What Is Age-Related Macular Degeneration?
Age-related macular degeneration (AMD) is a degenerative disease affecting the macula -- the central area of the retina responsible for sharp, detailed vision. It is the leading cause of severe, irreversible central vision loss in people over age 50 in developed countries. AMD does not affect peripheral vision, so patients retain mobility and independence but often cannot read, drive, or recognize faces.
Dry AMD (Non-Exudative)
Dry AMD accounts for approximately 85-90% of all AMD cases. It is characterized by:
- Drusen -- yellowish deposits of debris beneath the retinal pigment epithelium (RPE). Small hard drusen are normal aging; large soft drusen are a risk factor for progression.
- RPE changes -- pigment irregularities, hyper- and hypopigmentation
- Geographic atrophy (GA) -- advanced dry AMD where large areas of RPE and photoreceptors are lost, causing a scotoma (blind spot)
Dry AMD progresses slowly over years. There is no treatment that reverses dry AMD, but nutritional supplementation (AREDS2 formula) can slow progression in intermediate-to-advanced AMD.
💡 Clinical Tip: The AREDS2 formula (lutein/zeaxanthin, vitamin C, vitamin E, zinc, copper) has been shown in clinical trials to reduce the risk of advanced AMD in patients with intermediate AMD or advanced AMD in one eye. The CPOA may educate patients about supplementation and monitor for conversion to wet AMD.
Wet AMD (Exudative / Neovascular)
Wet AMD accounts for only 10-15% of AMD cases but causes about 90% of severe vision loss from AMD. It involves:
- Growth of abnormal new blood vessels from the choroid beneath the RPE and retina (choroidal neovascularization, CNV)
- These vessels are fragile and leak fluid and blood into the retinal layers (subretinal or intraretinal fluid)
- Symptoms: rapid distortion or blurring of central vision, metamorphopsia (straight lines appear wavy), central scotoma
Wet AMD can progress rapidly (days to weeks) and requires urgent treatment.
Risk Factors
- Advanced age (greatest risk factor)
- Smoking (doubles the risk)
- Family history / genetic variants (CFH and ARMS2 genes)
- Caucasian race
- Cardiovascular disease, obesity, hypertension
- UV exposure
Diagnosis and Monitoring
The CPOA plays a key role in AMD monitoring through:
- Amsler grid testing: Patient fixates on the central dot and reports any distortion, blurring, or missing areas in the grid. The standard Amsler grid detects metamorphopsia and scotomas. Changes from the patient's baseline may indicate wet AMD conversion.
- OCT imaging: The primary tool for detecting and monitoring wet AMD. OCT shows drusen, fluid under or within the retina (subretinal fluid, intraretinal fluid), CNV, and retinal thickness.
- Fundus photography: Documents drusen distribution and geographic atrophy extent.
- Fluorescein angiography (FA) or OCT-A: Identifies CNV and guides treatment decisions.
⚠️ Common Mistake: If a patient with dry AMD reports sudden new distortion or vision change, do not schedule a routine follow-up -- alert the physician immediately. Conversion to wet AMD requires urgent treatment within days to preserve vision.
Treatment
Dry AMD
- AREDS2 nutritional supplements for intermediate/advanced AMD
- Lifestyle modification (smoking cessation, diet, exercise)
- Low vision rehabilitation for geographic atrophy
Wet AMD
Anti-VEGF intravitreal injections are the standard of care. VEGF (vascular endothelial growth factor) drives CNV formation. Anti-VEGF agents suppress this:
- Ranibizumab (Lucentis)
- Bevacizumab (Avastin, off-label)
- Aflibercept (Eylea)
- Faricimab (Vabysmo)
Injections are given monthly initially, then spaced based on treatment response (treat-and-extend or PRN protocols). The CPOA prepares the patient, instills anesthetic drops, and ensures sterile preparation.
Key Takeaways
- AMD is the leading cause of central vision loss in adults over 50; peripheral vision is preserved
- Dry AMD (90%): drusen and RPE changes; geographic atrophy in advanced disease; AREDS2 slows progression
- Wet AMD (10%): CNV causes rapid vision loss from fluid/blood; requires urgent anti-VEGF injection
- Amsler grid at home monitors for metamorphopsia; changes require urgent physician notification
- OCT is the primary imaging tool for monitoring AMD
- Smoking cessation is the most important modifiable risk factor