Key result
SGLT2 inhibitors linked to ~29% lower one-year HF mortality, enhanced by intensified background therapy.
Why the study?
Although SGLT2 inhibitors improve outcomes in heart failure, their effects may depend on background medical therapy, prompting evaluation of whether the Heart Failure Collaboratory score modifies this benefit.
Does SGLT2 inhibitors reduce one-year all-cause mortality in patients with heart failure, and is this effect modified by the intensity of background medical therapy?
Cohort (n=4,077)
Yes
Does SGLT2 inhibitors reduce one-year all-cause mortality in patients with heart failure, and is this effect modified by the intensity of background medical therapy?
The mortality benefit of SGLT2 inhibitors in heart failure is significantly enhanced when patients are concurrently treated with adequately dosed background guideline-directed medical therapies.
Answers are grounded in this paper and cite their sources.
HF Collaboratory score may modify SGLT2i mortality benefit in HF; hypothesis-generating and requires prospective validation.
SGLT2 inhibitors (SGLT2is) improve outcomes in patients with heart failure (HF), but their effects may depend on background medical therapy. The Heart Failure Collaboratory score, which incorporates medication type and dose, may modify the benefit of SGLT2is. To evaluate the association between the scoring system and the mortality benefit of SGLT2 inhibitors in patients with heart failure. This retrospective multicenter cohort study used real-world data from the Chinese Cardiovascular Association Database–HF Center (HFC) Registry. 52 hospitals were selected with 26 HFCs and 26 NHFCs. Patients with a diagnosis of HF and one-year follow-up from July 1, 2022, to March 31, 2023, were included. The primary outcome was one-year all-cause mortality. Cox regression and multivariable fractional polynomial interaction (MFPI) models were used to assess the effect of SGLT2is on mortality risk across Heart Failure Collaboratory scores. A total of 4,077 patients (median age 70.0 years; 60.1% male) were included. SGLT2is was associated with reduced mortality risk in the overall population (adjusted hazard ratio (aHR) 0.71, 95% CI 0.60–0.85). A significant interaction was observed with the score (P interaction = 0.009), with SGLT2is therapy associated with a greater reduction in mortality risk among patients scoring ≥ 5 (aHR 0.60, 95% CI 0.46–0.78), whereas no significant association was observed in those scoring < 5 (aHR 0.98, 95% CI 0.76–1.26). MFPI analysis further demonstrated greater mortality risk reduction in SGLT2is user than nonuser, as the score increased (P interaction = 0.003), and also in patients with LVEF > 40% (P interaction = 0.021). The mortality benefit was more pronounced when other triple therapy agents were adequately applied. ChiCTR1800017226
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Zhang et al. (2026) conducted a cohort in Heart failure (n=4,077). SGLT2 inhibitors vs. Nonusers was evaluated on One-year all-cause mortality (aHR 0.71, 95% CI 0.60-0.85, p=<0.001). SGLT2 inhibitor use was associated with a 29% lower risk of one-year all-cause mortality (aHR 0.71) in patients with heart failure, with the benefit significantly enhanced by intensified background therapy.
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