Glaucomatous damage of the macula

被引:673
作者
Hood, Donald C. [1 ,2 ]
Raza, Ali S. [1 ,3 ]
de Moraes, Carlos Gustavo V. [4 ,5 ]
Liebmann, Jeffrey M. [4 ,5 ]
Ritch, Robert [4 ,6 ]
机构
[1] Columbia Univ, Dept Psychol, New York, NY 10027 USA
[2] Columbia Univ, Dept Ophthalmol, New York, NY 10027 USA
[3] Columbia Univ, Dept Neurobiol & Behav, New York, NY 10027 USA
[4] New York Eye & Ear Infirm, Einhorn Clin Res Ctr, New York, NY 10003 USA
[5] NYU, Dept Ophthalmol, New York, NY 10016 USA
[6] New York Med Coll, Dept Ophthalmol & Visual Sci, Valhalla, NY 10595 USA
关键词
Glaucoma; OCT; Macula; Retinal ganglion cell; Visual field; NERVE-FIBER LAYER; RETINAL GANGLION-CELL; VISUAL-FIELD LOSS; OPTICAL COHERENCE TOMOGRAPH; FREQUENCY-DOMAIN OCT; THICKNESS MEASUREMENTS; TENSION GLAUCOMA; LAMINA-CRIBROSA; SENSITIVITY; LOCATION;
D O I
10.1016/j.preteyeres.2012.08.003
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
There is a growing body of evidence that early glaucomatous damage involves the macula. The anatomical basis of this damage can be studied using frequency domain optical coherence tomography (fdOCT), by which the local thickness of the retinal nerve fiber layer (RNFL) and local retinal ganglion cell plus inner plexiform (RGC+) layer can be measured. Based upon averaged fdOCT results from healthy controls and patients, we show that: 1. For healthy controls, the average RGC+ layer thickness closely matches human histological data; 2. For glaucoma patients and suspects, the average RGC+ layer shows greater glaucomatous thinning in the inferior retina (superior visual field (VF)); and 3. The central test points of the 6 VF grid (24-2 test pattern) miss the region of greatest RGC+ thinning. Based upon fdOCT results from individual patients, we have learned that: 1. Local RGC+ loss is associated with local VF sensitivity loss as long as the displacement of RGCs from the foveal center is taken into consideration; and 2. Macular damage is typically arcuate in nature and often associated with local RNFL thinning in a narrow region of the disc, which we call the macular vulnerability zone (MVZ). According to our schematic model of macular damage, most of the inferior region of the macula projects to the MVZ, which is located largely in the inferior quadrant of the disc, a region that is particularly susceptible to glaucomatous damage. A small (cecocentral) region of the inferior macula, and all of the superior macula (inferior VF), project to the temporal quadrant, a region that is less susceptible to damage. The overall message is clear; clinicians need to be aware that glaucomatous damage to the macula is common, can occur early in the disease, and can be missed and/or underestimated with standard VF tests that use a 6 degrees grid, such as the 24-2 VF test. (C) 2012 Elsevier Ltd. All rights reserved.
引用
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页码:1 / 21
页数:21
相关论文
共 66 条
[1]  
AIRAKSINEN PJ, 1983, ACTA OPHTHALMOL, V61, P186
[2]  
ANCTIL JL, 1984, ARCH OPHTHALMOL-CHIC, V102, P363
[3]  
Araie M, 1995, Curr Opin Ophthalmol, V6, P36
[4]  
AULHORN E., 1967, P151
[5]  
Aulhorn E, 1977, DOC OPHTHALMOL P SER, P75
[6]  
BIXENMAN WW, 1982, OPHTHALMOLOGY, V89, P58
[7]   Determinants of normal retinal nerve fiber layer thickness measured by stratus OCT [J].
Budenz, Donald L. ;
Anderson, Douglas R. ;
Varma, Rohit ;
Schuman, Joel ;
Cantor, Louis ;
Savell, Jonathan ;
Greenfeld, David S. ;
Patella, Vincent Michael ;
Quigley, Harry A. ;
Tielsch, James .
OPHTHALMOLOGY, 2007, 114 (06) :1046-1052
[8]   TOPOGRAPHY OF GANGLION-CELLS IN HUMAN RETINA [J].
CURCIO, CA ;
ALLEN, KA .
JOURNAL OF COMPARATIVE NEUROLOGY, 1990, 300 (01) :5-25
[9]   Human Chorioretinal Layer Thicknesses Measured in Macula-wide, High-Resolution Histologic Sections [J].
Curcio, Christine A. ;
Messinger, Jeffrey D. ;
Sloan, Kenneth R. ;
Mitra, Arnab ;
McGwin, Gerald ;
Spaide, Richard F. .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2011, 52 (07) :3943-3954
[10]   QUANTITATIVE REGIONAL STRUCTURE OF THE NORMAL HUMAN LAMINA-CRIBROSA - A RACIAL COMPARISON [J].
DANDONA, L ;
QUIGLEY, HA ;
BROWN, AE ;
ENGER, C .
ARCHIVES OF OPHTHALMOLOGY, 1990, 108 (03) :393-398