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Cardiac magnetic resonance defines mechanisms of sex-based differences in outcomes following cardiac resynchronization therapy
BACKGROUND: Mechanisms of sex-based differences in outcomes following cardiac resynchronization therapy (CRT) are poorly understood. OBJECTIVE: To use cardiac magnetic resonance (CMR) to define mechanisms of sex-based differences in outcomes after CRT and describe distinct CMR-based phenotypes of CR...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9521735/ https://www.ncbi.nlm.nih.gov/pubmed/36186999 http://dx.doi.org/10.3389/fcvm.2022.1007806 |
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author | Bivona, Derek J. Tallavajhala, Srikar Abdi, Mohamad Oomen, Pim J. A. Gao, Xu Malhotra, Rohit Darby, Andrew Monfredi, Oliver J. Mangrum, J. Michael Mason, Pamela Mazimba, Sula Salerno, Michael Kramer, Christopher M. Epstein, Frederick H. Holmes, Jeffrey W. Bilchick, Kenneth C. |
author_facet | Bivona, Derek J. Tallavajhala, Srikar Abdi, Mohamad Oomen, Pim J. A. Gao, Xu Malhotra, Rohit Darby, Andrew Monfredi, Oliver J. Mangrum, J. Michael Mason, Pamela Mazimba, Sula Salerno, Michael Kramer, Christopher M. Epstein, Frederick H. Holmes, Jeffrey W. Bilchick, Kenneth C. |
author_sort | Bivona, Derek J. |
collection | PubMed |
description | BACKGROUND: Mechanisms of sex-based differences in outcomes following cardiac resynchronization therapy (CRT) are poorly understood. OBJECTIVE: To use cardiac magnetic resonance (CMR) to define mechanisms of sex-based differences in outcomes after CRT and describe distinct CMR-based phenotypes of CRT candidates based on sex and non-ischemic/ischemic cardiomyopathy type. MATERIALS AND METHODS: In a prospective study, sex-based differences in three short-term CRT response measures [fractional change in left ventricular end-systolic volume index 6 months after CRT (LVESVI-FC), B-type natriuretic peptide (BNP) 6 months after CRT, change in peak VO(2) 6 months after CRT], and long-term survival were evaluated with respect to 39 baseline parameters from CMR, exercise testing, laboratory testing, electrocardiograms, comorbid conditions, and other sources. CMR was also used to quantify the degree of left-ventricular mechanical dyssynchrony by deriving the circumferential uniformity ratio estimate (CURE-SVD) parameter from displacement encoding with stimulated echoes (DENSE) strain imaging. Statistical methods included multivariable linear regression with evaluation of interaction effects associated with sex and cardiomyopathy type (ischemic and non-ischemic cardiomyopathy) and survival analysis. RESULTS: Among 200 patients, the 54 female patients (27%) pre-CRT had a smaller CMR-based LVEDVI (p = 0.04), more mechanical dyssynchrony based on the validated CMR CURE-SVD parameter (p = 0.04), a lower frequency of both late gadolinium enhancement (LGE) and ischemic cardiomyopathy (p < 0.0001), a greater RVEF (p = 0.02), and a greater frequency of LBBB (p = 0.01). After categorization of patients into four groups based on cardiomyopathy type (ischemic/non-ischemic cardiomyopathy) and sex, female patients with non-ischemic cardiomyopathy had the lowest CURE-SVD (p = 0.003), the lowest pre-CRT BNP levels (p = 0.01), the lowest post-CRT BNP levels (p = 0.05), and the most favorable LVESVI-FC (p = 0.001). Overall, female patients had better 3-year survival before adjustment for cardiomyopathy type (p = 0.007, HR = 0.45) and after adjustment for cardiomyopathy type (p = 0.009, HR = 0.67). CONCLUSION: CMR identifies distinct phenotypes of female CRT patients with non-ischemic and ischemic cardiomyopathy relative to male patients stratified by cardiomyopathy type. The more favorable short-term response and long-term survival outcomes in female heart failure patients with CRT were associated with lower indexed CMR-based LV volumes, decreased presence of scar associated with prior myocardial infarction and ICM, and greater CMR-based dyssynchrony with the CURE-SVD. |
format | Online Article Text |
