A patient with primary open-angle glaucoma (POAG) on latanoprost monotherapy has insufficient IOP control. The treating physician adds brimonidine. What is the mechanism of brimonidine that makes it useful as an add-on therapy in POAG beyond IOP reduction?
- A Alpha-2 adrenergic receptor agonism providing direct neuroprotection ✓
- B Prostaglandin E2 receptor agonism enhancing uveoscleral outflow
- C Carbonic anhydrase inhibition reducing aqueous humor production
- D Beta-1 receptor blockade reducing aqueous secretion from ciliary epithelium
Explanation
Brimonidine is a selective alpha-2 adrenergic agonist. Beyond lowering IOP by reducing aqueous production and increasing uveoscleral outflow, it has demonstrated neuroprotective properties in animal models by reducing glutamate excitotoxicity and upregulating BDNF (brain-derived neurotrophic factor), protecting retinal ganglion cells independently of IOP reduction. This is a clinically significant property that distinguishes it from beta-blockers and CAIs.
Reference: Khurana Comprehensive Ophthalmology, 7th ed.
High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP
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