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Erschienen in: Documenta Ophthalmologica 3/2018

Open Access 22.06.2018 | ISCEV Standards

ISCEV extended protocol for the photopic On–Off ERG

verfasst von: Maja Sustar, Graham E. Holder, Jan Kremers, Claire S. Barnes, Bo Lei, Naheed W. Khan, Anthony G. Robson

Erschienen in: Documenta Ophthalmologica | Ausgabe 3/2018

Abstract

The International Society for Clinical Electrophysiology of Vision (ISCEV) standard for full-field electroretinography (ERG) describes a minimum procedure, but encourages more extensive testing. This ISCEV extended protocol describes an extension to the ERG standard, namely the photopic On–Off ERG, and outlines common clinical applications. A light stimulus duration of 150–200 ms is used in the presence of a rod-suppressing background to elicit cone-driven On- and Off-system ERG components. The On-response occurs after the stimulus onset and has a negative a-wave and positive b-wave. The Off d-wave is a positive component evoked by stimulus offset. Common diagnoses that may benefit from additional photopic On–Off ERG testing include retinal dystrophies and retinal disorders that cause dysfunction at a level that is post-phototransduction or post-receptoral. On–Off ERGs assess the relative involvement of On- and Off-systems and may be of use in the diagnosis of disorders such as complete and incomplete congenital stationary night blindness (complete and incomplete CSNB), melanoma-associated retinopathy, and some forms of autoimmune retinopathy. The photopic On–Off ERGs may also be useful in X-linked retinoschisis, Batten disease, Duchenne muscular dystrophy, spinocerebellar degeneration, quinine toxicity, and other retinal disorders.

Introduction

The International Society for Clinical Electrophysiology of Vision (ISCEV) standard for full-field electroretinography (ERG) describes a minimum set of tests but encourages the use of additional ERG protocols for clinical ERG testing [1]. This extended protocol describes the photopic On–Off ERG, as a specialized procedure which is well established and broadly accepted by experts in the field. The protocol was prepared by the authors in accordance with ISCEV procedures http://​www.​iscev.​org/​standards/​index.​html), and was approved by the ISCEV Board of Directors on 25th March 2018.

Scope and applications

The standard light-adapted (LA) 3.0 ERG b-wave is evoked with flashes of a short duration (< 5 ms) on a rod-saturating background and largely reflects overlapping contributions from the On- and Off-bipolar cell pathways. Separation of the function of the On- and Off-pathways requires long-duration stimuli (e.g., 150–200 ms) in the presence of a rod-saturating background. The photopic On–Off ERG has two major components, the On-response and the Off-response. The On-response occurs after the stimulus onset and consists of two prominent waves, the negative polarity a-wave and the positive b-wave. The Off-response, or d-wave, is a positive polarity component in response to stimulus offset [24]. The sources of On- and Off-responses were elucidated by experimental pharmacological studies in non-human primates, whose ERGs are very similar to those in humans. These studies showed that the a-wave of the On-response originates from cone photoreceptors, with a significant contribution from Off- (hyperpolarizing) bipolar cells [5]. The b-wave of the On-response reflects the function of the On- (depolarizing) bipolar cells, although its amplitude and shape may be influenced by Off-bipolar and horizontal cells [6]. The d-wave is a complex response; the initial rapid phase originates from Off-bipolar cell activity, but cone photoreceptors contribute to the later slow phase and On-bipolar cells act in an opposite polarity direction [7, 8].
Common diagnoses that may benefit from additional photopic On–Off ERG testing include retinal dystrophies and retinal disorders that cause dysfunction post-phototransduction or at a post-receptoral level. The photopic On–Off ERG allows evaluation of the relative or selective involvement of On- and Off-pathways, not fully enabled by the standard LA 3.0 ERG responses [24, 915]. Common forms of congenital stationary night blindness (CSNB) are good illustrative examples. In complete CSNB, there is generalized On-bipolar cell dysfunction, and the waveform shows an electronegative On-response but a preserved Off-response. In contrast, incomplete CSNB is associated with abnormalities affecting both the On- and Off-responses [2]. Other retinal disorders associated with selective On-pathway dysfunction include melanoma-associated retinopathy, early cases of phosphomannomutase deficiency (PMM2-CDG) [12], and some forms of autoimmune retinopathy [15]. The photopic On–Off ERGs may also be useful in X-linked retinoschisis, Batten disease, Duchenne muscular dystrophy, spinocerebellar degeneration, quinine toxicity, and other disorders [16, 17].

Patient population

Patients of all ages able to tolerate Ganzfeld stimulation, referred for investigation of possible retinal dysfunction, especially those with decreased light-adapted and/or dark-adapted ERG b-wave and relatively preserved a-wave (electronegative ERG or low b:a ratio), suggesting dysfunction post-phototransduction or at the level of the bipolar cells.

Technical issues

The photopic On–Off ERG protocol will follow the specifications of the current ISCEV standard ERG [1]. Additional considerations include the following:
(a) Stimulus duration. The duration of the light stimulus should be long enough to separate the On- and Off-responses. Most studies used durations of between 150 and 200 ms (Table 1 in appendix), based on the largest d-wave amplitude attained, although statistically, smaller amplitudes are reported only for flash durations shorter than 75 ms [18]. Further increase in the d-wave amplitude was observed with stimuli up to 900 ms duration [19], but responses to such long durations take longer to record. Patient comfort and minimizing possible eye closure and blink artefacts are considerations when selecting the light duration.
(b) Stimulus wavelength. The flash and background wavelength for the ISCEV standard ERG are defined as visibly white, with CIE coordinates near x = 0.31, y = 0.32. Both white and chromatic (blue and green) stimuli have been used to elicit On–Off ERGs of similar waveform [18]. Some laboratories use orange stimuli in the presence of green background, for more selective stimulation of L-and M-cone system with simultaneous suppression of the rods and S-cones [17, 20]. These stimuli are effective at eliciting On- and Off-responses and have been shown to be informative in numerous studies. Longer wavelength stimuli (red) may decrease the d-wave and change the shape of the b-wave [18, 19] and should be avoided.
(c) Stimulus strength and background luminance. Brighter backgrounds require stronger stimuli to elicit detectable responses [18]. If stimuli are too weak, responses are small. If stimuli are too strong the b-wave becomes broader and peak time variable and difficult to determine [18], while the d-wave becomes either decreased or dominated by a component of longer peak time (the basis of the photopic hill phenomenon) [21]. Strong stimuli and backgrounds may also be poorly tolerated by some patients.

