Key result
Lower serum tetranectin levels show no independent link to all-cause mortality.
Why the study?
Heart failure with LVEF >45% lacks reliable biomarkers for risk stratification, complicating management across HFpEF and HFmrEF.
Does serum tetranectin level predict disease severity and mortality in patients with heart failure with ejection fraction >45%?
Cohort (n=116)
No
Does serum tetranectin level predict disease severity and mortality in patients with heart failure with ejection fraction >45%?
Effect estimate: HR 1.22 (95% CI 0.94-1.86)
p-value: p=0.112
Serum tetranectin levels are inversely associated with heart failure severity in patients with LVEF >45%, but do not independently predict mortality when adjusted for age and NT-proBNP.
Does not independently predict mortality after adjustment; leaves open tetranectin's role in HF severity assessment with LVEF >45%.
Background and Objectives Heart failure (HF) with left ventricle ejection fraction (LVEF) >45% lacks reliable biomarkers for risk stratification complicating its management, as it encompasses both heart failure with preserved ejection fraction (HFpEF, LVEF ≥50%) and mildly reduced ejection fraction (HFmrEF, LVEF 45–49.9%). This study aimed to evaluate serum tetranectin (TETRA) as a novel biomarker for assessing disease severity and predicting mortality in patients with HF with EF >45%. Materials and Methods In a prospective cohort study including 116 patients HF with EF>45% from a single center in Arad, Romania, stratified by NYHA class (G1: NYHA I, n=48; G2: NYHA II, n=37; G3: NYHA III–IV, n=31), serum TETRA levels were measured using ELISA. Echocardiographic parameters (E/e’ ratio, LAVI, LAS, GLS, LVEF) and NT-proBNP were assessed at baseline, with all-cause mortality (9 deaths) tracked over a 12-month follow-up. Results Median TETRA levels decreased with worsening NYHA class (G1: 48.9 ng/mL, G2: 33.2 ng/mL, G3: 27.6 ng/mL; p < 0.001) and correlated negatively with NT-proBNP (rho = −0.66, p < 0.001), E/e’ ratio (rho = −0.58, p = 0.003), and LAVI (rho = −0.52, p = 0.010), while positively correlating with LAS (rho = 0.55, p = 0.005). In univariable Cox analysis, lower TETRA levels were associated with higher all-cause mortality (HR = 1.38 per 10 ng/mL decrease, 95% CI: 1.06–1.81, p = 0.045), but this association was not significant after adjustment for age and NT-proBNP (HR = 1.22, 95% CI: 0.94–1.86, p = 0.112). Conclusions TETRA levels are inversely associated with severity in heart failure with EF>45% and may reflect disease progression.
No takes yet. Share an insight, caveat, or question.
Vulciu et al. (2025) conducted a cohort in Heart failure with ejection fraction >45% (n=116). Serum tetranectin (TETRA) was evaluated on All-cause mortality (HR 1.22, 95% CI 0.94-1.86, p=0.112). Lower serum tetranectin levels were not significantly associated with all-cause mortality after adjustment for age and NT-proBNP (HR 1.22; 95% CI 0.94-1.86; p=0.112).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: