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      Gradients of refractive index in the crystalline lens and transient changes in refraction among patients with diabetes

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          Abstract

          Transient hyperopic refractive shifts occur on a timescale of weeks in some patients after initiation of therapy for hyperglycemia, and are usually followed by recovery to the original refraction. Possible lenticular origin of these changes is considered in terms of a paraxial gradient index model. Assuming that the lens thickness and curvatures remain unchanged, as observed in practice, it appears possible to account for initial hyperopic refractive shifts of up to a few diopters by reduction in refractive index near the lens center and alteration in the rate of change between center and surface, so that most of the index change occurs closer to the lens surface. Restoration of the original refraction depends on further change in the refractive index distribution with more gradual changes in refractive index from the lens center to its surface. Modeling limitations are discussed.

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          Most cited references30

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          Refractive index distribution and optical properties of the isolated human lens measured using magnetic resonance imaging (MRI).

          Using a non-invasive MRI technique for measuring the refractive index distribution through the crystalline lens, refractive index maps were obtained through 20 intact isolated human lenses (7-82years). Focal length measurements, obtained by simulated light ray propagation through each index map were found to be in agreement with direct measurements performed on a scanning laser apparatus. With increasing age, the refractive index profiles became flatter in the central region, accompanied by steepening of the profile in the periphery. This appears to be an important mechanism underlying the observed changes in power and longitudinal aberration of the human lens.
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            The lens in diabetes.

            This paper reviews the changes which occur in the human lens in diabetes. They include refractive changes and cataract and age-related increases in thickness, curvatures, light scattering, autofluorescence and yellowing. The incidence of cataract is greatly increased over the age of 50 years, slightly more so in women, compared with non-diabetics. Experimental models of sugar cataract provide some evidence for the mechanism of the uncommon, but morphologically distinct, juvenile form of human diabetic cataract, where an osmotic mechanism due to sugar alcohol accumulation has been thoroughly studied in diabetic or galactose-fed rats. The discrepancy between the ready accumulation of sugar alcohol in the lens in model systems and the very slow kinetics of aldose reductase (AR) has not been satisfactorily explained and suggests that the mechanism of polyol formation is not yet fully understood in mammalian systems. The activity of AR in the human lens lies mainly in the epithelium and there appears to be a marginal expectation that sufficient sorbitol accumulates in cortical lens fibres to explain the lens swelling and cataract on an osmotic basis. This is even more so in the cataracts of adult diabetics, which resemble those of age-related non-diabetic cataracts in appearance. The very low levels of sorbitol in adult diabetic lenses make an osmotic mechanism for the increased risk of cataract even less likely. Other mechanisms, including glycation and oxidative stress, are discussed. The occurrence of cataract is a predictor for increased mortality in the diabetic.
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              In vivo study of changes in refractive index distribution in the human crystalline lens with age and accommodation.

              Magnetic resonance imaging (MRI) was used to map the refractive index distribution in human eye lenses in vivo and to investigate changes with age and accommodation. Whole-eye MR images were obtained for sagittal and transverse axial planes in one eye each of 15 young (19-29 years) and 15 older (60-70 years) subjects when viewing a far ( approximately 6 m) target and at individual near points in the young subjects. Refractive index maps of the crystalline lens were calculated by using a procedure previously validated in vitro. A central high refractive index plateau region and sharp decline in refractive index at the periphery were seen in all three groups. The peripheral decline was steepest in the older lenses and least steep in the young accommodated lenses. Average lens thickness increased (+0.27 mm; P < 0.05) and equatorial diameter decreased (-0.35 mm; P < 0.05) with accommodation. Axial thickness (+0.96 mm; P < 0.05) and equatorial diameter (+0.28 mm; P < 0.05) increased with age. The central index (1.409 +/- 0.008) did not differ between groups. The axial thickness of the central plateau increased with age (+0.83 mm; P < 0.05) but not significantly with accommodation. The equatorial diameter of the central plateau increased with age (+0.56 mm; P < 0.01) and decreased with accommodation (-0.43 mm; P < 0.05). The refractive index of the central plateau region does not change significantly with accommodation or ageing, but its size increases with age and the peripheral decline in refractive index becomes steeper in older lenses.
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                Author and article information

                Journal
                Biomed Opt Express
                Biomed Opt Express
                BOE
                Biomedical Optics Express
                Optical Society of America
                2156-7085
                31 October 2012
                01 December 2012
                31 October 2012
                : 3
                : 12
                : 3033-3042
                Affiliations
                [1 ]Faculty of Life Sciences, University of Manchester, Manchester M13 9PT, UK
                [2 ]School of Optometry & Vision Science and Institute of Health & Biomedical Innovation, Queensland University of Technology, 60 Musk Avenue, Kelvin Grove Q 4059, Australia
                Author notes
                Article
                173378
                10.1364/BOE.3.003033
                3521312
                23243557
                22371227-bdaf-43d1-b0a9-2fb656a3467e
                ©2012 Optical Society of America

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially.

                History
                : 27 July 2012
                : 6 October 2012
                : 16 October 2012
                Categories
                Ophthalmology Applications
                Custom metadata
                True
                0

                Vision sciences
                (330.4460) ophthalmic optics and devices,(330.7326) visual optics, modeling

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