Calibration

The protocol is technically similar to that for the ISCEV standard ERG, and the calibration and frequency of calibration should follow the latest ISCEV standard [1]. The strength of the stimulus and background luminance should be specified in photopic candelas per meter squared (phot cd m−2).

Protocol specification

Patient preparation follows that for the current ISCEV standard ERG [1]. It is suggested that for routine applications the photopic On–Off ERG is added to the ISCEV standard protocol after the other LA ERGs. This extended protocol has the following additional specifications.
(a) Stimulus duration. A stimulus duration of 150 ms or 200 ms. To allow clear separation of On- and Off- responses, efficient signal averaging and to maintain consistency with the majority of published clinical studies to date.
(b) Stimulus wavelength. A white stimulus on a white background (as used in the majority of published studies) or a chromatic light on a chromatic background (to suppress rods and S-cones) may be used providing longer wavelength (red) stimuli are avoided. Orange (620 nm) stimuli in the presence of green (560 nm) background may allow more selective stimulation of L-and M-cone systems with simultaneous suppression of the rods and S-cones.
(c) Stimulus strength and background luminance. Stimulus luminance for white stimuli is 250 cd m−2 or within the range phot 150–350 cd m−2 with a background luminance of 30 cd m−2.
(d) Frequency of stimulus presentation. A stimulus rate of ≤ 2 per second (inter-stimulus interval ≥ 0.5 s), as for the current ISCEV Standard LA 3.0 ERG.

Response evaluation

The photopic On–Off ERG response consists of three prominent waves, the a- and b-waves as part of the On-response and the Off-response complex, mainly the d-wave (Fig. 1). A negative a-wave appears in response to the onset of the stimulus, followed by the positive-going On-response b-wave. The d-wave of the Off-response is the positive peak, which occurs after stimulus offset. The amplitude of the a-wave is measured from the baseline to the first negative trough. The amplitude of the b-wave is measured from the trough of the a-wave to the peak of the b-wave. The amplitude of the d-wave is measured from the time point of stimulus offset to the peak of the d-wave. Peak times of On-response components are measured from the beginning of the stimulus to the trough of the a-wave and peak of the b-wave; Off-response peak time is measured from stimulus offset to the peak of the d-wave. The amplitude and peak time values should be evaluated and compared with reference normative data, established in each laboratory for its own equipment, recording protocols and patient population.

Reporting

This protocol is intended to be used for routine applications as an extension to the standard ERG protocol, and reporting should follow the latest ISCEV standard for ERG [1]. Additionally, the spectral characteristics of the stimulus and background should be acknowledged if different from the standard LA ERG (e.g., peak wavelength and bandwidth). The duration of the light stimulus should be stated and luminance (in phot cd m−2) of stimulus and background should be stated. Unless already embedded within the ISCEV standard ERG protocol, pupil size and duration of light adaption should be stated. The amplitude of the a-, b-, and d-waves and respective time to peaks may be reported along with age-appropriate laboratory reference normative data. It is acknowledged that in diagnostic studies involving ISCEV standard ERGs, it may be sufficiently informative to describe the relative involvement of On–Off ERG a-, b-, and d-waves qualitatively.

Acknowledgements

We would like to thank the ISCEV membership for suggestions during the consultation period and in particular Daphne McCulloch and Mineo Kondo.

Compliance with ethical standards

Conflict of interest

The authors have no conflicts of interest.

Statement of human rights

The study involved no research on Human participants and consent is not applicable.

Statement on the welfare of animals

The study involved no research on animals.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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Appendix

