Evidence map›Paper›PMID 39527738›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Functional alterations of the magnocellular subdivision of the visual sensory thalamus in autism.

Stefanie Schelinski, Louise Kauffmann, Alejandro Tabas, Christa Müller-Axt, Katharina von Kriegstein

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. 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. Article
  2. Visual function and autism spectrum disorder.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Review
  3. Functional alterations of the magnocellular subdivision of the visual sensory thalamus in autism.Proceedings of the National Academy of Sciences of the United States of America · 2024
    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

5 authors.

Stefanie SchelinskiChair of Cognitive and Clinical Neuroscience, Faculty of Psychology, Dresden University of Technology, Dresden 01187, Germany.ORCID 0000-0001-5398-0020
Louise KauffmannMax Planck Institute for Human Cognitive and Brain Sciences, Leipzig 04303, Germany.ORCID 0000-0002-8733-7508
Alejandro TabasMax Planck Institute for Human Cognitive and Brain Sciences, Leipzig 04303, Germany.ORCID 0000-0002-8643-1543
Christa Müller-AxtChair of Cognitive and Clinical Neuroscience, Faculty of Psychology, Dresden University of Technology, Dresden 01187, Germany.ORCID 0000-0003-4983-7461
Katharina von KriegsteinChair of Cognitive and Clinical Neuroscience, Faculty of Psychology, Dresden University of Technology, Dresden 01187, Germany.ORCID 0000-0001-7989-5860

Funding

EC | ERC | HORIZON EUROPE European Research Council (ERC) grant agreement No 647051Federal Ministry of Education and Research (BMBF) grant No 01EW2213Max Planck Research Group Grant NN
6 · The paper itself

Abstract

The long-standing hypothesis that autism is linked to changes in the visual magnocellular system of the human brain has never been directly examined due to technological constraints. Here, we used a recently developed 7-Tesla functional MRI (fMRI) approach to investigate this hypothesis within the visual sensory thalamus (lateral geniculate nucleus, LGN). The LGN is a crucial component of the primary visual pathway. It is particularly suited to investigate the magnocellular visual system, because within the LGN, the magnocellular (mLGN) uniquely segregates from the parvocellular (pLGN) system. Our results revealed diminished mLGN blood-oxygenation-level-dependent (BOLD) responses in the autism group compared to controls. pLGN responses were comparable across groups. The mLGN alterations were observed specifically for stimuli optimized for mLGN function, i.e., visual displays with low spatial frequency and high temporal flicker frequency. The results confirm the long-standing hypothesis of magnocellular visual system alterations in autism. They substantiate the emerging perspective that sensory processing variations are part of autism symptomatology.

Indexed as

Autistic DisorderGeniculate BodiesMagnetic Resonance ImagingVisual PathwaysAdolescentAdultFemaleHumansMalePhotic StimulationThalamusYoung Adult7T-fMRIAutismlateral geniculate nucleusmagnocellularvisual motion

Identifiers

PMID39527738
PMCPMC11588090

What OpenQuestion holds

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Registered trials

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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.