J Am Acad Audiol
DOI: 10.1055/s-0043-1772582
Research Article

Clinical Saccadometry: Establishing Evaluative Standards Using a Simplified Video Oculography Protocol in the Adult Population

Daniel Demian
1   Venn Med, Toronto, Ontario, Canada
2   Interacoustics, Middelfart, Denmark
,
Michelle Petrak
2   Interacoustics, Middelfart, Denmark
3   Northwest Speech and Hearing, Arlington Heights, Illinois
,
Glen Zielinski
2   Interacoustics, Middelfart, Denmark
4   Northwest Functional Neurology, Lake Oswego, Oregon
,
Shelly Massingale
2   Interacoustics, Middelfart, Denmark
5   Banner Sports Medicine and Concussion Specialists, Phoenix, Arizona
,
Amy Alexander
2   Interacoustics, Middelfart, Denmark
5   Banner Sports Medicine and Concussion Specialists, Phoenix, Arizona
,
Liz Fuemmeler
2   Interacoustics, Middelfart, Denmark
6   Hearing and Balance Specialists of Kansas City, Kansas City, Missouri
,
Chia-Cheng Lin
7   Department of Physical Therapy, East Carolina University, Greenville, North Carolina
› Author Affiliations

Abstract

Background Saccadometry is an advanced ocular motor test battery that allows for the functional evaluation of the varied brain regions and circuits involved in the generation of fast, purposeful, and accurate saccadic eye movements. The test battery is composed of prosaccade (PS) and antisaccade (AS) tests that progressively increase cognitive demand. Existing saccadometry protocols qualitatively describe trends across the lifespan, but have not been widely adopted by clinicians.

Purpose The aims of this study are to design an efficient and simplified clinical saccadometry protocol using video oculography (VOG) equipment and establish associated evaluative standards across the lifespan.

Study Sample Data were reported on 273 adults ages 18 to 69 years.

Results Evaluative data on four measures: directional error rate (DE), latency (Lat), peak velocity (Vel), and accuracy (Acc) during PS and AS measurements were provided. Age-group differences were found in Lat (p < 0.01) and Vel (p = 0.04) during PS and age-group differences were found in DE (p = 0.04), Lat (p < 0.01) and Vel (p < 0.01) during AS. Gender differences were found in DE (p = 0.01) and Lat (p < 0.01) during AS.

Conclusions This study established a standardized and time-efficient protocol with evaluative standards for individuals ages 18 to 69 years old to enable the use of saccadometry as an objective measure in the clinic. Saccadometry allows clinicians to look beyond the traditional saccade test and evaluate complex oculomotor and cognitive functions that will better help clinicians differentiate between peripheral and central diagnoses.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author, upon reasonable request.


Author Contributions

Daniel Demian, Michelle Petrak, Glen Zielinski, Shelly Massingale, Liz Fuemmeler, and Amy Alexander collected and charted data. Chia-Cheng Lin provided the statistical analysis. All authors reviewed the text and approved the final paper for submission.




Publication History

Received: 16 September 2022

Accepted: 13 December 2022

Article published online:
21 November 2023

© 2023. American Academy of Audiology. This article is published by Thieme.

Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA

 
  • References

  • 1 Hallett PE. Primary and secondary saccades to goals defined by instructions. Vision Res 1978; 18 (10) 1279-1296
  • 2 Leigh R, Zee D. The Neurology of Eye Movements. Oxford: Oxford University Press; 1999
  • 3 Leigh RJ, Kennard C. Using saccades as a research tool in the clinical neurosciences. Brain 2004; 127 (Pt 3): 460-477
  • 4 Everling S, Fischer B. The antisaccade: a review of basic research and clinical studies. Neuropsychologia 1998; 36 (09) 885-899
  • 5 Munoz DP, Everling S. Look away: the anti-saccade task and the voluntary control of eye movement. Nat Rev Neurosci 2004; 5 (03) 218-228
  • 6 Coe BC, Munoz DP. Mechanisms of saccade suppression revealed in the anti-saccade task. Philos Trans R Soc Lond B Biol Sci 2017; 372 (1718): 20160192
  • 7 Hoffmann A, Ettinger U, Montoro C, Reyes Del Paso GA, Duschek S. Cerebral blood flow responses during prosaccade and antisaccade preparation in major depression. Eur Arch Psychiatry Clin Neurosci 2019; 269 (07) 813-822
  • 8 Hu Y, Liao R, Chen W. et al. Investigating behavior inhibition in obsessive-compulsive disorder: evidence from eye movements. Scand J Psychol 2020; 61 (05) 634-641
  • 9 Obyedkov I, Skuhareuskaya M, Skugarevsky O. et al. Saccadic eye movements in different dimensions of schizophrenia and in clinical high-risk state for psychosis. BMC Psychiatry 2019; 19 (01) 110
  • 10 Reilly JL, Frankovich K, Hill S. et al. Elevated antisaccade error rate as an intermediate phenotype for psychosis across diagnostic categories. Schizophr Bull 2014; 40 (05) 1011-1021
  • 11 LeVasseur AL, Flanagan JR, Riopelle RJ, Munoz DP. Control of volitional and reflexive saccades in Tourette's syndrome. Brain 2001; 124 (Pt 10): 2045-2058
  • 12 Tajik-Parvinchi DJ, Sandor P. Enhanced antisaccade abilities in children with Tourette syndrome: the gap-effect reversal. Front Hum Neurosci 2013; 7: 768
  • 13 Siqueiros Sanchez M, Falck-Ytter T, Kennedy DP. et al. Volitional eye movement control and ADHD traits: a twin study. J Child Psychol Psychiatry 2020; 61 (12) 1309-1316
  • 14 Fernandez-Ruiz J, Hakvoort Schwerdtfeger RM, Alahyane N, Brien DC, Coe BC, Munoz DP. Dorsolateral prefrontal cortex hyperactivity during inhibitory control in children with ADHD in the antisaccade task. Brain Imaging Behav 2020; 14 (06) 2450-2463
  • 15 MacAskill MR, Anderson TJ. Eye movements in neurodegenerative diseases. Curr Opin Neurol 2016; 29 (01) 61-68
  • 16 Pretegiani E, Optican LM. Eye movements in Parkinson's disease and inherited Parkinsonian syndromes. Front Neurol 2017; 8: 592
  • 17 Molitor RJ, Ko PC, Ally BA. Eye movements in Alzheimer's disease. J Alzheimers Dis 2015; 44 (01) 1-12
  • 18 Kahana Levy N, Lavidor M, Vakil E. Prosaccade and antisaccade paradigms in persons with Alzheimer's disease: a meta-analytic review. Neuropsychol Rev 2018; 28 (01) 16-31
  • 19 Stuart S, Parrington L, Martini D, Peterka R, Chesnutt J, King L. The measurement of eye movements in mild traumatic brain injury: a structured review of an emerging area. Front Sports Act Living 2020; 2: 5
  • 20 Webb B, Humphreys D, Heath M. Oculomotor executive dysfunction during the early and later stages of sport-related concussion recovery. J Neurotrauma 2018; 35 (16) 1874-1881
  • 21 Yep R, Smorenburg ML, Riek HC. et al. Interleaved pro/anti-saccade behavior across the lifespan. Front Aging Neurosci 2022; 14: 842549
  • 22 Munoz DP, Broughton JR, Goldring JE, Armstrong IT. Age-related performance of human subjects on saccadic eye movement tasks. Exp Brain Res 1998; 121 (04) 391-400
  • 23 Antoniades C, Ettinger U, Gaymard B. et al. An internationally standardised antisaccade protocol. Vision Res 2013; 84: 1-5
  • 24 Shepard NT, Jacobson GP. Balance Function Assessment and Management. 2nd ed.. Plural Publishing; 2016
  • 25 Dixon WJ. Processing data for outliers. Biometrics 1953; 9: 74-89
  • 26 Hopf S, Liesenfeld M, Schmidtmann I, Ashayer S, Pitz S. Age dependent normative data of vertical and horizontal reflexive saccades. PLoS One 2018; 13 (09) e0204008
  • 27 Klein C, Foerster F, Hartnegg K, Fischer B. Lifespan development of pro- and anti-saccades: multiple regression models for point estimates. Brain Res Dev Brain Res 2005; 160 (02) 113-123
  • 28 Evdokimidis I, Smyrnis N, Constantinidis TS. et al. The antisaccade task in a sample of 2,006 young men. I. Normal population characteristics. Exp Brain Res 2002; 147 (01) 45-52
  • 29 Liu C-L, Chiau HY, Tseng P. et al. Antisaccade cost is modulated by contextual experience of location probability. J Neurophysiol 2010; 103 (03) 1438-1447
  • 30 Ting WK-C, Schweizer TA, Topolovec-Vranic J, Cusimano MD. Antisaccadic eye movements are correlated with corpus callosum white matter mean diffusivity, Stroop performance, and symptom burden in mild traumatic brain injury and concussion. Front Neurol 2016; 6: 271
  • 31 Connolly JD, Goodale MA, DeSouza JF, Menon RS, Vilis T. A comparison of frontoparietal fMRI activation during anti-saccades and anti-pointing. J Neurophysiol 2000; 84 (03) 1645-1655
  • 32 Wilcockson TDW, Mardanbegi D, Xia B. et al. Abnormalities of saccadic eye movements in dementia due to Alzheimer's disease and mild cognitive impairment. Aging (Albany NY) 2019; 11 (15) 5389-5398
  • 33 Mack DJ, Heinzel S, Pilotto A. et al. The effect of age and gender on anti-saccade performance: results from a large cohort of healthy aging individuals. Eur J Neurosci 2020; 52 (09) 4165-4184