Skip to main content

Main menu

  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Current Issue
    • Issue Archive
    • Collections
    • Podcast
  • ALERTS
  • FOR AUTHORS
    • Information for Authors
    • Fees
    • Journal Clubs
    • eLetters
    • Submit
  • EDITORIAL BOARD
  • ABOUT
    • Overview
    • Advertise
    • For the Media
    • Rights and Permissions
    • Privacy Policy
    • Feedback
  • SUBSCRIBE

User menu

  • Log in
  • My Cart

Search

  • Advanced search
Journal of Neuroscience
  • Log in
  • My Cart
Journal of Neuroscience

Advanced Search

Submit a Manuscript
  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Current Issue
    • Issue Archive
    • Collections
    • Podcast
  • ALERTS
  • FOR AUTHORS
    • Information for Authors
    • Fees
    • Journal Clubs
    • eLetters
    • Submit
  • EDITORIAL BOARD
  • ABOUT
    • Overview
    • Advertise
    • For the Media
    • Rights and Permissions
    • Privacy Policy
    • Feedback
  • SUBSCRIBE
PreviousNext
Research Articles, Behavioral/Cognitive

Preservation of Eye Movements in Parkinson's Disease Is Stimulus- and Task-Specific

Jolande Fooken, Pooja Patel, Christina B. Jones, Martin J. McKeown and Miriam Spering
Journal of Neuroscience 19 January 2022, 42 (3) 487-499; DOI: https://doi.org/10.1523/JNEUROSCI.1690-21.2021
Jolande Fooken
1Centre for Neuroscience Studies, Queen's University, Kingston, Ontario, Canada K7L 3N6
2Ophthalmology & Visual Sciences, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Pooja Patel
2Ophthalmology & Visual Sciences, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Christina B. Jones
5Medicine, Division of Neurology, University of British Columbia, Vancouver, British Columbia, Canada V6T 2B5
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Martin J. McKeown
3Graduate Program in Neuroscience, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3
4Djavad Mowafaghian Center for Brain Health, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3
5Medicine, Division of Neurology, University of British Columbia, Vancouver, British Columbia, Canada V6T 2B5
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Miriam Spering
2Ophthalmology & Visual Sciences, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3
3Graduate Program in Neuroscience, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3
4Djavad Mowafaghian Center for Brain Health, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3
6Institute for Computing, Information and Cognitive Systems, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z4
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & Data
  • Info & Metrics
  • eLetters
  • PDF
Loading

Article Figures & Data

Figures

  • Tables
  • Figure 1.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 1.

    Stimulus characteristics and movement requirements in a battery of oculomotor tasks.

  • Figure 2.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 2.

    Flowchart of participant inclusion by participant group, task, and medication status.

  • Figure 3.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 3.

    Sequence of events and eye movements in the pro-saccade task. A, Each trial started with a drift correction followed by a fixation period. Participants had to saccade to the cued target square. B, 2D eye position in pro-saccade task for a representative PD patient (purple) and control participant (green). For illustration purposes, eye and target position data were flipped to always depict the saccade target on the right. C, Main sequence (saccade velocity vs amplitude) for 2 representative patients (purple circles) and 2 control participants (green circles). Each circle represents one trial. D, Saccade latency distributions (relative frequency of binned saccade latencies) for patients and controls. E, Mean saccade amplitude as a function of saccade latency. Each dot represents the mean saccade amplitude in a 50 ms time bin across all patients (purple) and controls (green). Vertical lines indicate SE. **p < 0.01; ***p < 0.001; ranked sum test.

  • Figure 4.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 4.

    Sequence of events and eye movements in the anti-saccade task. A, Each trial started with a drift correction followed by a fixation period. Participants had to saccade to the uncued target square. B, 2D eye position in pro-saccade task for a representative PD patient (purple) and control participant (green). For illustration purposes, eye and target position data were flipped to always depict the saccade target on the right. C, Saccade latency distributions (relative frequency of binned saccade latencies) for patients and controls. Blue bins represent changes of mind. Red bins represent direction errors. D, Task performance (percentage of saccades toward uncued location without any corrections) as a function of saccade latency. ***p < 0.001 (ranked sum test).

  • Figure 5.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 5.

