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      Changes in corneal parameters at confocal microscopy in treated glaucoma patients

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          Abstract

          Background:

          The purpose of this study was to evaluate corneal parameters in treated glaucoma patients, nontreated glaucoma patients, and normal subjects using confocal microscopy.

          Methods:

          Forty patients with primary open-angle glaucoma and 22 untreated controls underwent confocal microscopy of the cornea using the Heidelberg retinal tomograph cornea module. The glaucoma group was divided into two subgroups, ie, patients on medical treatment for at least two years before inclusion (with beta-blockers or prostaglandin analogs) and nontreated glaucoma patients. The following corneal parameters were evaluated: endothelial cell density and number, reflectivity, and tortuosity of sub-basal nerves. For reflectivity and tortuosity, a dedicated grading scale ranging from 0 to 4 was used. Differences between treatments were also evaluated in the treated glaucoma group.

          Results:

          Number of fibers and reflectivity of the sub-basal plexus were significantly lower in glaucoma patients as compared with controls (2.5 ± 0.7 versus 2.9 ± 0.9, P = 0.006, and 2.3 ± 0.8 versus 2.7 ± 0.9, P = 0.04, respectively), whereas tortuosity was significantly higher (2.6 ± 1 versus 2.0 ± 0.8, P = 0.007). Endothelial cell density (measured as cells per mm 2) was lower in the glaucoma group comparing treated patients with nontreated patients (2826 ± 285 versus 3124 ± 272, P = 0.0003). Comparing treated patients with nontreated patients, relevant differences were found in number (2.3 ± 0.7 versus 2.8 ± 0.8, P = 0.004), tortuosity (2.8 ± 1 versus 2.2 ± 0.8, P = 0.004), and reflectivity (2.2 ± 0.8 versus 2.6 ± 0.8, P = 0.04). No differences in corneal parameters were found between beta-blockers and prostaglandin analogs.

          Conclusion:

          This study shows that differences in corneal parameters between glaucoma patients and controls may be due to the medical treatments used for glaucoma. These data should be taken into consideration in long-standing medical glaucoma treatment and in potential candidates for surgery.

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          Most cited references8

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          To preserve or not to preserve, is that the question?

          L. Wilson (1996)
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            Cellular cytotoxicity of antiglaucoma drugs in cultured corneal endothelial cells.

            In this study, the various antiglaucoma drugs including betaxolol, timolol, levobunolol, carteolol, brimonidine, dipivefrin, dorzolamide, brinzolamide, latanoprost, unoprostone, and pilocarpine were used to investigate the effects of cellular cytotoxicity in cultured bovine corneal endothelial cells. After exposure to the drugs in three dilutions, 1/100, 1/1,000, and 1/10,000, for 100 minutes, cells were estimated based on the release assay of lactate dehydrogenase (LDH) enzyme. It was found that cellular LDH was significantly released in the medium only at 1/100th dilution of betaxolol, brimonidine, dorzolamide, dipivefrin, latanoprost and unoprostone to 130%, 123%, 145%, 157%, 128% and 237%, respectively, compared with controls upon exposure to drugs for 100 minutes. Moreover, benzalkonium chloride preservative at the concentrations ranging from 0.001 to 0.00001 mg/mL did not affect cellular LDH release in bovine corneal endothelial cells. These results indicate that high concentrations of antiglaucoma drugs may induce cytotoxicity in corneal endothelial cells.
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              [Cytotoxicity of antiglaucoma ophthalmic solutions for human corneal endothelial cells].

              The cytotoxicity of a range of commercial antiglaucoma ophthalmic solutions was assessed in human corneal endothelial cells using in vitro techniques.
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                Author and article information

                Journal
                Clin Ophthalmol
                Clinical Ophthalmology
                Clinical Ophthalmology (Auckland, N.Z.)
                Dove Medical Press
                1177-5467
                1177-5483
                2011
                2011
                26 July 2011
                : 5
                : 1037-1042
                Affiliations
                [1 ]Eye Clinic, San Giuseppe Hospital, University of Milan, Milan, Italy;
                [2 ]GB Bietti Foundation for Study and Research in Ophthalmology, Rome, Italy;
                [3 ]Eye Clinic, Department of Medicine, San Paolo Hospital, University of Milan, Milan, Italy
                Author notes
                Correspondence: Stefano Ranno, Via San Vittore 12, Milan, Italy, Tel/Fax +39 02 8599 4974, Email stefanoranno@ 123456yahoo.it
                Article
                opth-5-1037
                10.2147/OPTH.S22874
                3151567
                21845031
                15fd9894-dc0c-4c3d-afde-3f5928dd7acc
                © 2011 Ranno et al, publisher and licensee Dove Medical Press Ltd.

                This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.

                History
                : 25 July 2011
                Categories
                Original Research

                Ophthalmology & Optometry
                sub-basal nerves,cornea,confocal microscopy,endothelial cells,glaucoma
                Ophthalmology & Optometry
                sub-basal nerves, cornea, confocal microscopy, endothelial cells, glaucoma

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