Neuroinflammation in Radiation Maculopathy: A Pathophysiologic and Imaging Perspective.
Giulia Midena1, Raffaele Parrozzani2, Marisa Bruno1
1IRCCS-Fondazione Bietti, 00198 Rome, Italy.
Cancers
|August 14, 2025
Summary
Radiation maculopathy (RM) is now understood to be driven by neuroinflammation, not just vascular issues. Neuroinflammatory hyperreflective foci (I-HRF) detected by OCT are early biomarkers for preclinical diagnosis and treatment.
Area of Science:
- Ophthalmology
- Neuroscience
- Radiology
Background:
- Radiation maculopathy (RM) is a severe complication of ocular radiotherapy.
- Emerging evidence highlights neuroinflammation, involving microglial activation and cytokine dysregulation, as central to RM pathogenesis.
- Hyperreflective retinal foci of neuroinflammatory origin (I-HRF) are critical early biomarkers.
Purpose of the Study:
- To review the pathophysiology of neuroinflammation in RM.
- To explore associated imaging parameters, particularly I-HRF.
- To synthesize experimental and clinical findings on RM biomarkers.
Main Methods:
- Literature review of experimental and clinical studies.
- Synthesis of data on neuroinflammation in RM.
- Focus on optical coherence tomography (OCT) for imaging biomarkers.
Main Results:
- I-HRF are significant early indicators of neuroinflammation in RM.
- OCT facilitates the identification and quantification of I-HRF.
- These biomarkers correlate with microglial activation and cytokine changes.
Conclusions:
- RM pathophysiology is shifting from a vascular to a neuroinflammatory paradigm.
- I-HRF serve as crucial early biomarkers for RM.
- I-HRF enable potential preclinical diagnosis and therapeutic strategies for RM.
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