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The effect of exercise training on endothelial function in postmenopausal women with breast cancer under aromatase inhibitor therapy

BACKGROUND: Breast cancer is the leading non‐cardiovascular cause of death in women. In endocrine receptor positive women, aromatase inhibitors (AI) are the therapy of choice despite the fact that a decrease in systemic estrogen levels may result in endothelial dysfunction and eventually in cardiova...

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Autores principales: Mayr, Barbara, Reich, Bernhard, Greil, Richard, Niebauer, Josef
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/PMC9761059/
https://www.ncbi.nlm.nih.gov/pubmed/35585836
http://dx.doi.org/10.1002/cam4.4833
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author Mayr, Barbara
Reich, Bernhard
Greil, Richard
Niebauer, Josef
author_facet Mayr, Barbara
Reich, Bernhard
Greil, Richard
Niebauer, Josef
author_sort Mayr, Barbara
collection PubMed
description BACKGROUND: Breast cancer is the leading non‐cardiovascular cause of death in women. In endocrine receptor positive women, aromatase inhibitors (AI) are the therapy of choice despite the fact that a decrease in systemic estrogen levels may result in endothelial dysfunction and eventually in cardiovascular disease. In this study, we assessed whether exercise training (ET), which has repeatedly shown to lead to an improvement of endothelial dysfunction, will also exert this effect in postmenopausal women with AI treated breast cancer. METHODS: Thirty two postmenopausal women with AI treated breast cancer were randomized to an intervention group (ET; 6 months, supervised training plus 6 months without intervention) or control group of usual care (UC; 12 months without intervention plus initial exercise counseling). Endothelial function was assessed via Reactive Hyperemia Index (RHI) measured non‐invasively with the EndoPAT‐System at baseline, 6 and 12 months. RESULTS: After 6 months of supervised ET, changes in maximal exercise capacity were significantly greater in ET than in UC (∆W: 24.1 ± 11.5 vs. 1.1 ± 8.2 watts; p < 0.001). Even though 43.8% of all participants had endothelial dysfunction at baseline, there were no significant group differences in the changes of RHI between ET (∆RHI: −0.1 ± 1.04) and UC (0.02 ± 0.75; p = 0.323) after 6 months. CONCLUSION: Even though ET led to significantly greater improvement in exercise capacity in postmenopausal women with AI treated breast cancer than exercise counseling only, it did not exert any measurable effects on endothelial dysfunction.
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spelling pubmed-97610592022-12-20 The effect of exercise training on endothelial function in postmenopausal women with breast cancer under aromatase inhibitor therapy Mayr, Barbara Reich, Bernhard Greil, Richard Niebauer, Josef Cancer Med RESEARCH ARTICLES BACKGROUND: Breast cancer is the leading non‐cardiovascular cause of death in women. In endocrine receptor positive women, aromatase inhibitors (AI) are the therapy of choice despite the fact that a decrease in systemic estrogen levels may result in endothelial dysfunction and eventually in cardiovascular disease. In this study, we assessed whether exercise training (ET), which has repeatedly shown to lead to an improvement of endothelial dysfunction, will also exert this effect in postmenopausal women with AI treated breast cancer. METHODS: Thirty two postmenopausal women with AI treated breast cancer were randomized to an intervention group (ET; 6 months, supervised training plus 6 months without intervention) or control group of usual care (UC; 12 months without intervention plus initial exercise counseling). Endothelial function was assessed via Reactive Hyperemia Index (RHI) measured non‐invasively with the EndoPAT‐System at baseline, 6 and 12 months. RESULTS: After 6 months of supervised ET, changes in maximal exercise capacity were significantly greater in ET than in UC (∆W: 24.1 ± 11.5 vs. 1.1 ± 8.2 watts; p < 0.001). Even though 43.8% of all participants had endothelial dysfunction at baseline, there were no significant group differences in the changes of RHI between ET (∆RHI: −0.1 ± 1.04) and UC (0.02 ± 0.75; p = 0.323) after 6 months. CONCLUSION: Even though ET led to significantly greater improvement in exercise capacity in postmenopausal women with AI treated breast cancer than exercise counseling only, it did not exert any measurable effects on endothelial dysfunction. John Wiley and Sons Inc. 2022-05-18 /pmc/articles/PMC9761059/ /pubmed/35585836 http://dx.doi.org/10.1002/cam4.4833 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Mayr, Barbara
Reich, Bernhard
Greil, Richard
Niebauer, Josef
The effect of exercise training on endothelial function in postmenopausal women with breast cancer under aromatase inhibitor therapy
title The effect of exercise training on endothelial function in postmenopausal women with breast cancer under aromatase inhibitor therapy
title_full The effect of exercise training on endothelial function in postmenopausal women with breast cancer under aromatase inhibitor therapy
title_fullStr The effect of exercise training on endothelial function in postmenopausal women with breast cancer under aromatase inhibitor therapy
title_full_unstemmed The effect of exercise training on endothelial function in postmenopausal women with breast cancer under aromatase inhibitor therapy
title_short The effect of exercise training on endothelial function in postmenopausal women with breast cancer under aromatase inhibitor therapy
title_sort effect of exercise training on endothelial function in postmenopausal women with breast cancer under aromatase inhibitor therapy
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761059/
https://www.ncbi.nlm.nih.gov/pubmed/35585836
http://dx.doi.org/10.1002/cam4.4833
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