# Impact of Nutritional Status on Mortality in Older Patients Hospitalized for Acute Heart Failure

**Authors:** Tsukasa Murakami, Keisuke Kojima, Masanori Takenoya, Kentaro Jujo, Ryusuke Ae, Masanari Kuwabara

PMC · DOI: 10.3390/nu18040623 · Nutrients · 2026-02-13

## TL;DR

This study shows that the nutritional status of older patients admitted for heart failure is strongly linked to their risk of death within a year.

## Contribution

The study demonstrates that the Geriatric Nutritional Risk Index (GNRI) is a better predictor of mortality than other nutritional scores in older heart failure patients.

## Key findings

- Moderate and severe GNRI risk categories were associated with significantly higher all-cause mortality in older patients with acute heart failure.
- GNRI showed better risk reclassification compared to the CONUT score and the PNI for predicting 1-year mortality.
- The inverse association between GNRI and mortality was consistent even in patients aged 85 years and older.

## Abstract

Backgrounds/Objectives: Advances in prevention and medical care in the field of cardiology have led to an increase in the number of older patients with heart failure. In this population, assessment of nutritional status is particularly important. However, the prognostic impact of severity-based nutritional assessment at admission remains unclear. We conducted a study to elucidate the impact of malnutrition severity at admission on the prognosis of older patients hospitalized for acute heart failure (AHF). Methods: This study investigated the relationship between the Geriatric Nutritional Risk Index (GNRI) at admission and prognosis in 214 older patients aged ≥65 years who were hospitalized for AHF (mean age, 85 ± 8 years; male, 49%) between 2019 and 2023. GNRI was assessed by dividing patients into four groups: GNRI > 98 as normal (n = 64), 92 ≤ GNRI < 98 as mild risk (n = 54), 82 ≤ GNRI < 92 as moderate risk (n = 66), and GNRI < 82 as severe risk (n = 30). The discriminative performance of GNRI for 1-year all-cause mortality was compared with that of the Controlling Nutritional Status (CONUT) score and the Prognostic Nutritional Index (PNI). Results: During a median follow-up of 356 days, 76 deaths were observed. Worse GNRI categories were associated with older age, underweight, frailty, and anemia. Multivariable Cox proportional hazards models revealed that moderate GNRI risk (hazard ratio (HR), 2.69; 95% confidence interval (CI), 1.34–5.40) and severe GNRI risk (HR, 9.75; 95% CI, 4.30–22.10) were associated with higher all-cause mortality when compared with normal GNRI, along with age (HR per 1-year increase, 1.07; 95% CI, 1.03–1.11). Sensitivity analysis using GNRI as a continuous variable demonstrated similar results; GNRI was inversely associated with all-cause mortality (HR per 1 GNRI increase, 0.92; 95% CI, 0.90–0.95). In a subgroup analysis of age ≥85 years, the inverse association between GNRI and all-cause mortality was consistent. For 1-year all-cause mortality, GNRI showed moderate discrimination (area under the curve (AUC), 0.71; 95% CI, 0.63–0.80). Although the AUC of GNRI was not significantly different from that of the CONUT score or the PNI, GNRI demonstrated significantly better risk reclassification (net reclassification improvement, 0.47 vs. CONUT, p = 0.05; 0.43 vs. PNI, p = 0.02). Conclusions: In older patients with AHF including the oldest-old, nutritional status assessed by the GNRI at admission was predictive of prognosis. The importance of evaluating nutritional status at admission in clinical settings is reaffirmed.

## Linked entities

- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** NR3C2 (nuclear receptor subfamily 3 group C member 2) [NCBI Gene 4306] {aka MCR, MLR, MR, NR3C2VIT}, SERPINE2 (serpin family E member 2) [NCBI Gene 5270] {aka GDN, GDNPF, PI-7, PI7, PN-1, PN1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}, AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}, ACE (angiotensin I converting enzyme) [NCBI Gene 1636] {aka ACE1, CD143, DCP, DCP1}
- **Diseases:** cardiopulmonary arrest (MESH:D006323), AR (MESH:D013734), edema (MESH:D004487), impaired (MESH:D060825), acute myocardial infarction (MESH:D009203), cancer (MESH:D009369), diabetes mellitus (MESH:D003920), valve disease (MESH:D006349), atrial fibrillation (MESH:D001281), dyslipidemia (MESH:D050171), death (MESH:D003643), CONUT (MESH:D044342), terminally ill (MESH:D007153), malabsorption (MESH:D008286), hypertension (MESH:D006973), muscle wasting (MESH:D009133), inflammation (MESH:D007249), Anemia (MESH:D000740), injury to (MESH:D014947), hypercatabolism (MESH:C565476), MR (MESH:D008944), CFS (MESH:D000073496), nutritional deterioration (MESH:D009748), absorption (MESH:C564600), aortic regurgitation (MESH:D001022), COPD (MESH:D029424), heart diseases (MESH:D006331), appetite suppression (MESH:D001068), coronary artery disease (MESH:D003324), underweight (MESH:D013851), peripheral artery disease (MESH:D058729), aortic stenosis (MESH:D001024), AHF (MESH:D006333)
- **Chemicals:** MRA (MESH:C502936), cholesterol (MESH:D002784)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942728/full.md

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Source: https://tomesphere.com/paper/PMC12942728