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Advanced forms of age‐related macular degeneration (AMD), characterised by atrophic and neovascular changes, are a leading cause of vision loss in the elderly population worldwide. Prior to the development of advanced AMD, a myriad of risk factors from the early and intermediate stages of AMD have been published in the scientific literature over the last years. The ability to precisely recognise structural and anatomical changes in the ageing macula, altogether with the understanding of the individual risk implications of each one of them is key for an accurate and personalised diagnostic assessment. The present review aims to summarise updated evidence of the relative risk conferred by diverse macular signs, commonly seen on optical coherence tomography, in terms of progression to geographic atrophy or macular neovascularization. This information may also serve as a basis for tailored follow‐up monitoring visits. [ABSTRACT FROM AUTHOR]

Purpose: To evaluate the structural changes in the choroid by binarization method in intermediate age-related macular degeneration (AMD) and to examine the correlation between parafoveal external retinal and internal retinal thinning. Material method: Enhanced depth imaging optical coherence tomography images of 50 patients diagnosed with intermediary AMD and age matched 30 healthy subjects were analyzed retrospectively. Results: Compared to the control group in the AMD group; the central choroidal thickness, choroidal area, stroma area and lumen area were found to be significantly reduced. There was no significant difference in the choroidal vascular index (CVI) compared to the control group in intermediate AMD. In the AMD group, significant thinning was found in the parafoveal inner and outer retinal thickness compared to the control group. When the correlation between parafoveal inner and outer retinal thicknesses and choroidal parameters were evaluated individually in the AMD group, no significant correlation was found. Discussion: In non-neovascular intermediate AMD cases, there was a decrease in inner and outer retinal thicknesses, central choroidal thickness, lumen and stroma area of the choroid, however, the decrease in CVI was not prominent. No correlation was found to support the hypothesis that inner retinal thinning develops due to choroidal and/or outer retinal changes. [ABSTRACT FROM AUTHOR]

Purpose: To investigate the value of visual acuity and patient-perceived visual function test when subretinal drusenoid deposits (SDD) are incorporated into the classification of age-related macular degeneration (AMD). A total of 50 participants were recruited into the study in these groups: healthy ageing (n = 11), intermediate AMD (iAMD) with no SDD (n = 17), iAMD with SDD (n = 11) and non-foveal atrophic AMD (n = 11) confirmed by two retinal imaging modalities. Best-corrected visual acuity (BCVA) and low luminance visual acuity (LLVA) were measured and low luminance deficit (LLD) was calculated. Participants were also interviewed with the low luminance questionnaire (LLQ). Linear regression was used to assess function–function relations. Compared with healthy participants, BCVA and LLVA scores were significantly reduced in the atrophic AMD group (p < 0.0001 and p = 0.00016, respectively) and in patients with SDD (p = 0.028 and p = 0.045, respectively). Participants with atrophy also had reduced BCVA (p = 0.001) and LLVA (p = 0.009) compared with the iAMD no SDD group. However, there were no differences in visual function tests between healthy aging and iAMD without SDD and between iAMD with SDD and atrophic AMD groups. The LLD score did not differ between groups. BCVA and LLVA correlated well. The LLQ did not correlate with visual function tests. This study shows that LLD is not a marker of disease severity as assessed clinically. Although LLQ is a good marker for disease severity using the current AMD classification, it does not differentiate between eyes with and without SDD. Eyes with non-macular geographic atrophy and SDD had lower function than eyes with no SDD and healthy controls. [ABSTRACT FROM AUTHOR]