Skip to main content
Top
Published in: Documenta Ophthalmologica 1/2008

01-07-2008 | Original Research Article

Amax to scotopic Imax diagnoses feline hereditary rod cone degeneration more efficiently than any other combination of long protocol electroretinogram parameters

Authors: Vaegan, Kristina Narfström

Published in: Documenta Ophthalmologica | Issue 1/2008

Login to get access

Abstract

Aim To evaluate two recent methods for detecting feline hereditary rod cone degeneration with maximum efficiency from a long full-field flash ERG protocol. One combines 12 of these measures in an equation that is derived from iterative principal components factor analysis. The other uses the amplitude of the a-wave to the brightest available flash alone. Methods We tested the original 12-parameter equation, by applying it to 50 new ERG series in 23 backcrossed cats. They were necessarily either heterozygous or homozygous for hereditary rod cone degeneration. A masked observer compared the ERG score and fundus examinations. We reanalyzed the old, new and combined data sets. Data sets with only one session per animal were analysed to avoid problems from non-random sampling. A two factor linear model of the a-wave was evaluated. Results The prior equation, applied to the new data, discriminated the groups as well as it had initially. In the reanalysis, group separation continued to increase with even fewer measures compared to the previously reported study. Eventually, one measure, the amplitude of the a-wave (amax) to the brightest scotopic flash (Imax) discriminated the groups better than any other measure or combination of measures in all analyses, including data sets using only one session for each animal and in a two factor linear model of the a-wave. Conclusion Amax to Imax alone proved to be the best diagnostic criterion in all analyses. No linear model is likely to discriminate affected from unaffected animals more effectively because additional variables increased variance more rapidly than they increased discrimination. Amax to Imax may detect other rod and rod/cone dystrophies equally efficiently.
Footnotes
1
Principal component factor analysis mathematically reduces the intercorrelation matrix of a set of normally distributed variables to a set of hypothetical underlying dimensions (called factors). In principal component factor analysis the factors are kept orthogonal to each other i.e. uncorrelated and independent. The factors can be rotated and various rules have been proposed. In the most common ‘Varimax’ procedure, which we used, an effort is made to rotate the factors so as to minimise the number of the factors associated with each variable. Factors can be ranked in size, by their ‘eigenvalues’ which is a dimensionless number reflecting the amount of variance in the data they ‘explain’. Only eigenvalues above 1 are likely to occur beyond chance. The variables are correlated to (or loaded on) these dimensions to different degrees. Typically, on examination, variables loading highly on a factor can be recognised as having similar characteristics. Factors can be given generic names associated with these characteristics. As the number of factors is reduced, the amount of unexplained variance increases but, because factors are ranked by their eigenvalues and eigenvalues below 1 can be rejected, it is often the case that most of the intercorrelations and variance in the data can be reduced to many less factors than there were original variables. Individuals also have a score on each factor and can be given a single weighted sum of factor scores [15].
 
