Relationship Between Soluble Transferrin Receptor and Clinical Outcomes in Patients With Heart Failure According to...

Iron deficiency (ID) is highly prevalent in patients with heart failure (HF) but its impact on prognosis in HF with preserved ejection fraction (HFpEF) remains unclear. We assessed whether ID defined by soluble transferrin receptor (sTfR) criteria is independently associated with all-cause mortality in patients with HFpEF, and evaluated its comparative prognostic performance to ID definitions in common clinical use.

Data were analyzed from 788 patients (36% HFpEF) in a prospective multicenter HF cohort study. Baseline plasma samples were analyzed with respect to 4 definitions of ID: sTfR of ≥1.59 mg/L (ID_sTfR1), sTfR of ≥1.76 mg/L (ID_sTfR2), ferritin of <100 µg/L, or ferritin of 100-300 µg/L + transferrin saturation of <20% (ID_Ferritin), and transferrin saturation of <20% (ID_Tsat). In multivariable Cox models ID_sTfR2 (hazard ratio [HR] 1.84, 95% confidence interval [CI] 1.23-2.75) and ID_Tsat (HR, 1.69, 95% CI 1.10-2.59) were both independently associated with all-cause mortality in patients with HFpEF, whereas ID_sTfR1 (HR 1.41, 95% CI 0.92-2.16) and ID_Ferritin (HR 1.19, 95% CI 0.77-1.85) were not. On inclusion of patients with HF with reduced EF, ID_sTfR1 (HR 1.45, 95% CI 1.13-1.86) gained significance, but ID_Ferritin (HR 1.21, 95% CI 0.95-1.54) did not. For each pair of definitions intra-patient concordance was approximately 65%.

ID defined by sTfR criteria is independently associated with all-cause mortality in patients with HFpEF. Poor concordance between ID definitions suggests that iron biomarkers do not reflect the same pathological process in the complex relationship between iron and HF. Therefore, which definition should guide iron replacement needs further evaluation.