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Characterization of subclinical diastolic dysfunction by cardiac magnetic resonance feature-tracking in adult survivors of non-Hodgkin lymphoma treated with anthracyclines

dc.contributor.authorBarbosa, Maurício Fregonesi [UNESP]
dc.contributor.authorFusco, Daniéliso Renato [UNESP]
dc.contributor.authorGaiolla, Rafael Dezen [UNESP]
dc.contributor.authorWerys, Konrad
dc.contributor.authorTanni, Suzana Erico [UNESP]
dc.contributor.authorFernandes, Rômulo Araújo [UNESP]
dc.contributor.authorRibeiro, Sergio Marrone [UNESP]
dc.contributor.authorSzarf, Gilberto
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversity of Oxford
dc.contributor.institutionHospital Israelita Albert Einstein
dc.date.accessioned2021-06-25T10:28:04Z
dc.date.available2021-06-25T10:28:04Z
dc.date.issued2021-12-01
dc.description.abstractBackground: The use of anthracycline-based chemotherapy is associated with the development of heart failure, even years after the end of treatment. Early detection of cardiac dysfunction could identify a high-risk subset of survivors who would eventually benefit from early intervention. Cardiac magnetic resonance feature-tracking (CMR-FT) analysis offers a practical and rapid method to calculate systolic and diastolic strains from routinely acquired cine images. While early changes in systolic function have been described, less data are available about late effects of chemotherapy in diastolic parameters by CMR-FT. The main goal of this study was to determine whether left ventricular (LV) early diastolic strain rates (GDSR-E) by CMR-FT are impaired in long-term adult survivors of non-Hodgkin lymphoma (NHL). Our secondary objective was to analyze associations between GDSR-E with cumulative anthracycline dose, systolic function parameters and myocardial tissue characteristics. Methods: This is a single center cross-sectional observational study of asymptomatic patients in remission of NHL who previously received anthracycline therapy. All participants underwent their CMR examination on a 3.0-T scanner, including cines, T2 mapping, T1 mapping and late gadolinium enhancement imaging. Derived myocardial extracellular volume fraction was obtained from pre- and post-contrast T1 maps. CMR-FT analysis was performed using Trufi Strain software. The data obtained were compared between anthracycline group and volunteers without cardiovascular disease or neoplasia. Results: A total of 18 adult survivors of NHL, 14 (77.8%) males, at mean age of 57.6 (± 14.7) years-old, were studied 88.2 (± 52.1) months after exposure to anthracycline therapy (median 400 mg/m2). Compared with controls, anthracycline group showed impaired LV global early diastolic circumferential strain rate (GCSR-E) [53.5%/s ± 19.3 vs 72.2%/s ± 26.7, p = 0.022], early diastolic longitudinal strain rate (GLSR-E) [40.4%/s ± 13.0 vs 55.9%/s ± 17.8, p = 0.006] and early diastolic radial strain rate (GRSR-E) [− 114.4%/s ± 37.1 vs − 170.5%/s ± 48.0, p < 0.001]. Impaired LV GCSR-E, GLSR-E and GRSR-E correlated with increased anthracycline dose and decreased systolic function. There were no correlations between GDSR-E and myocardial tissue characteristics. Conclusions: Left ventricular early diastolic strain rates by CMR-FT are impaired late after anthracycline chemotherapy in adult survivors of non-Hodgkin lymphoma.en
dc.description.affiliationDepartment of Diagnostic Imaging Universidade Federal de São Paulo (UNIFESP), Rua Napoleão de Barros 800, Vila Clementino
dc.description.affiliationDepartment of Tropical Diseases and Diagnostic Imaging Universidade Estadual Paulista (UNESP)
dc.description.affiliationCardiology Division Internal Medicine Department Universidade Estadual Paulista (UNESP)
dc.description.affiliationHematology Division Internal Medicine Department Universidade Estadual Paulista (UNESP)
dc.description.affiliationUniversity of Oxford Centre for Clinical Magnetic Resonance Research (OCMR) University of Oxford
dc.description.affiliationPneumology Division Internal Medicine Department Universidade Estadual Paulista (UNESP)
dc.description.affiliationDepartment of Physical Education Universidade Estadual Paulista (UNESP)
dc.description.affiliationHospital Israelita Albert Einstein
dc.description.affiliationUnespDepartment of Tropical Diseases and Diagnostic Imaging Universidade Estadual Paulista (UNESP)
dc.description.affiliationUnespCardiology Division Internal Medicine Department Universidade Estadual Paulista (UNESP)
dc.description.affiliationUnespHematology Division Internal Medicine Department Universidade Estadual Paulista (UNESP)
dc.description.affiliationUnespPneumology Division Internal Medicine Department Universidade Estadual Paulista (UNESP)
dc.description.affiliationUnespDepartment of Physical Education Universidade Estadual Paulista (UNESP)
dc.identifierhttp://dx.doi.org/10.1186/s12872-021-01996-6
dc.identifier.citationBMC Cardiovascular Disorders, v. 21, n. 1, 2021.
dc.identifier.doi10.1186/s12872-021-01996-6
dc.identifier.issn1471-2261
dc.identifier.scopus2-s2.0-85104159254
dc.identifier.urihttp://hdl.handle.net/11449/206193
dc.language.isoeng
dc.relation.ispartofBMC Cardiovascular Disorders
dc.sourceScopus
dc.subjectCancer
dc.subjectChemotherapy
dc.subjectDiastolic dysfunction
dc.subjectFeature-tracking
dc.subjectStrain
dc.titleCharacterization of subclinical diastolic dysfunction by cardiac magnetic resonance feature-tracking in adult survivors of non-Hodgkin lymphoma treated with anthracyclinesen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0002-6557-2275[1]
unesp.author.orcid0000-0002-9456-0150[2]
unesp.author.orcid0000-0002-9480-4995[3]
unesp.author.orcid0000-0002-2334-2359[4]
unesp.author.orcid0000-0002-2587-2759[5]
unesp.author.orcid0000-0003-1576-8090[6]
unesp.author.orcid0000-0003-0732-2814[7]
unesp.author.orcid0000-0002-1941-7899[8]

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