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Quantitative cone contrast threshold testing in patients with differing pathophysiological mechanisms causing retinal diseases

International Journal of Retina and Vitreous volume 9, Article number: 9 (2023) Cite this article

Abstract

Background

Cone contrast threshold testing (CCT) provides quantitative measurements of color and contrast function to reveal changes in vision quality that are not standard endpoints in clinical trials. We utilize CCT to measure visual function in patients with multiple sclerosis (MS), age-related macular degeneration (AMD), epiretinal membrane (ERM), and retinal vein occlusion (RVO).

Methods

Retrospective data was gathered from 237 patients of the Gavin Herbert Eye Institute. Subjects included 17 patients with MS, 45 patients with AMD, 41 patients with ERM, 11 patients with RVO, and 123 healthy controls. Patients underwent the primary measurement outcome, CCT testing, as well as Sloan visual acuity test and spectral domain optical coherence tomography during normal care.

Results

Color and contrast deficits were present in MS patients regardless of history of optic neuritis. AMD with intermediate or worse disease demonstrated reduced CCT scores. All 3 stages of ERM demonstrated cone contrast deficits. Despite restoration of visual acuity, RVO-affected eyes demonstrated poorer CCT performance than unaffected fellow eyes.

Conclusions

CCT demonstrates color and contrast deficits for multiple retinal diseases with differing pathophysiology. Further prospective studies of CCT in other disease states and with larger samples sizes is warranted.

Background

Human trichromatic vision has been predicted to detect 2.3 million colors with discrimination between wavelength differences of as little as 0.25 nm. [1, 2] Despite 50 percent of visual information originating from color-sensitive cones in the fovea, clinical visual function testing is largely limited to visual acuity (VA) which quantifies minimal angle of resolution under maximal contrast (black-on-white) conditions [3]. Visual acuity, the widely used “gold standard” for retinal disease clinical trials, have had extensive techniques developed to mitigate the variability in visual acuity charts test results, including the Early Treatment of Diabetic Retinopathy Study (ETDRS) [4]. However, the contributions of color and contrast to visual function are merely noted qualitatively in patients with ophthalmic disease. Routine color vision deficit (CVD) testing in practice is typically reserved for neuro-ophthalmic disease, orbital compressive pathologies, and hereditary retinopathies [5,6,7,8] with both advantages and disadvantages for the various color and contrast assays [3]. The anomaloscope, considered the “gold standard” quantitative matching test for assessing CVD [3, 9], is rarely used because it is laborious, time-consuming, and restricted to quantifying CVD in the red-green axis. Instead, pseudoisochromatic plates are frequently used because they are easy to administer, rapid, and inexpensive; however, they provide low resolution quantitative results [3, 9]. Quantitative arrangement tests like the Farnsworth Munsell 100 [10] and computerized adaptations [11] are lengthy and performance is confounded by external factors including nonverbal intelligence. [12]

The ColorDx Cone Contrast Threshold Test (CCT) (ColorDx HD, Konan Medical, Irvine, CA), a computerized CVD test developed for the US Air Force, uses an adaptive algorithm to consecutively evaluate contrast sensitivity in L-, M-, and S-cones [13]. Individuals are presented with a series of tumbling Landolt-C optotypes in a randomized orientation of cone contrasted against an isochromatic photopic (~ 74 cd/m2) background (Fig. 1a) and prompted to indicate the orientation within 5 s. ColorDx generates a continuous quantitative output of contrast sensitivity for each of the 3 cone opsins (Fig. 1b). This test is 4–8 min long, is easy to administer, and can be standardized between testing centers with pre-programed color and luminance calibration on an anti-glare screen. Although not approved by the Food and Drug Administration as a primary endpoint for clinical trials, CCT has demonstrated its use as an indicator of eye function in multiple studies [3, 14]. Military screenings using CCT demonstrate 96–100% sensitivity and specificity for protan, deutan, and tritan CVD compared to the anomaloscope [3, 14]. Our study team has also demonstrated that there was no learning effect, or improvement in scores, when individuals repeated this test multiple times [15].

