Kinetics of visual field loss in Usher syndrome type II

被引:68
作者
Iannaccone, A
Kritchevsky, SB
Ciccarelli, ML
Tedesco, SA
Macalus, C
Kimberling, WJ
Somes, GW
机构
[1] Univ Tennessee, Ctr Hlth Sci, Dept Ophthalmol, Memphis, TN 38163 USA
[2] Univ Tennessee, Ctr Hlth Sci, Dept Prevent Med, Memphis, TN 38163 USA
[3] Fatebenefratelli Hosp, Div Ophthalmol, Rome, Italy
[4] Univ Parma, Dept Ophthalmol, I-43100 Parma, Italy
[5] Boys Town Natl Res Hosp, Omaha, NE 68131 USA
关键词
D O I
10.1167/iovs.03-0906
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. To characterize the kinetics of visual field decay in Usher syndrome type II. METHODS. The area of 137 Goldmann visual fields (GVFs) delimited with the I4e and V4e targets was measured in each eye of 19 patients with an established diagnosis of Usher syndrome type II, and the average interocular GVF area for each patient at each time point was calculated. The average follow-up was 5.58 years. Symptomatic disease duration was defined as years elapsed after symptoms were first noted. The data set (n = 67 for the We target; n = 70 for the V4e target) was analyzed with a random coefficient mixed model to identify the best-fit model describing the decay of visual field size over time. The half-life of the residual visual field area (t(0.5)) was also calculated. RESULTS. The variable that best explained the decay of the GVF area was the duration of symptomatic disease. In an exponential model, the slope estimate for the natural log of the GVF area was -0.172 for the We target and -0.136 for the V4e target for each year of symptomatic disease. Accordingly, t(0.5) was approximately 4 years for the I4e target and 5 years for the V4e target. These estimates are very similar to those in previous studies of nonsyndromic retinitis pigmentosa (RP). CONCLUSIONS. This study suggests that the kinetics of GVF decline in Usher syndrome type 11 are, on average, very similar to other forms of RP and that, once the disease becomes symptomatic, GVF deterioration follows stereotyped kinetics, even in patients with late-onset retinal disease.
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页码:784 / 792
页数:9
相关论文
共 30 条
[1]   NATURAL COURSE OF RETINITIS PIGMENTOSA OVER A 3-YEAR INTERVAL [J].
BERSON, EL ;
SANDBERG, MA ;
ROSNER, B ;
BIRCH, DG ;
HANSON, AH .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1985, 99 (03) :240-251
[2]   A RANDOMIZED TRIAL OF VITAMIN-A AND VITAMIN-E SUPPLEMENTATION FOR RETINITIS-PIGMENTOSA [J].
BERSON, EL ;
ROSNER, B ;
SANDBERG, MA ;
HAYES, KC ;
NICHOLSON, BW ;
WEIGELDIFRANCO, C ;
WILLETT, W .
ARCHIVES OF OPHTHALMOLOGY, 1993, 111 (06) :761-772
[3]  
BHATTACHARYA S, 1995, LANCET, V345, P739
[4]   Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod dystrophy [J].
Birch, DG ;
Anderson, JL ;
Fish, GE .
OPHTHALMOLOGY, 1999, 106 (02) :258-268
[5]  
DAGNELIE G, 1990, CLIN VISION SCI, V5, P95
[6]  
Edwards A, 1998, ARCH OPHTHALMOL-CHIC, V116, P165
[7]   USHERS SYNDROME - OPHTHALMIC AND NEURO-OTOLOGIC FINDINGS SUGGESTING GENETIC-HETEROGENEITY [J].
FISHMAN, GA ;
KUMAR, A ;
JOSEPH, ME ;
TOROK, N ;
ANDERSON, RJ .
ARCHIVES OF OPHTHALMOLOGY, 1983, 101 (09) :1367-1374
[8]   PREVALENCE OF FOVEAL LESIONS IN TYPE-1 AND TYPE-2 USHERS SYNDROME [J].
FISHMAN, GA ;
ANDERSON, RJ ;
LAM, BL ;
DERLACKI, DJ .
ARCHIVES OF OPHTHALMOLOGY, 1995, 113 (06) :770-773
[9]   Patterns of visual field progression in patients with retinitis pigmentosa [J].
Grover, S ;
Fishman, GA ;
Brown, J .
OPHTHALMOLOGY, 1998, 105 (06) :1069-1075
[10]   A longitudinal study of visual function in carriers of X-linked recessive retinitis pigmentosa [J].
Grover, S ;
Fishman, GA ;
Anderson, RJ ;
Lindeman, M .
OPHTHALMOLOGY, 2000, 107 (02) :386-396