4.3 Article

Arterial spin labeling fMRI measurements of decreased blood flow in primary visual cortex correlates with decreased visual function in human glaucoma

Journal

VISION RESEARCH
Volume 60, Issue -, Pages 51-60

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.visres.2012.03.012

Keywords

Functional MRI; Brain imaging; Optic nerve; Degeneration; Visual function testing; Visual pathway

Funding

  1. The Glaucoma Foundation
  2. NIH [EY11008, EY008208]
  3. Carl Zeiss Meditec Inc.
  4. Heidelberg Engineering GmbH
  5. Optovue Inc.
  6. Topcon Medical Systems Inc.
  7. Pfizer, Inc.
  8. Carl Zeiss Meditec
  9. Novartis
  10. Optovue.
  11. Topcon Medical Systems
  12. Haag-Streit

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Purpose: Altered metabolic activity has been identified as a potential contributing factor to the neurodegeneration associated with primary open angle glaucoma (POAG). Consequently, we sought to determine whether there is a relationship between the loss of visual function in human glaucoma and resting blood perfusion within primary visual cortex (VI). Methods: Arterial spin labeling (ASL) functional magnetic resonance imaging (fMRI) was conducted in 10 participants with POAG. Resting cerebral blood flow (CBF) was measured from dorsal and ventral VI. Behavioral measurements of visual function were obtained using standard automated perimetry (SAP), short-wavelength automated perimetry (SWAP), and frequency-doubling technology perimetry (FDT). Measurements of CBF were compared to differences in visual function for the superior and inferior hemifield. Results: Differences in CBF between ventral and dorsal V1 were correlated with differences in visual function for the superior versus inferior visual field. A statistical bootstrapping analysis indicated that the observed correlations between fMRI responses and measurements of visual function for SAP (r = 0.49), SWAP (r = 0.63), and FDT (r = 0.43) were statistically significant (all p < 0.05). Conclusions: Resting blood perfusion in human VI is correlated with the loss of visual function in POAG. Altered CBF may be a contributing factor to glaucomatous optic neuropathy, or it may be an indication of post-retinal glaucomatous neurodegeneration caused by damage to the retinal ganglion cells. (C) 2012 Elsevier Ltd. All rights reserved.

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