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Optical microangiography (OMAG) is a powerful optical angio-graphic tool to visualize micro-vascular flow in vivo. Despite numerous demonstrations for the past several years of the qualitative relationship between OMAG and flow, no convincing quantitative relationship has been proven. In this paper, we attempt to quantitatively correlate the OMAG signal with flow. Specifically, we develop a simplified analytical model of the complex OMAG, suggesting that the OMAG signal is a product of the number of particles in an imaging voxel and the decorrelation of OCT (optical coherence tomography) signal, determined by flow velocity, inter-frame time interval, and wavelength of the light source. Numerical simulation with the proposed model reveals that if the OCT amplitudes are correlated, the OMAG signal is related to a total number of particles across the imaging voxel cross-section per unit time (flux); otherwise it would be saturated but its strength is proportional to the number of particles in the imaging voxel (concentration). The relationship is validated using microfluidic flow phantoms with various preset flow metrics. This work suggests OMAG is a promising quantitative tool for the assessment of vascular flow.
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http://dx.doi.org/10.1364/BOE.7.002709 | DOI Listing |
Am J Ophthalmol
November 2021
Keck School of Medicine of the University of Southern California, Los Angeles, California, USA. Electronic address:
Purpose: To compare dynamic ranges and steps to measurement floors of peripapillary and macular metrics from a complex signal-based optical microangiography (OMAG) optical coherence tomography angiography (OCTA) device for glaucoma with those of OCT measurements.
Design: Cross-sectional study.
Methods: Imaging of 252 eyes from 173 patients with glaucoma and 123 eyes from 92 subjects without glaucoma from a glaucoma clinic was quantified using custom and commercial software.
J Glaucoma
August 2021
Glaucoma Services, Dr Shroff's Charity Eye Hospital, New Delhi, India.
Precis: The vessel density (VD) and perfusion density (PD) generated by optical microangiography (OMAG) is significantly affected by the signal strength (SS). Sex, hypertension, diabetes, and axial length did not have any statistically significant effect on these measurements.
Purpose: The aim was to assess the effect of subject-related factors (age, sex, systemic hypertension, diabetes, and axial length) and machine-related factor (SS) on VD and PD generated by OMAG in peripapillary and macular regions.
J Cereb Blood Flow Metab
August 2021
Department of Anesthesiology & Perioperative Medicine, Oregon Health & Science University, Portland, OR, USA.
Local blood flow in the brain is tightly coupled to metabolic demands, a phenomenon termed functional hyperemia. Both capillaries and arterioles contribute to the hyperemic response to neuronal activity via different mechanisms and timescales. The nature and specific signaling involved in the hyperemic response of capillaries versus arterioles, and their temporal relationship are not fully defined.
View Article and Find Full Text PDFQuant Imaging Med Surg
March 2021
Department of Bioengineering, University of Washington, Seattle, WA, USA.
Background: Photoplethysmography (PPG) is routinely used to detect the blood pulse signal from skin tissue beds in clinics. However, the origin of the PPG signal remains controversial. The purpose of this study is to explore optical coherence tomography angiography (OCTA) to indicate pulsatile waveforms in the papillary plexus and dermal plexus separately under different hand elevations.
View Article and Find Full Text PDFJ Biomed Opt
September 2020
University of Washington, Department of Bioengineering, Seattle, Washington, United States.
Significance: Cerebral blood flow (CBF) regulation at neurovascular coupling (NVC) plays an important role in normal brain functioning to support oxygen delivery to activating neurons. Therefore, studying the mechanisms of CBF adjustment is crucial for the improved understanding of brain activity.
Aim: We investigated the temporal profile of hemodynamic signal change in mouse cortex caused by neural activation and its variation over cortical depth.