Skip to main content

Advertisement

Log in

The 2-global flash mfERG in glaucoma: attempting to increase sensitivity by reducing the focal flash luminance and changing filter settings

  • Original Research Article
  • Published:
Documenta Ophthalmologica Aims and scope Submit manuscript

Abstract

Purpose

To test a new 2-flash multifocal electroretinogram (mfERG) paradigm in glaucoma using a reduced light intensity of the m-frame flash as opposed to the global flash, as it has been suggested that this may increase the responses induced by the global flash, which has been the part of the mfERG response where most changes have been noted in glaucoma.

Methods

A mfERG was recorded from one eye of 22 primary open angle glaucoma (POAG) patients [16 normal tension glaucoma (NTG), 6 high tension glaucoma (HTG)] and 20 control subjects. A binary m-sequence (2^13-1, L max 100 cd/m2, L min <1 cd/m2), followed by two global flashes (L max 200 cd/m2) at an interval of 26 ms (VERIS 6.0™, FMSIII), was used. The stimulus array consisted of 103 hexagons. Retinal signals were amplified (gain = 50 K) and bandpass filtered at 1–300 Hz. For each focal response, the root mean square was calculated. We analyzed 5 larger response averages (central 15° and 4 adjoining quadrants) as well as 8 smaller response averages (central 10° and 7 surrounding response averages of approximately 7° radius each). Three epochs were analyzed: the direct component at 15–45 ms (DC) and the following two components induced by the effects of the preceding focal flash on the response to the global flashes at 45–75 ms (IC-1) and at 75–105 ms (IC-2). Statistical analysis was performed using linear mixed effects models adjusted for age.

Results

Responses differed significantly between POAG patients and controls in all central response averages. This difference was larger for the central 10° than for the response average of the central 15°. While these observations held true for all response epochs analyzed, the DC differed least and the IC-1 most when POAG was compared to control. For POAG, the most sensitive differential measure was IC-1 of the central 10° with an area under the ROC curve of 0.78. With a cutoff value of 12.52 nV/deg2, 80 % of the POAG patients (100 % HTG, 69 % NTG) were correctly classified as abnormal, while 77 % of the control subjects were correctly classified as normal. When the results of the mfERG were compared to the visual fields, there was a tendency for the mfERG to decrease as the mean defect increased. However, this correlation was only significant in the superior nasal quadrant when the IC-1 of the mfERG was compared to the corresponding area of the visual field.

Conclusion

When compared to findings from previous studies, reducing the luminance of the m-frame flash in the 2-global flash paradigm did not increase the sensitivity and specificity of the mfERG to detect glaucoma further.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  1. Quigley HA (2011) Glaucoma. Lancet 377:1367–1377

    Article  PubMed  Google Scholar 

  2. Heijl A, Leske MC, Hyman L, Yang Z, Bengtsson B (2010) Intraocular pressure reduction with a fixed treatment protocol in the Early Manifest Glaucoma Trial. Acta Ophthalmol 89(8):749–754

    PubMed  Google Scholar 

  3. Hirneiss C, Niedermaier A, Kernt M, Kampik A, Neubauer AS (2010) Gesundheitsökonomische Aspekte des Glaukomscreenings. Ophthalmologe 107:143–149

    Article  PubMed  CAS  Google Scholar 

  4. Quigley HA, Addicks EM, Green WR (1982) Optic nerve damage in human glaucoma III. Quantitative correlation of nerve fiber loss and visual field defect in glaucoma, ischemic neuropathy, papilledema, and toxic neuropathy. Arch Ophtalmol 100(1):135–146

    Article  CAS  Google Scholar 

  5. Kerrigan-Baumrind LA, Quigley HA, Pease ME, Kerrigan DF, Mitchell RS (2000) Number of ganglion cells in glaucoma eyes compared with threshold visual field tests in the same persons. Invest Ophthalmol Vis Sci 41(3):741–748

    PubMed  CAS  Google Scholar 

  6. Hood DC, Kardon RH (2007) A framework for comparing structural and functional measures of glaucomatous damage. Prog Retin Eye Res 26(6):688–710

    Article  PubMed  Google Scholar 

  7. Palmowski AM, Allgayer R, Heinemann-Vernaleken B (2000) The multifocal ERG in open angle glaucoma—a comparison of high and low contrast recordings in high- and low-tension open angle glaucoma. Doc Ophthalmol 101(1):35–49

    Article  PubMed  CAS  Google Scholar 

  8. Palmowski AM, Ruprecht KW (2004) Follow up in open angle glaucoma. A comparison of static perimetry and the fast stimulation mfERG. Doc Ophthalmol 108:55–60

    Article  PubMed  Google Scholar 

  9. Hood DC, Greenstein VC, Holopigian K, Bauer R, Firoz B, Liebmann JM, Odel JG, Ritch R (2000) An attempt to detect glaucomatous damage to the inner retina with the multifocal ERG. Invest Ophthalmol Vis Sci 41(6):1570–1579

