Abstract
Purpose
To quantify the response dynamics of fast adaptation mechanisms of the scotopic ERG in younger and older adults using full-field m-sequence flash stimulation.
Methods
Scotopic ERGs were measured for a series of flashes separated by 65 ms over a range of 260 ms in 16 younger (20–26, 22.2 ± 2.1; range mean ±1 SD) and 16 older (65–85, 71.2 ± 7) observers without retinal pathology. A short-wavelength (λ peak = 442 nm) LED was used for scotopic stimulation, and the flashes ranged from 0.0001 to 0.01 cd s m−2. The complete binary kernel series was derived from the responses to the m-sequence flash stimulation, and the first- and second-order kernel responses were analyzed. The first-order kernel represented the response to a single, isolated flash, while the second-order kernels reflected the adapted flash responses that followed a single flash by one or more base intervals. B-wave amplitudes of the adapted flash responses were measured and plotted as a function of interstimulus interval to describe the recovery of the scotopic ERG. A linear function was fitted to the linear portion of the recovery curve, and the slope of the line was used to estimate the rate of fast adaptation recovery.
Results
The amplitudes of the isolated flash responses and rates of scotopic fast adaptation recovery were compared between the younger and older participants using a two-way ANOVA. The isolated flash responses and rates of recovery were found to be significantly lower in the older adults. However, there was no difference between the two age groups in response amplitude or recovery rate after correcting for age-related changes in the density of the ocular media.
Conclusions
These results demonstrated that the rate of scotopic fast adaptation recovery of normal younger and older adults is similar when stimuli are equated for retinal illuminance.
Similar content being viewed by others
References
Jackson GR, Owsley C, McGwin G (1999) Aging and dark adaptation. Vis Res 39:3975–3982
McMurdo MET, Gaskell A (1991) Dark adaptation and falls in the elderly. Gerontology 37:221–224
Mortimer RG, Fell JC (1989) Older drivers: their night fatal crash involvement and risk. Accid Anal Prev 21:273–282
Panda-Jonas S, Jonas JB, Jakobczyk-Zmija M (1995) Retinal photoreceptor density decreases with age. Ophthalmology 102:1853–1859
Gao H, Hollyfield JG (1992) Aging of the human retina. Differential loss of neurons and retinal pigment epithelial cells. Invest Ophthalmol Vis Sci 33:1–17
Curcio CA, Millican CL, Allen KA, Kalina RE (1993) Aging of the human photoreceptor mosaic: evidence for selective vulnerability of rods in central retina. Invest Ophthalmol Vis Sci 34:3278–3296
Jackson GR, Owsley C, Cordle EP, Finley CD (1998) Aging and scotopic sensitivity. Vis Res 38:3655–3662
Birch DG, Hood DC, Nusinowitz S, Pepperberg DR (1995) Abnormal activation and inactivation mechanisms of rod transduction in patients with autosomal dominant retinitis pigmentosa and the pro-23-his mutation. Invest Ophthalmol Vis Sci 36:1603–1614
Pugh Jr EN, Falsini B, Lyubarsky AL (1998) The origin of the major rod-and cone-driven components of the rodent electroretinogram and the effect of age and light-rearing history on the magnitude of these components. In: Williams TP, Thistle AB (eds) Photostasis and related phenomena. Springer, New york, pp 93–128
Jackson GR, McGwin G, Phillips JM et al (2006) Impact of aging and age-related maculopathy on inactivation of the a-wave of the rod-mediated electroretinogram. Vis Res 46:1422–1431
Menz MK, Sutter EE, Fendick M (2012) The adaptation recovery of the flash ERG. Invest Ophthalmol Vis Sci 53:2471
Sutter EE (1991) The fast m-transform: a fast computation of cross-correlations with binary m-sequences. SIAM J Comput 20:686–694
Sutter EE, Tran D (1992) The field topography of ERG components in man—I. The photopic luminance response. Vis Res 32:433–446
Sutter E (2000) The interpretation of multifocal binary kernels. Doc Ophthalmol 100:49–75
Sutter EE (2001) Imaging visual function with the multifocal m-sequence technique. Vis Res 41:1241–1255
Gerth C, Sutter EE, Werner JS (2003) mfERG response dynamics of the aging retina. Invest Ophthalmol Vis Sci 44:4443–4450
McCulloch DL, Marmor MF, Brigell MG et al (2015) ISCEV Standard for full-field clinical electroretinography (2015 update). Doc Ophthalmol 130:1–12
