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ResearchSpace@Auckland

In vivo confocal microscopy of the cornea in health and disease

Abstract

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.

Degree

thesis:*
Name thesis:degree_name
PhD
Level thesis:degree_level
Doctoral
Discipline thesis:degree_discipline
Ophthalmology
Grantor dc:publisher
ResearchSpace@Auckland
Year dc:date.issued
2005

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Patel, Dipika
Advisor dc:contributor.advisor
  • Professor Charles McGhee

Rights

dc:rights
Statement dc:rights
  • Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
Language dc:language.iso
en

Identifiers

dc:identifier.*
Handle dc:identifier.uri
https://hdl.handle.net/2292/615
OAI identifier oai:identifier
oai:researchspace.auckland.ac.nz:2292/615

Chain of custody

source
Harvested from
University of Auckland
Base URL
researchspace.auckland.ac.nz/server/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
related terms
citation

Patel, Dipika. In vivo confocal microscopy of the cornea in health and disease. Doctoral thesis, ResearchSpace@Auckland, 2005. https://hdl.handle.net/2292/615