id | pubmed-9521735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95217352022-09-30 Cardiac magnetic resonance defines mechanisms of sex-based differences in outcomes following cardiac resynchronization therapy Bivona, Derek J. Tallavajhala, Srikar Abdi, Mohamad Oomen, Pim J. A. Gao, Xu Malhotra, Rohit Darby, Andrew Monfredi, Oliver J. Mangrum, J. Michael Mason, Pamela Mazimba, Sula Salerno, Michael Kramer, Christopher M. Epstein, Frederick H. Holmes, Jeffrey W. Bilchick, Kenneth C. Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Mechanisms of sex-based differences in outcomes following cardiac resynchronization therapy (CRT) are poorly understood. OBJECTIVE: To use cardiac magnetic resonance (CMR) to define mechanisms of sex-based differences in outcomes after CRT and describe distinct CMR-based phenotypes of CRT candidates based on sex and non-ischemic/ischemic cardiomyopathy type. MATERIALS AND METHODS: In a prospective study, sex-based differences in three short-term CRT response measures [fractional change in left ventricular end-systolic volume index 6 months after CRT (LVESVI-FC), B-type natriuretic peptide (BNP) 6 months after CRT, change in peak VO(2) 6 months after CRT], and long-term survival were evaluated with respect to 39 baseline parameters from CMR, exercise testing, laboratory testing, electrocardiograms, comorbid conditions, and other sources. CMR was also used to quantify the degree of left-ventricular mechanical dyssynchrony by deriving the circumferential uniformity ratio estimate (CURE-SVD) parameter from displacement encoding with stimulated echoes (DENSE) strain imaging. Statistical methods included multivariable linear regression with evaluation of interaction effects associated with sex and cardiomyopathy type (ischemic and non-ischemic cardiomyopathy) and survival analysis. RESULTS: Among 200 patients, the 54 female patients (27%) pre-CRT had a smaller CMR-based LVEDVI (p = 0.04), more mechanical dyssynchrony based on the validated CMR CURE-SVD parameter (p = 0.04), a lower frequency of both late gadolinium enhancement (LGE) and ischemic cardiomyopathy (p < 0.0001), a greater RVEF (p = 0.02), and a greater frequency of LBBB (p = 0.01). After categorization of patients into four groups based on cardiomyopathy type (ischemic/non-ischemic cardiomyopathy) and sex, female patients with non-ischemic cardiomyopathy had the lowest CURE-SVD (p = 0.003), the lowest pre-CRT BNP levels (p = 0.01), the lowest post-CRT BNP levels (p = 0.05), and the most favorable LVESVI-FC (p = 0.001). Overall, female patients had better 3-year survival before adjustment for cardiomyopathy type (p = 0.007, HR = 0.45) and after adjustment for cardiomyopathy type (p = 0.009, HR = 0.67). CONCLUSION: CMR identifies distinct phenotypes of female CRT patients with non-ischemic and ischemic cardiomyopathy relative to male patients stratified by cardiomyopathy type. The more favorable short-term response and long-term survival outcomes in female heart failure patients with CRT were associated with lower indexed CMR-based LV volumes, decreased presence of scar associated with prior myocardial infarction and ICM, and greater CMR-based dyssynchrony with the CURE-SVD. Frontiers Media S.A. 2022-09-15 /pmc/articles/PMC9521735/ /pubmed/36186999 http://dx.doi.org/10.3389/fcvm.2022.1007806 Text en Copyright © 2022 Bivona, Tallavajhala, Abdi, Oomen, Gao, Malhotra, Darby, Monfredi, Mangrum, Mason, Mazimba, Salerno, Kramer, Epstein, Holmes and Bilchick. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cardiovascular Medicine Bivona, Derek J. Tallavajhala, Srikar Abdi, Mohamad Oomen, Pim J. A. Gao, Xu Malhotra, Rohit Darby, Andrew Monfredi, Oliver J. Mangrum, J. Michael Mason, Pamela Mazimba, Sula Salerno, Michael Kramer, Christopher M. Epstein, Frederick H. Holmes, Jeffrey W. Bilchick, Kenneth C. Cardiac magnetic resonance defines mechanisms of sex-based differences in outcomes following cardiac resynchronization therapy |
title | Cardiac magnetic resonance defines mechanisms of sex-based differences in outcomes following cardiac resynchronization therapy |
title_full | Cardiac magnetic resonance defines mechanisms of sex-based differences in outcomes following cardiac resynchronization therapy |
title_fullStr | Cardiac magnetic resonance defines mechanisms of sex-based differences in outcomes following cardiac resynchronization therapy |
title_full_unstemmed | Cardiac magnetic resonance defines mechanisms of sex-based differences in outcomes following cardiac resynchronization therapy |
title_short | Cardiac magnetic resonance defines mechanisms of sex-based differences in outcomes following cardiac resynchronization therapy |
title_sort | cardiac magnetic resonance defines mechanisms of sex-based differences in outcomes following cardiac resynchronization therapy |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9521735/ https://www.ncbi.nlm.nih.gov/pubmed/36186999 http://dx.doi.org/10.3389/fcvm.2022.1007806 |
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