Relationships between causative genes and epiretinal membrane formation in Japanese patients with retinitis pigmentosa

Graefes Arch Clin Exp Ophthalmol. 2024 Nov;262(11):3553-3558. doi: 10.1007/s00417-024-06534-6. Epub 2024 Jun 5.

Abstract

Purpose: To investigate the relationships between macular complications and causative genes frequently found in Japanese patients with retinitis pigmentosa (RP).

Methods: In the retrospective and observational study, we analyzed the data of 75 patients with RP (EYS-RP: 42 patients; USH2A-RP: 19 patients; RHO-RP: 14 patients) who were followed-up at Kyushu University Hospital and whose causative genes had been identified. Macular complications including epiretinal membrane (ERM), macular edema (ME), and macular hole (MH) were evaluated using optical coherence tomography and fundus photography. Main outcome was the proportion of macular complications.

Results: The proportion of ERM was 35.7% in the EYS group, 10.5% in the USH2A group and 14.3% in the RHO group. The proportion of ME was 7.1% in the EYS group, 5.3% in the USH2A group and 14.3% in the RHO group, and that of MH was 2.4% in the EYS group, 5.3% in the USH2A group and 0% in the RHO group. In the EYS group, the proportion of ERM was relatively higher (p = 0.06), and the presence of EYS was significantly associated with a higher age- and sex-adjusted OR for ERM (OR = 5.67, 95% CI = 1.59-25.20). There was no significant difference in the proportion of MH or ME among causative genes.

Conclusions: EYS causative gene may be associated with higher rate of ERM complication in RP.

Keywords: EYS-RP gene; Causative genes; Epiretinal membrane; Macular complications; Retinitis pigmentosa.

Publication types

  • Observational Study

MeSH terms

  • Adult
  • Aged
  • DNA / genetics
  • East Asian People
  • Epiretinal Membrane* / diagnosis
  • Epiretinal Membrane* / genetics
  • Extracellular Matrix Proteins / genetics
  • Eye Proteins / genetics
  • Female
  • Follow-Up Studies
  • Fundus Oculi
  • Humans
  • Japan / epidemiology
  • Macula Lutea / diagnostic imaging
  • Macula Lutea / pathology
  • Male
  • Middle Aged
  • Mutation
  • Retinitis Pigmentosa* / diagnosis
  • Retinitis Pigmentosa* / genetics
  • Retrospective Studies
  • Tomography, Optical Coherence* / methods
  • Visual Acuity*
  • Young Adult

Substances

  • Extracellular Matrix Proteins
  • USH2A protein, human
  • Eye Proteins
  • DNA