Trending Topic

23 mins

Trending Topic

Developed by Touch
Mark CompleteCompleted
BookmarkBookmarked
Luke G Qin, Michael T Pierce, Rachel C Robbins

The uvea is a vascular stratum that includes the iris, ciliary body and choroid. Uveitis is defined as inflammation of a part of the uvea or its entirety, but it is also used to describe inflammatory processes of any part of the eye, such as the vitreous or peripheral retina. The clinical taxonomy of uveitis […]

Evaluation of the Optic Nerve and Retinal Nerve Fiber Layer in Myopic Individuals

Ahmad A Aref, Donald L Budenz
Share
Facebook
X (formerly Twitter)
LinkedIn
Via Email
Mark CompleteCompleted
BookmarkBookmarked
Copy LinkLink Copied
Download as PDF
Published Online: Jun 21st 2012 US Ophthalmic Review, 2012;5(2):91-3 DOI: http://doi.org/10.17925/USOR.2012.05.02.91
Select a Section…
1

Abstract

Overview

Clinical discrimination between myopic tilted optic discs and glaucomatous optic neuropathy is often challenging, especially when considering that myopia is a risk factor for the development of glaucoma. Myopic tilted discs are usually larger than average, with associated relative cupping and thinner neuroretinal rim tissue. Histopathologic study has revealed thinner parapapillary retinal tissue in these eyes. Optical coherence tomography (OCT)-measured average retinal nerve fiber layer (RNFL) thickness has been found to decrease with longer axial length and higher myopic refractive error. Parapapillary RNFL quadrant and clock-hour analyses result in a higher false-positive rate in myopic eyes. Careful slit-lamp examination, quality baseline stereoscopic disc photographs, and frequent serial visual field testing are essential to the follow-up of myopic individuals with suspected glaucoma. A novel diagnostic parameter, OCT-derived ganglion cell analysis, may prove to be useful in the diagnosis and follow-up of these individuals.

Keywords

Retinal nerve fiber layer, myopia, glaucoma, optical coherence tomography, optic nerve

2

Article

According to pooled data from large, population-based eye surveys, the estimated prevalence of myopic refractive error (-1 diopter [D] or less) in individuals >40 years old is 25.4, 26.6, and 16.4 % in the US, Europe, and Australia, respectively. For myopia less than -5 D, the prevalence estimates are 4.5, 4.6, and 2.8 %, respectively.1 The prevalence of myopic refractive error is indeed substantial and is the highest of any ocular disorder in this age group.

Furthermore, optic nerve and visual field abnormalities associated with high myopia are notoriously difficult to differentiate from those associated with glaucomatous optic neuropathy. The challenge of distinguishing otherwise healthy myopic eyes from those afflicted with glaucoma becomes even more complex when considering that myopic refractive error is a risk factor for open-angle glaucoma. Marcus and colleagues2 performed a systematic review and meta-analysis of population-based cross-sectional studies published between 1994 and 2010, in order to determine the association between myopia and glaucoma. Analysis of seven studies that reported risk estimates for both low and high myopia revealed a pooled odds ratio of 1.65 (95 % confidence interval [CI] 1.26–2.17) between low myopia and open-angle glaucoma. The pooled odds ratio for the association between high myopia (-3 D or less) and open-angle glaucoma was found to be 2.46 (95 % CI 1.93–3.15). The authors acknowledge that, due to the presence of myopic visual field defects and relatively larger optic nerve cups in myopic individuals, studies included in this meta-analysis may have overestimated the prevalence of glaucoma and therefore they cite a single longitudinal study3 (deemed to be less prone to misdiagnosis of glaucoma) that yielded the same overall results. High myopic error does indeed appear to be an independent risk factor for open-angle glaucoma; however, clinicians must be aware of myriad clinical features that may confound an accurate diagnosis. This article aims to shed light on these clinical features and also to provide practical tips for the examination and follow-up of myopic individuals with suspected open-angle glaucoma.

To view the full article in PDF or eBook formats, please click on the icons above.

2

References

  1. The Eye Diseases Prevalence Research Group, The prevalence
    of refractive errors among adults in the United States, Western
    Europe, and Australia, Arch Ophthalmol, 2004;122:495–505.

  2. Marcus MW, de Vries MM, Montolio FG, Jansonius MM, Myopia
    as a risk factor for open-angle glaucoma: a systematic review
    and meta-analysis, Ophthalmology, 2011;118:1989–94.e2.

  3. Czudowska MA, Ramdas WD, Wolfs RC, et al., Incidence of
    glaucomatous visual field loss: a ten-year follow-up from
    the Rotterdam study, Ophthalmology, 2010;117:1705–12.

  4. Jonas JB, Gusek GC, Naumann GO, Optic disk morphometry in
    high myopia, Graefes Arch Clin Exp Ophthalmol, 1988;226:587–90.

  5. Jonas JB, Optic disk size correlated with refractive error,
    Am J Ophthalmol, 2005;139:346–8.

  6. Goldschmidt E, Fledelius HC, Clinical features in high myopia.
    A Danish cohort study of high myopia cases followed from
    age 14 to age 60, Acta Ophthalmol, 2011;89:97–8.

  7. Jonas JB, Jonas SB, Jonas RA, et al., Histology of the
    parapapillary region in high myopia, Am J Ophthalmol,
    2011;152:1021–9.

  8. Saw SM, Gazzard G, Shih-Yen EC, Chua WH, Myopia and
    associated pathological complications, Ophthalmic Physiol Opt,
    2005;25:381–91.