    Comparison of pro- and anti-saccade task performance. A, Relationship between the frequency of express saccades during the pro-saccade task and the error rate (saccade toward the cued target) in the anti-saccade task. Each circle represents a patient (purple) and control participant (green). Significant regression results in patient group: ***p < 0.001. B, Saccade distributions of a control participant (C57; green) and patient (P35; purple) who had a similar rate of express saccades.

  • Figure 6.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 6.

    Sequence of events and eye movements in sinusoidal pursuit task. A, Each trial started with a drift correction followed by five cycles of sinusoidal target motion in either horizontal or vertical direction. B, 2D eye position for a horizontally moving target at a speed of 16 deg/s for a representative PD patient (purple) and control participant (green). Saturated segments represent saccades. Lighter segments represent smooth pursuit.

  • Figure 7.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 7.

    Sequence of events and eye movements in go/no-go track-intercept task. A, Each trial started with a fixation period. Participants viewed a moving, disappearing target and had to judge whether the target would miss or pass a strike box. B, 2D eye position in track-intercept task for a representative PD patient (purple) and control participant (green). C, First catch-up saccade latency distributions (relative frequency of binned saccade latencies) for patients and controls. Red bins indicate trials in which the go/no-go decision was incorrect. D, Go/no-go decision accuracy as a function of initial catch-up saccade latency for patients (purple) and controls (green). Circles represent group mean for given saccade interval. **p < 0.01 (ranked sum test).

  • Figure 8.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 8.

    Hand movement dynamics in track-intercept task. A, Hand movement velocity across time for individual (thin lines) patients (purple) and controls (green). Thick lines indicate group average. B, Interception timing error for patients and controls. Positive timing errors indicate that participants intercepted too early; negative timing error indicates late interceptions.

Tables

  • Figures
    • View popup
    Table 1.

    Characteristics of study participantsa

    Subject codeAge (yr)HandednessSexETDRSMoCADisease duration (yr)Hoehn-Yahr stage (0-5)bUPDRS score (0-132)cDominant arm rigidity (0-4)Test orderCombination levodopa (mg)d
    P2367RHM20/40-22732442NA0
    P2478RHF20/25-12762441OFF/ON750
    P2684RHM20/25-124142493ON/OFF2250
    P2971RHM20/202782483ON/OFF1625
    P3061RHF20/16-2309.52351ON/OFF812.5
    P3167RHM20/16-2270.52343ON/OFF687.5
    P3261RHM20/16-12882402OFF/ON2000
    P3465RHM20/25-12742141ON/OFF1000
    P3578RHF20/50-227162392ON1625
    P3667RHM20/20-126102150OFF/ON1000
    P3765RHM20/25-128202292OFF/ON750
    P3858RHF20/2027253542ON1000
    P4372RHM20/25-22852182OFF/ON1187.5
    P4458RHM20/20-13042362ON/OFF937.5
    P4541RHF20/12.5-13032212OFF/ON800
    P4970RHM20/20-12613280ON1875
    Mean ± SD66.4 ± 9.920/22-1 ± 0.227.4 ± 1.69.71 ± 7.02.1 ± 0.333 ± 13.91.75 ± 0.91143.8 ± 584.0
    C2574RHM20/25-126
    C2781RHF20/16-228
    C2860RHM20/32-125
    C3968LHF20/20-128
    C4064RHF20/20-130
    C4161LHM20/2527
    C4269RHM20/16-129
    C4662RHM20/16-229
    C4761RHMmissing29
    C4874LHM20/12.5-228
    C5069RHF20/20-126
    C5178RHM20/20-226
    C5271RHM20/25-128
    C5369RHM20/16-129
    C5479RHM20/2030
    C5588RHM20/2528
    C5665RHM20/50-130
    C5743RHF20/2030
    Mean ± SD68.7 ± 10.020/22 ± 0.228.1 ± 1.6
    • ↵aETDRS, Early Treatment of Diabetic Retinopathy Study, visual acuity chart “R” (Precision Vision); MoCA, Montreal Cognitive Assessment, a test that rates cognitive ability on a scale from 0 to 30 (Nasreddine et al., 2005).

    • ↵bHoehn and Yahr (1967) staging scale for symptom severity, ranging from 1 (unilateral involvement only) to 5 (confinement to bed or wheelchair).