R Core Team (2014) R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna
Weale RA (1988) Age and the transmittance of the human crystalline lens. J Physiol 395:577
Pokorny J, Smith VC, Lutze M (1987) Aging of the human lens. Appl Opt 26:1437–1440
Sterling P, Freed MA, Smith RG (1988) Architecture of rod and cone circuits to the on-beta ganglion cell. J Neurosci 8:623–642
Liets LC, Eliasieh K, van der List DA, Chalupa LM (2006) Dendrites of rod bipolar cells sprout in normal aging retina. Proc Natl Acad Sci 103:12156–12160
Eliasieh K, Liets LC, Chalupa LM (2007) Cellular reorganization in the human retina during normal aging. Invest Ophthalmol Vis Sci 48:2824–2830
Li ZY, Kljavin IJ, Milam AH (1995) Rod photoreceptor neurite sprouting in retinitis pigmentosa. J Neurosci 15:5429–5438
Karpe G, Rickenbach K, Thomasson S (1950) The clinical electroretinogram. Acta Ophthalmol (Copenh) 28:301–305
Weleber RG (1981) The effect of age on human cone and rod Ganzfeld electroretinograms. Invest Ophthalmol Vis Sci 20:392–399
Birch DG, Anderson JL (1992) Standardized full-field electroretinography: normal values and their variation with age. Arch Ophthalmol 110:1571–1576
Gerth C, Garcia SM, Ma L et al (2002) Multifocal electroretinogram: age-related changes for different luminance levels. Graefes Arch Clin Exp Ophthalmol 240:202–208
Fortune B, Johnson CA (2002) Decline of photopic multifocal electroretinogram responses with age is due primarily to preretinal optical factors. J Opt Soc Am A 19:173–184
Jackson GR, De Leon Ortega J, Girkin C et al (2002) Aging-related changes in the multifocal electroretinogram. J Opt Soc Am A 19:185–189
Tam W-K, Chan H, Brown B et al (2006) Aging and mfERG topography. Eye Lond Engl 20:18–24. doi:10.1038/sj.eye.6701777
Tam W-K, Chan H, Brown B et al (2005) Comparing the multifocal electroretinogram topography before and after cataract surgery. Curr Eye Res 30:593–599. doi:10.1080/02713680590968565
Mohidin N, Yap MKH, Jacobs RJ (1999) Influence of age on the multifocal electroretinography. Ophthalmic Physiol Opt 19:481–488
Tzekov RT, Gerth C, Werner JS (2004) Senescence of human multifocal electroretinogram components: a localized approach. Graefes Arch Clin Exp Ophthalmol 242:549–560
Hood DC, Seiple W, Holopigian K, Greenstein V (1997) A comparison of the components of the multifocal and full-field ERGs. Vis Neurosci 14:533–544
Boettner EA, Wolter JR (1962) Transmission of the ocular media. Invest Ophthalmol Vis Sci 1:776–783
Desai P, Reidy A, Minassian DC et al (1996) Gains from cataract surgery: visual function and quality of life. Br J Ophthalmol 80:868–873
Lamoureux EL, Fenwick E, Pesudovs K, Tan D (2011) The impact of cataract surgery on quality of life. Curr Opin Ophthalmol 22:19–27
Pfoff DS, Werner JS (1994) Effect of cataract surgery on contrast sensitivity and glare in patients with 20/50 or better Snellen acuity. J Cataract Refract Surg 20:620–625
Acknowledgments
This study was supported by the NIH/National Institute on Aging (AG04058) and Research to Prevent Blindness. The authors thank Susan Garcia, Kyle McDermott, and Erich Sutter.
Funding
This study was funded by the NIH/National Institute on Aging (AG04058) and Research to Prevent Blindness.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
All authors declare that they have no conflict of interest.
Ethical approval
All procedures performed in studies involving human participants were in accordance with the ethical standard of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Statements of human rights
All procedures performed in this study were in accordance with the ethical standard of the Office of Human Research Protection of the University of California, Davis, School of Medicine and with the 1964 Helsinki Declaration and its later amendments.
Informed consent
Informed consent was obtained from all individual participants included in the study.
Rights and permissions
About this article
Cite this article
Tillman, M.A., Panorgias, A. & Werner, J.S. Age-related change in fast adaptation mechanisms measured with the scotopic full-field ERG. Doc Ophthalmol 132, 201–212 (2016). https://doi.org/10.1007/s10633-016-9541-2
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10633-016-9541-2