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Biological corneal inlay for presbyopia derived from small incision lenticule extraction (SMILE)

Corneal inlays are a relatively new treatment option for presbyopia. Using biological inlays, derived from lenticules extracted from small incision lenticule extraction, may offer advantages over commercialized synthetic inlays in the aspect of biocompatibility. We conducted a non-human primate stud...

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Autores principales: Liu, Yu-Chi, Teo, Ericia Pei Wen, Ang, Heng Pei, Seah, Xin Yi, Lwin, Nyein Chan, Yam, Gary Hin Fai, Mehta, Jodhbir S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789881/
https://www.ncbi.nlm.nih.gov/pubmed/29382905
http://dx.doi.org/10.1038/s41598-018-20267-7
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author Liu, Yu-Chi
Teo, Ericia Pei Wen
Ang, Heng Pei
Seah, Xin Yi
Lwin, Nyein Chan
Yam, Gary Hin Fai
Mehta, Jodhbir S.
author_facet Liu, Yu-Chi
Teo, Ericia Pei Wen
Ang, Heng Pei
Seah, Xin Yi
Lwin, Nyein Chan
Yam, Gary Hin Fai
Mehta, Jodhbir S.
author_sort Liu, Yu-Chi
collection PubMed
description Corneal inlays are a relatively new treatment option for presbyopia. Using biological inlays, derived from lenticules extracted from small incision lenticule extraction, may offer advantages over commercialized synthetic inlays in the aspect of biocompatibility. We conducted a non-human primate study to evaluate the safety, predictability, efficacy and tissue response after autogeneic, decellularized xenogeneic and xenogeneic lenticule implantation. The lenticule implantation effectively resulted in central corneal steepening (simulated keratometric values increased by 1.8–2.3 diopters), central hyper-prolate changes (asphericity Q values changed by −0.26 to −0.36), corneal anterior surface elevation (7.7–9.3 μm) and reasonable effective zone (1.5–1.8 times of the lenticule physical diameter), with no differences among the three groups. Slit lamp microscopy, transmission electron microscopy, confocal microscopy, histology and immunohistochemistry analyses confirmed the biocompatibility of the autogeneic and decellularized lenticules, whereas one eye in the xenogeneic group developed corneal stromal rejection during the study period. Our results showed that lenticule implantation has the potential for the management of presbyopia, and provide the basis for future clinical studies. The decellularization process may increase the potential utilization of lenticules without changing the efficacy.
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spelling pubmed-57898812018-02-15 Biological corneal inlay for presbyopia derived from small incision lenticule extraction (SMILE) Liu, Yu-Chi Teo, Ericia Pei Wen Ang, Heng Pei Seah, Xin Yi Lwin, Nyein Chan Yam, Gary Hin Fai Mehta, Jodhbir S. Sci Rep Article Corneal inlays are a relatively new treatment option for presbyopia. Using biological inlays, derived from lenticules extracted from small incision lenticule extraction, may offer advantages over commercialized synthetic inlays in the aspect of biocompatibility. We conducted a non-human primate study to evaluate the safety, predictability, efficacy and tissue response after autogeneic, decellularized xenogeneic and xenogeneic lenticule implantation. The lenticule implantation effectively resulted in central corneal steepening (simulated keratometric values increased by 1.8–2.3 diopters), central hyper-prolate changes (asphericity Q values changed by −0.26 to −0.36), corneal anterior surface elevation (7.7–9.3 μm) and reasonable effective zone (1.5–1.8 times of the lenticule physical diameter), with no differences among the three groups. Slit lamp microscopy, transmission electron microscopy, confocal microscopy, histology and immunohistochemistry analyses confirmed the biocompatibility of the autogeneic and decellularized lenticules, whereas one eye in the xenogeneic group developed corneal stromal rejection during the study period. Our results showed that lenticule implantation has the potential for the management of presbyopia, and provide the basis for future clinical studies. The decellularization process may increase the potential utilization of lenticules without changing the efficacy. Nature Publishing Group UK 2018-01-30 /pmc/articles/PMC5789881/ /pubmed/29382905 http://dx.doi.org/10.1038/s41598-018-20267-7 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liu, Yu-Chi
Teo, Ericia Pei Wen
Ang, Heng Pei
Seah, Xin Yi
Lwin, Nyein Chan
Yam, Gary Hin Fai
Mehta, Jodhbir S.
Biological corneal inlay for presbyopia derived from small incision lenticule extraction (SMILE)
title Biological corneal inlay for presbyopia derived from small incision lenticule extraction (SMILE)
title_full Biological corneal inlay for presbyopia derived from small incision lenticule extraction (SMILE)
title_fullStr Biological corneal inlay for presbyopia derived from small incision lenticule extraction (SMILE)
title_full_unstemmed Biological corneal inlay for presbyopia derived from small incision lenticule extraction (SMILE)
title_short Biological corneal inlay for presbyopia derived from small incision lenticule extraction (SMILE)
title_sort biological corneal inlay for presbyopia derived from small incision lenticule extraction (smile)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789881/
https://www.ncbi.nlm.nih.gov/pubmed/29382905
http://dx.doi.org/10.1038/s41598-018-20267-7
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