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      Revealing speckle obscured living human retinal cells with artificial intelligence assisted adaptive optics optical coherence tomography

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          Abstract

          Background

          In vivo imaging of the human retina using adaptive optics optical coherence tomography (AO-OCT) has transformed medical imaging by enabling visualization of 3D retinal structures at cellular-scale resolution, including the retinal pigment epithelial (RPE) cells, which are essential for maintaining visual function. However, because noise inherent to the imaging process (e.g., speckle) makes it difficult to visualize RPE cells from a single volume acquisition, a large number of 3D volumes are typically averaged to improve contrast, substantially increasing the acquisition duration and reducing the overall imaging throughput.

          Methods

          Here, we introduce parallel discriminator generative adversarial network (P-GAN), an artificial intelligence (AI) method designed to recover speckle-obscured cellular features from a single AO-OCT volume, circumventing the need for acquiring a large number of volumes for averaging. The combination of two parallel discriminators in P-GAN provides additional feedback to the generator to more faithfully recover both local and global cellular structures. Imaging data from 8 eyes of 7 participants were used in this study.

          Results

          We show that P-GAN not only improves RPE cell contrast by 3.5-fold, but also improves the end-to-end time required to visualize RPE cells by 99-fold, thereby enabling large-scale imaging of cells in the living human eye. RPE cell spacing measured across a large set of AI recovered images from 3 participants were in agreement with expected normative ranges.

          Conclusions

          The results demonstrate the potential of AI assisted imaging in overcoming a key limitation of RPE imaging and making it more accessible in a routine clinical setting.

          Plain language summary

          The retinal pigment epithelium (RPE) is a single layer of cells within the eye that is crucial for vision. These cells are unhealthy in many eye diseases, and this can result in vision problems, including blindness. Imaging RPE cells in living human eyes is time consuming and difficult with the current technology. Our method substantially speeds up the process of RPE imaging by incorporating artificial intelligence. This enables larger areas of the eye to be imaged more efficiently. Our method could potentially be used in the future during routine eye tests. This could lead to earlier detection and treatment of eye diseases, and the prevention of some causes of blindness.

          Abstract

          Das and colleagues develop and evaluate a parallel discriminator generative adversarial network (P-GAN) for improved in-vivo imaging of retinal cellular structures. The P-GAN network improves retinal pigment epithelium contrast 3.5-fold and the overall throughput 99-fold.

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          Most cited references61

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          U-Net: Convolutional Networks for Biomedical Image Segmentation

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            In situ click chemistry generation of cyclooxygenase-2 inhibitors

            Cyclooxygenase-2 isozyme is a promising anti-inflammatory drug target, and overexpression of this enzyme is also associated with several cancers and neurodegenerative diseases. The amino-acid sequence and structural similarity between inducible cyclooxygenase-2 and housekeeping cyclooxygenase-1 isoforms present a significant challenge to design selective cyclooxygenase-2 inhibitors. Herein, we describe the use of the cyclooxygenase-2 active site as a reaction vessel for the in situ generation of its own highly specific inhibitors. Multi-component competitive-binding studies confirmed that the cyclooxygenase-2 isozyme can judiciously select most appropriate chemical building blocks from a pool of chemicals to build its own highly potent inhibitor. Herein, with the use of kinetic target-guided synthesis, also termed as in situ click chemistry, we describe the discovery of two highly potent and selective cyclooxygenase-2 isozyme inhibitors. The in vivo anti-inflammatory activity of these two novel small molecules is significantly higher than that of widely used selective cyclooxygenase-2 inhibitors.
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              Image-to-Image Translation with Conditional Adversarial Networks

                Author and article information

                Contributors
                johnny@nih.gov
                Journal
                Commun Med (Lond)
                Commun Med (Lond)
                Communications Medicine
                Nature Publishing Group UK (London )
                2730-664X
                10 April 2024
                10 April 2024
                2024
                : 4
                : 68
                Affiliations
                [1 ]GRID grid.94365.3d, ISNI 0000 0001 2297 5165, National Eye Institute, , National Institutes of Health, ; Bethesda, MD 20892 USA
                [2 ]Center for Devices and Radiological Health, U.S. Food and Drug Administration, ( https://ror.org/007x9se63) Silver Spring, MD 20993 USA
                Author information
                http://orcid.org/0000-0001-9114-1455
                http://orcid.org/0000-0003-1645-5950
                http://orcid.org/0000-0003-2845-2490
                http://orcid.org/0000-0001-9864-3896
                http://orcid.org/0000-0003-0863-596X
                http://orcid.org/0000-0001-8019-2054
                http://orcid.org/0000-0003-0532-1914
                http://orcid.org/0000-0003-2300-0567
                Article
                483
                10.1038/s43856-024-00483-1
                11006674
                38600290
                ad18c416-29ea-4d17-b79c-597e11c46c1a
                © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2024

                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
                : 18 April 2023
                : 13 March 2024
                Funding
                Funded by: Intramural Research Program of the National Institutes of Health, National Eye Institute
                Categories
                Article
                Custom metadata
                © Springer Nature Limited 2024

                optical imaging,retina,three-dimensional imaging,interference microscopy

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