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Safety and tolerability of SGLT2 inhibitors in cardiac amyloidosis — a clinical feasibility study

Please always quote using this URN: urn:nbn:de:bvb:20-opus-356024
  • Sodium-glucose transport protein 2 inhibitors (SGLT2i) slow the progression of renal dysfunction and improve the prognosis of patients with heart failure. Amyloidosis constitutes an important subgroup for which evidence is lacking. Amyloidotic fibrils originating from misfolded transthyretin and light chains are the causal agents in ATTR and AL amyloidosis. In these most frequent subtypes, cardiac involvement is the most common organ manifestation. Because cardiac and renal function frequently deteriorate over time, even under best availableSodium-glucose transport protein 2 inhibitors (SGLT2i) slow the progression of renal dysfunction and improve the prognosis of patients with heart failure. Amyloidosis constitutes an important subgroup for which evidence is lacking. Amyloidotic fibrils originating from misfolded transthyretin and light chains are the causal agents in ATTR and AL amyloidosis. In these most frequent subtypes, cardiac involvement is the most common organ manifestation. Because cardiac and renal function frequently deteriorate over time, even under best available treatment, SGLT2i emerge as a promising treatment option due to their reno- and cardioprotective properties. We retrospectively analyzed patients with cardiac amyloidosis, who received either dapagliflozin or empagliflozin. Out of 79 patients, 5.1% had urinary tract infections; 2 stopped SGLT2i therapy; and 2.5% died unrelated to the intake of SGLT2i. No genital mycotic infections were observed. As expected, a slight drop in the glomerular filtration rate was noted, while the NYHA functional status, cardiac and hepatic function, as well as the 6 min walk distance remained stable over time. These data provide a rationale for the use of SGLT2i in patients with amyloidosis and concomitant cardiac or renal dysfunction. Prospective randomized data are desired to confirm safety and to prove efficacy in this increasingly important group of patients.show moreshow less

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Metadaten
Author: Maximilian J. SteinhardtORCiD, Vladimir CejkaORCiD, Mengmeng Chen, Sabrina Bäuerlein, Julia Schäfer, Ali Adrah, Sandra M. Ihne-Schubert, Aikaterini Papagianni, K. Martin KortümORCiD, Caroline MorbachORCiD, Stefan StörkORCiD
URN:urn:nbn:de:bvb:20-opus-356024
Document Type:Journal article
Faculties:Medizinische Fakultät / Neurologische Klinik und Poliklinik
Medizinische Fakultät / Medizinische Klinik und Poliklinik I
Medizinische Fakultät / Medizinische Klinik und Poliklinik II
Medizinische Fakultät / Deutsches Zentrum für Herzinsuffizienz (DZHI)
Language:English
Parent Title (English):Journal of Clinical Medicine
ISSN:2077-0383
Year of Completion:2024
Volume:13
Issue:1
Article Number:283
Source:Journal of Clinical Medicine (2024) 13:1, 283. https://doi.org/10.3390/jcm13010283
DOI:https://doi.org/10.3390/jcm13010283
Sonstige beteiligte Institutionen:Interdisziplinäres Amyloidosezentrum Nordbayern
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Tag:SGLT2 inhibitors; amyloidosis; chronic kidney disease; heart failure
Release Date:2024/06/10
Date of first Publication:2024/01/04
Licence (German):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International