Selective loss of the photopic negative response in patients with optic nerve atrophy.

OBJECTIVE To determine how the photopic negative response (PhNR) is altered in patients with optic nerve atrophy. METHODS Ten patients with optic nerve atrophy induced by compression, trauma, or inflammation were examined. There were 6 men and 4 women with a mean age of 52.4 years. Ten age-matched control subjects were examined with the same protocol. Full-field electroretinograms were recorded, and the retinal nerve fiber layer thickness surrounding the optic nerve head was measured by means of optical coherence tomography. RESULTS The amplitudes of the rod, maximum, cone, and 30-Hz flicker electroretinograms of the affected eyes were not different from those of the corresponding waves of the contralateral unaffected eyes or control eyes. In contrast, the amplitude of the PhNR was significantly smaller in the affected eyes than in the contralateral (P =.005) or control (P<.001) eyes. The decrease in amplitude of the PhNR preceded thinning of the retinal nerve fiber layer. There was a significant correlation between the PhNR amplitude and retinal nerve fiber layer thickness in eyes with optic nerve atrophy (r = 0.879; P<.001). CONCLUSIONS Selective reduction and loss of the PhNR amplitude was found in eyes with optic nerve atrophy, which suggests that the PhNR can be used to evaluate the function of ganglion cells or their axons.

[1]  P. Sieving,et al.  Contribution of the Photopic Negative Response to the Photopic ERG in Rats With Inherited Photoreceptor Degeneration , 2002 .

[2]  M. Mita,et al.  A new wavelet in the multifocal electroretinogram, probably originating from ganglion cells. , 2002, Investigative ophthalmology & visual science.

[3]  N. Gellrich,et al.  Quantification of histological changes after calibrated crush of the intraorbital optic nerve in rats , 2002, The British journal of ophthalmology.

[4]  L. Zangwill,et al.  Using optical imaging summary data to detect glaucoma. , 2001, Ophthalmology.

[5]  H. Grossniklaus,et al.  Quantification of optic nerve axon loss associated with a relative afferent pupillary defect in the monkey. , 2001, Archives of ophthalmology.

[6]  J. Robson,et al.  The photopic negative response of the flash electroretinogram in primary open angle glaucoma. , 2001, Investigative ophthalmology & visual science.

[7]  D. Zurakowski,et al.  Ganglion cell loss after optic nerve crush mediated through AMPA-kainate and NMDA receptors. , 2000, Investigative ophthalmology & visual science.

[8]  J. Robson,et al.  The uniform field and pattern ERG in macaques with experimental glaucoma: removal of spiking activity. , 2000, Investigative ophthalmology & visual science.

[9]  L. Scullica,et al.  Photopic negative response of the human ERG: losses associated with glaucomatous damage. , 2000, Investigative ophthalmology & visual science.

[10]  M. Vidal-Sanz,et al.  Microglial cells in the retina of Carassius auratus: Effects of optic nerve crush , 2000, The Journal of comparative neurology.

[11]  Earl L. Smith,et al.  The photopic negative response of the macaque electroretinogram: reduction by experimental glaucoma. , 1999, Investigative ophthalmology & visual science.

[12]  M. Marmor,et al.  Standard for clinical electroretinography (1999 update) , 1998, Documenta Ophthalmologica.

[13]  S. Bloomfield Effect of spike blockade on the receptive-field size of amacrine and ganglion cells in the rabbit retina. , 1996, Journal of neurophysiology.

[14]  J G Fujimoto,et al.  Evaluation of focal defects of the nerve fiber layer using optical coherence tomography. , 1996, Ophthalmology.

[15]  Eberhart Zrenner,et al.  Standard for clinical electroretinography , 1989, Documenta Ophthalmologica.

[16]  P. Sieving,et al.  Scotopic threshold response (STR) of the human electroretinogram. , 1988, Investigative ophthalmology & visual science.

[17]  L. Halperin,et al.  Afferent pupillary defect caused by hyphema. , 1988, American journal of ophthalmology.

[18]  L. Frishman,et al.  Scotopic threshold response of proximal retina in cat. , 1986, Journal of neurophysiology.

[19]  L. Maffei,et al.  Pattern ERG in the monkey after section of the optic nerve , 1986, Behavioural Brain Research.

[20]  J J Corbett,et al.  How to measure the relative afferent pupillary defect. , 1981, Survey of ophthalmology.

[21]  A. Fiorentini,et al.  Electroretinographic responses to alternating gratings before and after section of the optic nerve. , 1981, Science.

[22]  T. Narahashi Chemicals as tools in the study of excitable membranes. , 1974, Physiological reviews.

[23]  Y. Gotoh [Photopic negative response of eyes with normal-tension glaucoma]. , 2002, Nippon Ganka Gakkai zasshi.

[24]  M. Kondo,et al.  A contact lens electrode with built-in high intensity white light-emitting diodes. A contact lens electrode with built-in white LEDs. , 2001, Documenta ophthalmologica. Advances in ophthalmology.

[25]  R S Harwerth,et al.  The scotopic electroretinogram of macaque after retinal ganglion cell loss from experimental glaucoma. , 1996, Investigative ophthalmology & visual science.

[26]  W. Spileers,et al.  The human erg evoked by a ganzfeld stimulator powered by red and green light emitting diodes , 1993 .

[27]  P. Sieving Retinal ganglion cell loss does not abolish the scotopic threshold response (STR) of the cat and human ERG , 1991 .