Key result
SGLT2i initiation linked to LV reverse remodelling in ~73% of heart failure patients.
Why the study?
Although SGLT2i improve outcomes in heart failure, the baseline characteristics associated with left ventricular changes after SGLT2i initiation in routine practice are incompletely defined.
Does initiation of SGLT2 inhibitors improve left ventricular volumes and ejection fraction at 6 months in patients with predominantly HFrEF?
Cohort (n=101)
Yes
Does initiation of SGLT2 inhibitors improve left ventricular volumes and ejection fraction at 6 months in patients with predominantly HFrEF?
In routine clinical practice, SGLT2i initiation in patients with predominantly HFrEF is associated with modest reductions in left ventricular volumes and a small improvement in LVEF at 6 months.
Answers are grounded in this paper and cite their sources.
SGLT2 inhibitor use was associated with LVEDV reduction; leaves open whether this drives clinical benefit in randomized trials.
Background: Sodium–glucose cotransporter-2 inhibitors (SGLT2i) improve outcomes in heart failure (HF), but baseline characteristics associated with left ventricular (LV) changes after their initiation in routine practice are incompletely defined. Methods: In this retrospective two-centre study, 101 patients with HF (94 HFrEF, 6 HFmrEF, 1 HFpEF) initiating an SGLT2i underwent echocardiography at baseline and 6 months. For the purposes of this study, LV reverse remodelling was defined as a simultaneous reduction in LV end-diastolic (LVEDV) and end-systolic volume (LVESV); LVESV reductions ≥10% and ≥15% were used as stringent definitions. Associations were explored with Firth logistic regression adjusted for age and baseline LVEF. Death or HF hospitalisation after the 6-month visit was analysed in relation to 6-month changes (landmark analysis). Results: Median LVEF increased from 28.8% at baseline to 31.6% at 6 months, and the medians of individual paired changes in LVEDV and LVESV were −13.0% and −16.3% (all p < 0.001). The operational definition was met by 74 patients (73.3%) and an LVESV reduction ≥15% by 56 (55.4%). Higher BMI and larger baseline LVEDV were associated with LV volume reduction, and lower TAPSE with LVEF response, LVESV reduction ≥15% and NYHA improvement. No statistically significant association was observed between 6-month changes in LVEF or LV volumes and subsequent death or HF hospitalisation; confidence intervals were wide. Conclusions: In this uncontrolled cohort, SGLT2i initiation was followed by modest LV volume reduction and a small LVEF increase. These associations are exploratory and hypothesis-generating.
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Tricarico et al. (2026) conducted a cohort in Heart failure (predominantly HFrEF) (n=101). Sodium-glucose cotransporter-2 inhibitors (SGLT2i) vs. Baseline (pre-initiation) was evaluated on LV reverse remodelling (simultaneous reduction in LVEDV and LVESV at 6 months) (p=<0.001). SGLT2i initiation in heart failure was associated with LV reverse remodelling in 73.3% of patients and increased median LVEF from 28.8% to 31.6% at 6 months.
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