SGLT2 inhibitor therapy for transthyretin amyloid cardiomyopathy: early tolerance and clinical response to dapagliflozin.


Journal

ESC heart failure
ISSN: 2055-5822
Titre abrégé: ESC Heart Fail
Pays: England
ID NLM: 101669191

Informations de publication

Date de publication:
Feb 2023
Historique:
revised: 06 09 2022
received: 27 07 2022
accepted: 19 09 2022
pubmed: 20 10 2022
medline: 26 1 2023
entrez: 19 10 2022
Statut: ppublish

Résumé

Sodium-glucose cotransporter 2 inhibitors (SGLT2i) improve clinical outcomes in heart failure patients with reduced and preserved left ventricular ejection fraction (LVEF), but have not yet been investigated in transthyretin amyloid cardiomyopathy (ATTR-CM). This study aimed to evaluate tolerability, clinical outcomes, and changes in NT-proBNP levels and glomerular filtration rate (GFR) in ATTR-CM patients treated with dapagliflozin. Patients with stable, tafamidis-treated ATTR-CM were retrospectively evaluated at the initiation of dapagliflozin and 3 months thereafter. Tafamidis-treated ATTR-CM patients without SGLT2i served as a reference cohort. Overall, SLGT2i therapy was initiated in 34 patients. Seventeen patients with stable disease on tafamidis, who were subsequently started on dapagliflozin, were included in the analysis. Patients selected for SGLT2i presented with signs of advanced disease, evidenced by higher Gillmore disease stage (stage ≥2: 53% vs. 27.5%; P = 0.041), baseline median NT-proBNP [median (IQR) 2668 pg/mL (1314-3451) vs. 1424 (810-2059); P = 0.038] and loop diuretic demand (76.5% vs. 45% of patients; P = 0.044), and lower LVEF (46.6 ± 12.9 vs. 53.7 ± 8.7%; P = 0.019) and GFR (51.8 ± 16.5 vs. 68.5 ± 18.6 mL/min; P = 0.037) compared with the reference cohort. At 3-month follow-up, a numerical decrease in NT-proBNP levels was observed in 13/17 (76.5%) patients in the dapagliflozin (-190 pg/mL, IQR: -1,028-71, P = 0.557) and 27/40 (67.5%) of patients in the control cohort (-115 pg/mL, IQR: -357-105, P = 0.551). Other disease parameters remained stable and no adverse events occurred. In tafamidis-treated ATTR-CM patients, initiation of dapagliflozin was well tolerated. The efficacy of SGLT2i therapy in patients with ATTR-CM needs to be studied in randomized controlled trials.

Identifiants

pubmed: 36259276
doi: 10.1002/ehf2.14188
pmc: PMC9871707
doi:

Substances chimiques

dapagliflozin 1ULL0QJ8UC
Prealbumin 0
Sodium-Glucose Transporter 2 Inhibitors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

397-404

Subventions

Organisme : Pfizer

Informations de copyright

© 2022 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

Références

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Auteurs

Stephan Dobner (S)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Benedikt Bernhard (B)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Babken Asatryan (B)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Stephan Windecker (S)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Stefan Stortecky (S)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Thomas Pilgrim (T)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Christoph Gräni (C)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Lukas Hunziker (L)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

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Classifications MeSH