  9. Fong DS, Epstein DL, Allingham RR, Glaucoma and myopia:
    are they related?, Int Ophthalmol Clin, 1990;30:215–8.

  10. Chang RT, Knight OJ, Feuer WJ, Budenz DL, Sensitivity and
    specificity of time-domain versus spectral-domain optical
    coherence tomography in diagnosing early to moderate
    glaucoma, Ophthalmology, 2009;116:2294–9.

  11. Kim MJ, Lee EJ, Kim TW, Peripapillary retinal nerve fiber layer
    thickness profile in subjects with myopia measured using the
    stratus optical coherence tomography, Br J Ophthalmol,
    2010;94:115–20.

  12. Kim NR, Lim H, Kim JH, et al., Factors associated with false
    positives in retinal nerve fiber layer color codes from
    spectral-domain optical coherence tomography,
    Ophthalmology, 2011;118:1774–81.

  13. Vernon SA, Rotchford AP, Negi A, et al., Peripapillary retinal
    nerve fibre layer thickness in highly myopic Caucasians as
    measured by stratus optical coherence tomography,
    Br J Ophthalmol, 2008;92:1076–80.

  14. Rauscher FM, Sekhon N, Feuer WJ, Budenz DL, Myopia affects
    retinal nerve fiber layer measurements as determined by
    optical coherence tomography, J Glaucoma, 2009;18:501–5.

  15. Kim NR, Lim H, Kim JH, et al., Factors associated with false
    positives in retinal nerve fiber layer color codes from
    spectral-domain optical coherence tomography,
    Ophthalmology, 2011;118:1774–81.

  16. Leung CK, Lam S, Weinreb RN, et al., Retinal nerve fiber layer
    imaging with spectral-domain optical coherence tomography:
    Analysis of the retinal nerve fiber layer map for glaucoma
    detection, Ophthalmology, 2010;117:1684–91.

  17. Kim MJ, Lee EJ, Kim TW, Peripapillary retinal nerve fibre layer
    thickness profile in subjects with myopia measured using
    the stratus optical coherence tomography, Br J Ophthalmol,
    2010;94:115–20.

  18. Chung JK, Yoo YC, Correct calculation circle location of
    optical coherence tomography in measuring retinal nerve
    fiber layer thickness in eyes with a myopic tilted disc,
    Invest Ophthalmol Vis Sci, 2011;52:7894–7900.

  19. Budde WM, Jonas JM, Martus P, Gründler AE, Influence of optic
    disc size on neuroretinal rim shape in healthy eyes, J Glaucoma,
    2000;9:357–62.

  20. Xu L, Li Y, Wang S, et al., Characteristics of highly myopic eyes:
    the Beijing Eye Study, Ophthalmology, 2007;114:121–6.

  21. Teng CC, De Moraes CG, Prata TS, et al., Beta-zone
    parapapillary atrophy and the velocity of glaucoma
    progression, Ophthalmology, 2010;117:909–15.

  22. Teng CC, De Moraes CG, Prata TS, et al., The region of largest
    beta-zone parapapillary atrophy area predicts the location
    of most rapid visual field progression, Ophthalmology,
    2011;118:2409–13.

  23. Doshi A, Kreidl KO, Lombardi L, et al., Nonprogressive
    glaucomatous cupping and visual field abnormalities in
    young Chinese males, Ophthalmology, 2007;114:472–9.

  24. Budenz DL, Anderson DR, Feuer WJ, et al., Detection and
    prognostic significance of optic disc hemorrhages during
    the ocular hypertension treatment study, Ophthalmology,
    2006;113:2137–43.

  25. Mwanza JC, Chang RT, Budenz DL, et al., Reproducibility of
    peripapillary retinal nerve fiber layer thickness and optic
    nerve head parameters measured with cirrus HD-OCT
    in glaucomatous eyes, Invest Ophthalmol Vis Sci,
    2010;51:5724–30.

  26. Tan O, Chopra V, Lu AT, et al., Detection of macular ganglion
    cell loss in glaucoma by fourier-domain optical coherence
    tomography, Ophthalmology, 2009;116:2305–14.

  27. Mwanza JC, Durbin MK, Budenz DL, et al., Profile and predictors
    of normal ganglion cell-inner plexiform layer thickness
    measured with frequency domain optical coherence
    tomography, Invest Ophthalmol Vis Sci, 2011;52:7872–9.

  28. Asrani S, Rosdahl JA, Allingham RR, Novel software strategy
    for glaucoma diagnosis: asymmetry analysis of retinal
    thickness, Arch Ophthalmol, 2011;129:1205–11.

  29. Mwanza JC, Oakley JD, Budenz DL, et al., Macular ganglion
    cell-inner plexiform layer: automated detection and thickness
    reproducibility with spectral-domain optical coherence
    tomography in glaucoma, Invest Ophthalmol Vis Sci, 2011;52:8323–9.

  30. Ang GS, Mustafa MS, Scott N, et al., Perimetric progression
    in open angle glaucoma and the visual field index (VFI),
    J Glaucoma, 2011;20:223–7.

  31. Vuori ML, Mantyjarvi M, Tilted disc syndrome may mimic false
    visual field deterioration, Acta Ophthalmol, 2008;86:622–5.

3

Article Information

Disclosure

The authors have no conflicts of interest to declare.

Correspondence

Donald L Budenz, MD, MPH, Department of Ophthalmology, University of North Carolina School of Medicine, 5151 Bioinformatics, CB 7040, Chapel Hill, NC 27599-7040, US. E: dbudenz@med.unc.edu

Received

2011-10-11T00:00:00

4

Further Resources

Share
Facebook
X (formerly Twitter)
LinkedIn
Via Email
Mark CompleteCompleted
BookmarkBookmarked
Copy LinkLink Copied
Download as PDF

This Functionality is for
Members Only

Explore the latest in medical education and stay current in your field. Create a free account to track your learning.

Close Popup