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V体育官网 - Interleukin-6 in heart failure with reduced ejection fraction and the effect of dapagliflozin : an exploratory analysis of the dapagliflozin and prevention of adverse outcomes in heart failure trial

Docherty, K. F. et al. (2025) Interleukin-6 in heart failure with reduced ejection fraction and the effect of dapagliflozin : an exploratory analysis of the dapagliflozin and prevention of adverse outcomes in heart failure trial. JACC: Heart Failure, 13(7), 102393. (doi: 10. 1016/j. jchf. 2024. 12 VSports. 012) (PMID:40088234) .

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V体育官网 - Abstract

Background: Inflammation may play an important pathophysiological role in the development and progression of heart failure (HF). Interleukin (IL)-6 is a circulating cytokine and is the main regulator of the release of C-reactive protein (CRP). Objectives: The authors examined the association between IL-6 and high-sensitivity (hs)-CRP and outcomes in patients with HFrEF in the DAPA-HF trial and their relationship with the effect of dapagliflozin. Methods: Inclusion criteria included: 1) NYHA functional class II-IV; 2) left ventricular ejection fraction ≤40%; 3) elevated N-terminal pro–B-type natriuretic peptide; and 4) estimated glomerular filtration rate ≥30 mL/min/1. 73 m2. The primary outcome was a composite of a worsening HF event or cardiovascular death. IL-6 and hs-CRP were measured at baseline and 12 months (Roche Diagnostics). The associations between IL-6 and hs-CRP and outcomes were adjusted for known prognostic variables, including NT-proBNP. Results: Among 2,940 patients, median IL-6 and hs-CRP at baseline were 6. 01 pg/mL (Q1-Q3: 4. 18-9. 28 pg/mL) and 2. 05 mg/L (Q1-Q3: 0. 83-4. 9 mg/L), respectively VSports app下载. Baseline IL-6 tertiles (T) were: T1 ≤4. 72 pg/mL; T2 4. 73-7. 89 pg/mL; and T3 ≥7. 90 pg/mL. The adjusted risks of the primary outcome relative to T1 were as follows: T2 = HR 1. 34 (95% CI: 1. 04-1. 73) and T3 = HR 1. 80 (95% CI: 1. 41-2. 31). A rise in IL-6 between baseline and 12 months was associated with worse outcomes. The beneficial effect of dapagliflozin on the primary outcome was consistent regardless of IL-6 concentration (continuous interaction P = 0. 57), with similar results for hs-CRP. Dapagliflozin did not reduce IL-6 or hs-CRP at 12 months. Conclusions: In DAPA-HF, elevated IL-6 and hs-CRP levels were each associated with the risk of worsening HF or cardiovascular death. Dapagliflozin reduced the risk of adverse outcomes regardless of baseline IL-6 or hs-CRP. (Study to Evaluate the Effect of Dapagliflozin on the Incidence of Worsening Heart Failure or Cardiovascular Death in Patients With Chronic Heart Failure [DAPA-HF]; NCT03036124).

Item Type:Articles
Keywords:Heart failure, inflammation, interleukin-6, SGLT2i.
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:McDowell, Dr Kirsty and Docherty, Dr Kieran and Jhund, Professor Pardeep and Welsh, Professor Paul and Kober, Professor Lars and Petrie, Professor Mark and Sattar, Professor Naveed and McMurray, Professor John
Authors: Docherty, K. F., McDowell, K., Welsh, P., Petrie, M. C., Anand, I., Berg, D. D., de Boer, R. A., Køber, L., Kosiborod, M. N., Martinez, F. A., O'Meara, E., Morrow, D. A., Ponikowski, P., Sabatine, M. S., Sattar, N., Schou, M., Hammarstedt, A., Sjöstrand, M., Langkilde, A. M., Jhund, P. S., Solomon, S. D., and McMurray, J. J.V.
College/School:College of Medical Veterinary and Life Sciences > School of Cardiovascular & Metabolic Health
Journal Name:JACC: Heart Failure
Publisher:Elsevier
ISSN:2213-1779
ISSN (Online):2213-1787
Published Online:12 March 2025
Copyright Holders:Copyright © 2025 The Authors
First Published:First published in JACC: Heart Failure 13(7): 102393
Publisher Policy:Reproduced under a Creative Commons license

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Project Code
Award No
Project Name
Principal Investigator
Funder's Name
Funder Ref
Lead Dept
BHF Centre of Excellence
Colin Berry
RE/18/6/34217
SCMH - Cardiovascular & Metabolic Health

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