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



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.


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.


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-R2, 0.35 vs 0.22). In clinical terms, the improvement in prediction (i) translated to improved classification agreement with the FI (Cohen’s kw, 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.


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.

Peer Review reports


With the fast-aging population worldwide, accurate screening for individuals early in their trajectory towards frailty is an urgent and unmet need [1]. Over 60 frailty instruments have been developed to measure frailty amongst which the Cardiovascular Health Study (CHS) physical frailty phenotype (PFP) [2] and the frailty index (FI) [3] are widely used [4]. The multi-dimensional FI measures frailty by the accumulation of deficits across the domains of medical health and physical, social, and cognitive functioning. As a continuous measure, the FI is a sensitive measure of frailty [5, 6]. However, comprising at least 30 deficit items, the FI may not be suitable for large-scale frailty screening. The PFP measures frailty by assessing 5 biologic manifestations of frailty that are primarily physical in nature—that is, reduced gait speed, muscle strength, body mass, physical activity, and energy levels. The PFP is constructed by dichotomizing these 5 criterion predictors and summed to produce a count-based measure. Presumably, this dichotomization approach to creating a PFP count score facilitates ease-of-use and clinical interpretability; however, it has limitations.

First, a count-based approach assumes that the PFP criterion predictors weigh equally—an assumption that may be invalid in light of findings that individual predictors may have varying prognostic or predictive associations with FI [5, 7] and clinical outcomes [8, 9]. Second, constructing the PFP score, originally described by Fried et al. [2], necessitates dichotomizing its criterion predictors using the 20th percentile population cut-point. However, the appropriate reference population data are often not available in many settings, thereby reducing the feasibility of the PFP [10]. In the absence of population-specific cut-points, a population-independent or literature-derived cut-point approach has been advocated and widely adopted [11]. However, for a given PFP criterion (e.g., gait speed), several cut-points have been proposed in the literature [11,12,13,14,15], potentially resulting in varying prevalence estimates of prefrailty/frailty which hinder harmonization and comparison of findings.

Third, dichotomization discards information and decreases the discrimination power of the predictors [16]. This information loss leads to assumptions that are clinically unrealistic. For example, predictor dichotomization assumes participants with similar gait speed values on opposite sides of a 1.0m/s cut-point—for example, 0.95m/s and 1.05m/s—are classified differently as having “slow” and “normal” gait speed, respectively. Given these assumptions, the ability of the count-based PFP to finely grade the degree of frailty is likely to be adversely affected.

Taken altogether, a count-based dichotomization approach reduces the full predictive potential of the PFP, which may partially explain why (i) the FI had reportedly at least comparable but often better predictive performance than the PFP [7, 17,18,19] and (ii) the PFP was reportedly less adept than the FI in discriminating levels of frailty particularly at the early stages of frailty [6, 19]. Furthermore, we believe it is possible for the often-reported poor-to-fair classification agreement [7, 18,19,20] between the PFP and FI to be attributed not only to the conceptual differences between the 2 instruments but also to the discrimination loss from predictor dichotomization.

Against this background, we propose a more feasible approach to computing the PFP by developing and validating a regression model for FI in community-dwelling older adults using criterion predictors of the PFP (termed “model-based PFP” henceforth). Specifically, (i) analyzing the FI as the response variable capitalizes on its continuous nature [5] whilst (ii) analyzing the PFP components as continuous (or ordinal) variables in the regression model overcomes problems of information loss and arbitrary predictor stratification using cut-points that have tended to vary across time and studies.


Participants and procedures

This prospective cohort study comprised 998 community-dwelling ambulant adults aged ≥50 years who participated in “Individual Physical Proficiency Test for Seniors” (IPPT-S)—an ongoing community-based program designed to promote fitness and to prevent or delay sarcopenia and frailty in older adults [21]. The institutional review board approved the study (SingHealth CIRB 2018/2115, Singapore), and all participants provided written informed consent. Consenting participants completed a questionnaire-based multi-domain geriatric screen and a physical fitness assessment at baseline assessment, and they were followed up 1 year later via telephone interview.

Frailty index (FI)

The 36-item FI was constructed following a standardized procedure which included medical comorbidities, functional performance deficits, cognitive and sensory impairments, and psychosocial problems [3] (Additional file 1: Appendix A details the FI items and their associated scores.) The FI is the proportion of deficits present and similar to previous studies [7, 19], and the participants were classified as being robust (≤0.10), pre-frail (>0.10–0.21), and frail (>0.21).

