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      Retinal neurodegeneration may precede microvascular changes characteristic of diabetic retinopathy in diabetes mellitus

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          Significance

          Diabetic retinopathy (DR), a primary cause of blindness, is characterized by microvascular abnormalities. Recent evidence suggests that retinal diabetic neuropathy (RDN) also occurs in people with diabetes, but little is known about the temporal relationship between DR and RDN. This longitudinal study in people with diabetes with no or minimal DR shows that RDN precedes signs of microvasculopathy and that RDN is progressive and independent of glycated hemoglobin, age, and sex. This finding was further confirmed in human donor eyes and in two experimental mouse models of diabetes. The results suggest that RDN is not ischemic in origin and represent a shift in our understanding of the pathophysiology of this complication of diabetes that potentially affects vision in all people with diabetes mellitus.

          Abstract

          Diabetic retinopathy (DR) has long been recognized as a microvasculopathy, but retinal diabetic neuropathy (RDN), characterized by inner retinal neurodegeneration, also occurs in people with diabetes mellitus (DM). We report that in 45 people with DM and no to minimal DR there was significant, progressive loss of the nerve fiber layer (NFL) (0.25 μm/y) and the ganglion cell (GC)/inner plexiform layer (0.29 μm/y) on optical coherence tomography analysis (OCT) over a 4-y period, independent of glycated hemoglobin, age, and sex. The NFL was significantly thinner (17.3 μm) in the eyes of six donors with DM than in the eyes of six similarly aged control donors (30.4 μm), although retinal capillary density did not differ in the two groups. We confirmed significant, progressive inner retinal thinning in streptozotocin-induced “type 1” and B6.BKS(D)-Lepr db /J “type 2” diabetic mouse models on OCT; immunohistochemistry in type 1 mice showed GC loss but no difference in pericyte density or acellular capillaries. The results suggest that RDN may precede the established clinical and morphometric vascular changes caused by DM and represent a paradigm shift in our understanding of ocular diabetic complications.

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          Most cited references39

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          Diabetic retinopathy: seeing beyond glucose-induced microvascular disease.

          Diabetic retinopathy remains a frightening prospect to patients and frustrates physicians. Destruction of damaged retina by photocoagulation remains the primary treatment nearly 50 years after its introduction. The diabetes pandemic requires new approaches to understand the pathophysiology and improve the detection, prevention, and treatment of retinopathy. This perspective considers how the unique anatomy and physiology of the retina may predispose it to the metabolic stresses of diabetes. The roles of neural retinal alterations and impaired retinal insulin action in the pathogenesis of early retinopathy and the mechanisms of vision loss are emphasized. Potential means to overcome limitations of current animal models and diagnostic testing are also presented with the goal of accelerating therapies to manage retinopathy in the face of ongoing diabetes.
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            Death of retinal neurons in streptozotocin-induced diabetic mice.

            Neuronal cell death has been reported in retinas of humans with diabetic retinopathy and in diabetic rat models. Little is known about neuronal cell death in mouse models of diabetic retinopathy. This study was designed to determine whether neurons are lost in diabetic mouse retinas and whether the loss involves an apoptotic process. Three-week-old C57Bl/6 mice were made diabetic with streptozotocin. They were studied over the course of 14 weeks after onset of diabetes. Eyes were processed for morphometric analysis and detection of apoptotic cells by TUNEL analysis and activated caspase-3 and were subjected to electron microscopy. Morphometric analysis of retinal cross sections of mice that had been diabetic 14 weeks showed approximately 20% to 25% fewer cells in the ganglion cell layer compared with age-matched control mice. There was a modest, but significant, decrease in the thickness of the whole retina and the inner and outer nuclear layers in mice that had been diabetic for 10 weeks. TUNEL analysis and detection of active caspase-3 revealed that cells of the ganglion cell layer were dying by apoptosis. Electron microscopic analysis detected morphologic features characteristic of apoptosis, including margination of chromatin and crenated nuclei of cells in the ganglion cell layer. The data suggest that in diabetic mouse retinas, neurons in the ganglion cell layer die, and this death occurs through an apoptotic pathway. Diabetic mice may be appropriate and valuable models for studies of neuronal cell death in diabetes. Copyright Association for Research in Vision and Ophthalmology
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              Effects of age, sex, and axial length on the three-dimensional profile of normal macular layer structures.

