Publication

Retinal vessel oximetry in children with inherited retinal diseases

Journal Paper/Review - Jun 22, 2020

Units
PubMed
Doi

Citation
Della Volpe Waizel M, Scholl H, Valmaggia C, Todorova M. Retinal vessel oximetry in children with inherited retinal diseases. Acta Ophthalmol 2020; 99:52-60.
Type
Journal Paper/Review (English)
Journal
Acta Ophthalmol 2020; 99
Publication Date
Jun 22, 2020
Issn Electronic
1755-3768
Pages
52-60
Brief description/objective

BACKGROUND
Retinal vessel oximetry (RO) has been used to show altered metabolic function in patients with inherited retinal diseases (IRDs). The aim of this study was to investigate RO parameters of children with IRDs and presumed IRD carriers (pIRDc) and to compare them to controls.

METHODS
In this cross-sectional cohort study, 142 eyes from 71 Caucasian subjects were included: 40 eyes with IRDs, 26 eyes with pIRDc and 76 control eyes. The oxygen saturation was measured with the Retinal Vessel Analyser (IMEDOS Systems UG, Jena, Germany). Mean oxygen saturations in the peripapillary retinal arterioles (A-SO ; %) and venules (V-SO ; %) were estimated, and their difference (A-V SO ; %) was calculated. In addition, we evaluated the mean diameter in all major retinal arterioles (D-A; μm) and venules (D-V; μm). anova-based linear mixed-effects models were calculated with SPSS .

RESULTS
In general, children suffering from IRDs differed from controls when the A-SO and A-V SO were taken into account: both the A-SO and the A-V SO were significantly increased (p = 0.012). In subgroup analyses, children suffering from rod-cone dystrophy (RCD) presented an A-SO increase (99.12 ± 8.24%) when compared to controls (91.33 ± 10.34%, p = 0.014) and pIRDc (92.37 ± 6.57%, p = 0.065). For V-SO significant changes in RCD (67.42 ± 9.19%) were found in comparison with controls (58.24 ± 11.74%, p < 0.041), pIRDc (56.67 ± 7.16%, p = 0.007), cone-rod dystrophies (CRD, 52.17 ± 5.32%, p < 0.001) and inherited macular dystrophies (IMD, 55.74 ± 6.96%, p = 0.004), In addition, A-V SO was decreased in RCD (31.69 ± 3.92%) when measured against CRD (41.9 ± 8.87%, p = 0.017) or IMD (39.52 ± 8.95%, p = 0.059).

CONCLUSION
In general, we found that children with IRDs presented early metabolic changes. Within IRDs, children with RCD showed more affected metabolic changes. Thus, RO may support early screening to rule out IRDs in children, and more precisely may help to differentiate those suffering from RCD.