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Correlation of Clinical Fibrillar Layer Detection and Corneal Thickness in Advanced Fuchs Endothelial Corneal Dystrophy.

Orlando ÖzerMert MestanogluAntonia HowaldtThomas ClahsenPetra SchillerSebastian SiebelmannNiklas ReinkingClaus CursiefenBjörn O BachmannMario Matthaei
Published in: Journal of clinical medicine (2022)
Central subendothelial geographic deposits are formed as a fibrillar layer (FL) in advanced Fuchs endothelial corneal dystrophy (FECD). Previous studies demonstrated a significant decrease in corneal endothelial cell (CEC) density and an increase in focal corneal backscatter in the FL area. The present study investigated the association of the FL with edema formation and its localization. Patients ( n = 96) presenting for Descemet membrane endothelial keratoplasty (DMEK) for advanced FECD were included. Slit-lamp biomicroscopy with FECD grading was followed by Scheimpflug imaging with en face backscatter analysis and pachymetric analysis. FL dimensions were measured, and correlation with pachymetric values was performed. An FL was detected in 74% of all eyes ( n = 71). Pachymetric values in FL-positive versus FL-negative eyes were for corneal thickness at the apex (ACT) 614 ± 52 µm and 575 ± 46 µm ( p = 0.001), for peripheral corneal thickness at 1 mm (PCT 1mm ) 616 ± 50 µm and 580 ± 44 µm ( p = 0.002), for PCT 2mm 625 ± 48 µm and 599 ± 41 µm ( p = 0.017), for PCT 3mm 651 ± 46 µm and 635 ± 40 µm ( p = 0.128) and for PCT 4mm 695 ± 52 µm and 686 ± 43 µm ( p = 0.435), respectively. Correlation analysis indicated a weak correlation for the FL maximum vertical caliper diameter with ACT and PCT 1mm values but no further relevant correlations. In FL-positive eyes, increased focal corneal backscatter and increased corneal thickness showed primarily central and inferotemporal localization. In conclusion, Scheimpflug imaging shows an association of the FL with increased corneal thickness in advanced FECD and shows localization of the FL and increased corneal thickness in the central and inferotemporal region. This may provide important information for progression assessment and therapeutic decision making in FECD patients in the future.
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