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Diagnosis and Progression
Diagnosis and Progression

Diagnostic Hallmarks of AMD Progression to GA

Early AMD: Drusen Development Image courtesy of Dr. Mohammad Rafieetary.
Early AMD: Drusen Development

Drusen are a hallmark of early age-related macular degeneration (AMD), which can be observed by direct examination of CFP or OCT.1,2 Drusen come in various sizes—the larger the drusen, the greater the chance of progression to an advanced form of AMD such as GA.1

Early AMD—marked by white arrows—is associated with multiple small (<63 µm) and a few intermediate (63-124 µm) drusen, or retinal pigment epithelium (RPE) abnormalities.1

Intermediate AMD: Degenerative Changes

Intermediate AMD: Degenerative Changes Image courtesy of Dr. Arshad Khanani.
Intermediate AMD: Degenerative Changes Image courtesy of Dr. Arshad Khanani.

Intermediate AMD is associated with extensive intermediate drusen (63-124 µm) or more
than 1 large drusen (≥125 µm).1 Degenerative changes in the retinal layers may also be observed.1

Images are from separate patients.

Intermediate drusen (white arrows) can be visualized clearly on OCT and CFP.2 Pigmentary changes (wedges) visualized on CFP may precede atrophic changes.1

Advanced AMD (GA): Lesion Enlargement

The progression to GA is characterized by the development of new atrophic lesions, expansion of individual areas, or coalescence of multiple lesions in the retinal layers. GA can be detected using various imaging modalities, such as OCT, which are commonly available in most clinics.1

Advanced AMD (GA): Lesion Enlargement

    Image courtesy of Dr. Mohammad Rafieetary.

Advanced AMD (GA): Lesion Enlargement

   Image courtesy of Dr. Arshad Khanani.

Advanced AMD (GA): Lesion Enlargement

   Image courtesy of Dr. David Lally.

Images are from separate patients.

Atrophic lesions represent a loss of the RPE, overlying photoreceptors, and underlying
choriocapillaris.1 Atrophic regions (white arrows) are represented on CFP, OCT, and FAF.

Noninvasive Imaging to Identify GA Early

While GA progression is highly variable, lesions in the perifoveal macula are typically first to appear, expanding over time to include the fovea.1

Optical Coherence Tomography (OCT)

Optical Coherence Tomography (OCT) Image courtesy of Dr. Arshad Khanani.

Intermediate AMD

Optical Coherence Tomography (OCT) Image courtesy of Dr. Arshad Khanani.

Advanced AMD (GA)

Key Features1

(1) Degeneration of overlying photoreceptors increases reflectivity below Bruch’s membrane

(2) Hyper-reflective foci correspond to attenuation or disruption of the RPE

(3) Atrophy of the RPE 

(4) Area of choroidal hypertransmission

Images are from separate patients.

Colour Fundus Photography (CFP)

Colour Fundus Photography (CFP) Image courtesy of Dr. Arshad Khanani.

Intermediate AMD

Colour Fundus Photography (CFP) Image courtesy of Dr. Mohammad Rafieetary.

Advanced AMD (GA)

Key Features2

(1) Drusen and (2) fundus abnormalities are identifiable as hyperpigmented areas


(3) GA lesion borders are sharply demarcated with increased choroidal vessel visibility (dashed circle)

Images are from separate patients.

Fundus Autofluorescence (FAF)

Fundus Autofluorescence (FAF) Image courtesy of Dr. Arshad Khanani.

Intermediate AMD

Fundus Autofluorescence (FAF) Image courtesy of Dr. David Lally.

Advanced AMD (GA)

Key Features1

(1) Reticular pseudodrusen appearing as multiple, clustered, regularly networked, round areas of low-contrast hypo-autofluorescence may be prognostic of advancing AMD
(2) Abnormal patterns of hyperautofluorescence surrounding atrophic lesions
(3) Areas of hypo-autofluorescence with sharply demarcated borders indicate atrophic lesions

Images are from separate patients.

Monitoring Can Help Predict for Progression

Lesion patterns can be predictive of slower or faster progressing disease.1,3

Monitoring Can Help Predict for Progression
Monitoring Can Help Predict for Progression

Lesion size, location, and focality may be predictive of the rate of lesion progression in GA. GA progression is faster in lesions that are larger, outside of the fovea, or multifocal.1


References:

  1. Fleckenstein M, et al. Ophthalmology. 2018;125(3):369-390.

  2. Monés J, et al. Ophthalmol Retina. 2017;1(6):461-473.

  3. Regillo CD, et al. Clin Ophthalmol. 2024;18:325-335.