Literature
1.
go back to reference Narfström K (1985) Progressive retinal atrophy in the Abyssinian cat: clinical characteristics. Invest Ophthalmol Vis Sci 26:193–200PubMed Narfström K (1985) Progressive retinal atrophy in the Abyssinian cat: clinical characteristics. Invest Ophthalmol Vis Sci 26:193–200PubMed
2.
go back to reference Narfström K, Nilsson SE (1985) Hereditary retinal degeneration in the Abyssinian cat: correlation of ophthalmoscopic and electroretinographic findings. Doc Ophthalmol 60(2):183–187PubMedCrossRef Narfström K, Nilsson SE (1985) Hereditary retinal degeneration in the Abyssinian cat: correlation of ophthalmoscopic and electroretinographic findings. Doc Ophthalmol 60(2):183–187PubMedCrossRef
3.
go back to reference Narfström K, Nilsson SE, Andersson BE (1985) Progressive retinal atrophy in the Abyssinian cat. Studies of the DC-recorded electroretinogram and the standing potential of the eye. Br J Ophthalmol 9:618–623CrossRef Narfström K, Nilsson SE, Andersson BE (1985) Progressive retinal atrophy in the Abyssinian cat. Studies of the DC-recorded electroretinogram and the standing potential of the eye. Br J Ophthalmol 9:618–623CrossRef
4.
go back to reference Narfström K, Wilen M, Andersson BE (1988) Hereditary retinal degeneration in the Abyssinian cat: developmental studies using clinical electroretinography. Doc Ophthalmol 69(2):111–118PubMedCrossRef Narfström K, Wilen M, Andersson BE (1988) Hereditary retinal degeneration in the Abyssinian cat: developmental studies using clinical electroretinography. Doc Ophthalmol 69(2):111–118PubMedCrossRef
5.
go back to reference Narfström K, Arden GB, Nilsson SE (1989) Retinal sensitivity in hereditary retinal degeneration in Abyssinian cats: electrophysiological similarities between man and cat. Br J Ophthalmol 73(7):516–521PubMedCrossRef Narfström K, Arden GB, Nilsson SE (1989) Retinal sensitivity in hereditary retinal degeneration in Abyssinian cats: electrophysiological similarities between man and cat. Br J Ophthalmol 73(7):516–521PubMedCrossRef
6.
go back to reference Jacobson SG, Kemp CM, Narfström K, Nilsson SE (1989) Rhodopsin levels and rod-mediated function in Abyssinian cats with hereditary retinal degeneration. Exp Eye Res 49(5):843–852PubMedCrossRef Jacobson SG, Kemp CM, Narfström K, Nilsson SE (1989) Rhodopsin levels and rod-mediated function in Abyssinian cats with hereditary retinal degeneration. Exp Eye Res 49(5):843–852PubMedCrossRef
7.
go back to reference Ekesten B, Narfström K (2004) Abnormal dark-adapted ERG in cats heterozygous for a recessively inherited rod-cone degeneration. Vet Ophthalmol 7(1):63–67PubMedCrossRef Ekesten B, Narfström K (2004) Abnormal dark-adapted ERG in cats heterozygous for a recessively inherited rod-cone degeneration. Vet Ophthalmol 7(1):63–67PubMedCrossRef
8.
go back to reference Narfström K, Andersson BE, Andreasson S, Gouras P (1995) Clinical electroretinography in the dog with ganzfeld stimulation: a practical method of examining rod and cone function. Doc Ophthalmol 90(3):279–290PubMedCrossRef Narfström K, Andersson BE, Andreasson S, Gouras P (1995) Clinical electroretinography in the dog with ganzfeld stimulation: a practical method of examining rod and cone function. Doc Ophthalmol 90(3):279–290PubMedCrossRef
9.
go back to reference Hyman JA, Vaegan, Lei B, Narfström KL (2005) Electrophysiologic differentiation of homozygous and heterozygous Abyssinian-crossbred cats with late-onset hereditary retinal degeneration. Am J Vet Res 66(11):1914–1921PubMedCrossRef Hyman JA, Vaegan, Lei B, Narfström KL (2005) Electrophysiologic differentiation of homozygous and heterozygous Abyssinian-crossbred cats with late-onset hereditary retinal degeneration. Am J Vet Res 66(11):1914–1921PubMedCrossRef
10.
go back to reference Vaegan, Narfström K (2004) Optimal discrimination of an Abyssinian cat recessive retinal degeneration: a short electroretinogram protocol is more efficient than a long one. Clin Experiment Ophthalmol 32(6):619–625PubMedCrossRef Vaegan, Narfström K (2004) Optimal discrimination of an Abyssinian cat recessive retinal degeneration: a short electroretinogram protocol is more efficient than a long one. Clin Experiment Ophthalmol 32(6):619–625PubMedCrossRef
