Clinical and microstructural analysis of patients with hyper-reflective corneal endothelial nuclei imaged by in vivo confocal microscopy

被引:14
作者
Patel, DV [1 ]
Phua, YS [1 ]
McGhee, CNJ [1 ]
机构
[1] Univ Auckland, Fac Med & Hlth Sci, Dept Ophthalmol, Auckland 1, New Zealand
关键词
cornea; confocal microscopy; endothelium; nucleic; in vivo;
D O I
10.1016/j.exer.2005.09.006
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
The purpose of this study was to determine the significance of hyper-reflective corneal endothelial nuclei imaged by in vivo confocal microscopy. A retrospective analysis was performed using a database of 505 patients that had undergone in vivo confocal microscopy of the cornea. All subjects with hyper-reflective endothelial nuclei were identified and these images were analysed to determine corneal endothelial cell density and morphology. The clinical notes of these patients were reviewed and corresponding data regarding corneal thickness was obtained from a related database of Orbscan II pachymetry. Hyper-reflective endothelial nuclei were identified in 41 eyes of 39 (7.7%) patients. Diagnoses included previous cataract surgery or penetrating keratoplasty, posterior polymorphous dystrophy, Fuchs' endothelial dystrophy and irido-comeal endothelial syndrome. No patients with clinically and endothelial normal corneas exhibited bright endothelial nuclei. The mean endothelial cell density in this group was 1325 +/- 872 cells mm(-2) density was below age-adjusted normal values in 69.2% of patients. Both cellular polymegathism (coefficient of variation of cell area 33.9 +/- 7.4%) and cellular pleomorphism were noted (51.8 +/- 9.0% hexagonal cells). The mean central corneal thickness was 582 +/- 52 mu m. There was no significant difference in endothelial density and morphology compared to cases that had low enclothelial density but did not exhibit bright nuclei. In conclusion, this study is the first to investigate the significance of bright endothelial nuclei detected by in vivo confocal microscopy. The strong association with corneal disease states suggests that the most likely explanation for this appearance is the alteration in cellular/nuclear morphology, composition or function. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:682 / 687
页数:6
相关论文
共 11 条
[1]   Behavior of corneal endothelial density over a lifetime [J].
Abib, FC ;
Barreto, J .
JOURNAL OF CATARACT AND REFRACTIVE SURGERY, 2001, 27 (10) :1574-1578
[2]   Pathology of late endothelial failure: Late endothelial failure of penetrating keratoplasty: Study with light and electron microscopy [J].
Bell, KD ;
Campbell, RJ ;
Bourne, WM .
CORNEA, 2000, 19 (01) :40-46
[3]   Fuchs' endothelial dystrophy: a fresh look at an aging disease [J].
Bergmanson, JPG ;
Sheldon, TM ;
Goosey, JD .
OPHTHALMIC AND PHYSIOLOGICAL OPTICS, 1999, 19 (03) :210-222
[4]   Clinical responses of the corneal endothelium [J].
Bourne, WM ;
McLaren, JW .
EXPERIMENTAL EYE RESEARCH, 2004, 78 (03) :561-572
[5]   Orbscan corneal topography system in evaluating the anterior structures of the human eye [J].
Cosar, CB ;
Sener, AB .
CORNEA, 2003, 22 (02) :118-121
[6]   CHANGES IN NUCLEAR-DNA CONTENT AND CELL-SIZE OF INJURED HUMAN CORNEAL ENDOTHELIUM [J].
IKEBE, H ;
TAKAMATSU, T ;
ITOI, M ;
FUJITA, S .
EXPERIMENTAL EYE RESEARCH, 1988, 47 (02) :205-215
[7]   AGE-DEPENDENT CHANGES IN NUCLEAR-DNA CONTENT AND CELL-SIZE OF PRESUMABLY NORMAL HUMAN CORNEAL ENDOTHELIUM [J].
IKEBE, H ;
TAKAMATSU, T ;
ITOI, M ;
FUJITA, S .
EXPERIMENTAL EYE RESEARCH, 1986, 43 (02) :251-258
[8]   Corneal endothelial cell morphology in patients undergoing cataract surgery [J].
Inoue, K ;
Tokuda, Y ;
Inoue, Y ;
Amano, S ;
Oshika, T ;
Inoue, J .
CORNEA, 2002, 21 (04) :360-363
[9]   COALESCENCE OF ENDOTHELIAL-CELLS IN THE TRAUMATIZED CORNEA .2. CLINICAL OBSERVATIONS [J].
LAING, RA ;
NEUBAUER, L ;
LEIBOWITZ, HM ;
OAK, SS .
ARCHIVES OF OPHTHALMOLOGY, 1983, 101 (11) :1712-1715
[10]  
WARING GO, 1982, OPHTHALMOLOGY, V89, P531