Fig. 1
figure 1

a Cone contrast threshold test isolates cone opsins by providing photopic background to suppress rod function and adjusts Landolt C optotype contrast for each cone opsin. b The quantitative output indicates a mean score with error for each individual cone opsin and these are reported as normal, borderline or abnormal

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We report visual function changes beyond visual acuity in patients with 4 diseases affecting the neurosensory retina. Loss of retinal ganglion cells with or without [15] optic neuritis (ON) in multiple sclerosis (MS) has established serial color vision testing as standard care for optic neuropathies [17, 18]. However, color and contrast vision is not standard care in diseases affecting the retina. Age-related macular degeneration (AMD) is a common cause of vision loss primarily due to metabolic dysfunction [19] and death [20] of the photoreceptors and retinal pigmented epithelium, and CCT has been shown to be reduced in the intermediate stage of the disease [21]. Epiretinal membranes (ERM) are thin fibrocellular membranes which exert mechanical force from the inner retina to the outer retina to reduce visual quality and acuity, but little is known about their effect on color and contrast vision [22,23,24]. Visual acuity loss from retinal edema associated with retinal vein occlusion (RVO), a vascular disease of the inner retina, is well-treated with injectable medications [25,26,27,28]; however, many patients still note poor vision despite good visual acuity recovery. In AMD, ERM, and RVO, patients subjectively report qualitative reductions in vision despite normal visual acuity (Additional files 1, 2, Additional file 3: Figs. S1–S3). The aim of this study is to analyze CCT quantitative cone contrast vision testing in patients with MS, AMD, ERM, and RVO to characterize visual function deficits beyond BCVA.

Methods

Human subjects

We performed a retrospective chart review on all patients seen at the Gavin Herbert Eye Institute during the period of May 2018 through December 2019 who met inclusion criteria. Institutional Review Board (IRB)/Ethics Committee approval was obtained, and the described research adhered to the tenets of the Declaration of Helsinki. We included patients if they had one of several diagnoses including MS with and without previous ON, AMD, ERM, or RVO. ColorDx is not a visual acuity test but requires 20/120 vision or better to complete the test. All subjects across the various disease states and in the healthy control groups had to meet the following criteria: age 18 or older, no history of other ocular comorbidities except for age-related cataracts, VA of 20/60 or better, and no prior history of ocular surgery except for cataract extraction. To avoid any concern that VA would play any role in a subject’s CCT performance, we elected to conservatively double the minimal acuity for resolution in our population. MS patients were compared to a group of healthy control subjects who met the same inclusion and exclusion criteria as stated above and have no other ocular conditions apart from age-related cataracts and refractive error. A unique group was the set of RVO patients. Given that this disease state affects only one eye in each of our included patients, healthy fellow eyes were compared to disease-impacted eyes within this population to eliminate potential confounding variables between participants. Additionally, in the RVO group, inclusion criteria were broadened in this group to 20/100 or better, which allowed for a larger number of participants while still meeting the 20/120 criteria required by the CCT test. All subjects had previously obtained CCT and VA assessments (Snellen letter set, Sloan characters with ETDRS spacing as is customary on M&S Technologies digital visual acuity charts) as a part of routine care at the Gavin Herbert Eye Institute.

Retina specialists made the diagnosis of AMD, ERM, and RVO (AB, MM). Neurologists in consultation with neuro-ophthalmologists made the diagnosis of MS (CB, WC). Specialists performed dilated retinal exam and optical coherence tomography (OCT) to diagnose and grade AMD by evaluating the extent of pigmentary changes, drusen number, and drusen size [29, 30]. Dilated retinal exam and SD-OCT imaging confirmed the presence of ERM. Two independent retina specialists determined severity and grading of ERM (AB, DF), with a third retina specialist available in the case there was any disagreement between graders [31]. In brief, Grade 1 ERMs have a foveal depres­sion, are thin, and distinguishable retinal layers. Grade 2 membranes have a disruption in their foveal depression, the retina is distorted with widening of layers in particular the outer nuclear layers, however individual layers can still be distinguished. Grade 3 membranes have new continuous ectopic inner foveal layers, but retinal layers can still be distinguished. Grade 4 membranes were not included in this study. Patients were excluded if they were actively receiving treatment for AMD, defined as having received any injections of steroid or anti-VegF within 3 months of performing the CCT assessment. Eyes affected by ERM were compared to a subset of fellow healthy eyes with trace or no ERM and drusen and belonging to patients aged 50 years or older. Eyes affected by AMD were compared to a subset of healthy eyes with no sign of early AMD belonging to patients aged 64 years or older. Age ranges for healthy control groups were restricted to correspond with the age distributions of patients in the diseased groups to minimize age as a possible confounding factor of the study. Diagnosis of RVO was based on clinical examination and a historical onset of more than 6 months and no active macular edema after treatment.

