Skip to main content

Operationalization of a frailty index among older adults in the InCHIANTI study: predictive ability for all-cause and cardiovascular disease mortality



The frailty index (FI) is a sensitive instrument to measure the degree of frailty in older adults, and is increasingly used in cohort studies on aging.


To operationalize an FI among older adults in the “Invecchiare in Chianti” (InCHIANTI) study, and to validate its predictive capacity for mortality.


Longitudinal data were used from 1129 InCHIANTI participants aged ≥ 65 years. A 42-item FI was operationalized following a standard procedure using baseline data (1998/2000). Associations of the FI with 3- and 6-year all-cause and cardiovascular disease (CVD) mortality were studied using Cox regression. Predictive accuracy was estimated by the area under the ROC curve (AUC), for a continuous FI score and for different cut-points.


The median FI was 0.13 (IQR 0.08–0.21). Scores were higher in women, and at advanced age. The FI was associated with 3- and 6-year all-cause and CVD mortality (HR range per 0.01 FI increase = 1.03–1.07, all p < 0.001). The continuous FI score predicted the mortality outcomes with moderate-to-good accuracy (AUC range 0.72–0.83). When applying FI cut-offs between 0.15 and 0.35, the accuracy of this FI for predicting mortality was moderate (AUC range 0.61–0.76). Overall, the predictive accuracy of the FI was higher in women than in men.


The FI operationalized in the InCHIANTI study is a good instrument to grade the risk of all-cause mortality and CVD mortality. More measurement properties, such as the responsiveness of this FI when used as outcome measure, should be investigated in future research.


In aging societies, there is increasing attention for the concept of frailty [1, 2]. This is an age-related condition, which has been defined as a decline in multiple physiological systems and increased vulnerability to stressors. Frailty is strongly related to various adverse health outcomes, such as functional decline, delirium, hospital admission, and mortality [3].

In the past decades, many frailty instruments have been developed [4], of which the frailty index (FI) is one of the most commonly used [5]. The FI defines frailty as a gradient from fit to frail, based on the accumulation of health deficits [5]. A critical mass of health deficits (at least 30), including diseases, disabilities, signs, and symptoms, is used to arithmetically generate a continuous score ranging from 0 to 1. As a result, the FI seems to be a sensitive instrument to distinguish the degree of frailty in older adults [6].

Because of its sensitivity, the FI is increasingly recognized as particularly useful for longitudinal studies on aging, as predictor of adverse health events or as outcome measure. As an outcome measure, the FI can be used to monitor the individual`s changes in frailty over time [7, 8]. Recently, FIs have been developed in various longitudinal studies on aging, such as the English Longitudinal Study of Aging (ELSA) [9], the Longitudinal Aging Study Amsterdam (LASA) [10, 11], the Health and Retirement Study (HRS) [12], the Survey of Health, Aging and Retirement in Europe (SHARE) [13, 14], and the Gothenburg H70 Birth Cohort Studies (H70 Studies) [15]. This is a promising development, as this enables comparisons between different populations, countries, and settings.

The FI was originally developed to be used as a continuous scale [16]. However, dichotomizing a measure is sometimes necessary to be able to identify the presence of certain conditions and to inform clinicians in the development of diagnostic/therapeutic plans. Although cut-offs are controversial, they have also been applied to the FI to determine the presence of frailty. Some studies have reported an FI cut-off of 0.2 to identify a frail state [17], but a cut-point of 0.25 has most often been used (e.g., [16, 18,19,20]). Interestingly, there is a lack of validation studies for these cut-offs with regard to outcome prediction. Therefore, optimal FI cut-offs for predicting specific adverse health outcomes are largely unknown. Furthermore, most FIs have been validated for all-cause mortality (e.g., [11, 13]. Very few studies have investigated the predictive validity for specific causes of death, such as cardiovascular disease (CVD) mortality [21].

