Effects of SGLT2 inhibitors on parameters of renal venous congestion in intrarenal Doppler ultrasonography.

congestive nephropathy estimated glomerular filtration rate heart failure intrarenal Doppler sonography renal venous congestion

Journal

Clinical kidney journal
ISSN: 2048-8505
Titre abrégé: Clin Kidney J
Pays: England
ID NLM: 101579321

Informations de publication

Date de publication:
Sep 2024
Historique:
received: 23 05 2024
medline: 11 9 2024
pubmed: 11 9 2024
entrez: 11 9 2024
Statut: epublish

Résumé

Cardiorenal syndrome is a common condition in clinical practice in which renal venous congestion (VC) plays an important role. Intrarenal Doppler ultrasound (IRD) is a non-invasive method to assess and quantify renal VC. The current study aims to investigate the effects of SGLT2 inhibitor (SGLT2i) therapy on IRD parameters of renal VC. This prospective observational study included patients with chronic kidney disease (CKD) with or without type 2 diabetes mellitus and/or heart failure (HF) with reduced and preserved ejection fraction who had an indication for standard of care SGLT2i therapy. IRD, assessing venous impedance index (VII), and intrarenal venous flow pattern (IRVF) analysis were performed within the interlobar vessels of the right kidney before and 6 months after initiation of SGLT2i therapy. A number of 64 patients with CKD and a cardiorenal risk profile were included (mean eGFR 42.9 ml/min/1.73 m In this study, SGLT2i therapy resulted in a reduction in renal VC as assessed by IRD. These findings underscore the potential haemodynamic benefits of SGLT2 inhibitors in cardiorenal syndrome and warrant further investigation into their clinical implications.

Sections du résumé

Background UNASSIGNED
Cardiorenal syndrome is a common condition in clinical practice in which renal venous congestion (VC) plays an important role. Intrarenal Doppler ultrasound (IRD) is a non-invasive method to assess and quantify renal VC. The current study aims to investigate the effects of SGLT2 inhibitor (SGLT2i) therapy on IRD parameters of renal VC.
Methods UNASSIGNED
This prospective observational study included patients with chronic kidney disease (CKD) with or without type 2 diabetes mellitus and/or heart failure (HF) with reduced and preserved ejection fraction who had an indication for standard of care SGLT2i therapy. IRD, assessing venous impedance index (VII), and intrarenal venous flow pattern (IRVF) analysis were performed within the interlobar vessels of the right kidney before and 6 months after initiation of SGLT2i therapy.
Results UNASSIGNED
A number of 64 patients with CKD and a cardiorenal risk profile were included (mean eGFR 42.9 ml/min/1.73 m
Conclusions UNASSIGNED
In this study, SGLT2i therapy resulted in a reduction in renal VC as assessed by IRD. These findings underscore the potential haemodynamic benefits of SGLT2 inhibitors in cardiorenal syndrome and warrant further investigation into their clinical implications.

Identifiants

pubmed: 39258260
doi: 10.1093/ckj/sfae234
pii: sfae234
pmc: PMC11384228
doi:

Types de publication

Journal Article

Langues

eng

Pagination

sfae234

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the ERA.

Déclaration de conflit d'intérêts

M.W. declares lecture fees from AstraZeneca. M.J.K. declares lecture fees from Boehringer Ingelheim, Lilly, and AstraZeneca. For the present study, there are no conflict of interest from any of the other authors.

Auteurs

Manuel Wallbach (M)

Department of Nephrology and Rheumatology, University Medical Center Göttingen, Germany.
German Center for Cardiovascular Research (DZHK), Partner Site Göttingen, Germany.

Jamil Ajrab (J)

Department of Nephrology and Rheumatology, University Medical Center Göttingen, Germany.

Bilgin Bayram (B)

Department of Nephrology and Rheumatology, University Medical Center Göttingen, Germany.

Dennis Pieper (D)

Department of Nephrology and Rheumatology, University Medical Center Göttingen, Germany.

Ann-Kathrin Schäfer (AK)

Department of Nephrology and Rheumatology, University Medical Center Göttingen, Germany.

Stephan Lüders (S)

Department of Nephrology and Rheumatology, University Medical Center Göttingen, Germany.
Department of Nephrology, St.-Josefs-Hospital, Cloppenburg, Germany.

Fani Delistefani (F)

Department of Nephrology and Rheumatology, University Medical Center Göttingen, Germany.

Dieter Müller (D)

GIZ Nord Poison Centre, Göttingen, Germany.

Michael Koziolek (M)

Department of Nephrology and Rheumatology, University Medical Center Göttingen, Germany.
German Center for Cardiovascular Research (DZHK), Partner Site Göttingen, Germany.

Classifications MeSH