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Visualising and quantifying microvascular structure and function in patients with heart failure using optical coherence tomography

ABSTRACT: Heart failure (HF) is characterised by abnormal conduit and resistance artery function in humans. Microvascular function in HF is less well characterised, due in part to the lack of tools to image these vessels in vivo. The skin microvasculature is a surrogate for systemic microvascular fu...

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Autores principales: Sciarrone, David F. G., McLaughlin, Robert A., Argarini, Raden, To, Minh‐Son, Naylor, Louise H., Bolam, Lucy M., Carter, Howard H., Green, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541462/
https://www.ncbi.nlm.nih.gov/pubmed/35869823
http://dx.doi.org/10.1113/JP282940
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author Sciarrone, David F. G.
McLaughlin, Robert A.
Argarini, Raden
To, Minh‐Son
Naylor, Louise H.
Bolam, Lucy M.
Carter, Howard H.
Green, Daniel J.
author_facet Sciarrone, David F. G.
McLaughlin, Robert A.
Argarini, Raden
To, Minh‐Son
Naylor, Louise H.
Bolam, Lucy M.
Carter, Howard H.
Green, Daniel J.
author_sort Sciarrone, David F. G.
collection PubMed
description ABSTRACT: Heart failure (HF) is characterised by abnormal conduit and resistance artery function in humans. Microvascular function in HF is less well characterised, due in part to the lack of tools to image these vessels in vivo. The skin microvasculature is a surrogate for systemic microvascular function and health and plays a key role in thermoregulation, which is dysfunctional in HF. We deployed a novel optical coherence tomography (OCT) technique to visualise and quantify microvascular structure and function in 10 subjects with HF and 10 age‐ and sex‐matched controls. OCT images were obtained from the ventral aspect of the forearm, at baseline (33°C) and after 30 min of localised skin heating. At rest, OCT‐derived microvascular density (20.3 ± 8.7%, P = 0.004), diameter (35.1 ± 6.0 μm, P = 0.006) and blood flow (82.9 ± 41.1 pl/s, P = 0.021) were significantly lower in HF than CON (27.2 ± 8.0%, 40.4 ± 5.8 μm, 110.8 ± 41.9 pl/s), whilst blood speed was not significantly lower (74.3 ± 11.0 μm/s vs. 81.3 ± 9.9 μm/s, P = 0.069). After local heating, the OCT‐based density, diameter, blood speed and blood flow of HF patients were similar (all P > 0.05) to CON. Although abnormalities exist at rest which may reflect microvascular disease status, patients with HF retain the capacity to dilate cutaneous microvessels in response to localised heat stress. This is a novel in vivo human observation of microvascular dysfunction in HF, illustrating the feasibility of OCT to directly visualise and quantify microvascular responses to physiological stimuli in vivo. [Image: see text] KEY POINTS: Microvessels in the skin are critical to human thermoregulation, which is compromised in participants with heart failure (HF). We have developed a powerful new non‐invasive optical coherence tomography (OCT)‐based approach for the study of microvascular structure and function in vivo. Our approach enabled us to observe and quantify abnormal resting microvascular function in participants with HF. Patients with HF were able to dilate skin microvessels in response to local heat stress, arguing against an underlying structural abnormality. This suggests that microvascular functional regulation is the primary abnormality in HF. OCT can be used to directly visualise and quantify microvascular responses to physiological stimuli in vivo.
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spelling pubmed-95414622022-10-14 Visualising and quantifying microvascular structure and function in patients with heart failure using optical coherence tomography Sciarrone, David F. G. McLaughlin, Robert A. Argarini, Raden To, Minh‐Son Naylor, Louise H. Bolam, Lucy M. Carter, Howard H. Green, Daniel J. J Physiol Techniques for Physiology ABSTRACT: Heart failure (HF) is characterised by abnormal conduit and resistance artery function in humans. Microvascular function in HF is less well characterised, due in part to the lack of tools to image these vessels in vivo. The skin microvasculature is a surrogate for systemic microvascular function and health and plays a key role in thermoregulation, which is dysfunctional in HF. We deployed a novel optical coherence tomography (OCT) technique to visualise and quantify microvascular structure and function in 10 subjects with HF and 10 age‐ and sex‐matched controls. OCT images were obtained from the ventral aspect of the forearm, at baseline (33°C) and after 30 min of localised skin heating. At rest, OCT‐derived microvascular density (20.3 ± 8.7%, P = 0.004), diameter (35.1 ± 6.0 μm, P = 0.006) and blood flow (82.9 ± 41.1 pl/s, P = 0.021) were significantly lower in HF than CON (27.2 ± 8.0%, 40.4 ± 5.8 μm, 110.8 ± 41.9 pl/s), whilst blood speed was not significantly lower (74.3 ± 11.0 μm/s vs. 81.3 ± 9.9 μm/s, P = 0.069). After local heating, the OCT‐based density, diameter, blood speed and blood flow of HF patients were similar (all P > 0.05) to CON. Although abnormalities exist at rest which may reflect microvascular disease status, patients with HF retain the capacity to dilate cutaneous microvessels in response to localised heat stress. This is a novel in vivo human observation of microvascular dysfunction in HF, illustrating the feasibility of OCT to directly visualise and quantify microvascular responses to physiological stimuli in vivo. [Image: see text] KEY POINTS: Microvessels in the skin are critical to human thermoregulation, which is compromised in participants with heart failure (HF). We have developed a powerful new non‐invasive optical coherence tomography (OCT)‐based approach for the study of microvascular structure and function in vivo. Our approach enabled us to observe and quantify abnormal resting microvascular function in participants with HF. Patients with HF were able to dilate skin microvessels in response to local heat stress, arguing against an underlying structural abnormality. This suggests that microvascular functional regulation is the primary abnormality in HF. OCT can be used to directly visualise and quantify microvascular responses to physiological stimuli in vivo. John Wiley and Sons Inc. 2022-08-10 2022-09-01 /pmc/articles/PMC9541462/ /pubmed/35869823 http://dx.doi.org/10.1113/JP282940 Text en © 2022 The Authors. The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://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 Techniques for Physiology
Sciarrone, David F. G.
McLaughlin, Robert A.
Argarini, Raden
To, Minh‐Son
Naylor, Louise H.
Bolam, Lucy M.
Carter, Howard H.
Green, Daniel J.
Visualising and quantifying microvascular structure and function in patients with heart failure using optical coherence tomography
title Visualising and quantifying microvascular structure and function in patients with heart failure using optical coherence tomography
title_full Visualising and quantifying microvascular structure and function in patients with heart failure using optical coherence tomography
title_fullStr Visualising and quantifying microvascular structure and function in patients with heart failure using optical coherence tomography
title_full_unstemmed Visualising and quantifying microvascular structure and function in patients with heart failure using optical coherence tomography
title_short Visualising and quantifying microvascular structure and function in patients with heart failure using optical coherence tomography
title_sort visualising and quantifying microvascular structure and function in patients with heart failure using optical coherence tomography
topic Techniques for Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541462/
https://www.ncbi.nlm.nih.gov/pubmed/35869823
http://dx.doi.org/10.1113/JP282940
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