Glaucoma is a neurodegenerative disease, our study aimed to evaluate the potential effects of Palmitoylethanolamide (PEA) supplementation on RGCs function by PERG examination, and to record effects on intraocular pressure, visual field and quality of life. It was a single centre, randomized, prospective, single blind, two treatment, two period crossover study on stable glaucoma patients on topical monotherapy comparing current topical therapy alone or additioned with PEA 600 mg one tablet a day. At baseline, at 4 and at 8 months, all patients underwent to complete ophthalmic examination, pattern electroretinogram, visual field, and quality of life evaluation. 40 patients completed the study: mean age 66.6 ± 7.6 years; 21 (52.5%) male; 35 POAG (87.5%). At baseline, most patients had an early visual field defect, the IOP was well controlled. At the end of the PEA 600 mg supplementation, a significantly higher (mean 0.56 μV, 95% CI 0.30-0.73, p < 0.001) in the P50-wave amplitude was observed; in the PEA period a significantly lower IOP (− 1.6 mmHg, 95% CI − 2 to 1.2, p < 0.001) and higher quality of life scores (+ 6.7, 95% CI 4-9.9, p < 0.001) were observed. Our study is the first to show promising effects of PEA on PERG and on quality of life in glaucoma patients. Glaucoma is a progressive and multifactorial neurodegeneration in which pro-apoptotic signals are developed towards the retinal ganglion cells (RGC) and their axons: neurodegeneration is the progressive loss of structure or function of neurons resulting from the imbalance between protective factors and harmful influences on RGCs. It is widely recognized that the high outflow resistance in the trabecular meshwork outflow pathways causes an increase in intra-ocular pressure (IOP) and that the IOP levels cause deformation of the lamina cribrosa resulting in axonal damage and consequent apoptosis of the RGCs. Therefore, currently, the only approach proven to be efficient in preserving visual function is lowering IOP in both the initial and advanced stages 1-4. Many glaucoma patients experience damage that continues despite tonometric compensation, therefore other possible treatment areas have been studied, including ocular blood flow and neuroprotection. Neuroprotection can be defined as a therapeutic approach aimed at preventing, blocking and, in some cases, reversing neuronal cell damage 5. Numerous compounds have been shown to be neuroprotective in animal models of experimental glaucoma, such as memantine 6 and brimonidine 7 : but so far, no compound has reached a level of evidence sufficient to be considered a neuroprotective agent in humans 8. Blood flow abnormalities in the optic nerve head may initiate the glaucomatous cascade leading to neuroaxonal damage 9,10 , although perfusion pressure may be relevant in glaucoma but very difficult to measure 11. Secondary trans-synaptic degeneration may also involve higher visual centers and treatment strategies to prevent
The aim of this study was to evaluate the in vivo effects at 3 years of preservative-free tafluprost on corneal health. It was a prospective, masked, study on consecutive patients with a new prescription of preservative-free (PF) tafluprost (naïve-N or switched-S, 44 and 14 patients), and preserved (P) bimatoprost 0.003% or travoprost 0.004% (P-group, 35 patients). A complete ophthalmic examination and an in vivo corneal confocal microscopy evaluation were performed at baseline and every 6 months for 3 years. Ninety-three patients were enrolled, clinical parameters were similar in the groups at baseline, apart from intraocular pressure (IOP) which was lower in the S-group (p = 0.012). Both at baseline and over time, confocal microscopy parameters had different trends. At baseline, keratocyte activation was similar in the three groups (p = 0.43) but over the next months naïve patients treated with PF-tafluprost presented a significant (p = 0.004) reduction in keratocyte activation. Sub-basal nerves tended to increase in patients switched to PF-tafluprost (p = 0.07) while were stable in the other two groups (p = 0.11 in PF and 0.40 in P group). Grade of tortuosity was stable over time in the three groups. Beading-like formations were stable over time for the P- and the PF-group, while significantly increased in the S-group (p = 0.027). Endothelial density values were statistically different at baseline (p = 0.007), they decreased both in PF-group and in S-group (p = 0.048 and 0.001, respectively), while increased in P-group (p = 0.006). Our study is the first to show that a PF-tafluprost formulation does not significantly alter the corneal structures as examined by confocal microscopy after 36 months of topical daily therapy, while improving corneal alterations due to chronic preserved therapies.
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