Physical frailty phenotype

The modified PFP comprised the 5 criteria of (i) slowness, (ii) weakness, (iii) shrinking, (iv) low physical activity, and (v) exhaustion. The “slowness” criterion was measured by the 10-m habitual gait-speed test, and slow gait speed was defined by a cut-point of <1.0 m/s [13, 22]. The “weakness” criterion was measured by the handgrip strength test, which was measured using a Jamar digital dynamometer (Sammons USA), and the testing procedures followed the Southampton protocol [23]. Consistent with recent recommendations [4], the maximal reading from all trials (2 trials for each hand) was analyzed, and weak handgrip strength was defined using cut-points of <28 kg for men and <18 kg for women [22]. The “shrinking” criterion was defined by a body mass index (BMI) of ≤18.5kg/m2 [24].

The “low physical activity level” criterion was measured by the total walking time per week (hours/week). Notably, physical activity was operationally defined by walking time—the most common form of physical activity amongst older adults [25]—to facilitate external validation of the model-based PFP in established studies that have tended to use different physical activity questionnaires. In our study, low physical activity level was defined by a total waking time < 2 h (or 120 min)/week [26]. Finally, the “exhaustion” criterion was measured by 2 questions about effort and motivation from the Center for Epidemiological Studies-Depression Scale [27].

The count-based PFP was graded using the number of criteria satisfied, and the participants were classified as being robust (0 criterion), pre-frail (1-2 criteria), and frail (≥3 criteria) [2]. For the model-based PFP, the PFP component criteria and sex were included in a Bayesian model which generated a continuous FI measure (described later), from which the 3 frailty categories could be derived using FI-defined cut-points (Table 1 details the operational definitions).

Table 1 Operational definition of count- and model-based physical frailty phenotype

Clinical outcomes

Clinical outcomes were self-reported (i) incident falls resulting in emergency department visits and (ii) all-cause hospitalization within 1 year after baseline assessment.

Statistical analysis

We used means with SDs and medians with IQRs for continuous variables and frequencies with percentages for categorical variables. Amongst those with non-missing FI, all PFP criterion predictors were missing at very low levels (0.2 to 1.5%). Thus, we used the transcan function in the Hmisc [28] R package to singly impute missing values.

Model and prior specification

To develop the model-based PFP, we fitted a Bayesian multivariable beta regression model, which included (i) FI as the response variable and (ii) PFP component criteria and sex as predictors. A Bayesian analytical framework was used because it aligned closely with our objectives of (i) modeling the 2 PFP “exhaustion” criterion items flexibly as monotonic ordered predictors [29] and (i) providing interpretable uncertainty estimates of the predicted FI values. Beta regression was used because it is a flexible approach to model the FI—a continuous proportion with a non-normal distribution [30]. The model-based PFP was reported according to the transparent reporting of a multivariable prediction model for Individual Prognosis or Diagnosis (TRIPOD) guidelines [31].

Our goal was to optimize the predictive accuracy of the PFP by preserving information in its criterion predictors. Thus, gait speed, handgrip strength, body weight, body height, and total walking time were treated as continuous variables. For total walking time, this variable was first transformed using its cube root to reduce the potential influence of extreme values. To allow prior distributions to be scaled for other predictors, we standardized them as z scores. To avoid assuming linearity for all continuous predictors, we modeled them with thin-plate splines [32]. For the 2 “exhaustion” variables, we modeled these ordinal predictors using the “monotonic effects” function [29] which allows ordinal categories to exert individual conditional effects whilst maintaining monotonically (same directionality).

In our analyses, we set weakly informative prior distributions for the model parameters to reduce the likelihood of estimating unrealistic values without excluding reasonable values [33]. All Bayesian models were fitted using Stan [34] through the brms [35] R package. Stan implements the Hamiltonian Monte Carlo with No-U-Turn sampling algorithm [34], and each model used 4 chains, 3000 iterations per chain, to generate the posterior samples for all parameters (Additional file 1: Appendix B provides the model implementation details.). From these samples, we derived the posterior predictive distribution of the FI which could be interpreted as the predictions of possible mean FI values for a given individual characterized by a given set of PFP criterion values. To summarize this distribution, we used mean as point estimate and 95% credible interval (CrI) as the interval with 95% probability of containing the true FI, given our prior knowledge and observed data.

