Optical Coherence Tomography Angiography Assessment in Congenital Aniridia.


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:
09 2023
Historique:
received: 19 02 2023
revised: 05 04 2023
accepted: 07 04 2023
medline: 18 8 2023
pubmed: 15 4 2023
entrez: 14 4 2023
Statut: ppublish

Résumé

This study aims to characterize foveal vasculature assessed by optical coherence tomography angiography (OCT-A) in congenital aniridia which is hallmarked by foveal hypoplasia (FH). Cross-sectional case-control analysis. At the National Referral Center for congenital aniridia, patients with confirmed PAX6-related aniridia and FH diagnosed on spectral-domain OCT (SD-OCT) with available OCT-A and matched control subjects were included. OCT-A was performed in patients with aniridia and control subjects. Foveal avascular zone (FAZ) and vessel density (VD) were collected. VD in the foveal and parafoveal areas at the level of the superficial and deep capillary plexi (SCP and DCP, respectively) were compared between the 2 groups. In patients with congenital aniridia, correlation between VD and the grading of FH was assessed. Among 230 patients with confirmed PAX6-related aniridia, high-quality macular B-scans and OCT-A were available in 10 patients. On the foveal area, mean VD was higher in aniridia patients (41.10%, n = 10) than in control subjects (22.65%, n = 10) at the level of the SCP and the DCP (P = .0020 and P = .0273, respectively). On the parafoveal area, mean VD was lower in patients with aniridia (42.34%, n = 10) than in healthy subjects (49.24%, n = 10) at the level of both plexi (P = .0098 and P = .0371, respectively). In patients with congenital aniridia, a positive correlation was found between the grading of FH and the foveal VD at the SCP (r = 0.77, P = .0106). Vasculature is altered in PAX6-related congenital aniridia, higher in foveal and lower in parafoveal areas, especially when FH is severe, which is consistent with the concept that the absence of retinal blood vessels is essential for foveal pit development.

Identifiants

pubmed: 37059316
pii: S0002-9394(23)00170-8
doi: 10.1016/j.ajo.2023.04.004
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

44-48

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Auteurs

Alexandre Dentel (A)

From the Ophthalmology Department (A.D., M.F., M.P.R., D.B-G., A.D.), Necker-Enfants Malades University Hospital, Paris. Electronic address: dentel_alexandre@orange.fr.

Marco Ferrari (M)

From the Ophthalmology Department (A.D., M.F., M.P.R., D.B-G., A.D.), Necker-Enfants Malades University Hospital, Paris.

Matthieu P Robert (MP)

From the Ophthalmology Department (A.D., M.F., M.P.R., D.B-G., A.D.), Necker-Enfants Malades University Hospital, Paris; Borelli Centre (M.P.R.), UMR 9010, CNRS-SSA-ENS Paris Saclay-Paris Cité University, Paris.

Sophie Valleix (S)

INSERM (S.V., D.B-G., A.D.), UMRS1138, Team 17, From Physiopathology of Ocular Diseases to Clinical Development, Sorbonne Paris Cité University, Centre de Recherche des Cordeliers, Paris; Genomic Medicine Department of Systemic and Organ Diseases (S.V.), Cochin Hospital, Paris City University, Paris, France.

Dominique Bremond-Gignac (D)

From the Ophthalmology Department (A.D., M.F., M.P.R., D.B-G., A.D.), Necker-Enfants Malades University Hospital, Paris; INSERM (S.V., D.B-G., A.D.), UMRS1138, Team 17, From Physiopathology of Ocular Diseases to Clinical Development, Sorbonne Paris Cité University, Centre de Recherche des Cordeliers, Paris.

Alejandra Daruich (A)

From the Ophthalmology Department (A.D., M.F., M.P.R., D.B-G., A.D.), Necker-Enfants Malades University Hospital, Paris; INSERM (S.V., D.B-G., A.D.), UMRS1138, Team 17, From Physiopathology of Ocular Diseases to Clinical Development, Sorbonne Paris Cité University, Centre de Recherche des Cordeliers, Paris.

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