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An Ex Vivo Choroid Sprouting Assay of Ocular Microvascular Angiogenesis
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Choroidal Microvascular Dropout in Pseudoexfoliation Glaucoma.

Zia S Pradhan1, Harsha L Rao1,2, Shivani Dixit1

  • 1Narayana Nethralaya, Rajajinagar, Bangalore, India.

Investigative Ophthalmology & Visual Science
|May 21, 2019
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Choroidal microvasculature dropout (CMvD) is less common in pseudoexfoliation glaucoma (PXG) than in primary open-angle glaucoma (POAG). This finding suggests differences in glaucoma pathophysiology and vascular involvement between these conditions.

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Area of Science:

  • Ophthalmology
  • Glaucoma Research
  • Vascular Imaging

Background:

  • Pseudoexfoliation glaucoma (PXG) and primary open-angle glaucoma (POAG) are common forms of glaucoma.
  • Understanding the underlying pathophysiology, including vascular changes, is crucial for diagnosis and treatment.
  • Choroidal microvasculature dropout (CMvD) is a potential indicator of vascular compromise in glaucoma.

Purpose of the Study:

  • To compare the prevalence of choroidal microvasculature dropout (CMvD) between eyes with PXG and POAG.
  • To assess if CMvD differs in glaucoma patients with similar disease severity.

Main Methods:

  • A cross-sectional study included 39 PXG eyes and 39 age- and disease-severity-matched POAG eyes.
  • Optical coherence tomography angiography (OCTA) was used to evaluate CMvD on choroidal slabs.
  • Visual fields and optical coherence tomography (OCT) were performed to confirm glaucoma severity.

Main Results:

  • Groups had similar visual field mean deviation and peripapillary retinal nerve fiber layer thickness.
  • Prevalence of CMvD was significantly lower in PXG eyes (46.2%) compared to POAG eyes (79.5%), with P=0.002.
  • Multivariate analysis confirmed significantly lower odds of CMvD in PXG eyes (OR: 0.18-0.21, P < 0.01).

Conclusions:

  • The prevalence of CMvD is significantly lower in pseudoexfoliation glaucoma compared to primary open-angle glaucoma.
  • This suggests a potentially different role of vascular changes in the pathogenesis of PXG versus POAG.