Evidence map›Paper›PMID 29214728›Full record

ArticleHuman brain mapping2018

Disruption of network for visual perception of natural motion in primary dystonia.

Koji Fujita, Wataru Sako, An Vo, Susan B Bressman, David Eidelberg

Open access · bronzeAbstract read
In one paragraph

Article in Human brain mapping, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. An 18-fluorodeoxyglucose-PET study inBrain communications · 2026
    Article
  4. Brain network pathophysiology in dystonia.Dystonia (Lausanne, Switzerland) · 2025
    Article
  5. Article
  6. 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 at 2 institutions in 1 country.

Koji FujitaCenter for Neurosciences, The Feinstein Institute for Medical Research, Manhasset, NY, 11030.
Wataru SakoCenter for Neurosciences, The Feinstein Institute for Medical Research, Manhasset, NY, 11030.
An VoCenter for Neurosciences, The Feinstein Institute for Medical Research, Manhasset, NY, 11030.
Susan B BressmanMirken Department of Neurology, Mount Sinai Beth Israel, New York, NY, 10003.
David EidelbergCenter for Neurosciences, The Feinstein Institute for Medical Research, Manhasset, NY, 11030.ORCID 0000-0002-0854-864X
Feinstein Institute for Medical Research · 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 NS072514
6 · The paper itself

Abstract

In healthy subjects, brain activation in motor regions is greater during the visual perception of "natural" target motion, which complies with the two-thirds power law, than of "unnatural" motion, which does not. It is unknown whether motion perception is normally mediated by a specific network that can be altered in the setting of disease. We used block-design functional magnetic resonance imaging and covariance analysis to identify normal network topographies activated in response to "natural" versus "unnatural" motion. A visual motion perception-related pattern (VPRP) was identified in 12 healthy subjects, characterized by covarying activation responses in the inferior parietal lobule, frontal operculum, lateral occipitotemporal cortex, amygdala, and cerebellum (Crus I). Selective VPRP activation during "natural" motion was confirmed in 12 testing scans from healthy subjects. Consistent network activation was not seen, however, in 29 patients with dystonia, a neurodevelopmental disorder in which motion perception pathways may be involved. Using diffusion tractography, we evaluated the integrity of anatomical connections between the major VPRP nodes. Indeed, fiber counts in these pathways were substantially reduced in the dystonia subjects. In aggregate, the findings associate normal motion perception with a discrete brain network which can be disrupted under pathological conditions.

Indexed as

AdultBrainBrain MappingDiffusion Tensor ImagingDystonic DisordersFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedMotion PerceptionNeural Pathwaysamygdaladiffusion tensor imagingdystoniafMRImotion perception

Identifiers

PMID29214728
PMCPMC5807185
OpenAlexW2775507673

What OpenQuestion holds

Textmetadata
LicenceTDM
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.