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In Vivo Multimodal Imaging and Analysis of Mouse Laser-Induced Choroidal Neovascularization Model
Published on: January 21, 2018
Riesgo a Largo Plazo de Mortalidad y Morbilidad Sistémica en el Glaucoma Neovascular: Un Estudio de Cohorte
Ryan Margolis1, Pranav Vasu2, Syril K Dorairaj3
1Department of Medicine, Renaissance School of Medicine at Stony Brook University, New York, United States.
Purpose:
To evaluate long-term systemic risks associated with neovascular glaucoma (NVG) using a large, real-world dataset from the TriNetX Research Network.
Design:
Retrospective Cohort Study SUBJECTS: Adults > 40 years old with central retinal vein occlusion (CRVO) or proliferative diabetic retinopathy (PDR) were compared based on whether they did or did not subsequently develop NVG.
Methods:
Patients were propensity score matched 1:1 based on demographics and comorbidities. Outcomes were assessed at 1, 5, and 10 years using hazard ratios (HRs) with 95% confidence intervals (CIs). Subgroup analysis compared outcomes in NVG+PDR versus CRVO+NVG. NVG patients were also compared to a cataract control cohort.
Main Outcome Measures:
Risk of all-cause mortality, stroke, myocardial infarction (MI), end-stage renal disease (ESRD), and deep-vein thrombosis (DVT).
Results:
Patients with PDR who developed NVG had a higher long-term risk than PDR alone, including elevated 10-year mortality (HR 1.34, 95% CI 1.14-1.57) and ESRD (HR 1.43, 95% CI 1.23-1.67). Among patients with CRVO, development of NVG increased 10-year mortality (HR 1.61, 95% CI 1.17-2.20) and stroke (HR 1.86, 95% CI 1.19-2.90), while MI and ESRD were not significantly different. DVT risk was not significantly different. Subgroup comparison showed that PDR-NVG had higher 10-year risk of mortality (HR 1.56, 95% CI 1.17-2.07), MI (HR 1.94, 95% CI 1.13-3.32), and ESRD (HR 4.04, 95% CI 2.43-6.73) compared with CRVO-NVG. Compared with cataract control at 10 years, NVG was associated with higher risks of mortality (HR 2.66, 95% CI 2.40-2.94), stroke (HR 2.17, 95% CI 1.85-2.54), MI (HR 1.89, 95% CI 1.60-2.23), and ESRD (HR 3.34, 95% CI 2.89-3.88).
Conclusions:
NVG itself appears to add systemic risk beyond underlying PDR or CRVO, suggesting that the onset of NVG may represent a critical breakpoint in the spectrum of systemic vascular disease. Our results highlight the importance of coordinated ophthalmic and multispecialty care at the time of diagnosis.
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