Adaptive optics-assisted identification of preferential erythrocyte aggregate pathways in the human retinal microvasculature

To characterize human parafoveal blood flow using adaptive optics scanning laser ophthalmoscopy (AO-SLO). In 5 normal subjects, erythrocyte aggregate distributions were analyzed on 3 different days. Erythrocyte aggregates were described as a "dark tail" in AO-SLO. The characteristics of th...

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Veröffentlicht in:PloS one 2014-02, Vol.9 (2), p.e89679-e89679
Hauptverfasser: Arichika, Shigeta, Uji, Akihito, Ooto, Sotaro, Miyamoto, Kazuaki, Yoshimura, Nagahisa
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Uji, Akihito
Ooto, Sotaro
Miyamoto, Kazuaki
Yoshimura, Nagahisa
description To characterize human parafoveal blood flow using adaptive optics scanning laser ophthalmoscopy (AO-SLO). In 5 normal subjects, erythrocyte aggregate distributions were analyzed on 3 different days. Erythrocyte aggregates were described as a "dark tail" in AO-SLO. The characteristics of the pathways with dark tail flow in the parafovea were measured. Additionally, the tendency for dark tail flow before and after bifurcations was analyzed to study the blood flow in detail. Average velocity in parent vessels with dark tail flow was 1.30±0.27 mm/s. Average velocity in daughter vessels with dark tail flow was 1.12±0.25 mm/s, and the average velocity of plasma gaps in daughter vessels without dark tail flow was 0.64±0.11 mm/s. Downstream from the bifurcations, the velocity in vessels with dark tail flow was higher than that in those without it (p
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subjects Adaptive optics
Average velocity
Bifurcations
Biology
Blood
Blood flow
Blood Flow Velocity
Blood pressure
Blood vessels
Diabetes
Diabetic retinopathy
Engineering
Erythrocyte Aggregation
Erythrocytes
Family medical history
Flow
Hemodynamics
Humans
Lasers
Medical imaging
Medicine
Microcirculation
Microvasculature
Microvessels
Ophthalmoscopy - methods
Optics
Optics and Photonics
Pathways
Photoreceptors
Retina
Retinal Vessels - physiology
Systemic diseases
University graduates
Velocity
title Adaptive optics-assisted identification of preferential erythrocyte aggregate pathways in the human retinal microvasculature
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