TY - JOUR
T1 - Pro-Permeability Factors after Dexamethasone Implant in Retinal Vein Occlusion; The Ozurdex for Retinal Vein Occlusion (ORVO) Study
AU - Campochiaro, Peter A.
AU - Hafiz, Gulnar
AU - Mir, Tahreem A.
AU - Scott, Adrienne W.
AU - Sophie, Raafay
AU - Shah, Syed M.
AU - Ying, Howard S.
AU - Lu, Lili
AU - Chen, Connie
AU - Campbell, J. Peter
AU - Kherani, Saleema
AU - Zimmer-Galler, Ingrid
AU - Wenick, Adam
AU - Han, Ian
AU - Paulus, Yannis
AU - Sodhi, Akrit
AU - Wang, Guohua
AU - Qian, Jiang
N1 - Funding Information:
All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Financial Disclosures: Peter A. Campochiaro: Consultant, Genentech, South San Francisco, California; Regeneron, Tarrytown, New York; Aerpio, Cincinnati, Ohio; Alimera, Atlanta, Georgia; Allegro, San Diego, California; Eleven, Cambridge, Massachusetts; Kala, Cambridge, Massachusetts; Applied Genetic Technologies Corporation, Gainesville, Florida; Ocata Therapeutics, Marlborough, Massachusetts; and AsclepiX, Baltimore, Maryland; Institutional Grants: Allergan, Irvine, California; Genentech, South San Francisco, California; Regeneron, Tarrytown, New York; Aerpio, Cincinnati, Ohio, Abbvie, North Chicago, Illinois; Genzyme, Cambridge, Massachusetts; Oxford Biomedica, Oxford, United Kingdom; Roche, Basel, Switzerland; GlaxoSmithKline, Middlesex, United Kingdom; AscepiX, Baltimore, Maryland, Graybug, Baltimore, Maryland. Howard S. Ying: Institutional Grant, Regeneron, Tarrytown, New York. Adam Wenick: Consultant, Bristol-Myers Squibb, New York, New York; Institutional Grant, Novo Nordisk, Bagsvaerd, Denmark. This study was supported by a grant from Allergan (Irvine, California, USA). The authors would like to acknowledge the Wilmer Biostatistics Core Grant EY01765 . All authors attest that they meet the current ICMJE requirements to qualify as authors.
Publisher Copyright:
© 2015 Elsevier Inc. All rights reserved.
PY - 2015/8/1
Y1 - 2015/8/1
N2 - Purpose To correlate aqueous vasoactive protein changes with macular edema after dexamethasone implant in retinal vein occlusion (RVO). Design Prospective, interventional case series. Methods Twenty-three central RVO (CRVO) and 17 branch RVO (BRVO) subjects with edema despite prior anti-vascular endothelial growth factor (VEGF) treatment had aqueous taps at baseline and 4 and 16 weeks after dexamethasone implant. Best-corrected visual acuity (BCVA) and center subfield thickness were measured every 4 weeks. Aqueous vasoactive protein levels were measured by protein array or enzyme-linked immunosorbent assay. Results Thirty-two vasoactive proteins were detected in aqueous in untreated eyes with macular edema due to RVO. Reduction in excess foveal thickness after dexamethasone implant correlated with reduction in persephin and pentraxin 3 (Pearson correlation coefficients = 0.682 and 0.638, P =.014 and P =.003). Other protein changes differed among RVO patients as edema decreased, but ≥50% of patients showed reductions in hepatocyte growth factor, endocrine gland VEGF, insulin-like growth factor binding proteins, or endostatin by ≥30%. Enzyme-linked immunosorbent assay in 18 eyes (12 CRVO, 6 BRVO) showed baseline levels of hepatocyte growth factor and VEGF of 168.2 ± 20.1 pg/mL and 78.7 ± 10.0 pg/mL, and each was reduced in 12 eyes after dexamethasone implant. Conclusions Dexamethasone implants reduce several pro-permeability proteins providing a multitargeted approach in RVO. No single protein in addition to VEGF can be implicated as a contributor in all patients. Candidates for contribution to chronic edema in subgroups of patients that deserve further study include persephin, hepatocyte growth factor, and endocrine gland VEGF.
AB - Purpose To correlate aqueous vasoactive protein changes with macular edema after dexamethasone implant in retinal vein occlusion (RVO). Design Prospective, interventional case series. Methods Twenty-three central RVO (CRVO) and 17 branch RVO (BRVO) subjects with edema despite prior anti-vascular endothelial growth factor (VEGF) treatment had aqueous taps at baseline and 4 and 16 weeks after dexamethasone implant. Best-corrected visual acuity (BCVA) and center subfield thickness were measured every 4 weeks. Aqueous vasoactive protein levels were measured by protein array or enzyme-linked immunosorbent assay. Results Thirty-two vasoactive proteins were detected in aqueous in untreated eyes with macular edema due to RVO. Reduction in excess foveal thickness after dexamethasone implant correlated with reduction in persephin and pentraxin 3 (Pearson correlation coefficients = 0.682 and 0.638, P =.014 and P =.003). Other protein changes differed among RVO patients as edema decreased, but ≥50% of patients showed reductions in hepatocyte growth factor, endocrine gland VEGF, insulin-like growth factor binding proteins, or endostatin by ≥30%. Enzyme-linked immunosorbent assay in 18 eyes (12 CRVO, 6 BRVO) showed baseline levels of hepatocyte growth factor and VEGF of 168.2 ± 20.1 pg/mL and 78.7 ± 10.0 pg/mL, and each was reduced in 12 eyes after dexamethasone implant. Conclusions Dexamethasone implants reduce several pro-permeability proteins providing a multitargeted approach in RVO. No single protein in addition to VEGF can be implicated as a contributor in all patients. Candidates for contribution to chronic edema in subgroups of patients that deserve further study include persephin, hepatocyte growth factor, and endocrine gland VEGF.
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U2 - 10.1016/j.ajo.2015.04.025
DO - 10.1016/j.ajo.2015.04.025
M3 - Article
C2 - 25908486
AN - SCOPUS:84937513600
SN - 0002-9394
VL - 160
SP - 313-321.e19
JO - American Journal of Ophthalmology
JF - American Journal of Ophthalmology
IS - 2
ER -