Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which causes coronavirus disease 2019 (COVID-19), affects the pulmonary systems via angiotensin-converting enzyme-2 (ACE-2) receptor, being an entry to systemic infection. As COVID-19 disease features ACE-2 deficiency, a link to microcirculation is proposed. Optical coherence tomography angiography (OCT-A) enables non-invasive analysis of retinal microvasculature. Thus, an impaired systemic microcirculation might be mapped on retinal capillary system. As recent OCT-A studies, analyzing microcirculation in two subdivided layers, yielded contrary results, an increased subdivision of retinal microvasculature might offer an even more fine analysis. The aim of the study was to investigate retinal microcirculation by OCT-A after COVID-19 infection in three subdivided layers (I). In addition, short-term retinal affections were monitored during COVID-19 disease (II). Considering (I), a prospective study (33 patientspost−COVID and 28 controls) was done. Macula and peripapillary vessel density (VD) were scanned with the Spectralis II. Macula VD was measured in three layers: superficial vascular plexus (SVP), intermediate capillary plexus (ICP), and deep capillary plexus (DCP). Analysis was done by the EA-Tool, including an Anatomical Positioning System and an analysis of peripapillary VD by implementing Bruch's membrane opening (BMO) landmarks. Overall, circular (c1, c2, and c3) and sectorial VD (s1-s12) was analyzed. Considering (II), in a retrospective study, 29 patients with severe complications of COVID-19 infection, hospitalized at the intensive care unit, were monitored for retinal findings at bedside during hospitalization. (I) Overall (p = 0.0133) and circular (c1, p = 0.00257; c2, p = 0.0067; and c3, p = 0.0345). VD of the ICP was significantly reduced between patientspost−COVID and controls, respectively. Overall (p = 0.0179) and circular (c1, p = 0.0189) peripapillary VD was significantly reduced between both groups. Subgroup analysis of hospitalized vs. non-hospitalized patientspost−COVID yielded a significantly reduced VD of adjacent layers (DCP and SVP) with increased severity of COVID-19 disease. Clinical severity parameters showed a negative correlation with VD (ICP) and peripapillary VD. (II) Funduscopy yielded retinal hemorrhages and cotton wool spots in 17% of patients during SARS-CoV-2 infection. As VD of the ICP and peripapillary regions was significantly reduced after COVID-19 disease and showed a link to clinical severity markers, we assume that the severity of capillary impairment after COVID-19 infection is mapped on retinal microcirculation, visualized by non-invasive OCT-A.

Highlights

  • In December 2019, several cases of a severe and unknown pneumonia were diagnosed in Wuhan [1]

  • After age correction of the vessel density (VD) data, additional regional variations of macula VD were observed in the superficial vascular plexus (SVP) (p < 0.0001), intermediate capillary plexus (ICP) (p < 0.0001), and deep capillary plexus (DCP) (p < 0.0001)

  • Considering severity of COVID-19 disease, the more increased the level of D-dimers and GPT were observed during hospitalization, the more reduced the peripapillary VD was measured in Optical coherence tomography angiography (OCT-A) scans

Read more

Summary

Introduction

In December 2019, several cases of a severe and unknown pneumonia were diagnosed in Wuhan [1]. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was identified as a disease causative agent, and clinical features were summarized as coronavirus disease 2019 (COVID-19). SARS-CoV-2 enters human cells via the angiotensin-converting enzyme-2 (ACE-2) receptor [2, 3]. ACE-2 and Ang-1-7 are assumed to prevent atherosclerosis and protect endothelial cells via inhibition of inflammation [8]. The latter one was seen to reduce oxidative stress via the MAS receptor [9, 10]. It is hypothesized that SARS-CoV-2 targeting the ACE-2 receptor features molecular characteristics of ACE-2 deficiency [16, 17]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call