    PubMed  CAS  Google Scholar 

  10. Palmowski AM, Allgayer R, Heinemann-Vernaleken B, Ruprecht KW (2002) Multifocal electroretinogram with a multiflash stimulation technique in open-angle glaucoma. Ophthalmic Res 34:83–89

    Article  PubMed  CAS  Google Scholar 

  11. Fortune B, Bearse MA Jr, Coiffi GA, Johnson CA (2002) Selective loss of an oscillatory component from temporal retinal multifocal ERG responses in glaucoma. Invest Ophthalmol Vis Sci 43:2638–2647

    PubMed  Google Scholar 

  12. Palmowski-Wolfe AM, Todorova MG, Orguel S, Flammer J, Brigell M (2007) The two global flash mfERG in high and normal tension primary open-angle glaucoma. Doc Ophthalmol 114:9–19

    Article  PubMed  Google Scholar 

  13. Chu PH, Chan HH, Brown B (2006) Glaucoma detection is facilitated by luminance modulation of the global flash multifocal electroretinogram. Invest Ophthalmol Vis Sci 47(3):929–937

    Article  PubMed  Google Scholar 

  14. Shimada Y, Bearse MA Jr, Sutter EE (2005) Multifocal electroretinograms combined with periodic flashes: direct responses and induced components. Graefe’s Arch Clin Exp Ophthalmol 243:132–141

    Article  Google Scholar 

  15. Hood DC, Bach M, Brigell M, Keating D, Kondo M, Lyons JS, Marmor MF, McCulloch DL, Palmowski-Wolfe AM, For the International Society For Clinical Electrophysiology of Vision (2012) ISCEV standard for clinical multifocal electroretinography (mfERG) (2011 edition). Doc Ophthalmol 124(1):1–13

    Article  PubMed  Google Scholar 

  16. Machida S, Toba Y, Ohtaki A, Gotoh Y, Kaneko M, Kurosaka D (2008) Photoptic negative response of focal electroretinograms in glaucomatous eyes. Invest Ophthalmol Vis Sci 49(12):5636–5644

    Article  PubMed  Google Scholar 

  17. Lou X, Patel NB, Harwerth RS, Frishman LJ (2011) Loss of the low-frequency component of the global-flash multifocal electroretinogram in primate eyes with experimental glaucoma. Invest Ophthalmol Vis Sci 52(6):3792–3804

    Article  Google Scholar 

  18. R Development Core Team (2010) R, version 2.10.1, accessed on Dec 2009: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. ISBN 3-900051-07-0. http://www.R-project.org/

  19. Palmowski AM, Sutter EE, Bearse MA Jr, Fung W (1997) Mapping of retinal function in diabetic retinopathy using the multifocal electroretinogram. Invest Ophthalmol Vis Sci 38(12):2586–2596

    PubMed  CAS  Google Scholar 

  20. Glovinsky Y, Quigley HA, Pease ME (1993) Foveal ganglion cell loss is size dependent in experimental glaucoma. Invest Ophthalmol Vis Sci 34:395–400

    PubMed  CAS  Google Scholar 

  21. Kanadani FN, Hood DC, Grippo TM, Wangsupadilok B, Harizman N, Greenstein VC, Liebmann JM, Ritch R (2006) Structural and functional assessment of the macular region in patient with glaucoma. Br J Ophthalmol 90:1393–1397

    Article  PubMed  CAS  Google Scholar 

  22. Hood DC, Rasa AS, De Morales CGV, Oder JG, Greenstein VC, Liebmann JM, Ritch R (2011) Initial arcuate defects within the central 10 degrees in glaucoma. Invest Ophthalmol Vis Sci 52(2):940–946

    Article  PubMed  Google Scholar 

  23. Wang M, Hood DC, Cho HS, Ghadiali Q, De Morales CG, Zhang X, Ritch R, Liebmann JM (2009) Measurement of local retinal ganglion cell layer thickness in patients with glaucoma using frequency-domain optical coherence tomography. Arch Ophthalmol 127(7):875–881

    Article  PubMed  Google Scholar 

  24. Kaltwasser Ch, Horn FK, Kremers J, Juenemann A (2009) A comparison of the suitability of cathode ray tube (CRT) and liquid crystal display (LCD) monitors as visual stimulators in mfERG diagnostics. Doc Ophthalmol 118(3):179–189

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

This study was supported by the SNF (Swiss National Fund, 32003B-135219, PAM) and the LHW Stiftung Lichtenstein. The data were presented in part at ARVO 2011, Abstract number: 5482 A283.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to S. A. Kramer.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kramer, S.A., Ledolter, A.A., Todorova, M.G. et al. The 2-global flash mfERG in glaucoma: attempting to increase sensitivity by reducing the focal flash luminance and changing filter settings. Doc Ophthalmol 126, 57–67 (2013). https://doi.org/10.1007/s10633-012-9360-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10633-012-9360-z

Keywords

Navigation