    • ↵cUnified Parkinson's Disease Rating Scale (Movement Disorder Society Task Force 2003). Motor Score only.

    • ↵dMost patients were on combination drugs containing levodopa and carbidopa (e.g., Sinemet, Levocarb). Table states total daily dose in milligrams across equivalent combination drugs.

    • View popup
    Table 2.

    Saccadic eye-movement accuracy in pro- and anti-saccade task

    PD patientsControlsTwo-sample unpaired t tests
    Pro-saccades
        Amplitude (deg)
    Velocity (deg/s)
    Latency (ms)
    10.5 ± 1.0
    242 ± 56
    268 ± 52
    12.0 ± 0.6
    298 ± 53
    264 ± 60
    t(25.3) = 5.17; p < 0.001; d = 1.80a
    t(31.1) = 3.00; p = 0.005; d = 1.03a
    t(31.9) = 0.20; p = 0.84; d = 0.07
    Anti-saccades
        Direction error (%)
    Changes of mind (%)
    Amplitudeb (deg)
    Velocityb (deg/s)
    Latency (ms)
    10.1 ± 13.4
    24.4 ± 17.0
    12.0 ± 1.9
    247 ± 61
    343 ± 76
    4.2 ± 6.3
    9.4 ± 8.4
    11.6 ± 2.8
    293 ± 51
    314 ± 80
    t(20.7) = 1.60; p = 0.12; d = 0.56
    t(21.3) = 3.21; p = 0.004; d = 1.12a
    t(30.1) = 0.48; p = 0.64; d = 0.16
    t(29.3) = 2.35; p = 0.03; d = 0.81a
    t(31.8) = 1.06; p = 0.30; d = 0.36
    • ↵aSignificant results.

    • ↵bOnly trials in which participants made a saccade into the correct (uncued) direction are included.

    • View popup
    Table 3.

    Saccadic eye-movement variability in pro- and anti-saccade task

    PD patientsControlsTwo-sample unpaired t tests
    Pro-saccades
        Amplitude (deg)
    Velocity (deg/s)
    Latency (ms)
    3.3 ± 1.5
    72 ± 34
    106 ± 35
    0.8 ± 0.4
    29 ± 21
    55 ± 21
    t(16.9) = 6.45; p < 0.001; d = 2.27a
    t(24.4) = 4.40; p < 0.001; d = 1.53a
    t(24.3) = 5.14; p < 0.001; d = 1.79a
    Anti-saccades
        Amplitudeb (deg)
    Velocityb (deg/s)
    Latency (ms)
    3.1 ± 2.0
    66 ± 44
    115 ± 29
    1.5 ± 1.2
    30 ± 19
    73 ± 26
    t(23.8) = 2.83; p = 0.009; d = 0.99a
    t(19.8) = 3.01; p = 0.007; d = 1.06a
    t(30.5) = 4.45; p < 0.001; d = 1.53a
    • ↵aSignificant results.

    • ↵bOnly trials in which participants made a saccade into the correct (uncued) direction are included.

    • View popup
    Table 4.

    Eye movement accuracy during sinusoidal pursuit and track-intercept task

    PD patientsControlsTwo-sample unpaired t tests
    Sinusoidal pursuit
        Eye velocity gain
    Position error (deg)
    Saccade rate (sac/s)
    1.08 ± 0.23
    2.2 ± 1.0
    4.6 ± 1.1
    1.01 ± 0.21
    1.9 ± 0.7
    4.0 ± 0.7
    t(30.5) = 0.87; p = 0.39; d = 0.30
    t(25.4) = 0.79; p = 0.44; d = 0.27
    t(24.4) = 2.05; p = 0.05; d = 0.71a
    Track-intercept
        Pursuit latency (ms)
    Initial eye velocity
        (deg/s)
    Position error (deg)
    Saccade latency (ms)
    88 ± 48
    5.8 ± 1.6
    1.3 ± 0.3
    275 ± 32
    49 ± 51
    6.1 ± 1.6
    1.2 ± 0.3
    241 ± 26
    t(26.8) = 2.14; p = 0.04; d = 0.79a
    t(27.2) = 0.46; p = 0.65; d = 0.17
    t(26.1) = 1.47; p = 0.15; d = 0.54
    t(27.9) = 3.18; p = 0.004; d = 1.16a
    • ↵aSignificant results.

