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Original Contribution |

Pervasive Ocular Tremor in Patients With Parkinson Disease

George T. Gitchel, MS; Paul A. Wetzel, PhD; Mark S. Baron, MD
Arch Neurol. 2012;69(8):1011-1017. doi:10.1001/archneurol.2012.70.
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Published online

Objective  To further assess oculomotor control of patients with Parkinson disease (PD) during fixation and with movement.

Design  Case-control study.

Setting  A Parkinson disease research, education, and clinical center.

Patients  One hundred twelve patients with PD, including 18 de novo untreated patients, and 60 age-matched controls.

Intervention  Modern, precise eye tracking technology was used to assess oculomotor parameters. Oculomotor function was compared between groups during fixation and while tracking a randomly displaced target on a PC monitor.

Main Outcome Measures  Fixation stability and saccadic parameters.

Results  All patients with PD and 2 of 60 control subjects showed oscillatory fixation instability (ocular tremor), with an average fundamental frequency of 5.7 Hz and average magnitude of 0.27°. Saccadic parameters and occurrences of square wave jerks did not differ between subjects with PD and controls. The amplitude and frequency of fixation instability did not correlate with disease duration, clinical Unified Parkinson's Disease Rating Scale scores, or dopa-equivalent dosing. No differences in oculomotor parameters were found between medicated and unmedicated patients with PD.

Conclusions  All patients with PD exhibited persistent ocular tremor that prevented stability during fixation. The pervasiveness and specificity of this feature suggest that modern, precise oculomotor testing could provide a valuable early physiological biomarker for diagnosing PD.

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Figures

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Figure 1. Normal oculomotor behavior contrasted with tremulous fixations in patients with Parkinson disease (PD). A, Recordings from a control subject demonstrate stable fixations. B-D, In distinction, in representative medicated (B and C) and unmedicated (D) patients with PD, fixations are unstable anddominated by ocular tremor. Black circles represent horizontal eye movements, with positive values indicating rightward eye movements, while red triangles indicate rotational head movement along the azimuth.

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Figure 2. Root mean square (RMS) velocity and absolute velocity during fixation for the control and Parkinson disease (PD) groups. Oscillatory fixation instability in patients with PD results in a greater RMS velocity (A) and absolute velocity (B) of the eye during fixation. Middle bars inside the boxes represent sample means, while the edges of the boxes indicate first and third quartiles. Bottom and top bars represent minimum and maximum, respectively. Circles denote outliers, while an asterisk denotes an extreme outlier.

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Figure 3. Fixation variability for comparison between the control and Parkinson disease (PD) groups. The illustrated data consist of all sample points from 1 randomly selected fixation per subject (n = 94 fixations in medicated patients with PD and 45 control fixations), located at the origin, and with duration of at least 250 milliseconds. Note the major ocular fixation instability in patients with PD compared with the stable clustering of the controls.

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Figure 4. The product of peak velocity and duration vs amplitude of saccades for the medicated patients with Parkinson disease (PD) and controls. Regression line formulae and correlation indicate no differences between the PD and control groups in the dynamics of reflexive saccades made to randomly displaced targets.

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