11.
go back to reference Vaegan, Narfström K (2005) A(max) is the best a-wave measure for classifying Abyssinian cat rod/cone dystrophy. Doc Ophthalmol 111(1):33–38PubMedCrossRef Vaegan, Narfström K (2005) A(max) is the best a-wave measure for classifying Abyssinian cat rod/cone dystrophy. Doc Ophthalmol 111(1):33–38PubMedCrossRef
12.
go back to reference Kang Derwent JJ, Padnick-Silver L, McRipley M, Giuliano E, Linsenmeier RA, Narfström K (2006) The electroretinogram (ERG) components in Abyssinian cats with hereditary retinal degeneration. Invest Ophthalmol and Vis Sci 47(8):3673–3682CrossRef Kang Derwent JJ, Padnick-Silver L, McRipley M, Giuliano E, Linsenmeier RA, Narfström K (2006) The electroretinogram (ERG) components in Abyssinian cats with hereditary retinal degeneration. Invest Ophthalmol and Vis Sci 47(8):3673–3682CrossRef
13.
go back to reference Seeliger MW, Narfström K (2000) Functional assessment of the regional distribution of disease in a cat model of hereditary retinal degeneration. Invest Ophthalmol Vis Sci 41(7):1998–2005PubMed Seeliger MW, Narfström K (2000) Functional assessment of the regional distribution of disease in a cat model of hereditary retinal degeneration. Invest Ophthalmol Vis Sci 41(7):1998–2005PubMed
14.
go back to reference Menotti-Raymond M, David VA, Schaffer AA, Stephens R, Wells D, Kumar-Singh R et al (2007) Mutation in CEP290 discovered for cat model of human retinal degeneration. J Hered 98(3):211–220PubMedCrossRef Menotti-Raymond M, David VA, Schaffer AA, Stephens R, Wells D, Kumar-Singh R et al (2007) Mutation in CEP290 discovered for cat model of human retinal degeneration. J Hered 98(3):211–220PubMedCrossRef
15.
go back to reference Kendall MG (1980) Multivariate analysis, 2nd edn. Griffin, London Kendall MG (1980) Multivariate analysis, 2nd edn. Griffin, London
16.
go back to reference Vaegan, Narfström K (2004) A blind trial verification and rules for use of an optimized equation, combining selected ERG scores, to efficiently detect recessive rod cone degeneration in Abyssinian cats. Investig Ophthalmol and Vis Sci (ARVO Abstr Suppl) 2004; Fort Lauderdale, Fl, USA: ARVO, 2004. p Abstr # 5086 Vaegan, Narfström K (2004) A blind trial verification and rules for use of an optimized equation, combining selected ERG scores, to efficiently detect recessive rod cone degeneration in Abyssinian cats. Investig Ophthalmol and Vis Sci (ARVO Abstr Suppl) 2004; Fort Lauderdale, Fl, USA: ARVO, 2004. p Abstr # 5086
17.
go back to reference Hood DC, Birch DG (1990) The a-wave of the human electroretinogram and rod receptor function. Invest Ophthalmol Vis Sci 31(10):2070–2081PubMed Hood DC, Birch DG (1990) The a-wave of the human electroretinogram and rod receptor function. Invest Ophthalmol Vis Sci 31(10):2070–2081PubMed
18.
go back to reference Hood DC, Birch DG (1997) Assessing abnormal rod photoreceptor activity with the a-wave of the ERG: applications and methods. Doc Ophthalmol 92:253–267CrossRef Hood DC, Birch DG (1997) Assessing abnormal rod photoreceptor activity with the a-wave of the ERG: applications and methods. Doc Ophthalmol 92:253–267CrossRef
19.
go back to reference Lamb TD, Pugh EN Jr (1992) A quantitative account of the activation steps involved in phototransduction in amphibian photoreceptors. J Physiol 449:719–758PubMed Lamb TD, Pugh EN Jr (1992) A quantitative account of the activation steps involved in phototransduction in amphibian photoreceptors. J Physiol 449:719–758PubMed
20.
go back to reference Hood DC, Birch DG (2005) Measuring the health of the human photoreceptors with the leading edge of the a-wave. In: Heckenlively JR, Arden GB (eds) Principles and practice of clinical electrophysiology of vision, 2nd edn. MIT Press, Boston Hood DC, Birch DG (2005) Measuring the health of the human photoreceptors with the leading edge of the a-wave. In: Heckenlively JR, Arden GB (eds) Principles and practice of clinical electrophysiology of vision, 2nd edn. MIT Press, Boston
