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Ageing effect on flicker‐induced diameter changes in retinal microvessels of healthy individuals

PURPOSE: To compare flicker‐induced retinal vessel diameter changes in varying age groups with low cardiovascular risk. METHODS: Retinal vascular reactivity to flicker light was assessed by means of dynamic retinal vessel analysis in 57 participants aged 19–30 years, 75 participants aged 31–50 years...

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Detalles Bibliográficos
Autores principales: Seshadri, Swathi, Ekart, Aniko, Gherghel, Doina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5034828/
https://www.ncbi.nlm.nih.gov/pubmed/26149453
http://dx.doi.org/10.1111/aos.12786
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author Seshadri, Swathi
Ekart, Aniko
Gherghel, Doina
author_facet Seshadri, Swathi
Ekart, Aniko
Gherghel, Doina
author_sort Seshadri, Swathi
collection PubMed
description PURPOSE: To compare flicker‐induced retinal vessel diameter changes in varying age groups with low cardiovascular risk. METHODS: Retinal vascular reactivity to flicker light was assessed by means of dynamic retinal vessel analysis in 57 participants aged 19–30 years, 75 participants aged 31–50 years and 62 participants aged 51–70 years participants. Other assessments included carotid intima–media thickness (c‐IMT), augmentation index (AIx), blood pressure profiles, blood lipid metabolism markers and Framingham risk scores (FRS). RESULTS: Retinal arterial dilation amplitude (DA) and postflicker percentage constriction (MC%) were significantly decreased in the oldest group compared to the middle‐aged (p = 0.028; p = 0.021) and youngest group (p = 0.003; p = 0.026). The arterial constriction slope (Slope(AC)) was also decreased in the oldest group compared to the youngest group (p = 0.027). On the venous side, MC% was decreased in the middle‐aged and oldest groups in comparison with the youngest group (p = 0.015; p = 0.010, respectively). Additionally, men exhibited increased arterial DA (p = 0.007), and percentage dilation (MD%, p < 0.001) in comparison with women, but only in the youngest age group. Both AIx and c‐IMT scores increased with age (both p < 0.001); however, no correlations were found between the observed differences in the measured retinal vascular function and systemic parameters. CONCLUSION: In individuals with low cardiovascular risk, there are age‐related differences in flicker‐induced retinal vessel diameter changes throughout the entire functional response curve for arteries and veins. Gender differences mainly affect the arterial dilatory phase and are only present in young individuals.
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spelling pubmed-50348282016-10-03 Ageing effect on flicker‐induced diameter changes in retinal microvessels of healthy individuals Seshadri, Swathi Ekart, Aniko Gherghel, Doina Acta Ophthalmol Original Articles PURPOSE: To compare flicker‐induced retinal vessel diameter changes in varying age groups with low cardiovascular risk. METHODS: Retinal vascular reactivity to flicker light was assessed by means of dynamic retinal vessel analysis in 57 participants aged 19–30 years, 75 participants aged 31–50 years and 62 participants aged 51–70 years participants. Other assessments included carotid intima–media thickness (c‐IMT), augmentation index (AIx), blood pressure profiles, blood lipid metabolism markers and Framingham risk scores (FRS). RESULTS: Retinal arterial dilation amplitude (DA) and postflicker percentage constriction (MC%) were significantly decreased in the oldest group compared to the middle‐aged (p = 0.028; p = 0.021) and youngest group (p = 0.003; p = 0.026). The arterial constriction slope (Slope(AC)) was also decreased in the oldest group compared to the youngest group (p = 0.027). On the venous side, MC% was decreased in the middle‐aged and oldest groups in comparison with the youngest group (p = 0.015; p = 0.010, respectively). Additionally, men exhibited increased arterial DA (p = 0.007), and percentage dilation (MD%, p < 0.001) in comparison with women, but only in the youngest age group. Both AIx and c‐IMT scores increased with age (both p < 0.001); however, no correlations were found between the observed differences in the measured retinal vascular function and systemic parameters. CONCLUSION: In individuals with low cardiovascular risk, there are age‐related differences in flicker‐induced retinal vessel diameter changes throughout the entire functional response curve for arteries and veins. Gender differences mainly affect the arterial dilatory phase and are only present in young individuals. John Wiley and Sons Inc. 2015-07-06 2016-02 /pmc/articles/PMC5034828/ /pubmed/26149453 http://dx.doi.org/10.1111/aos.12786 Text en © 2015 The Authors. Acta Ophthalmologica published by John Wiley & Sons Ltd on behalf of Acta Ophthalmologica Scandinavica Foundation. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Seshadri, Swathi
Ekart, Aniko
Gherghel, Doina
Ageing effect on flicker‐induced diameter changes in retinal microvessels of healthy individuals
title Ageing effect on flicker‐induced diameter changes in retinal microvessels of healthy individuals
title_full Ageing effect on flicker‐induced diameter changes in retinal microvessels of healthy individuals
title_fullStr Ageing effect on flicker‐induced diameter changes in retinal microvessels of healthy individuals
title_full_unstemmed Ageing effect on flicker‐induced diameter changes in retinal microvessels of healthy individuals
title_short Ageing effect on flicker‐induced diameter changes in retinal microvessels of healthy individuals
title_sort ageing effect on flicker‐induced diameter changes in retinal microvessels of healthy individuals
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5034828/
https://www.ncbi.nlm.nih.gov/pubmed/26149453
http://dx.doi.org/10.1111/aos.12786
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