Effect of ertugliflozin on left ventricular function in type 2 diabetes and pre-heart failure: the Ertu-GLS randomized clinical trial

Bibliographic Details
Title: Effect of ertugliflozin on left ventricular function in type 2 diabetes and pre-heart failure: the Ertu-GLS randomized clinical trial
Authors: Soo Lim, Jae Hyun Bae, Heran Oh, In-Chang Hwang, Yeonyee E. Yoon, Goo-Yeong Cho
Source: Cardiovascular Diabetology, Vol 23, Iss 1, Pp 1-9 (2024)
Publisher Information: BMC, 2024.
Publication Year: 2024
Collection: LCC:Diseases of the circulatory (Cardiovascular) system
Subject Terms: Angiotensin-converting enzyme 2, Angiotensin (1–7), Diabetes mellitus, type 2, Ertugliflozin, Global longitudinal strain, Heart function tests, Diseases of the circulatory (Cardiovascular) system, RC666-701
More Details: Abstract Background The therapeutic effects of ertugliflozin, a sodium-glucose cotransporter 2 inhibitor, on cardiovascular outcome are not fully understood. This study aimed to evaluate the efficacy and safety of ertugliflozin on cardiac function in people with type 2 diabetes and pre-heart failure. Methods We conducted a 24-week randomized, double-blind, placebo-controlled trial involving individuals with type 2 diabetes inadequately controlled with antidiabetic medications. Participants with left ventricular hypertrophy, E/e’ >15, or impaired left ventricular global longitudinal strain (LVGLS) were randomized 1:1 to receive either ertugliflozin (5 mg once daily) or a placebo. The primary outcome was the change in LVGLS. Secondary outcomes included changes in left ventricular mass index (LVMI) and left ventricular ejection fraction (LVEF). Prespecified exploratory outcomes, including angiotensin-converting enzyme 2 (ACE2) and angiotensin (1–7) levels, were also assessed. Results A total of 102 individuals (mean age, 63.9 ± 9.2 years; 38% women) were included. The ertugliflozin group showed a significant improvement in LVGLS (− 15.5 ± 3.1% to − 16.6 ± 2.8%, P = 0.004) compared to the placebo group (− 16.7 ± 2.7% to − 16.4 ± 2.6%, P = 0.509), with a significant between-group difference (P = 0.013). Improvements in LVMI and LVEF were also observed. Additionally, significant reductions in HbA1c, systolic blood pressure, whole-body and visceral fat, uric acid, proteinuria, N-terminal pro–B-type natriuretic peptide, and lipoprotein(a) were noted. ACE2 and angiotensin (1–7) levels significantly increased in the ertugliflozin group compared to the placebo group and correlated with changes in LVGLS [r = 0.456, P
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1475-2840
Relation: https://doaj.org/toc/1475-2840
DOI: 10.1186/s12933-024-02463-0
Access URL: https://doaj.org/article/e7aab2e61d5649d0b29bf334e60887fa
Accession Number: edsdoj.7aab2e61d5649d0b29bf334e60887fa
Database: Directory of Open Access Journals
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More Details
ISSN:14752840
DOI:10.1186/s12933-024-02463-0
Published in:Cardiovascular Diabetology
Language:English