Model performance

To evaluate the model-based PFP in relation to current practice, we developed a “referent” model that had the PFP count score as its only predictor. Given that gait speed was, amongst the PFP criterion predictors, reportedly the strongest predictor of FI and clinical outcomes [5, 7,8,9], we also fitted a “gait speed” model which included gait speed and covariates [5] routinely and easily obtained in the clinical setting–namely, age, sex, body weight, and body height. To evaluate whether the performance of the model-based PFP could simply be the result of overfitting a more complex model, we used approximate Bayesian leave-one-out (LOO) cross-validation—a technique that assesses how well a model potentially generalizes to new individuals [36]. Notably, the approximate LOO cross-validation technique, based on Pareto smoothed importance sampling [36], was chosen because the full LOO cross-validation process is computationally burdensome in the Bayesian setting. Accordingly, for all models, we computed (i) their respective approximate LOO cross-validated R2 (LOO-R2) and (ii) the paired difference between their respective approximate LOO cross-validated expected log-predictive density (denoted using ELPDdiff). Notably, as ELPDdiff was estimated with respect to the best-performing model, an absolute ELPDdiff of greater than twice its standard error was taken as evidence that the best-performing model had better out-of-sample predictive performance than the alternative model. Finally, we evaluated calibration of the referent model and the model-based PFP using locally weighted scatterplot smoothing calibration plots.

Classification performance

To assess agreement of the various models with the ordinal FI-defined frailty categories, we stratified participants by their mean posterior predicted FI values into robust (posterior predicted FI≤0.10), pre-frail (>0.10–0.21), and frail (FI>0.21), and we computed Cohen’s quadratic weighted kappa coefficient. To assess discriminative performance, we compared the ability of count- and model-based PFP to identify participants with FI-defined prefrailty/frailty (FI>0.10) using the area under the receiver-operating characteristics curve (AUC) with DeLong’s test. To assess the clinical relevance of the improvement in discriminative performance over the count-based PFP, we computed the categorical net reclassification index (NRI) statistic [37]. To provide a clinical view on the consequences of reclassification, similar to previous analyses [20], we compared participants with discrepant frailty classifications by FI and PFP on their demographic and clinical characteristic variables.

Prognostic performance

To assess prognostic performance of the count- and model-based PFP in predicting clinical outcomes, we fitted separate binary logistic regression models for 1-year incident falls and hospitalization. In these models, count-based PFP was modeled as a count variable whilst model-based PFP was modeled as a continuous variable based on the posterior predicted FI values. The AUCs of the models were compared using the DeLong’s test. To evaluate whether model-based PFP provided incremental prognostic information over the conventional count-based PFP, we compared nested binary logistic regression models with a likelihood ratio χ2 test. To summarize its added prognostic value, we computed the proportion of explainable variation that was explained by the model-based PFP (calculated as 1 minus the ratio of variances of predicted values before and after adding model-based PFP to the model containing only count-based PFP) [38]. In all analyses, we have chosen to perform complete-case analyses because (i) we did not have strong auxiliary outcome variables for multiple imputation and (ii) we have observed that the baseline characteristics of participants without outcome data were similar to those of participants with outcome data (Additional file 1: Appendix C).



Table 2 shows that the mean age of all 998 participants was 68 years (SD, 6) and women accounted for accounted for nearly three-quarters (74%) of the sample. Based on the FI, 49% (n=485) of participants had pre-frailty/frailty based on the count- and model-based PFP, 38% and 55%, respectively. At 1-year follow-up, 561 patients (56%) completed at least a telephone interview and incidence rates for falls and all-cause hospitalization were 14% and 12%, respectively.

Table 2 Sample characteristics

Predictive performance

All models converged and the LOO cross-validation process was reliable with all Pareto k values below 0.5. (Additional file 1: Appendix D shows the trace plots of all model parameters). For the model-based PFP, all PFP criterion predictors were predictive of FI and Fig. 1 shows their multivariable associations—including nonlinear relations—with FI. Overall, the model-based PFP had better predictive performance (LOO-R2, 0.35; Table 3) than either the referent model containing the count-based PFP (0.22) or the gait speed model (0.26). Formal model validation and comparison using approximate LOO cross-validation showed that the model-based PFP potentially generalized to new individuals better than the referent model (ELPDdiff [SE] = −91 [15]) and the gait speed model (ELPDdiff [SE] = −51 [13]). Besides having better predictive performance, the model-based PFP showed good calibration with the observed FI (Fig. 2).

