Topographic Correlation between β-Zone Parapapillary Atrophy and Retinal Nerve Fiber Layer Defect

Objective To investigate whether a topographic correlation exists between β-zone parapapillary atrophy (PPA) and retinal nerve fiber layer (RNFL) defect. The location and extent of the β-zone were examined. Design Retrospective, cross-sectional study. Participants One hundred twenty-eight eyes from...

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Veröffentlicht in:Ophthalmology (Rochester, Minn.) Minn.), 2013-03, Vol.120 (3), p.528-534
Hauptverfasser: Cho, Bum-Joo, MD, Park, Ki Ho, MD, PhD
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Sprache:eng
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Zusammenfassung:Objective To investigate whether a topographic correlation exists between β-zone parapapillary atrophy (PPA) and retinal nerve fiber layer (RNFL) defect. The location and extent of the β-zone were examined. Design Retrospective, cross-sectional study. Participants One hundred twenty-eight eyes from 128 consecutive patients with primary open-angle glaucoma (POAG) and a single localized RNFL defect were included. Methods Digital optic disc photographs of the enrolled eyes were reviewed and eyes with β-zone PPA were identified. The topographic parameters of β-zone PPA and RNFL defect were measured on optic disc photographs and digital red-free RNFL photographs. The association between these parameters was examined statistically. Main Outcome Measures Angular location and angular extent of β-zone PPA and RNFL defect, angular location of point of maximum radial extent (PMRE) of β-zone PPA, and β-zone PPA-to-disc area ratio. Results Eighty-two (64.1%) of the 128 eyes with a single localized RNFL defect had β-zone PPA. Patients with β-zone PPA were younger (by 6.6 years) than those without β-zone PPA ( P = 0.001). β-Zone PPA was located most commonly inferotemporally (65.9%). The RNFL defect was located in the same hemifield as the β-zone PPA in 76% of eyes and was located in the same hemifield as PMRE in 88% of eyes. The angular location of the RNFL defect showed a linear correlation with those of β-zone PPA ( r = 0.390; P
ISSN:0161-6420
1549-4713
DOI:10.1016/j.ophtha.2012.09.004