Cone contrast threshold and imaging

ColorDx is a CCT test that presents a Landolt C optotype in 4 different orientations in the center of a photopic gray screen. Patients use a response pad with arrows to indicate optotype orientation. Following color and luminance calibration on an anti-glare screen, the device presented tumbling Landolt-C optotypes. A Bayesian thresholding method, the Psi-Marginal Adaptive Technique, adjusted the contrast for subsequent tests based on preceding answers [13] and a Psi-marginal calculation yielded the final CCT value. Scores ranged from 175 to 0, with scores below 75 considered as color deficiency in accordance to pass/fail criteria developed by the United States Air Force [3]. The test is performed separately on each eye and generates a separate contrast threshold score for each of the 3 color cones.

The device utilizes an adaptive algorithm per manufacturer specifications to increase or decrease the contrast of the displayed optotype in accordance with the test subject’s response accuracy. All CCT testing was performed with BCVA under photopic and monocular conditions at 2 feet. BCVA, age, and phakic status were recorded for all subjects. SD-OCT (Cirrus, Carl Zeiss Meditiec, USA or Spectralis Heidelberg Engineering Heidelberg Germany) imaging was acquired for all subjects in the disease state groups. The images acquired were horizontal raster scans on either a Zeiss Cirrus 5000 (Karl Zeiss Meditec, Dublin CA) or a Heidelberg Spectralis (Heidelberg Engineering, Heidelberg) through the fovea extending throughout the perifovea. In the MS patient group, OCT images of the retinal nerve fiber layer were analyzed as well. Researchers chose to focus analysis on the average RNFL thickness value as well as temporal RNFL region, which is the most commonly affected region in MS [46]. Additionally, prior literature has demonstrated that thinning of the temporal region has the closest association with disease burden in MS and it is increasingly being utilized to monitor disease state in MS patients with optic neuritis [47, 48].

Statistical analysis

As each patient’s eyes were subject to different retinal conditions, each eye was considered a separate unit of analysis. Sample characteristics (mean, standard deviation, and range) with respect to age and visual acuity (logMAR) were calculated for all eyes across groups. We then performed linear regression models to estimate the mean differences in CCT scores for each cone class by ERM grade, AMD severity, and, among MS patients, by diagnosis of active optic neuritis and total RNFL thickness (G) or temporal RNFL octant thickness (T) each compared to healthy controls as the reference group. To assess RVO status, we used linear regression models to compare affected vs unaffected eye in each patient. All models were estimated using generalized estimating equations (GEE) to account for clustering within persons and adjusted for age, visual acuity and phakia. For each analysis, individual CCT score distributions for each cone class were visually compared using violin plots with overlying mean CCT score differences with 95% confidence intervals (CIs) for each group. Comparisons for significance were made with healthy controls using adjusted regression model estimates with Pearson’s r correlation coefficients (Additional file 4: Table S1). We conducted all analyses using R version 1.2 [32].

Results

Table 1 summarizes the distribution of age and visual acuity of all subjects. CCT results are represented in violin plots that follow (Figs. 2, 3, 4, 5). Each violin plot is a distribution of patients on the horizontal axis with the group CCT scores plotted from 0 to 150 on the vertical axis. The adjusted mean and 95% confidence interval for each plot are overlaid. Significant differences from healthy controls are represented by asterisks.

