Enhancement of Under Corrected Visual Acuity and Contrast Sensitivity in Myopic Children Using NeuroVision’s Neural Vision Correction (NVC) Technology.

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Enhancement of Under Corrected Visual Acuity and Contrast Sensitivity in Myopic Children Using NeuroVision’s Neural Vision Correction (NVC) Technology Kit Ian 1, Donald Tan 2,3,4, Allan Fong 2,3, Wei Han Chua 2,3 R&D Dept, Essilor R&D Centre Singapore 1 ; Singapore Eye Research Institute (SERI) 2 ; Singapore National Eye Centre (SNEC) 3 ; Department of Ophthalmology, Yong Loo Lin School of Medicine, National University of Singapore 4 Figure 1. UBM images of a patient demonstrating plateau iris pre- and post-LI in the inferior quadrant Figure 2. UBM images of a patient showing plateau iris pre- LI only in the temporal quadrant Figure 3. UBM images of a patient demonstrating plateau iris post- LI only in the temporal quadrant Singapore Eye Research Institute Introduction NeuroVision™ NVC vision correction technology is a non-invasive, patient-specific treatment based on visual stimulation and facilitation of neural connections responsible for vision. The technology involves the use of an internet-based computer generated visual training exercise regime using sets of patient specific stimuli based on Gabor patches, to sharpen contrast sensitivity and visual acuity. Children with highly progressive Myopia often use under-corrected eyeglasses, due to: improper prescription, intentional under-correction or simply due to the high progression of their Myopia. We evaluated the efficacy of NVC treatment in the enhancement of under-corrected visual acuity and contrast sensitivity function in Myopic children in Singapore. We also monitored the Myopia progression in these children for a 12 months period after the end of the NVC treatment. Scientific Background Cortical neurons in the visual cortex function as highly specialized image analyzers or filters, responding only to specific parameters of a visual image, such as orientation and spatial frequency, and visual processing involves the integrated activity of many neurons, with inter-neural interactions effecting both excitation and inhibition 1. Visual contrast activates neurons involved in vision processing, and neural interactions determine the sensitivity for visual contrast at each spatial frequency, and the combination of neural activities set Contrast Sensitivity Function (CSF) 1,2. The relationship between neuronal responses and perception are mainly determined by the signal-to-noise ratio (S/N ratio) of neuronal activity, and the brain pools responses across many neurons to average out noisy activity of single cells, thus improving S/N ratio, leading to improved visual performance and acuity 3. Studies have shown that the noise of individual neurons can be brought under experimental control by appropriate choice of stimulus conditions, and CSF can be increased dramatically through control of stimulus parameters 4-8. This precise control of stimulus conditions leading to increased neuronal efficiency is fundamental in initiating the neural modifications that are the basis for brain plasticity 9,10. Brain plasticity (the ability to adapt to changed conditions in acquiring new skills) has been demonstrated in many basic tasks, with evidence pointing to physical modifications in the adult cortex during repetitive performance NeuroVision’s technology probes specific neuronal interactions, using a set of patient- specific stimuli that improve neuronal efficiency 6,13 and induce improvement of CSF due to a reduction of noise and increase in signal strength. As visual perception quality depends both on the input received through the eye and the processing in the visual cortex, NeuroVision’s technology compensates for blurred (myopic) inputs, coming from the retina, by enhancing neural processing. Technology Implementation The building block of these visual stimulations is the Gabor patch (Figure 1), which efficiently activates and matches the shape of receptive field in the Visual Cortex. Figure 1: The Gabor Patch Myopic Children In Singapore The Singapore Cohort Study of the Risk factors for Myopia (SCORM) found that about 50% of Myopic children (age 7-9) do not wear proper eyeglasses prescription. 57% out of these children have a 6/12 or worse VA in both eyes. Out of the 50% Myopic children who do use a proper prescription, 47% have a 6/9 or worse VA in at least one of their eyes. According to the SCORM study, the Myopia progression in Myopic Children (At least -1.0D in both eyes) age 7 to 9 is: 0.944D a year. This rapid progression of Myopia means that effectively children in Singapore are most of the time significantly under-corrected even when they are annually prescribed with new corrective eyeglasses. In this pilot study we evaluated: 1)The efficacy of the NeuroVision NVC technology in enhancing quality of vision ie. under- corrected visual acuity (UC-VA) and contrast sensitivity function (UC-CSF) in myopic children when they use an under-corrected prescription 2)The progression rate of Myopia in children who use daily a significantly under-corrected prescription (by approximately 1D) after completion of the NeuroVision NVC treatment. Methods 33 children aged 7 to 9 having a myopic refraction of at least -1.0DS in both eyes (mean cycloplegic SE of -2.88D, range -1.0D to -6.00D) completed NVC treatment over a period of 3-4 months. During the course of treatment, subjects were prescribed with eyeglasses that are 0.5D under their full manifest refraction. Investigations included: manifest and cycloplegic refraction, axial length measurements and under-Corrected (1.0DS) VA and CSF. Investigation were done pre- and post- NeuroVision treatment and every 3 months for the period of 12 months following the end of treatment. After the end of the NVC treatment, children were prescribed with the highest possible under- correction that allows them a 6/12 binocular VA. 27 Children have been followed up for a complete 12 month period while wearing daily the new under-corrected prescription. Results Baseline Under-Corrected (1D Spheric) was 0.47 logMAR, improving by 2.2 lines to logMAR at the end of the treatment. 