Fei Wu, Monica Lavoie, Mélanie Hébert, Ali Dirani, Robert Laforce
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引用次数: 0
Abstract
Background: Optical coherence tomography (OCT) and OCT angiography (OCT-A) have been studied as biomarkers for Alzheimer's disease (AD), with promising results. Nevertheless, their potential in the logopenic variant of primary progressive aphasia (lvPPA), which shares the same amyloid pathology, has not yet been explored. This work aimed to characterize retinal changes in lvPPA compared to healthy controls.
Methods: Ten participants with lvPPA and eleven controls underwent OCT and OCT-A imaging. Amyloid pathology in lvPPA was confirmed by lumbar puncture. Retinal parameters included retinal nerve fiber layer (RNFL) thickness and foveal avascular zone (FAZ).
Results: Compared to controls, lvPPA participants exhibited reduced RNFL thickness in the temporal sector (p = 0.013) and significantly decreased FAZ circularity (p = 0.002).
Discussion: RNFL thinning may reflect trans-synaptic degeneration from cortical atrophy, while reduced FAZ circularity suggests early microvascular changes related to amyloid burden. Our findings support OCT and OCT-A as potential biomarkers for lvPPA.
Highlights: For the first time, OCT and OCT-A are studied as potential biomarkers for lvPPA.Compared to healthy controls, retinal nerve thickness is decreased in lvPPA patients.Retinal vasculature exhibits structural alterations in lvPPA patients.
期刊介绍:
Alzheimer''s & Dementia: Diagnosis, Assessment & Disease Monitoring (DADM) is an open access, peer-reviewed, journal from the Alzheimer''s Association® that will publish new research that reports the discovery, development and validation of instruments, technologies, algorithms, and innovative processes. Papers will cover a range of topics interested in the early and accurate detection of individuals with memory complaints and/or among asymptomatic individuals at elevated risk for various forms of memory disorders. The expectation for published papers will be to translate fundamental knowledge about the neurobiology of the disease into practical reports that describe both the conceptual and methodological aspects of the submitted scientific inquiry. Published topics will explore the development of biomarkers, surrogate markers, and conceptual/methodological challenges. Publication priority will be given to papers that 1) describe putative surrogate markers that accurately track disease progression, 2) biomarkers that fulfill international regulatory requirements, 3) reports from large, well-characterized population-based cohorts that comprise the heterogeneity and diversity of asymptomatic individuals and 4) algorithmic development that considers multi-marker arrays (e.g., integrated-omics, genetics, biofluids, imaging, etc.) and advanced computational analytics and technologies.