Table 1 Age and visual acuity demographics for healthy control eyes and various retinal disease states
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Fig. 2
figure 2

CCT in patients with MS compared to healthy controls. a CCT scores in eyes with and without a history of optic neuritis. b CCT scores in patients with RNFL thinning in the temporal (T) octant, or the average (G) of all octants. ON = Optic neuritis, RNFL = retinal nerve fiber layer. Estimated means (95% CI) are adjusted for age, visual acuity and phakic status. Asterisks indicate significant differences (vs healthy) at p < 0.05

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Fig. 3
figure 3

CCT scores in patients with age-related macular degeneration at different stages compared to healthy controls ≥ 64 years old. Estimated means (95% CI) are adjusted for age, visual acuity and phakic status. Asterisks indicate significant differences (versus healthy) at p < 0.05

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Fig. 4
figure 4

CCT scores in patients with epiretinal membranes increasing in severity compared to healthy controls ≥ 50 years old. Estimated means (95% CI) are adjusted for age, visual acuity and phakic status. Asterisks indicate significant differences (versus healthy) at p < 0.05

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Fig. 5
figure 5

CCT in patients with retinal vein occlusion. Estimated means (95% CI) are adjusted for age, visual acuity and phakic status. Asterisks indicate significant differences (vs healthy) at p < 0.05

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Multiple sclerosis

Not all patients with MS were able to complete CCT in both eyes as some patients had monocular vision loss which precluded test performance. MS patients with a history (9 eyes) and without a history (22 eyes) of ON demonstrated reduced CCT scores compared to the healthy control subject group. Likewise, MS was associated with statistically significant reductions in CCT scores for all cone classes even among those with normal RNFL, except for L-opsin in which normal RNFL was not associated with a significant reduction in CCT (Fig. 2). There was a downtrend in CCT performance in eyes with abnormal RNFL compared to normal RNFL across all 3 color cones that was not statistically significant. There were no statistically significant correlations between VA and CCT score or VA and RNFL.

Age-related macular degeneration

All classification stages for AMD, except early AMD, demonstrated significant (p < 0.05) reduction in CCT scores compared to healthy control eyes aged 64 and older (Fig. 3). Advanced AMD with or without neovascularization represents the largest reduction in CCT scores demonstrated by widening of the lowest portions of the violin plots. Additionally, no subjects had normal M-cone and L-cone CCT with rare patients in the neovascular AMD retaining some tritan vision (s-cone plot is taller for neovascular AMD than advanced non-neovascular AMD).

Epiretinal membranes

Two independent retina specialists classified subjects diagnosed on clinical exam and SD-OCT into ERM grades and we evaluated each group’s CCT results (Fig. 4). Each grade of ERM demonstrated a statistically significant reduction in CCT compared with healthy controls aged 50 and older (p < 0.05). Both S- and M-cones demonstrate a nominal reduction in CCT with advancing ERM grade which is not observed with the L-cone, though these differences by ERM grade are not statistically significant.

Retinal vein occlusion

All patients with RVO (n = 11) who were evaluated with CCT in this study had achieved steady state resolution of macular edema and had sufficient visual acuity scores to reliably complete CCT testing (ranging 20/25 to 20/100). All eleven patients (86%) had visual acuity of 20/60 or better (twice the minimum angle of resolution to reliably complete CCT testing). There was no significant correlation observed between visual acuity and CCT. RVO demonstrated reduced CCT for all 3 cone populations (Fig. 5). For example, one patient with 20/100 visual acuity had near zero CCT results which were similar to other eyes with 20/25 visual acuity. Another patient with 20/80 visual acuity had diminished, but not zero, CCT scores equivalent to other eyes affected by RVO and 20/25 vision.

Discussion

We analyzed cone contrast threshold testing of patients with a variety of diseases with differing pathophysiological mechanisms for vision loss. CCT performance has been shown to quantify contrast and color vision. For these various diseases, we sought to determine if CCT reveals diminished visual function beyond VA alone. We started by verifying color vision deficits in a disease for which color vision testing is performed as standard of care. Color vision testing is routinely performed in patients with optic neuropathies and diseases like MS which can present with optic neuritis. We then evaluated CCT testing in retinal diseases for which color and contrast vision is not routinely tested.

