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Sympathomodulation in Heart Failure with High vs. Normal Ejection Fraction
BACKGROUND: 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 in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242566/ https://www.ncbi.nlm.nih.gov/pubmed/37288333 http://dx.doi.org/10.1016/j.shj.2022.100073 |
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author | Fengler, Karl Kresoja, Karl-Patrik Rommel, Karl-Philipp Rosch, Sebastian Roeder, Maximilian v. Desch, Steffen Thiele, Holger Lurz, Philipp |
author_facet | Fengler, Karl Kresoja, Karl-Patrik Rommel, Karl-Philipp Rosch, Sebastian Roeder, Maximilian v. Desch, Steffen Thiele, Holger Lurz, Philipp |
author_sort | Fengler, Karl |
collection | PubMed |
description | BACKGROUND: 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: 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(20)). RESULTS: 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 (p < 0.01). Ees was higher and VPED(20) was lower in the HEF than those in the NEF. Both were changed significantly at follow-up in the HEF but not in the NEF. Ees/Ea was lower in the NEF (0.95 ± 0.22 vs 1.15 ± 0.27, p < 0.01) and was significantly increased in the NEF (by 0.08 ± 0.20, p < 0.05) but not in the HEF. CONCLUSIONS: Beneficial effects of RDN were observed in the NEF and HEF, supporting the further investigation of sympathomodulating treatments for HFpEF in future trials. |
format | Online Article Text |
id | pubmed-10242566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-102425662023-06-07 Sympathomodulation in Heart Failure with High vs. Normal Ejection Fraction Fengler, Karl Kresoja, Karl-Patrik Rommel, Karl-Philipp Rosch, Sebastian Roeder, Maximilian v. Desch, Steffen Thiele, Holger Lurz, Philipp Struct Heart Original Research BACKGROUND: 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: 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(20)). RESULTS: 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 (p < 0.01). Ees was higher and VPED(20) was lower in the HEF than those in the NEF. Both were changed significantly at follow-up in the HEF but not in the NEF. Ees/Ea was lower in the NEF (0.95 ± 0.22 vs 1.15 ± 0.27, p < 0.01) and was significantly increased in the NEF (by 0.08 ± 0.20, p < 0.05) but not in the HEF. CONCLUSIONS: Beneficial effects of RDN were observed in the NEF and HEF, supporting the further investigation of sympathomodulating treatments for HFpEF in future trials. Elsevier 2022-08-02 /pmc/articles/PMC10242566/ /pubmed/37288333 http://dx.doi.org/10.1016/j.shj.2022.100073 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Fengler, Karl Kresoja, Karl-Patrik Rommel, Karl-Philipp Rosch, Sebastian Roeder, Maximilian v. Desch, Steffen Thiele, Holger Lurz, Philipp Sympathomodulation in Heart Failure with High vs. Normal Ejection Fraction |
title | Sympathomodulation in Heart Failure with High vs. Normal Ejection Fraction |
title_full | Sympathomodulation in Heart Failure with High vs. Normal Ejection Fraction |
title_fullStr | Sympathomodulation in Heart Failure with High vs. Normal Ejection Fraction |
title_full_unstemmed | Sympathomodulation in Heart Failure with High vs. Normal Ejection Fraction |
title_short | Sympathomodulation in Heart Failure with High vs. Normal Ejection Fraction |
title_sort | sympathomodulation in heart failure with high vs. normal ejection fraction |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242566/ https://www.ncbi.nlm.nih.gov/pubmed/37288333 http://dx.doi.org/10.1016/j.shj.2022.100073 |
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