# Beyond the MNA: A Biological Vulnerability Phenotype Associated with Prolonged Hospitalization in Older Adults

**Authors:** Virginia Boccardi, Francesca Mancinetti, Cesare Balducci, Valeria Labbozzetta, Elena Ercolanetti, Carmelinda Ruggiero, Sara Ercolani, Patrizia Mecocci

PMC · DOI: 10.3390/nu18040586 · Nutrients · 2026-02-11

## TL;DR

This study shows that a biological definition of occult malnutrition in older hospitalized patients is linked to longer hospital stays, even when standard nutritional screening tools like MNA suggest they are fine.

## Contribution

The study introduces a biological vulnerability phenotype defined by serum markers that improves risk stratification in older hospitalized adults.

## Key findings

- Occult malnutrition, defined by abnormal biological markers, was present in 54.7% of hospitalized older adults.
- Patients with occult malnutrition had significantly longer hospital stays and higher rates of prolonged LOS compared to those without.
- Occult malnutrition remained independently associated with prolonged LOS even after adjusting for MNA scores and other factors.

## Abstract

Background/Objectives: Nutritional status in hospitalized older adults is usually evaluated using screening tools such as the Mini Nutritional Assessment (MNA). During acute illness, however, these tools may overlook biologically relevant vulnerability related to inflammation and metabolic stress, a condition often described as occult malnutrition. The clinical implications of applying a more stringent biological definition of this phenotype are still poorly defined. Methods: We conducted an observational cohort study including 172 hospitalized older adults (mean age 86.7 ± 6.0 years) in an acute geriatric setting with complete data on MNA, serum albumin, hemoglobin, and C-reactive protein (CRP). Occult malnutrition was defined by the coexistence of at least two abnormal biological markers: hypoalbuminemia (albumin < 3.5 g/dL), anemia (Hb < 12 g/dL), and elevated CRP (>0.5 mg/dL). Prolonged length of stay (LOS) was defined as LOS above the 75th percentile. Associations between occult malnutrition, MNA categories, and prolonged LOS were examined using chi-square tests and multivariable logistic regression models adjusted for age ≥ 85 years, sex, primary reason for hospital admission and comorbidity burden. Results: Among 172 acutely hospitalized older adults (mean age 86.7 ± 6.0 years), hypoalbuminemia, anemia, and elevated CRP were observed in 42.4%, 46.5%, and 72.1% of patients, respectively. Occult malnutrition was identified in 54.7% of the cohort. Prolonged length of stay (LOS > 75th percentile) occurred in 50.0% of patients. Compared with patients without occult malnutrition, those with occult malnutrition were older, had significantly longer hospital stays, and a higher prevalence of prolonged LOS (59.6% vs. 38.5%, p = 0.006). The prevalence of occult malnutrition increased across worsening MNA categories (p = 0.022) and was present in 40.7% of patients with a normal MNA score. Occult malnutrition was independently associated with prolonged LOS in multivariable models adjusting for age, sex, admission reason, comorbidity burden, and MNA (adjusted OR range 1.97–2.14, all p < 0.05), whereas MNA itself was not independently associated with prolonged hospitalization. Conclusions: A stringent biological definition of occult malnutrition identifies a large subgroup of hospitalized older adults at increased risk of prolonged hospitalization, including patients considered nutritionally normal by standard screening. These findings underline the limitations of screening-based assessment alone and support the use of simple biological markers to refine risk stratification in acute geriatric care.

## Linked entities

- **Proteins:** LOC100189571 (uncharacterized LOC100189571)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** Syncope (MESH:D013575), injury to (MESH:D014947), Anemia (MESH:D000740), impaired metabolic and inflammatory homeostasis (MESH:D001928), sarcopenia (MESH:D055948), Cardio (MESH:D059347), inflammation (MESH:D007249), muscle catabolism (MESH:D019042), MNA (MESH:D044342), Failure-to-thrive (MESH:D005183), cancer (MESH:D009369), impaired (MESH:D060825), length (MESH:D007870), infection (MESH:D007239), weight loss (MESH:D015431), Depression (MESH:D003866), febrile (MESH:D000071072), Fall (MESH:C537863), Abdominal symptoms (MESH:D000007), synthesis (MESH:C536766), Hypoalbuminemia (MESH:D034141), systemic (MESH:D015619), Vertigo (MESH:D014717), acute illness (MESH:D000208), Prolonged length of stay (MESH:D008133), oncologic disease (MESH:D000072716), metabolic dysregulation (MESH:D021081), related, (MESH:D019973), Neurological (MESH:D009461), metabolic (MESH:D008659), renal, (MESH:D006030), Sepsis (MESH:D018805), Infectious (MESH:D003141), Cognitive (MESH:D003072), Gastrointestinal/Bleeding (MESH:D006471)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943111/full.md

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Source: https://tomesphere.com/paper/PMC12943111