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  • 0 scripts, each with its path and the digest of its content;
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Data

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Versions

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Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 5 authors, 7 keywords, 10 MeSH terms, 7 funders, 80 references.

Cite

This paper

Demirayak, P., Fleming, L. L., Stewart, P., Chua, R., & Visscher, K. M. (2026). Increased Attentive Use Is Linked to More Idiosyncratic Functional Connections. The Journal of neuroscience : the official journal of the Society for Neuroscience, 46(36), e2178252026. https://doi.org/10.1523/jneurosci.2178-25.2026

BibTeX

@article{demirayak2026increased,
author = {Demirayak, Pinar and Fleming, Leland L. and Stewart, Pauline and Chua, Rachel and Visscher, Kristina M.},
title = {{Increased Attentive Use Is Linked to More Idiosyncratic Functional Connections}},
journal = {The Journal of neuroscience : the official journal of the Society for Neuroscience},
year = {2026},
month = sep,
volume = {46},
number = {36},
pages = {e2178252026},
publisher = {Society for Neuroscience},
issn = {0270-6474},
doi = {10.1523/jneurosci.2178-25.2026},
url = {https://doi.org/10.1523/jneurosci.2178-25.2026},
pmid = {42562649},
pmcid = {PMC13560913}
}

RIS

TY - JOUR
AU - Demirayak, Pinar
AU - Fleming, Leland L.
AU - Stewart, Pauline
AU - Chua, Rachel
AU - Visscher, Kristina M.
TI - Increased Attentive Use Is Linked to More Idiosyncratic Functional Connections
T2 - The Journal of neuroscience : the official journal of the Society for Neuroscience
J2 - J Neurosci
PY - 2026
DA - 2026/09/09
VL - 46
IS - 36
SP - e2178252026
SN - 0270-6474
PB - Society for Neuroscience
DO - 10.1523/jneurosci.2178-25.2026
UR - https://doi.org/10.1523/jneurosci.2178-25.2026
LA - en
ER -

CSL-JSON

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