Cone Spacing Correlates With Retinal Thickness and Microperimetry in Patients With Inherited Retinal Degenerations.


Journal

Investigative ophthalmology & visual science
ISSN: 1552-5783
Titre abrégé: Invest Ophthalmol Vis Sci
Pays: United States
ID NLM: 7703701

Informations de publication

Date de publication:
01 03 2019
Historique:
entrez: 30 3 2019
pubmed: 30 3 2019
medline: 24 8 2019
Statut: ppublish

Résumé

To determine whether high-resolution retinal imaging measures of macular structure correlate with visual function over 36 months in retinal degeneration (RD) patients and normal subjects. Twenty-six eyes of 16 RD patients and 16 eyes of 8 normal subjects were studied at baseline; 15 eyes (14 RD) and 11 eyes (6 normal) were studied 36 months later. Adaptive Optics Scanning Laser Ophthalmoscopy (AOSLO) was used to identify regions of interest (ROIs) with unambiguous cones at baseline to measure cone spacing. AOSLO images were aligned with spectral-domain optical coherence tomography (SD-OCT) and fundus-guided microperimetry results to correlate structure and function at the ROIs. SD-OCT images were segmented to measure inner segment (IS) and outer segment (OS) thickness. Correlations between cone spacing, IS and OS thickness and sensitivity were assessed using Spearman correlation coefficient ρ with bootstrap analyses clustered by person. Cone spacing (ρ = 0.57, P < 0.001) and macular sensitivity (ρ = 0.19, P = 0.14) were significantly correlated with eccentricity in patients. Controlling for eccentricity, cone spacing Z-scores were inversely correlated with IS (ρ = -0.29, P = 0.002) and OS thickness (ρ = -0.39, P < 0.001) in RD patients only, and with sensitivity in normal subjects (ρ = -0.22, P < 0.001) and RD patients (ρ = -0.38, P < 0.001). After 36 months, cone spacing increased (P < 0.001) and macular sensitivity decreased (P = 0.007) compared to baseline in RD patients. Cone spacing increased and macular sensitivity declined significantly in RD patients over 36 months. High resolution images of cone structure correlated with retinal sensitivity, and may be appropriate outcome measures for clinical trials in RD.

Identifiants

pubmed: 30924848
pii: 2729835
doi: 10.1167/iovs.18-25688
pmc: PMC6440525
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Langues

eng

Pagination

1234-1243

Subventions

Organisme : NEI NIH HHS
ID : P30 EY002162
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY023591
Pays : United States
Organisme : NEI NIH HHS
ID : T32 EY007043
Pays : United States

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Auteurs

Katharina G Foote (KG)

School of Optometry and Vision Science Graduate Group, University of California, Berkeley, Berkeley, California, United States.
Ophthalmology, University of California, San Francisco, California, United States.

Irina De la Huerta (I)

Ophthalmology, University of California, San Francisco, California, United States.

Kevin Gustafson (K)

Ophthalmology, University of California, San Francisco, California, United States.

Angela Baldwin (A)

Ophthalmology, University of California, San Francisco, California, United States.

Shiri Zayit-Soudry (S)

Ophthalmology, University of California, San Francisco, California, United States.

Nicholas Rinella (N)

Ophthalmology, University of California, San Francisco, California, United States.

Travis C Porco (TC)

Ophthalmology, University of California, San Francisco, California, United States.
Francis I. Proctor Foundation, University of California, San Francisco, California, United States.

Austin Roorda (A)

School of Optometry and Vision Science Graduate Group, University of California, Berkeley, Berkeley, California, United States.

Jacque L Duncan (JL)

Ophthalmology, University of California, San Francisco, California, United States.

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Classifications MeSH