The “Invecchiare in Chianti”, (i.e., Aging in the Chianti area; InCHIANTI) study is a population-based cohort study of older adults in Tuscany, Italy. The study is well known for its contribution to the frailty research field, especially with regard to insights into determinants and onset of physical frailty in later life [22,23,24,25,26,27,28]. Nevertheless, all previous InCHIANTI studies measured frailty using the frailty phenotype [29]. An FI has not yet been established in this cohort study. Therefore, our aim was to operationalize an FI in the InCHIANTI study, and to validate it by investigating its predictive ability for all-cause mortality and CVD mortality. Both continuous scores and different cut-offs were used to study the predictive accuracy of this FI.


Study sample

The InCHIANTI study is a prospective population-based cohort study among older adults aged 65 years and over in Tuscany, Italy. Participants were randomly selected from population registers in this area. The study started in 1998 and is still ongoing. Follow-up measurements are conducted every 3 years. The main focus of InCHIANTI is mobility decline in later life and related factors. The data collection is based on a home interview and clinical measurements at the study clinic. Details on the sampling and design of InCHIANTI have been described in a previous publication [30]. The InCHIANTI study was approved by the ethical committee of the Italian National Institute of Research and Care on Aging. All study participants provided written informed consent.

In the current study, we included people with valid data at baseline (1998–2000) and valid data on the outcome measure (mortality) during follow-up. Of the 1155 InCHIANTI participants at baseline, 24 (2.1%) had no valid frailty score due to missing data and 2 (0.2%) had no data on level of education. Vital status at follow-up was available for all participants, resulting in a sample of 1129 people that were included in the analyses.

Frailty index

An FI of health deficits was operationalized following a standard procedure, as described by Searle et al. [17]. In the current study, this was done with data from the InCHIANTI baseline. However, we made sure that the included variables are available at all InCHIANTI follow-up waves, so that future longitudinal studies may use this FI as well. Variables were included in the FI if they met various criteria: (a) variables must be health-related deficits, such as symptoms, signs, diseases, or disabilities, all associated with adverse outcomes (b) the deficits are biologically meaningful and represent multiple organ systems, (c) deficits increase with age, but do not saturate too early (i.e., high prevalence at young age), and (d) variables contain less than 5% missing values.

The questionnaires and clinical measurements of InCHIANTI were screened for variables that could be included in the FI. This resulted in a list of health deficits from various functional domains that were used to construct a 42-item FI. The FI included the following variables: major medical conditions (hypertension, myocardial infarction, congestive heart failure, chronic liver disease, cancer, peripheral arterial disease, stroke, Parkinson`s disease, diabetes, chronic lung disease, angina pectoris, and knee/hip arthritis) based on disease ascertainment algorithms (including information from medical records, medication use, signs and symptoms, medical history, and hospital records); having difficulties with various (instrumental) activities of daily living (ADL/IADL, including bathing, dressing/undressing, eating, toileting, continence, walking across a small room, walking up/down staircase ten steps, getting in/out of bed, food preparation, shopping, heavy housework, using telephone, lifting/carry shopping bag, using public transportation, medication use, and managing finances); self-rated health assessed with the question “How would you evaluate your current health?”; five items from the Center for Epidemiologic Studies Depression (CES-D) scale (feel depressed, feel everything is an effort, could not get going, feel lonely, and feel happy) [31]; four sub-domains of the Mini-Mental State Examination (MMSE, domains: orientation time, orientation place, attention, and recall) [32]; self-reported weight loss in the last 12 months; physical activity level in the last year; and two physical performance measures (gait speed, grip strength). Details of the items included in the FI and their cut-offs are shown in Table 1.

Table 1 Frailty index items and coding

In line with previous studies, we only calculated an FI for participants with less than 20% missing variables [11, 33]. Most older adults in the initial InCHIANTI sample had no missing variables on the FI (65.4%) or 1–3 missing variables (27.2%) out of the total of 42 variables. Only 2.1% had more than 20% missing variables. An FI ranging from 0 (no deficits present) to 1 (all deficits present) was calculated for individual participants by dividing the sum of the items present out of the sum of all the possible ones measured in the FI. To illustrate, if a person presents with 10 altered items out of 42, the corresponding FI score is 10/42 = 0.24.


