Cargando…

Left Ventricular Systolic Function in Long-Term Survivors of Allogeneic Hematopoietic Stem Cell Transplantation

BACKGROUND: Allogeneic hematopoietic stem cell transplantation (allo-HSCT), a potentially curative therapy for malignant and nonmalignant diseases, is being increasingly used in younger patients. Although allo-HSCT survivors have an established increased risk of cardiovascular disease, there is limi...

Descripción completa

Detalles Bibliográficos
Autores principales: Massey, Richard J., Diep, Phoi P., Ruud, Ellen, Burman, Marta M., Kvaslerud, Anette B., Brinch, Lorentz, Aakhus, Svend, Gullestad, Lars L., Beitnes, Jan O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8352258/
https://www.ncbi.nlm.nih.gov/pubmed/34396253
http://dx.doi.org/10.1016/j.jaccao.2020.06.011
_version_ 1783736142363885568
author Massey, Richard J.
Diep, Phoi P.
Ruud, Ellen
Burman, Marta M.
Kvaslerud, Anette B.
Brinch, Lorentz
Aakhus, Svend
Gullestad, Lars L.
Beitnes, Jan O.
author_facet Massey, Richard J.
Diep, Phoi P.
Ruud, Ellen
Burman, Marta M.
Kvaslerud, Anette B.
Brinch, Lorentz
Aakhus, Svend
Gullestad, Lars L.
Beitnes, Jan O.
author_sort Massey, Richard J.
collection PubMed
description BACKGROUND: Allogeneic hematopoietic stem cell transplantation (allo-HSCT), a potentially curative therapy for malignant and nonmalignant diseases, is being increasingly used in younger patients. Although allo-HSCT survivors have an established increased risk of cardiovascular disease, there is limited knowledge of the long-term effects on cardiac function in survivors. OBJECTIVES: The purpose of this study was to describe left ventricular (LV) systolic function in long-term allo-HSCT survivors treated in childhood, adolescence, or early adulthood. METHODS: Our cross-sectional cohort study included 104 patients (56% women), age 18 ± 10 years at time allo-HSCT with 17 ± 6 years of follow-up. Echocardiography included 2-dimensional (2D) and 3-dimensional (3D) analyses and speckle tracking imaging. In total, 55 healthy control subjects with a similar age, sex, and body mass index were used for comparison. Left ventricular systolic dysfunction (LVSD) was defined as reduced 2D left ventricular ejection fraction (LVEF) of <52% in men and <54% in women, and/or a reduced global longitudinal strain (GLS) of ≥−17%. Multivariable linear regression was used to determine independent predictors of 2D-LVEF and GLS. RESULTS: Allo-HSCT survivors had significantly reduced LV systolic function compared with control subjects: 2D-LVEF (55.2 ± 5.8% vs. 59.0 ± 2.9%; p < 0.001), 3D LVEF (54.0 ± 5.1% vs. 57.6 ± 2.7%; p < 0.001), and GLS (−17.5 ± 2.2% vs. −19.8 ± 1.4%; p < 0.001). LVSD was found in 44.2%, of whom 28.3% were symptomatic. Clinical factors independently associated with 2D-LVEF and/or GLS included age, anthracyclines, graft versus host disease (GVHD), heart rate, and hypertension. In the 45% of survivors pre-treated with anthracyclines, the effect of anthracyclines on 2D-LVEF and GLS was dose-dependent. CONCLUSIONS: LVSD is common in long-term survivors of allo-HSCT treated in their youth. Pre-HSCT therapies with anthracyclines, age, heart rate, hypertension, and graft versus host disease are associated with measures of LV function.
format Online
Article
Text
id pubmed-8352258
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-83522582021-08-13 Left Ventricular Systolic Function in Long-Term Survivors of Allogeneic Hematopoietic Stem Cell Transplantation Massey, Richard J. Diep, Phoi P. Ruud, Ellen Burman, Marta M. Kvaslerud, Anette B. Brinch, Lorentz Aakhus, Svend Gullestad, Lars L. Beitnes, Jan O. JACC CardioOncol Original Research BACKGROUND: Allogeneic hematopoietic stem cell transplantation (allo-HSCT), a potentially curative therapy for malignant and nonmalignant diseases, is being increasingly used in younger patients. Although allo-HSCT survivors have an established increased risk of cardiovascular disease, there is limited knowledge of the long-term effects on cardiac function in survivors. OBJECTIVES: