Relevance of subclinical right ventricular dysfunction measured by feature-tracking cardiac magnetic resonance in non-ischemic dilated cardiomyopathy

dc.contributor.authorUrmeneta Ulloa, Javier
dc.contributor.authorPozo Osinalde, Eduardo
dc.contributor.authorCabrera Rodríguez, José Ángel
dc.contributor.authorRecio Rodríguez, Manuel
dc.contributor.authorThuissard Vasallo, Israel John
dc.contributor.authorAndreu Vázquez, Cristina
dc.contributor.authorIslas, Fabian
dc.contributor.authorMarcos Alberca, Pedro
dc.contributor.authorMahía, Patricia
dc.contributor.authorMartínez de Vega, Vicente
dc.contributor.authorEt al.
dc.date.accessioned2023-03-01T15:41:16Z
dc.date.available2023-03-01T15:41:16Z
dc.date.issued2023
dc.description.abstractRight ventricular (RV) dysfunction in patients with non-ischemic dilated cardiomyopathy (NICM) is associated with cardiovascular events. To analyze the feasibility of assessing RV myocardial deformation by feature tracking (FT)-cardiac magnetic resonance (CMR), and its usefulness as a prognostic marker. Retrospective study of NICM patients undergoing CMR. Longitudinal FT-RV free wall (LFT-RVFW) and fractional area change (FAC) were obtained. Correlation with standard RV parameters was studied. An association with combined event (heart failure (HF), ICD implantation or cardiovascular death) was assessed using a logistic regression model. Results 98 patients (64±13 years) were included. Left ventricular (LV) systolic function (LVEF 29.5±9.6%, 47% with LVEF≥30%) and RV (RVEF 52.2±14.6%, 72% with RVEF≥45%). Follow-up of 38±17 months, 26.5% presented at least one admission for HF. An excellent correlation of LFT-RVFW (r=0.82) and FAC (r=0.83) with RVEF was evident. No association of RV-FT parameters with prognosis entire study population was found. However, in patients with LVEF≥30%, admissions for HF were associated with lower LFT-RVFW (−21.6 ± 6.6% vs −31.3 ± 10%; p = 0.006) and FAC (36.6 ± 9.6% vs 50.5 ± 13.4%; p < 0.001) values. Similar diferences were observed when only patients with RVEF≥45% were considered. An LFT-RVFW cut-of point of -19.5% and FAC of 36.5% showed good prognostic performance. Decreased LFT-RVFW or FAC represented an independent predictor of combined event in patients with LVEF≥30%. Conclusions In NICM patients without severe LV dysfunction, decreased values of LFT-RVFW and/or FAC were associated with HF admissions, independently of RVEF.spa
dc.description.filiationUEMspa
dc.description.impact2.0 Q3 JCR 2023spa
dc.description.impact0.646 Q2 SJR 2023spa
dc.description.impactNo data IDR 2023spa
dc.description.sponsorshipSin financiaciónspa
dc.identifier.citationUrmeneta Ulloa, J., Pozo Osinalde, E., Cabrera, J. A., Recio Rodríguez, M., Thuissard-Vasallo, I. J., Andreu-Vázquez, C., Islas, F., Pérez de Isla, L., Marcos-Alberca, P., Mahía, P., Cobos, M. A., Cabeza, B., Rodríguez-Hernández, J. L., Luaces Méndez, M., Gómez de Diego, J. J., Bustos, A., Pérez-Villacastín, J., Agustín, A., & Martínez De Vega, V. (2023). Relevance of subclinical right ventricular dysfunction measured by feature-tracking cardiac magnetic resonance in non-ischemic dilated cardiomyopathy. BMC Cardiovascular Disorders, 23(1), 13. https://doi.org/10.1186/s12872-023-03044-xspa
dc.identifier.doi10.1186/s12872-023-03044-x
dc.identifier.issn1471-2261
dc.identifier.urihttp://hdl.handle.net/11268/11860
dc.language.isoengspa
dc.peerreviewedSispa
dc.relation.publisherversionhttps://doi.org/10.1186/s12872-023-03044-xspa
dc.rightsAttribution 4.0 Internacional*
dc.rights.accessRightsopen accessspa
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.otherImagen por resonancia magnéticaspa
dc.subject.otherCardiomiopatía dilatadaspa
dc.subject.otherDisfunción ventricular derechaspa
dc.subject.unescoEnfermedad cardiovascularspa
dc.subject.unescoMedicina preventivaspa
dc.subject.unescoTecnología médicaspa
dc.titleRelevance of subclinical right ventricular dysfunction measured by feature-tracking cardiac magnetic resonance in non-ischemic dilated cardiomyopathyspa
dc.typejournal articlespa
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscovery744ef0de-0c66-4902-9653-6aa4802312c3

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