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Retinal pigment epithelial characteristics in eyes with neovascular age-related macular degeneration

Long-term retinal changes under anti-vascular endothelial growth factor treatment

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Summary

Purpose

The aim of this study was to assess retinal pigment epithelial (RPE) and retinal structural changes in eyes with neovascular age-related macular degeneration (AMD) treated with anti-vascular endothelial growth factor (anti-VEGF) during long-term follow-up and to evaluate morphological markers potentially influencing prognosis.

Methods

A total of 18 eyes of 18 patients with neovascular AMD were examined subsequent to completion of the Avastin Versus Lucentis in Age Related Macular Degeneration (MANTA) study following a mean period of 84 months (range 69–93 months). After receiving a loading dose of 3 intravitreal anti-VEGF injections subsequent to baseline of the MANTA study, patients were treated as needed (pro re nata, PRN). Functional and morphological changes were assessed, the latter using spectral domain optical coherence tomography (SD-OCT).

Results

Retinal/RPE atrophy generally increased significantly during follow-up compared to baseline (fibrosis 28% vs. 89%, p = 0.0001, geographic atrophy, GA 0% vs. 67%, p = 0.0002, RPE porosity 61% vs. 100%, p = 0.009) whereas regenerative alterations tendentially increased until 3 months and then subsequently declined until the last visit (RPE thickening 28% vs. 11%, p = 0.22 and intraretinal hyperreflective foci 89% vs. 78%, p = 0.39).

Conclusion

Atrophic alterations of the retina and RPE are progressive and may partly be induced by anti-VEGF. Morphological findings may aid in the identification of prognostic markers in the progression of neovascular AMD. This could lead to a more targeted education of affected patients.

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References

  1. Klein R, Klein BE, Linton KL. Prevalence of age-related maculopathy. The beaver dam eye study. Ophthalmology. 1992;99(6):933–43.

    Article  CAS  Google Scholar 

  2. Friedman DS, O’Colmain BJ, Munoz B. Prevalence of age-related macular degeneration in the United States. Arch Ophthalmol. 2004;122(4):564–72.

    Article  Google Scholar 

  3. Chakravarthy U, Harding SP, Rogers CA, et al. Ranibizumab versus bevacizumab to treat neovascular age-related macular degeneration: one-year findings from the IVAN randomized trial. Ophthalmology. 2012;119:1399–411.

    Article  Google Scholar 

  4. Tufail A, Patel PJ, Egan C, Hykin P, et al. Bevacizumab for neovascular age related macular degeneration (ABC Trial): multicenter randomised double masked study. BMJ. 2010; https://doi.org/10.1136/bmj.c2459.

    Article  PubMed  Google Scholar 

  5. Busbee BG, Ho AC, Brown DM, HARBOR Study Group.. Twelve-month efficacy and safety of 0.5 mg or 2.0 mg ranibizumab in patients with subfoveal neovascular age-related macular degeneration. Ophthalmology. 2013;120(5):1046–56.

    Article  Google Scholar 

  6. Chang TS, Bressler NM, Fine JT, MARINA Study Group, et al. Improved vision-related function after ranibizumab treatment of neovascular age-related macular degeneration: results of a randomized clinical trial. Arch Ophthalmol. 2007;125(11):1460–9.

    Article  CAS  Google Scholar 

  7. Fung AE, Lalwani GA, Rosenfeld PJ, Dubovy SR, et al. An optical coherence tomography-guided, variable dosing regimen with intravitreal ranibizumab (lucentis) for neovascular age-related macular degeneration. Am J Ophthalmol. 2007;143:566–83.

    Article  CAS  Google Scholar 

  8. CATT Research Group, Martin DF, Maguire MG, et al. Ranibizumab and bevacizumab for neovascular age-related macular degeneration. N Engl J Med. 2011;364:1897–908.

    Article  Google Scholar 

  9. IVAN Study Investigators, Chakravarthy U, Harding SP, et al. Ranibizumab versus bevacizumab to treat neovascular age-related macular degeneration: one-year findings from the IVAN randomized trial. Ophthalmology. 2012;119:1399–411.

    Article  Google Scholar 

  10. Regatieri CV, Branchini L, Fujimoto JG, et al. Choroidal imaging using spectral-domain optical coherence tomography. Retina. 2012;32:865–76.

    Article  Google Scholar 

  11. Regatieri CV, Branchini L, Duker JS. The role of spectral-domain OCT in the diagnosis and management of neovascular age-related macular degeneration. Ophthalmic Surg Lasers Imaging. 2011;42:S56–66.

    Article  Google Scholar 

  12. Kumar N, Mrejen S, Fung AT, et al. Retinal pigment epithelial cell loss assessed by fundus autofluorescence imaging in neovascular age-related macular degeneration. Ophthalmology. 2013;120:334–41.

