Onset of Retinal Pigment Epithelium Atrophy Subsequent to Anti-VEGF Therapy in Patients with Neovascular Age-Related Macular Degeneration

Autor: Lebriz Altay, Manuel M. Hermann, Philip Enders, Sascha Fauser, Philipp S. Muether, Vasilena Sitnilska
Rok vydání: 2018
Předmět:
Male
Vascular Endothelial Growth Factor A
Time Factors
Angiogenesis Inhibitors
Retinal Pigment Epithelium
01 natural sciences
chemistry.chemical_compound
0302 clinical medicine
Risk Factors
Prospective Studies
Fluorescein Angiography
Aged
80 and over

General Medicine
Middle Aged
Sensory Systems
Vascular endothelial growth factor
Bevacizumab
medicine.anatomical_structure
Treatment Outcome
Intravitreal Injections
Female
Tomography
Optical Coherence

medicine.medical_specialty
Fundus Oculi
Recombinant Fusion Proteins
03 medical and health sciences
Atrophy
Ophthalmology
Ranibizumab
Post-hoc analysis
medicine
Humans
0101 mathematics
Risk factor
Aged
Retinal pigment epithelium
Dose-Response Relationship
Drug

business.industry
010102 general mathematics
Odds ratio
Macular degeneration
medicine.disease
eye diseases
Receptors
Vascular Endothelial Growth Factor

chemistry
Concomitant
030221 ophthalmology & optometry
Wet Macular Degeneration
sense organs
business
Follow-Up Studies
Zdroj: Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde. 241(3)
ISSN: 1423-0267
Popis: Purpose: The aim of this study was to evaluate risk factors for the development of retinal pigment epithelium (RPE) atrophy in patients with neovascular age-related macular degeneration (nAMD). Procedures: This post hoc analysis of the prospective RESPONSE study includes 52 therapy-naive nAMD patients without baseline RPE atrophy, who were treated with ≥9 anti-vascular endothelial growth factor (VEGF) injections for ≥3 years. RPE atrophy was assessed via multimodal imaging. Baseline aqueous VEGF and serum complement levels (C3d/C3) were measured. Risk factors for atrophy development were evaluated via logistic regression analysis. Results: Atrophy onset was significantly associated with the duration of nAMD (mean 5.34 years; odds ratio = 1.83, p = 0.012). Anti-VEGF injection number, age, C3d/C3 ratio, baseline intraocular VEGF, or delay to the first treatment had no influence on RPE atrophy. Conclusions: The duration of treatment-requiring nAMD was identified as primary risk factor for the onset of concomitant RPE atrophy after commencing therapy. Targeting concomitant atrophy in nAMD patients might improve the long-term prognosis of the disease.
Databáze: OpenAIRE