Journal article
Aortic stiffness is associated with changes in retinal arteriole flow pulsatility mediated by local vasodilation in healthy young/middle-age adults
Journal of applied physiology (1985), Vol.129(1), pp.84-93
07/01/2020
DOI: 10.1152/japplphysiol.00252.2020
PMID: 32437246
Abstract
By using the human retinal microvasculature as an end-organ in vivo model, we confirm that aortic stiffness and related increases in central pulse pressure are inversely correlated with retinal arteriole lumen diameter and increased microvascular resistance among heathy young/middle-age adults. Additionally, higher aortic stiffness is not associated with excessive flow pulsatility in the retinal microvasculature under tonic conditions but may be related to limited reductions in retinal arteriole flow pulsatility in response to local vasodilation.
Aortic stiffness is associated with augmented pressure pulsatility in large conduit arteries and remodeling of the microcirculation. However, studies in humans examining the relation between aortic stiffness and end-organ microvascular flow pulsatility are limited. Therefore, we used the retinal microvasculature as an end-organ in vivo model to examine the hypothesis that aortic stiffness would be positively associated with microvascular flow pulsatility index (PI) (flow pulse amplitude/mean flow) in humans. In 40 young/middle-age healthy adults (25–60 yr old, 50% women), aortic stiffness (carotid-femoral pulse wave velocity, CFPWV) and retinal arteriole flow (laser speckle flowgraphy) were examined at rest and during metabolic vasodilation (light flicker). CFPWV and related increases in central pulse pressure (PP) were inversely correlated with arteriole lumen diameter independent of age (CFPWV: R = −0.52, P = 0.001; Central PP: R = −0.39, P = 0.014). Accordingly, microvascular resistance was positively related to CFPWV independent of age ( R = 0.35, P = 0.031). Multiple linear regression showed that CFPWV was not a significant determinant of resting arteriole flow PI (β = −0.10, P = 0.64). However, during reduced retinal microvascular resistance using light flicker ( P < 0.001), CFPWV was a significant determinant of the percent change in arteriole flow PI (β = 0.58, P = 0.046), but not mean flow (β = −0.17, P = 0.54), where reductions in arteriole flow PI were associated with lower CFPWV. In summary, our findings suggest that higher aortic stiffness and the related increase in central PP in healthy young/middle-age adults are associated with retinal arteriole narrowing and smaller reductions in arteriole flow pulsatility in response to dynamic conditions such as local metabolic vasodilation. NEW & NOTEWORTHY By using the human retinal microvasculature as an end-organ in vivo model, we confirm that aortic stiffness and related increases in central pulse pressure are inversely correlated with retinal arteriole lumen diameter and increased microvascular resistance among heathy young/middle-age adults. Additionally, higher aortic stiffness is not associated with excessive flow pulsatility in the retinal microvasculature under tonic conditions but may be related to limited reductions in retinal arteriole flow pulsatility in response to local vasodilation.
Details
- Title: Subtitle
- Aortic stiffness is associated with changes in retinal arteriole flow pulsatility mediated by local vasodilation in healthy young/middle-age adults
- Creators
- Seth W Holwerda - Department of Health and Human Physiology, University of Iowa, Iowa City, Iowa, Abboud Cardiovascular Research Center, University of Iowa, Iowa City, Iowa, Department of Anesthesiology, University of Kansas Medical Center, Kansas City, KansasRandy H Kardon - Iowa City Veterans Affairs Center for Prevention and Treatment of Visual Loss, Iowa City, Iowa, Department of Veteran Affairs Hospital Iowa City, Iowa City, Iowa, Department of Ophthalmology and Visual Sciences, University of Iowa, Iowa City, IowaRyuya Hashimoto - Department of Ophthalmology and Visual Sciences, University of Iowa, Iowa City, IowaJan M Full - Department of Ophthalmology and Visual Sciences, University of Iowa, Iowa City, IowaJulie K Nellis - Department of Ophthalmology and Visual Sciences, University of Iowa, Iowa City, IowaLyndsey E DuBose - Division of Geriatric Medicine, University of Colorado Anschutz Medical Campus, Aurora, ColoradoJess G Fiedorowicz - Abboud Cardiovascular Research Center, University of Iowa, Iowa City, Iowa, Department of Psychiatry, University of Iowa, Iowa City, Iowa, Department of Epidemiology, University of Iowa, Iowa City, Iowa, Department of Internal Medicine, University of Iowa, Iowa City, IowaGary L Pierce - Department of Health and Human Physiology, University of Iowa, Iowa City, Iowa, Abboud Cardiovascular Research Center, University of Iowa, Iowa City, Iowa
- Resource Type
- Journal article
- Publication Details
- Journal of applied physiology (1985), Vol.129(1), pp.84-93
- DOI
- 10.1152/japplphysiol.00252.2020
- PMID
- 32437246
- NLM abbreviation
- J Appl Physiol (1985)
- ISSN
- 8750-7587
- eISSN
- 1522-1601
- Grant note
- DOI: 10.13039/100000968, name: American Heart Association, award: 17POST33440101, 13SDG143400012; DOI: 10.13039/100000050, name: HHS | NIH | National Heart, Lung, and Blood Institute, award: T32 HL07121; DOI: 10.13039/100008893, name: University of Iowa, award: U54 TR001356; name: Iowa City VA Center for the Prevention and Treatment of Visual Loss, award: C9251-c (RX003002)
- Language
- English
- Date published
- 07/01/2020
- Academic Unit
- Psychiatry; Epidemiology; Iowa Neuroscience Institute; Health, Sport, and Human Physiology ; Internal Medicine; Ophthalmology and Visual Sciences
- Record Identifier
- 9984070214102771
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