N-Terminal Pro Brain Natriuretic Peptide, sST2, and Galectin-3 Levels in Breast Cancer Survivors
NT-proBNP, soluble ST2 (sST2), and galectin-3 are biomarkers of cardiac dysfunction that have been proposed as identifiers of patients experiencing asymptomatic cardiac dysfunction after anthracycline-based chemotherapy. This study aimed to compare the proportion of breast cancer (BC) survivors with...
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doaj-4b92e43644c44ff4b61bde5e3f603a292021-08-06T15:26:46ZengMDPI AGJournal of Clinical Medicine2077-03832021-07-01103313331310.3390/jcm10153313N-Terminal Pro Brain Natriuretic Peptide, sST2, and Galectin-3 Levels in Breast Cancer SurvivorsShruti Rajesh Patel0Joerg Herrmann1Robert A. Vierkant2Janet E. Olson3Fergus J. Couch4Antonious Hazim5Jeff A. Sloan6Charles L. Loprinzi7Kathryn J. Ruddy8Department of Internal Medicine, Mayo Clinic, Rochester, MN 55901, USADepartment of Cardiovascular Disease, Mayo Clinic, Rochester, MN 55901, USAHealth Sciences Research, Mayo Clinic, Rochester, MN 55901, USAHealth Sciences Research, Mayo Clinic, Rochester, MN 55901, USADepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55901, USADepartment of Internal Medicine, Mayo Clinic, Rochester, MN 55901, USAHealth Sciences Research, Mayo Clinic, Rochester, MN 55901, USADepartment of Oncology, Mayo Clinic, Rochester, MN 55901, USADepartment of Oncology, Mayo Clinic, Rochester, MN 55901, USANT-proBNP, soluble ST2 (sST2), and galectin-3 are biomarkers of cardiac dysfunction that have been proposed as identifiers of patients experiencing asymptomatic cardiac dysfunction after anthracycline-based chemotherapy. This study aimed to compare the proportion of breast cancer (BC) survivors with elevated serum levels of these three putative biomarkers by prior receipt of anthracycline (yes vs. no). Five-hundred-eighty survivors of BC who had received anthracycline-based chemotherapy were matched by age and time between diagnosis and serum storage to 580 who had not. Cardiac biomarker levels were analyzed using immunoassays. Analyses were carried out using linear and logistic regression models. Anthracycline recipients had higher values of NT-proBNP than non-recipients (mean 116.0 ng/L vs. 97.0 ng/L, respectively; <i>p</i> < 0.001). Values for ST2 and galectin-3 did not significantly differ by receipt of anthracycline. After further adjustment for age at breast cancer diagnosis, ethnicity, and receipt of trastuzumab, associations between receipt of anthracycline and higher NT-proBNP persisted (<i>p</i> < 0.001), showing that NT-proBNP may be a biomarker of cardiovascular toxicity after receipt of anthracycline-based chemotherapy. Further research to assess the clinical utility of NT-proBNP testing after receipt of anthracycline is recommended. sST2 and galectin-3 do not appear to differentiate between anthracycline recipients and non-recipients amongst breast cancer survivors.https://www.mdpi.com/2077-0383/10/15/3313breast canceranthracycline toxicitycardio-oncology |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shruti Rajesh Patel Joerg Herrmann Robert A. Vierkant Janet E. Olson Fergus J. Couch Antonious Hazim Jeff A. Sloan Charles L. Loprinzi Kathryn J. Ruddy |
spellingShingle |
Shruti Rajesh Patel Joerg Herrmann Robert A. Vierkant Janet E. Olson Fergus J. Couch Antonious Hazim Jeff A. Sloan Charles L. Loprinzi Kathryn J. Ruddy N-Terminal Pro Brain Natriuretic Peptide, sST2, and Galectin-3 Levels in Breast Cancer Survivors Journal of Clinical Medicine breast cancer anthracycline toxicity cardio-oncology |
author_facet |
Shruti Rajesh Patel Joerg Herrmann Robert A. Vierkant Janet E. Olson Fergus J. Couch Antonious Hazim Jeff A. Sloan Charles L. Loprinzi Kathryn J. Ruddy |
author_sort |
Shruti Rajesh Patel |
title |
N-Terminal Pro Brain Natriuretic Peptide, sST2, and Galectin-3 Levels in Breast Cancer Survivors |
title_short |
N-Terminal Pro Brain Natriuretic Peptide, sST2, and Galectin-3 Levels in Breast Cancer Survivors |
title_full |
N-Terminal Pro Brain Natriuretic Peptide, sST2, and Galectin-3 Levels in Breast Cancer Survivors |
title_fullStr |
N-Terminal Pro Brain Natriuretic Peptide, sST2, and Galectin-3 Levels in Breast Cancer Survivors |
title_full_unstemmed |
N-Terminal Pro Brain Natriuretic Peptide, sST2, and Galectin-3 Levels in Breast Cancer Survivors |
title_sort |
n-terminal pro brain natriuretic peptide, sst2, and galectin-3 levels in breast cancer survivors |
publisher |
MDPI AG |
series |
Journal of Clinical Medicine |
issn |
2077-0383 |
publishDate |
2021-07-01 |
description |
NT-proBNP, soluble ST2 (sST2), and galectin-3 are biomarkers of cardiac dysfunction that have been proposed as identifiers of patients experiencing asymptomatic cardiac dysfunction after anthracycline-based chemotherapy. This study aimed to compare the proportion of breast cancer (BC) survivors with elevated serum levels of these three putative biomarkers by prior receipt of anthracycline (yes vs. no). Five-hundred-eighty survivors of BC who had received anthracycline-based chemotherapy were matched by age and time between diagnosis and serum storage to 580 who had not. Cardiac biomarker levels were analyzed using immunoassays. Analyses were carried out using linear and logistic regression models. Anthracycline recipients had higher values of NT-proBNP than non-recipients (mean 116.0 ng/L vs. 97.0 ng/L, respectively; <i>p</i> < 0.001). Values for ST2 and galectin-3 did not significantly differ by receipt of anthracycline. After further adjustment for age at breast cancer diagnosis, ethnicity, and receipt of trastuzumab, associations between receipt of anthracycline and higher NT-proBNP persisted (<i>p</i> < 0.001), showing that NT-proBNP may be a biomarker of cardiovascular toxicity after receipt of anthracycline-based chemotherapy. Further research to assess the clinical utility of NT-proBNP testing after receipt of anthracycline is recommended. sST2 and galectin-3 do not appear to differentiate between anthracycline recipients and non-recipients amongst breast cancer survivors. |
topic |
breast cancer anthracycline toxicity cardio-oncology |
url |
https://www.mdpi.com/2077-0383/10/15/3313 |
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