Fig. 1
figure 1

Multivariable associations (black lines or points) of physical frailty phenotype criterion predictors (expressed on their natural scales for interpretability) with Frailty Index. Predicted mean frailty index values were calculated from a Bayesian beta regression model using thin-plate splines for continuous predictors and the monotonic effects approach for ordinal predictors. For all predictors, ribbons are 95% (light blue), 80% (medium blue), and 50% (dark blue) credible intervals

Table 3 Model performance and classification accuracy statisticsa
Fig. 2
figure 2

Visual assessment of model calibration for frailty index (FI). Predicted FI were derived from a model using the count-based physical frailty phenotype (PFP) as the only predictor (left panel) and a model using non-dichotomized PFP criterion predictors (right panel). Solid line represents the identity line. Dotted line represents a lowess smoother through the data points, showing good calibration (linear relation) between observed and predicted FI values for the model-based PFP

Classification performance

In terms of classification agreement, frailty classifications by the count-based PFP showed fair agreement with those by FI (kw= 0.36; 95%CI, 0.30 to 0.42) whilst model-based PFP showed greater (moderate) agreement (kw= 0.47; 95%CI, 0.42 to 0.52). In terms of model discrimination ability to separate participants with and without FI-defined prefrailty/frailty, the AUROC for the model-based PFP (0.77, 95% CI, 0.74 to 0.80) was higher than the count-based PFP (0.67; 95% CI, 0.64to 0.69; Delong’s P<0.001). In terms of the ability of the model-based PFP to correctly reclassify participants over the count-based PFP, as shown in Table 3 and Additional file 1: Appendix E, model-based PFP resulted in a 23% (110/484) net increase in FI-defined “prefrail/frail” participants correctly classified (event NRI, 0.23; 95% CI, 0.18 to 0.27) but a 11% (59/514) net loss in FI-defined “robust” participants correctly classified (non-event NRI, −0.11; 95% CI, −0.07 to −0.16), with an overall NRI of 0.11 (95% CI, 0.05 to 0.18). Across all performance metrics, the referent model did not outperform the gait speed model, with the latter model having potentially better model generalizability (ELPDdiff [SE] comparing gait speed vs referent models = −40 [10]) and discrimination ability (AUROC, 0.72; P<0.05).

Prognostic performance

Overall, the model-based PFP showed stronger prognostic performance than count-based PFP in predicting incident falls and hospitalization. When predicting the risk of incident falls, the model-based PFP had an AUC of 0.56 whist the count-based PFP had an AUC of 0.51 (P=0.10 for difference between 2 models). Using the likelihood ratio χ2 test for nested models, the model-based PFP predictor added statistically significant incremental predictive value (P<0.01) to a model comprising the conventional count-based PFP predictor. In a model comprising both predictors, ~93% of its prognostic information was attributed to the model-based PFP predictor. When predicting the risk of incident hospitalization, the model-based PFP showed higher AUC (0.63 vs 0.55; P=0.01) and it provided statistically significant incremental prognostic value above count-based PFP (P<0.01). In a model comprising both predictors, ~87% of its prognostic information was attributed to the model-based PFP predictor.


In 998 community-dwelling older adults, we developed a model-based PFP which showed better prognostic performance for clinical outcomes and predicted FI more accurately than the count-based PFP. Specifically, a modeling approach that (i) avoided dichotomizing the PFP criterion predictors and (ii) avoided assuming that predictors act equally or linearly better captured the relationship between the PFP and FI (LOO-R2, 0.35 vs 0.22). In clinical terms, the improvement in prediction translates to improved classification agreement with the FI (kw, 0.47 vs 0.36) and an overall net correct reclassification of 11% for FI-defined prefrailty/frailty. Importantly, model validation using approximate LOO cross-validation indicated that this improvement in predictive and classification performance was unlikely to be achieved by over-fitting a more complex model. Overall, our findings of lower predictive and classification accuracy for the count-based PFP are consistent with those from both clinical [39] and simulation [40] studies demonstrating the substantial loss of information and predictive power from predictor dichotomization. Indeed, our count-based PFP comprising 5 elaborately-obtained—but eventually dichotomized—criterion predictors did not even outperform a model comprising a non-dichotomized gait speed predictor and standard covariates, further attesting to the toll of dichotomization.