Experimental procedures excluded from this extended protocol
ERG recordings with long-duration stimuli can be affected by technical issues, and blink and squint artefacts may disturb the recordings. Some authors suggest that this may be alleviated by using stimuli with sawtooth luminance profiles. The recordings are typically performed at photopic luminances. Instead of a stimulus upon a background, these stimuli are modulated around a mean. The stimulus strength is quantified by Michelson contrast (C): C = (Lmax + Lmin)/(Lmax − Lmin) in which Lmax and Lmin are the maximal and minimal luminance in the stimulus. Since this stimulus is given repetitively with a frequency between 2 and 8 Hz, blink artefacts do not play a large role. Higher frequencies are not recommended because the responses to subsequent stimuli may merge. On- and Off-responses are obtained separately by using rapid-ON and rapid-OFF stimuli. They have been used in a variety of disorders [2227] and may have benefits, but have not been widely available on commercial systems. On- and Off-responses may not be the same for all stimulus types. It has been reported that On- and Off-responses originating in the L-cones have the same morphology as those obtained with luminance stimuli. In contrast, M-cone-driven On-responses resemble Off-responses with L-cone isolating and luminance stimuli and vice versa, suggesting that cone opponent processes may be involved [2830]. Beside the sawtooth stimulation, increment and decrement stimulation is another way of eliciting the d-wave without a major impact of blink artefacts [31].
An alternative method extracts On- and Off-responses from the LA 3.0 ERG through the quantification of wavelet coefficients by discrete wavelet transform (DWT) analyses [32]. This approach suggests the activity of the retinal On-pathway to be related to a 20 Hz component of the photopic ERG, while the Off-pathway activity is reflected by a 40-Hz component. This finding was based on the fact that 20 and 40 Hz components of the photopic b-wave are selectively attenuated in case of imbalanced dysfunction of the On- and Off-pathways in some diseases [32], confirmed with the DWT of the photopic On–Off ERGs [33].
Since the photopic On–Off ERG is potentially valuable ERG method in animal studies, researchers should be aware that positive On- and Off-responses, as those in humans, can only be recorded in some non-human primates, while On- and Off-responses with electronegative waveform are present in rodents including mice and rats [34].
Justification for the protocol details
A literature review was performed with Medline search engine to find publications that reported photopic On–Off ERG using following keywords: electroretinogram or full-field ERG or long-duration flash, b-wave or ON-response, d-wave or OFF-response. Studies from the year 1986 to 2016 were reviewed and those that specified stimulus parameters are summarized in Table 1. For the purposes of developing a clinical protocol animal studies were excluded, as were studies using multifocal, focal and saw tooth type of stimulation and studies focusing on the function of rod or ganglion cell systems. Other exclusions included responses obtained by silent substitution [2830] and analyses of On and Off components derived from discrete wavelet transform (DWT) analyses of the LA 3 ERG [32, 33]. Studies from the year 1986 to 2016 were reviewed and those that specified stimulus parameters are summarized in Table 1.
Table 1
Previously published recording parameters
References
Stimulus strength
Background luminance
Stimulus duration (ms)
Stimulus and background wavelength
[4]
185 cd m−2
43 cd m−2
150
White stimulus on white background
[3]
3.7 log cd m−2 (5011 cd m−2)
2.1 log cd m−2 (125 cd m−2)
5–100
White stimulus on white background
[9, 53]
3 cd s m−2 (15 cd m−2)a
10 cd m−2
200 and 250
Red and green stimulus on white background
[10]
750 cd m−2
42 cd m−2
500
White stimulus on white background
[11]
3 cd s m−2 (12 cd m−2)
10 cd m−2
256
630 nm stimulus on white background
[12]
200 cd m−2
43 cd m−2
90, 120
White 6500K
[13]
3 log cd s m−2 (5000 cd m−2)
2 log cd m−2 (100 cd m−2)
200
White stimulus on white background
[14]
398 cd m−2
48 cd m−2
200
White stimulus on white background
[21]
0.6–3.5 log cd m−2 (4–3162 cd m−2)
40 cd m−2
250
White stimulus on white background
[18, 56]
0.4–2.1 log cd s m−2 (12.5–629 cd m−2)
20-50 cd m−2
5–200
White, 460, 508 and 667 nm stimulus on white background
[15, 17, 20, 38, 41, 52]
560 cd m−2
160 cd m−2
150–200
620 nm stimulus on 530 nm background
[35]
440 cd m−2
160 cd m−2
200
612 nm stimulus on 530 nm background
[36]
133 cd m−2
43 cd m−2
120
White 6500K
[37]
1.7 log cd s m−2 (250 cd m−2)
40 cd m−2
200
White stimulus (6500K) on white background
[39]
1 cd s/m2 (4 cd m−2)
30 cd m−2
250
White 6500K
[40]
200 cd m−2
42 cd m−2
150
White stimulus on white background
[42]
4 log ph td (200 cd m−2)b
3.3 log ph td (40 cd m−2)b
150
White stimulus on white background
[43]
200 cd m−2
30 cd m−2
100
White stimulus on white background
[44]
225 cd m−2
30 cd m−2
188
White stimulus on white background
[4548]
300 cd m−2
40 cd m−2
150