Mortality is one of the most studied endpoints in the context of frailty [34]. In the current study, outcome measures were 3-year and 6-year all-cause mortality and CVD mortality. Vital status, date of death, and cause of death (International Classification of Disease, 9th revision (ICD-9) codes) were retrieved from regional and municipality registers. CVD mortality was determined by ICD-9 codes 390–459.

Statistical analysis

Descriptive analyses were conducted to show the characteristics of the study sample. T tests, Chi-square tests, and Mann–Whitney tests were performed to determine differences in baseline characteristics by sex. Next, descriptive statistics were generated to provide insight into the general characteristics of the FI at baseline. The distribution of the FI was displayed in a histogram. Mean frailty scores were plotted by age and sex. To investigate the predictive ability of the FI, various analyses were performed. First, associations of the FI (continuous score) with each outcome (3-year and 6-year all-cause mortality and CVD mortality) were studied using Cox proportional hazard models, without and with adjustment for confounders. Three models were tested: a crude model (Model 1), a model adjusted for age and sex (Model 2), and a model additionally adjusted for partner status, educational level, and smoking (Model 3). In the Cox regression analyses, survivors were censored at the end of follow-up (3 or 6 years after baseline). People who died within 3 or 6 years were censored at the time of death. In the analyses on CVD mortality, those who died because of other reasons than CVD were also censored at time of death. Second, the predictive accuracy of the continuous FI score was estimated by the area under the ROC curve (AUC). An AUC of 1.0 indicates perfect sensitivity and specificity for the outcome of interest, 0.9–0.99 is excellent, 0.8–0.89 is good, 0.7–0.79 is moderate, and everything below 0.70 is poor [35]. Next, to find optimal FI cut-offs for predicting mortality, we calculated the sensitivity, the specificity, and AUCs for various cut-points (between 0.15 and 0.35) around the commonly used cut-point of 0.25 [16, 18]. All analyses on predictive ability of the FI for all-cause mortality were done for the total population and stratified by sex, as sex differences in frailty have often been reported, with higher frailty levels among women [36]. For CVD mortality, the number of events was too low to perform sex-stratified analyses. All analyses were done in SPSS 24 (IBM corp, Armonk, NY, USA).


Baseline characteristics are shown in Table 2. The analytical sample consisted of 1129 older adults, of which 642 (56.9%) were female. The participants had a mean age of 75.2 years (SD = 7.4) and a mean educational level of 5.3 years (SD = 3.3). The distribution of the FI is displayed in Fig. 1. The FI is skewed to the right and ranges from 0.01 to 0.72. The median FI score was 0.13 (IQR = 0.08–0.21) and the 99% upper limit was 0.64. When applying cut-offs, the prevalence of frailty ranged from 10.4% (≥ 0.35 cut-off) to 39.9% (≥ 0.15 cut-off). Frailty scores were higher in women than in men (median = 0.14 vs. median = 0.10, p < 0.001). Figure 2 shows that the FI scores tend to be higher with advancing age in both men and women.

Table 2 Baseline characteristics
Fig. 1

Distribution of the frailty index at baseline

Fig. 2

Association between age and baseline frailty index score for men and womena. aThe circles and squares indicate frailty index scores by age rounded to nearest whole number, and may represent more than one individual

Table 3 shows the associations of the continuous FI score with all-cause mortality for the total sample as well as after stratification by sex. In the total sample (n = 1129), 112 people (9.9%) died within 3 years of follow-up and 267 people (23.6%) died within 6 years of follow-up. Mortality was higher in men than women (3-year mortality = 11.5% vs. 8.7%; 6-year mortality = 27.9% vs. 20.4%, respectively). An increase in all-cause mortality by FI score was observed for both men and women (Fig. 3). Table 3 also shows CVD mortality for the total population. During 3 years and 6 years of follow-up, 53 (4.7%) and 128 people (11.3%) died because of CVD, respectively. The FI showed statistically significant associations with all outcomes in all models. For example, 0.01 increment in the FI score was associated with 3-year all-cause mortality (HR 1.04, 95% CI 1.03–1.06) and 3-year CVD mortality (HR 1.05, 95% CI 1.03–1.06) in models adjusted for age, sex, partner status, educational level, and smoking. The associations between the FI score and all-cause mortality were stronger among women than among men (p interaction FI*sex was < 0.05, not shown in table) for both 3-year and 6-year mortality.

