Dapagliflozin significantly increased left ventricular ejection fraction from approximately 35% to 40% over 12 months in patients with heart failure and type 2 diabetes, without altering total body water.
Observational (n=64)
No
Does SGLT-2 inhibitor therapy improve left ventricular ejection fraction and fluid compartment dynamics in patients with heart failure and type 2 diabetes?
SGLT-2 inhibitor therapy in patients with HF and T2DM improves cardiac function and reduces hospitalizations without measurable changes in total body water, suggesting mechanisms beyond simple volume reduction.
Absolute Event Rate: 40% vs 35%
p-value: p=<0.001
To evaluate the longitudinal changes in body fluid compartments and their association with cardiac recovery in patients with concomitant heart failure (HF) and type 2 diabetes mellitus (T2DM) receiving sodium-glucose cotransporter-2 (SGLT-2) inhibitor therapy. In this prospective, single-center study, 64 patients diagnosed with both HF and T2DM were initiated on SGLT-2 inhibitor therapy and followed up for 12 months. Clinical and laboratory parameters, along with bioelectrical impedance analysis (BIA), were evaluated at baseline, 6 months, and 12 months. The key analytical parameters included left ventricular ejection fraction (LVEF), NT-proBNP levels, peripheral edema scores, hospitalization rates, and fluid metrics such as total body water (TBW), extracellular water (ECW), intracellular water (ICW), absolute fluid overload (FO), and relative fluid overload (RFO). A statistically significant increase in LVEF was observed during the 12-month follow-up period (p 0.05). Although an increase in RFO was noted at 12 months (p = 0.012), the primary fluid compartments remained stable. SGLT-2 inhibitor therapy in patients with HF and T2DM is associated with improved cardiac function, reduced myocardial stress, regression of peripheral edema, and a substantial decrease in the hospitalization rate. The absence of measurable changes in total body water suggests that the cardioprotective effects of SGLT-2 inhibitors extend beyond simple volume reduction, potentially involving direct myocardial and metabolic mechanisms.
KANTAR et al. (Tue,) conducted a observational in Heart failure and type 2 diabetes mellitus (n=64). Dapagliflozin vs. Baseline was evaluated on Change in left ventricular ejection fraction (LVEF) (p=<0.001). Dapagliflozin significantly increased left ventricular ejection fraction from approximately 35% to 40% over 12 months in patients with heart failure and type 2 diabetes, without altering total body water.
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