Erschienen in:
01.10.2019 | Original Paper
Increased choroidal thickness in primary angle closure measured by swept-source optical coherence tomography in Caucasian population
verfasst von:
Diem-Trang Nguyen, Audrey Giocanti-Aurégan, Nassima Benhatchi, Nicolas Greliche, Helene Beaussier, Pierre Sustronck, Sirine Hammoud, Marie-Nathalie Jeanteur, Gilles Kretz, Olivia Abitbol, Yves Lachkar
Erschienen in:
International Ophthalmology
|
Ausgabe 1/2020
Einloggen, um Zugang zu erhalten
Abstract
Purpose
A role of the choroid has been suggested in the pathophysiology of angle closure. We assessed the choroidal thickness (CT) in Caucasian patients with primary angle closure (PAC) and in a subgroup of patients with plateau iris using swept-source optical coherence tomography (SS-OCT) compared to normal eyes.
Methods
This prospective cohort study in a hospital-based population in a tertiary center compared consecutive patients with PAC to healthy controls. A subgroup analysis of patients with plateau iris was also performed. Choroidal thickness was measured by SS-OCT in the subfoveal area (SFCT) and at 1- and 3-mm eccentricity superiorly, inferiorly, nasally and temporally from the fovea.
Results
Compared to the 25 eyes of 13 control patients [7 women, mean (SD) age, 56.6 (15.7) years], the 45 eyes of 25 patients with PAC [15 women, mean (SD) age, 55.7 (10.7) years] had a significantly increased SFCT. SFCT was 355.36 μm (SD 85.97) in PAC eyes versus 286.08 μm (SD 98.09) in control eyes (p = 0.009). The CT was also significantly increased compared to control eyes in other macular areas (p < 0.05), except at 3 mm temporal to the fovea. In the plateau iris subgroup, a not significant (except 3 mm nasal to the fovea) trend toward an increased CT was observed in all studied macular areas compared to control eyes.
Conclusion
In eyes of Caucasian patients with PAC, the CT is increased compared to controls. Increased CT could contribute to the pathophysiology of PAC with a possible choroidal expansion and dysfunction of choroidal ganglion cells.