TY - JOUR
T1 - Predictive Factors for the Rate of Visual Field Progression in the Advanced Imaging for Glaucoma Study
AU - Advanced Imaging for Glaucoma Study Group
AU - Zhang, Xinbo
AU - Parrish, Richard K.
AU - Greenfield, David S.
AU - Francis, Brian A.
AU - Varma, Rohit
AU - Schuman, Joel S.
AU - Tan, Ou
AU - Huang, David
N1 - Funding Information:
Funding/Support: Supported by US National Institutes of Health grants R01 EY013516 and R01 EY023285, Bethesda, Maryland. Financial Disclosures: Dr. Huang and Dr. Tan have financial interests in Optovue, Inc. Dr. Greenfield receives research support from Optovue,Inc., Carl Zeiss Meditec, Inc. and Heidelberg Engineering. Dr. Varma has received research grants, honoraria, and travel support from Carl Zeiss Meditec, Inc. Heidelberg Engineering, and Optovue,Inc. Dr. Zhang and Dr. Francis have no financial disclosures. All authors attest that they meet the current ICMJE criteria for authorship.
Funding Information:
Funding/Support: Supported by US National Institutes of Health grants R01 EY013516 and R01 EY023285 , Bethesda, Maryland. Financial Disclosures: Dr. Huang and Dr. Tan have financial interests in Optovue, Inc. Dr. Greenfield receives research support from Optovue,Inc. , Carl Zeiss Meditec , Inc., and Heidelberg Engineering . Dr. Varma has received research grants, honoraria, and travel support from Carl Zeiss Meditec , Inc., Heidelberg Engineering , and Optovue,Inc . Dr. Zhang and Dr. Francis have no financial disclosures. All authors attest that they meet the current ICMJE criteria for authorship.
Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2019/6
Y1 - 2019/6
N2 - Purpose: To investigate predictive factors associated with the rate of visual field (VF) loss in open-angle glaucoma. Design: Prospective multicenter cohort study. Methods: Perimetric glaucoma patients of the Advanced Imaging for Glaucoma study were selected for analysis if they had 9 completed visits. Confirmed rapid significant progression (CRSP) of VF was defined as a significant (P < 0.05) negative VF index (VFI) slope of −1%/year or a mean deviation slope of −0.5 dB/year, confirmed at 2 consecutive follow-up visits. Slow progression was defined as VFI slope greater than −0.5%/year or a mean deviation slope of −0.25 dB/year. Fourier-domain optical coherence tomography (FD-OCT) measured optic disc, peripapillary retinal nerve fiber layer (NFL), and macular ganglion cell complex (GCC) thicknesses. Logistic regression was used to identify baseline predictors for CRSP and slow progression. Linear regression was used to identify baseline predictors for the VFI and mean deviation slope. Results: Eyes (n = 150) of 103 participants were included. Slow progression was observed in 80 eyes (53.3%) and CRSP in 23 eyes (15.3%). Larger NFL and GCC baseline focal loss volume (FLV), thinner central corneal thickness, and lower VFI were significant (P < 0.05) baseline predictors of more rapid progression on univariate analysis. The predictor with the highest odds ratio (OR) was NFL-FLV, which was also the most significant non-VF predictor in the multivariate analysis. Eyes with NFL-FLV >8.5% had an OR of 2.67 for CRSP and 0.42 for slow progression. Disc hemorrhage during the follow-up was also important, with an OR of 2.61 for CRSP and 0.23 for slow progression for each occurrence. Conclusions: Focal loss measured by FD-OCT or VF along with CCT are strong baseline predictors for the rate of glaucoma progression.
AB - Purpose: To investigate predictive factors associated with the rate of visual field (VF) loss in open-angle glaucoma. Design: Prospective multicenter cohort study. Methods: Perimetric glaucoma patients of the Advanced Imaging for Glaucoma study were selected for analysis if they had 9 completed visits. Confirmed rapid significant progression (CRSP) of VF was defined as a significant (P < 0.05) negative VF index (VFI) slope of −1%/year or a mean deviation slope of −0.5 dB/year, confirmed at 2 consecutive follow-up visits. Slow progression was defined as VFI slope greater than −0.5%/year or a mean deviation slope of −0.25 dB/year. Fourier-domain optical coherence tomography (FD-OCT) measured optic disc, peripapillary retinal nerve fiber layer (NFL), and macular ganglion cell complex (GCC) thicknesses. Logistic regression was used to identify baseline predictors for CRSP and slow progression. Linear regression was used to identify baseline predictors for the VFI and mean deviation slope. Results: Eyes (n = 150) of 103 participants were included. Slow progression was observed in 80 eyes (53.3%) and CRSP in 23 eyes (15.3%). Larger NFL and GCC baseline focal loss volume (FLV), thinner central corneal thickness, and lower VFI were significant (P < 0.05) baseline predictors of more rapid progression on univariate analysis. The predictor with the highest odds ratio (OR) was NFL-FLV, which was also the most significant non-VF predictor in the multivariate analysis. Eyes with NFL-FLV >8.5% had an OR of 2.67 for CRSP and 0.42 for slow progression. Disc hemorrhage during the follow-up was also important, with an OR of 2.61 for CRSP and 0.23 for slow progression for each occurrence. Conclusions: Focal loss measured by FD-OCT or VF along with CCT are strong baseline predictors for the rate of glaucoma progression.
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U2 - 10.1016/j.ajo.2019.02.015
DO - 10.1016/j.ajo.2019.02.015
M3 - Article
C2 - 30794787
AN - SCOPUS:85064587542
SN - 0002-9394
VL - 202
SP - 62
EP - 71
JO - American Journal of Ophthalmology
JF - American Journal of Ophthalmology
ER -