Table 3 Cox regression: associations between frailty index score and mortality
Fig. 3

Percentage of all-cause mortality at follow-up by baseline frailty index score for A men and B women

The predictive accuracy of the continuous FI score for the studied outcomes (Tables 4 and 5) ranged from moderate to good (AUC range 0.72–0.83), and was a bit higher among women (AUC range 0.80–0.83) compared to men (AUC range 0.72–0.77). For the total population, the AUC was the same for predicting 3-year and 6-year all-cause mortality (AUC 0.76), and nearly the same for predicting 3-year and 6-year CVD mortality (AUC 0.79 vs. AUC 0.78). Tables 4 and 5 also show the predictive accuracy of different FI cut-offs. For prediction of mortality, all cut-offs between 0.15 and 0.35 had moderate accuracy (AUC < 0.80). In the Online Appendix, ROC curves and optimal cut-offs for all outcomes are graphically displayed (see Online Appendix 1). The optimal cut-off for predicting 3-year mortality was 0.198 (AUC 0.71), for 6-year mortality 0.191 (AUC 0.72), for 3-year CVD mortality 0.201 (AUC 0.76), and for 6-year CVD mortality 0.201 (AUC 0.73). Sex differences can be observed with regard to the optimal FI cut-point for outcome prediction. For example, for men, the optimal cut-off for predicting 3-year mortality was around ≥ 0.17, while for women, the optimal cut-off was around ≥ 0.28 (Tables 4 and 5, Online Appendix 1).

Table 4 Predictive accuracy of continuous frailty index scores and various frailty index cut-offs for 3-year mortality
Table 5 Predictive accuracy of continuous frailty index scores and various frailty index cut-offs for 6-year mortality


In the present study, we operationalized a 42-item FI in the InCHIANTI study, a large population-based cohort study. We validated this FI for predicting mortality, and investigated optimal cut-offs for outcome prediction. Our results showed that this FI is associated with 3-year and 6-year all-cause and CVD mortality. It is, therefore, a good instrument to grade the risk of mortality in older adults. The FI predicted mortality with moderate-to-good accuracy, and showed slightly better predictive accuracy in women than in men. Interestingly, the optimal FI cut-off for predicting mortality differed between men and women.

The characteristics of the FI developed in the InCHIANTI study are in line with previously published FIs in older population-based samples. In fact, our FI had a skewed right distribution, a 99% upper limit below 0.70, and higher values in women and persons with more advanced age [11, 17, 37]. The median FI score of 0.13 did not differ much from the FI that was reported in the Longitudinal Aging Study Amsterdam (median = 0.16) in the same time period (late 1990s) [11]. Furthermore, we validated the FI against mortality. Consistent with results from a large number of earlier studies (e.g., [11, 34, 38,39,40]), a higher FI score in the InCHIANTI study was associated with increased all-cause mortality. A novel finding is that the FI was also related to CVD mortality.

Although sex differences in frailty have been reported in many studies, relatively little attention has been paid to sex differences in the association between frailty and adverse outcomes [36]. A common observation from previous research is that men have higher mortality rates in combination with lower average frailty scores [36]. Our results showed that, even with greater mortality rates among men, a stronger relationship between the FI score and all-cause mortality was observed among women. Perhaps, this association is influenced by the greater increase in mortality in the highest FI categories among women, as can be observed in Fig. 3. These findings suggest that a sex-specific approach to frailty is warranted when the FI is used to predict adverse outcomes. More research is needed to investigate whether sex differences are also present for associations with other outcomes than mortality.