The purpose of this study was to describe left ventricular (LV) systolic function in long-term allo-HSCT survivors treated in childhood, adolescence, or early adulthood. METHODS: Our cross-sectional cohort study included 104 patients (56% women), age 18 ± 10 years at time allo-HSCT with 17 ± 6 years of follow-up. Echocardiography included 2-dimensional (2D) and 3-dimensional (3D) analyses and speckle tracking imaging. In total, 55 healthy control subjects with a similar age, sex, and body mass index were used for comparison. Left ventricular systolic dysfunction (LVSD) was defined as reduced 2D left ventricular ejection fraction (LVEF) of <52% in men and <54% in women, and/or a reduced global longitudinal strain (GLS) of ≥−17%. Multivariable linear regression was used to determine independent predictors of 2D-LVEF and GLS. RESULTS: Allo-HSCT survivors had significantly reduced LV systolic function compared with control subjects: 2D-LVEF (55.2 ± 5.8% vs. 59.0 ± 2.9%; p < 0.001), 3D LVEF (54.0 ± 5.1% vs. 57.6 ± 2.7%; p < 0.001), and GLS (−17.5 ± 2.2% vs. −19.8 ± 1.4%; p < 0.001). LVSD was found in 44.2%, of whom 28.3% were symptomatic. Clinical factors independently associated with 2D-LVEF and/or GLS included age, anthracyclines, graft versus host disease (GVHD), heart rate, and hypertension. In the 45% of survivors pre-treated with anthracyclines, the effect of anthracyclines on 2D-LVEF and GLS was dose-dependent. CONCLUSIONS: LVSD is common in long-term survivors of allo-HSCT treated in their youth. Pre-HSCT therapies with anthracyclines, age, heart rate, hypertension, and graft versus host disease are associated with measures of LV function. Elsevier 2020-09-15 /pmc/articles/PMC8352258/ /pubmed/34396253 http://dx.doi.org/10.1016/j.jaccao.2020.06.011 Text en © 2020 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Massey, Richard J.
Diep, Phoi P.
Ruud, Ellen
Burman, Marta M.
Kvaslerud, Anette B.
Brinch, Lorentz
Aakhus, Svend
Gullestad, Lars L.
Beitnes, Jan O.
Left Ventricular Systolic Function in Long-Term Survivors of Allogeneic Hematopoietic Stem Cell Transplantation
title Left Ventricular Systolic Function in Long-Term Survivors of Allogeneic Hematopoietic Stem Cell Transplantation
title_full Left Ventricular Systolic Function in Long-Term Survivors of Allogeneic Hematopoietic Stem Cell Transplantation
title_fullStr Left Ventricular Systolic Function in Long-Term Survivors of Allogeneic Hematopoietic Stem Cell Transplantation
title_full_unstemmed Left Ventricular Systolic Function in Long-Term Survivors of Allogeneic Hematopoietic Stem Cell Transplantation
title_short Left Ventricular Systolic Function in Long-Term Survivors of Allogeneic Hematopoietic Stem Cell Transplantation
title_sort left ventricular systolic function in long-term survivors of allogeneic hematopoietic stem cell transplantation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8352258/
https://www.ncbi.nlm.nih.gov/pubmed/34396253
http://dx.doi.org/10.1016/j.jaccao.2020.06.011
work_keys_str_mv AT masseyrichardj leftventricularsystolicfunctioninlongtermsurvivorsofallogeneichematopoieticstemcelltransplantation
AT diepphoip leftventricularsystolicfunctioninlongtermsurvivorsofallogeneichematopoieticstemcelltransplantation
AT ruudellen leftventricularsystolicfunctioninlongtermsurvivorsofallogeneichematopoieticstemcelltransplantation
AT burmanmartam leftventricularsystolicfunctioninlongtermsurvivorsofallogeneichematopoieticstemcelltransplantation
AT kvaslerudanetteb leftventricularsystolicfunctioninlongtermsurvivorsofallogeneichematopoieticstemcelltransplantation
AT brinchlorentz leftventricularsystolicfunctioninlongtermsurvivorsofallogeneichematopoieticstemcelltransplantation
AT aakhussvend leftventricularsystolicfunctioninlongtermsurvivorsofallogeneichematopoieticstemcelltransplantation
AT gullestadlarsl leftventricularsystolicfunctioninlongtermsurvivorsofallogeneichematopoieticstemcelltransplantation
AT beitnesjano leftventricularsystolicfunctioninlongtermsurvivorsofallogeneichematopoieticstemcelltransplantation