Macular Vascularity in Ischemic Optic Neuropathy Compared to Glaucoma by Projection-Resolved Optical Coherence Tomography Angiography.


Journal

American journal of ophthalmology
ISSN: 1879-1891
Titre abrégé: Am J Ophthalmol
Pays: United States
ID NLM: 0370500

Informations de publication

Date de publication:
01 2020
Historique:
received: 05 06 2019
revised: 12 08 2019
accepted: 17 09 2019
pubmed: 29 9 2019
medline: 18 4 2020
entrez: 29 9 2019
Statut: ppublish

Résumé

To compare macular vasculature in patients with primary open-angle glaucoma (POAG) and atrophic nonarteritic anterior ischemic optic neuropathy (NAION). Prospective, cross-sectional study. Thirty-seven eyes with moderate and advanced POAG, 19 eyes with atrophic NAION, and 40 eyes of normal subjects were imaged using optical coherence tomography angiography (OCT-A). Macular ganglion cell complex (GCC) and peripapillary retinal nerve fiber layer (RNFL) thicknesses were measured in addition to macular superficial and deep vasculature after projection removal using custom software. Linear models showed that while averaged peripapillary RNFL and macular GCC were not different between NAION and POAG eyes, both were significantly thinner than control eyes. Whole image macular superficial vessel density was significantly lower in NAION and glaucoma eyes (P = .003 and <.001, respectively) than in normal eyes, with lower vessel density in glaucoma than in NAION eyes (P = .01). Whole image and parafoveal deep macular vessels in glaucoma eyes (21.0%±8.7%, 24.4%±9.6%) were significantly lower than in control eyes (27.4%±8.6%, 31.9%±10.6%) (P = .01 and P = .01, respectively). No significant differences in deep vessels were observed between NAION and control eyes. Glaucomatous eyes had lower temporal and inferior parafoveal deep vasculature values than NAION eyes (P = .007 and .03, respectively). In NAION and POAG with similar RNFL and macular damage, macular OCT-A shows less involvement of superficial and deep vascular plexus in NAION in contrast to POAG, which might show a primary vascular insult in addition to secondary vascular damage due to ganglion cell damage.

Identifiants

pubmed: 31562857
pii: S0002-9394(19)30473-8
doi: 10.1016/j.ajo.2019.09.015
pii:
doi:

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

27-34

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Masoud Aghsaei Fard (MA)

Farabi Eye Hospital, Tehran University of Medical Science, Iran. Electronic address: masood219@gmail.com.

Ghasem Fakhraee (G)

Farabi Eye Hospital, Tehran University of Medical Science, Iran.

Hossein Ghahvechian (H)

Farabi Eye Hospital, Tehran University of Medical Science, Iran.

Alireza Sahraian (A)

Farabi Eye Hospital, Tehran University of Medical Science, Iran.

Sasan Moghimi (S)

Farabi Eye Hospital, Tehran University of Medical Science, Iran; Department of Ophthalmology, Shiley Eye Institute, University of California, San Diego, California; and the Einhorn Clinical Research Center, New York Eye and Ear Infirmary of Mount Sinai, New York, New York, USA.

Robert Ritch (R)

Department of Ophthalmology, Shiley Eye Institute, University of California, San Diego, California; and the Einhorn Clinical Research Center, New York Eye and Ear Infirmary of Mount Sinai, New York, New York, USA.

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Classifications MeSH