# An Immuno-Fragile Profile Is Associated with Mortality Risk in Patients with Chronic Kidney Disease

**Authors:** Noemí Ceprián, Irene Martínez de Toda, Paula Jara Caro, Claudia Yuste, Gemma Valera-Arévalo, Ignacio González de Pablos, Andrea Figuer, Matilde Alique, Rafael Ramírez, Enrique Morales, Julia Carracedo

PMC · DOI: 10.3390/biomedicines13102370 · Biomedicines · 2025-09-27

## TL;DR

This study finds that a combination of immune dysfunction and frailty, called an immuno-fragile profile, is linked to higher mortality in chronic kidney disease patients.

## Contribution

The study introduces the concept of an 'immuno-fragile profile' as a novel prognostic tool for CKD mortality.

## Key findings

- CKD patients, especially those on hemodialysis, show reduced lymphocyte counts and increased proinflammatory monocytes.
- Frailty is most common in hemodialysis patients and correlates with higher mortality risk.
- The immuno-fragile profile independently predicts mortality in CKD patients.

## Abstract

Background/Objectives: Patients with chronic kidney disease (CKD) face higher risks of infections, poor vaccine responses, and cardiovascular diseases, leading to increased morbidity and mortality due to immune dysfunction and frailty. This study aims to evaluate immune status and frailty in CKD patients across different treatments, examine the influence of frailty on immune status, and link these factors to mortality. Methods: A total of 174 participants were included (end-stage renal disease, ESRD n = 40; hemodialysis, HD n = 40; peritoneal dialysis, n = 36; kidney transplant patients, n = 40; healthy subjects n = 18). Immunophenotyping of lymphocyte and monocyte subpopulations was performed, and frailty was assessed using the Edmonton Frail Scale. Principal component analysis (PCA) integrated immune and frailty variables to define an “immuno-fragile profile,” and survival was monitored for up to six years. Results: CKD patients, especially those on HD, showed decreased lymphocyte counts and proinflammatory monocyte subpopulations with increased expression of costimulatory molecules (B7.2/CD86 and ICAM-1/CD54). Frailty was most prevalent in HD patients (53%), with notable sex differences. PCA identified three components—lymphocyte counts, monocyte co-stimulatory expression, and frailty—that together explained 70% of the variance. Survival analysis revealed that patients with lower lymphocyte counts and higher frailty scores had increased mortality risk, especially in the HD and ESRD groups. Cox regression confirmed that the immuno-fragile profile independently predicted mortality. Conclusions: The integration of immune alterations and frailty defines an immuno-fragile profile strongly associated with mortality in CKD patients, which may serve as a robust prognostic tool to improve risk stratification and guide personalized interventions in clinical practice.

## Linked entities

- **Diseases:** chronic kidney disease (MONDO:0005300), end-stage renal disease (MONDO:0004375)

## Full-text entities

- **Genes:** CD86 (CD86 molecule) [NCBI Gene 942] {aka B7-2, B7.2, B70, BU63, CD28LG2, CD86 v6}, ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}
- **Diseases:** ESRD (MESH:D007676), infections (MESH:D007239), immune dysfunction (MESH:D007154), Frail (MESH:D000073496), CKD (MESH:D051436), HD (MESH:D006816), cardiovascular diseases (MESH:D002318)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12561049/full.md

## References

89 references — full list in the complete paper: https://tomesphere.com/paper/PMC12561049/full.md

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Source: https://tomesphere.com/paper/PMC12561049