White stimulus on white background
[49]
650 cd m−2
160 cd m−2
120, 200
Orange stimulus on green background
[50]
200 cd m−2
42 cd m−2
150
White stimulus on white background
[51]
1700 cd m−2
28 cd m−2
125
White stimulus on white background
[54]
360 cd m−2
40 cd m−2
100
White stimulus on white background
[55, 57]
1120 cd m−2
30 cd m−2
200
White stimulus on white background
[58]
40,60,80 cd m−2
20 cd m−2
240
White stimulus on white background
[59]
2.5 log cd m−2 (316 cd m−2)
40 cd m−2
150
White stimulus on white background
aTime integrated luminance divided by the length of the stimulus in seconds
bCalculated for 8 mm pupil diameter
Literatur
1.
Zurück zum Zitat McCulloch DL, Marmor MF, Brigell MG, Hamilton R, Holder GE, Tzekov R, Bach M (2015) ISCEV Standard for full-field clinical electroretinography (2015 update). Doc Ophthalmol 130:1–12CrossRefPubMed McCulloch DL, Marmor MF, Brigell MG, Hamilton R, Holder GE, Tzekov R, Bach M (2015) ISCEV Standard for full-field clinical electroretinography (2015 update). Doc Ophthalmol 130:1–12CrossRefPubMed
2.
Zurück zum Zitat Miyake Y, Yagasaki K, Horiguchi M, Kawase Y (1987) On- and off responses in photopic electroretinogram in complete and incomplete types of congenital stationary night blindness. Jpn J Ophthalmol 31:81–87PubMed Miyake Y, Yagasaki K, Horiguchi M, Kawase Y (1987) On- and off responses in photopic electroretinogram in complete and incomplete types of congenital stationary night blindness. Jpn J Ophthalmol 31:81–87PubMed
3.
Zurück zum Zitat Alexander KR, Fishman GA, Peachey NS, Marchese AL, Tso MOM (1992) ‘On’ response defect in paraneoplastic night blindness with cutaneous malignant melanoma. Invest Ophthalmol Vis Sci 33:477–483PubMed Alexander KR, Fishman GA, Peachey NS, Marchese AL, Tso MOM (1992) ‘On’ response defect in paraneoplastic night blindness with cutaneous malignant melanoma. Invest Ophthalmol Vis Sci 33:477–483PubMed
4.
Zurück zum Zitat Sieving PA (1993) Photopic ON- and OFF-pathway abnormalities in retinal dystrophies. Trans Am Ophthalmol Soc 91:701–773PubMedPubMedCentral Sieving PA (1993) Photopic ON- and OFF-pathway abnormalities in retinal dystrophies. Trans Am Ophthalmol Soc 91:701–773PubMedPubMedCentral
5.
Zurück zum Zitat Bush RA, Sieving PA (1994) A proximal retinal component in the primate photopic ERG a-wave. Invest Ophthalmol Vis Sci 35:635–645PubMed Bush RA, Sieving PA (1994) A proximal retinal component in the primate photopic ERG a-wave. Invest Ophthalmol Vis Sci 35:635–645PubMed
6.
Zurück zum Zitat Sieving PA, Murayama K, Naarendorp F (1994) Push-pull model of the primate photopic electroretinogram: a role for hyperpolarizing neurons in shaping the b-wave. Vis Neurosci 11:519–532CrossRefPubMed Sieving PA, Murayama K, Naarendorp F (1994) Push-pull model of the primate photopic electroretinogram: a role for hyperpolarizing neurons in shaping the b-wave. Vis Neurosci 11:519–532CrossRefPubMed
7.
Zurück zum Zitat Ueno S, Kondo M, Ueno M, Miyata K, Terasaki H, Miyake Y (2006) Contribution of retinal neurons to d-wave of primate photopic electroretinograms. Vision Res 46:658–664CrossRefPubMed Ueno S, Kondo M, Ueno M, Miyata K, Terasaki H, Miyake Y (2006) Contribution of retinal neurons to d-wave of primate photopic electroretinograms. Vision Res 46:658–664CrossRefPubMed
8.
Zurück zum Zitat Khan NW, Kondo M, Hiriyanna KT, Jamison JA, Bush RA, Sieving PA (2005) Primate retinal signaling pathways: suppressing ON-pathway activity in monkey with glutamate analogues mimics human CSNB1-NYX genetic night blindness. J Neurophysiol 93:481–492CrossRefPubMed Khan NW, Kondo M, Hiriyanna KT, Jamison JA, Bush RA, Sieving PA (2005) Primate retinal signaling pathways: suppressing ON-pathway activity in monkey with glutamate analogues mimics human CSNB1-NYX genetic night blindness. J Neurophysiol 93:481–492CrossRefPubMed
9.
Zurück zum Zitat Ruether K, Kellner U (1998) Inner retinal function in hereditary retinal dystrophies. Acta Anat (Basel) 162:169–177CrossRef Ruether K, Kellner U (1998) Inner retinal function in hereditary retinal dystrophies. Acta Anat (Basel) 162:169–177CrossRef
10.
Zurück zum Zitat Quigley M, Roy MS, Barsoum-Homsy M, Chevrette L, Jacob JL, Milot J (1996) On- and off-responses in the photopic electroretinogram in complete-type congenital stationary night blindness. Doc Ophthalmol 92:159–165CrossRefPubMed Quigley M, Roy MS, Barsoum-Homsy M, Chevrette L, Jacob JL, Milot J (1996) On- and off-responses in the photopic electroretinogram in complete-type congenital stationary night blindness. Doc Ophthalmol 92:159–165CrossRefPubMed
11.
Zurück zum Zitat Kellner U, Bornfeld N, Foerster MH (1995) Severe course of cutaneous melanoma associated paraneoplastic retinopathy. Br J Ophthalmol 79:746–752CrossRefPubMedPubMedCentral Kellner U, Bornfeld N, Foerster MH (1995) Severe course of cutaneous melanoma associated paraneoplastic retinopathy. Br J Ophthalmol 79:746–752CrossRefPubMedPubMedCentral
12.
Zurück zum Zitat Thompson DA, Lyons RJ, Liasis A, Russell-Eggitt I, Jägle H, Grünewald S (2012) Retinal on-pathway deficit in congenital disorder of glycosylation due to phosphomannomutase deficiency. Arch Ophthalmol 130:712–719PubMed Thompson DA, Lyons RJ, Liasis A, Russell-Eggitt I, Jägle H, Grünewald S (2012) Retinal on-pathway deficit in congenital disorder of glycosylation due to phosphomannomutase deficiency. Arch Ophthalmol 130:712–719PubMed