Multiple Sclerosis is associated with earlier and more pronounced color and contrast vision dysfunction compared to other eye diseases [33]. Color vision loss in MS was previously thought to occur secondary to ON due to direct damage to the optic nerve and resulting damage to the retinal ganglion cell layer [16]. More recently, retinal fiber nerve layer atrophy and reduced macular volume have been described in MS patients with no history of ON [16]. One theory suggests a secondary retinopathy in MS due to retrograde axonal degeneration [17].

Our study demonstrated that MS with no history of ON exhibited a statistically significant reduction in CCT compared to controls (Fig. 2a). This supports the theory that color vision loss occurs as a result of a separate disease process from optic nerve inflammation. The downtrend in CCT scores with abnormal RNFL compared to normal RNFL suggests a correlation between functional vision loss and RNFL, although a larger sample size is needed to further verify this relationship as it did not reach statistical significance (Fig. 2b).

The temporal octant of the optic nerve transmits visual signals from the fovea and perifovea. Thinning of the temporal octant is associated with a significant reduction in CCT scores, and the same is true for the global nerve fiber layer thickness in the optic nerve. Even after adjusting for visual acuity, visual quality subjectively declines, which is corroborated by a decline in CCT performance. Because global and temporal changes in RNFL thickness correlate with CCT reduction, but only the temporal RNFL serves CCT performance, changes in analogous visual quality features may continue in the eccentric and peripheral vision.

Age-related macular degeneration is characterized by the physical presence of drusen with an associated disruption in normal retinal anatomy, physiology, and vision [34]. Early AMD is functionally indistinguishable from normal aging [21]; however, intermediate disease produces reduced color and contrast sensitivity with poor low-light vision which can precede the onset of visual acuity loss. Advanced AMD extinguishes central visual acuity and contrast vision. Clinical trials directed at treating or slowing progression of diseases like non-neovascular (dry) AMD rely exclusively on subjective VA determinations and objective structural imaging [35]. Some new treatments show promise because they slow structural damage [36] while other potential treatments are discarded after multimillion dollar clinical trials because they do not show the same structural benefits [37]. While retinal structure and visual acuity do correlate, subjective measures of visual function extend beyond visual acuity to contrast sensitivity, color perception, and the ability to respond to changing lighting conditions (Additional file 1: Fig. S1). These other subjective visual function tests are not routinely performed because they are slow, require trained technical administration, demand reliable patient participation, and do not integrate easily with a busy clinic schedule.

AMD patients described in this report confirm similar findings to Cocce et. al [23]. with CCT results insignificantly changed in early AMD, but intermediate and advanced AMD yield large reductions in color vision. There is partial agreement with the data presented by Oza et. al [38]. which found significant CCT changes in all 3 color vision tests in intermediate AMD; they also found changes in early AMD when tracking patients over the course of 12 and 24 months, which was not in the scope of the current study. CCT may be used as a clinical endpoint for interventions directed at intermediate AMD and beyond. Inability for conventional testing to identify functional endpoints for early AMD highlights our communities need for novel assays sensitive to early disease.

Epiretinal membranes are thin avascular fibrocellular membranes which develop on the inner surface of the retina [22, 39]. ERMs can be asymptomatic or alter macular structure to produce metamorphopsia and reduced visual acuity [22,23,24]. SD-OCT studies of the ERM reveal retinal disruptions that may impair cone function such as blurred, interrupted, or absent cone outer segment tip lines (COST) [21]. Additionally, the ectopic inner foveal layers (EIFLs) within ERMs have been associated with significant visual function loss [31]. Disruptions of the COST line has been associated with macular diseases and may indicate photoreceptor dysfunction [40]. Recovery of the COST after ERM surgery correlates with better outcomes in VA, with COST thickness prior to ERM surgery correlating well to postoperative VA [41, 42]. While some patients subjectively report metamorphopsia and reduced acuity, others additionally report reduced quality in their vision (Additional file 2: Fig. S2). However, little is known about the qualitative changes in vision beyond visual acuity.