    Article  Google Scholar 

  13. Grunwald JE, Daniel E, Huang J. Risk of geographic atrophy in the comparison of age-related macular degeneration treatments trials. Ophthalmology. 2014;121:150–61.

    Article  Google Scholar 

  14. Schütze C, Wedl M, Baumann B, et al. Progression of retinal pigment epithelial atrophy in antiangiogenic therapy of neovascular age-related macular degeneration. Am J Ophthalmol. 2015;159:1100–14.

    Article  Google Scholar 

  15. Grunwald JE, Pistilli M, Ying GS, et al. Comparison of age-related macular degeneration treatments trials research group. Incidence and growth of geographic atrophy during 5 years of comparison of Age-related macular degeneration treatments trials. Ophthalmology. 2017;124:97–104.

    Article  Google Scholar 

  16. Krebs I, Schmetterer L, Boltz A, MANTA Research Group, et al. A randomised double-masked trial comparing the visual outcome after treatment with ranibizumab or bevacizumab in patients with neovascular age-related macular degeneration. Br J Ophthalmol. 2013;97:266–71.

    Article  Google Scholar 

  17. Schmitz-Valckenberg S, Fleckenstein M, Göbel AP, et al. Optical coherence tomography and autofluorescence findings in areas with geographic atrophy due to age-related macular degeneration. Invest Ophthalmol Vis Sci. 2011;52:1–6.

    Article  Google Scholar 

  18. Bird AC, Phillips RL, Hageman GS. Geographic atrophy: a histopathological assessment. JAMA Ophthalmol. 2014;132:338–45.

    Article  Google Scholar 

  19. Jaffe GJ, Martin DF, Toth CA, et al. Comparison of age-related macular degeneration treatments trials research group. Macular morphology and visual acuity in the comparison of age-related macular degeneration treatments trials. Ophthalmology. 2013;120:1860–70.

    Article  Google Scholar 

  20. Thavikulwat AT, Jacobs-El N, Kim JS, Agrón E, et al. Evolution of geographic atrophy in participants treated with ranibizumab for neovascular age-related macular degeneration. Ophthalmol Retina. 2017;1:34–41.

    Article  Google Scholar 

  21. Tsuboi S, Pederson JE, Toris CB. Functional recovery of retinal pigment epithelial damage in experimental retinal detachment. Invest Ophthalmol Vis Sci. 1987;28(11):1788–94.

    CAS  PubMed  Google Scholar 

  22. Ho J, Witkin AJ, Liu J, et al. Documentation of intraretinal retinal pigment epithelium migration via high-speed ultrahigh-resolution optical coherence tomography. Ophthalmology. 2011;118:687–93.

    Article  Google Scholar 

  23. Lee JY, Folgar FA, Maguire MG. Outer retinal tubulation in the comparison of age-related macular degeneration treatments trials (CATT). Ophthalmology. 2014;121:2423–31.

    Article  Google Scholar 

  24. Zweifel SA, Engelbert M, Laud K, et al. Outer retinal tubulation a novel optical coherence tomography finding. Arch Ophthalmol. 2009;127:1596–602.

    Article  Google Scholar 

  25. Curcio CA, Zanzottera EC, Ach T, et al. Activated retinal pigment epithelium, an optical coherence tomography biomarker for progression in age-related macular degeneration. Invest Ophthalmol Vis Sci. 2017;58(6):211–26.

    Google Scholar 

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Funding

The research did not receive any funding. It was performed as part of the employment of the authors. All authors are employed at Hietzing Hospital, department of ophthalmology, and further at the Karl Landsteiner Institute for Process Optimization and Quality Management in Cataract Surgery.

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Correspondence to Pia-Veronika Vécsei-Marlovits MD, MBA.

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Conflict of interest

C. Ebner, C. Wernigg, C. Schütze, B. Weingessel, and P.-V. Vécsei-Marlovits declare that they have no financial interests in context with this study. Each of the authors warrants that there are no commercial associations that might pose a conflict of interest in context with the submitted article.

Ethical standards

Signed informed consent was obtained from each patient prior to enrolment. The local ethics committee approved the study protocol that followed the ethical tenets of the Declaration of Helsinki.

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Registration site: ClinicalTrials. Registration number: NCT03679156

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Ebner, C., Wernigg, C., Schütze, C. et al. Retinal pigment epithelial characteristics in eyes with neovascular age-related macular degeneration. Wien Klin Wochenschr 133, 123–130 (2021). https://doi.org/10.1007/s00508-020-01718-6

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  • DOI: https://doi.org/10.1007/s00508-020-01718-6

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