Tear proteome profile in eyes with keratoconus after intracorneal ring segment implantation or corneal crosslinking

• Published in: Acta ophthalmologica (Oxford, England) Vol. 100; no. S275
• Main Authors: Goñi, Nahia, Martínez‐Soroa, Itziar, Ibarrondo, Oliver, Azkargorta, Mikel, Elortza, Felix, Galarreta, David, Bidaguren, Aritz, Juaristi, Leire, Acera, Arantxa
• Format: Journal Article
• Language: English
• Published: Malden Wiley Subscription Services, Inc 01.12.2022
• Subjects: A kinase-anchoring protein; Collagen; Cornea; Cytoskeleton; Immune response; Keratoconus; Kinases; Liquid chromatography; Mass spectroscopy; Patients; Protein biosynthesis; Proteins; Proteomes; Surgery; Tears
• ISSN: 1755-375X; 1755-3768
• DOI: 10.1111/j.1755-3768.2022.0520

Purpose: Intracorneal Ring Segment (ICRS) and Corneal collagen Crosslinking (CXL) are widely used treatments in keratoconus (KC) disease, but the alterations they cause in biomechanical mediators in the cornea, are still poorly understood. The aim of this study was to analyse the tear proteome profile before and after treatments to identify biomarkers altered by surgery. Methods: An observational, prospective, case–control pilot study was conducted, analysing tear samples from KC patients by nano‐liquid chromatography‐mass spectrometry (nLC‐MS/MS). Patients with KC who underwent ICRS surgery (n = 4), CXL (n = 4), and healthy subjects (CT, n = 4) were included in this study. Clinical parameters were measured and tear samples were collected before and 18 months after surgery. Proteins with ≥2 expression change and p‐value <0.05 between groups and times were selected to study their role in postoperative corneal changes. Results: These analyses led to the identification of 447 tear proteins. In comparisons between the two surgical groups and CTs, the biological processes that were altered in KC patients at baseline were those that were dysregulated as a consequence of the disease. Among the biological processes seen to be altered were: immune responses, cytoskeleton components, protein synthesis, and metabolic reactions. When comparing the two treatment groups, A‐kinase anchor protein 13 (AKAP‐13) was the most overexpressed protein before and after surgery in CXL group. Conclusions: The changes observed in tears after 18 months postoperatively could be due to the treatments performed and the pathology. Among the deregulated proteins detected, AKAP‐13 deserves special attention for its involvement in corneal thinning, and for its strong overexpression in the tears of patients with more active KC and faster disease progression. However, it should be kept in mind that this is a pilot study conducted on a small number of patients.