Sympathomodulation in Heart Failure with High vs. Normal Ejection Fraction.

Heart failure with preserved ejection fraction Single-beat estimation Sympathomodulation

Journal

Structural heart : the journal of the Heart Team
ISSN: 2474-8714
Titre abrégé: Struct Heart
Pays: United States
ID NLM: 101743256

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 01 04 2022
revised: 15 06 2022
accepted: 27 06 2022
medline: 8 6 2023
pubmed: 8 6 2023
entrez: 8 6 2023
Statut: epublish

Résumé

Despite recent advances in the treatment of heart failure with preserved ejection fraction (HFpEF), the overall outcome is poor and evidence-based therapeutic options are scarce. So far, the only evidence-based therapy in HFpEF, sodium glucose linked transporter 2 inhibitors, has only insignificant effects in patients with a high EF (EF > 60%, HEF) when compared to a normal EF (EF 50%-60%, NEF). This could be explained by different biomechanical and cellular phenotypes of HFpEF across the range of EFs rather than a uniform pathophysiology. We aimed to investigate the concept of different phenotypes in the HEF and NEF using noninvasive single-beat estimations and to observe alterations in pressure-volume relations in both groups following sympathomodulation using renal denervation (RDN). Patients from a previous study on RDN in HFpEF were stratified by having HFpEF with an HEF or NEF. Single-beat estimations were used to derive arterial elastance (Ea), end-systolic elastance (Ees), and diastolic capacitance (VPED Overall, 63 patients were classified as having an HEF, and 36 patients were classified as having an NEF. Ea did not differ between the groups and was reduced at follow-up in both groups ( Beneficial effects of RDN were observed in the NEF and HEF, supporting the further investigation of sympathomodulating treatments for HFpEF in future trials.

Sections du résumé

Background UNASSIGNED
Despite recent advances in the treatment of heart failure with preserved ejection fraction (HFpEF), the overall outcome is poor and evidence-based therapeutic options are scarce. So far, the only evidence-based therapy in HFpEF, sodium glucose linked transporter 2 inhibitors, has only insignificant effects in patients with a high EF (EF > 60%, HEF) when compared to a normal EF (EF 50%-60%, NEF). This could be explained by different biomechanical and cellular phenotypes of HFpEF across the range of EFs rather than a uniform pathophysiology. We aimed to investigate the concept of different phenotypes in the HEF and NEF using noninvasive single-beat estimations and to observe alterations in pressure-volume relations in both groups following sympathomodulation using renal denervation (RDN).
Methods UNASSIGNED
Patients from a previous study on RDN in HFpEF were stratified by having HFpEF with an HEF or NEF. Single-beat estimations were used to derive arterial elastance (Ea), end-systolic elastance (Ees), and diastolic capacitance (VPED
Results UNASSIGNED
Overall, 63 patients were classified as having an HEF, and 36 patients were classified as having an NEF. Ea did not differ between the groups and was reduced at follow-up in both groups (
Conclusions UNASSIGNED
Beneficial effects of RDN were observed in the NEF and HEF, supporting the further investigation of sympathomodulating treatments for HFpEF in future trials.

Identifiants

pubmed: 37288333
doi: 10.1016/j.shj.2022.100073
pii: S2474-8706(22)01863-2
pmc: PMC10242566
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100073

Informations de copyright

© 2022 The Author(s).

Déclaration de conflit d'intérêts

P.L. and K.F. received modest institutional fees from ReCor Medical (Palo Alto, CA, USA) and Medtronic (Minneapolis, MN, USA). The remaining authors have nothing to disclosure.

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Auteurs

Karl Fengler (K)

Department of Cardiology, Heart Center Leipzig at University of Leipzig, Leipzig, Germany.

Karl-Patrik Kresoja (KP)

Department of Cardiology, Heart Center Leipzig at University of Leipzig, Leipzig, Germany.

Karl-Philipp Rommel (KP)

Department of Cardiology, Heart Center Leipzig at University of Leipzig, Leipzig, Germany.

Sebastian Rosch (S)

Department of Cardiology, Heart Center Leipzig at University of Leipzig, Leipzig, Germany.

Maximilian V Roeder (MV)

Department of Cardiology, Heart Center Leipzig at University of Leipzig, Leipzig, Germany.

Steffen Desch (S)

Department of Cardiology, Heart Center Leipzig at University of Leipzig, Leipzig, Germany.

Holger Thiele (H)

Department of Cardiology, Heart Center Leipzig at University of Leipzig, Leipzig, Germany.

Philipp Lurz (P)

Department of Cardiology, Heart Center Leipzig at University of Leipzig, Leipzig, Germany.

Classifications MeSH