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Pattern recognition can detect subtle field defects in eyes of HIV individuals without retinitis under HAART

OBJECTIVES: To use machine learning classifiers (MLCs) to seek differences in visual fields (VFs) between normal eyes and eyes of HIV+ patients; to find the effect of immunodeficiency on VFs and to compare the effectiveness of MLCs to commonly-used Statpac global indices in analyzing standard automa...

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Autores principales: Goldbaum, Michael H., Kozak, Igor, Hao, Jiucang, Sample, Pamela A., Lee, TeWon, Grant, Igor, Freeman, William R.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3070878/
https://www.ncbi.nlm.nih.gov/pubmed/20865422
http://dx.doi.org/10.1007/s00417-010-1511-x
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author Goldbaum, Michael H.
Kozak, Igor
Hao, Jiucang
Sample, Pamela A.
Lee, TeWon
Grant, Igor
Freeman, William R.
author_facet Goldbaum, Michael H.
Kozak, Igor
Hao, Jiucang
Sample, Pamela A.
Lee, TeWon
Grant, Igor
Freeman, William R.
author_sort Goldbaum, Michael H.
collection PubMed
description OBJECTIVES: To use machine learning classifiers (MLCs) to seek differences in visual fields (VFs) between normal eyes and eyes of HIV+ patients; to find the effect of immunodeficiency on VFs and to compare the effectiveness of MLCs to commonly-used Statpac global indices in analyzing standard automated perimetry (SAP). METHODS: The high CD4 group consisted of 70 eyes of 39 HIV-positive patients with good immune status (CD4 counts were never <100/ml). The low CD4 group had 59 eyes of 38 HIV-positive patients with CD4 cell counts <100/ml at some period of time lasting for at least 6 months. The normal group consisted of 61 eyes of 52 HIV-negative individuals. We used a Humphrey Visual Field Analyzer, SAP full threshold program 24-2, and routine settings for evaluating VFs. We trained and tested support vector machine (SVM) machine learning classifiers to distinguish fields from normal subjects and high and CD4 groups separately. Receiver operating characteristic (ROC) curves measured the discrimination of each classifier, and areas under ROC were statistically compared. RESULTS: Low CD4 HIV patients: with SVM, the AUROC was 0.790 ± 0.042. SVM and MD each significantly differed from chance decision, with p < .00005. High CD4 HIV patients: the SVM AUROC of 0.664 ± 0.047 and MD were each significantly better than chance (p = .041, p = .05 respectively). CONCLUSIONS: Eyes from both low and high CD4 HIV+ patients have VFs defects indicating retinal damage. Generalized learning classifier, SVM, and a Statpac classifier, MD, are effective at detecting HIV eyes that have field defects, even when these defects are subtle.
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spelling pubmed-30708782011-05-02 Pattern recognition can detect subtle field defects in eyes of HIV individuals without retinitis under HAART Goldbaum, Michael H. Kozak, Igor Hao, Jiucang Sample, Pamela A. Lee, TeWon Grant, Igor Freeman, William R. Graefes Arch Clin Exp Ophthalmol Retinal Disorders OBJECTIVES: To use machine learning classifiers (MLCs) to seek differences in visual fields (VFs) between normal eyes and eyes of HIV+ patients; to find the effect of immunodeficiency on VFs and to compare the effectiveness of MLCs to commonly-used Statpac global indices in analyzing standard automated perimetry (SAP). METHODS: The high CD4 group consisted of 70 eyes of 39 HIV-positive patients with good immune status (CD4 counts were never <100/ml). The low CD4 group had 59 eyes of 38 HIV-positive patients with CD4 cell counts <100/ml at some period of time lasting for at least 6 months. The normal group consisted of 61 eyes of 52 HIV-negative individuals. We used a Humphrey Visual Field Analyzer, SAP full threshold program 24-2, and routine settings for evaluating VFs. We trained and tested support vector machine (SVM) machine learning classifiers to distinguish fields from normal subjects and high and CD4 groups separately. Receiver operating characteristic (ROC) curves measured the discrimination of each classifier, and areas under ROC were statistically compared. RESULTS: Low CD4 HIV patients: with SVM, the AUROC was 0.790 ± 0.042. SVM and MD each significantly differed from chance decision, with p < .00005. High CD4 HIV patients: the SVM AUROC of 0.664 ± 0.047 and MD were each significantly better than chance (p = .041, p = .05 respectively). CONCLUSIONS: Eyes from both low and high CD4 HIV+ patients have VFs defects indicating retinal damage. Generalized learning classifier, SVM, and a Statpac classifier, MD, are effective at detecting HIV eyes that have field defects, even when these defects are subtle. Springer-Verlag 2010-09-24 2011 /pmc/articles/PMC3070878/ /pubmed/20865422 http://dx.doi.org/10.1007/s00417-010-1511-x Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Retinal Disorders
Goldbaum, Michael H.
Kozak, Igor
Hao, Jiucang
Sample, Pamela A.
Lee, TeWon
Grant, Igor
Freeman, William R.
Pattern recognition can detect subtle field defects in eyes of HIV individuals without retinitis under HAART
title Pattern recognition can detect subtle field defects in eyes of HIV individuals without retinitis under HAART
title_full Pattern recognition can detect subtle field defects in eyes of HIV individuals without retinitis under HAART
title_fullStr Pattern recognition can detect subtle field defects in eyes of HIV individuals without retinitis under HAART
title_full_unstemmed Pattern recognition can detect subtle field defects in eyes of HIV individuals without retinitis under HAART
title_short Pattern recognition can detect subtle field defects in eyes of HIV individuals without retinitis under HAART
title_sort pattern recognition can detect subtle field defects in eyes of hiv individuals without retinitis under haart
topic Retinal Disorders
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3070878/
https://www.ncbi.nlm.nih.gov/pubmed/20865422
http://dx.doi.org/10.1007/s00417-010-1511-x
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