              To identify sex-related differences and age-related changes in individual retinal layer thicknesses in a population of healthy eyes across the lifespan, using spectral domain optical coherence tomography (SD-OCT). In seven institutes in Japan, mean thicknesses of the retinal nerve fiber layer (RNFL), ganglion cell layer (GCL), inner plexiform layer (IPL), inner nuclear layer (INL), outer plexiform layer (OPL), outer nuclear layer (ONL), photoreceptor inner segment (IS), and photoreceptor outer segment (OS) were measured using SD-OCT with a new automated segmentation protocol in 256 healthy subjects. Interoperator coefficients of variability for measurements of each layer ranged from 0.012 to 0.038. The RNFL, GCL, IPL, and INL were thinnest in the foveal area, whereas the OPL+ONL and OS were thickest in this area. Mean thicknesses of the INL and the OPL+ONL were significantly greater in men (P = 0.002 and 0.001, respectively). However, mean RNFL thickness was greater in women (P = 0.006). Thicknesses of the RNFL, GCL, IPL, INL, and IS correlated negatively with age. Thickness of the OPL+ONL was not correlated with age, and thickness of the OS correlated positively with age. Inner retinal (RNFL+GCL+IPL) thickness over the whole macula correlated negatively with age (P < 0.001), but outer retinal (OPL+ONL+IS+OS) thickness did not. Thicknesses of layers did not correlate with axial length. Macular layer thicknesses measured on SD-OCT images in healthy eyes showed significant variations by sex and age. These findings should inform macular layer thickness analyses in SD-OCT studies of retinal diseases and glaucoma.
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                Author and article information

                Journal
                Proc Natl Acad Sci U S A
                Proc. Natl. Acad. Sci. U.S.A
                pnas
                pnas
                PNAS
                Proceedings of the National Academy of Sciences of the United States of America
                National Academy of Sciences
                0027-8424
                1091-6490
                10 May 2016
                25 April 2016
                : 113
                : 19
                : E2655-E2664
                Affiliations
                [1] aStephen A. Wynn Institute for Vision Research, Department of Ophthalmology, University of Iowa , Iowa City, IA 52242;
                [2] bDepartment of Ophthalmology, Academic Medical Center, University of Amsterdam , 1105 AZ Amsterdam, The Netherlands;
                [3] cDepartment of Global Health, Academic Medical Center, University of Amsterdam , 1105 AZ Amsterdam, The Netherlands;
                [4] d Oogziekenhuis Rotterdam , 3011 BH Rotterdam, The Netherlands;
                [5] eDepartment of Endocrinology, Academic Medical Center, University of Amsterdam , 1105 AZ Amsterdam, The Netherlands;
                [6] fIowa Institute for Biomedical Imaging, University of Iowa , Iowa City, IA 52242;
                [7] gDepartment of Electrical and Computer Engineering, University of Iowa , Iowa City, IA 52242;
                [8] hDepartment of Biomedical Engineering and Physics, Academic Medical Center, University of Amsterdam , 1105 AZ Amsterdam, The Netherlands;
                [9] iIowa City VA Health Care System , Iowa City, IA 52246;
                [10] jDepartment of Biomedical Engineering, University of Iowa, Iowa City, IA 52242
                Author notes
                2To whom correspondence should be addressed. Email: michael-abramoff@ 123456uiowa.edu .

                Edited by Artur V. Cideciyan, University of Pennsylvania, Philadelphia, PA, and accepted by the Editorial Board March 23, 2016 (received for review December 17, 2015)

                Author contributions: E.H.S., H.W.v.D., C.J., J.H.D., R.O.S., F.D.V., and M.D.A. designed research; E.H.S., H.W.v.D., C.J., P.H.B.K., W.J., N.D., A.G., F.W., M.K., M.E.J.v.V., J.H.D., R.F.M., M.H.K., R.O.S., F.D.V., and M.D.A. performed research; M.S. and M.D.A. contributed new reagents/analytic tools; E.H.S., C.J., F.W., F.D.V., and M.D.A. analyzed data; E.H.S., H.W.v.D., F.D.V., and M.D.A. wrote the paper; H.W.v.D., C.J., P.H.B.K., W.J., N.D., A.G., M.K., M.E.J.v.V., R.F.M., M.H.K., F.D.V., and M.D.A. managed data acquisition; and E.H.S., C.J., F.W., R.F.M., M.H.K., R.O.S., M.S., F.D.V., and M.D.A. provided administrative, technical, or material support.

                1E.H.S. and H.W.v.D. contributed equally to this work.

                Article
                PMC4868487 PMC4868487 4868487 201522014
                10.1073/pnas.1522014113
                4868487
                27114552
                176d1edc-467a-452d-a597-e4790998844f
                History
                Page count
                Pages: 10
                Funding
                Funded by: HHS | NIH | National Eye Institute (NEI) 100000053
                Award ID: R01EY018853
                Funded by: HHS | NIH | National Eye Institute (NEI) 100000053
                Award ID: R01EY019112
                Funded by: HHS | NIH | National Eye Institute (NEI) 100000053
                Award ID: R01EY016379
                Funded by: HHS | NIH | National Eye Institute (NEI) 100000053
                Award ID: R01EY017066
                Funded by: HHS | NIH | National Institute of Biomedical Imaging and Bioengineering (NIBIB) 100000070
                Award ID: R01EB004640
                Categories
                PNAS Plus
                Biological Sciences
                Medical Sciences
                PNAS Plus

                retina,diabetes,neurodegeneration,diabetic retinopathy,optical coherence tomography

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