Mediators of Corneal Haze Following Implantation of Presbyopic Corneal Inlays

To identify protein mediators of corneal haze following presbyopic corneal inlay surgery. Tears were collected from eyes with corneal haze following surgery with a shape-changing corneal inlay. Samples were subjected to quantitative proteomic analysis using iTRAQ and proteins significantly increased...

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Veröffentlicht in:Investigative ophthalmology & visual science 2019-03, Vol.60 (4), p.868-876
Hauptverfasser: Fenner, Beau J, Liu, Yu-Chi, Koh, Siew Kwan, Gao, Yan, Deng, Lu, Beuerman, Roger W, Zhou, Lei, Theng, Julian T S, Mehta, Jodhbir S
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Sprache:eng
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Zusammenfassung:To identify protein mediators of corneal haze following presbyopic corneal inlay surgery. Tears were collected from eyes with corneal haze following surgery with a shape-changing corneal inlay. Samples were subjected to quantitative proteomic analysis using iTRAQ and proteins significantly increased or decreased (1.3-fold or more) in haze eyes relative to fellow eyes were identified. Expression ratios were compared to postoperative eyes without corneal haze to identify proteins selectively increased or decreased in corneal haze eyes. Inlay-associated haze occurred in 35% of eyes (6 of 17). Of 1443 unique tear proteins identified, eight proteins were selectively reduced in tears from postoperative haze eyes and one protein selectively increased. Proteins reduced in haze eyes included complement 4a (level relative to nonhaze eyes 0.464, P = 0.037), complement factor H (0.589, P = 0.048), immunoglobulin kappa variable 2-29 (0.128, P = 0.006), immunoglobulin kappa variable 2D-28 (0.612, P = 0.025), immunoglobulin lambda variable 7-46 (0.482, P = 0.007), S100 calcium binding protein A4 (0.614, P = 0.048), Shootin-1 (0.614, P = 0.048), and tissue inhibitor of metalloproteinase-1 (0.736, P = 0.023). The Xaa-Pro aminopeptidase 1 was increased in haze eyes relative to nonhaze eyes (1.517, P = 0.023). Corneal haze following corneal inlay surgery is associated with reduction in levels of known inflammatory and immune mediators. These findings represent a starting point for elucidation of pathways involved in corneal haze following synthetic inlay implantation and may enable development of targeted therapies that modulate the haze response.
ISSN:1552-5783
1552-5783
DOI:10.1167/iovs.18-25761