TY - JOUR
T1 - Effect of SGLT2 inhibitors on cardiac structure and function assessed by cardiac magnetic resonance
T2 - a systematic review and meta-analysis
AU - Leo, Isabella
AU - Salerno, Nadia
AU - Figliozzi, Stefano
AU - Cersosimo, Angelica
AU - Ielapi, Jessica
AU - Stankowski, Kamil
AU - Bisaccia, Giandomenico
AU - Dellegrottaglie, Santo
AU - Canino, Giovanni
AU - De Rosa, Salvatore
AU - Sorrentino, Sabato
AU - Bucciarelli-Ducci, Chiara
AU - Torella, Daniele
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Background and aim: Sodium-glucose cotransporter-2 inhibitors (SGLT2i) improve outcomes in patients with heart failure (HF) but underlying mechanisms remain incompletely understood. Cardiac magnetic resonance (CMR) is key in evaluating cardiac structure and function, enabling accurate assessment of reverse remodeling. Aim of this systematic review and meta-analysis was to assess the effects of SGLT2i on cardiac remodeling evaluated by CMR changes. Methods: We conducted a systematic review and meta-analysis of studies assessing changes in CMR parameters in patients treated with SGLT2i (PROSPERO registration: CRD42024574302). Databases were searched through April 30, 2025. Random-effects models were used to pool mean changes in left and right ventricular volumes, mass, function, stroke volume, global longitudinal strain, left atrial volume, and tissue characterization indices. Meta-regression and sensitivity analyses were performed to evaluate potential sources of heterogeneity. Results: Twenty-three studies and 1008 patients were included. Treatment with SGLT2i was associated with significant reductions in left ventricular (LV) end-diastolic volume (− 7.10 mL; 95% CI: −13.01 to − 1.19, p = 0.023), left ventricular mass (− 4.24 g; 95% CI: −7.88 to − 0.60, p = 0.027) and epicardial adipose tissue (-4.94 ml; 95% CI: -9.06, -0.82, p = 0.019). A subgroup analysis in patients with reduced LV ejection fraction showed improvement in LV stroke volume. Meta-regression revealed no significant effect of age, male sex or diabetes prevalence on pooled estimates. Conclusions: SGLT2i are associated with reductions in LV volumes and mass in line with an overall favorable reverse remodeling effects as assessed by CMR.
AB - Background and aim: Sodium-glucose cotransporter-2 inhibitors (SGLT2i) improve outcomes in patients with heart failure (HF) but underlying mechanisms remain incompletely understood. Cardiac magnetic resonance (CMR) is key in evaluating cardiac structure and function, enabling accurate assessment of reverse remodeling. Aim of this systematic review and meta-analysis was to assess the effects of SGLT2i on cardiac remodeling evaluated by CMR changes. Methods: We conducted a systematic review and meta-analysis of studies assessing changes in CMR parameters in patients treated with SGLT2i (PROSPERO registration: CRD42024574302). Databases were searched through April 30, 2025. Random-effects models were used to pool mean changes in left and right ventricular volumes, mass, function, stroke volume, global longitudinal strain, left atrial volume, and tissue characterization indices. Meta-regression and sensitivity analyses were performed to evaluate potential sources of heterogeneity. Results: Twenty-three studies and 1008 patients were included. Treatment with SGLT2i was associated with significant reductions in left ventricular (LV) end-diastolic volume (− 7.10 mL; 95% CI: −13.01 to − 1.19, p = 0.023), left ventricular mass (− 4.24 g; 95% CI: −7.88 to − 0.60, p = 0.027) and epicardial adipose tissue (-4.94 ml; 95% CI: -9.06, -0.82, p = 0.019). A subgroup analysis in patients with reduced LV ejection fraction showed improvement in LV stroke volume. Meta-regression revealed no significant effect of age, male sex or diabetes prevalence on pooled estimates. Conclusions: SGLT2i are associated with reductions in LV volumes and mass in line with an overall favorable reverse remodeling effects as assessed by CMR.
KW - Cardiovascular magnetic resonance
KW - Heart failure
KW - Reverse cardiac remodeling
KW - Sodium-glucose transport protein 2
UR - https://www.scopus.com/pages/publications/105013971629
U2 - 10.1186/s12933-025-02904-4
DO - 10.1186/s12933-025-02904-4
M3 - Article
C2 - 40841653
AN - SCOPUS:105013971629
SN - 1475-2840
VL - 24
JO - Cardiovascular Diabetology
JF - Cardiovascular Diabetology
IS - 1
M1 - 345
ER -