Key result
Baseline IGFBP7 concentrations in the highest tertile predicted an increased risk of HF hospitalization or cardiovascular death (HR 2.00, 95% CI 1.28-3.10, p=0.002) regardless of ejection fraction.
Why the study?
The role of IGFBP7 as a prognostic biomarker across the full ejection fraction spectrum of heart failure, and the effect of empagliflozin on its levels, remained less well understood.
Does baseline IGFBP7 predict cardio-renal outcomes in heart failure, and does empagliflozin alter its concentrations?
Observational (n=1,125)
Yes
Does baseline IGFBP7 predict cardio-renal outcomes in heart failure, and does empagliflozin alter its concentrations?
Effect estimate: HR 2.00 (95% CI 1.28-3.10)
p-value: p=0.002
IGFBP7 is a strong prognostic biomarker for adverse cardio-renal outcomes in heart failure across the ejection fraction spectrum, though its levels are not modified by empagliflozin.
AIMS: Insulin-like growth factor binding protein-7 (IGFBP7) is a biomarker of tissue senescence with a role in cardio-renal pathophysiology. The role of IGFBP7 as a prognostic biomarker across the full ejection fraction (EF) spectrum of heart failure (HF) remains less well understood. We examined associations between IGFBP7 and risk of cardio-renal outcomes regardless of EF and the effect of empagliflozin treatment on IGFBP7 concentrations among individuals with HF. METHODS AND RESULTS: IGFBP7 was measured in 1125 study participants from the EMPEROR-Reduced and EMPEROR-Preserved trials. Cox regression was used to study associations with outcomes. Study participants with IGFBP7 levels in the highest tertile had a higher-risk clinical profile. In Cox proportional hazards models adjusted for clinical variables, N-terminal pro-B-type natriuretic peptide and high-sensitivity cardiac troponin T, baseline IGFBP7 values in the highest tertile predicted an increased risk of HF hospitalization or cardiovascular death (hazard ratio [HR] 2.00, 95% confidence interval [CI] 1.28-3.10, p = 0.002, p for trend <0.001) and higher risk of the renal composite endpoint (HR 4.66, 95% CI 1.61-13.53, p = 0.005, p for trend = 0.001), regardless of EF. Empagliflozin reduced risk for cardiovascular death/HF hospitalization irrespective of baseline IGFBP7 (p for trend across IGFBP7 tertiles = 0.26). Empagliflozin treatment was not associated with meaningful change in IGFBP7 at 12 or 52 weeks. CONCLUSION: Across the entire left ventricular EF spectrum in the EMPEROR Programme, concentrations of the senescence-associated biomarker IGFBP7 were associated with higher risk clinical status and predicted adverse cardio-renal outcomes even in models adjusted for conventional biomarkers. Empagliflozin did not significantly affect IGFBP7 levels over time.
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Ferreira et al. (2024) conducted an observational in Chronic Heart Failure (n=1,125). Empagliflozin was evaluated on HF hospitalization or cardiovascular death (HR 2.00, 95% CI 1.28-3.10, p=0.002). Baseline IGFBP7 concentrations in the highest tertile predicted an increased risk of HF hospitalization or cardiovascular death (HR 2.00, 95% CI 1.28-3.10, p=0.002) regardless of ejection fraction.
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