Frailty in ageing persons with multiple sclerosis

Author:

Ayrignac Xavier1ORCID,Larochelle Catherine2,Keezer Mark3,Roger Elaine2,Poirier Josée2,Lahav Boaz2,Girard Marc2,Prat Alexandre2,Duquette Pierre2

Affiliation:

1. Clinique de Sclérose en plaques du Centre de Recherche du Centre Hospitalier de l’Université de Montréal (CRCHUM), Montreal, QC, Canada/Department of Neurosciences, Faculty of Medicine, Université de Montréal, Montreal, QC, Canada/Département de Neurologie, CRC sclérose en plaques, CHU Montpellier, INSERM, Université Montpellier, Montpellier, France

2. Clinique de Sclérose en plaques du Centre de Recherche du Centre Hospitalier de l’Université de Montréal (CRCHUM), Montreal, QC, Canada/Department of Neurosciences, Faculty of Medicine, Université de Montréal, Montreal, QC, Canada

3. Department of Neurosciences, Université de Montréal, Montreal, QC, Canada/Centre Hospitalier de l’Université de Montréal (CHUM), Montreal, QC, Canada/Department of Social and Preventative Medicine, Université de Montréal, Montreal, QC, Canada/Centre de Recherche du Centre Hospitalier de l’Université de Montréal (CRCHUM), Montréal, QC, Canada

Abstract

Background: Recent progress in multiple sclerosis (MS) management has contributed to a greater life expectancy in persons with MS. Ageing with MS comes with unique challenges and bears the potential to greatly affect quality of life and socioeconomic burden. Objectives: To compare frailty in ageing persons with multiple sclerosis (pwMS) and controls; to correlate frailty with MS clinical characteristics. Methods: PwMS and controls over 50 years old were recruited in a cross-sectional study. Two validated frailty measures were assessed: the frailty index and the Fried’s phenotype. Several multiple linear regressions accounting for demographic and clinical characteristics were performed. Results: Eighty pwMS (57 females, mean age 58.5 ± 6 years old) and 37 controls (24 females, mean age 61 ± 6.5 years old) were recruited. Multivariable analysis identified significantly higher frailty index in pwMS (0.21 ± 0.12 vs 0.11 ± 0.08, p < 0.0001). Similarly, according to Fried’s phenotype, a significantly higher percentage of pwMS were frail compared to controls (28% vs 8%). In pwMS, frailty index was independently associated with expanded disability status scale (EDSS), comorbidities, education level and disease duration. Conclusion: Our results suggest that frailty can be routinely assessed in pwMS. Increased frailty in MS patients suggests that, along with MS therapeutics, a tailored multidisciplinary approach of ageing pwMS is needed.

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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