Aims/Purpose: Pseudoexfoliation glaucoma (PEG), is the most prevalent of the secondary glaucomas, characterized by the accumulation of fibrillar extracellular material in the anterior eye chamber. The miRNAs are regulators of gene expression, as epigenetic effectors. Our aim is to identify candidate miRNAs that may be involved in PEG physiopathology.Methods: A collaborative, longitudinal, prospective, case‐control study was set up in 120 participants, of both sexes, that were classified as: PEG patients (n = 60) and healthy individuals (CG n = 60). Sociodemographic and opththalmologic data were recorded. Aqueous humor was collected at the onset of glaucoma surgery, labelled and stored at. ‐80° until processing. Total ARN was obtained, and expression and quantitation of the miRNAs ‐122‐5p, ‐146a‐5p and ‐320a‐3p, were assayed by real time quantitative polimerase chain reaction (RT qPCR) in both study groups. Databases DIANA TOOLS, miRDB, TargetScanHuman 7.2 were used to connect the target genes with its biological functions. Data were processed by IBM SPSS 28.0 statistical program.Results: Mean age was 73 ± 11 years. Gender distribution was 32 % men/68 % women. Mean intraocular pressure was 17 mmHg in the right eye (RE) and 19 mmHg in the left eye (LE). Mean retinal nerve fiber layer thickness was 73 μm in RE and 71 μm in LE. MiRNAs ‐122‐5p (p = 0.02),146a‐5p (p = 0.02) and ‐320a‐3p (p = 0.04) showed a significantly higher expression in the aqueous humor of PEG versus CG.Conclusions: miRNAs ‐122‐5p, ‐146a‐5p and ‐320a‐3p are involved in PEG pathogenesis, epigenetically affecting the expression of target genes and protein translation, by means of their biological functions, in relation to extracellular matrix, metalloproteinases, glutamate, and the signaling pathways MAPK and RhoA/ROCK. We may suggest to investigate new biological therapies on the basis of the above miRNAs in PEG patients.
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