Optical Coherence Tomography Biomarkers for Conversion to Exudative Neovascular Age-related Macular Degeneration.


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:
03 2023
Historique:
received: 27 07 2022
revised: 04 09 2022
accepted: 20 09 2022
pubmed: 14 10 2022
medline: 3 3 2023
entrez: 13 10 2022
Statut: ppublish

Résumé

To identify optical coherence tomography (OCT) biomarkers, including thin and thick double-layer sign (DLS) for the progression from intermediate AMD (iAMD) to exudative macular neovascularization (MNV) over 24 months. Retrospective cohort study. Setting: Retina consultants of Texas. 458 eyes of 458 subjects with iAMD in at least 1 eye with 24 months of follow-up data. The following biomarkers were assessed at baseline: high central drusen volume (≥0.03 mm During follow-up, 18.1% (83 of 458) of eyes with iAMD progressed to exudative MNV. Thick DLS, IHRF, and fellow eye exudative MNV were found to be independent predictors for the development of exudative MNV within 2 years. The baseline frequencies, odds ratios, 95% confidence intervals, and P values for these biomarkers were as follows: thick DLS (9.6%, 4.339, 2.178-8.644; P < .001), IHRF (36.0%, 2.340, 1.396-3.922; P = 0.001), and fellow eye exudative MNV (35.8%, 1.694, 1.012-2.837; P = .045). Thick DLS, IHRF, and fellow eye exudative MNV were associated with an increased risk of progression from iAMD to exudative MNV. These biomarkers, which are readily identified by the review of OCT volume scans, may aid in risk prognostication for patients and for identifying patients for early intervention trials.

Identifiants

pubmed: 36228779
pii: S0002-9394(22)00375-0
doi: 10.1016/j.ajo.2022.09.018
pii:
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

137-144

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Auteurs

Yu Wakatsuki (Y)

From the Doheny Eye Institute, Los Angeles, California (Y.W., K.H., K.M.M., G.C., S.R.S.); Department of Ophthalmology, David Geffen School of Medicine at UCLA, Los Angeles, California, USA (Y.W., K.H., G.C., S.R.S.).

Kazutaka Hirabayashi (K)

From the Doheny Eye Institute, Los Angeles, California (Y.W., K.H., K.M.M., G.C., S.R.S.); Department of Ophthalmology, David Geffen School of Medicine at UCLA, Los Angeles, California, USA (Y.W., K.H., G.C., S.R.S.).

Hannah J Yu (HJ)

Retina Consultants of Texas, Retina Consultants of America, Houston, Texas (H.J.Y., C.C.W.).

Kenneth M Marion (KM)

From the Doheny Eye Institute, Los Angeles, California (Y.W., K.H., K.M.M., G.C., S.R.S.).

Giulia Corradetti (G)

From the Doheny Eye Institute, Los Angeles, California (Y.W., K.H., K.M.M., G.C., S.R.S.); Department of Ophthalmology, David Geffen School of Medicine at UCLA, Los Angeles, California, USA (Y.W., K.H., G.C., S.R.S.).

Charles C Wykoff (CC)

Retina Consultants of Texas, Retina Consultants of America, Houston, Texas (H.J.Y., C.C.W.).

Srinivas R Sadda (SR)

From the Doheny Eye Institute, Los Angeles, California (Y.W., K.H., K.M.M., G.C., S.R.S.); Department of Ophthalmology, David Geffen School of Medicine at UCLA, Los Angeles, California, USA (Y.W., K.H., G.C., S.R.S.). Electronic address: ssadda@doheny.org.

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