Cargando…

Myocardial Function in Premenopausal Women Treated With Ovarian Function Suppression and an Aromatase Inhibitor

BACKGROUND: Premenopausal women with high-risk hormone receptor (HR)-positive breast cancer often receive ovarian function suppression (OFS) with aromatase inhibitor therapy; however, abrupt menopause induction, together with further decrements in estrogen exposure through aromatase inhibition, may...

Descripción completa

Detalles Bibliográficos
Autores principales: Jordan, Jennifer H, D’Agostino, Ralph B, Ansley, Katherine, Douglas, Emily, Melin, Susan, Sorscher, Steven, Vasu, Sujethra, Park, Sung, Kotak, Anuj, Romitti, Paul A, O’Connell, Nathanial S, Hundley, William G, Thomas, Alexandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406435/
https://www.ncbi.nlm.nih.gov/pubmed/34476341
http://dx.doi.org/10.1093/jncics/pkab071
_version_ 1783746511636529152
author Jordan, Jennifer H
D’Agostino, Ralph B
Ansley, Katherine
Douglas, Emily
Melin, Susan
Sorscher, Steven
Vasu, Sujethra
Park, Sung
Kotak, Anuj
Romitti, Paul A
O’Connell, Nathanial S
Hundley, William G
Thomas, Alexandra
author_facet Jordan, Jennifer H
D’Agostino, Ralph B
Ansley, Katherine
Douglas, Emily
Melin, Susan
Sorscher, Steven
Vasu, Sujethra
Park, Sung
Kotak, Anuj
Romitti, Paul A
O’Connell, Nathanial S
Hundley, William G
Thomas, Alexandra
author_sort Jordan, Jennifer H
collection PubMed
description BACKGROUND: Premenopausal women with high-risk hormone receptor (HR)-positive breast cancer often receive ovarian function suppression (OFS) with aromatase inhibitor therapy; however, abrupt menopause induction, together with further decrements in estrogen exposure through aromatase inhibition, may affect cardiovascular microcirculatory function. We examined adenosine-induced changes in left ventricular (LV) myocardial T1, a potential subclinical marker of LV microcirculatory function in premenopausal women undergoing treatment for breast cancer. METHODS: Twenty-one premenopausal women (14 with HR-positive breast cancer receiving OFS with an aromatase inhibitor and 7 comparator women with triple-negative breast cancer [TNBC] who had completed primary systemic therapy) underwent serial resting and adenosine cardiovascular magnetic resonance imaging measurements of LV myocardial T1 and LV volumes, mass, and ejection fraction. All statistical tests were 2-sided. RESULTS: After a median of 4.0 months (range = 3.1-5.7 months), the stress to resting ratio of LV myocardial T1 declined in women with HR-positive breast cancer (−1.3%, 95% confidence interval [CI] = −3.4% to 0.7%) relative to those with TNBC (3.2%, 95% CI = −1.2% to 7.6%, P = .02). After accounting for age, LV stroke volume, LV ejection fraction, diastolic blood pressure, and breast cancer subtype women with HR-positive breast cancer experienced a blunted T1 response after adenosine relative to women with TNBC (difference = −4.7%, 95% CI = −7.3% to −2.1%, P(difference) = .002). CONCLUSIONS: Over the brief interval examined, women with HR-positive breast cancer receiving OFS with an aromatase inhibitor experienced reductions in adenosine-associated changes in LV myocardial T1 relative to women who received nonhormonal therapy for TNBC. These findings suggest a possible adverse impact on LV myocardial microcirculatory function in premenopausal women with breast cancer receiving hormone deprivation therapy.
format Online
Article
Text
id pubmed-8406435
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-84064352021-09-01 Myocardial Function in Premenopausal Women Treated With Ovarian Function Suppression and an Aromatase Inhibitor Jordan, Jennifer H D’Agostino, Ralph B Ansley, Katherine Douglas, Emily Melin, Susan Sorscher, Steven Vasu, Sujethra Park, Sung Kotak, Anuj Romitti, Paul A O’Connell, Nathanial S Hundley, William G Thomas, Alexandra JNCI Cancer Spectr Article BACKGROUND: Premenopausal women with high-risk hormone receptor (HR)-positive breast cancer often receive ovarian function suppression (OFS) with aromatase inhibitor therapy; however, abrupt menopause induction, together with further decrements in estrogen exposure through aromatase inhibition, may affect cardiovascular microcirculatory function. We examined adenosine-induced changes in left ventricular (LV) myocardial T1, a potential subclinical marker of LV microcirculatory function in premenopausal women undergoing