The predictive accuracy of the continuous FI score for mortality was similar to findings from other population-based cohort studies. We observed AUCs of 0.76 for predicting both 3-year and 6-year mortality. This was comparable to the previous work in the SHARE study, which found AUCs for predicting 2-year and 5-year mortality of 0.77 and 0.75, respectively [33]. And it is also not very different from other risk indicators that have been used in older populations, such as gait speed measurement, which also showed moderate predictive accuracy for mortality with AUCs around 0.70 [41]. Nevertheless, it is very likely that the predictive accuracy of the FI differs across settings and subpopulations. For example, in an earlier Italian study, a slightly higher AUC (0.81) for predicting 2-year mortality was observed [38]. The FI was of similar size as ours (40 items), but the main difference is that our study was conducted in a population-based sample, while this previous study was done in a specific sample in a clinical setting. Another study conducted in a clinical setting found; however, moderate predictive accuracy for 1-year, 3-year, and 5-year mortality (AUC ≤ 0.75) when operationalizing a frailty index using data from electronic medical records [39]. This highlights the need for more research into the predictive accuracy of the FI across different settings. Future studies should explore to what extent the predictive ability of the FI in clinical settings differs from that in population-based samples, and whether there is consistency in the predictive ability of the FI within specific settings. It is, for example, possible that the FI is less predictive in long-term care facilities, where average frailty levels are much higher than in other settings [42].

One of the main advantages of using an FI is that the content is not fixed. As long as several conditions are met, such as the type and number of included health deficits (at least 30 items), the combination of health deficits does not matter [17]. The key characteristics of the FI are consistent across data sets with different FI operationalizations [37]. Because of this flexibility, FIs can be constructed with almost any comprehensive health database in both research and clinical settings. The FI that was constructed in the current study contains 42 items from various domains of functioning. However, our aim was not to construct an FI that is completely fixed. In future research with InCHIANTI data, it is still possible to replace items or to add more items, if this is needed for specific research questions.

The FI is not meant to be dichotomized, as Rockwood et al. described in their paper from 2007 [16]. However, when a cut-point is needed, an arbitrary cut-off of ≥ 0.25 has usually been proposed for community-dwelling older adults. Until now, this cut-point has been used in many studies [18,19,20]. In the present study, we explored the use of various cut-offs around this commonly used cut-point. Whereas the predictive accuracy of the continuous FI was moderate-to-good, the dichotomized scores had slightly lower levels of accuracy. Remarkably, we observed sex differences with regard to the optimal cut-off for outcome prediction. The optimal cut-off for men for predicting 3-year mortality was around 0.17, while for women, this was around 0.28. This could just be an expression of the male–female health-survival paradox (i.e., a higher life expectancy that is accompanied by higher rates of poor health in women compared to men) [36]. It should be noted that for some higher cut-off values, especially among men, the sensitivity was low. It depends on the purpose of the study, but if a dichotomized FI would be used as screening instrument, one would prefer high sensitivity as this would select the highest number of true positive cases (people that experience the adverse health event). Additional research in other cohorts is, therefore, needed, to further investigate optimal FI cut-offs for specific outcomes.

The current study has several strengths. We used data from a large population-based cohort of older adults in Italy to validate an FI that was constructed based on existing FI methodology. Our study expands previous research in various ways. First, this is one the few studies that tests various FI cut-offs for outcome prediction. Second, this study contributes to insights into sex differences in frailty, by providing detailed information on the predictive accuracy of the FI for men and women separately. And, finally, in addition to all-cause mortality, we have also investigated CVD mortality as outcome. Specific causes of death have seldom been studied in relation to the FI [21].

The study also has some limitations. First, we validated the FI only for mortality, an important outcome measure, but other outcomes should be considered in future research, such as falls, functional decline, and healthcare utilization [3]. Second, we only have studied the main characteristics and the predictive accuracy of the FI. More measurement properties need to be investigated. For example, the instrument has great potential to be used as outcome measure. A crucial next step is to test the responsiveness of this FI when used as outcome in longitudinal research. Another important direction for future research is the performance of comparative research, to see to what extent the predictive ability of this FI differs from that of other risk indicators for mortality or other frailty measures.

The application of the FI is not only limited to research settings. It has been suggested that the FI is a good instrument to select older adults in clinical practice that may benefit from additional care or specific interventions [39, 40]. However, this field is in an early stage of development. For example, in the UK, an electronic frailty index (eFI) is currently being implemented for older adults in primary care [39]. Based on generic cut-points of the eFI, the general practitioner has to carry out additional actions for those with moderate-to-severe frailty. Although this is a promising development, it is possible that some refinement and further specificity of cut-points for use in clinical practice are needed in the future. The results of the current study would, for example, implicate that cut-points need to be sex-specific, as men are at risk of mortality at lower FI levels than women.

To conclude, we have operationalized an FI in the InCHIANTI study and validated this FI for predicting mortality. This FI is a good instrument to grade the risk of 3-year and 6-year all-cause and CVD mortality in older adults. The predictive accuracy of the FI was slightly better among women compared to men. Future research should investigate the responsiveness of the FI when using this instrument as outcome measure.


  1. 1.

    Cesari M, Marzetti E, Thiem U et al (2016) The geriatric management of frailty as paradigm of "The end of the disease era". Eur J Intern Med 31:11–14

    Article  PubMed  Google Scholar 

  2. 2.

    Hoogendijk EO, Afilalo J, Ensrud KE et al (2019) Frailty: implications for clinical practice and public health. Lancet 394:1365–1375

    PubMed  PubMed Central  Article  Google Scholar 

  3. 3.

    Clegg A, Young J, Iliffe S et al (2013) Frailty in elderly people. Lancet 381:752–762

    Article  PubMed  Google Scholar 

  4. 4.

    Dent E, Kowal P, Hoogendijk EO (2016) Frailty measurement in research and clinical practice: a review. Eur J Intern Med 31:3–10

    Article  PubMed  Google Scholar 

  5. 5.

    Rockwood K, Mitnitski A (2007) Frailty in relation to the accumulation of deficits. J Gerontol A 62:722–727

    Article  Google Scholar 

  6. 6.

    Rockwood K, Mitnitski A (2011) Frailty defined by deficit accumulation and geriatric medicine defined by frailty. Clin Geriatr Med 27:17–26

    Article  PubMed  Google Scholar 

  7. 7.

    Cesari M, Gambassi G, Abellan van Kan G, Vellas B (2014) The frailty phenotype and the frailty index: different instruments for different purposes. Age Ageing 43:10–12

    Article  PubMed  Google Scholar 

  8. 8.

    Hoogendijk EO, Rockwood K, Theou O et al (2018) Tracking changes in frailty throughout later life: results from a 17-year longitudinal study in the Netherlands. Age Ageing 47:727–733

    Article  PubMed  Google Scholar 

  9. 9.

    Wade KF, Marshall A, Vanhoutte B et al (2017) Does pain predict frailty in older men and women? Findings from the English Longitudinal Study of Ageing (ELSA). J Gerontol A 72:403–409

    Google Scholar 

  10. 10.

    Hoogendijk EO, Deeg DJH, de Breij S et al (2019) The Longitudinal Aging Study Amsterdam: cohort update 2019 and additional data collections. Eur J Epidemiol.

    Article  PubMed  PubMed Central  Google Scholar 

  11. 11.

    Hoogendijk EO, Theou O, Rockwood K et al (2017) Development and validation of a frailty index in the Longitudinal Aging Study Amsterdam. Aging Clin Exp Res 29:927–933

    Article  PubMed  Google Scholar 

  12. 12.

    Mezuk B, Lohman MC, Rock AK et al (2016) Trajectories of body mass indices and development of frailty: evidence from the Health and Retirement Study. Obesity 24:1643–1647

    Article  PubMed  Google Scholar 

  13. 13.

    Romero-Ortuno R, Kenny RA (2012) The frailty index in Europeans: association with age and mortality. Age Ageing 41:684–689

    Article  PubMed  PubMed Central  Google Scholar 

  14. 14.

    Stolz E, Mayerl H, Waxenegger A et al (2017) Impact of socioeconomic position on frailty trajectories in 10 European countries: evidence from the Survey of Health, Ageing and Retirement in Europe (2004–2013). J Epidemiol Community Health 71:73–80

    Article  PubMed  Google Scholar 

  15. 15.

