Abstract

PurposeMultimodal imaging was used to identify and characterize the cause of hyperpigmentation seen on color fundus images (CFIs) of eyes with intermediate age-related macular degeneration (iAMD).DesignRetrospective review of a prospective study.ParticipantsPatients with iAMD.MethodsColor fundus images with macular hyperpigmentation were compared with same-day images obtained using fundus autofluorescence (FAF), near infrared reflectance (NIR), and swept-source (SS) OCT imaging. Two SS OCT en face slabs were generated: a retinal slab to identify hyperreflective foci within the retina and a slab from beneath the retinal pigment epithelium (RPE; the sub-RPE slab) that was used to detect regions that cause decreased light transmission into the choroid, also known as hypotransmission defects. All images were registered to allow for qualitative comparisons by 2 independent graders.Main Outcome MeasuresComparison between foci of macular hyperpigmentation seen on CFIs with the detection of these regions on FAF, NIR, and SS OCT en face images.ResultsCompared with CFIs, FAF imaging seemed to be the least sensitive method for the detection of hyperpigmentation, whereas NIR and SS OCT imaging reliably detected these hyperpigmented areas. Although NIR imaging detected most of the hyperpigmentation seen in CFIs, SS OCT imaging detected all the areas of hyperpigmentation and anatomically localized these areas by using both en face and B-scan images. En face OCT slabs of the retina and sub-RPE region were registered to the CFIs, and areas of hyperpigmentation were shown to correspond to hyperreflective foci in the retina and regions of thickened RPE seen on OCT B-scans. Although both hyperpigmentation and early atrophic lesions appeared bright on NIR imaging, en face SS OCT imaging was able to distinguish these lesions because hyperpigmentary changes appeared dark and early atrophic lesions appeared bright on the sub-RPE slab.ConclusionsEn face OCT imaging in conjunction with OCT B-scans were able to identify and localize the hyperpigmentation seen in CFIs reliably. This hyperpigmentation was not only associated with intraretinal hyperreflective foci, but also corresponded to areas with a thickened RPE.

Highlights

  • Hyperpigmentation in the macula of eyes with age-related macular degeneration (AMD) has been recognized as a risk factor for disease progression.[1,2,3,4,5] In the 9-step severity scale from the Age-Related Macular Degeneration Disease Study (AREDS),[1] the presence of these pigmentary deposits was recognized as one of several important risk factors for disease progression

  • While near infrared reflectance (NIR) imaging detected most of the hyperpigmentation seen in color fundus images (CFIs), SS-optical coherence tomography (OCT) imaging detected all the areas of hyperpigmentation and anatomically localized these areas by using both en face and B

  • -p ro of the CFIs and areas of hyperpigmentation were shown to correspond to hyper-reflective foci in the retina and regions of thickened retinal pigment epithelium (RPE) seen on OCT B-scans

Read more

Summary

Introduction

Hyperpigmentation in the macula of eyes with age-related macular degeneration (AMD) has been recognized as a risk factor for disease progression.[1,2,3,4,5] In the 9-step severity scale from the Age-Related Macular Degeneration Disease Study (AREDS),[1] the presence of these pigmentary deposits was recognized as one of several important risk factors for disease progression. In the simplified AREDS severity scale,[2] only the presence of drusen and pigmentary changes were needed to assess the overall risk of disease progression. Due to the ability of OCT imaging to provide crosssectional imaging of the macular anatomy in AMD, the Classification of Atrophy

Methods
Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.