April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
Progression of Patterns (POP) Using Independent Component Analysis Identifies Glaucoma Progression
Author Affiliations & Notes
  • Michael H. Goldbaum
    Ophthalmology, Univ of California-San Diego, La Jolla, California
  • Intae Lee
    Ophthalmology, Univ of California-San Diego, La Jolla, California
  • GilJin Jang, V
    Ophthalmology, Univ of California-San Diego, La Jolla, California
  • Christopher Bowd
    Ophthalmology, Univ of California-San Diego, La Jolla, California
  • Madhu Balasubramanian
    Ophthalmology, Univ of California-San Diego, La Jolla, California
  • Robert N. Weinreb
    Ophthalmology, Univ of California-San Diego, La Jolla, California
  • Linda M. Zangwill
    Ophthalmology, Univ of California-San Diego, La Jolla, California
  • Jeffrey M. Liebmann
    Ophthalmology, NYU School of Medicine, New York, New York
  • Christopher A. Girkin
    Ophthalmology, Univ of Alabama at Birmingham, Birmingham, Alabama
  • Pamela A. Sample
    Ophthalmology, Univ of California-San Diego, La Jolla, California
  • Footnotes
    Commercial Relationships  Michael H. Goldbaum, None; Intae Lee, None; GilJin Jang, V, None; Christopher Bowd, Lace Elettronica (R); Madhu Balasubramanian, None; Robert N. Weinreb, Carl Zeiss Meditec (C, R), Heidelberg Engineering (R), Topcon (C, R); Linda M. Zangwill, Carl Zeiss Meditec (R), Heidelberg Engineering (R), Optovue, Topcon (R); Jeffrey M. Liebmann, Carl Zeiss Meditec (C, R), Optovue (C, R), Topcon (C, R); Christopher A. Girkin, Carl Zeiss Meditec (R), Optovue (R), Topcon (R); Pamela A. Sample, Carl Zeiss Meditec (R), Haag-Streit (R), Welch-Allyn (R)
  • Footnotes
    Support  NIH Grants EY08208, EY11008, EY13928, EY13959, EY14267; Eyesight Foundation, Pfizer, David & Marilyn Dunn Fund
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 4151. doi:
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      Michael H. Goldbaum, Intae Lee, GilJin Jang, V, Christopher Bowd, Madhu Balasubramanian, Robert N. Weinreb, Linda M. Zangwill, Jeffrey M. Liebmann, Christopher A. Girkin, Pamela A. Sample; Progression of Patterns (POP) Using Independent Component Analysis Identifies Glaucoma Progression. Invest. Ophthalmol. Vis. Sci. 2011;52(14):4151.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract
 
Purpose:
 

We evaluated Progression of Patterns (POP) for its ability to identify and quantify progression of glaucomatous visual field defects.

 
Methods:
 

POP uses the variational Bayesian independent component mixture model (VIM) [TAOS 2009]. VIM separated Swedish Interactive Thresholding Algorithm (SITA) visual fields (VFs) from a set of 2085 normal and glaucoma eyes into 9 axes of maximally different patterns of VF defects. POP used a second set of 55 eyes with 5 VFs collected within 4 weeks (D.R. Anderson) to simulate stability and a third set of 4,186 VFs from 628 eyes from the Diagnostic Innovations in Glaucoma Study and the African Descent and Glaucoma Evaluation Study to test for progression (mean+sd 6.67+1.66 VFs followed 4.01+1.40 years). Eyes were classified into diagnostic categories based on VFs and optic disk photographs and whether they had photographic evidence of progressive glaucomatous optic neuropathy (PGON). Each sequence of fields was projected on 7 VIM glaucoma axes. POP concentrated on change detection of the VF defect axis with maximal change. Using linear regression (LR), which incorporated 95% confidence limits of stable eyes and variability in an evaluated eye’s sequence of VFs, the probability of progression in the third set of eyes was estimated for POP and compared to the LR of Humphrey Visual Field Index (VFI), and AGIS scores.

 
Results:
 

The evaluated populations had suspicious disk or pressure (suspects), glaucomatous fields (VF only), glaucomatous fields and GON (VF+GON), or PGON. Table shows percent progressing at specificity set at 95%.

 
Conclusions:
 

The automatic algorithm in POP 1) could give probability of progression, 2) identified more progressing eyes in groups at higher risk for progression, and 3) found change of a specific VIM defect pattern to be a sensitive indicator of progression in more progressing eyes than did change in global indices.  

 
Keywords: visual fields • clinical (human) or epidemiologic studies: prevalence/incidence 
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