    Backman K, Joas E, Falk H et al (2017) Changes in the lethality of frailty over 30 years: evidence from two cohorts of 70-year-olds in Gothenburg Sweden. J Gerontol A 72:945–950

    Google Scholar 

  16. 16.

    Rockwood K, Andrew M, Mitnitski A (2007) A comparison of two approaches to measuring frailty in elderly people. J Gerontol A 62:738–743

    Article  Google Scholar 

  17. 17.

    Searle SD, Mitnitski A, Gahbauer EA et al (2008) A standard procedure for creating a frailty index. BMC Geriatr 8:24

    Article  PubMed  PubMed Central  Google Scholar 

  18. 18.

    Song X, Mitnitski A, Rockwood K (2010) Prevalence and 10-year outcomes of frailty in older adults in relation to deficit accumulation. J Am Geriatr Soc 58:681–687

    Article  PubMed  Google Scholar 

  19. 19.

    Wou F, Gladman JR, Bradshaw L et al (2013) The predictive properties of frailty-rating scales in the acute medical unit. Age Ageing 42:776–781

    Article  PubMed  PubMed Central  Google Scholar 

  20. 20.

    Eeles EM, White SV, O'Mahony SM et al (2012) The impact of frailty and delirium on mortality in older inpatients. Age Ageing 41:412–416

    Article  PubMed  Google Scholar 

  21. 21.

    Jiang M, Foebel AD, Kuja-Halkola R et al (2017) Frailty index as a predictor of all-cause and cause-specific mortality in a Swedish population-based cohort. Aging 9:2629–2646

    Article  PubMed  PubMed Central  Google Scholar 

  22. 22.

    Bartali B, Frongillo EA, Bandinelli S et al (2006) Low nutrient intake is an essential component of frailty in older persons. J Gerontol A Biol Sci Med Sci 61:589–593

    Article  PubMed  PubMed Central  Google Scholar 

  23. 23.

    Cesari M, Leeuwenburgh C, Lauretani F et al (2006) Frailty syndrome and skeletal muscle: results from the Invecchiare in Chianti study. Am J Clin Nutr 83:1142–1148

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. 24.

    Shardell M, D'Adamo C, Alley DE et al (2012) Serum 25-hydroxyvitamin D, transitions between frailty states, and mortality in older adults: the Invecchiare in Chianti Study. J Am Geriatr Soc 60:256–264

    Article  PubMed  PubMed Central  Google Scholar 

  25. 25.

    Talegawkar SA, Bandinelli S, Bandeen-Roche K et al (2012) A higher adherence to a Mediterranean-style diet is inversely associated with the development of frailty in community-dwelling elderly men and women. J Nutr 142:2161–2166

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. 26.

    Rabassa M, Zamora-Ros R, Urpi-Sarda M et al (2015) Association of habitual dietary resveratrol exposure with the development of frailty in older age: the Invecchiare in Chianti study. Am J Clin Nutr 102:1534–1542

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. 27.

    Urpi-Sarda M, Andres-Lacueva C, Rabassa M et al (2015) The relationship between urinary total polyphenols and the frailty phenotype in a community-dwelling older population: the InCHIANTI Study. J Gerontol A Biol Sci Med Sci 70:1141–1147

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. 28.

    Stenholm S, Ferrucci L, Vahtera J et al (2019) Natural course of frailty components in people who develop frailty syndrome: evidence from two cohort studies. J Gerontol A Biol Sci Med Sci 74:667–674

    Article  PubMed  Google Scholar 

  29. 29.

    Fried LP, Tangen CM, Walston J et al (2001) Frailty in older adults: evidence for a phenotype. J Gerontol A Biol Sci Med Sci 56:M146–156

    Article  CAS  PubMed  Google Scholar 

  30. 30.

    Ferrucci L, Bandinelli S, Benvenuti E et al (2000) Subsystems contributing to the decline in ability to walk: bridging the gap between epidemiology and geriatric practice in the InCHIANTI study. J Am Geriatr Soc 48:1618–1625

    Article  CAS  PubMed  Google Scholar 

  31. 31.

