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Lower endothelium-dependent microvascular function in adult breast cancer patients receiving radiation therapy
PURPOSE: Cancer patients with a history of radiotherapy are at an increased risk of ischemic heart disease. Preclinical animal studies demonstrate markedly impaired acetylcholine (ACh)-mediated endothelium-dependent vasorelaxation within days to weeks post-irradiation, however, whether microvascular...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117502/ https://www.ncbi.nlm.nih.gov/pubmed/33985593 http://dx.doi.org/10.1186/s40959-021-00104-z |
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author | Banister, Heather R. Hammond, Stephen T. Parr, Shannon K. Sutterfield, Shelbi L. Turpin, Vanessa-Rose G. Treinen, Scott Bell, Martin J. Ade, Carl J. |
author_facet | Banister, Heather R. Hammond, Stephen T. Parr, Shannon K. Sutterfield, Shelbi L. Turpin, Vanessa-Rose G. Treinen, Scott Bell, Martin J. Ade, Carl J. |
author_sort | Banister, Heather R. |
collection | PubMed |
description | PURPOSE: Cancer patients with a history of radiotherapy are at an increased risk of ischemic heart disease. Preclinical animal studies demonstrate markedly impaired acetylcholine (ACh)-mediated endothelium-dependent vasorelaxation within days to weeks post-irradiation, however, whether microvascular function is affected in the intact human circulation during cancer radiation therapy has yet to be determined. MATERIALS AND METHODS: Using laser-Doppler flowmetry, microvascular endothelium-dependent and independent responses were evaluated through iontophoresis of acetylcholine (ACh) (part 1, n = 7) and sodium nitroprusside (SNP) (part 2, n = 8), respectively, in women currently receiving unilateral chest adjuvant radiation therapy for breast cancer. Measurements were performed at the site of radiation treatment and at a contralateral control, non-radiated site. Cutaneous vascular conductance (CVC) was calculated by normalizing for mean arterial pressure. RESULTS AND CONCULSIONS: In part 1, patients received an average radiation dose of 2104 ± 236 cGy. A significantly lower peak ACh-mediated endothelium-dependent vasodilation was observed within the radiated microvasculature when compared to non-radiated (radiated: 532 ± 167%, non-radiated 1029 ± 263%; P = 0.02). In part 2, the average radiation dose received was 2251 ± 196 cGy. Iontophoresis of SNP elicited a similar peak endothelium-independent vasodilator response in radiated and non-radiated tissue (radiated: 179 ± 58%, non-radiated: 310 ± 158; P = 0.2). The time to 50% of the peak response for ACh and SNP was similar between radiated and non-radiated microvasculature (P < 0.05). These data provide evidence of early endothelium-dependent microvascular dysfunction in cancer patients currently receiving chest radiation and provide the scientific premise for future work evaluating coronary endothelial function and vasomotor reactivity using more detailed and invasive procedures. |
format | Online Article Text |
id | pubmed-8117502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81175022021-05-13 Lower endothelium-dependent microvascular function in adult breast cancer patients receiving radiation therapy Banister, Heather R. Hammond, Stephen T. Parr, Shannon K. Sutterfield, Shelbi L. Turpin, Vanessa-Rose G. Treinen, Scott Bell, Martin J. Ade, Carl J. Cardiooncology Research PURPOSE: Cancer patients with a history of radiotherapy are at an increased risk of ischemic heart disease. Preclinical animal studies demonstrate markedly impaired acetylcholine (ACh)-mediated endothelium-dependent vasorelaxation within days to weeks post-irradiation, however, whether microvascular function is affected in the intact human circulation during cancer radiation therapy has yet to be determined. MATERIALS AND METHODS: Using laser-Doppler flowmetry, microvascular endothelium-dependent and independent responses were evaluated through iontophoresis of acetylcholine (ACh) (part 1, n = 7) and sodium nitroprusside (SNP) (part 2, n = 8), respectively, in women currently receiving unilateral chest adjuvant radiation therapy for breast cancer. Measurements were performed at the site of radiation treatment and at a contralateral control, non-radiated site. Cutaneous vascular conductance (CVC) was calculated by normalizing for mean arterial pressure. RESULTS AND CONCULSIONS: In part 1, patients received an average radiation dose of 2104 ± 236 cGy. A significantly lower peak ACh-mediated endothelium-dependent vasodilation was observed within the radiated microvasculature when compared to non-radiated (radiated: 532 ± 167%, non-radiated 1029 ± 263%; P = 0.02). In part 2, the average radiation dose received was 2251 ± 196 cGy. Iontophoresis of SNP elicited a similar peak endothelium-independent vasodilator response in radiated and non-radiated tissue (radiated: 179 ± 58%, non-radiated: 310 ± 158; P = 0.2). The time to 50% of the peak response for ACh and SNP was similar between radiated and non-radiated microvasculature (P < 0.05). These data provide evidence of early endothelium-dependent microvascular dysfunction in cancer patients currently receiving chest radiation and provide the scientific premise for future work evaluating coronary endothelial function and vasomotor reactivity using more detailed and invasive procedures. BioMed Central 2021-05-13 /pmc/articles/PMC8117502/ /pubmed/33985593 http://dx.doi.org/10.1186/s40959-021-00104-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Banister, Heather R. Hammond, Stephen T. Parr, Shannon K. Sutterfield, Shelbi L. Turpin, Vanessa-Rose G. Treinen, Scott Bell, Martin J. Ade, Carl J. Lower endothelium-dependent microvascular function in adult breast cancer patients receiving radiation therapy |
title | Lower endothelium-dependent microvascular function in adult breast cancer patients receiving radiation therapy |
title_full | Lower endothelium-dependent microvascular function in adult breast cancer patients receiving radiation therapy |
title_fullStr | Lower endothelium-dependent microvascular function in adult breast cancer patients receiving radiation therapy |
title_full_unstemmed | Lower endothelium-dependent microvascular function in adult breast cancer patients receiving radiation therapy |
title_short | Lower endothelium-dependent microvascular function in adult breast cancer patients receiving radiation therapy |
title_sort | lower endothelium-dependent microvascular function in adult breast cancer patients receiving radiation therapy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117502/ https://www.ncbi.nlm.nih.gov/pubmed/33985593 http://dx.doi.org/10.1186/s40959-021-00104-z |
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