Dichotomizing the criterion predictors to create the count-based PFP requires the availability of a contemporary reference population, from which the lowest quintile cut-points derive [2]. In the absence of population normative data, several cut-points have been proposed in the literature even for the same criterion. For example, proposed cut-points for gait speed have included 0.8m/s [11, 12], 0.9m/s [14], 1.0m/s [13], and 1.1m/s [15]. Collectively, these cut-points led to the question: Do optimal cut-points exist? In our analyses, we allowed potential nonlinear effects for the criterion predictors, and we found that whilst nonlinear in form (Fig. 1), their associations with FI did not evince sharp inflection points which argue against the existence of universal cut-points. In the absence of apparent thresholds, recent simulation [40] and clinical [41] studies have indicated that it is unlikely for the study-specific predictor cut-points to generalize. Thus, although our findings await further confirmation, we believe the concept of population-independent cut-points should be interpreted with some caution. Consistent with previous recommendations [40, 41], we urge future studies aspiring to propose new optimal predictor cut-points to first inspect the relationship between the PFP criterion predictors and various clinical outcomes and explore whether optimal thresholds are apparent.

In our study, classification agreement between count-based PFP and FI was fair (kw = 0.36)—a finding consistent with several previous studies [7, 18,19,20]. When compared to previous studies [7, 18, 20], another consistent finding was that amongst participants with discrepant frailty classifications, proportionally more were classified as prefrail/frail by the FI (228 vs 112; Additional file 1: Appendix F1). Different from previous studies, however, our findings shed further light by showing that classification agreement improved to moderate (kw = 0.47) with the model-based PFP. Amongst participants with discrepant frailty classifications, participants classified as prefrail/frail by the FI but not by the model-based PFP substantially reduced in number (n=181 vs 228) and they were less likely to report having stair climbing difficulties (Additional file 1: Appendix F2). Given this improvement in sensitivity (event NRI, 23%; Table 3), the model-based PFP may be less prone to the criticism often made of the PFP—that the (count-based) PFP may be less adept than the FI in discriminating levels of frailty particularly at the early stages of frailty [6, 19]. Further studies are needed to confirm the improved sensitivity of model-based PFP over the count-based PFP.

Besides predictive and discriminative accuracy, ease-of-use and result interpretability are keys to adoption and implementation. Although model complexity and ease-of-use are often seen as competing factors, we argue that they need not be trade-offs. Indeed, whilst the flexible modeling of predictors and the inclusion of spline terms may have complicated the underlying algorithm of the model-based PFP, this approach has removed the need for predictor cut-points which likely facilitates usage and feasibility. Furthermore, to promote ease-of-use, we have incorporated the model into an online calculator (, and the approximated model equation can be found in Additional file 1: Appendix G. To facilitate results interpretability, we have used (i) a Bayesian modeling framework to generate continuous predicted FI scores and (ii) established FI cut-points to generate frailty classifications based on the predicted FI scores. Given this flexibility and depending on the context and purpose, the model-based PFP could potentially be used as a continuous variable for prediction and longitudinal tracking purposes or as a categorical variable for risk-stratification purposes. That said, we should clearly state that the model-based PFP was developed into an online calculator purely as a proof-of-concept and a thought-starter for encouraging similar validation work across the diverse populations and settings where both PFP and FI measures have already been collected. Hence, pending external validation, its use should be confined to research purposes at present.


Our study has limitations. First, the model-based PFP was developed and validated in Asian older adults; hence, it may not directly apply to non-Asians. Nonetheless, our study should be rightly viewed as a proof-of-concept for the potential use of the model-based PFP, and we hope it will encourage similar work in other racial/ethnic groups. Second, our use of the FI as the reference standard may be criticized as it is not the gold standard frailty measure. In the absence of a gold standard, however, we believe the FI is a sensible choice because of (i) its continuous nature, (ii) its positive association with the count-based PFP [7, 42], and (iii) and its comparable—and if not often better—predictive performance than the count-based PFP [7, 17,18,19]. Third, we did not have follow-up clinical outcomes of 44% of the participants; however, included and excluded participants did not differ meaningfully in baseline characteristics and frailty status (Additional file 1: Appendix C). Whilst our analyses focused on the relative prognostic performance of the count-based and model-based PFP, it is unknown how the missing data would impact the results. Fourth, we validated the model-based PFP using approximate LOO cross-validation but this strategy could be criticized for not representing a true external validation procedure performed in samples geographically and temporally different from our development sample. Nonetheless, given the current study findings and existing knowledge about the limitations of predictor dichotomization, we expect the model-based PFP to have better predictive and classification performance than the count-based PFP in other settings.


In community-dwelling older adults, we developed and validated a model-based PFP which predicted adverse clinical outcomes and FI more strongly than did the count-based PFP. By not needing population-specific predictor cut-points, the model-based approach represents a potentially feasible and innovative method to compute the PFP. As many cohort studies have obtained both PFP and FI measures, it is our hope that this work could efficiently leverage on existing studies to further evaluate the model-based PFP. Future work should also aim to obtain clear evidence on the benefits of this model-based approach compared with the conventional count-based approach.