treatment for breast cancer. METHODS: Twenty-one premenopausal women (14 with HR-positive breast cancer receiving OFS with an aromatase inhibitor and 7 comparator women with triple-negative breast cancer [TNBC] who had completed primary systemic therapy) underwent serial resting and adenosine cardiovascular magnetic resonance imaging measurements of LV myocardial T1 and LV volumes, mass, and ejection fraction. All statistical tests were 2-sided. RESULTS: After a median of 4.0 months (range = 3.1-5.7 months), the stress to resting ratio of LV myocardial T1 declined in women with HR-positive breast cancer (−1.3%, 95% confidence interval [CI] = −3.4% to 0.7%) relative to those with TNBC (3.2%, 95% CI = −1.2% to 7.6%, P = .02). After accounting for age, LV stroke volume, LV ejection fraction, diastolic blood pressure, and breast cancer subtype women with HR-positive breast cancer experienced a blunted T1 response after adenosine relative to women with TNBC (difference = −4.7%, 95% CI = −7.3% to −2.1%, P(difference) = .002). CONCLUSIONS: Over the brief interval examined, women with HR-positive breast cancer receiving OFS with an aromatase inhibitor experienced reductions in adenosine-associated changes in LV myocardial T1 relative to women who received nonhormonal therapy for TNBC. These findings suggest a possible adverse impact on LV myocardial microcirculatory function in premenopausal women with breast cancer receiving hormone deprivation therapy. Oxford University Press 2021-07-26 /pmc/articles/PMC8406435/ /pubmed/34476341 http://dx.doi.org/10.1093/jncics/pkab071 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Article
Jordan, Jennifer H
D’Agostino, Ralph B
Ansley, Katherine
Douglas, Emily
Melin, Susan
Sorscher, Steven
Vasu, Sujethra
Park, Sung
Kotak, Anuj
Romitti, Paul A
O’Connell, Nathanial S
Hundley, William G
Thomas, Alexandra
Myocardial Function in Premenopausal Women Treated With Ovarian Function Suppression and an Aromatase Inhibitor
title Myocardial Function in Premenopausal Women Treated With Ovarian Function Suppression and an Aromatase Inhibitor
title_full Myocardial Function in Premenopausal Women Treated With Ovarian Function Suppression and an Aromatase Inhibitor
title_fullStr Myocardial Function in Premenopausal Women Treated With Ovarian Function Suppression and an Aromatase Inhibitor
title_full_unstemmed Myocardial Function in Premenopausal Women Treated With Ovarian Function Suppression and an Aromatase Inhibitor
title_short Myocardial Function in Premenopausal Women Treated With Ovarian Function Suppression and an Aromatase Inhibitor
title_sort myocardial function in premenopausal women treated with ovarian function suppression and an aromatase inhibitor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406435/
https://www.ncbi.nlm.nih.gov/pubmed/34476341
http://dx.doi.org/10.1093/jncics/pkab071
work_keys_str_mv AT jordanjenniferh myocardialfunctioninpremenopausalwomentreatedwithovarianfunctionsuppressionandanaromataseinhibitor
AT dagostinoralphb myocardialfunctioninpremenopausalwomentreatedwithovarianfunctionsuppressionandanaromataseinhibitor
AT ansleykatherine myocardialfunctioninpremenopausalwomentreatedwithovarianfunctionsuppressionandanaromataseinhibitor
AT douglasemily myocardialfunctioninpremenopausalwomentreatedwithovarianfunctionsuppressionandanaromataseinhibitor
AT melinsusan myocardialfunctioninpremenopausalwomentreatedwithovarianfunctionsuppressionandanaromataseinhibitor
AT sorschersteven myocardialfunctioninpremenopausalwomentreatedwithovarianfunctionsuppressionandanaromataseinhibitor
AT vasusujethra myocardialfunctioninpremenopausalwomentreatedwithovarianfunctionsuppressionandanaromataseinhibitor
AT parksung myocardialfunctioninpremenopausalwomentreatedwithovarianfunctionsuppressionandanaromataseinhibitor
AT kotakanuj myocardialfunctioninpremenopausalwomentreatedwithovarianfunctionsuppressionandanaromataseinhibitor
AT romittipaula myocardialfunctioninpremenopausalwomentreatedwithovarianfunctionsuppressionandanaromataseinhibitor
AT oconnellnathanials myocardialfunctioninpremenopausalwomentreatedwithovarianfunctionsuppressionandanaromataseinhibitor
AT hundleywilliamg myocardialfunctioninpremenopausalwomentreatedwithovarianfunctionsuppressionandanaromataseinhibitor
AT thomasalexandra myocardialfunctioninpremenopausalwomentreatedwithovarianfunctionsuppressionandanaromataseinhibitor