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Genotype-Specific Lesion Growth Rates in Stargardt Disease.
Heath Jeffery, Rachael C; Thompson, Jennifer A; Lo, Johnny; Lamey, Tina M; McLaren, Terri L; McAllister, Ian L; Constable, Ian J; De Roach, John N; Chen, Fred K.
Affiliation
  • Heath Jeffery RC; Centre for Ophthalmology and Visual Science (Incorporating Lions Eye Institute), The University of Western Australia, Nedlands, WA 6009, Australia.
  • Thompson JA; Department of Ophthalmology, Royal Perth Hospital, Perth, WA 6000, Australia.
  • Lo J; Australian Inherited Retinal Disease Registry and DNA Bank, Department of Medical Technology and Physics, Sir Charles Gairdner Hospital, Nedlands, WA 6009, Australia.
  • Lamey TM; School of Science, Edith Cowan University, Joondalup, WA 6027, Australia.
  • McLaren TL; Centre for Ophthalmology and Visual Science (Incorporating Lions Eye Institute), The University of Western Australia, Nedlands, WA 6009, Australia.
  • McAllister IL; Australian Inherited Retinal Disease Registry and DNA Bank, Department of Medical Technology and Physics, Sir Charles Gairdner Hospital, Nedlands, WA 6009, Australia.
  • Constable IJ; Centre for Ophthalmology and Visual Science (Incorporating Lions Eye Institute), The University of Western Australia, Nedlands, WA 6009, Australia.
  • De Roach JN; Australian Inherited Retinal Disease Registry and DNA Bank, Department of Medical Technology and Physics, Sir Charles Gairdner Hospital, Nedlands, WA 6009, Australia.
  • Chen FK; Centre for Ophthalmology and Visual Science (Incorporating Lions Eye Institute), The University of Western Australia, Nedlands, WA 6009, Australia.
Genes (Basel) ; 12(12)2021 12 14.
Article in En | MEDLINE | ID: mdl-34946930
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° × 30° 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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: ATP-Binding Cassette Transporters / Stargardt Disease Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Genes (Basel) Year: 2021 Document type: Article Affiliation country: Australia Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: ATP-Binding Cassette Transporters / Stargardt Disease Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Genes (Basel) Year: 2021 Document type: Article Affiliation country: Australia Country of publication: Switzerland