Utilizing CCT, we demonstrate significant color and contrast deficits in patients with ERM’s of mild to severe grade. While not statistically significant, there was a downtrend in CCT performance with worsening ERM grade in S and M cones and further research is warranted to determine if disease severity correlates with the degree of color and contrast vision loss.

Retinal vein occlusion remains one of the most investigated retinal disease conditions because intraocular anti-VEGF and steroid injections demonstrate profound improvements in retinal anatomy seen on OCT and visual acuity [43]. RVO, like diabetic retinopathy, is an inner retinal vascular disease affecting cells in the ganglion cell layer and inner nuclear layer. Clinical trials to treat eyes affected by RVO focus on visual acuity and OCT anatomy as the primary outcome for therapeutic success. However, patients who have recovered visual acuity suitable for reading or driving remain dissatisfied with the quality of their vision (Additional file 3: Fig. S3).

CCT testing in patients who have recovered optimal visual acuity and retinal anatomy highlights the residual loss of color and contrast vision in eyes affected by RVO when compared with unaffected fellow eyes. This finding was present for both eyes with 20/40 vision or better (n = 8), and eyes with vision worse than 20/40 (n = 6). CCT, therefore, presents a practical quantitative endpoint for therapies aimed at optimizing visual quality in addition to visual acuity. These results agree with Matsumoto et. al. [44], who demonstrated similar findings in statistically significant loss of all S, M, and L cones testing in eyes affected by RVO when compared to the healthy eye.

Overall, the data presented in this report demonstrates an agreement with previous studies that there are various disease states associated with reduced CCT scores. Improvement of S and M scores were seen after cataract surgery, suggesting worsening S and M CCT scores with cataract development.15 Worsened M and S CCT scores have been demonstrated in glaucoma. Our data demonstrated MS was associated with reductions in CCT scores, except for L-opsin in which MS patients with normal RNFL did not have significant reduction in CCT. Prior studies on AMD agreed with the current data that there are reductions in CCT scores across all cones in intermediate AMD and advanced AMD [23, 38]. We found no statistically significant changes in early AMD, which partially disagrees with Oza et. al [38]. who found changes in early AMD when tracking patients over time. Regarding ERM, our data demonstrated statistically significant worsened CCT scores across S, M, and L cones compared to healthy controls, however there was no statistically significant differences in scores across worsening ERM grades. Finally, we found worsened S, M, and L cone CCT scores in eyes affected by RVO compared to unaffected fellow eyes, which agrees with published studies [44].

Results of this study are likely impacted by its retrospective nature, and limited sample size, particularly for the higher grade ERM states. ETDRS testing was not used because all data was collected during standard course of care where the M&S technologies digital display for visual acuity testing. Additionally, it is worth noting that while healthy control eyes were restricted to age ranges of the corresponding AMD and ERM disease state eyes, there were statistically significant increases in the ages for intermediate, advanced, and neovascular AMD as well as trace ERM overall when compared to their healthy control groups. While this report highlights changes in color and contrast vision with disease, further prospective studies with larger sample sizes are warranted.

Conclusion

As one of the first studies to utilize CCT testing in MS, AMD, ERM, and RVO patients, we present novel quantitative data describing cone-specific visual function across all 3 cone classes in these disease states. We observed that inner retinal vascular and inner retinal mechanical disease states both diminish CCT test results, suggesting that CCT performance is affected by multiple mechanisms downstream of photoreceptors.

Availability of data and materials

The datasets generated and/or analyzed during the current study are available from the corresponding author on reasonable request.

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Acknowledgements

The authors would like to thank Donald Frambach MD for assistance with grading ERM and Konan medical for an unrestricted donation of ColorDX CCT devices.

Several abstracts were previously presented at American Academy of Ophthalmology Annual Meeting, Vancouver Canada, 2019.

Funding

This project was supported by the National Center for Research Resources and the National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, through RPB unrestricted grant to UCI Department of Ophthalmology.

