Abnormal eye movement features in patients with depression: Preliminary findings based on eye tracking technology

眼球运动 萧条(经济学) 眼动 心理学 眼电学 物理医学与康复 运动(音乐) 医学 验光服务 眼科 计算机视觉 计算机科学 艺术 经济 宏观经济学 美学
作者
Mingzhou Gao,Rongrong Xin,Qingxiang Wang,Dongmei Gao,Jieqiong Wang,Yanhong Yu
出处
期刊:General Hospital Psychiatry [Elsevier BV]
卷期号:84: 25-30 被引量:19
标识
DOI:10.1016/j.genhosppsych.2023.04.010
摘要

Saccadic eye movement (SEM) has been considered a non-invasive potential biomarker for the diagnosis of depression in recent years, but its application is not yet mature. In this study, we used eye-tracking technology to identify the eye movements of patients with depression to develop a new method for objectively identifying depression.Thirty-six patients with depression as the depression group, while thirty-six matched healthy individuals as the control group were recruited and completed eye movement tests, including two tasks: the prosaccade task and the antisaccade task. iViewX RED 500 eye-tracking instruments from SMI were used to collect eye movement data for both groups.In the prosaccade task, there was no difference between the depression and control groups(t = 0.019, P > 0.05). In general, with increasing angle, both groups showed significantly higher peak velocity (F = 81.72, P < 0.0001), higher mean velocity (F = 32.83, P = 0.000), and greater SEM amplitude (F = 24.23, P < 0.0001). In the antisaccade task, there were significant differences in correct rate (t = 3.219, P = 0.002) and mean velocity (F = 3.253, P < 0.05) between the depression group and the control group. In the anti-effect analysis, there were significant differences in correct rate (F = 67.44, P < 0.0001) and accuracy (F = 79.02, P < 0.0001) between the depression group and the control group. Both groups showed longer latency and worse correct rate and precision in the antisaccade task compared with the prosaccade task.Patients with depression showed different eye movement features, which could be potential biomarkers for clinical identification. Further studies must validate these results with larger sample sizes and more clinical populations.
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