June 2023
Volume 64, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2023
Macula Deformability as a Potential Biomarker for High Myopia Eyes at Risk of Developing Glaucoma and Pathologic Myopia
Author Affiliations & Notes
  • Quan V Hoang
    Singapore Eye Research Institute, Singapore National Eye Centre, Duke-NUS Medical School, Singapore, Singapore
    Ophthalmology, Columbia University, New York, New York, United States
  • Thanadet Chuangsuwanich
    Ophthalmic Engineering & Innovation Laboratory, Department of Biomedical Engineering, National University of Singapore, Singapore, Singapore
  • Tin A Tun
    Singapore Eye Research Institute, Singapore National Eye Centre, Duke-NUS Medical School, Singapore, Singapore
    Ophthalmic Engineering & Innovation Laboratory, Department of Biomedical Engineering, National University of Singapore, Singapore, Singapore
  • Tin Aung
    Singapore Eye Research Institute, Singapore National Eye Centre, Duke-NUS Medical School, Singapore, Singapore
  • Michael J A Girard
    Singapore Eye Research Institute, Singapore National Eye Centre, Duke-NUS Medical School, Singapore, Singapore
    Ophthalmic Engineering & Innovation Laboratory, Department of Biomedical Engineering, National University of Singapore, Singapore, Singapore
  • Footnotes
    Commercial Relationships   Quan Hoang None; Thanadet Chuangsuwanich None; Tin Tun None; Tin Aung None; Michael Girard Abyss Processing Pte Ltd, Code S (non-remunerative)
  • Footnotes
    Support  Singapore National Medical Research Council (Grant CSA/MOH-000151/2019, QVH)
Investigative Ophthalmology & Visual Science June 2023, Vol.64, 5094. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Quan V Hoang, Thanadet Chuangsuwanich, Tin A Tun, Tin Aung, Michael J A Girard; Macula Deformability as a Potential Biomarker for High Myopia Eyes at Risk of Developing Glaucoma and Pathologic Myopia. Invest. Ophthalmol. Vis. Sci. 2023;64(8):5094.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Purpose : To assess the macula deformation following IOP elevation in healthy, highly myopic (HM) eyes, highly myopic eyes with glaucoma (HMG) and pathologic myopia (PM).

Methods : We recruited 328 subjects, which comprised of 32 emmetropic controls, 50 HM (>26 mm in axial length), 108 HMG and 138 PM subjects (PM defined as HM + staphyloma and/or myopic macular degeneration). For each subject, we imaged the macula using Spectral-domain optical coherence tomography (OCT) under at baseline and under acute intraocular pressure (IOP) elevation through ophthalmodynamometry to ~40mmHg. Macula scans were manually-aligned using 4 choroidal landmarks to allow comparison of scans of a given eye at baseline vs. during IOP elevation. We then automatically segmented the sclera and the choroid tissues using a deep-learning algorithm and extracted the point clouds of the sclera-choroid interface. Macula curvatures were calculated by fitting a second-degree polynomial to the sclera-choroid points cloud along the nasal-temporal direction at 100-micron intervals).

Results : IOP elevation resulted in a high macula curvature change in the PM (10.5±10.2 micron-1) and HMG (5.2±5.1 micron-1) eyes as compared to HM (3.1±2.7 micron-1) eyes (both p < 0.05). Interestingly, HM eyes had the same curvature change as emmetropic eyes (4.2±4.3 micron-1).

Conclusions : We found that the macula of pathologic eye (i.e. eyes with HMG and/or PM) were more sensitive to IOP elevation as compared to HM eyes and emmetropic eyes. These preliminary results indicate that macula curvature changes may serve as a biomarker for HM eyes at risk of developing other pathologies (e.g. glaucoma and staphyloma).

This abstract was presented at the 2023 ARVO Annual Meeting, held in New Orleans, LA, April 23-27, 2023.

×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×