Retinal microvascular attenuation in mental cognitive impairment and Alzheimer's disease by optical coherence

Jing Wu1,2, Xiaojun Zhang3, Guliqiwaer Azhati1

  • 1Department of Ophthalmology, Shanghai Tenth People's Hospital, Tongji University, Shanghai, China.

Acta Ophthalmologica
|March 11, 2020
PubMed
Abstract

Insights

Macular microvascular density loss is evident in mild cognitive impairment (MCI) and Alzheimer's disease (AD) patients, particularly in the deep retinal capillary plexuses. Optical coherence tomography angiography (OCT-A) can detect these early signs, aiding in monitoring disease progression.

Area of Science:

  • Ophthalmology
  • Neurology
  • Medical Imaging

Background:

  • Macular microvasculature changes are implicated in neurodegenerative diseases.
  • Early detection of Alzheimer's disease (AD) and mild cognitive impairment (MCI) is crucial for timely intervention.
  • Optical coherence tomography angiography (OCT-A) offers high-resolution imaging of retinal microvasculature.

Purpose of the Study:

  • To investigate regional variations in macular microvasculature in patients with MCI and AD.
  • To assess the association between retinal microvascular parameters and the progression of preclinical AD.

Main Methods:

  • Prospective study involving healthy controls (HC), MCI patients, and AD patients.
  • Utilized Optical coherence tomography angiography (OCT-A) to quantify foveal avascular zone (FAZ) areas and retinal capillary plexus densities.
  • Analyzed superficial retinal capillary plexuses (SRCP) and deep retinal capillary plexuses (DRCP) in inner and outer annular rings, divided into four quadrants.

Main Results:

  • AD patients exhibited significantly lower microvascular densities in the DRCP across all parafoveal and perifoveal quadrants compared to HC.
  • MCI patients showed significant microvascular loss in most parafoveal sectors and the SE sector of the DRCP compared to HC.
  • No significant differences in SRCP microvascular density were observed among groups, except for the SI quadrant between AD and HC.

Conclusions:

  • Macular microvascular attenuation is evident in both MCI and AD patients, with more pronounced loss in the DRCP.
  • OCT-A is effective in identifying early microvascular abnormalities associated with MCI and AD.
  • Quantified microvascular density in the DRCP may serve as a potential biomarker for early AD detection and monitoring preclinical progression.

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