Availability of data and materials

All data generated or analyzed during this study are included in this published article [and its supplementary information files].


  1. Bandeen-Roche K, Gross AL, Varadhan R, Buta B, Carlson MC, Huisingh-Scheetz M, et al. Principles and issues for physical frailty measurement and its clinical application. J Gerontol A Biol Sci Med Sci. 2020;75:1107–12.

    Article  Google Scholar 

  2. Fried LP, Tangen CM, Walston J, Newman AB, Hirsch C, Gottdiener J, et al. Frailty in older adults: evidence for a phenotype. J Gerontol A Biol Sci Med Sci. 2001;56:M146–56.

    Article  CAS  Google Scholar 

  3. Searle SD, Mitnitski A, Gahbauer EA, Gill TM, Rockwood K. A standard procedure for creating a frailty index. BMC Geriatr. 2008;8:24.

    Article  Google Scholar 

  4. Buta BJ, Walston JD, Godino JG, Park M, Kalyani RR, Xue Q-L, et al. Frailty assessment instruments: systematic characterization of the uses and contexts of highly-cited instruments. Ageing Res Rev. 2016;26:53–61.

    Article  Google Scholar 

  5. Hoogendijk EO, van Kan GA, Guyonnet S, Vellas B, Cesari M. Components of the frailty phenotype in relation to the frailty index: results from the toulouse frailty platform. J Am Med Dir Assoc. 2015;16:855–9.

    Article  Google Scholar 

  6. Blodgett J, Theou O, Kirkland S, Andreou P, Rockwood K. Frailty in NHANES: comparing the frailty index and phenotype. Arch Gerontol Geriatr. 2015;60:464–70.

    Article  Google Scholar 

  7. Ryan J, Espinoza S, Ernst ME, Ekram ARMS, Wolfe R, Murray AM, et al. Validation of a deficit-accumulation frailty index in the ASPirin in reducing events in the elderly study and its predictive capacity for disability-free survival. J Gerontol A Biol Sci Med Sci. 2022;77:19–26.

    Article  Google Scholar 

  8. Bouillon K, Sabia S, Jokela M, Gale CR, Singh-Manoux A, Shipley MJ, et al. Validating a widely used measure of frailty: are all sub-components necessary? Evidence from the Whitehall II cohort study. Age (Dordr). 2013;35:1457–65.

    Article  CAS  Google Scholar 

  9. Sanchis J, Ruiz V, Sastre C, Bonanad C, Ruescas A, Fernández-Cisnal A, et al. Frailty tools for assessment of long-term prognosis after acute coronary syndrome. Mayo Clin Proc Innov Qual Outcomes. 2020;4:642–8.

    Article  Google Scholar 

  10. Romero-Ortuno R, Soraghan C. A Frailty Instrument for primary care for those aged 75 years or more: findings from the Survey of Health, Ageing and Retirement in Europe, a longitudinal population-based cohort study (SHARE-FI75+). BMJ Open. 2014;4:e006645.

    Article  Google Scholar 

  11. Saum K-U, Müller H, Stegmaier C, Hauer K, Raum E, Brenner H. Development and evaluation of a modification of the Fried frailty criteria using population-independent cutpoints. J Am Geriatr Soc. 2012;60:2110–5.

    Article  Google Scholar 

  12. Clegg A, Rogers L, Young J. Diagnostic test accuracy of simple instruments for identifying frailty in community-dwelling older people: a systematic review. Age Ageing. 2015;44.Clegg A, Rogers L, Young J. Diagnostic test accuracy of simple instruments for identifying frailty in community-dwelling older people: a systematic review. Age Ageing . 2015 Jan;44(1):148-52

  13. Satake S, Arai H. The revised Japanese version of the cardiovascular health study criteria (revised J-CHS criteria). Geriatr Gerontol Int. 2020;20:992–3.

    Article  Google Scholar 

  14. Auyeung TW, Lee JSW, Leung J, Kwok T, Woo J. The selection of a screening test for frailty identification in community-dwelling older adults. J Nutr Health Aging. 2014;18:199–203.

    Article  CAS  Google Scholar 

  15. Rodríguez-Laso Á, Martín-Lesende I, Sinclair A, Sourdet S, Tosato M, Rodríguez-Mañas L. Diagnostic accuracy of the FRAIL scale plus functional measures for frailty screening: a cross-sectional study. BJGP Open. 2022;6(3).

