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Contrast Acuity and the King-Devick Test in Huntington's Disease
Ali G Hamedani1, Tanya Bardakjian1, Laura J Balcer2
1Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Insights
Huntington's disease (HD) is linked to poorer low-contrast vision and slower number naming on the King-Devick test. These simple tests can objectively measure visual changes in HD patients.
Area of Science:
- Neuroscience
- Ophthalmology
- Genetics
Background:
- Saccadic eye movement abnormalities are early indicators of Huntington's disease (HD), but bedside quantification is challenging.
- Afferent visual pathway involvement in HD remains poorly understood.
Purpose of the Study:
- To evaluate afferent and efferent visual function in individuals with manifest Huntington's disease.
- To identify objective, quantifiable measures of visual impairment in HD.
Main Methods:
- Participants with manifest HD (n=19) and controls (n=20) underwent the King-Devick test for rapid number naming.
- Binocular high and low-contrast acuities were measured using Sloan letter charts.
- Pupillometry and validated questionnaires (NEI-VFQ-25) assessed visual function and quality of life.
Main Results:
- Patients with HD showed significantly slower King-Devick test times (102.9s vs 48.2s, p < .01).
- Low-contrast acuity was significantly reduced in HD patients, correlating with UHDRS motor scores (p < .05).
- No significant differences were observed in pupillary reactivity or self-reported vision-related quality of life.
Conclusions:
- Huntington's disease is associated with impaired low-contrast visual acuity and abnormal rapid number naming.
- The King-Devick test and low-contrast acuity measurement offer objective, quantifiable assessments of visual function in HD.
- These tests could be integrated into clinical rating scales for optimized HD monitoring.
Abstract:
Saccadic eye movement abnormalities are among the earliest manifestations of Huntington's disease (HD) but are difficult to quantify at the bedside. Similarly, afferent visual pathway involvement in HD is poorly characterised. The objective was to evaluate afferent and efferent visual function in HD. Participants with manifest HD (n = 19) and healthy controls (n = 20) performed the King-Devick test, a timed test of rapid number naming. Binocular high and low-contrast (2.5% and 1.25%) acuities were measured using low-contrast Sloan letter charts, and pupillometric recordings were made using a handheld NeurOptics PLR-3000 pupillometer. The NEI-VFQ-25 questionnaire with 10-item neuro-ophthalmic supplement were also completed. Unified Huntington's Disease Rating Scale (UHDRS) motor score and other clinical and demographic variables were collected. Comparisons between manifest HD and controls were performed using linear regression adjusted for confounders. Mean King-Devick time scores were 102.9 seconds in patients with manifest HD and 48.2 seconds in controls (p < .01, t-test). In unadjusted analyses, binocular high contrast acuity was seven letters (one Snellen line equivalent) lower in manifest HD than controls (p = .043). This effect was similar for low-contrast acuity, but only low-contrast acuity remained statistically significant after adjusting for covariates. Low-contrast acuity also correlated with UHDRS motor score. There were no differences in pupillary reactivity or self-reported vision-related quality of life. In conclusion, HD is associated with reduced low-contrast acuity and abnormal performance on the King-Devick test of rapid number naming. These tests are easy to administer, providing an objective quantitative measure of visual function which could be incorporated into optimised rating scales.
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