Publication

The impact of macular edema on microvascular and metabolic alterations in retinitis pigmentosa

Journal Paper/Review - Sep 10, 2020

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PubMed
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Citation
Todorova M, Scholl H, Della Volpe Waizel M. The impact of macular edema on microvascular and metabolic alterations in retinitis pigmentosa. Graefes Arch Clin Exp Ophthalmol 2020; 259:643-652.
Type
Journal Paper/Review (English)
Journal
Graefes Arch Clin Exp Ophthalmol 2020; 259
Publication Date
Sep 10, 2020
Issn Electronic
1435-702X
Pages
643-652
Brief description/objective

PURPOSE
The primary aim of our study was to evaluate retinal microvascular anomalies recorded with optical coherence tomography angiography (OCTA) and the retinal metabolic function measured with retinal oximetry (RO) in patients with retinitis pigmentosa (RP). The secondary aim of the study was to link the presence of macular edema to microvascular and metabolic parameters in RP.

METHODS
OCTA and RO were performed on 94 eyes: 64 eyes diagnosed with RP with (ME-RP) and without (no-ME-RP) macular edema were compared with 30 control eyes. Study end points were as follows: mean superficial (FAZ-S) and deep foveal avascular zone (FAZ-D) determined by OCTA. In addition, we evaluated the mean arterial (A-SO; %), venular (V-SO; %) oxygen saturation, their difference (A-V SO; %), as well as the corresponding mean diameter of the retinal arterioles (D-A; μm) and venules (D-V; μm).

RESULTS
RP patients differed from controls by enlarged FAZ-S and FAZ-D (p ≤ 0.001), attenuated retinal vessels (p ≤ 0.001), and increased retinal vessel oxygen saturation (p ≤ 0.010). Subgroup analyses within RP patients revealed more pronounced alterations of microvascular parameters and metabolic function in the presence of macular edema. In the no-ME-RP subgroup, significant interactions were present between FAZ-S, A-SO, and V-SO, whereas in the ME-RP subgroup, we found significant correlations between FAZ-D and D-A.

CONCLUSION
A combined microvascular structure-metabolic function approach enhances our understanding of inherited retinal diseases. The presence of macular edema in RP seems to be a result of more altered microvascular-metabolic function. Macular edema should thus be taken into consideration when evaluating microvascular and/or metabolic changes in RP.