In vivo confocal microscopy of the cornea in health and disease

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dc.contributor.advisor Professor Charles McGhee en
dc.contributor.author Patel, Dipika en
dc.date.accessioned 2007-07-03T22:22:14Z en
dc.date.available 2007-07-03T22:22:14Z en
dc.date.issued 2005 en
dc.identifier.citation Thesis (PhD--Ophthalmology)--University of Auckland, 2005. en
dc.identifier.uri http://hdl.handle.net/2292/615 en
dc.description.abstract The cornea is the transparent structure forming the anterior eye. Principal functions include: transmitting and focusing light onto the retina, containing intraocular pressure, and providing a protective interface with the environment. The specialized microstructural organization of the cornea is key to these functions and maintenance of corneal integrity. In vivo confocal microscopy enables examination of the living human cornea at the microstructural level. This technique, in combination with computerized topography, corneal aesthesiometry and other clinical assessments has been utilized in a series of inter-related studies of the human cornea. Both slit scanning and laser scanning in vivo confocal microscopes were used and the attributes and performance of the two types of microscope were compared, demonstrating marked differences. Quantitative analysis of the sub-basal nerve plexus in the normal cornea and the inherited ectatic condition of keratoconus was correlated with central corneal sensitivity, revealing that nerve density does not change with increasing age and that nerve density is positively correlated with corneal sensitivity. However, in keratoconus, central corneal sensation, sub-basal nerve density, and basal epithelial density are all significantly lower than normal. A novel technique developed to map the corneal sub-basal nerve plexus enabled elucidation of the previously enigmatic architecture, revealing an overall radial pattern with a clockwise whorl at the area of convergence, inferior to the corneal apex. Keratoconic corneas demonstrated gross abnormalities of the nerve plexus even in mild cases. A two-dimensional reconstruction of the inferior limbus was also produced using this method. IV Analysis of the corneal endothelium in posterior polymorphous dystrophy revealed that endothelial density does not correlate with the clinical severity of this dystrophy. Key observations included hyper-reflective endothelial nuclei and apparent aggregation of keratocytes around the endothelial lesions. Investigation of hyper-reflective corneal endothelial nuclei per se, revealed that these are not seen in the normal cornea but are associated with endothelial trauma, intraocular surgery or disease states that primarily affect the endothelium. In conclusion, using in vivo confocal microscopy, these studies have provided important qualitative and quantitative data that add to our knowledge of the human cornea, at the microstructural level, in health and disease states. en
dc.format Scanned from print thesis en
dc.language.iso en en
dc.publisher ResearchSpace@Auckland en
dc.relation.ispartof PhD Thesis - University of Auckland en
dc.relation.isreferencedby UoA1599376 en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.title In vivo confocal microscopy of the cornea in health and disease en
dc.type Thesis en
thesis.degree.discipline Ophthalmology en
thesis.degree.grantor The University of Auckland en
thesis.degree.level Doctoral en
thesis.degree.name PhD en
dc.rights.holder Copyright: The author en
pubs.local.anzsrc 11 - Medical and Health Sciences en
pubs.org-id Faculty of Medical & Hlth Sci en


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