Author information

Authors and Affiliations

  1. Department of Ophthalmology, Gavin Herbert Eye Institute, University of California, Irvine, CA, 92617, USA

    Itamar Livnat, Urmi V. Mehta, M. Cristina Kenney, Mitul C. Mehta, Chantal J. Boisvert, Wade R. Crow & Andrew W. Browne

  2. Center for Translational Vision Research, University of California, Irvine, CA, 92617, USA

    M. Cristina Kenney & Andrew W. Browne

  3. School of Medicine, University of California, Irvine, CA, 92617, USA

    Kayla M. White & Caroline R. Frambach

  4. Department of Biomedical Engineering, University of California, Irvine, CA, 92617, USA

    Andrew W. Browne

  5. Institute for Mathematical Behavioral Sciences, University of California, Irvine, CA, 92617, USA

    Kimberly A. Jameson

  6. Institute for Clinical and Translational Sciences University, Department of Physical Medicine and Rehabilitation, University of California, Irvine, CA, 92617, USA

    Anton M. Palma & Andrew W. Browne

  7. University of California, Irvine, CA, 92617, USA

    Clara Yuh

  8. Western University of Health Sciences, Pomona, CA, 91766, USA

    Urmi V. Mehta & Clara Yuh

  9. Medical College of Wisconsin, Wauwatosa, WI, 53226, USA

    John Doan

  10. Duke Eye Center, Department of Ophthalmology, Duke University School of Medicine, Durham, NC, 27705, USA

    Chantal J. Boisvert

  11. Case Western Reserve University Ophthalmology, 10900 Euclid Ave, Cleveland, OH, 44106, USA

    Kayla M. White

  12. Kaiser Permanente Santa Clara Internal Medicine, Santa Clara, CA, 95051, USA

    John Doan

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Contributions

KMW contributed to design of the work, acquisition/analysis/interpretation of data, and writing on the draft. IL contributed to interpretation of data and writing on the draft. CRF, JD, UVM, CY, AMP, KAJ contributed to design of the work and acquisition/analysis/interpretation of data. CK, MCM, CJB, WRC contributed to design of the work and acquisition/analysis/interpretation, revision of the draft. AWB contributed to design of the work, acquisition/analysis/interpretation of data, and writing on the draft. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Itamar Livnat.

Ethics declarations

Ethical approval and consent to participate

Institutional Review Board (IRB)/Ethics Committee approval was obtained. The study was conducted in accordance with the Declaration of Helsinki. The collection and evaluation of all protected patient health information was performed in a Health Insurance Portability and Accountability Act (HIPAA)-compliant manner.

Competing interests

The authors declare that there is no conflict of interests with respect to the research, authorship, and/or publication of this article.

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Supplementary Information

Additional file 1: Fig. S1.

94-year-old pseudophakic male with quiescent nvAMD in his right eye and non-nvAMD in his left eye. The patient reports that color blocks in the CCT report appear black in his right eye (VA: 20/40), and washed out in his 20/20 left eye (VA: 20/20).

Additional file 2: Fig. S2.

72-year-old pseudophakic female reports visual distortion and 20/40 vision OD with normal 20/20 vision OS. SD-OCT imaging of right eye demonstrates ERM with corresponding reduction in CCT. *Orange line denotes cut-off point for normal cone contrast scores.

Additional file 3: Fig. S3

. a) Fundus Autofluorescence images and visual acuities for 65-year-old phakic female who presented with acute onset blurry vision OD was found to have an inferior hemiretinal RVO and cystoid macular edema. b) After anti-VEGF therapy the patient’s vision improved from 20/60 to 20/30 but she remained very symptomatic for “poor” vision. CCT scores OD were significantly lower and near zero OD compared to OS even when visual acuity was 20/30 and 20/15.

Additional file 4:

Table S1. Regression model beta coefficients, 95% confidence intervals (CIs) and p-values for model predictors.

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White, K.M., Livnat, I., Frambach, C. et al. Quantitative cone contrast threshold testing in patients with differing pathophysiological mechanisms causing retinal diseases. Int J Retin Vitr 9, 9 (2023). https://doi.org/10.1186/s40942-023-00442-3

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Keywords

International Journal of Retina and Vitreous

ISSN: 2056-9920

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