Macular Microvascular Density as a Diagnostic Biomarker for Alzheimer's Disease

J Alzheimers Dis. 2022;90(1):139-149. doi: 10.3233/JAD-220482.

Abstract

Background: Some previous studies showed abnormal pathological and vascular changes in the retina of patients with Alzheimer's disease (AD). However, whether retinal microvascular density is a diagnostic indicator for AD remains unclear.

Objective: This study evaluated the macular vessel density (m-VD) in the superficial capillary plexus and fovea avascular zone (FAZ) area in AD, explored their correlations with clinical parameters, and finally confirmed an optimal machine learning model for AD diagnosis.

Methods: 77 patients with AD and 145 healthy controls (HCs) were enrolled. The m-VD and the FAZ area were measured using optical coherence tomography angiography (OCTA) in all participants. Additionally, AD underwent neuropsychological assessment, brain magnetic resonance imaging scan, cerebrospinal fluid (CSF) biomarker detection, and APOE ɛ4 genotyping. Finally, the performance of machine learning algorithms based on the OCTA measurements was evaluated by Python programming language.

Results: The m-VD was noticeably decreased in AD compared with HCs. Moreover, m-VD in the fovea, superior inner, inferior inner, nasal inner subfields, and the whole inner ring declined significantly in mild AD, while it was more serious in moderate/severe AD. However, no significant difference in the FAZ was noted between AD and HCs. Furthermore, we found that m-VD exhibited a significant correlation with cognitive function, medial temporal atrophy and Fazekas scores, and APOE ɛ4 genotypes. No significant correlations were observed between m-VD and CSF biomarkers. Furthermore, results revealed the Adaptive boosting algorithm exhibited the best diagnostic performance for AD.

Conclusion: Macular vascular density could serve as a diagnostic biomarker for AD.

Keywords: Alzheimer’s disease; diagnosis; machine learning; optical coherence tomography angiography; vessel density.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease* / diagnostic imaging
  • Alzheimer Disease* / genetics
  • Apolipoproteins E
  • Biomarkers
  • Fluorescein Angiography / methods
  • Humans
  • Microvascular Density*
  • Retinal Vessels / diagnostic imaging
  • Retinal Vessels / pathology
  • Tomography, Optical Coherence / methods

Substances

  • Biomarkers
  • Apolipoproteins E