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      Vitrectomized versus non-vitrectomized eyes in diabetic macular edema response to ranibizumab—retinal layers thickness as prognostic biomarkers

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          Abstract

          To evaluate the role of the vitreous in the management of diabetic macular edema with ranibizumab intravitreal injections in a pro re nata regimen. Prospective study of 50 consecutive eyes with diabetic macular edema treated with ranibizumab and 12 months of follow-up. Primary endpoint: to assess differences between non-vitrectomized and vitrectomized eyes in the number injections needed to control the edema. Secondary endpoints: comparison of groups regarding best corrected visual acuity, central foveal thickness and thickness of seven retinal layers. 46 eyes from 38 patients, 10 vitrectomized and 36 non-vitrectomized, completed the follow-up. At month 12, the two groups achieved an equivalent anatomical outcome and needed a similar number of ranibizumab intravitreal injections. In vitrectomized eyes final visual acuity was worse when baseline retinal nerve fiber layers in the central foveal subfield were thicker, showing a strong correlation (r = − 0.942, p < 0.001). A similar, albeit moderate correlation was observed in non-vitrectomized eyes (r = − 0.504, p = 0.002). A decrease of retinal nerve fiber layers inner ring thickness was correlated with a better final visual acuity only in vitrectomized eyes (r = 0.734, p = 0.016). The effect of diabetic macular edema seems to be worse in vitrectomized eyes, with a thinner inner retina reservoir.

          Clinicaltrials.govNCT04387604.

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          Most cited references40

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          Guidelines for the Management of Diabetic Macular Edema by the European Society of Retina Specialists (EURETINA)

          Diabetic retinal disease is envisioned to become the plague of the coming decades with a steep increase of worldwide diabetes incidence followed by a substantial rise in retinal disease. Improvements in diagnostic and therapeutic care have to cope with this dilemma in a clinically and socioeconomically efficient manner. Laser treatment has found a less destructive competitor in pharmacological treatments. As a consequence of recent rigorous clinical trials, laser photocoagulation is no longer recommended for the treatment of diabetic macular edema (DME), and anti-vascular endothelial growth factor therapy has emerged as first-line therapy. Steroids have maintained a role in the management of chronically persistent DME. The paradigm shifts in therapy are accompanied by a substantial break-through in diagnostics. The following guidance for the management of DME has been composed from the best updated knowledge of leading experts in Europe and represents another volume in the series of EURETINA recommendations for the management of retinal disease.
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            Neurodegeneration in diabetic retinopathy: does it really matter?

            The concept of diabetic retinopathy as a microvascular disease has evolved, in that it is now considered a more complex diabetic complication in which neurodegeneration plays a significant role. In this article we provide a critical overview of the role of microvascular abnormalities and neurodegeneration in the pathogenesis of diabetic retinopathy. A special emphasis is placed on the pathophysiology of the neurovascular unit (NVU), including the contributions of microvascular and neural elements. The potential mechanisms linking retinal neurodegeneration and early microvascular impairment, and the effects of neuroprotective drugs are summarised. Additionally, we discuss how the assessment of retinal neurodegeneration could be an important index of cognitive status, thus helping to identify individuals at risk of dementia, which will impact on current procedures for diabetes management. We conclude that glial, neural and microvascular dysfunction are interdependent and essential for the development of diabetic retinopathy. Despite this intricate relationship, retinal neurodegeneration is a critical endpoint and neuroprotection, itself, can be considered a therapeutic target, independently of its potential impact on microvascular disease. In addition, interventional studies targeting pathogenic pathways that impact the NVU are needed. Findings from these studies will be crucial, not only for increasing our understanding of diabetic retinopathy, but also to help to implement a timely and efficient personalised medicine approach for treating this diabetic complication. Electronic supplementary material The online version of this article (10.1007/s00125-018-4692-1) contains a slideset of the figures for download, which is available to authorised users.
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              Aflibercept, Bevacizumab, or Ranibizumab for Diabetic Macular Edema: Two-Year Results from a Comparative Effectiveness Randomized Clinical Trial.

              To provide 2-year results comparing anti-vascular endothelial growth factor (VEGF) agents for center-involved diabetic macular edema (DME) using a standardized follow-up and retreatment regimen.
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                Author and article information

                Contributors
                bbtpessoa@gmail.com
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                29 November 2021
                29 November 2021
                2021
                : 11
                : 23055
                Affiliations
                [1 ]GRID grid.5808.5, ISNI 0000 0001 1503 7226, Departamento de Oftalmologia, Hospital de Santo António, , Centro Hospitalar Universitário do Porto, ; Largo Prof. Abel Salazar—Edifício Neoclássico, 4099-001 Porto, Portugal
                [2 ]GRID grid.5808.5, ISNI 0000 0001 1503 7226, Instituto de Ciências Biomédicas Abel Salazar (ICBAS), , Universidade do Porto, ; Porto, Portugal
                [3 ]Departamento de Oftalmologia, Hospital de Santa Maria Maior de Barcelos, Barcelos, Portugal
                [4 ]GRID grid.9983.b, ISNI 0000 0001 2181 4263, Instituto de Saúde Ambiental, Faculdade de Medicina, , Universidade de Lisboa, ; Lisbon, Portugal
                [5 ]GRID grid.28911.33, ISNI 0000000106861985, Centro Hospitalar e Universitário de Coimbra, ; Coimbra, Portugal
                [6 ]GRID grid.8051.c, ISNI 0000 0000 9511 4342, Faculty of Medicine, , University of Coimbra, ; Coimbra, Portugal
                [7 ]GRID grid.422199.5, ISNI 0000 0004 6364 7450, Association for Innovation and Biomedical Research On Light and Image, ; Coimbra, Portugal
                Article
                2532
                10.1038/s41598-021-02532-4
                8630028
                34845300
                35a14ed4-779f-40f9-8395-91ce13a6b2e4
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 10 January 2021
                : 13 October 2021
                Categories
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                © The Author(s) 2021

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                medical research,biomarkers
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                medical research, biomarkers

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