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Discriminating retinal microvascular and neuronal differences related to migraines: Deep Learning based Crossectional Study

2024-07-30 · Feilong Tang, Matt Trinh, Annita Duong, Angelica Ly, Fiona Stapleton, Zhe Chen, ZongYuan Ge, Imran Razzak

Migraine, a prevalent neurological disorder, has been associated with various ocular manifestations suggestive of neuronal and microvascular deficits. However, there is limited understanding of the extent to which retinal imaging may discriminate between individuals with migraines versus without migraines. In this study, we apply convolutional neural networks to color fundus photography (CFP) and optical coherence tomography (OCT) data to investigate differences in the retina that may not be apparent through traditional human-based interpretations of retinal imaging. Retrospective data of CFP type 1 [posterior pole] and type 2 [optic nerve head (ONH)] from 369 and 336 participants respectively were analyzed. All participants had bilaterally normal optic nerves and maculae, with no retinal-involving diseases. CFP images were concatenated with OCT default ONH measurements, then inputted through three convolutional neural networks - VGG-16, ResNet-50, and Inceptionv3. The primary outcome was performance of discriminating between with migraines versus without migraines, using retinal microvascular and neuronal imaging characteristics. Using CFP type 1 data, discrimination (AUC [95% CI]) was high (0.84 [0.8, 0.88] to 0.87 [0.84, 0.91]) and not significantly different between VGG-16, ResNet-50, and Inceptionv3. Using CFP type 2 [ONH] data, discrimination was reduced and ranged from poor to fair (0.69 [0.62, 0.77] to 0.74 [0.67, 0.81]). OCT default ONH measurements overall did not significantly contribute to model performance. Class activation maps (CAMs) highlighted that the paravascular arcades were regions of interest. The findings suggest that individuals with migraines demonstrate microvascular differences more so than neuronal differences in comparison to individuals without migraines.

📄 PDF Abstract BibTeX arXiv:2408.07293

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