13.
Zurück zum Zitat Cibis GW, Fitzgerald KM (2001) The negative ERG is not synonymous with nightblindness. Trans Am Ophthalmol Soc 99:171–176PubMedPubMedCentral Cibis GW, Fitzgerald KM (2001) The negative ERG is not synonymous with nightblindness. Trans Am Ophthalmol Soc 99:171–176PubMedPubMedCentral
14.
Zurück zum Zitat Allen LE, Zito I, Bradshaw K, Patel RJ, Bird AC, Fitzke F, Yates JR, Trump D, Hardcastle AJ, Moore AT (2003) Genotype-phenotype correlation in British families with X linked congenital stationary night blindness. Br J Ophthalmol 87:1413–1420CrossRefPubMedPubMedCentral Allen LE, Zito I, Bradshaw K, Patel RJ, Bird AC, Fitzke F, Yates JR, Trump D, Hardcastle AJ, Moore AT (2003) Genotype-phenotype correlation in British families with X linked congenital stationary night blindness. Br J Ophthalmol 87:1413–1420CrossRefPubMedPubMedCentral
15.
Zurück zum Zitat Robson AG, Richardson EC, Koh AH, Pavesio CE, Hykin PG, Calcagni A, Graham EM, Holder GE (2005) Unilateral electronegative ERG of non-vascular aetiology. Br J Ophthalmol 89:1620–1626CrossRefPubMedPubMedCentral Robson AG, Richardson EC, Koh AH, Pavesio CE, Hykin PG, Calcagni A, Graham EM, Holder GE (2005) Unilateral electronegative ERG of non-vascular aetiology. Br J Ophthalmol 89:1620–1626CrossRefPubMedPubMedCentral
16.
Zurück zum Zitat Kim JM, Payne JF, Yan J, Barnes CS (2012) Negative electroretinograms in the pediatric and adult population. Doc Ophthalmol 124:41–48CrossRefPubMed Kim JM, Payne JF, Yan J, Barnes CS (2012) Negative electroretinograms in the pediatric and adult population. Doc Ophthalmol 124:41–48CrossRefPubMed
17.
Zurück zum Zitat Audo I, Robson AG, Holder GE, Moore AT (2008) The negative ERG: clinical phenotypes and disease mechanisms of inner retinal dysfunction. Surv Ophthalmol 53:16–40CrossRefPubMed Audo I, Robson AG, Holder GE, Moore AT (2008) The negative ERG: clinical phenotypes and disease mechanisms of inner retinal dysfunction. Surv Ophthalmol 53:16–40CrossRefPubMed
18.
Zurück zum Zitat Sustar M, Hawlina M, Brecelj J (2006) ON- and OFF-response of the photopic electroretinogram in relation to stimulus characteristics. Doc Ophthalmol 113:43–52CrossRefPubMed Sustar M, Hawlina M, Brecelj J (2006) ON- and OFF-response of the photopic electroretinogram in relation to stimulus characteristics. Doc Ophthalmol 113:43–52CrossRefPubMed
19.
Zurück zum Zitat Evers HU, Gouras P (1986) Three cone mechanisms in the primate electroretinogram: two with, one without off-center bipolar responses. Vision Res 26:245–254CrossRefPubMed Evers HU, Gouras P (1986) Three cone mechanisms in the primate electroretinogram: two with, one without off-center bipolar responses. Vision Res 26:245–254CrossRefPubMed
20.
Zurück zum Zitat Audo I, Michaelides M, Robson AG, Hawlina M, Vaclavik V, Sandbach JM, Neveu MM, Hogg CR, Hunt DM, Moore AT, Bird AC, Webster AR, Holder GE (2008) Phenotypic variation in enhanced S-cone syndrome. Invest Ophthalmol Vis Sci 49:2082–2093CrossRefPubMed Audo I, Michaelides M, Robson AG, Hawlina M, Vaclavik V, Sandbach JM, Neveu MM, Hogg CR, Hunt DM, Moore AT, Bird AC, Webster AR, Holder GE (2008) Phenotypic variation in enhanced S-cone syndrome. Invest Ophthalmol Vis Sci 49:2082–2093CrossRefPubMed
21.
Zurück zum Zitat Kondo M, Piao CH, Tanikawa A, Horiguchi M, Terasaki H, Miyake Y (2000) Amplitude decrease of photopic ERG b-wave at higher stimulus intensities in humans. Jpn J Ophthalmol 44:20–28CrossRefPubMed Kondo M, Piao CH, Tanikawa A, Horiguchi M, Terasaki H, Miyake Y (2000) Amplitude decrease of photopic ERG b-wave at higher stimulus intensities in humans. Jpn J Ophthalmol 44:20–28CrossRefPubMed
22.
Zurück zum Zitat Barnes CS, Alexander KR, Fishman GA (2002) A distinctive form of congenital stationary night blindness with cone ON-pathway dysfunction. Ophthalmology 109:575–583CrossRefPubMed Barnes CS, Alexander KR, Fishman GA (2002) A distinctive form of congenital stationary night blindness with cone ON-pathway dysfunction. Ophthalmology 109:575–583CrossRefPubMed
23.
Zurück zum Zitat Dryja TP, McGee TL, Berson EL, Fishman GA, Sandberg MA, Alexander KR, Derlacki DJ, Rajagopalan AS (2005) Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6. Proc Natl Acad Sci USA 102:4884–4889CrossRefPubMed Dryja TP, McGee TL, Berson EL, Fishman GA, Sandberg MA, Alexander KR, Derlacki DJ, Rajagopalan AS (2005) Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6. Proc Natl Acad Sci USA 102:4884–4889CrossRefPubMed
24.
Zurück zum Zitat Alexander KR, Barnes CS, Fishman GA, Milam AH (2002) Nature of the cone ON-pathway dysfunction in melanoma-associated retinopathy. Invest Ophthalmol Vis Sci 43:1189–1197PubMed Alexander KR, Barnes CS, Fishman GA, Milam AH (2002) Nature of the cone ON-pathway dysfunction in melanoma-associated retinopathy. Invest Ophthalmol Vis Sci 43:1189–1197PubMed
25.
