Early Detection of Progressive Visual Loss in Glaucoma Using Deep Learning
使用深度学习早期检测青光眼进行性视力丧失
基本信息
- 批准号:10424899
- 负责人:
- 金额:--
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-06-01 至 2026-05-31
- 项目状态:未结题
- 来源:
- 关键词:AffectAmbulatory Care FacilitiesAreaArtificial IntelligenceBackBinocular VisionBlindnessClinicClinicalClinical DataCommunitiesComputersDataDefectDiseaseEarly DiagnosisEarly treatmentEyeFutureGanglion Cell LayerGlaucomaGlobal ChangeGoalsImageIndividualInner Plexiform LayerInterventionLearningMapsMeasuresMethodsModelingMonitorMorphologyOptic DiskOptic NerveOptical Coherence TomographyOutcomeOutcome MeasureOutputPatientsPatternQuality of lifeReportingRetinaSeriesSeveritiesStandardizationStructureTestingThickTimeTrainingVariantVeteransVisionVisualVisual FieldsVisuospatialaggressive therapyautoencoderbaseclinical practicedeep learningdenoisingdiagnostic valueexpectationexperiencefield studyganglion cellinstrumentinterestmaculanovelnovel strategiesoptic cuppreservationretinal nerve fiber layersuccesstreatment planningtrend analysisvisual map
项目摘要
Glaucoma, a leading cause of irreversible blindness, disproportionately affects veterans. While often progressing
slowly, glaucoma can also progress rapidly, and especially given the variability of standard visual-field (VF) tests
to monitor progression, it currently can be challenging to determine those individuals needing a more aggressive
treatment plan. Veterans may experience permanent loss of vision (and corresponding vision-related quality of
life) while waiting for subsequent tests to show VF loss progression (and thus indicating a change in treatment
is needed). Structural optical coherence tomography (OCT) measures, such as the thickness of the macular
ganglion cell layer (GCL), retinal nerve fiber layer (RNFL) and optic disc morphology can also be used to help
monitor progression. However, existing clinical use of global parameters to assess glaucoma progression may
be insensitive to worsening of focal defects. It is also not known how differing spatial patterns of progression
affects quality of life. There is an unmet clinical need for simple-to-use approaches to more accurately estimate
future progression and corresponding quality-of-life measures. We will use a specific type of deep-learning
approach, called deep variational autoencoders (VAEs) to provide a novel standardized and sensitive approach
to monitoring glaucomatous progression, comparable to a glaucoma expert. Our specific aims are as follows:
1. Evaluate how well image-based deep-learning variational autoencoder (VAE) models can be used
to monitor a patient’s current glaucomatous progression. This aim will first involve training and
evaluating a separate deep VAE model for each image-based structure of interest as well as a deep VAE
model for 24-2 visual field threshold data. Once trained, each VAE model will allow for the extraction of the
so-called latent variable values given the input image. The ability of these latent variable values to monitor
change over time will be compared (in an independent test set) to standard global and regional parameters.
Because of their ability to naturally capture both global and local changes, the latent-variable approach will
be able to better detect changes over time compared to current clinical reports.
2. Evaluate how well image-based deep-learning variational autoencoder (VAE) models can be used
to predict a patient’s future glaucomatous progression. In this aim, we will first develop an approach
for predicting future latent-variable representations of structure/function based on learning from a prior time
series of values. Once determined, future latent values will be mapped back to their original
structure/function representations using the trained “decoder” part of the VAE. Such an approach will
provide a clear advantage for a clinician in having visual spatial representations of future structure and
function trajectories to optimize early treatment decisions.
3. Evaluate how latent variables from a novel binocular VAE model relate to visual quality-of-life
measures. In this aim, we will first develop an additional VAE model to take into account binocular vision
(what the patient sees with both eyes open) and then relate latent factors from each model to quality-of-
life measures in a cross-sectional fashion. We hypothesize that binocular VAE models of structure and
function will be more predictive of visual quality-of-life measures than current methods, helping to
prioritize and guide treatment.
Successful completion of these aims is expected to have positive impact to help veteran glaucomatous
patients avoid permanent vision loss at an early disease stage and maintain vision-related quality of life.
