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Development and validation of a physical frailty phenotype index-based model to estimate the frailty index

BACKGROUND: The conventional count-based physical frailty phenotype (PFP) dichotomizes its criterion predictors—an approach that creates information loss and depends on the availability of population-derived cut-points. This study proposes an alternative approach to computing the PFP by developing a...

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Detalles Bibliográficos
Autores principales: Pua, Yong-Hao, Tay, Laura, Clark, Ross Allan, Thumboo, Julian, Tay, Ee-Ling, Mah, Shi-Min, Lee, Pei-Yueng, Ng, Yee-Sien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029224/
https://www.ncbi.nlm.nih.gov/pubmed/36941719
http://dx.doi.org/10.1186/s41512-023-00143-3
Descripción
Sumario:BACKGROUND: The conventional count-based physical frailty phenotype (PFP) dichotomizes its criterion predictors—an approach that creates information loss and depends on the availability of population-derived cut-points. This study proposes an alternative approach to computing the PFP by developing and validating a model that uses PFP components to predict the frailty index (FI) in community-dwelling older adults, without the need for predictor dichotomization. METHODS: A sample of 998 community-dwelling older adults (mean [SD], 68 [7] years) participated in this prospective cohort study. Participants completed a multi-domain geriatric screen and a physical fitness assessment from which the count-based PFP and the 36-item FI were computed. One-year prospective falls and hospitalization rates were also measured. Bayesian beta regression analysis, allowing for nonlinear effects of the non-dichotomized PFP criterion predictors, was used to develop a model for FI (“model-based PFP”). Approximate leave-one-out (LOO) cross-validation was used to examine model overfitting. RESULTS: The model-based PFP showed good calibration with the FI, and it had better out-of-sample predictive performance than the count-based PFP (LOO-R(2), 0.35 vs 0.22). In clinical terms, the improvement in prediction (i) translated to improved classification agreement with the FI (Cohen’s k(w), 0.47 vs 0.36) and (ii) resulted primarily in a 23% (95%CI, 18–28%) net increase in FI-defined “prefrail/frail” participants correctly classified. The model-based PFP showed stronger prognostic performance for predicting falls and hospitalization than did the count-based PFP. CONCLUSION: The developed model-based PFP predicted FI and clinical outcomes more strongly than did the count-based PFP in community-dwelling older adults. By not requiring predictor cut-points, the model-based PFP potentially facilitates usage and feasibility. Future validation studies should aim to obtain clear evidence on the benefits of this approach. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41512-023-00143-3.