3.8 Review

Optical Coherence Tomography in Patients with Alzheimer's Disease: What Can It Tell Us?

Journal

EYE AND BRAIN
Volume 13, Issue -, Pages 1-20

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/EB.S235238

Keywords

optical coherence tomography; optical coherence tomography angiography; Alzheimer's disease; mild cognitive impairment; dementia

Categories

Funding

  1. National Eye Institute [1K23EY030897-01]

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The review found that OCT and OCTA have great potential in the diagnosis of AD, especially in comparing AD patients with healthy controls, with most studies indicating significant structural and functional decline in AD patients. While the analysis of MCI groups yielded more mixed results, a similar pattern of decline was often noted among patients with MCI compared to healthy controls.
Purpose: Although Alzheimer's disease (AD) is a leading cause of dementia worldwide, its clinical diagnosis remains a challenge. Optical coherence tomography (OCT) and OCT with angiography (OCTA) are non-invasive ophthalmic imaging tools with the potential to detect retinal structural and microvascular changes in patients with AD, which may serve as biomarkers for the disease. In this systematic review, we evaluate whether certain OCT and OCTA parameters are significantly associated with AD and mild cognitive impairment (MCI). Methods: PubMed database was searched using a combination of MeSH terms to identify studies for review. Studies were organized by participant diagnostic groups, type of imaging modality, and OCT/OCTA parameters of interest. Participant demographic data was also collected and baseline descriptive statistics were calculated for the included studies. Results: Seventy-one studies were included for review, representing a total of 6757 patients (2350 AD, 793 MCI, 2902 healthy controls (HC), and 841 others with a range of other neurodegenerative diagnoses). The mean baseline ages were 72.78 +/- 3.69, 71.52 +/- 2.88, 70.55 +/- 3.85 years for AD, MCI and HC groups, respectively. The majority of studies noted significant structural and functional decline in AD patients when compared to HC. Although analysis of MCI groups yielded more mixed results, a similar pattern of decline was often noted amongst patients with MCI relative to HC. OCT and OCTA measurements were also shown to correlate with established measures of AD such as neuropsychological testing or neuroimaging. Conclusion: OCT and OCTA show great potential as non-invasive technologies for the diagnosis of AD. However, further research is needed to determine whether there are AD-specific patterns of structural or microvascular change in the retina and optic nerve that distinguish AD from other neurodegenerative diseases. Development of sensitive and specific OCT/OCTA parameters will be necessary before they can be used to detect AD in clinical settings.

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