PROGRESSION OF ABCA4-RELATED RETINOPATHY Prognostic value of demographic, functional, genetic, and imaging parameters


Por: Müller PL, Pfau M, Treis T, Pascual-Camps I, Birtel J, Lindner M, Herrmann P and Holz FG

Publicada: 1 dic 2020 Ahead of Print: 8 ene 2020
Resumen:
Purpose: To investigate the prognostic value of demographic, functional, genetic, and imaging parameters on retinal pigment epithelium atrophy progression secondary to ABCA4-related retinopathy. Methods: Patients with retinal pigment epithelium atrophy secondary to ABCA4-related retinopathy were examined longitudinally with fundus autofluorescence imaging. Lesion area, perimeter, circularity, caliper diameters, and focality of areas with definitely decreased autofluorescence were determined. A model was used to predict the lesion enlargement rate based on baseline variables. Sample size calculations were performed to model the power in a simulated interventional study. Results: Sixty-eight eyes of 37 patients (age range, 14-78 years) with a follow-up time of 10 to 100 months were included. The mean annual progression of retinal pigment epithelium atrophy was 0.89 mm(2). The number of atrophic areas, the retina-wide functional impairment, and the age-of-onset category constituted significant predictors for future retinal pigment epithelium atrophy growth, explaining 25.7% of the variability. By extension of a simulated study length and/or specific patient preselection based on these baseline characteristics, the required sample size could significantly be reduced. Conclusion: Trial design based on specific shape-descriptive factors and patients' baseline characteristics and the adaption of the trial duration may provide potential benefits in required cohort size and absolute number of visits.
ISSN: 15392864





RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES
Editorial
Lippincott Williams & Wilkins Ltd., 530 WALNUT ST, PHILADELPHIA, PA 19106-3621 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 40 Número: 12
Páginas: 2343-2356
WOS Id: 000618957100012
ID de PubMed: 33214501

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