A Convolutional Neural Network to Identify Parkinson’s Disease using Multimodal Retinal Images

Abstract Background Retinal structure and microvasculature may be used as a surrogate for parallel processes in the brain. Previous studies have revealed differences in retinal structure and microvasculature in patients with Parkinson’s disease (PD) compared to cognitively normal controls[1]. Previous work developed a convolutional neural network (CNN) trained on multimodal retinal images that was able to identify Alzheimer’s dementia with an area under the curve (AUC) of 0.841[2]. Herein, we developed a CNN to identify PD. Methods Building upon a pretrained VGG19 architecture, we trained a CNN to receive inputs of ganglion cell‐inner plexiform layer (GC‐IPL) thickness color maps, optical coherence tomography angiography (OCTA) superficial capillary plexus 6x6mm en face images centered on the fovea obtained using the Zeiss Cirrus HD‐5000 with AngioPlex (v11.0.0.29946), ultra‐widefield (UWF) fundus color and autofluorescence (FAF) scanning laser ophthalmoscopy (Optos California) images from patients with a clinical diagnosis of PD and from controls without PD or cognitive impairment. The model consisted of a shared convolutional encoder, parallel image modality specific feature transformations, and prediction heads for all modalities that converge into a single output. Results 1,784 images from 371 eyes of 249 control subjects and 75 eyes of 52 PD subjects were used for development and testing. 296 (80%) control eyes were used for training, 36 (10%) for validation, and 39 (10%) for testing. 59 (79%) PD eyes were used for training, 6 for validation (8%), and 10 (14%) for testing. Our best performing model had an AUC of 0.918. UWF color images proved to be the most effective imaging input (highest AUC 0.838), and GCL‐IPL color maps were the least effective (highest AUC 0.630). Conclusions This CNN was able to successfully identify individuals with a clinical diagnosis of PD. Further work is ongoing to expand the number of images and the diversity of the population to improve translatability. Ma, J.P., et al., Retinal vascular changes in Parkinson’s disease on ultra‐widefield retinal imaging. Investigative Ophthalmology & Visual Science, 2021. 62(8): p. 1779‐1779. Wisely, C.E., et al., Convolutional neural network to identify symptomatic Alzheimer’s disease using multimodal retinal imaging. British Journal of Ophthalmology, 2020. 106: p. 388 ‐ 395.

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Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.089793
Citations
1
Primary Topic
Retinal Imaging and Analysis
Type
article
Field-Weighted Citation Impact
0.40
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article

A Convolutional Neural Network to Identify Parkinson’s Disease using Multimodal Retinal Images

Sharon Fekrat, Dilraj Singh Grewal, B.L. Scott, Ricardo Henao et al.
1 citations
Alzheimer s & Dementia
Retinal Imaging and Analysis
0.40
article

A Convolutional Neural Network to Identify Parkinson’s Disease using Multimodal Retinal Images

Sharon Fekrat, Dilraj Singh Grewal, B.L. Scott, Ricardo Henao, Anita Kundu, Terry Lee, Alexander Richardson
article en
1 citations

Abstract

Abstract Background Retinal structure and microvasculature may be used as a surrogate for parallel processes in the brain. Previous studies have revealed differences in retinal structure and microvasculature in patients with Parkinson’s disease (PD) compared to cognitively normal controls[1]. Previous work developed a convolutional neural network (CNN) trained on multimodal retinal images that was able to identify Alzheimer’s dementia with an area under the curve (AUC) of 0.841[2]. Herein, we developed a CNN to identify PD. Methods Building upon a pretrained VGG19 architecture, we trained a CNN to receive inputs of ganglion cell‐inner plexiform layer (GC‐IPL) thickness color maps, optical coherence tomography angiography (OCTA) superficial capillary plexus 6x6mm en face images centered on the fovea obtained using the Zeiss Cirrus HD‐5000 with AngioPlex (v11.0.0.29946), ultra‐widefield (UWF) fundus color and autofluorescence (FAF) scanning laser ophthalmoscopy (Optos California) images from patients with a clinical diagnosis of PD and from controls without PD or cognitive impairment. The model consisted of a shared convolutional encoder, parallel image modality specific feature transformations, and prediction heads for all modalities that converge into a single output. Results 1,784 images from 371 eyes of 249 control subjects and 75 eyes of 52 PD subjects were used for development and testing. 296 (80%) control eyes were used for training, 36 (10%) for validation, and 39 (10%) for testing. 59 (79%) PD eyes were used for training, 6 for validation (8%), and 10 (14%) for testing. Our best performing model had an AUC of 0.918. UWF color images proved to be the most effective imaging input (highest AUC 0.838), and GCL‐IPL color maps were the least effective (highest AUC 0.630). Conclusions This CNN was able to successfully identify individuals with a clinical diagnosis of PD. Further work is ongoing to expand the number of images and the diversity of the population to improve translatability. Ma, J.P., et al., Retinal vascular changes in Parkinson’s disease on ultra‐widefield retinal imaging. Investigative Ophthalmology & Visual Science, 2021. 62(8): p. 1779‐1779. Wisely, C.E., et al., Convolutional neural network to identify symptomatic Alzheimer’s disease using multimodal retinal imaging. British Journal of Ophthalmology, 2020. 106: p. 388 ‐ 395.

Alzheimer s & DementiaVol. 20(S2)
Duke University (US)
Openalex Percentile: Top 31%
Retinal Imaging and Analysis
0.40
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