Literature DB >> 3335434

Central visual fields for short wavelength sensitive pathways in glaucoma and ocular hypertension.

G Heron1, A J Adams, R Husted.   

Abstract

While conventional clinical visual acuity and kinetic visual fields may be essentially normal in ocular hypertension and early stages of glaucoma, other foveal aspects of vision (eg color, spatial and temporal contrast sensitivity) may be quite abnormal. Specifically, a selective vulnerability of the short wavelength sensitive (SWS) visual pathways in these conditions has previously been noted. Here we studied the central visual fields of 33 primary open angle glaucoma (POAG) patients, 32 ocular hypertensives (OHT), and 24 age-matched normal controls using blue and yellow test flashes on bright yellow backgrounds. SWS cone and MWS and/or LWS cone pathway sensitivities were measured at the fovea and at 2.5 degrees, 5 degrees, 10 degrees and 15 degrees eccentricities, in either the inferior temporal (for OHT) or horizontal nasal retina (for POAG). As expected, all groups had normal sensitivity to yellow flashes--detected by LWS and/or MWS cones--in these meridians. By comparison, for the blue flashes--detected by the SWS cones--the POAG and OHT groups had sensitivity deficits, uniformly across the central visual field, of about 6X and 1.8X, respectively, compared to normals. While six of 31 (19%) OHT subjects had localized glaucomatous field defects (greater than 0.4 log units) in the non-foveal inferior temporal retina, none of the 12 OHT subjects who were also tested in the horizontal nasal retina showed loss in this meridian. Finally, while no POAG subjects had localized sensitivity loss for yellow flashes in the horizontal nasal retina, four did show local field defects with blue test flashes.(ABSTRACT TRUNCATED AT 250 WORDS)

Entities:  

Mesh:

Year:  1988        PMID: 3335434

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  8 in total

Review 1.  Acquired colour vision defects in glaucoma-their detection and clinical significance.

Authors:  M Pacheco-Cutillas; D F Edgar; A Sahraie
Journal:  Br J Ophthalmol       Date:  1999-12       Impact factor: 4.638

2.  Blue-yellow perimetry in the detection of early glaucomatous damage.

Authors:  L A De Jong; C E Snepvangers; T J van den Berg; C T Langerhorst
Journal:  Doc Ophthalmol       Date:  1990-10       Impact factor: 2.379

3.  Interpretation of the Humphrey Matrix 24-2 test in the diagnosis of preperimetric glaucoma.

Authors:  Jin A Choi; Na Young Lee; Chan Kee Park
Journal:  Jpn J Ophthalmol       Date:  2009-01-30       Impact factor: 2.447

Review 4.  Selective cell death in glaucoma: does it really occur?

Authors:  J E Morgan
Journal:  Br J Ophthalmol       Date:  1994-11       Impact factor: 4.638

5.  Automated perimetry and short wavelength sensitivity in patients with asymmetric intraocular pressures.

Authors:  R A Lewis; C A Johnson; A J Adams
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1993-05       Impact factor: 3.117

6.  The influence of induced forward light scatter on the normal blue-on-yellow perimetric profile.

Authors:  I D Moss; J M Wild
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1994-07       Impact factor: 3.117

7.  Use of a blue filter in visual field analysis.

Authors:  C E Hugkulstone; S A Vernon
Journal:  Br J Ophthalmol       Date:  1991-03       Impact factor: 4.638

8.  Differential Effects of Experimental Retinal Detachment on S- and M/L-Cones in Rats.

Authors:  Glyn Chidlow; Weng Onn Chan; John P M Wood; Robert J Casson
Journal:  Mol Neurobiol       Date:  2021-10-11       Impact factor: 5.590

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.