Role of heart rate recovery in chronic heart failure : results from the MyoVasc study

dc.contributor.authorVelmeden, David
dc.contributor.authorSöhne, Jakob
dc.contributor.authorSchuch, Alexander
dc.contributor.authorZeid, Silav
dc.contributor.authorSchulz, Andreas
dc.contributor.authorTröbs, Sven-Oliver
dc.contributor.authorMüller, Felix
dc.contributor.authorHeidorn, Marc W.
dc.contributor.authorBuch, Gregor
dc.contributor.authorBelanger, Noémie
dc.contributor.authorDinh, Wilfried
dc.contributor.authorMondritzki, Thomas
dc.contributor.authorLackner, Karl J.
dc.contributor.authorGori, Tommaso
dc.contributor.authorMünzel, Thomas
dc.contributor.authorWild, Philipp S.
dc.contributor.authorProchaska, Jürgen H.
dc.date.accessioned2025-12-02T11:06:51Z
dc.date.issued2025
dc.description.abstractBackground: Cardiac autonomic dysfunction is associated with heart failure (HF). Reduced heart rate recovery (HRR) indicates impaired parasympathetic reactivation after physical activity. Heart rate recovery 60 seconds after peak effort (HRR60) is linked to autonomic dysfunction, but data on its relevance across HF phenotypes are scarce. This study aimed to identify clinical determinants of HRR60 in an HF cohort and assess its relationship with clinical outcomes. Methods: Data from the MyoVasc study (NCT04064450; N=3289) were analyzed. Participants underwent standardized clinical phenotyping including cardiopulmonary exercise testing. HRR60 was defined as the heart rate decline 60 seconds after exercise termination. Clinical determinants of HRR60 were evaluated using multivariate regression, whereas Cox regression analyses assessed all‐cause death and worsening of HF. Results: The analysis sample comprised 1289 individuals (median age, 66.0 [interquartile range {IQR}, 58.0–73.0] years, 30.4% women) ranging from stage B to stage C/D according to the universal definition of HF. Age, sex, smoking, obesity, peripheral artery disease, and chronic kidney disease were identified as determinants of HRR60. HRR60 showed a strong association with all‐cause death (hazard ratio [HR]HRR60 [10 bpm], 1.56 [95% CI, 1.32–1.85]; P<0.0001) and worsening of HF (HRHRR60 [10 bpm], 1.36 [95% CI, 1.10–1.69]; P=0.0052) independent of age, sex, and clinical profile. Sensitivity analysis showed a stronger association with worsening HF in HF with preserved left ventricular ejection fraction (Pinteraction=0.027). Conclusions: HRR60 was associated with clinical outcome in chronic HF. Because it showed a stronger association with outcomes in HF with preserved ejection fraction, future research should consider phenotype‐specific differences.en_GB
dc.identifier.doihttps://doi.org/10.25358/openscience-13761
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/13782
dc.language.isoeng
dc.rightsCC-BY-NC-ND-4.0
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleRole of heart rate recovery in chronic heart failure : results from the MyoVasc studyen_GB
dc.typeZeitschriftenaufsatzde_DE
jgu.apc.netprice2400,00
jgu.apc.price2568,00
jgu.apc.taxrate7
jgu.apc.transformationcontractWiley (DEAL)
jgu.dfg.year2025
jgu.identifier.uuid0d5fc40f-808a-47d7-a6c7-242cfc2fd3f4
jgu.journal.issue10
jgu.journal.titleJournal of the American Heart Association
jgu.journal.volume14
jgu.nationalcurrency.eur2400,00
jgu.organisation.departmentFB 04 Medizinde_DE
jgu.organisation.nameJohannes Gutenberg-Universität Mainzde_DE
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternativee039792
jgu.publisher.doi10.1161/JAHA.124.039792
jgu.publisher.eissn2047-9980
jgu.publisher.nameAssociation
jgu.publisher.placeNew York, NY
jgu.publisher.year2025
jgu.rights.accessrightsopenAccessen_GB
jgu.subject.ddccode610
jgu.subject.dfgLebenswissenschaftende_DE
jgu.type.contenttypeScientific articleen_GB
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTexten_GB
jgu.type.versionPublished versionen_GB

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