Genotype-Specific Lesion Growth Rates in Stargardt Disease

被引:7
|
作者
Heath Jeffery, Rachael C. [1 ,2 ]
Thompson, Jennifer A. [3 ,4 ]
Lo, Johnny [5 ]
Lamey, Tina M. [1 ,3 ,4 ]
McLaren, Terri L. [1 ,3 ,4 ]
McAllister, Ian L. [1 ]
Constable, Ian J. [1 ]
De Roach, John N. [1 ,3 ,4 ]
Chen, Fred K. [1 ,2 ,3 ,4 ]
机构
[1] Univ Western Australia, Inc Lions Eye Inst, Ctr Ophthalmol & Visual Sci, Nedlands, WA 6009, Australia
[2] Royal Perth Hosp, Dept Ophthalmol, Perth, WA 6000, Australia
[3] Sir Charles Gairdner Hosp, Australian Inherited Retinal Dis Registry, Nedlands, WA 6009, Australia
[4] Sir Charles Gairdner Hosp, DNA Bank, Dept Med Technol & Phys, Nedlands, WA 6009, Australia
[5] Edith Cowan Univ, Sch Sci, Joondalup, WA 6027, Australia
基金
英国医学研究理事会;
关键词
Stargardt disease; ABCA4; fundus autofluorescence; growth rate; natural history study; VARIANTS;
D O I
10.3390/genes12121981
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Reported growth rates (GR) of atrophic lesions in Stargardt disease (STGD1) vary widely. In the present study, we report the longitudinal natural history of patients with confirmed biallelic ABCA4 mutations from five genotype groups: c.6079C>T, c.[2588G>C;5603A>T], c.3113C>T, c.5882G>A and c.5603A>T. Fundus autofluorescence (AF) 30 degrees x 30 degrees images were manually segmented for boundaries of definitely decreased autofluorescence (DDAF). The primary outcome was the effective radius GR across five genotype groups. The age of DDAF formation in each eye was calculated using the x-intercept of the DDAF effective radius against age. Discordance between age at DDAF formation and symptom onset was compared. A total of 75 eyes from 39 STGD1 patients (17 male [44%]; mean +/- SD age 45 +/- 19 years; range 21-86) were recruited. Patients with c.3113C>T or c.6079C>T had a significantly faster effective radius GR at 0.17 mm/year (95% CI 0.12 to 0.22; p < 0.001 and 0.14 to 0.21; p < 0.001) respectively, as compared to those patients harbouring c.5882G>A at 0.06 mm/year (95% CI 0.03-0.09), respectively. Future clinical trial design should consider the effect of genotype on the effective radius GR and the timing of DDAF formation relative to symptom onset.
引用
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页数:6
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