Electrophysiologic differentiation of homozygous and heterozygous Abyssinian-crossbred cats with late-onset hereditary retinal degeneration

被引:12
作者
Hyman, JA
Vaegan
Lei, B
Narfström, KL
机构
[1] Eye Care Anim, Overland Pk, KS 66210 USA
[2] Univ New S Wales, Dept Optometry, Sch Optometry & Vis Sci, Sydney, NSW 2052, Australia
[3] Univ Missouri, Dept Vet Med & Surg, Coll Vet Med, Columbia, MO 65211 USA
[4] Univ Missouri, Dept Ophthalmol, Mason Eye Inst, Sch Med, Columbia, MO 65211 USA
关键词
D O I
10.2460/ajvr.2005.66.1914
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Objective-To develop a method to electrophysiologically differentiate heterozygous-carrier Abyssinian-crossbred cats from homozygous-affected Abyssinian-crossbred cats before clinical onset of inherited rodcone retinal degeneration. Animals-14 back-crossed Abyssinian-crossbred cats of unknown genotype (homozygous or heterozygous) for inherited rod-cone retinal degeneration, 24 age-matched mixed-breed control cats, 6 age-matched heterozygous Abyssinian-crossbred cats, and 6 homozygous Abyssinian cats. Procedure-Electroretinography (ERG) of heterozygous and homozygous cats revealed differences, especially for scotopic recordings. Frequent ophthalmoscopy and ERG (2 to 5 times; at intervals of 3 to 6 months) of back-crossed cats were performed. Amplitudes and implicit times were analyzed by use of a graphic representation of results. Ratios for amplitudes of the b-waves to amplitudes of the a-waves (b-wave:a-wave) were compared. Results-8 back-crossed cats had decreased a-wave amplitudes, increased b-wave implicit times, and abnormal ERG waveforms. Values for the b-wave:a-wave for the highest scotopic light intensity were significantly higher for those same 8 cats. Conclusions and Clinical Relevance-The 8 back-crossed Abyssinian-crossbred cats with abnormal results developed fundus changes over time consistent with disease. A graphic representation of ERG results can be used to differentiate between genotypes prior to funduscopic changes. Values for the b-wave:a-wave ratio provide confirmation. These ERG analyses may be applied clinically in the diagnosis of retinal degenerations in various species. Impact for Human Medicine-Cats with hereditary rod-cone degeneration may be a useful model for comparative studies in relation to retinitis pigmentosa in humans. Similar evaluations of ERG results could possibly be used for humans with suspected generalized retinal degeneration.
引用
收藏
页码:1914 / 1921
页数:8
相关论文
共 23 条
[1]   VARIATION IN RETINAL DEGENERATION PHENOTYPE INHERITED AT THE PRCD LOCUS [J].
AGUIRRE, GD ;
ACLAND, GM .
EXPERIMENTAL EYE RESEARCH, 1988, 46 (05) :663-687
[2]   AUTOSOMAL DOMINANT PROGRESSIVE RETINAL ATROPHY IN ABYSSINIAN CATS [J].
BARNETT, KC ;
CURTIS, R .
JOURNAL OF HEREDITY, 1985, 76 (03) :168-170
[3]  
CURTIS R, 1987, INVEST OPHTH VIS SCI, V28, P131
[4]   Abnormal dark-adapted ERG in cats heterozygous for a recessively inherited rod-cone degeneration [J].
Ekesten, B ;
Narfström, K .
VETERINARY OPHTHALMOLOGY, 2004, 7 (01) :63-67
[5]   Cone positive off-response in normal and dystrophic cats [J].
Ekesten, B ;
Narfström, K .
DOCUMENTA OPHTHALMOLOGICA, 1999, 97 (01) :9-21
[6]   DEVELOPMENT AND DEGENERATION OF RETINA IN RDS MUTANT MICE - PHOTORECEPTOR ABNORMALITIES IN THE HETEROZYGOTES [J].
HAWKINS, RK ;
JANSEN, HG ;
SANYAL, S .
EXPERIMENTAL EYE RESEARCH, 1985, 41 (06) :701-720
[7]   RHODOPSIN LEVELS AND ROD-MEDIATED FUNCTION IN ABYSSINIAN CATS WITH HEREDITARY RETINAL DEGENERATION [J].
JACOBSON, SG ;
KEMP, CM ;
NARFSTROM, K ;
NILSSON, SEG .
EXPERIMENTAL EYE RESEARCH, 1989, 49 (05) :843-852
[8]   Impaired retinal function in young Labrador retriever dogs heterozygous for late onset rod-cone degeneration [J].
Kommonen, B ;
Kylma, T ;
Karhunen, U ;
Dawson, WW ;
Penn, JS .
VISION RESEARCH, 1997, 37 (03) :365-370
[9]   Neural remodeling in retinal degeneration [J].
Marc, RE ;
Jones, BW ;
Watt, CB ;
Strettoi, E .
PROGRESS IN RETINAL AND EYE RESEARCH, 2003, 22 (05) :607-655
[10]   HEREDITARY PROGRESSIVE RETINAL ATROPHY IN THE ABYSSINIAN CAT [J].
NARFSTROM, K .
JOURNAL OF HEREDITY, 1983, 74 (04) :273-276