USH2A-Related Retinitis Pigmentosa: Staging of Disease Severity and Morpho-Functional Studies

Benedetto Falsini, Angelo Maria Minnella, Martina Maceroni, Pietro Chiurazzi, Stanislao Rizzo, Giorgio Placidi, Maria Cristina Savastano, Elisa De Siena, Giulia Midena, Lucia Ziccardi, Vincenzo Parisi, Matteo Bertelli, Paolo Enrico Maltese

Risultato della ricerca: Contributo in rivistaArticolo in rivistapeer review


Usher syndrome type 2A (USH2A) is a genetic disease characterized by bilateral neuro-sensory hypoacusia and retinitis pigmentosa (RP). While several methods, including electroretinogram (ERG), describe retinal function in USH2A patients, structural alterations can be assessed by optical coherence tomography (OCT). According to a recent collaborative study, RP can be staged considering visual acuity, visual field area and ellipsoid zone (EZ) width. The aim of this study was to retrospectively determine RP stage in a cohort of patients with USH2A gene variants and to correlate the results with age, as well as additional functional and morphological parameters. In 26 patients with established USH2A genotype, RP was staged according to recent international standards. The cumulative staging score was correlated with patients' age, amplitude of full-field and focal flicker ERGs, and the OCT-measured area of sub-Retinal Pigment Epithelium (RPE) illumination (SRI). RP cumulative score (CS) was positively correlated (r = 0.6) with age. CS was also negatively correlated (rho = -0.7) with log10 ERG amplitudes and positively correlated (r = 0.5) with SRI. In USH2A patients, RP severity score is correlated with age and additional morpho-functional parameters not included in the international staging system and can reliably predict their abnormality at different stages of disease.
Lingua originaleEnglish
pagine (da-a)213-N/A
Numero di pagine7
Stato di pubblicazionePubblicato - 2021


  • Usher 2A gene
  • Usher syndrome
  • electroretinogram
  • sub-RPE illumination (SRI)
  • retinitis pigmentosa
  • staging
  • retinal pigment epithelium (RPE) and outer retina atrophy (RORA)

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