Evidence map›Paper›PMID 26419798›Full record

ArticleBrain : a journal of neurology2015

The visual perception of natural motion: abnormal task-related neural activity in DYT1 dystonia.

Wataru Sako, Koji Fujita, An Vo, Janet C Rucker, John-Ross Rizzo, Martin Niethammer, Maren Carbon, Susan B Bressman, Aziz M Uluğ, David Eidelberg

Open access · bronzeAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 15% of its field
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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Structural Alterations in the Gray Matter Volume in Rapid-Onset Dystonia-Parkinsonism.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
  4. Brain network pathophysiology in dystonia.Dystonia (Lausanne, Switzerland) · 2025
    Article
  5. MR spectroscopy and imaging-derived measurements in the supplementary motor area for biomarkers of amyotrophic lateral sclerosis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021
    Article
  6. Contemporary functional neuroanatomy and pathophysiology of dystonia.Journal of neural transmission (Vienna, Austria : 1996) · 2021
    Review
  7. Article
  8. Article
  9. Spontaneous brain activity in the sensorimotor cortex in amyotrophic lateral sclerosis can be negatively regulated by corticospinal fiber integrity.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2017
    Article
  10. Review
  11. Article
  12. 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

10 authors at 5 institutions in 2 countries.

Wataru Sako1 Center for Neurosciences, The Feinstein Institute for Medical Research, Manhasset, NY 11030, USA.
Koji Fujita1 Center for Neurosciences, The Feinstein Institute for Medical Research, Manhasset, NY 11030, USA.
An Vo1 Center for Neurosciences, The Feinstein Institute for Medical Research, Manhasset, NY 11030, USA.
Janet C Rucker2 Department of Neurology, NYU Langone Medical Center, New York, NY 10016, USA.
John-Ross Rizzo3 Department of Rehabilitation Medicine, NYU Langone Medical Center, New York, NY 10016, USA.
Martin Niethammer1 Center for Neurosciences, The Feinstein Institute for Medical Research, Manhasset, NY 11030, USA.
Maren Carbon1 Center for Neurosciences, The Feinstein Institute for Medical Research, Manhasset, NY 11030, USA.
Susan B Bressman4 Mirken Department of Neurology, Beth Israel Medical Center, New York, NY 10003, USA.
Aziz M Uluğ1 Center for Neurosciences, The Feinstein Institute for Medical Research, Manhasset, NY 11030, USA 5 Department of Radiology, Albert Einstein College of Medicine, Bronx, NY 10461, USA 6 Institute of Biomedical Engineering, Boğaziçi University, Istanbul, Turkey.
David Eidelberg1 Center for Neurosciences, The Feinstein Institute for Medical Research, Manhasset, NY 11030, USA david1@nshs.edu.
Center for Neurosciences · USFeinstein Institute for Medical Research · USNYU Langone Health · USAlbert Einstein College of Medicine · USMount Sinai Beth Israel · US

Funding

Structure-Function Relationships in Dystonia: A Network ApproachR01NS072514 · NINDS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI EIDELBERG, DAVID · 2011 to 2014
$2.4M
NINDS NIH HHS R01 NS 072514NINDS NIH HHS R01 NS072514
6 · The paper itself

Abstract

Although primary dystonia is defined by its characteristic motor manifestations, non-motor signs and symptoms have increasingly been recognized in this disorder. Recent neuroimaging studies have related the motor features of primary dystonia to connectivity changes in cerebello-thalamo-cortical pathways. It is not known, however, whether the non-motor manifestations of the disorder are associated with similar circuit abnormalities. To explore this possibility, we used functional magnetic resonance imaging to study primary dystonia and healthy volunteer subjects while they performed a motion perception task in which elliptical target trajectories were visually tracked on a computer screen. Prior functional magnetic resonance imaging studies of healthy subjects performing this task have revealed selective activation of motor regions during the perception of 'natural' versus 'unnatural' motion (defined respectively as trajectories with kinematic properties that either comply with or violate the two-thirds power law of motion). Several regions with significant connectivity changes in primary dystonia were situated in proximity to normal motion perception pathways, suggesting that abnormalities of these circuits may also be present in this disorder. To determine whether activation responses to natural versus unnatural motion in primary dystonia differ from normal, we used functional magnetic resonance imaging to study 10 DYT1 dystonia and 10 healthy control subjects at rest and during the perception of 'natural' and 'unnatural' motion. Both groups exhibited significant activation changes across perceptual conditions in the cerebellum, pons, and subthalamic nucleus. The two groups differed, however, in their responses to 'natural' versus 'unnatural' motion in these regions. In healthy subjects, regional activation was greater during the perception of natural (versus unnatural) motion (P < 0.05). By contrast, in DYT1 dystonia subjects, activation was relatively greater during the perception of unnatural (versus natural) motion (P < 0.01). To explore the microstructural basis for these functional changes, the regions with significant interaction effects (i.e. those with group differences in activation across perceptual conditions) were used as seeds for tractographic analysis of diffusion tensor imaging scans acquired in the same subjects. Fibre pathways specifically connecting each of the significant functional magnetic resonance imaging clusters to the cerebellum were reconstructed. Of the various reconstructed pathways that were analysed, the ponto-cerebellar projection alone differed between groups, with reduced fibre integrity in dystonia (P < 0.001). In aggregate, the findings suggest that the normal pattern of brain activation in response to motion perception is disrupted in DYT1 dystonia. Thus, it is unlikely that the circuit changes that underlie this disorder are limited to primary sensorimotor pathways.

Indexed as

Motion PerceptionAdultBrainBrain MappingCase-Control StudiesCerebellumDiffusion Tensor ImagingDystonia Musculorum DeformansFemaleHumansMagnetic Resonance ImagingMaleNeural PathwaysPonsSubthalamic Nucleusdiffusion tensor imagingDYT1 dystoniafunctional MRImotion perceptiontwo-thirds power law

Identifiers

PMID26419798
PMCPMC4840548
OpenAlexW2266085241

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.