Publication

Linking the Presence of Macular Oedema to Structural and Functional Alterations in Retinitis Pigmentosa

Journal Paper/Review - Apr 14, 2021

Units
PubMed
Doi

Citation
Friesacher A, Lopez Torres L, Valmaggia C, Rüesch R, Todorova M. Linking the Presence of Macular Oedema to Structural and Functional Alterations in Retinitis Pigmentosa. Klin Monbl Augenheilkd 2021; 238:418-427.
Type
Journal Paper/Review (English)
Journal
Klin Monbl Augenheilkd 2021; 238
Publication Date
Apr 14, 2021
Issn Electronic
1439-3999
Pages
418-427
Brief description/objective

OBJECTIVE
To investigate the association between the central retinal thickness (CRT), the retinal nerve fibre layer thickness (RNFL), and the functional alterations in retinitis pigmentosa (RP) patients.

METHODS
Forty-three patients with typical RP and nineteen age-matched controls, who underwent SD-OCT (macular and optic disc OCT protocols) and electrophysiology, were included. The RP group was divided into two subgroups: with clinical appearance of macular oedema (ME-RP; 30 eyes) and without macular oedema (no-ME; 44 eyes). Central retinal thickness OCT data were averaged in three zones (zone 1 [0°-3°], zone 2 [3°-8°], and zone 3 [8°-15°]) and were evaluated in relation to the RNFL thickness and electrophysiological data.

RESULTS
The ME-RP group showed increased CRT (zone 1) and RNFL thickness compared to the controls and no-ME-RP (p ≤ 0.002). The no-ME-RP group had reduced CRT thickness (all zones; p ≤ 0.018) compared to the controls and ME-RP, whereas the RNFL thickness in the no-ME-RP group was reduced only compared to the ME-RP group (p < 0.001). The ME-RP group showed significantly more attenuated functional responses than the no-ME-RP patients. A significant positive interaction was found between the CRT (zones 1 and 2) and the RNFL thickness within ME-RP (p ≤ 0.010). Significant negative interactions were found between CRT, RNFL thickness, and functional findings within ME-RP (p ≤ 0.049).

CONCLUSION
The presence of macular oedema correlated well with increased RNFL thickness and residual function in RP patients. Such association provides evidence of an underlying transneuronal mechanism of retinal degeneration. Simultaneous monitoring of CRT and RNFL thickness may help in the future to evaluate the progression of the disease and the efficacy of treatments in RP patients.