Zurück zum Zitat Alexander KR, Fishman GA, Barnes CS, Grover S (2001) ON-response deficit in the electroretinogram of the cone system in X-linked retinoschisis. Invest Ophthalmol Vis Sci 42:453–459PubMed Alexander KR, Fishman GA, Barnes CS, Grover S (2001) ON-response deficit in the electroretinogram of the cone system in X-linked retinoschisis. Invest Ophthalmol Vis Sci 42:453–459PubMed
26.
Zurück zum Zitat Pangeni Lämmer GR, Tornow RP, Horn FK, Kremers J (2012) On- and Off- response ERGs elicited by sawtooth stimuli in normal subjects and glaucoma patients. Doc Ophthalmol 124:237–248CrossRefPubMed Pangeni Lämmer GR, Tornow RP, Horn FK, Kremers J (2012) On- and Off- response ERGs elicited by sawtooth stimuli in normal subjects and glaucoma patients. Doc Ophthalmol 124:237–248CrossRefPubMed
27.
Zurück zum Zitat Barboni MTS, Nagy BV, de Araújo Moura AL, Damico FM, da Costa MF, Kremers J, Ventura DF (2013) ON and OFF electroretinogram and contrast sensitivity in Duchenne muscular dystrophy. Invest Ophthalmol Vis Sci 54:3195–3204CrossRefPubMed Barboni MTS, Nagy BV, de Araújo Moura AL, Damico FM, da Costa MF, Kremers J, Ventura DF (2013) ON and OFF electroretinogram and contrast sensitivity in Duchenne muscular dystrophy. Invest Ophthalmol Vis Sci 54:3195–3204CrossRefPubMed
28.
Zurück zum Zitat McKeefry D, Kremers J, Kommanapalli D, Challa NK, Murray IJ, Maguire J, Parry NRA (2014) Incremental and decremental L- and M-cone driven ERG responses: I. Square-wave pulse stimulation. J Opt Soc Am A 31:A159–A169CrossRef McKeefry D, Kremers J, Kommanapalli D, Challa NK, Murray IJ, Maguire J, Parry NRA (2014) Incremental and decremental L- and M-cone driven ERG responses: I. Square-wave pulse stimulation. J Opt Soc Am A 31:A159–A169CrossRef
29.
Zurück zum Zitat Kremers J, Pangeni G, Tsaousis KT, McKeefry D, Murray IJ, Parry NRA (2014) Incremental and decremental L- and M-cone driven ERG responses: II. Sawtooth stimulation. J Opt Soc Am A 31:A170–A178CrossRef Kremers J, Pangeni G, Tsaousis KT, McKeefry D, Murray IJ, Parry NRA (2014) Incremental and decremental L- and M-cone driven ERG responses: II. Sawtooth stimulation. J Opt Soc Am A 31:A170–A178CrossRef
30.
Zurück zum Zitat Tsai TI, Jacob MM, McKeefry D, Murray IJ, Parry NRA, Kremers J (2016) Spatial properties of L- and M-cone driven incremental (On-) and decremental (Off-) electroretinograms: evidence for the involvement of multiple post-receptoral mechanisms. J Opt Soc Am A 33:A1–A11CrossRef Tsai TI, Jacob MM, McKeefry D, Murray IJ, Parry NRA, Kremers J (2016) Spatial properties of L- and M-cone driven incremental (On-) and decremental (Off-) electroretinograms: evidence for the involvement of multiple post-receptoral mechanisms. J Opt Soc Am A 33:A1–A11CrossRef
31.
Zurück zum Zitat Vukmanic E, Godwin K, Shi P, Hughes A, DeMarco P Jr (2014) Full-field electroretinogram response to increment and decrement stimuli. Doc Ophthalmol 129:85–95CrossRefPubMed Vukmanic E, Godwin K, Shi P, Hughes A, DeMarco P Jr (2014) Full-field electroretinogram response to increment and decrement stimuli. Doc Ophthalmol 129:85–95CrossRefPubMed
32.
Zurück zum Zitat Gauvin M, Little JM, Lina JM, Lachapelle P (2015) Functional decomposition of the human ERG based on the discrete wavelet transform. J Vis 15:14CrossRefPubMed Gauvin M, Little JM, Lina JM, Lachapelle P (2015) Functional decomposition of the human ERG based on the discrete wavelet transform. J Vis 15:14CrossRefPubMed
33.
Zurück zum Zitat Gauvin M, Sustar M, Little JM, Brecelj J, Lina JM, Lachapelle P (2017) Quantifying the ON and OFF contributions to the flash ERG with the discrete wavelet transform. Transl Vis Sci Technol 10(6):3CrossRef Gauvin M, Sustar M, Little JM, Brecelj J, Lina JM, Lachapelle P (2017) Quantifying the ON and OFF contributions to the flash ERG with the discrete wavelet transform. Transl Vis Sci Technol 10(6):3CrossRef
34.
Zurück zum Zitat Lei B (2003) The ERG of guinea pig (Cavis porcellus): comparison with I-type monkey and E-type rat. Doc Ophthalmol 106:243–249CrossRefPubMed Lei B (2003) The ERG of guinea pig (Cavis porcellus): comparison with I-type monkey and E-type rat. Doc Ophthalmol 106:243–249CrossRefPubMed
35.
Zurück zum Zitat Kabanarou SA, Holder GE, Bird AC, Webster AR, Stanga PE, Vickers S, Harney BA (2004) Congenital stationary night blindness and a “Schubert-Bornschein” type electrophysiology in a family with dominant inheritance. Br J Ophthalmol 88:1018–1022CrossRefPubMedPubMedCentral Kabanarou SA, Holder GE, Bird AC, Webster AR, Stanga PE, Vickers S, Harney BA (2004) Congenital stationary night blindness and a “Schubert-Bornschein” type electrophysiology in a family with dominant inheritance. Br J Ophthalmol 88:1018–1022CrossRefPubMedPubMedCentral
36.
Zurück zum Zitat Constable PA, Gaigg SB, Bowler DM, Jägle H, Thompson DA (2016) Full-field electroretinogram in autism spectrum disorder. Doc Ophthalmol 132:83–99CrossRefPubMed Constable PA, Gaigg SB, Bowler DM, Jägle H, Thompson DA (2016) Full-field electroretinogram in autism spectrum disorder. Doc Ophthalmol 132:83–99CrossRefPubMed
37.
