Optical coherence tomography angiography changes in cardiovascular systemic diseases and risk factors: A Review

Inês Monteiro-Henriques1, Amândio Rocha-Sousa2,3, João Barbosa-Breda2,3,4

  • 1Faculty of Medicine of the University of Porto, Porto, Portugal.

Acta Ophthalmologica
|March 30, 2021
PubMed

Insights

Optical Coherence Tomography Angiography (OCTA) reveals ocular microvasculature changes linked to cardiovascular risk factors. These non-invasive findings may aid in assessing patient cardiovascular risk profiles.

Area of Science:

  • Ophthalmology
  • Cardiology
  • Medical Imaging

Background:

  • Cardiovascular disease (CVD) is a leading global cause of mortality.
  • Assessing cardiovascular risk factors (CVRF) is crucial for CVD prevention.
  • Retinal vascular alterations may indicate systemic processes, including CVRF.

Purpose of the Study:

  • To systematically review ocular microvasculature changes detected by OCTA.
  • To compare changes in patients with systemic conditions affecting the CV system versus healthy subjects.
  • To identify non-invasive OCTA markers for CVRF assessment.

Main Methods:

  • Systematic review of studies from PubMed, Scopus, Cochrane, and Web of Science.
  • Inclusion of 47 articles, excluding case reports and reviews.
  • Analysis of OCTA findings in patients with hypertension, diabetes, kidney disease, preeclampsia, CAD, carotid stenosis, OSA, and in healthy subjects with varying conditions.

Main Results:

  • Patients with various systemic conditions generally exhibit lower retinal/choroidal Vessel Density (VD) and Vessel Length (VL).
  • Increased foveal avascular zone area and perimeter are observed in these patients.
  • Factors like smoking, hypoxia, and race in healthy individuals also correlate with ocular vascular changes.

Conclusions:

  • OCTA is a promising non-invasive tool for evaluating cardiovascular risk.
  • OCTA findings may be integrated into diagnostic and prognostic algorithms for CVD.
  • Ocular microvasculature changes detected by OCTA serve as potential biomarkers for CVRF.

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