Key result
Combined ARNI and SGLT2i linked to ~608 mL higher day-1 urine volume in acute heart failure.
Why the study?
To explore changes in diuretic and renal outcomes following initiation of combined ARNI and SGLT2 inhibitor therapy post-hemodynamic stabilization in acute heart failure patients.
Does combined ARNI and SGLT2 inhibitor therapy improve diuretic response and cardiac biomarkers in patients with acute heart failure and LVEF ≤40%?
Does combined ARNI and SGLT2 inhibitor therapy improve diuretic response and cardiac biomarkers in patients with acute heart failure and LVEF ≤40%?
Combined ARNI and SGLT2 inhibitor therapy in acute heart failure may improve short-term diuresis and cardiac biomarkers without worsening renal function.
Hypothesis-generating for combined ARNI/SGLT2i in AHF; randomized trials needed before clinical adoption.
Acute heart failure (AHF) requires immediate intervention, with diuretics central to managing volume overload. We conducted a prospective single-arm study to explore changes in diuretic and renal outcomes following initiation of combined angiotensin receptor neprilysin inhibitor (ARNI) and sodium-glucose cotransporter 2 (SGLT2) inhibitors therapy in AHF patients. We enrolled 120 patients with left ventricular ejection fraction ≤40% and signs of fluid overload, initiation of combined ARNI and SGLT2 inhibitor therapy post-hemodynamic stabilization. Urine volume, renal function, and cardiovascular biomarkers were assessed over 9 days. Urine volume and diuretic response increased significantly on day 1, stabilizing above baseline levels. Cardiovascular biomarkers showed improvements, with decreased NT-proBNP and increased LVEF, without affecting eGFR. Increased diuresis and improved cardiac function parameters were observed during combination therapy. These hypothesis-generating findings support the need for randomized controlled trials to evaluate the clinical utility of this combination in AHF management. The short-term nature of the study and lack of a control group are limitations, which preclude definitive causal attribution of the observed effects. This study has been registered with the Chinese Clinical Trial Registry under registration number ChiCTR2600118845. Clinical Trial RegistrationChinese Clinical Trial Registry (ChiCTR2600118845).
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Zhang et al. (2026) studied Acute heart failure (AHF) (n=120). ARNI (sacubitril/valsartan) and SGLT2 inhibitor (dapagliflozin) vs. Baseline (single-arm study) was evaluated on Change in 24-hour urine volume from baseline to Day 0 (p=<0.001). Combined ARNI and SGLT2 inhibitor therapy significantly increased 24-hour urine volume by 608 mL on day 1 compared to baseline in patients with acute heart failure.
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