Glaucoma, a leading cause of irreversible blindness, disproportionately affects veterans. While often progressing
Slowly, glaucoma can also progress rapidly, and especially given the variability of standard visual-field (VF) tests
to monitor progression, it currently can be challenged to determine those individuals need a more aggressive
treatment plan. Veterans may experience permanent loss of vision (and corresponding vision-related quality of
life) while waiting for subsequent tests to show VF loss progression (and thus indicating a change in treatment
is needed). Structural optical coherence tomography (OCT) measures, such as the thickness of the macular
ganglion cell layer (GCL), retinal nerve fiber layer (RNFL) and optic disc morphology can also be used to help
monitor progression. However, existing clinical use of global parameters to assess glaucoma progression may
be insensitive to worry of focal defects. It is also not known how differentiating spatial patterns of progression
affects quality of life. There is an unmet clinical need for simple-to-use approaches to more accurately estimate
Future progression and corresponding quality-of-life measures. We will use a specific type of deep-learning
approach, called deep variational autoencoders (VAEs) to provide a novel standardized and sensitive approach
to monitor glaucomatous progression, comparable to a glaucoma expert.我们的具体目的如下:
1. Evaluate how well image-based deep-learning variational autoencoder (VAE) models can be used
to monitor a patient’s current glaucomatous progression. This aim will first involve training and
evaluating a separate deep VAE model for each image-based structure of interest as well as a deep VAE
model for 24-2 visual field threshold data. Once trained, each VAE model will allow for the extraction of the
so-called latent variable values given the input image. The ability of these latent variable values to monitor
change over time will be compared (in an independent test set) to standard global and regional parameters.
Because of their ability to naturally capture both global and local changes, the latent-variable approach will
be able to better detect changes over time compared to current clinical reports.
2. Evaluate how well image-based deep-learning variational autoencoder (VAE) models can be used
to predict a patient’s future glaucomatous progression. In this aim, we will first develop an approach
for predicting future latent-variable representations of structure/function based on learning from a prior time
series of values. Once determined, future latent values will be mapped back to their original
structure/function representations using the trained “decoder” part of the VAE. Such an approach will
Provide a clear advantage for a clinical in having visual spatial representations of future structure and
function trajectories to optimize early treatment decisions.
3. Evaluate how latent variables from a novel binocular VAE model relate to visual quality-of-life
措施。 In this aim, we will first develop an additional VAE model to take into account binocular vision
(what the patient sees with both eyes open) and then relate latent factors from each model to quality-of-
life measures in a cross-sectional fashion. We hypothesize that binocular VAE models of structure and
function will be more predictive of visual quality-of-life measures than current methods, helping to
Prioritize and guide treatment.
Successful completion of these aims is expected to have positive impact to help veteran glaucomatous
patients avoid permanent vision loss at an early disease stage and maintain vision-related quality of life.
项目成果
期刊论文数量(0)
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MONA K. GARVIN其他文献
MONA K. GARVIN的其他文献
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{{ truncateString('MONA K. GARVIN', 18)}}的其他基金
Early Detection of Progressive Visual Loss in Glaucoma Using Deep Learning
使用深度学习早期检测青光眼进行性视力丧失
- 批准号:
10623178 - 财政年份:2022
- 资助金额:
-- - 项目类别:
IEEE International Symposium on Biomedical Imaging (ISBI) 2020
IEEE 国际生物医学成像研讨会 (ISBI) 2020
- 批准号:
9914410 - 财政年份:2020
- 资助金额:
-- - 项目类别:
Automated Assessment of Optic Nerve Edema with Low-Cost Imaging
通过低成本成像自动评估视神经水肿
- 批准号:
9569310 - 财政年份:2016
- 资助金额:
-- - 项目类别:
3D Image Analysis Approach to Determine Severity and Cause of Optic Nerve Edema
3D 图像分析方法确定视神经水肿的严重程度和原因
- 批准号:
8477880 - 财政年份:2013
- 资助金额:
-- - 项目类别:
3D Image Analysis Approach to Determine Severity and Cause of Optic Nerve Edema
3D 图像分析方法确定视神经水肿的严重程度和原因
- 批准号:
8842639 - 财政年份:2013
- 资助金额:
-- - 项目类别:
3D Image Analysis Approach to Determine Severity and Cause of Optic Nerve Edema
3D 图像分析方法确定视神经水肿的严重程度和原因
- 批准号:
8652462 - 财政年份:2013
- 资助金额:
-- - 项目类别:
Glaucoma Assessment Using A Multimodality Image Analysis Approach
使用多模态图像分析方法进行青光眼评估
- 批准号:
8425995 - 财政年份:2012
- 资助金额:
-- - 项目类别:
Glaucoma Assessment Using A Multimodality Image Analysis Approach
使用多模态图像分析方法进行青光眼评估
- 批准号:
8838199 - 财政年份:2012
- 资助金额:
-- - 项目类别:
Glaucoma Assessment Using A Multimodality Image Analysis Approach
使用多模态图像分析方法进行青光眼评估
- 批准号:
8202660 - 财政年份:2012
- 资助金额:
-- - 项目类别:
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