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Contributions of Brain Microstructures and Metabolism to Visual Field Loss Patterns in Glaucoma Using Archetypal and Information Gain Analyses.
Pang, Yueyin; Bang, Ji Won; Kasi, Anisha; Li, Jeremy; Parra, Carlos; Fieremans, Els; Wollstein, Gadi; Schuman, Joel S; Wang, Mengyu; Chan, Kevin C.
Affiliation
  • Pang Y; Department of Ophthalmology, New York University Grossman School of Medicine, New York, New York, United States.
  • Bang JW; Department of Ophthalmology, New York University Grossman School of Medicine, New York, New York, United States.
  • Kasi A; Department of Ophthalmology, New York University Grossman School of Medicine, New York, New York, United States.
  • Li J; Department of Ophthalmology, New York University Grossman School of Medicine, New York, New York, United States.
  • Parra C; Department of Ophthalmology, New York University Grossman School of Medicine, New York, New York, United States.
  • Fieremans E; Department of Radiology, New York University Grossman School of Medicine, New York, New York, United States.
  • Wollstein G; Department of Biomedical Engineering, Tandon School of Engineering, New York University, Brooklyn, New York, United States.
  • Schuman JS; Department of Ophthalmology, New York University Grossman School of Medicine, New York, New York, United States.
  • Wang M; Department of Biomedical Engineering, Tandon School of Engineering, New York University, Brooklyn, New York, United States.
  • Chan KC; Center for Neural Science, New York University, New York, New York, United States.
Invest Ophthalmol Vis Sci ; 65(8): 15, 2024 Jul 01.
Article in En | MEDLINE | ID: mdl-38975942
ABSTRACT

Purpose:

To investigate the contributions of the microstructural and metabolic brain environment to glaucoma and their association with visual field (VF) loss patterns by using advanced diffusion magnetic resonance imaging (dMRI), proton magnetic resonance spectroscopy (MRS), and clinical ophthalmic measures.

Methods:

Sixty-nine glaucoma and healthy subjects underwent dMRI and/or MRS at 3 Tesla. Ophthalmic data were collected from VF perimetry and optical coherence tomography. dMRI parameters of microstructural integrity in the optic radiation and MRS-derived neurochemical levels in the visual cortex were compared among early glaucoma, advanced glaucoma, and healthy controls. Multivariate regression was used to correlate neuroimaging metrics with 16 archetypal VF loss patterns. We also ranked neuroimaging, ophthalmic, and demographic attributes in terms of their information gain to determine their importance to glaucoma.

Results:

In dMRI, decreasing fractional anisotropy, radial kurtosis, and tortuosity and increasing radial diffusivity correlated with greater overall VF loss bilaterally. Regionally, decreasing intra-axonal space and extra-axonal space diffusivities correlated with greater VF loss in the superior-altitudinal area of the right eye and the inferior-altitudinal area of the left eye. In MRS, both early and advanced glaucoma patients had lower gamma-aminobutyric acid (GABA), glutamate, and choline levels than healthy controls. GABA appeared to associate more with superonasal VF loss, and glutamate and choline more with inferior VF loss. Choline ranked third for importance to early glaucoma, whereas radial kurtosis and GABA ranked fourth and fifth for advanced glaucoma.

Conclusions:

Our findings highlight the importance of non-invasive neuroimaging biomarkers and analytical modeling for unveiling glaucomatous neurodegeneration and how they reflect complementary VF loss patterns.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Visual Fields / Tomography, Optical Coherence / Visual Field Tests Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Invest Ophthalmol Vis Sci Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Visual Fields / Tomography, Optical Coherence / Visual Field Tests Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Invest Ophthalmol Vis Sci Year: 2024 Document type: Article