Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/113394
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dc.contributorSchool of Optometry-
dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.contributorResearch Centre for SHARP Vision-
dc.creatorMansoor, H-
dc.creatorLee, IXY-
dc.creatorLiu, C-
dc.creatorYu, M-
dc.creatorToh, CJL-
dc.creatorHsu, VWT-
dc.creatorLiu, F-
dc.creatorLu, D-
dc.creatorLam, TC-
dc.creatorTan, HC-
dc.creatorZhou, L-
dc.creatorYu-Chi Liu-
dc.date.accessioned2025-06-05T01:37:42Z-
dc.date.available2025-06-05T01:37:42Z-
dc.identifier.issn1542-0124-
dc.identifier.urihttp://hdl.handle.net/10397/113394-
dc.language.isoenen_US
dc.publisherElsevier Inc.en_US
dc.rights© 2025 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication Mansoor, H., Lee, I. X. Y., Liu, C., Yu, M., Toh, C. J. L., Hsu, V. W.-T., Liu, F., Lu, D., Lam, T. C., Tan, H. C., Zhou, L., & Liu, Y.-C. (2025). Fenofibrate ameliorates ocular surface inflammation in diabetic keratopathy. The Ocular Surface, 38, 31-40 is available at https://doi.org/10.1016/j.jtos.2025.05.010.en_US
dc.subjectApoptosisen_US
dc.subjectCorneaen_US
dc.subjectDiabetesen_US
dc.subjectFenofibrateen_US
dc.subjectInflammationen_US
dc.subjectOcular surfaceen_US
dc.titleFenofibrate ameliorates ocular surface inflammation in diabetic keratopathyen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage31-
dc.identifier.epage40-
dc.identifier.volume38-
dc.identifier.doi10.1016/j.jtos.2025.05.010-
dcterms.abstractPurpose: To investigate the efficacy of oral fenofibrate in the amelioration of ocular surface inflammation in diabetes mellitus (DM).-
dcterms.abstractMethods: In this open-label interventional study, 41 participants with type 2 DM received oral fenofibrate for 30 days. Forty age-matched healthy controls were recruited. Ocular surface objective and subjective assessment, in-vivo confocal microscopy (IVCM) imaging and quantification for corneal dendritic cells (DCs), epithelium and neuromas were performed. Tear inflammatory markers and proteomics were analyzed with enzyme-linked immunosorbent assay (ELISA) and Data Independent Acquisition experiments before and after treatment.-
dcterms.abstractResults: Oral fenofibrate treatment significantly improved tear film breakup time (p = 0.004), corneal staining evaluated with National Eye Institute-Corneal Fluorescein Staining scores (p = 0.005), and ocular surface symptoms assessed with the Ocular Surface Disease Index scores (p = 0.003), in DM patients. On IVCM, fenofibrate significantly reduced mean DC area (p = 0.01) and mean DC density (p = 0.02), while increasing mean DC elongation (p = 0.004) and length (p = 0.01), suggesting less DC activities. Fenofibrate also significantly increased corneal epithelial cell density (p = 0.04). 192 tear proteins were significantly altered after treatment. Fenofibrate significantly up-regulated the expression of anti-inflammatory interleukin-1 receptor antagonist, while significantly reduced the concentrations of pro-inflammatory and inflammatory proteins, including tumour necrosis factor α, nuclear factor kappa B, complement 4 B, cytochrome B5 Type A, and cytochrome B5 Type B (all p < 0.05) in tears, via regulation of tricarboxylic acid cycle, oxidative phosphorylation and liver X receptor/retinoid X receptor activation.-
dcterms.abstractConclusion: This first clinical trial demonstrated that oral fenofibrate ameliorates diabetic ocular surface inflammation, providing a novel therapeutic option for diabetic keratopathy.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationOcular surface, Oct. 2025, v. 38, p. 31-40-
dcterms.isPartOfOcular surface-
dcterms.issued2025-10-
dc.identifier.eissn1937-5913-
dc.description.validate202506 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera3633en_US
dc.identifier.SubFormID50532en_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextPolyU grant (P0043882)en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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