21.
go back to reference Johnson MA, Hood DC (1996) Rod photoreceptor transduction is affected in central retinal vein occlusion associated with iris neovascularization. J Opt Soc Am A 13(3):572–576CrossRef Johnson MA, Hood DC (1996) Rod photoreceptor transduction is affected in central retinal vein occlusion associated with iris neovascularization. J Opt Soc Am A 13(3):572–576CrossRef
22.
go back to reference Marmor MF, Holder GE, Seeliger MW, Yamamoto S (2004) Standard for clinical electroretinography (2004 update). Doc Ophthalmol 108:107–114PubMedCrossRef Marmor MF, Holder GE, Seeliger MW, Yamamoto S (2004) Standard for clinical electroretinography (2004 update). Doc Ophthalmol 108:107–114PubMedCrossRef
23.
go back to reference Robson JG, Frishman LJ (1998) Dissecting the dark-adapted electroretinogram. Doc Ophthalmol 95(3–4):187–215PubMedCrossRef Robson JG, Frishman LJ (1998) Dissecting the dark-adapted electroretinogram. Doc Ophthalmol 95(3–4):187–215PubMedCrossRef
24.
go back to reference Tsekov RT, Locke KG, Hood DC, Birch DG (2003) Cone and rod ERG phototransduction in retinitis pigmentosa. Invest Ophthalmol Vis Sci 44(9):3993–4000CrossRef Tsekov RT, Locke KG, Hood DC, Birch DG (2003) Cone and rod ERG phototransduction in retinitis pigmentosa. Invest Ophthalmol Vis Sci 44(9):3993–4000CrossRef
25.
go back to reference Birch DG, Hood DC, Locke KG, Hoffman DR, Tzekov RT (2002) Quantitative electroretinogram measures of phototransduction in cone and rod photoreceptors: normal aging, progression with disease and test-retest variability. Arch Ophthalmol 120:1045–1051PubMed Birch DG, Hood DC, Locke KG, Hoffman DR, Tzekov RT (2002) Quantitative electroretinogram measures of phototransduction in cone and rod photoreceptors: normal aging, progression with disease and test-retest variability. Arch Ophthalmol 120:1045–1051PubMed
26.
go back to reference Marcus M, Cabael L, Marmor MF (2006) Utility in clinical practice of standard vs. high-intensity ERG a-waves. Doc Ophthalmol 113(3):145–153PubMedCrossRef Marcus M, Cabael L, Marmor MF (2006) Utility in clinical practice of standard vs. high-intensity ERG a-waves. Doc Ophthalmol 113(3):145–153PubMedCrossRef
27.
go back to reference Vogel M (1978) Postnatal development of the cat’s retina. A concept of maturation obtained by qualitative and quantitative examination. Albrecht von Graefes Arch Klin Ophthalmol 208:93–107CrossRef Vogel M (1978) Postnatal development of the cat’s retina. A concept of maturation obtained by qualitative and quantitative examination. Albrecht von Graefes Arch Klin Ophthalmol 208:93–107CrossRef
28.
go back to reference Narfström K, Bragadottir R, Sjostrom A, Andersson BE (2001) Electrophysiological differentiation of homozygous, heterozygous and normal cats at an early stage in recessively inherited rod cone degeneration. Invest Ophthalmol Vis Sci 42:S182 Narfström K, Bragadottir R, Sjostrom A, Andersson BE (2001) Electrophysiological differentiation of homozygous, heterozygous and normal cats at an early stage in recessively inherited rod cone degeneration. Invest Ophthalmol Vis Sci 42:S182
29.
go back to reference Kang Derwent J, Linsenmeier RA, Padnick-Silver L, Narfström K (2000) Changes in photoreceptor oxidative metabolism in Abyssinian cats with hereditary rod-cone degeneration. ARVO 2000; Fort Lauderdale, FL, USA: ARVO, 2000, p S887 Kang Derwent J, Linsenmeier RA, Padnick-Silver L, Narfström K (2000) Changes in photoreceptor oxidative metabolism in Abyssinian cats with hereditary rod-cone degeneration. ARVO 2000; Fort Lauderdale, FL, USA: ARVO, 2000, p S887
Metadata
Title
Amax to scotopic Imax diagnoses feline hereditary rod cone degeneration more efficiently than any other combination of long protocol electroretinogram parameters
Authors
Vaegan
Kristina Narfström
Publication date
01-07-2008
Publisher
Springer-Verlag
Published in
Documenta Ophthalmologica / Issue 1/2008
Print ISSN: 0012-4486
Electronic ISSN: 1573-2622
DOI
https://doi.org/10.1007/s10633-007-9096-3

Other articles of this Issue 1/2008

Documenta Ophthalmologica 1/2008 Go to the issue