Beyond sarcopenia: frailty in chronic haemodialysis patients

Author:

Souweine Jean-Sébastien1,Pasquier Grégoire2,Morena Marion1,Patrier Laure3,Rodriguez Annie3,Raynal Nathalie3,Ohresser Isabelle3,Benomar Racim4,Hayot Maurice5,Mercier Jacques5,Gouzi Farès5,Cristol Jean-Paul13ORCID

Affiliation:

1. PhyMedExp, University of Montpellier, INSERM, CNRS, Department of Biochemistry and Hormonology, University Hospital Center of Montpellier , Montpellier , France

2. University of Montpellier, Academic Hospital (CHU) of Montpellier, Department of Parasitology/Mycology , National Reference Centre (CNR) for Leishmaniosis, Montpellier , France

3. Fondation Charles Mion AIDER Santé , Montpellier , France

4. Department of Biochemistry and Hormonology, University Hospital Center of Montpellier , Montpellier , France

5. PhyMedExp, University of Montpellier, INSERM, CNRS, Department of Physiology, University Hospital Center of Montpellier , Montpellier , France

Abstract

ABSTRACT Background Frailty, characterized by vulnerability, reduced reserves and increased susceptibility to severe events, is a significant concern in chronic haemodialysis (HD) patients. Sarcopenia, corresponding to the progressive loss of muscle mass and strength, may contribute to frailty by reducing functional capacity, mobility and autonomy. However, consensus lacks on the optimal bedside frailty index for chronic HD patients. This study investigated the influence of frailty on chronic HD patient survival and explored the associated factors. Methods A total of 135 patients were enrolled from January to April 2019 and then followed up prospectively until April 2022. At inclusion, frailty was assessed by the Timed Up and Go (TUG) and Short Physical Performance Battery (SPPB) tests including gait speed, standing balance and lower limb muscle strength. Results From a total of 114 prevalent chronic HD patients (66% men, age 67.6 ± 15.1 years), 30 died during the follow-up period of 23.7 months (range 16.8–34.3). Deceased patients were older, had more comorbidities and a higher sarcopenia prevalence (P < .05). The TUG and SPPB test scores were significantly reduced in patients who had died [SPPB total score: 7.2 ± 3.3 versus 9.4 ± 2.5; TUG time 8.7 ± 5.8 versus 13.8 ± 10.5 (P < .05)]. Multivariate analysis showed that a higher SPPB score (total value >9) was associated with a lower mortality risk [hazard ratio 0.83 (95% confidence interval 0.74–0.92); P < .03). Each component of the SPPB test was also associated with mortality in univariate analysis, but only the SPPB balance test remained protective against mortality in multivariate analysis. Older age, lower handgrip strength and lower protein catabolic rate were associated with SPPB total scores <9, SPPB balance score and TUG time >10 s. Conclusions Screening for frailty is crucial in chronic HD patients, and incorporating SPPB, especially the balance test, provides valuable insights. Diminished muscle strength and inadequate protein intake negatively influence the SPPB score and balance in chronic HD patients. Effective identification and management of frailty can therefore improve outcomes. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov NCT03845452.

Publisher

Oxford University Press (OUP)

Reference40 articles.

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