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Updated: Feb 2, 2026

Doppler Optical Coherence Tomography of Retinal Circulation
Published on: September 18, 2012
Color vision testing versus pattern visual evoked potentials and optical coherence tomography parameters in
Burcu Yuksel1, Berna Dogan2, Belkıs Koctekin3
1Antalya Training and Research Hospital, Neurology Department, Muratpasa, 07050 Antalya, Turkey.
Color vision testing is not a reliable biomarker for detecting optic nerve damage in multiple sclerosis (MS) patients without a history of optic neuritis. Pattern visual evoked potentials (PVEP) and optical coherence tomography (OCT) are more effective indicators of neurodegeneration.
Area of Science:
- Neuro-ophthalmology
- Neuroimmunology
- Ophthalmology
Background:
- Acute idiopathic demyelinating optic neuritis is a common initial symptom of multiple sclerosis (MS).
- Early detection of optic nerve involvement is crucial for managing MS, even in patients without a history of optic neuritis.
Purpose of the Study:
- To evaluate the utility of color vision testing as a simple biomarker for detecting subclinical optic nerve damage in MS patients.
- To compare the effectiveness of color vision testing with pattern visual evoked potentials (PVEP) and spectral domain optical coherence tomography (SD-OCT) parameters in identifying optic nerve involvement.
Main Methods:
- Color vision was assessed using the Farnsworth-Munsell 100 (FM-100) hue test, calculating total error scores (TES), red-green axis (RGS), and blue-yellow axis (BYS).
- Ocular imaging included SD-OCT for retinal nerve fiber layer (RNFL), optic disc parameters, macular volume, central macular thickness, and retinal ganglion cell layer, and enhanced depth imaging OCT for choroidal thickness (CT).
- Pattern visual evoked potentials (PVEP) were recorded, and data were compared between 28 RRMS patients and 25 healthy controls.
Main Results:
- PVEP showed significantly delayed P100 latencies and reduced amplitudes in MS patients compared to controls.
- SD-OCT revealed statistically significant thinning in the temporal quadrant of the RNFL in MS patients.
- While color vision test scores (TES, RGS, BYS) were higher in MS patients, the differences were not statistically significant, and no correlation was found with PVEP or OCT parameters.
Conclusions:
- Color vision testing, using the FM-100 hue test, is not a sensitive biomarker for detecting subclinical optic nerve damage in MS patients without prior optic neuritis.
- PVEP and OCT-measured RNFL thickness are more valuable and reliable biomarkers for assessing neurodegeneration in the anterior visual pathway in MS.
- These findings suggest that PVEP and OCT should be prioritized over color vision testing for early detection of optic nerve involvement in MS.
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