    • View popup
    Table 5.

    Hand movement kinematics during track-intercept task

    PD patientsControlsTwo-sample unpaired t tests
    Latency (ms)
    Peak velocity (cm/s)
    Interception error (deg)
    712 ± 155
    25.6 ± 4.7
    4.4 ± 1.6
    868 ± 199
    32.0 ± 8.1
    4.4 ± 1.2
    t(24.5) = 2.38; p = 0.03; d = 0.88a
    t(20.2) = 2.55; p = 0.02; d = 0.95a
    t(27.1) = 0.13; p = 0.90; d = 0.05
    • ↵aSignificant results.

Back to top

In this issue

The Journal of Neuroscience: 42 (3)
Journal of Neuroscience
Vol. 42, Issue 3
19 Jan 2022
  • Table of Contents
  • Table of Contents (PDF)
  • About the Cover
  • Index by author
  • Ed Board (PDF)
Email

Thank you for sharing this Journal of Neuroscience article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
Preservation of Eye Movements in Parkinson's Disease Is Stimulus- and Task-Specific
(Your Name) has forwarded a page to you from Journal of Neuroscience
(Your Name) thought you would be interested in this article in Journal of Neuroscience.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Print
View Full Page PDF
Citation Tools
Preservation of Eye Movements in Parkinson's Disease Is Stimulus- and Task-Specific
Jolande Fooken, Pooja Patel, Christina B. Jones, Martin J. McKeown, Miriam Spering
Journal of Neuroscience 19 January 2022, 42 (3) 487-499; DOI: 10.1523/JNEUROSCI.1690-21.2021

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Respond to this article
Request Permissions
Share
Preservation of Eye Movements in Parkinson's Disease Is Stimulus- and Task-Specific
Jolande Fooken, Pooja Patel, Christina B. Jones, Martin J. McKeown, Miriam Spering
Journal of Neuroscience 19 January 2022, 42 (3) 487-499; DOI: 10.1523/JNEUROSCI.1690-21.2021
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • Introduction
    • Materials and Methods
    • Results
    • Discussion
    • Footnotes
    • References
  • Figures & Data
  • Info & Metrics
  • eLetters
  • PDF

Keywords

  • eye movements
  • Parkinson's disease
  • prediction
  • preservation of function
  • saccades
  • smooth pursuit

Responses to this article

Respond to this article

Jump to comment:

No eLetters have been published for this article.

Related Articles

Cited By...

More in this TOC Section

Research Articles

  • Elevated TNF-α Leads to Neural Circuit Instability in the Absence of Interferon Regulatory Factor 8
  • Maturational Indices of the Cognitive Control Network Are Associated with Inhibitory Control in Early Childhood
  • The MAP3Ks DLK and LZK Direct Diverse Responses to Axon Damage in Zebrafish Peripheral Neurons
Show more Research Articles

Behavioral/Cognitive

  • Maturational Indices of the Cognitive Control Network Are Associated with Inhibitory Control in Early Childhood
  • The Spatial Reach of Neuronal Coherence and Spike-Field Coupling across the Human Neocortex
  • Neural Correlates Underlying Social-Cue-Induced Value Change
Show more Behavioral/Cognitive
  • Home
  • Alerts
  • Visit Society for Neuroscience on Facebook
  • Follow Society for Neuroscience on Twitter
  • Follow Society for Neuroscience on LinkedIn
  • Visit Society for Neuroscience on Youtube
  • Follow our RSS feeds

Content

  • Early Release
  • Current Issue
  • Issue Archive
  • Collections

Information

  • For Authors
  • For Advertisers
  • For the Media
  • For Subscribers

About

  • About the Journal
  • Editorial Board
  • Privacy Policy
  • Contact
(JNeurosci logo)
(SfN logo)

Copyright © 2022 by the Society for Neuroscience.
JNeurosci Online ISSN: 1529-2401

The ideas and opinions expressed in JNeurosci do not necessarily reflect those of SfN or the JNeurosci Editorial Board. Publication of an advertisement or other product mention in JNeurosci should not be construed as an endorsement of the manufacturer’s claims. SfN does not assume any responsibility for any injury and/or damage to persons or property arising from or related to any use of any material contained in JNeurosci.