Evidence map›Paper›PMID 28769866›Full record

ArticleFrontiers in neurology2017

Eye Control Deficits Coupled to Hand Control Deficits: Eye-Hand Incoordination in Chronic Cerebral Injury.

John-Ross Rizzo, James K Fung, Maryam Hosseini, Azadeh Shafieesabet, Edmond Ahdoot, Rosa M Pasculli, Janet C Rucker, Preeti Raghavan, Michael S Landy, Todd E Hudson

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  5. Review
  6. Multiple processes independently predict motor learning.Journal of neuroengineering and rehabilitation · 2020
    Article
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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 2 institutions in 1 country.

John-Ross RizzoDepartment of Rehabilitation Medicine, New York University Langone Medical Center, New York, NY, United States.
James K FungDepartment of Rehabilitation Medicine, New York University Langone Medical Center, New York, NY, United States.
Maryam HosseiniDepartment of Rehabilitation Medicine, New York University Langone Medical Center, New York, NY, United States.
Azadeh ShafieesabetDepartment of Rehabilitation Medicine, New York University Langone Medical Center, New York, NY, United States.
Edmond AhdootDepartment of Rehabilitation Medicine, New York University Langone Medical Center, New York, NY, United States.
Rosa M PasculliDepartment of Rehabilitation Medicine, New York University Langone Medical Center, New York, NY, United States.
Janet C RuckerDepartment of Neurology, New York University Langone Medical Center, New York, NY, United States.
Preeti RaghavanDepartment of Rehabilitation Medicine, New York University Langone Medical Center, New York, NY, United States.
Michael S LandyDepartment of Psychology & Center for Neural Science, New York University, New York, NY, United States.
Todd E HudsonDepartment of Rehabilitation Medicine, New York University Langone Medical Center, New York, NY, United States.
NYU Langone Health · USNew York University · US

Funding

Project-005UL1TR001445 · NCATS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BREDELLA, MIRIAM ANTOINETTE, HOCHMAN, JUDITH S · 2015 to 2025
$103.5M
Institutional Clinical and Translational Science AwardUL1TR000038 · NCATS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CRONSTEIN, BRUCE NEIL, HOCHMAN, JUDITH S · 2012 to 2014
$16.8M
Vision Core Grant- Design and Fabrication ModuleP30EY013079 · NEI · NEW YORK UNIVERSITY · PI MOVSHON, J ANTHONY · 2000 to 2025
$14.2M
Rehabilitation Medicine Scientist Training (RMST) ProgramK12HD001097 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BONINGER, MICHAEL L. · 1995 to 2016
$14.1M
SHAPE REPRESENTATION AND MULTIPLE DEPTH CUESR01EY008266 · NEI · NEW YORK UNIVERSITY · PI MICHAEL S LANDY · 1989 to 2026
$7.7M
Strategies for recovery of dexterity post strokeR01HD071978 · NICHD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI RAGHAVAN, PREETI · 2013 to 2017
$3.4M
NCATS NIH HHS UL1 TR000038NCATS NIH HHS UL1 TR001445NEI NIH HHS P30 EY013079NEI NIH HHS R01 EY008266NICHD NIH HHS K12 HD001097NICHD NIH HHS R01 HD071978
6 · The paper itself

Abstract

It is widely accepted that cerebral pathology can impair ocular motor and manual motor control. This is true in indolent and chronic processes, such as neurodegeneration and in acute processes such as stroke or those secondary to neurotrauma. More recently, it has been suggested that disruptions in these control systems are useful markers for prognostication and longitudinal monitoring. The utility of examining the relationship or the coupling between these systems has yet to be determined. We measured eye and hand-movement control in chronic, middle cerebral artery stroke, relative to healthy controls, in saccade-to-reach paradigms to assess eye-hand coordination. Primary saccades were initiated significantly earlier by stroke participants relative to control participants. However, despite these extremely early initial saccades to the target, reaches were nevertheless initiated at approximately the same time as those of control participants. Control participants minimized the time period between primary saccade onset and reach initiation, demonstrating temporal coupling between eye and hand. In about 90% of all trials, control participants produced no secondary, or corrective, saccades, instead maintaining fixation in the terminal position of the primary saccade until the end of the reach. In contrast, participants with stroke increased the time period between primary saccade onset and reach initiation. During this temporal decoupling, multiple saccades were produced in about 50% of the trials with stroke participants making between one and five additional saccades. Reaches made by participants with stroke were both longer in duration and less accurate. In addition to these increases in spatial reach errors, there were significant increases in saccade endpoint errors. Overall, the magnitude of the endpoint errors for reaches and saccades were correlated across participants. These findings suggest that in individuals with otherwise intact visual function, the spatial and temporal relationships between the eye and hand are disrupted poststroke, and may need to be specifically targeted during neurorehabilitation. Eye-hand coupling may be a useful biomarker in individuals with cerebral pathology in the setting of neurovascular, neurotraumatic, and neurodegenerative pathology.

Indexed as

brain injurieseyeeye movementshandstroke

Identifiers

PMID28769866
PMCPMC5512342
OpenAlexW2735616173

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.