  16. Altman DG, Royston P. The cost of dichotomising continuous variables. BMJ. 2006;332:1080.

    Article  Google Scholar 

  17. Kojima G, Iliffe S, Walters K. Frailty index as a predictor of mortality: a systematic review and meta-analysis. Age Ageing. 2018;47:193–200.

    Article  Google Scholar 

  18. Kim DJ, Massa MS, Clarke R, Scarlett S, O’Halloran AM, Kenny RA, et al. Variability and agreement of frailty measures and risk of falls, hospital admissions and mortality in TILDA. Sci Rep. 2022;12:4878.

    Article  CAS  Google Scholar 

  19. Zhu Y, Liu Z, Wang Y, Wang Z, Shi J, Xie X, et al. Agreement between the frailty index and phenotype and their associations with falls and overnight hospitalizations. Arch Gerontol Geriatr. 2016;66:161–5.

    Article  Google Scholar 

  20. Xue Q-L, Tian J, Walston JD, Chaves PHM, Newman AB, Bandeen-Roche K. Discrepancy in frailty identification: move beyond predictive validity. J Gerontol A Biol Sci Med Sci. 2020;75:387–93.

    Article  Google Scholar 

  21. Tay LB, Chua MP, Tay EL, Chan HN, Mah SM, Latib A, et al. Multidomain geriatric screen and physical fitness assessment identify prefrailty/frailty and potentially modifiable risk factors in community-dwelling older adults. Ann Acad Med Singapore. 2019;48:171–80.

    Article  Google Scholar 

  22. Chen L-K, Woo J, Assantachai P, Auyeung T-W, Chou M-Y, Iijima K, et al. Asian working group for sarcopenia: 2019 consensus update on sarcopenia diagnosis and treatment. J Am Med Dir Assoc. 2020;21:300–307.e2.

    Article  Google Scholar 

  23. Roberts HC, Denison HJ, Martin HJ, Patel HP, Syddall H, Cooper C, et al. A review of the measurement of grip strength in clinical and epidemiological studies: towards a standardised approach. Age Ageing. 2011;40:423–9.

    Article  Google Scholar 

  24. Bandeen-Roche K, Xue Q-L, Ferrucci L, Walston J, Guralnik JM, Chaves P, et al. Phenotype of frailty: characterization in the women’s health and aging studies. J Gerontol A Biol Sci Med Sci. 2006;61:262–6.

    Article  Google Scholar 

  25. Centers for Disease Control and Prevention (CDC). Vital signs: walking among adults--United States, 2005 and 2010. MMWR Morb Mortal Wkly Rep. 2012;61.Centers for Disease Control and Prevention (CDC). Vital signs: walking among adults--United States, 2005 and 2010. MMWR Morb Mortal Wkly Rep. 2012;61(31);595–601.

  26. Kelly P, Kahlmeier S, Götschi T, Orsini N, Richards J, Roberts N, et al. Systematic review and meta-analysis of reduction in all-cause mortality from walking and cycling and shape of dose response relationship. Int J Behav Nutr Phys Act. 2014;11:132.

    Article  Google Scholar 

  27. Andresen EM, Malmgren JA, Carter WB, Patrick DL. Screening for depression in well older adults: evaluation of a short form of the CES-D (Center for Epidemiologic Studies Depression Scale). Am J Prev Med. 1994;10:77–84.

    Article  CAS  Google Scholar 

  28. Harrell Jr FE. Hmisc: Harrell Miscellaneous. R package version 4.7-0. 2022.

  29. Bürkner P-C, Charpentier E. Modelling monotonic effects of ordinal predictors in Bayesian regression models. Br J Math Stat Psychol. 2020;73:420–51.

    Article  Google Scholar 

  30. Smithson M, Verkuilen J. A better lemon squeezer? Maximum-likelihood regression with beta-distributed dependent variables. Psychol Methods. 2006;11:54–71.

    Article  Google Scholar 

  31. Moons KGM, Altman DG, Reitsma JB, Ioannidis JPA, Macaskill P, Steyerberg EW, et al. Transparent Reporting of a multivariable prediction model for Individual Prognosis or Diagnosis (TRIPOD): explanation and elaboration. Ann Intern Med. 2015;162:W1–73.

    Article  Google Scholar 

  32. Wood SN. Thin plate regression splines. J R Stat Soc Series B Stat Methodology. 2003;65:95–114.

    Article  Google Scholar 

  33. Gelman A, Jakulin A, Pittau MG, Su Y-S. A weakly informative default prior distribution for logistic and other regression models. Ann Appl Stat. 2008;2:1360–83.

