June 2015
Volume 56, Issue 7
ARVO Annual Meeting Abstract  |   June 2015
Early changes in structure and inner retinal function in experimental glaucoma
Author Affiliations & Notes
  • Lakshmi Priya Rajagopalan
    College of Optometry, University of Houston, Houston, TX
  • Nimesh Bhikhu Patel
    College of Optometry, University of Houston, Houston, TX
  • Kevin Ivers
    Devers Eye Institute, Portland, OR
  • Nripun Sredar
    Computer Science, University of Houston, Houston, TX
  • Suresh Viswanathan
    College of Optometry, State University of New York, New York, NY
  • Jason Porter
    College of Optometry, University of Houston, Houston, TX
  • Ronald S Harwerth
    College of Optometry, University of Houston, Houston, TX
  • Laura J Frishman
    College of Optometry, University of Houston, Houston, TX
  • Footnotes
    Commercial Relationships Lakshmi Rajagopalan, None; Nimesh Patel, None; Kevin Ivers, None; Nripun Sredar, None; Suresh Viswanathan, None; Jason Porter, None; Ronald Harwerth, None; Laura Frishman, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2015, Vol.56, 4827. doi:
  • Views
  • Share
  • Tools
    • Alerts
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Lakshmi Priya Rajagopalan, Nimesh Bhikhu Patel, Kevin Ivers, Nripun Sredar, Suresh Viswanathan, Jason Porter, Ronald S Harwerth, Laura J Frishman; Early changes in structure and inner retinal function in experimental glaucoma. Invest. Ophthalmol. Vis. Sci. 2015;56(7 ):4827.

      Download citation file:

      © ARVO (1962-2015); The Authors (2016-present)

  • Supplements

Purpose: To determine the relationships between structural and functional measures of glaucomatous neuropathy over the timecourse of experimental glaucoma in non-human primates.

Methods: Five macaque monkeys with unilaterally elevated intraocular pressure (IOP), induced by laser photocoagulation of the trabecular meshwork, were followed longitudinally using multifocal electroretinogram (mfERG) and optical coherence tomography (OCT). The stimulus display for mfERG, was a 35° X 34° array of 19 unstretched hexagons, each 7° across. The stimulus sequence consisted of five focal flashes followed by 25 dark frames repeating every 400ms. Global (averaged across all hexagons) and regional percent change in the experimental eye for the photopic negative response (mfPhNR), and retinal nerve fiber layer thickness (RNFLT), retinal ganglion cell inner plexiform layer thickness (GCIPLT) or optic nerve head (ONH) measures of minimum rim width, (MRW), and anterior lamina cribrosa surface depth (ALCSD) were compared longitudinally. Values in the experimental eye were considered to be reduced when the percent change exceeded the lower 95% confidence limit of the control eye values. The data were analyzed to model relationships between the local mfPhNR, peripapillary RNFLT, and macular GCIPLT.

Results: In the experimental eyes, sectoral mfPhNR amplitude (corresponding to at least one of the six different sectors of the temporal RNFL) was the first measure to be reduced after elevation of IOP. Global mfPhNR amplitude changed next, concurrently with ONH structural measurements of global MRW and global ALCSD, and all of these changed prior to global or sectoral changes in RNFLT. For the control eye, local mfPhNR amplitude was linearly related to RNFLT and GCIPLT in the corresponding retinal regions (RNFLT, r>0.85, P<0.0001: GCIPLT, r>0.75, P<0.0001). In experimental eyes, the relationship showed an initial nonlinearity due to reductions in mfPhNR amplitude that preceded reductions in retinal thickness measures.

Conclusions: The onset of changes in mfPhNR and ONH measures (MRW and ALCSD) occurred prior to the onset of changes in RNFLT. These results suggest that mfPhNR and ONH parameters reflect early changes in the timecourse of glaucomatous neuropathy.


This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.