83% of the participants achieved the treatment success criteria (2 lines of improvement in at least one of their eyes). Contrast Sensitivity improved in all spatial frequencies as shown in Figure 3. At the end of the NVC treatment, children were prescribed with an average under- correction of 1.147D, allowing them an average binocular VA of 0.22 logMAR. Table 1 details the Myopia progression during 12 months post end of the treatment. Figure 3: Contrast Sensitivity improvement at the end of the treatment Spatial Frequency UCVA=20/25 UCVA=20/44 End of Treatment Baseline Average change in same age group in SCORM Change in this Study 12 months Post treatment End of TreatmentInvestigation N/A-0.52D-3.57D-3.05DManifest Subjective N/A-0.50D-3.53D-3.03DCycloplegic Subjective -0.94D-0.68D-3.89D-3.12DCycloplegic Objective 0.40mm0.32mm24.81mm24.49mmAxial Length Table 1 – Myopia progression during 12 months post treatment end Conclusions Results of the NVC treatment suggest that this technology is able to improve under- corrected VA and CSF in myopic children. It appears to allow functional quality of vision even when the children use a significantly under-corrected prescription. It appears that using NeuroVision treatment followed by prescription of significantly under-corrected eyewear may slow down the progression of Myopia. We are in the planning stage of a large randomized controlled trial involving myopic Singaporean school children to validate these findings. References 1.Hubel, D. H. & Wiesel, T. N. Receptive fields, binocular interaction and functional architecture in the cat's visual cortex. J. Physiol. (Lond.) 160, (1962). 2.Polat, U. Functional architecture of long-range perceptual interactions. Spat Vis 12, (1999). 3.Geisler, W. S. & Albrecht, D. G. Visual cortex neurons in monkeys and cats: detection, discrimination, and identification. Vis Neurosci 14, (1997). 4.Kasamatsu, T., Polat, U., Pettet, M. W. & Norcia, A. M. Colinear facilitation promotes reliability of single-cell responses in cat striate cortex. Exp Brain Res 138, (2001). 5.Polat, U., Mizobe, K., Pettet, M. W., Kasamatsu, T. & Norcia, A. M. Collinear stimuli regulate visual responses depending on cell's contrast threshold. Nature 391, (1998). 6.Polat, U. & Sagi, D. Spatial interactions in human vision: from near to far via experience- dependent cascades of connections. Proc Natl Acad Sci U S A 91, (1994). 7.Polat, U. & Sagi, D. Lateral interactions between spatial channels: suppression and facilitation revealed by lateral masking experiments. Vision Res 33, (1993). 8.Polat, U. & Sagi, D. The architecture of perceptual spatial interactions. Vision Res 34, 73-8 (1994). 9.Dosher, B. A. & Lu, Z. L. Perceptual learning reflects external noise filtering and internal noise reduction through channel reweighting. Proc Natl Acad Sci U S A 95, (1998). 10.Dosher, B. A. & Lu, Z. L. Mechanisms of perceptual learning. Vision Res 39, (1999). 11.Sagi, D. & Tanne, D. Perceptual learning: learning to see. Curr Opin Neurobiol 4, (1994). 12.Gilbert, C. D. Adult Cortical Dynamics. Physiological Reviews 78, (1998). 13.Polat, U. & Sagi, D. in Maturational Windows and Adult Cortical Plasticity (eds. Julesz, B. & Kovâcs, I.) 1-15 (Addison-Wesley, 1995). 14.Polat, U., Ma-Naim, T. Belkin, M. Sagi, D. Improving vision in adult amblyopia by perceptual learning. PNAS 101, (2004). The fundamental stimulation-control technique is called “Lateral Masking”, where collinearly oriented flanking Gabors are displayed in addition to the target Gabor image. The patient is exposed to two short displays in succession, in a random order; the patient identifies which display contains the target Gabor image (Figure 2). Audio feedback is provided with an incorrect response. The task is repeated and a staircase is applied until the patient reaches their visual threshold level. The NeuroVision System The NeuroVision System is a software-based, interactive system tailored and continuously adaptive to the individual visual abilities. In the first stage, the subject is exposed to a set of visual perception tasks, aimed to analyze and identify each subject’s neural inefficiencies or deficiencies. Based on this analysis, a treatment plan is initialized, and subject specificity is achieved by administering patient-specific stimuli in a controlled environment. Each session is designed to train, directly and selectively, those functions in the visual cortex, which were diagnosed to be further enhanced. At each session an algorithm analyzes the patient's responses and accordingly adjusts the level of visual difficulty to the range most effective for further improvement. Between sessions, the progress of the patient is taken into account by the algorithm for the next session generation. Thus, for each subject an individual training schedule is designed based on the initial state of visual performance, severity of dysfunction and progress in course of treatment. The treatment is applied in successive 30- minute sessions, administered 2-3 times a week, a total of approximately 30 sessions. Every 5 sessions, subject’s visual acuity is tested in order to continuously monitor subject’s progress. The average entire treatment duration is around 3 months. Figure 2: Lateral Masking images Program Number: 1435 Commercial Relationships: K. Ian, Essilor, E; D.Tan, SERI, SNEC, NUS, N; A. Fong, SERI, SNEC, N; W.H. Chua, SERI, SNEC, N.