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Updated: Feb 5, 2026

Multifocal Electroretinograms
Published on: December 4, 2011
[Pattern electroretinogram and macular perfusion in glaucoma]
N I Kurysheva1, E V Maslova1, A V Trubilina1
1Consultative-diagnostic Department of Ophthalmology Center of the Federal Medical and Biological Agency, Burnasyan Federal Medical Biophysical Center of FMBA, Department of Ophthalmology at Institute of Advanced Training of FMBA, 15 Gamalei St., Moscow, Russian Federation, 123098.
Primary Open-Angle Glaucoma (POAG) is linked to reduced macular microcirculation and pattern electroretinogram (PERG) function in early stages. These circulatory and functional changes correlate in early POAG, highlighting potential diagnostic markers.
Area of Science:
- Ophthalmology
- Neuroscience
- Medical Imaging
Background:
- Primary Open-Angle Glaucoma (POAG) is a leading cause of irreversible blindness.
- Early detection and understanding of POAG pathophysiology are crucial for effective management.
- Microcirculatory and functional changes in the macula may precede overt optic nerve damage.
Purpose of the Study:
- To investigate microcirculatory and functional alterations within the macula of patients diagnosed with POAG.
- To explore the relationship between macular microcirculation, retinal nerve fiber layer thickness, and electrophysiological responses in POAG.
Main Methods:
- Employed Optical Coherence Tomography Angiography (OCT-A) to measure vessel density (wiVDRetina) in the foveal and parafoveal regions.
- Assessed macular thickness and ganglion cell complex (GCC) parameters using SD-OCT.
- Evaluated retrobulbar blood flow via Color Doppler Imaging (CDI) and retinal function using pattern electroretinogram (PERG).
Main Results:
- A significant decrease in t-PERG P50 amplitude was observed in early (2.8±1.6 µV) and advanced (2.3±1.5 µV) POAG compared to healthy controls (6.1±1.3 µV).
- Relative vessel density in the macular capillary bed was reduced in early (45.9±5.0%) and advanced (41.8±5.0%) POAG versus controls (51.3±3.0%).
- Correlations were found between OCT-A, CDI parameters, and morphological/functional measures in normal and early glaucomatous eyes.
Conclusions:
- Early-stage POAG is characterized by diminished macular microcirculation and impaired PERG function.
- Circulatory and functional deficits show significant correlations in the early stages of POAG, suggesting a common pathophysiological pathway.
- These findings underscore the potential of OCT-A and PERG as sensitive biomarkers for early POAG detection and monitoring.
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