Zurück zum Zitat Sustar M, Perovšek D, Cima I, Stirn-Kranjc B, Hawlina M, Brecelj J (2015) Electroretinography and optical coherence tomography reveal abnormal post-photoreceptoral activity and altered retinal lamination in patients with enhanced S-cone syndrome. Doc Ophthalmol 130:165–177CrossRefPubMed Sustar M, Perovšek D, Cima I, Stirn-Kranjc B, Hawlina M, Brecelj J (2015) Electroretinography and optical coherence tomography reveal abnormal post-photoreceptoral activity and altered retinal lamination in patients with enhanced S-cone syndrome. Doc Ophthalmol 130:165–177CrossRefPubMed
38.
Zurück zum Zitat Ba-Abbad R, Robson AG, Yap YC, Moore AT, Webster AR, Holder GE (2014) PRPH2 mutations as a cause of electronegative ERG. Retina 34:1235–1243CrossRefPubMed Ba-Abbad R, Robson AG, Yap YC, Moore AT, Webster AR, Holder GE (2014) PRPH2 mutations as a cause of electronegative ERG. Retina 34:1235–1243CrossRefPubMed
39.
Zurück zum Zitat Schatz A, Breithaupt M, Hudemann J, Niess A, Messias A, Zrenner E, Bartz-Schmidt KU, Gekeler F, Willmann G (2014) Electroretinographic assessment of retinal function during acute exposure to normobaric hypoxia. Graefes Arch Clin Exp Ophthalmol 252:43–50CrossRefPubMed Schatz A, Breithaupt M, Hudemann J, Niess A, Messias A, Zrenner E, Bartz-Schmidt KU, Gekeler F, Willmann G (2014) Electroretinographic assessment of retinal function during acute exposure to normobaric hypoxia. Graefes Arch Clin Exp Ophthalmol 252:43–50CrossRefPubMed
40.
Zurück zum Zitat Raghuram A, Hansen RM, Moskowitz A, Fulton AB (2013) Photoreceptor and postreceptor responses in congenital stationary night blindness. Invest Ophthalmol Vis Sci 54:4648–4658CrossRefPubMedPubMedCentral Raghuram A, Hansen RM, Moskowitz A, Fulton AB (2013) Photoreceptor and postreceptor responses in congenital stationary night blindness. Invest Ophthalmol Vis Sci 54:4648–4658CrossRefPubMedPubMedCentral
41.
Zurück zum Zitat Vincent A, Robson AG, Neveu MM, Wright GA, Moore AT, Webster AR, Holder GE (2013) A phenotype-genotype correlation study of X-linked retinoschisis. Ophthalmology 120:1454–1464CrossRefPubMed Vincent A, Robson AG, Neveu MM, Wright GA, Moore AT, Webster AR, Holder GE (2013) A phenotype-genotype correlation study of X-linked retinoschisis. Ophthalmology 120:1454–1464CrossRefPubMed
42.
Zurück zum Zitat Moskowitz A, Hansen RM, Eklund SE, Fulton AB (2012) Electroretinographic (ERG) responses in pediatric patients using vigabatrin. Doc Ophthalmol 124:197–209CrossRefPubMed Moskowitz A, Hansen RM, Eklund SE, Fulton AB (2012) Electroretinographic (ERG) responses in pediatric patients using vigabatrin. Doc Ophthalmol 124:197–209CrossRefPubMed
43.
Zurück zum Zitat Kondo M, Sanuki R, Ueno S, Nishizawa Y, Hashimoto N, Ohguro H, Yamamoto S, Machida S, Terasaki H, Adamus G, Furukawa T (2011) Identification of autoantibodies against TRPM1 in patients with paraneoplastic retinopathy associated with ON bipolar cell dysfunction. PLoS ONE 6(5):e19911CrossRefPubMedPubMedCentral Kondo M, Sanuki R, Ueno S, Nishizawa Y, Hashimoto N, Ohguro H, Yamamoto S, Machida S, Terasaki H, Adamus G, Furukawa T (2011) Identification of autoantibodies against TRPM1 in patients with paraneoplastic retinopathy associated with ON bipolar cell dysfunction. PLoS ONE 6(5):e19911CrossRefPubMedPubMedCentral
44.
Zurück zum Zitat Hankins MW, Jones SR, Jenkins A, Morland AB (2001) Diurnal daylight phase affects the temporal properties of both the b-wave and d-wave of the human electroretinogram. Brain Res 889:339–343CrossRefPubMed Hankins MW, Jones SR, Jenkins A, Morland AB (2001) Diurnal daylight phase affects the temporal properties of both the b-wave and d-wave of the human electroretinogram. Brain Res 889:339–343CrossRefPubMed
45.
Zurück zum Zitat Shinoda K, Ohde H, Mashima Y, Inoue R, Ishida S, Inoue M, Kawashima S, Oguchi Y (2001) On- and off-responses of the photopic electroretinograms in X-linked juvenile retinoschisis. Am J Ophthalmol 131:489–494CrossRefPubMed Shinoda K, Ohde H, Mashima Y, Inoue R, Ishida S, Inoue M, Kawashima S, Oguchi Y (2001) On- and off-responses of the photopic electroretinograms in X-linked juvenile retinoschisis. Am J Ophthalmol 131:489–494CrossRefPubMed
46.
Zurück zum Zitat Shinoda K, Ohde H, Ishida S, Inoue M, Oguchi Y, Mashima Y (2004) Novel 473-bp deletion in XLRS1 gene in a Japanese family with X-linked juvenile retinoschisis. Graefes Arch Clin Exp Ophthalmol 242:561–565CrossRefPubMed Shinoda K, Ohde H, Ishida S, Inoue M, Oguchi Y, Mashima Y (2004) Novel 473-bp deletion in XLRS1 gene in a Japanese family with X-linked juvenile retinoschisis. Graefes Arch Clin Exp Ophthalmol 242:561–565CrossRefPubMed
47.
Zurück zum Zitat Yamamoto S, Hayashi M, Tsuruoka M, Ogata K, Tsukahara I, Yamamoto T, Takeuchi S (2002) Selective reduction of S-cone response and on-response in the cone electroretinograms of patients with X-linked retinoschisis. Graefes Arch Clin Exp Ophthalmol 240:457–460CrossRefPubMed Yamamoto S, Hayashi M, Tsuruoka M, Ogata K, Tsukahara I, Yamamoto T, Takeuchi S (2002) Selective reduction of S-cone response and on-response in the cone electroretinograms of patients with X-linked retinoschisis. Graefes Arch Clin Exp Ophthalmol 240:457–460CrossRefPubMed
48.
