Key result
Higher CONUT score is linked to ~37% higher mortality in elderly patients with HFpEF.
Why the study?
Although malnutrition is common in elderly patients with HFpEF, its prognostic significance and the optimal screening tool remain unclear.
Does nutritional assessment using the CONUT score and GNRI predict all-cause mortality and clinical outcomes in patients aged ≥ 75 years with HFpEF?
Cohort (n=196)
Blinded outcome adjudication
No
Does nutritional assessment using the CONUT score and GNRI predict all-cause mortality and clinical outcomes in patients aged ≥ 75 years with HFpEF?
Hazard Ratio: 1.366 (95% CI 1.181–1.579)
p-value: p=<0.001
In very elderly patients (≥75 years) with HFpEF, both CONUT and GNRI independently predict all-cause mortality, with the CONUT score demonstrating superior prognostic accuracy compared to GNRI alone and no incremental benefit from combining the two scores over CONUT alone.
Background: Malnutrition is common in elderly patients with heart failure with preserved ejection fraction (HFpEF), but its prognostic significance and the optimal screening tool remain unclear. This retrospective, single-center study aimed to compare the application of the Geriatric Nutritional Risk Index (GNRI) and the Controlling Nutritional Status (CONUT) score in assessing nutritional status in very elderly patients with HFpEF, and to evaluate the association between nutritional status and clinical outcomes. Methods: A total of 196 patients aged ≥ 75 years (mean age 92.12 ± 4.28 years, 86.2% male) with HFpEF were enrolled. Nutritional status was categorized using CONUT and GNRI according to standard cut-offs. Results: Patients with higher CONUT scores or lower GNRI scores (indicating worse nutritional status) had significantly longer hospital stays, lower levels of nutrition-related indices (albumin, total cholesterol, low-density lipoprotein cholesterol (LDL-C), serum ferritin, transferrin saturation), lower lymphocyte counts, and higher NT-pro-B-type natriuretic peptide (NT-proBNP) and inflammatory markers (C-reactive protein (CRP), procalcitonin (PCT), interleukin-6 (IL-6)) (all P < 0.05). Over a median follow-up of 11.5 months, 83 patients (42.3%) died. In unadjusted analyses, patients with worse nutritional status had significantly higher rates of all-cause death, all-cause readmission, and heart failure-related readmission (all P < 0.05). Multivariable Cox regression revealed that CONUT (hazard ratio (HR) = 1.366, 95% confidence interval (CI): 1.181–1.579, P < 0.001) was an independent risk factor for all-cause mortality, while GNRI (HR = 0.962, 95% CI: 0.927–0.999, P = 0.043) was a protective factor. The CONUT and GNRI showed poor consistency (κ = 0.235, P < 0.01). Using receiver operating characteristic (ROC) analysis based on vital status at the end of follow-up, the area under the curve (AUC) for predicting all-cause mortality was 0.86 (95% CI: 0.80–0.91) for CONUT, 0.79 (95% CI: 0.73–0.86) for GNRI, and 0.87 (95% CI: 0.82–0.92) for a combined model incorporating both scores via logistic regression. Net reclassification improvement (NRI) analysis showed that compared with the GNRI score, the NRI of the CONUT score was 0.580 (95% CI: 0.309–0.852), and the NRI of the combined score was 0.760 (95% CI: 0.499–1.022), both reaching statistical significance (P < 0.01). By contrast, the NRI was 0.083 (95% CI: −0.197 to 0.363, P = 0.560) for the combined score versus the CONUT score. Conclusions: Malnutrition is common in elderly patients with HFpEF. CONUT and GNRI scores are associated with adverse outcomes. Compared with GNRI alone, the combined assessment of the two scores improves predictive performance for adverse prognosis in elderly patients with HFpEF, while no incremental benefit is observed over CONUT alone.
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Li et al. (2026) conducted a cohort in Heart failure with preserved ejection fraction (HFpEF) (n=196). Controlling Nutritional Status (CONUT) score and Geriatric Nutritional Risk Index (GNRI) vs. Normal nutritional status (CONUT 0-1 or GNRI > 98) / GNRI vs CONUT score comparison was evaluated on All-cause mortality (HR 1.366, 95% CI 1.181-1.579, p=<0.001). Higher CONUT scores independently predicted increased all-cause mortality (HR 1.366, 95% CI 1.181-1.579, P < 0.001) with superior discrimination over GNRI in patients aged ≥75 years with HFpEF.
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