High-Resolution Imaging of the Optic Nerve and Retina in Optic Nerve Hypoplasia

• Published in: Ophthalmology (Rochester, Minn.) Vol. 122; no. 7; pp. 1330 - 1339
• Main Authors: Pilat, Anastasia, Sibley, Daniel, McLean, Rebecca J., Proudlock, Frank A., Gottlob, Irene
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.07.2015; Elsevier
• Subjects: Adolescent; Adult; Child; Child, Preschool; Cross-Sectional Studies; Female; Humans; Infant; Male; Nerve Fibers - pathology; Ophthalmology; Optic Disk - pathology; Optic Nerve Diseases - congenital; Optic Nerve Diseases - diagnosis; Original; Prospective Studies; Retina - pathology; Retinal Ganglion Cells - pathology; Sensitivity and Specificity; Tomography, Optical Coherence; Visual Acuity - physiology; OCT; SD OCT; IPL; OS; RNFL; INL; RPE; ONH; SOD; IS; OPL; logMAR; GCL; ONHD; optic nerve hypoplasia; optical coherence tomography; septo-optic-dysplasia; inner nuclear layer; optic nerve head drusen; outer segment; retinal pigment epithelium; logarithm of the minimum angle of resolution; outer plexiform layer; retinal nerve fiber layer; ganglion cell layer; spectral-domain optical coherence tomography; inner plexiform layer; inner segment
• ISSN: 0161-6420; 1549-4713; 1549-4713
• DOI: 10.1016/j.ophtha.2015.03.020

To investigate the optic nerve and macular morphology in patients with optic nerve hypoplasia (ONH) using spectral-domain optical coherence tomography (SD OCT). Prospective, cross-sectional, observational study. A total of 16 participants with ONH (10 female and 6 male; mean age, 17.2 years; 6 bilateral involvement) and 32 gender-, age-, ethnicity-, and refraction-matched healthy controls. High-resolution SD OCT (Copernicus [Optopol Technology S.A., Zawiercie, Poland], 3 μm resolution) and handheld SD OCT (Bioptigen Inc [Research Triangle Park, NC], 2.6 μm resolution) devices were used to acquire horizontal scans through the center of the optic disc and macula. Horizontal optic disc/cup and rim diameters, cup depth, peripapillary retinal nerve fiber layer (RNFL), and thickness of individual retinal layers in participants with ONH and in controls. Patients with ONH had significantly smaller discs (P < 0.03 and P < 0.001 compared with unaffected eye and healthy controls, respectively), horizontal cup diameter (P < 0.02 for both), and cup depth (P < 0.02 and P < 0.01, respectively). In the macula, significantly thinner RNFL (nasally), ganglion cell layer (GCL) (nasally and temporally), inner plexiform layer (IPL) (nasally), outer nuclear layer (ONL) (nasally), and inner segment (centrally and temporally) were found in patients with ONH compared with the control group (P < 0.05 for all comparisons). Continuation of significantly thicker GCL, IPL, and outer plexiform layer in the central retinal area (i.e., foveal hypoplasia) was found in more than 80% of patients with ONH. Clinically unaffected fellow eyes of patients with ONH showed mild features of underdevelopment. Visual acuity and presence of septo-optic dysplasia were associated with changes in GCL and IPL. Sensitivity and specificity for the detection of ONH based on disc and retinal optical coherence tomography (OCT) parameters were >80%. Our study provides evidence of retinal changes in ONH. In addition to thinning of retina layers mainly involving the RNFL and GCL, signs reminiscent of foveal hypoplasia were observed in patients with ONH. Optic nerve and foveal parameters measured using OCT showed high sensitivity and specificity for detecting ONH, demonstrating their useful for clinical diagnosis.