    Article  Google Scholar 

  34. Stan Development Team. RStan: the R interface to Stan. R package version. 2021;2.21.3.Stan Development Team (2021). RStan: the R interface to Stan. R package version 2.21.3.

  35. Bürkner P-C. brms: an R package for Bayesian multilevel models using Stan. J Stat Softw. 2017;80:1–28.

    Article  Google Scholar 

  36. Vehtari A, Gelman A, Gabry J. Practical Bayesian model evaluation using leave-one-out cross-validation and WAIC. Stat Comput. 2017;27:1413–32.

    Article  Google Scholar 

  37. Leening MJG, Vedder MM, Witteman JCM, Pencina MJ, Steyerberg EW. Net reclassification improvement: computation, interpretation, and controversies: a literature review and clinician’s guide. Ann Intern Med. 2014;160:122–31.

    Article  Google Scholar 

  38. Harrell F. Statistical Thinking - Statistically efficient ways to quantify added predictive value of new measurements. 2018. Accessed 6 Jan 2023.

    Google Scholar 

  39. Fronczek J, Polok K, de Lange DW, Jung C, Beil M, Rhodes A, et al. Relationship between the Clinical Frailty Scale and short-term mortality in patients ≥ 80 years old acutely admitted to the ICU: a prospective cohort study. Crit Care. 2021;25:231.

    Article  Google Scholar 

  40. Giannoni A, Baruah R, Leong T, Rehman MB, Pastormerlo LE, Harrell FE, et al. Do optimal prognostic thresholds in continuous physiological variables really exist? Analysis of origin of apparent thresholds, with systematic review for peak oxygen consumption, ejection fraction and BNP. PLoS One. 2014;9:e81699.

    Article  Google Scholar 

  41. Potgieter D, Simmers D, Ryan L, Biccard B, Lurati-Buse G, Dm C, et al. N-terminal pro-B-type natriuretic peptides’ prognostic utility is overestimated in meta-analyses using study-specific optimal diagnostic thresholds. Anesthesiology. 2015;123.

  42. Verschoor CP, Tamim H. Frailty is inversely related to age at menopause and elevated in women who have had a hysterectomy: an analysis of the Canadian Longitudinal Study on Aging. J Gerontol A Biol Sci Med Sci. 2019;74:675–82.

    Article  CAS  Google Scholar 

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We thank the study participants, staff of the Senior Activity Centers, and Resident Committees in the northeast region of Singapore for their logistical and manpower support. We extend our gratitude to Vanessa Voong Zi Lin from the Sengkang General Hospital Department of Physiotherapy for their contributions towards this project.


The study was funded by the Singapore National Medical Research Council Centre Grants (CGAug16C027 and CGAug16M011) and the National Innovation Challenge on Active and Confident Aging Grant (MOH/NIC/HAIG04/2017), and the Singapore Ministry of Health’s National Medical Research Council under the Fellowship Programme by SingHealth Regional Health System, Population-based, Unified, Learning System for Enhanced and Sustainable (PULSES) Health Centre Grant (CG21APR1013).

Author information

Authors and Affiliations



LT and NYS were the study’s principal investigators were involved in the acquisition of the data. All authors were involved in the study conception and design. YHP analyzed the data and wrote the first draft of the manuscript. PYL and YHP developed the app. The authors revised the manuscript and gave final approval for submission.

Corresponding author

Correspondence to Yong-Hao Pua.

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The study was approved by the institutional review board (SingHealth CIRB 2018/2115, Singapore) and all participants provided written informed consent.

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Not applicable.

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The authors declare that they have no competing interests.

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Supplementary Information

Additional file 1: Appendix A.

36-Item frailty index. Appendix B. Model implementation details for model-based PFP. Appendix C. Demographic and clinical characteristics of participants with and without one-year follow-up clinical outcomes. Appendix D. Markov Chain Monte Carlo (MCMC) simulation diagnostics. Appendix E. Reclassification of participants by net reclassification index (NRI) with use of gait speed model or model-based PFP versus count-based PFP. Appendix F. Demographic and clinical characteristics of participants with discordant prefrailty/frailty classification by FI and count- or model-based PFP. Appendix G. Approximated model equation.

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Pua, YH., Tay, L., Clark, R.A. et al. Development and validation of a physical frailty phenotype index-based model to estimate the frailty index. Diagn Progn Res 7, 5 (2023).

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  • Frailty scales
  • Frailty phenotype
  • Frailty index
  • Geriatrics
  • Prediction