Visual Acuity Change over 12 Months in the Prospective Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study

被引:40
作者
Kong, Xiangrong [1 ,2 ,3 ]
Strauss, Rupert W. [4 ,5 ,6 ,7 ]
Cideciyan, Artur V. [8 ]
Michaelides, Michel [5 ,6 ]
Sahel, Jose-Alain [9 ]
Munoz, Beatriz [3 ]
Ahmed, Mohamed [3 ]
Ervin, Ann M. [2 ,3 ]
West, Sheila K. [3 ]
Cheetham, Janet K. [10 ]
Scholl, Hendrik P. N. [3 ,7 ]
机构
[1] Univ Massachusetts, Sch Publ Hlth & Hlth Sci, Amherst, MA 01003 USA
[2] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Baltimore, MD USA
[3] Johns Hopkins Univ, Wilmer Eye Inst, Baltimore, MD 21218 USA
[4] Johannes Kepler Univ Linz, Dept Ophthalmol, Linz, Austria
[5] Moorfields Eye Hosp, Dept Ophthalmol, London, England
[6] UCL, UCL Inst Ophthalmol, London, England
[7] Univ Basel, Dept Ophthalmol, Basel, Switzerland
[8] Univ Penn, Scheie Eye Inst, Perelman Sch Med, Philadelphia, PA 19104 USA
[9] Univ Pittsburgh, Brain Inst, Pittsburgh, PA USA
[10] Fdn Fighting Blindness, Columbia, MD USA
基金
美国国家卫生研究院; 奥地利科学基金会;
关键词
BULLS-EYE MACULOPATHY; RETINAL DEGENERATIONS; GENOTYPE CORRELATIONS; MACULAR DYSTROPHIES; GEOGRAPHIC ATROPHY; IMPROVEMENT; PHENOTYPE; GENETICS; FEATURES; ABCA4;
D O I
10.1016/j.ophtha.2017.04.026
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To estimate the yearly rate of change of best-corrected visual acuity (BCVA) and the risk of loss 1 line or more over 1 year and to identify risk factors for BCVA loss in patients with Stargardt disease (STGD1). Design: Multicenter, prospective cohort study. Participants: Two hundred fifty-nine patients (489 eyes) with molecularly confirmed STGD1 enrolled at 9 centers in the United States and Europe. Methods: Participants were followed up every 6 months, and data at the baseline and 6-and 12-month visits were analyzed. Best-corrected visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Standardized reporting forms were used to collect participants' characteristics and clinical observations. Linear mixed effects models were used to estimate the rate of BCVA loss. Linear models with generalized estimating equations were used to identify risk factors for BCVA loss of 1 line or more over 1 year. Main Outcome Measures: Change in BCVA over 1 year. Results: Cross-sectional analysis at baseline showed that earlier symptom onset and longer duration since onset was associated with worse BCVA. Longitudinal analysis showed no overall significant change of BCVA within 12 months, but the rate of BCVA change was significantly different by baseline BCVA (P < 0.001). The BCVA of eyes with baseline BCVA of 20/25 or better declined at a rate of 2.8 ETDRS letters per year (P = 0.10), eyes with baseline BCVA between 20/25 and 20/70 declined at a rate of 2.3 ETDRS letters per year (P = 0.002), eyes with baseline BCVA between 20/70 and 20/200 declined at a rate of 0.8 ETDRS letters per year (P = 0.08), and eyes with baseline BCVA worse than 20/200 showed a significant improvement of 2.3 ETDRS letters per year (P < 0.001). Overall, 12.9% of eyes lost 1 line or more, and the risk of such BCVA loss was different by baseline BCVA level (P = 0.016). Smoking and vitamin A use was not associated significantly with baseline BCVA, nor with rate of BCVA loss over 1 year. Conclusions: Change in BCVA in STGD1 patients over a 12-month period was small, but varied depending on baseline BCVA. Given the slow change during 1 year, BCVA is unlikely to be a sensitive outcome measure for STGD1 treatment trials with 1 year's duration. (C) 2017 by the American Academy of Ophthalmology
引用
收藏
页码:1640 / 1651
页数:12
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