Fibrillar Layer as a Marker for Areas of Pronounced Corneal Endothelial Cell Loss in Advanced Fuchs Endothelial Corneal Dystrophy

• Published in: American journal of ophthalmology 2021-02, Vol.222, p.292-301
• Main Authors: Hribek, Agathe, Clahsen, Thomas, Horstmann, Jens, Siebelmann, Sebastian, Loreck, Niklas, Heindl, Ludwig M., Bachmann, Björn O., Cursiefen, Claus, Matthaei, Mario
• Format: Article
• Language: English
• Subjects: Aged; Antibodies; Binding sites; Cataracts; Collagen; Cornea; Corneal Endothelial Cell Loss - diagnosis; Corneal Endothelial Cell Loss - etiology; Corneal Endothelial Cell Loss - surgery; Datasets; Descemet Stripping Endothelial Keratoplasty - methods; Edema; Endothelium; Endothelium, Corneal - pathology; Eye surgery; Female; Fuchs' Endothelial Dystrophy - complications; Fuchs' Endothelial Dystrophy - diagnosis; Humans; Male; Microscopy; Middle Aged; Normal distribution; Open source software; Prospective Studies; Slit Lamp Microscopy; Transplants & implants; Visual Acuity
• ISSN: 0002-9394; 1879-1891
• DOI: 10.1016/j.ajo.2020.09.030

We sought to assess the correlation of corneal endothelial cell (CEC) density to alterations of collagen composition of Descemet membrane (DM) in advanced Fuchs endothelial corneal dystrophy (FECD) and to image such changes by slit-lamp biomicroscopy in vivo. Prospective, observational consecutive case series. Fifty eyes (50 subjects) with advanced FECD were enrolled. After slit-lamp biomicroscopy and corneal Scheimpflug imaging, the Descemet endothelium complex (DEC) was retrieved during DM endothelial keratoplasty (DMEK) surgery. The expression of collagens I, III, and IV (COL I, COL III, and COL IV) and corresponding CEC density were analyzed by immunofluorescence flat mount-staining. Presence, diameter and surface area of collagen expression, and CEC density served as the main outcome measures. Immunofluorescence staining revealed central coherent collagen positive areas (mean surface area = 10 mm2 ± 6 mm2) corresponding to a fibrillar layer burying the guttae of DM in 84% (42/50) of DECs. CEC density overlying the fibrillar layer compared with the periphery was significantly reduced (−54.8%, P < .0001) with a steep decline of CEC density at its borders. Subgroup analysis revealed that the fibrillar layer may be imaged by slit-lamp biomicroscopy in vivo with significant positive correlation of mean maximum diameter detected by slit-lamp biomicroscopy (dSL max = 4.1 mm ± 0.9 mm) and by immunofluorescence staining (dIF max = 4.7 mm ± 1.1 mm; r = 0.76; P = .001). A fibrillar layer with a clear geographic pattern marks areas of pronounced loss of CEC density in advanced FECD eyes and may be imaged by slit-lamp biomicroscopy in vivo.