TY - JOUR
T1 - Baseline Fourier-Domain Optical Coherence Tomography Structural Risk Factors for Visual Field Progression in the Advanced Imaging for Glaucoma Study
AU - Zhang, Xinbo
AU - Dastiridou, Anna
AU - Francis, Brian A.
AU - Tan, Ou
AU - Varma, Rohit
AU - Greenfield, David S.
AU - Schuman, Joel S.
AU - Sehi, Mitra
AU - Chopra, Vikas
AU - Huang, David
N1 - Funding Information:
Funding/Support: Supported by NIH grants R01 EY013516 , R01 EY023285 (Bethesda, Maryland). Financial disclosures: David Huang and Ou Tan have a significant financial interest in Carl Zeiss Meditec, Inc (Dublin, California). Oregon Health & Science University (OHSU), David Huang, and Ou Tan have a significant financial interest in Optovue, Inc (Fremont, California), a company that may have a commercial interest in the results of this research and technology. These potential conflicts of interest have been reviewed and managed by OHSU. David Huang and Joel S. Schuman receive royalties for an optical coherence tomography patent owned and licensed by the Massachusetts Institute of Technology (Cambridge, Massachusetts) and Massachusetts Eye & Ear Infirmary to Carl Zeiss Meditec, Inc. David S. Greenfield receives research support from Optovue, Inc, Carl Zeiss Meditec, Inc, and Heidelberg Engineering (Carlsbad, California). Rohit Varma has received research grants, honoraria, and/or travel support from Carl Zeiss Meditec, Inc, Heidelberg Engineering, and Optovue, Inc. Vikas Chopra is a consultant to Allergan, Inc. The following authors have no financial interest to disclose: Xinbo Zhang, Anna Dastiridou, Brian A. Francis, and Mitra Sehi. All authors attest that they meet the current ICMJE criteria for authorship.
Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/12/1
Y1 - 2016/12/1
N2 - Purpose To identify baseline structural parameters that predict the progression of visual field (VF) loss in patients with open-angle glaucoma. Design Multicenter cohort study. Methods Participants from the Advanced Imaging for Glaucoma (AIG) study were enrolled and followed up. VF progression is defined as either a confirmed progression event on Humphrey Progression Analysis or a significant (P < .05) negative slope for VF index (VFI). Fourier-domain optical coherence tomography (FDOCT) was used to measure optic disc, peripapillary retinal nerve fiber layer (NFL), and macular ganglion cell complex (GCC) thickness parameters. Results A total of 277 eyes of 188 participants were followed up for 3.7 ± 2.1 years. VF progression was observed in 83 eyes (30%). Several baseline NFL and GCC parameters, but not disc parameters, were found to be significant predictors of progression on univariate Cox regression analysis. The most accurate single predictors were the GCC focal loss volume (FLV), followed closely by NFL-FLV. An abnormal GCC-FLV at baseline increased risk of progression by a hazard ratio of 3.1. Multivariate Cox analysis showed that combining age and central corneal thickness with GCC-FLV in a composite index called “Glaucoma Composite Progression Index” (GCPI) further improved the accuracy of progression prediction. GCC-FLV and GCPI were both found to be significantly correlated with the annual rate of change in VFI. Conclusion Focal GCC and NFL loss as measured by FDOCT are the strongest predictors for VF progression among the measurements considered. Older age and thinner central corneal thickness can enhance the predictive power using the composite risk model.
AB - Purpose To identify baseline structural parameters that predict the progression of visual field (VF) loss in patients with open-angle glaucoma. Design Multicenter cohort study. Methods Participants from the Advanced Imaging for Glaucoma (AIG) study were enrolled and followed up. VF progression is defined as either a confirmed progression event on Humphrey Progression Analysis or a significant (P < .05) negative slope for VF index (VFI). Fourier-domain optical coherence tomography (FDOCT) was used to measure optic disc, peripapillary retinal nerve fiber layer (NFL), and macular ganglion cell complex (GCC) thickness parameters. Results A total of 277 eyes of 188 participants were followed up for 3.7 ± 2.1 years. VF progression was observed in 83 eyes (30%). Several baseline NFL and GCC parameters, but not disc parameters, were found to be significant predictors of progression on univariate Cox regression analysis. The most accurate single predictors were the GCC focal loss volume (FLV), followed closely by NFL-FLV. An abnormal GCC-FLV at baseline increased risk of progression by a hazard ratio of 3.1. Multivariate Cox analysis showed that combining age and central corneal thickness with GCC-FLV in a composite index called “Glaucoma Composite Progression Index” (GCPI) further improved the accuracy of progression prediction. GCC-FLV and GCPI were both found to be significantly correlated with the annual rate of change in VFI. Conclusion Focal GCC and NFL loss as measured by FDOCT are the strongest predictors for VF progression among the measurements considered. Older age and thinner central corneal thickness can enhance the predictive power using the composite risk model.
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U2 - 10.1016/j.ajo.2016.09.015
DO - 10.1016/j.ajo.2016.09.015
M3 - Article
C2 - 27651070
AN - SCOPUS:84995906410
SN - 0002-9394
VL - 172
SP - 94
EP - 103
JO - American journal of ophthalmology
JF - American journal of ophthalmology
ER -