    Radloff L (1977) The CES-D scale: a self-report depression scale for research in the general population. Appl Psychol Meas 1:385–401

    Article  Google Scholar 

  32. 32.

    Folstein MF, Folstein SE, McHugh PR (1975) “Mini-mental state”. A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res 12:189–198

    Article  CAS  PubMed  Google Scholar 

  33. 33.

    Theou O, Brothers TD, Mitnitski A et al (2013) Operationalization of frailty using eight commonly used scales and comparison of their ability to predict all-cause mortality. J Am Geriatr Soc 61:1537–1551

    Article  PubMed  Google Scholar 

  34. 34.

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

    Article  PubMed  Google Scholar 

  35. 35.

    Carter JV, Pan J, Rai SN et al (2016) ROC-ing along: evaluation and interpretation of receiver operating characteristic curves. Surgery 159:1638–1645

    Article  PubMed  Google Scholar 

  36. 36.

    Gordon EH, Peel NM, Samanta M et al (2017) Sex differences in frailty: a systematic review and meta-analysis. Exp Gerontol 89:30–40

    Article  CAS  PubMed  Google Scholar 

  37. 37.

    Rockwood K, Mitnitski A (2006) Limits to deficit accumulation in elderly people. Mech Ageing Dev 127:494–496

    Article  PubMed  Google Scholar 

  38. 38.

    Abete P, Basile C, Bulli G et al (2017) The Italian version of the "frailty index" based on deficits in health: a validation study. Aging Clin Exp Res 29:913–926

    Article  PubMed  Google Scholar 

  39. 39.

    Clegg A, Bates C, Young J et al (2016) Development and validation of an electronic frailty index using routine primary care electronic health record data. Age Ageing 45:353–360

    Article  PubMed  PubMed Central  Google Scholar 

  40. 40.

    Drubbel I, de Wit NJ, Bleijenberg N et al (2013) Prediction of adverse health outcomes in older people using a frailty index based on routine primary care data. J Gerontol A 68:301–308

    Article  Google Scholar 

  41. 41.

    Studenski S, Perera S, Patel K et al (2011) Gait speed and survival in older adults. JAMA 305:50–58

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. 42.

    Rockwood K, McMillan M, Mitnitski A et al (2015) A frailty index based on common laboratory tests in comparison with a clinical frailty index for older adults in long-term care facilities. J Am Med Dir Assoc 16:842–847

    Article  PubMed  Google Scholar 

Download references


The content of this research is solely the responsibility of the authors, and does not reflect the views of the InCHIANTI study group. Emiel O. Hoogendijk was supported by an NWO/ZonMw Veni fellowship [Grant Number 91618067]. This study was in part funded by the Intramural Research Program at the National Institute on Aging. The InCHIANTI study baseline (1998–2000) was funded by the Italian Ministry of Health (ICS110.1/RF97.71) and in part by the U.S. National Institute on Aging, Bethesda, Maryland (Contracts 236 MD 916413 and 236 MD 821336). The InCHIANTI follow-up 1 (2001–2003) was funded by the U.S. National Institute on Aging (Contracts: N.1-AG-1–1 and N.1-AG-1–2111); the InCHIANTI follow-up 2 and 3 studies (2004–2010) were financed by the U.S. National Institute on Aging (Contract: N01-AG-5–0002).

Author information



Corresponding author

Correspondence to Emiel O. Hoogendijk.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Statement of human and animal rights

The InCHIANTI study was approved by the ethical committee of the Italian National Institute of Research and Care on Aging.

Informed consent

Signed informed consent was obtained from all study participants.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 126 kb)

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Hoogendijk, E.O., Stenholm, S., Ferrucci, L. et al. Operationalization of a frailty index among older adults in the InCHIANTI study: predictive ability for all-cause and cardiovascular disease mortality. Aging Clin Exp Res 32, 1025–1034 (2020).

Download citation


  • Frail elderly
  • Frailty index
  • Deficit accumulation
  • Risk prediction
  • Geriatrics