Foveolar Drusen Decrease Fixation Stability in Pre-Symptomatic AMD.


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 Jul 2024
Historique:
medline: 8 7 2024
pubmed: 8 7 2024
entrez: 8 7 2024
Statut: ppublish

Résumé

This study aims at linking subtle changes of fixational eye movements (FEM) in controls and in patients with foveal drusen using adaptive optics retinal imaging in order to find anatomo-functional markers for pre-symptomatic age-related macular degeneration (AMD). We recruited 7 young controls, 4 older controls, and 16 patients with presymptomatic AMD with foveal drusen from the Silversight Cohort. A high-speed research-grade adaptive optics flood illumination ophthalmoscope (AO-FIO) was used for monocular retinal tracking of fixational eye movements. The system allows for sub-arcminute resolution, and high-speed and distortion-free imaging of the foveal area. Foveal drusen position and size were documented using gaze-dependent imaging on a clinical-grade AO-FIO. FEM were measured with high precision (RMS-S2S = 0.0015 degrees on human eyes) and small foveal drusen (median diameter = 60 µm) were detected with high contrast imaging. Microsaccade amplitude, drift diffusion coefficient, and ISOline area (ISOA) were significantly larger for patients with foveal drusen compared with controls. Among the drusen participants, microsaccade amplitude was correlated to drusen eccentricity from the center of the fovea. A novel high-speed high-precision retinal tracking technique allowed for the characterization of FEM at the microscopic level. Foveal drusen altered fixation stability, resulting in compensatory FEM changes. Particularly, drusen at the foveolar level seemed to have a stronger impact on microsaccade amplitudes and ISOA. The unexpected anatomo-functional link between small foveal drusen and fixation stability opens up a new perspective of detecting oculomotor signatures of eye diseases at the presymptomatic stage.

Identifiants

pubmed: 38975944
pii: 2800407
doi: 10.1167/iovs.65.8.13
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

13

Auteurs

Jimmy Murari (J)

Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.

Josselin Gautier (J)

CHNO des Quinze-Vingts, INSERM-DGOS CIC, Paris, France.
LTSI, Inserm UMR 1099, University of Rennes, Rennes, France.

Joël Daout (J)

Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.

Léa Krafft (L)

Office National d'Etudes et de Recherches Aérospatiales (ONERA), Hauts-de-Seine, France.

Pierre Senée (P)

Office National d'Etudes et de Recherches Aérospatiales (ONERA), Hauts-de-Seine, France.
Quantel Medical SA, Cournon d'Auvergne, France.

Pedro Mecê (P)

Office National d'Etudes et de Recherches Aérospatiales (ONERA), Hauts-de-Seine, France.
Institut Langevin, CNRS, ESPCI, Paris, France.

Kate Grieve (K)

Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
CHNO des Quinze-Vingts, INSERM-DGOS CIC, Paris, France.

William Seiple (W)

Lighthouse Guild, New York, New York, United States.

Denis Sheynikhovich (D)

Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.

Serge Meimon (S)

Office National d'Etudes et de Recherches Aérospatiales (ONERA), Hauts-de-Seine, France.

Michel Paques (M)

CHNO des Quinze-Vingts, INSERM-DGOS CIC, Paris, France.

Angelo Arleo (A)

Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.

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Classifications MeSH