Frailty in rheumatoid arthritis and the general population: A cross-sectional analysis of the Groningen Frailty Indicator and Fried criteria.
cross_sectional · Level IV
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- Record sourced from PubMed, PMID 42308523.
- Also identified by DOI 10.1093/rheumatology/keag310.
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Abstract
To compare frailty prevalence and factors driving frailty between older adults with rheumatoid arthritis (RA) and controls, using two conceptually distinct frailty instruments. Cross-sectional data from the STudying Ageing in Rheumatoid arthritis (STAR) study were used, including 207 patients with RA and 214 population controls aged 55-85 years. Frailty was assessed using the Groningen Frailty Indicator (GFI; 15 yes/no items; physical, cognitive, social, psychological domains; frail≥4/15) in all participants and the Fried criteria (5 yes/no items; physical domain; prefrail=1-2, frail≥3, and combined frail/prefrail≥1 deficit) in a clinically assessed subgroup (RA: n = 88, controls: n = 96). Prevalence and overlap between instruments were described by group. Uni- and multivariable logistic (GFI: frailty vs. robust) and Poisson (Fried: frail/prefrail vs. robust) regressions assessed effects of age, group, the age*group interaction, and additional covariates. Frailty prevalence was higher in RA than controls for GFI-frailty (34% vs 18%) and Fried-frailty/prefrailty (72% vs 50%). Among GFI-frail persons, 88% of patients with RA compared to 69% of controls were also frail or prefrail by Fried. Age was not associated with frailty in uni- or multivariable analyses for either instrument, in RA or controls (p interaction age*group>0.10). The association with RA became insignificant after multivariable adjustment. Living alone, comorbidity score ≥1, higher fatigue, and anxiety were associated with GFI-frailty, and higher BMI and poorer physical function with Fried- frailty/prefrailty. Older adults with RA show higher (pre)frailty prevalence than controls, which is associated with disease-related consequences and vulnerability rather than age, questioning the added value of frailty assessment beyond routine clinical evaluation.