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Exercise training and high-sensitivity cardiac troponin-I in patients with heart failure with reduced ejection fraction.
Riveland, Egil; Valborgland, Torstein; Ushakova, Anastasia; Skadberg, Øyvind; Karlsen, Trine; Hole, Torstein; Støylen, Asbjørn; Dalen, Håvard; Videm, Vibeke; Koppen, Elias; Linke, Axel; Delagardelle, Charles; Van Craenenbroeck, Emeline M; Beckers, Paul; Prescott, Eva; Halle, Martin; Omland, Torbjørn; Ellingsen, Øyvind; Larsen, Alf Inge.
Afiliação
  • Riveland E; Department of Cardiology, Stavanger University Hospital, Stavanger, Norway.
  • Valborgland T; Institute of Clinical Science, University of Bergen, Stavanger, Norway.
  • Ushakova A; Department of Cardiology, Stavanger University Hospital, Stavanger, Norway.
  • Skadberg Ø; Department of Research, Section of Biostatistics, Stavanger University Hospital, Stavanger, Norway.
  • Karlsen T; Department of Biochemistry, Stavanger University Hospital, Stavanger, Norway.
  • Hole T; Faculty of Nursing and Health Sciences, Nord University, Bodø, Norway.
  • Støylen A; Department of Circulation and Medical Imaging, Cardiac Exercise Research Group, Norwegian University of Science and Technology, Trondheim, Norway.
  • Dalen H; Department of Circulation and Medical Imaging, Cardiac Exercise Research Group, Norwegian University of Science and Technology, Trondheim, Norway.
  • Videm V; Møre og Romsdal Health Trust, Ålesund Hospital, Ålesund, Norway.
  • Koppen E; Department of Circulation and Medical Imaging, Norwegian University of Science and Technology, Trondheim, Norway.
  • Linke A; Department of Circulation and Medical Imaging, Norwegian University of Science and Technology, Trondheim, Norway.
  • Delagardelle C; Department of Circulation and Medical Imaging, Norwegian University of Science and Technology, Trondheim, Norway.
  • Van Craenenbroeck EM; Department of Medicine, Levanger Hospital, Nord-Trøndelag Hospital Trust, Levanger, Norway.
  • Beckers P; Clinict of Cardiology, St. Olavs University Hospital, Trondheim, Norway.
  • Prescott E; Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
  • Halle M; Department of Immunology and Transfusion Medicine, St. Olavs University Hospital, Trondheim, Norway.
  • Omland T; Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
  • Ellingsen Ø; Technische Universität Dresden, Herzzentrum, Dresden, Germany.
  • Larsen AI; Hospital Centre of Luxembourg, Luxembourg, UK.
ESC Heart Fail ; 11(2): 1121-1132, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38268237
ABSTRACT

AIMS:

The aims of this sub-study of the SMARTEX trial were (1) to evaluate the effects of a 12-week exercise training programme on serum levels of high sensitivity cardiac troponin I (hs-cTnI) in patients with moderate chronic heart failure (CHF), in New York Heart Association class II-III with reduced ejection fraction (HFrEF) and (2) to explore the associations with left ventricular remodelling, functional capacity and filling pressures measured with N-terminal pro brain natriuretic peptide (NT-proBNP). METHODS AND

RESULTS:

In this sub-study, 196 patients were randomly assigned to high intensity interval training (HIIT, n = 70), moderate continuous training (MCT, n = 59) or recommendation of regular exercise (RRE), (n = 67) for 12 weeks. To reveal potential difference between structured intervention and control, HIIT and MCT groups were merged and named supervised exercise training (SET) group. The RRE group constituted the control group (CG). To avoid contributing factors to myocardial injury, we also evaluated changes in patients without additional co-morbidities (atrial fibrillation, hypertension, diabetes mellitus, and chronic obstructive pulmonary disease). The relationship between hs-cTnI and left ventricular end-diastolic diameter (LVEDD), VO2peak, and NT-proBNP was analysed by linear mixed models. At 12 weeks, Hs-cTnI levels were modestly but significantly reduced in the SET group from median 11.9 ng/L (interquartile ratio, IQR 7.1-21.8) to 11.5 ng/L (IQR 7.0-20.7), P = 0.030. There was no between-group difference (SET vs. CG, P = 0.116). There was a numerical but not significant reduction in hs-cTnI for the whole population (P = 0.067) after 12 weeks. For the sub-group of patients without additional co-morbidities, there was a significant between-group difference SET group (delta -1.2 ng/L, IQR -2.7 to 0.1) versus CG (delta -0.1 ng/L, IQR -0.4 to 0.7), P = 0.007. In the SET group, hs-cTnI changed from 10.9 ng/L (IQR 6.0-22.7) to 9.2 ng/L (IQR 5.2-20.5) (P = 0.002), whereas there was no change in the CG (6.4 to 5.8 ng/L, P = 0.64). Changes in hs-cTnI (all patients) were significantly associated with changes in; LVEDD, VO2peak, and NT-proBNP, respectively.

CONCLUSIONS:

In patients with stable HFrEF, 12 weeks of structured exercise intervention was associated with a modest, but significant reduction of hs-cTnI. There was no significant difference between intervention group and control group. In the sub-group of patients without additional co-morbidities, this difference was highly significant. The alterations in hs-cTnI were associated with reduction of LVEDD and natriuretic peptide concentrations as well as improved functional capacity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Disfunção Ventricular Esquerda / Insuficiência Cardíaca Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: ESC Heart Fail / ESC heart failure Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Noruega

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Disfunção Ventricular Esquerda / Insuficiência Cardíaca Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: ESC Heart Fail / ESC heart failure Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Noruega