Zurück zum Zitat Shinoda K, Ohde H, Inoue R, Ishida S, Mashima Y, Oguchi Y (2002) ON-pathway disturbance in two siblings. Acta Ophthalmol Scand 80:219–223CrossRefPubMed Shinoda K, Ohde H, Inoue R, Ishida S, Mashima Y, Oguchi Y (2002) ON-pathway disturbance in two siblings. Acta Ophthalmol Scand 80:219–223CrossRefPubMed
49.
Zurück zum Zitat Koh AH, Hogg CR, Holder GE (2001) The incidence of negative ERG in clinical practice. Doc Ophthalmol 102:19–30CrossRefPubMed Koh AH, Hogg CR, Holder GE (2001) The incidence of negative ERG in clinical practice. Doc Ophthalmol 102:19–30CrossRefPubMed
50.
Zurück zum Zitat Khan NW, Jamison JA, Kemp JA, Sieving PA (2001) Analysis of photoreceptor function and inner retinal activity in juvenile X-linked retinoschisis. Vision Res 41:3931–3942CrossRefPubMed Khan NW, Jamison JA, Kemp JA, Sieving PA (2001) Analysis of photoreceptor function and inner retinal activity in juvenile X-linked retinoschisis. Vision Res 41:3931–3942CrossRefPubMed
51.
Zurück zum Zitat Imaizumi M, Matsumoto CS, Kimoto K, Furushima M, Nakatsuka K (2002) “On” response dysfunction in multifocal posterior pigment epitheliopathy. Retina 22:33–36CrossRefPubMed Imaizumi M, Matsumoto CS, Kimoto K, Furushima M, Nakatsuka K (2002) “On” response dysfunction in multifocal posterior pigment epitheliopathy. Retina 22:33–36CrossRefPubMed
52.
Zurück zum Zitat Holder GE, Robson AG, Pavesio C, Graham EM (2005) Electrophysiological characterisation and monitoring in the management of birdshot chorioretinopathy. Br J Ophthalmol 89:709–718CrossRefPubMedPubMedCentral Holder GE, Robson AG, Pavesio C, Graham EM (2005) Electrophysiological characterisation and monitoring in the management of birdshot chorioretinopathy. Br J Ophthalmol 89:709–718CrossRefPubMedPubMedCentral
53.
Zurück zum Zitat Renner AB, Kellner U, Cropp E, Foerster MH (2006) Dysfunction of transmission in the inner retina: incidence and clinical causes of negative electroretinogram. Graefes Arch Clin Exp Ophthalmol 244:1467–1473CrossRefPubMed Renner AB, Kellner U, Cropp E, Foerster MH (2006) Dysfunction of transmission in the inner retina: incidence and clinical causes of negative electroretinogram. Graefes Arch Clin Exp Ophthalmol 244:1467–1473CrossRefPubMed
54.
Zurück zum Zitat Hotta K, Kondo M, Nakamura M, Hotta J, Terasaki H, Miyake Y, Hida T (2006) Negative electroretinograms in pericentral pigmentary retinal degeneration. Clin Exp Ophthalmol 34:89–92CrossRefPubMed Hotta K, Kondo M, Nakamura M, Hotta J, Terasaki H, Miyake Y, Hida T (2006) Negative electroretinograms in pericentral pigmentary retinal degeneration. Clin Exp Ophthalmol 34:89–92CrossRefPubMed
55.
Zurück zum Zitat Usui T, Tanimoto N, Ueki S, Miki A, Takagi M, Hasegawa S, Abe H (2005) Night blindness with depolarizing pattern of ON/OFF response in electroretinogram: a case report. Doc Ophthalmol 111:15–21CrossRefPubMed Usui T, Tanimoto N, Ueki S, Miki A, Takagi M, Hasegawa S, Abe H (2005) Night blindness with depolarizing pattern of ON/OFF response in electroretinogram: a case report. Doc Ophthalmol 111:15–21CrossRefPubMed
56.
Zurück zum Zitat Sustar M, Stirn-Kranjc B, Hawlina M, Brecelj J (2008) Photopic ON- and OFF-responses in complete type of congenital stationary night blindness in relation to stimulus intensity. Doc Ophthalmol 117:37–46CrossRefPubMed Sustar M, Stirn-Kranjc B, Hawlina M, Brecelj J (2008) Photopic ON- and OFF-responses in complete type of congenital stationary night blindness in relation to stimulus intensity. Doc Ophthalmol 117:37–46CrossRefPubMed
57.
Zurück zum Zitat Tanimoto N, Usui T, Ichibe M, Kuze M, Takagi M, Hasegawa S, Sato M, Tanaka K, Abe H (2006) Negative scotopic ERG and photopic ERG ON response impairment in a patient with normal dark adaptation. Doc Ophthalmol 113:171–177CrossRefPubMed Tanimoto N, Usui T, Ichibe M, Kuze M, Takagi M, Hasegawa S, Sato M, Tanaka K, Abe H (2006) Negative scotopic ERG and photopic ERG ON response impairment in a patient with normal dark adaptation. Doc Ophthalmol 113:171–177CrossRefPubMed
58.
Zurück zum Zitat Horn FK, Gottschalk K, Mardin CY, Pangeni G, Jünemann AG, Kremers J (2011) On and Off responses of the photopic full field ERG in normal subjects and glaucoma patients. Doc Ophthalmol 122:53–62CrossRefPubMed Horn FK, Gottschalk K, Mardin CY, Pangeni G, Jünemann AG, Kremers J (2011) On and Off responses of the photopic full field ERG in normal subjects and glaucoma patients. Doc Ophthalmol 122:53–62CrossRefPubMed
59.
Zurück zum Zitat Machida S, Ohguro H, Tateda M, Sato H, Kurosaka D (2011) Melanoma-associated retinopathy associated with intranasal melanoma. Doc Ophthalmol 122:191–197CrossRefPubMed Machida S, Ohguro H, Tateda M, Sato H, Kurosaka D (2011) Melanoma-associated retinopathy associated with intranasal melanoma. Doc Ophthalmol 122:191–197CrossRefPubMed
Metadaten
Titel
ISCEV extended protocol for the photopic On–Off ERG
verfasst von
Maja Sustar
Graham E. Holder
Jan Kremers
Claire S. Barnes
Bo Lei
Naheed W. Khan
Anthony G. Robson
Publikationsdatum
22.06.2018
Verlag
Springer Berlin Heidelberg
Erschienen in
Documenta Ophthalmologica / Ausgabe 3/2018
Print ISSN: 0012-4486
Elektronische ISSN: 1573-2622
DOI
https://doi.org/10.1007/s10633-018-9645-y

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